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CRB3P1 crumbs cell polarity complex component 3 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 106480279, updated on 10-Oct-2023

Summary

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Official Symbol
CRB3P1provided by HGNC
Official Full Name
crumbs cell polarity complex component 3 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:49684
See related
Ensembl:ENSG00000232563 AllianceGenome:HGNC:49684
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Location:
3p26.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (1394173..1394448, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (1388505..1388780, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (1435857..1436132, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene contactin 6 Neighboring gene uncharacterized LOC105376924 Neighboring gene uncharacterized LOC105376923 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:1277185-1278384 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:1642422-1642922 Neighboring gene ribosomal protein L23a pseudogene 38 Neighboring gene meiotic recombination hotspot S Neighboring gene ribosomal protein L23a pseudogene 39

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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Other Names

  • crumbs family member 3 pseudogene 1

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.

Genomic

  1. NG_044100.1 

    Range
    101..376
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    1394173..1394448 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    1388505..1388780 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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