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ZNF815P zinc finger protein 815, pseudogene [ Homo sapiens (human) ]

Gene ID: 401303, updated on 13-May-2022

Summary

Official Symbol
ZNF815Pprovided by HGNC
Official Full Name
zinc finger protein 815, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:22029
See related
AllianceGenome:HGNC:22029
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ZNF815
Expression
Ubiquitous expression in brain (RPKM 2.1), appendix (RPKM 1.2) and 24 other tissues See more
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Genomic context

See ZNF815P in Genome Data Viewer
Location:
7p22.1
Exon count:
7
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (5823160..5854435)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (5940921..5972186)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (5862791..5894066)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene ring finger protein 216 Neighboring gene RNF216 intronic transcript 1 Neighboring gene microRNA 6874 Neighboring gene Sharpr-MPRA regulatory region 1711 Neighboring gene RNA, 7SL, cytoplasmic 556, pseudogene Neighboring gene oncomodulin

Genomic regions, transcripts, and products

Expression

  • 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

Phenotypes

EBI GWAS Catalog

Description
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
EBI GWAS Catalog

General gene information

Markers

Other Names

  • Putative protein ZNF815
  • zinc finger protein pseudogene

Clone Names

  • FLJ38969

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.

RNA

  1. NR_023382.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC004983, AK096288, AK291169

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    5823160..5854435
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    5940921..5972186
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)