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PTCH1 patched 1 [ Homo sapiens (human) ]

Gene ID: 5727, updated on 5-Mar-2024

Summary

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Official Symbol
PTCH1provided by HGNC
Official Full Name
patched 1provided by HGNC
Primary source
HGNC:HGNC:9585
See related
Ensembl:ENSG00000185920 MIM:601309; AllianceGenome:HGNC:9585
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
PTC; BCNS; PTC1; PTCH; BCNS1; NBCCS
Summary
This gene encodes a member of the patched family of proteins and a component of the hedgehog signaling pathway. Hedgehog signaling is important in embryonic development and tumorigenesis. The encoded protein is the receptor for the secreted hedgehog ligands, which include sonic hedgehog, indian hedgehog and desert hedgehog. Following binding by one of the hedgehog ligands, the encoded protein is trafficked away from the primary cilium, relieving inhibition of the G-protein-coupled receptor smoothened, which results in activation of downstream signaling. Mutations of this gene have been associated with basal cell nevus syndrome and holoprosencephaly. [provided by RefSeq, Aug 2017]
Expression
Broad expression in endometrium (RPKM 11.5), testis (RPKM 8.7) and 24 other tissues See more
Orthologs
mouse all
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Genomic context

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See PTCH1 in Genome Data Viewer
Location:
9q22.32
Exon count:
28
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (95442980..95516971, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (107612621..107686610, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (98205262..98279253, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376155 Neighboring gene Sharpr-MPRA regulatory region 1060 Neighboring gene uncharacterized LOC105376156 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110630 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:98173297-98173917 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:98173918-98174537 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20065 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98196113-98196685 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98196686-98197257 Neighboring gene metallothionein 1 pseudogene 1 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98209829-98210813 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98224469-98225332 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:98225569-98226070 Neighboring gene uncharacterized LOC100507346 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98255961-98256702 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:98256703-98257442 Neighboring gene VISTA enhancer hs1258 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20067 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20069 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20068 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:98269229-98269862 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20071 Neighboring gene NANOG hESC enhancer GRCh37_chr9:98271448-98271997 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:98272951-98273714 Neighboring gene VISTA enhancer hs1417 Neighboring gene uncharacterized LOC105376157 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110687 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:98314166-98315130 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:98315131-98316095 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:98326699-98327200 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:98327201-98327700 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_110694 Neighboring gene uncharacterized LOC105376158 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:98362911-98363412 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:98363413-98363912

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. Mutations of PTCH1 gene in two pedigrees with bifid rib-basal cell nevus-jaw cyst syndrome. Peng X, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban, 2023 Apr 25. PMID 37283107, Free PMC Article
  2. Rs28446116 in PTCH1 is associated with non-syndromic cleft lip with or without palate in the Ningxia population, China. Ruan W, et al. Arch Oral Biol, 2023 May. PMID 36870116
  3. New insight into the role of PTCH1 protein in serous ovarian carcinomas. Karin-Kujundzic V, et al. Int J Oncol, 2022 Dec. PMID 36205138, Free PMC Article
  4. Orthokeratinized odontogenic cysts: A clinicopathologic study of 159 cases and molecular evidence for the absence of PTCH1 mutations. Wang YJ, et al. J Oral Pathol Med, 2022 Aug. PMID 35569117
  5. Impaired Wnt/beta-catenin and protein patched homolog 1 signaling in extraocular sebaceous carcinoma: A clinical and histopathological study. Cheng AY, et al. J Dermatol, 2022 Jun. PMID 35318716

