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ZNF962P zinc finger protein 962, pseudogene [ Homo sapiens (human) ]

Gene ID: 729501, updated on 10-Oct-2023

Summary

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Official Symbol
ZNF962Pprovided by HGNC
Official Full Name
zinc finger protein 962, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:39250
See related
Ensembl:ENSG00000215604 AllianceGenome:HGNC:39250
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 ZNF962P in Genome Data Viewer
Location:
13q11
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (18466319..18487412, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (17682946..17704030, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (19040459..19061552, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene putative ankyrin repeat domain-containing protein 30B-like Neighboring gene U6 spliceosomal RNA Neighboring gene vomeronasal 1 receptor 58 pseudogene Neighboring gene OCT4 hESC enhancer GRCh37_chr13:19101768-19102269 Neighboring gene long intergenic non-protein coding RNA 349 Neighboring gene LONRF2 pseudogene 2

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. The DNA sequence and analysis of human chromosome 13. Dunham A, et al. Nature, 2004 Apr 1. PMID 15057823, Free PMC Article

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

  • Putative zinc finger protein ENSP00000344568

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_023215.1 

    Range
    101..21194
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    18466319..18487412 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    17682946..17704030 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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