ATP7A

protein-coding gene in the species Homo sapiens

Class type of: protein-coding gene Q14884608

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Summary

ATP7A is a gene^[1]. ATP7A is a type of protein-coding gene^[2].

Key Facts

HomoloGene ID: 35^[3]
Genomic start: 77166194^[4], 77910690^[5]
Genomic end: 78050395^[6], 77305892^[7]
Ortholog: Atp7a^[8], CCC2^[9], cua-1^[10], ATP7^[11]
Encodes: ATPase copper transporting alpha^[12]
Found in taxon: Homo sapiens^[13]

⭐ Popularity Graph

15/100 established

🌐 Wiki Languages

5 / 428 langs

📈 Wikipedia Views · last 12 months

622 views trend: hourly, last 36h

Quick Facts

Instance of gene

Subclass of protein-coding gene

Properties

Chromosome human X chromosome

Cytogenetic location Xq21.1

Encodes ATPase copper transporting alpha

Expressed in buccal mucosa cell, trabecular bone, skin of thigh, germinal epithelium, corpus epididymis, tibia, Achilles tendon, parietal pleura, visceral pleura, skin of hip

Found in taxon Homo sapiens

Genetic association Menkes disease, occipital horn syndrome, X-linked distal spinal muscular atrophy type 3

Genomic end 78050395, 77305892

Genomic start 77166194, 77910690

Homologene id 35

Ortholog Atp7a, CCC2, Atp7a, atp7a, cua-1, ATP7

Strand orientation forward strand

Identifiers (13)

Image (Wikimedia Commons) Protein ATP7A PDB 1aw0.png ↗

Ensembl gene id ENSG00000165240

Ensembl transcript id ENST00000341514, ENST00000343533, ENST00000645094, ENST00000645454, ENST00000642651, ENST00000642523, ENST00000682742, ENST00000682475, ENST00000686515, ENST00000685208, ENST00000689649, ENST00000693398, ENST00000691456, ENST00000692908, ENST00000686543, ENST00000687599, ENST00000686050, ENST00000686999, ENST00000687082, ENST00000685264, ENST00000687086, ENST00000686255, ENST00000687416, ENST00000692729, ENST00000686688, ENST00000689891, ENST00000688746, ENST00000693387, ENST00000685885, ENST00000686560, ENST00000687984, ENST00000692110, ENST00000685434, ENST00000688165, ENST00000684798, ENST00000687325, ENST00000689514, ENST00000689731, ENST00000686133, ENST00000687628, ENST00000686464, ENST00000693051, ENST00000689541, ENST00000691152, ENST00000693167, ENST00000689767, ENST00000686896, ENST00000689872, ENST00000689530, ENST00000685033, ENST00000688249, ENST00000686033, ENST00000688338, ENST00000689083, ENST00000686480, ENST00000688889, ENST00000686416

Entrez gene id 538

Exact match identifiers.org

Freebase id /m/09mhmy

Hgnc gene symbol ATP7A

Hgnc id 869

Microsoft academic id (discontinued) 2779736553

Omim id 300011

Openalex id C2779736553

Refseq rna id NR_104109, NM_000052, NM_001282224

Umls cui C1412688

🌐 Available in 3 languages

enATP7A csATP7A ukATP7A

🏷️ Also known as

en ATP7A en ATPase copper transporting alpha en DSMAX en MK en MNK en SMAX3

🔗 Connections

Expressed in 5

tibia, Achilles tendon, trabecular bone, germinal epithelium, visceral pleura

Chromosome 1

human X chromosome

Found in taxon 1

Homo sapiens

Genetic association 1

Menkes disease

Instance of 1

gene

← Genetic association 1

Menkes disease

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

[2] ↑ ATP7A — subclass of (P279): protein-coding gene. NCBI homo sapiens annotation release 107. Retrieved 2016-10-03. wikidata.org.
[3] ↑ ATP7A — HomoloGene ID (P593): 35. NCBI Gene. Retrieved 2022-05-15. wikidata.org.
[4] ↑ ATP7A — genomic start (P644): 77166194. ensembl Release 106. wikidata.org.
[5] ↑ ATP7A — genomic start (P644): 77910690. ensembl Release 106. wikidata.org.
[6] ↑ ATP7A — genomic end (P645): 78050395. ensembl Release 106. wikidata.org.
[7] ↑ ATP7A — genomic end (P645): 77305892. ensembl Release 106. wikidata.org.
[8] ↑ ATP7A — ortholog (P684): Atp7a. HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
[9] ↑ ATP7A — ortholog (P684): CCC2. HomoloGene build68. wikidata.org.
[10] ↑ ATP7A — ortholog (P684): cua-1. HomoloGene build68. wikidata.org.
[11] ↑ ATP7A — ortholog (P684): ATP7. HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
[12] ↑ ATP7A — encodes (P688): ATPase copper transporting alpha. UniProt. Retrieved 2017-07-06. wikidata.org.
[13] ↑ ATP7A — found in taxon (P703): Homo sapiens. ensembl Release 106. wikidata.org.

Class ancestry

[1] ↑ ATP7A is an instance of gene (Q7187) [P31, primary]. Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). ATP7A. Retrieved October 28, 2026, from https://4ort.xyz/entity/atp7a

MLA “ATP7A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 28 Oct. 2026, https://4ort.xyz/entity/atp7a.

BibTeX

@misc{4ortxyz_atp7a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ATP7A}}, year = {2026}, url = {https://4ort.xyz/entity/atp7a}, note = {Accessed: 2026-10-28}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ATP7A — https://4ort.xyz/entity/atp7a (retrieved 2026-10-28)

Canonical URL: https://4ort.xyz/entity/atp7a · Last refreshed: October 28, 2026

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

23w ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗

Genetic association → Menkes disease, occipital horn syndrome, X-linked distal spinal muscular atrophy type 3

Subclass of → —

Chromosome → human X chromosome

Strand orientation → forward strand

+ 8 other properties edited (see Wikidata diff for full list)

"/* wbeditentity-update-languages-short:0||gsw */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/32527|batch #32527]]: human gene name and description in Alemannic"

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