See all (316) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. PTCH1-mutant human cerebellar organoids exhibit altered neural development and recapitulate early medulloblastoma tumorigenesis.
    Title: PTCH1-mutant human cerebellar organoids exhibit altered neural development and recapitulate early medulloblastoma tumorigenesis.
  2. PTCH1 gene variants rs357564, rs2236405, rs2297086 and rs41313327, mRNA and tissue expression in basal cell carcinoma patients from Western Mexico.
    Title: PTCH1 gene variants rs357564, rs2236405, rs2297086 and rs41313327, mRNA and tissue expression in basal cell carcinoma patients from Western Mexico.
  3. Mutations of PTCH1 gene in two pedigrees with bifid rib-basal cell nevus-jaw cyst syndrome.
    Title: Mutations of PTCH1 gene in two pedigrees with bifid rib-basal cell nevus-jaw cyst syndrome.
  4. Rs28446116 in PTCH1 is associated with non-syndromic cleft lip with or without palate in the Ningxia population, China.
    Title: Rs28446116 in PTCH1 is associated with non-syndromic cleft lip with or without palate in the Ningxia population, China.
  5. New insight into the role of PTCH1 protein in serous ovarian carcinomas.
    Title: New insight into the role of PTCH1 protein in serous ovarian carcinomas.
  6. Orthokeratinized odontogenic cysts: A clinicopathologic study of 159 cases and molecular evidence for the absence of PTCH1 mutations.
    Title: Orthokeratinized odontogenic cysts: A clinicopathologic study of 159 cases and molecular evidence for the absence of PTCH1 mutations.
  7. Impaired Wnt/beta-catenin and protein patched homolog 1 signaling in extraocular sebaceous carcinoma: A clinical and histopathological study.
    Title: Impaired Wnt/beta-catenin and protein patched homolog 1 signaling in extraocular sebaceous carcinoma: A clinical and histopathological study.
  8. Novel PTCH1 and concurrent TP53 mutations in four patients with numerous non-syndromic basal cell carcinomas: The paradigm of oncogenic synergy.
    Title: Novel PTCH1 and concurrent TP53 mutations in four patients with numerous non-syndromic basal cell carcinomas: The paradigm of oncogenic synergy.
  9. Differential promoter usages of PTCH1 and down regulation of HHIP are associated with HNSCC progression.
    Title: Differential promoter usages of PTCH1 and down regulation of HHIP are associated with HNSCC progression.
  10. Inherited rare and common variants in PTCH1 and PTCH2 contributing to the predisposition to reproductive cancers.
    Title: Inherited rare and common variants in PTCH1 and PTCH2 contributing to the predisposition to reproductive cancers.
Submit: New GeneRIF Correction See all GeneRIFs (241)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description Tests
Basal cell carcinoma, susceptibility to, 1
MedGen: C2751544 OMIM: 605462 GeneReviews: Not available
Compare labs
Basal cell nevus syndrome 1
MedGen: CN376810 OMIM: 109400 GeneReviews: Nevoid Basal Cell Carcinoma Syndrome
not available
Holoprosencephaly 7
MedGen: C1835820 OMIM: 610828 GeneReviews: Holoprosencephaly Overview
Compare labs

Copy number response

Description
Copy number response
Triplosensitivity

No evidence available (Last evaluated 2020-07-01)

ClinGen Genome Curation PagePubMed
Haploinsufficency

Sufficient evidence for dosage pathogenicity (Last evaluated 2020-07-01)

ClinGen Genome Curation PagePubMed

EBI GWAS Catalog

Description
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
EBI GWAS Catalog
Chemerin, a novel adipokine in the regulation of angiogenesis.
EBI GWAS Catalog
Genome-wide association analysis identifies 20 loci that influence adult height.
EBI GWAS Catalog
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
EBI GWAS Catalog
Hundreds of variants clustered in genomic loci and biological pathways affect human height.
EBI GWAS Catalog
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
EBI GWAS Catalog
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • FLJ26746, FLJ42602

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables cholesterol binding IDA
Inferred from Direct Assay
more info
 PubMed 
enables cyclin binding IPI
Inferred from Physical Interaction
more info
 PubMed 
enables hedgehog family protein binding IBA
Inferred from Biological aspect of Ancestor
more info
  
enables hedgehog family protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
enables hedgehog receptor activity IBA
Inferred from Biological aspect of Ancestor
more info
  
enables heparin binding IEA
Inferred from Electronic Annotation
more info
  
enables patched binding IEA
Inferred from Electronic Annotation
more info
  
enables protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
enables protein-containing complex binding IEA
Inferred from Electronic Annotation
more info
  
