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CDV3P1 CDV3 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100129736, updated on 10-Oct-2023

Summary

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Official Symbol
CDV3P1provided by HGNC
Official Full Name
CDV3 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:42387
See related
AllianceGenome:HGNC:42387
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:
3q11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (96776774..96777887)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (99480601..99481714)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (96495618..96496731)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene ribosomal protein L18a pseudogene 8 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:96513110-96513654 Neighboring gene uncharacterized LOC124909397 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14550 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14551 Neighboring gene regulator of chromosome condensation 2 pseudogene 5 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr3:96606342-96607541 Neighboring gene EPH receptor A6 Neighboring gene uncharacterized LOC107986103

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)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • CDV3 homolog 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_022257.2 

    Range
    26..1139
    Download
    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
    96776774..96777887
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    99480601..99481714
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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