ATP6V0CP1 ATPase H+ transporting V0 subunit c pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: ATP6V0CP1provided by HGNC
Official Full Name: ATPase H+ transporting V0 subunit c pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:31323
See related: AllianceGenome:HGNC:31323
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: ATCD1
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Genomic context

Location:: 17p13.2

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	17	NC_000017.11 (4856967..4857399, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	17	NC_060941.1 (4747157..4747589, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	17	NC_000017.10 (4760262..4760694, complement)

Chromosome 17 - NC_000017.11 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?

High glucose disrupts autophagy lysosomal pathway in gingival epithelial cells via ATP6V0C.
Title: High glucose disrupts autophagy lysosomal pathway in gingival epithelial cells via ATP6V0C.

Submit: New GeneRIF Correction

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

ATP synthase subunit C domain containing 1 pseudogene
ATPase H+ transporting subunit c pseudogene 1
ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c (ATP6VOC) pseudogene
ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c 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.