enables smoothened binding IBA
Inferred from Biological aspect of Ancestor
more info
  
enables smoothened binding IPI
Inferred from Physical Interaction
more info
 PubMed 
Process Evidence Code Pubs
involved_in animal organ morphogenesis ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in brain development ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in branching involved in ureteric bud morphogenesis IEA
Inferred from Electronic Annotation
more info
  
involved_in cell differentiation involved in kidney development IEA
Inferred from Electronic Annotation
more info
  
involved_in cell fate determination IEA
Inferred from Electronic Annotation
more info
  
involved_in cell proliferation involved in metanephros development IEA
Inferred from Electronic Annotation
more info
  
involved_in cellular response to cholesterol IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in cellular response to cholesterol ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in commissural neuron axon guidance IEA
Inferred from Electronic Annotation
more info
  
involved_in dorsal/ventral neural tube patterning IEA
Inferred from Electronic Annotation
more info
  
involved_in dorsal/ventral pattern formation ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in embryonic limb morphogenesis ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in embryonic organ development IEA
Inferred from Electronic Annotation
more info
  
involved_in epidermal cell fate specification IEA
Inferred from Electronic Annotation
more info
  
involved_in glucose homeostasis IEA
Inferred from Electronic Annotation
more info
  
involved_in heart morphogenesis IEA
Inferred from Electronic Annotation
more info
  
involved_in hindlimb morphogenesis IEA
Inferred from Electronic Annotation
more info
  
involved_in in utero embryonic development IEA
Inferred from Electronic Annotation
more info
  
involved_in keratinocyte proliferation IEA
Inferred from Electronic Annotation
more info
  
involved_in limb morphogenesis IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in liver regeneration IEA
Inferred from Electronic Annotation
more info
  
involved_in mammary gland duct morphogenesis IEA
Inferred from Electronic Annotation
more info
  
involved_in mammary gland epithelial cell differentiation IEA
Inferred from Electronic Annotation
more info
  
involved_in metanephric collecting duct development IEP
Inferred from Expression Pattern
more info
 PubMed 
involved_in negative regulation of DNA-binding transcription factor activity IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in negative regulation of cell division IEA
Inferred from Electronic Annotation
more info
  
involved_in negative regulation of keratinocyte proliferation IEA
Inferred from Electronic Annotation
more info
  
involved_in negative regulation of multicellular organism growth ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in negative regulation of osteoblast differentiation IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in negative regulation of smoothened signaling pathway IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in negative regulation of smoothened signaling pathway ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in negative regulation of smoothened signaling pathway TAS
Traceable Author Statement
more info
 PubMed 
involved_in negative regulation of stem cell proliferation IEA
Inferred from Electronic Annotation
more info
  
involved_in negative regulation of transcription by RNA polymerase II IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in neural plate axis specification ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in neural tube closure IEA
Inferred from Electronic Annotation
more info
  
involved_in neural tube patterning IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in pharyngeal system development IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in positive regulation of DNA-templated transcription IEA
Inferred from Electronic Annotation
more info
  
involved_in positive regulation of cholesterol efflux IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in positive regulation of epidermal cell differentiation IEA
Inferred from Electronic Annotation
more info
  
involved_in prostate gland development IEA
Inferred from Electronic Annotation
more info
  
involved_in protein localization to plasma membrane IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in protein processing ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in regulation of mitotic cell cycle IEA
Inferred from Electronic Annotation
more info
  
involved_in regulation of protein localization IEA
Inferred from Electronic Annotation
more info
  
involved_in regulation of smoothened signaling pathway ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in response to chlorate IEA
Inferred from Electronic Annotation
more info
  
involved_in response to estradiol IEA
Inferred from Electronic Annotation
more info
  
involved_in response to mechanical stimulus IEA
Inferred from Electronic Annotation
more info
  
involved_in response to retinoic acid IEA
Inferred from Electronic Annotation
more info
  
involved_in response to xenobiotic stimulus IEA
Inferred from Electronic Annotation
more info
  
involved_in smooth muscle tissue development IEP
Inferred from Expression Pattern
more info
 PubMed 
involved_in smoothened signaling pathway ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in somite development IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in spermatid development IEA
Inferred from Electronic Annotation
more info
  
involved_in spinal cord motor neuron differentiation IEA
Inferred from Electronic Annotation
more info
  
involved_in stem cell proliferation IEA
Inferred from Electronic Annotation
more info
  
