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TFIP11 tuftelin interacting protein 11 [ Homo sapiens (human) ]

Gene ID: 24144, updated on 7-Apr-2024

Summary

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Official Symbol
TFIP11provided by HGNC
Official Full Name
tuftelin interacting protein 11provided by HGNC
Primary source
HGNC:HGNC:17165
See related
Ensembl:ENSG00000100109 MIM:612747; AllianceGenome:HGNC:17165
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
NTR1; STIP; TIP39; STIP-1; Spp382; bK445C9.6
Summary
This gene encodes a protein component of the spliceosome that promotes the release of the lariat-intron during late-stage splicing through the recruitment of a pre-mRNA splicing factor called DEAH-box helicase 15. The encoded protein contains a G-patch domain, a hallmark of RNA-processing proteins, that binds DEAH-box helicase 15. This protein contains an atypical nuclear localization sequence as well as a nuclear speckle-targeting sequence, enabling it to localize to distinct speckled regions within the cell nucleus. Polymorphisms in this gene are associated with dental caries suggesting a role in amelogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Expression
Ubiquitous expression in testis (RPKM 20.2), bone marrow (RPKM 19.7) and 25 other tissues See more
Orthologs
mouse all
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Genomic context

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Location:
22q12.1
Exon count:
16
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (26491240..26512473, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (26953642..26974877, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (26887206..26908439, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13567 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13568 Neighboring gene Sharpr-MPRA regulatory region 14748 Neighboring gene RPS3A pseudogene 55 Neighboring gene ReSE screen-validated silencer GRCh37_chr22:26836513-26836669 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr22:26837982-26839181 Neighboring gene aspartate beta-hydroxylase domain containing 2 Neighboring gene HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:26866926-26868125 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13569 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 18791 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr22:26889254-26890453 Neighboring gene SRR1 domain containing Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13570 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr22:26902046-26903245 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 18792 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:26908724-26909261 Neighboring gene TFIP11 divergent transcript Neighboring gene tyrosylprotein sulfotransferase 2 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:26937311-26937812 Neighboring gene Sharpr-MPRA regulatory region 3066 Neighboring gene microRNA 548j

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. DHX15-independent roles for TFIP11 in U6 snRNA modification, U4/U6.U5 tri-snRNP assembly and pre-mRNA splicing fidelity. Duchemin A, et al. Nat Commun, 2021 Nov 17. PMID 34789764, Free PMC Article
  2. STIP Regulates ERK1/2 Signaling Pathway Involved in Interaction with PP1γ in Lymphoblastic Leukemia. Sun S, et al. Curr Mol Med, 2016. PMID 27758712
  3. STIP overexpression confers oncogenic potential to human non-small cell lung cancer cells by regulating cell cycle and apoptosis. Tang Y, et al. J Cell Mol Med, 2015 Dec. PMID 26354852, Free PMC Article
  4. TFIP11, CCNL1 and EWSR1 Protein-protein Interactions, and Their Nuclear Localization. Tannukit S, et al. Int J Mol Sci, 2008 Aug. PMID 19122807, Free PMC Article
  5. Spliceosomal small nuclear ribonucleoprotein particles repeatedly cycle through Cajal bodies. Stanek D, et al. Mol Biol Cell, 2008 Jun. PMID 18367544, Free PMC Article

See all (111) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. TFIP11 promotes replication fork reversal to preserve genome stability.
    Title: TFIP11 promotes replication fork reversal to preserve genome stability.
  2. DHX15-independent roles for TFIP11 in U6 snRNA modification, U4/U6.U5 tri-snRNP assembly and pre-mRNA splicing fidelity.
    Title: DHX15-independent roles for TFIP11 in U6 snRNA modification, U4/U6.U5 tri-snRNP assembly and pre-mRNA splicing fidelity.
  3. the high expression and activation effect on the ERK1/2 signaling of STIP in lymphoblastic leukemia suggest that STIP would be a potential therapy target or diagnosis marker for leukemia.
    Title: STIP Regulates ERK1/2 Signaling Pathway Involved in Interaction with PP1γ in Lymphoblastic Leukemia.
  4. We now report the identification of a novel molecular function of STIP that links USP7 to the p53-Mdm2 pathway
    Title: STIP is a critical nuclear scaffolding protein linking USP7 to p53-Mdm2 pathway regulation.
  5. Results suggest that Sip1/tuftelin-interacting protein (STIP, also referred to as TFIP11) may be a novel potential diagnostic and therapeutic target for non-small cell lung cancer (NSCLC).
    Title: STIP overexpression confers oncogenic potential to human non-small cell lung cancer cells by regulating cell cycle and apoptosis.
  6. the statistically significant association of rs2337359 upstream of TUFT1 with dental caries experience via meta-analysis across adult samples (p < 0.002) and the suggestive association for multiple variants in TFIP11 across child samples
    Title: Effects of enamel matrix genes on dental caries are moderated by fluoride exposures.
  7. Associations between TFIP11 (p=0.02), ENAM (p=0.00001), and AMELX (p=0.01) could be seen with caries independent of having MIH or genomic DNA copies of Streptococcus mutans detected by real time PCR in the Brazilian sample.
    Title: Genes expressed in dental enamel development are associated with molar-incisor hypomineralization.
  8. These data help define the mechanism of nuclear/nuclear speckle localization of the splicing factor TFIP11, with implications for it's function.
    Title: Identification of a novel nuclear localization signal and speckle-targeting sequence of tuftelin-interacting protein 11, a splicing factor involved in spliceosome disassembly.
  9. Observational study of gene-disease association. (HuGE Navigator)
    Title: Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients.
  10. Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)
    Title: Enamel formation genes are associated with high caries experience in Turkish children.
Submit: New GeneRIF Correction See all GeneRIFs (11)

