ATP5PDP4 ATP synthase peripheral stalk subunit d pseudogene 4 [Homo sapiens (human)] - Gene

Summary

Official Symbol: ATP5PDP4provided by HGNC
Official Full Name: ATP synthase peripheral stalk subunit d pseudogene 4provided by HGNC
Primary source: HGNC:HGNC:49626
See related: AllianceGenome:HGNC:49626
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: ATP5HP4
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Genomic context

Location:: 12q15

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	12	NC_000012.12 (68642445..68643038, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	12	NC_060936.1 (68621983..68622576, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	12	NC_000012.11 (69036225..69036818, complement)

Chromosome 12 - NC_000012.12 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

SHGC-32780 (e-PCR)
- UniSTS:18007

RH17542 (e-PCR)
- UniSTS:85647

Other Names

ATP synthase, H+ transporting, mitochondrial Fo complex subunit D pseudogene 4
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d pseudogene
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 4

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.