Component Evidence Code Pubs
colocalizes_with Golgi apparatus IDA
Inferred from Direct Assay
more info
 PubMed 
located_in apical part of cell IDA
Inferred from Direct Assay
more info
 PubMed 
located_in axonal growth cone IEA
Inferred from Electronic Annotation
more info
  
located_in caveola IDA
Inferred from Direct Assay
more info
 PubMed 
located_in ciliary membrane TAS
Traceable Author Statement
more info
  
located_in dendritic growth cone IEA
Inferred from Electronic Annotation
more info
  
located_in endocytic vesicle membrane TAS
Traceable Author Statement
more info
  
located_in intracellular membrane-bounded organelle IDA
Inferred from Direct Assay
more info
 PubMed 
located_in midbody IEA
Inferred from Electronic Annotation
more info
  
located_in perinuclear region of cytoplasm IDA
Inferred from Direct Assay
more info
 PubMed 
is_active_in plasma membrane IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in plasma membrane IDA
Inferred from Direct Assay
more info
 PubMed 

General protein information

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Preferred Names
protein patched homolog 1

NCBI Reference Sequences (RefSeq)

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NEW Try the new Transcript table

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_007664.1 RefSeqGene

    Range
    5001..78984
    Download
    GenBank, FASTA, Sequence Viewer (Graphics), LRG_515

mRNA and Protein(s)

  1. NM_000264.5 → NP_000255.2  protein patched homolog 1 isoform L

    See identical proteins and their annotated locations for NP_000255.2

    Status: REVIEWED

    Source sequence(s)
    AL161729
    Consensus CDS
    CCDS6714.1
    UniProtKB/Swiss-Prot
    A3KBI9, E9PEJ8, Q13463, Q13635, Q5R1U7, Q5R1U9, Q5R1V0, Q5VZC0, Q5VZC2, Q86XG7
    Related
    ENSP00000332353.6, ENST00000331920.11
    Conserved Domains (2) summary
    PHA03377
    Location:1253 → 1369
    PHA03377; EBNA-3C; Provisional
    TIGR00918
    Location:43 → 1206
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family

  2. NM_001083602.3 → NP_001077071.1  protein patched homolog 1 isoform M

    Status: REVIEWED

    Source sequence(s)
    AB189436, AB209495, AI417736, BC043542, BX117041, CR744004, U59464
    Consensus CDS
    CCDS47996.1
    UniProtKB/Swiss-Prot
    Q13635
    Related
    ENSP00000518556.1, ENST00000711046.1
    Conserved Domains (3) summary
    TIGR00918
    Location:2 → 1140
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family
    pfam07698
    Location:949 → 1095
    7TM-7TMR_HD; 7TM receptor with intracellular HD hydrolase
    pfam12349
    Location:396 → 550
    Sterol-sensing; Sterol-sensing domain of SREBP cleavage-activation

  3. NM_001083603.3 → NP_001077072.1  protein patched homolog 1 isoform L'

    Status: REVIEWED

    Source sequence(s)
    AB189437, AB209495, AI417736, AL161729, BX117041, CR744004, U59464
    Consensus CDS
    CCDS47995.1
    UniProtKB/Swiss-Prot
    Q13635
    Related
    ENSP00000389744.2, ENST00000437951.6
    Conserved Domains (3) summary
    TIGR00918
    Location:65 → 1205
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family
    pfam07698
    Location:1014 → 1160
    7TM-7TMR_HD; 7TM receptor with intracellular HD hydrolase
    pfam12349
    Location:461 → 615
    Sterol-sensing; Sterol-sensing domain of SREBP cleavage-activation