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

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

  • FLJ22086

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables nucleic acid binding IEA
Inferred from Electronic Annotation
more info
  
enables protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
Process Evidence Code Pubs
involved_in RNA processing IC
Inferred by Curator
more info
 PubMed 
involved_in biomineral tissue development IEA
Inferred from Electronic Annotation
more info
  
involved_in mRNA splicing, via spliceosome IC
Inferred by Curator
more info
 PubMed 
involved_in negative regulation of DNA ligase activity IC
Inferred by Curator
more info
 PubMed 
involved_in negative regulation of double-strand break repair via nonhomologous end joining ISS
Inferred from Sequence or Structural Similarity
more info
 PubMed 
involved_in negative regulation of protein binding IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in negative regulation of protein-containing complex assembly IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in protection from non-homologous end joining at telomere IC
Inferred by Curator
more info
 PubMed 
involved_in spliceosomal complex disassembly IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in spliceosomal complex disassembly IMP
Inferred from Mutant Phenotype
more info
 PubMed 
Component Evidence Code Pubs
part_of U2-type post-mRNA release spliceosomal complex IBA
Inferred from Biological aspect of Ancestor
more info
  
part_of U2-type post-mRNA release spliceosomal complex IDA
Inferred from Direct Assay
more info
 PubMed 
part_of catalytic step 2 spliceosome IDA
Inferred from Direct Assay
more info
 PubMed 
located_in chromosome, telomeric region IDA
Inferred from Direct Assay
more info
 PubMed 
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
  
located_in extracellular matrix IEA
Inferred from Electronic Annotation
more info
  
located_in nuclear speck IDA
Inferred from Direct Assay
more info
  
located_in nucleolus IDA
Inferred from Direct Assay
more info
 PubMed 
located_in nucleoplasm TAS
Traceable Author Statement
more info
  
part_of spliceosomal complex IDA
Inferred from Direct Assay
more info
 PubMed 

General protein information

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Preferred Names
tuftelin-interacting protein 11
Names
septin and tuftelin-interacting protein 1
sip1/tuftelin interacting protein

NCBI Reference Sequences (RefSeq)

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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.

mRNA and Protein(s)

  1. NM_001008697.3 → NP_001008697.1  tuftelin-interacting protein 11 isoform 1

    See identical proteins and their annotated locations for NP_001008697.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes isoform 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, AL050258, CT841511, Z95115
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000384297.1, ENST00000405938.5
    Conserved Domains (3) summary
    pfam01585
    Location:149 → 191
    G-patch; G-patch domain
    pfam07842
    Location:397 → 666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23 → 104
    TIP_N; Tuftelin interacting protein N terminal

  2. NM_001346857.2 → NP_001333786.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) uses an alternate splice site in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Conserved Domains (3) summary
    pfam01585
    Location:149 → 191
    G-patch; G-patch domain
    pfam07842
    Location:397 → 666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23 → 104
    TIP_N; Tuftelin interacting protein N terminal

  3. NM_001346858.2 → NP_001333787.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) uses an alternate splice site in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Conserved Domains (3) summary
    pfam01585
    Location:149 → 191
    G-patch; G-patch domain
    pfam07842
    Location:397 → 666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23 → 104
    TIP_N; Tuftelin interacting protein N terminal

  4. NM_001346859.2 → NP_001333788.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (5) differs in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, DC411331, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000385861.1, ENST00000407148.5
    Conserved Domains (3) summary
    pfam01585
    Location:149 → 191
    G-patch; G-patch domain
    pfam07842
    Location:397 → 666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23 → 104
    TIP_N; Tuftelin interacting protein N terminal

  5. NM_001346861.2 → NP_001333790.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (6) differs in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000480171.1, ENST00000619735.4
    Conserved Domains (3) summary
    pfam01585
    Location:149 → 191
    G-patch; G-patch domain
    pfam07842
    Location:397 → 666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23 → 104
    TIP_N; Tuftelin interacting protein N terminal

  6. NM_001346862.2 → NP_001333791.1  tuftelin-interacting protein 11 isoform 2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (7) differs in the 5' UTR, lacks an in-frame portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (2) is shorter and has a distinct N-terminus, compared to isoform 1.
    Source sequence(s)
    AI468631, Z95115, Z99714
    UniProtKB/TrEMBL
    Q8N523

  7. NM_012143.4 → NP_036275.1  tuftelin-interacting protein 11 isoform 1

    See identical proteins and their annotated locations for NP_036275.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an exon in the 5' UTR, compared to variant1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, AL050258, DC411331
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000384421.1, ENST00000407690.6
    Conserved Domains (3) summary
    pfam01585
    Location:149 → 191
    G-patch; G-patch domain
    pfam07842
    Location:397 → 666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23 → 104
    TIP_N; Tuftelin interacting protein N terminal

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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    26491240..26512473 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    26953642..26974877 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q9UBB9.1 GenPept UniProtKB/Swiss-Prot:Q9UBB9

Gene LinkOut

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