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C2orf69P2 chromosome 2 open reading frame 69 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 642614, updated on 17-Sep-2024

Summary

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Official Symbol
C2orf69P2provided by HGNC
Official Full Name
chromosome 2 open reading frame 69 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:51801
See related
AllianceGenome:HGNC:51801
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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See C2orf69P2 in Genome Data Viewer
Location:
16p11.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (35492323..35494220)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (38634710..38636607, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (34726694..34728591)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene retinoic acid receptor responder 2 pseudogene 10 Neighboring gene angiogenic factor with G-patch and FHA domains 1 pseudogene 6 Neighboring gene uncharacterized LOC105371204 Neighboring gene TP53 target 3 family member H, pseudogene Neighboring gene retinoic acid receptor responder 2 pseudogene 8

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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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_008611.2 

    Range
    101..1998
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    35492323..35494220
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    38634710..38636607 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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