  4. NM_001083604.3 → NP_001077073.1  protein patched homolog 1 isoform S

    See identical proteins and their annotated locations for NP_001077073.1

    Status: REVIEWED

    Source sequence(s)
    AB189438, AB209495, AI417736, BX117041, CR744004, U59464
    Consensus CDS
    CCDS43851.1
    UniProtKB/Swiss-Prot
    Q13635
    Conserved Domains (3) summary
    TIGR00918
    Location:1 → 1055
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family
    pfam07698
    Location:864 → 1010
    7TM-7TMR_HD; 7TM receptor with intracellular HD hydrolase
    pfam12349
    Location:311 → 465
    Sterol-sensing; Sterol-sensing domain of SREBP cleavage-activation

  5. NM_001083605.3 → NP_001077074.1  protein patched homolog 1 isoform S

    See identical proteins and their annotated locations for NP_001077074.1

    Status: REVIEWED

    Source sequence(s)
    AB189439, AB209495, AI417736, BX117041, CR744004, U59464
    Consensus CDS
    CCDS43851.1
    UniProtKB/Swiss-Prot
    Q13635
    Related
    ENSP00000510238.1, ENST00000692981.1
    Conserved Domains (3) summary
    TIGR00918
    Location:1 → 1055
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family
    pfam07698
    Location:864 → 1010
    7TM-7TMR_HD; 7TM receptor with intracellular HD hydrolase
    pfam12349
    Location:311 → 465
    Sterol-sensing; Sterol-sensing domain of SREBP cleavage-activation

  6. NM_001083606.3 → NP_001077075.1  protein patched homolog 1 isoform S

    See identical proteins and their annotated locations for NP_001077075.1

    Status: REVIEWED

    Source sequence(s)
    AB209495, AI358880, AI417736, AL161729, BX117041, CR744004, U43148
    Consensus CDS
    CCDS43851.1
    UniProtKB/Swiss-Prot
    Q13635
    Related
    ENSP00000414823.2, ENST00000429896.6
    Conserved Domains (3) summary
    TIGR00918
    Location:1 → 1055
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family
    pfam07698
    Location:864 → 1010
    7TM-7TMR_HD; 7TM receptor with intracellular HD hydrolase
    pfam12349
    Location:311 → 465
    Sterol-sensing; Sterol-sensing domain of SREBP cleavage-activation

  7. NM_001083607.3 → NP_001077076.1  protein patched homolog 1 isoform S

    See identical proteins and their annotated locations for NP_001077076.1

    Status: REVIEWED

    Source sequence(s)
    AB189440, AB209495, AI417736, BF195352, BX117041, CR744004, U59464
    Consensus CDS
    CCDS43851.1
    UniProtKB/Swiss-Prot
    Q13635
    Conserved Domains (3) summary
    TIGR00918
    Location:1 → 1055
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family
    pfam07698
    Location:864 → 1010
    7TM-7TMR_HD; 7TM receptor with intracellular HD hydrolase
    pfam12349
    Location:311 → 465
    Sterol-sensing; Sterol-sensing domain of SREBP cleavage-activation

  8. NM_001354918.2 → NP_001341847.1  protein patched homolog 1 isoform 8

    Status: REVIEWED

    Source sequence(s)
    AL161729
    UniProtKB/TrEMBL
    A0A1W5YLI7
    Conserved Domains (2) summary
    TIGR00918
    Location:43 → 1154
    2A060602; The Eukaryotic (Putative) Sterol Transporter (EST) Family
    cl27975
    Location:1201 → 1317
    EBV-NA3; Epstein-Barr virus nuclear antigen 3 (EBNA-3)

  9. NM_001354919.2 → NP_001341848.1  protein patched homolog 1 isoform 9

    Status: REVIEWED

    Source sequence(s)
    AL161729, BC043542
    Consensus CDS
    CCDS87661.1
    UniProtKB/TrEMBL
    A0A0C4DGJ5
    Related
    ENSP00000449745.1, ENST00000468211.6
    Conserved Domains (1) summary
    cl25655
    Location:2 → 183
    Patched; Patched family

RNA

  1. NR_149061.2 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL161729

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    95442980..95516971 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    107612621..107686610 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q13635.2 GenPept UniProtKB/Swiss-Prot:Q13635

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Chemical Information
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