HERC2P7 HERC2 pseudogene 7 [Homo sapiens (human)] - Gene

Summary

Official Symbol: HERC2P7provided by HGNC
Official Full Name: HERC2 pseudogene 7provided by HGNC
Primary source: HGNC:HGNC:4875
See related: AllianceGenome:HGNC:4875
Gene type: pseudo
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Annotation information: Note: On NCBI's Build 37.1, HGNC and NCBI annotated this gene, HERC2P7 (HGNC id: 4875), at chromosome 15:28573729..28580221(+). As of August 2010 it was determined by NCBI and HGNC that HERC2P7 should be located at chromosome 15:23377989..23403847(+) where LOC100132101 is annotated in Build 37.1. [13 Feb 2013]
Expression: Ubiquitous expression in testis (RPKM 2.5), skin (RPKM 2.5) and 24 other tissues See more
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Genomic context

Location:: 15q11.2

Exon count:: 3

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	15	NC_000015.10 (22479153..22482374, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	15	NC_060939.1 (20151268..20154489, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	15	NC_000015.9 (23390722..23393943)

Chromosome 15 - NC_000015.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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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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Markers

D11S2921 (e-PCR)
- UniSTS:152074

D8S2279 (e-PCR)
- UniSTS:473907

L18426 (e-PCR)
- UniSTS:34648

D1S1423 (e-PCR)
- UniSTS:149619

G44298 (e-PCR)
- UniSTS:95092

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.