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Chromosome 12 open reading frame 57

mammalian protein found in Homo sapiens
Protein protein Q21115577
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Chromosome 12 open reading frame 57

Summary

Chromosome 12 open reading frame 57 is a protein[1].

Key Facts

  • Chromosome 12 open reading frame 57's instance of is recorded as protein[2].
  • Chromosome 12 open reading frame 57's UniProt protein ID is recorded as Abraham Esau[3].
  • Chromosome 12 open reading frame 57's part of is recorded as Protein C10[4].
  • Chromosome 12 open reading frame 57's RefSeq protein ID is recorded as NP_001288763[5].
  • Chromosome 12 open reading frame 57's RefSeq protein ID is recorded as NP_001288765[6].
  • Chromosome 12 open reading frame 57's RefSeq protein ID is recorded as NP_001288766[7].
  • Chromosome 12 open reading frame 57's RefSeq protein ID is recorded as NP_001288767[8].
  • Chromosome 12 open reading frame 57's RefSeq protein ID is recorded as NP_612434[9].
  • Chromosome 12 open reading frame 57's molecular function is recorded as molecular function[10].
  • Chromosome 12 open reading frame 57's cell component is recorded as cytoplasm[11].
  • Chromosome 12 open reading frame 57's cell component is recorded as nuclear speck[12].
  • Chromosome 12 open reading frame 57's biological process is recorded as post-embryonic development[13].
  • Chromosome 12 open reading frame 57's biological process is recorded as regulation of skeletal muscle contraction[14].
  • Chromosome 12 open reading frame 57's biological process is recorded as corpus callosum morphogenesis[15].
  • Chromosome 12 open reading frame 57's biological process is recorded as third ventricle development[16].
  • Chromosome 12 open reading frame 57's biological process is recorded as psychomotor behavior[17].
  • Chromosome 12 open reading frame 57's biological process is recorded as camera-type eye morphogenesis[18].
  • Chromosome 12 open reading frame 57's biological process is recorded as cognition[19].
  • Chromosome 12 open reading frame 57's encoded by is recorded as C12orf57[20].
  • Chromosome 12 open reading frame 57's found in taxon is recorded as Homo sapiens[21].
  • Chromosome 12 open reading frame 57's Ensembl protein ID is recorded as ENSP00000229281[22].
  • Chromosome 12 open reading frame 57's Ensembl protein ID is recorded as ENSP00000440602[23].
  • Chromosome 12 open reading frame 57's Ensembl protein ID is recorded as ENSP00000440937[24].
  • Chromosome 12 open reading frame 57's Ensembl protein ID is recorded as ENSP00000475422[25].
  • Chromosome 12 open reading frame 57's Ensembl protein ID is recorded as ENSP00000475635[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . Q905695. Retrieved . wikidata.org.
  2. [3] ↑ . Q905695. Retrieved . wikidata.org.
  3. [4] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  4. [5] ↑ . Q20641742. Retrieved . wikidata.org.
  5. [6] ↑ . Q20641742. Retrieved . wikidata.org.
  6. [7] ↑ . Q20641742. Retrieved . wikidata.org.
  7. [8] ↑ . Q20641742. Retrieved . wikidata.org.
  8. [9] ↑ . Q20641742. Retrieved . wikidata.org.
  9. [10] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] ↑ . Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] ↑ . Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizures. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] ↑ . Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] ↑ . Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] ↑ . A newly recognized autosomal recessive syndrome affecting neurologic function and vision. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizures. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . A newly recognized autosomal recessive syndrome affecting neurologic function and vision. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . Q905695. Retrieved . wikidata.org.
  20. [21] ↑ . Q905695. Retrieved . wikidata.org.
  21. [22] ↑ . Ensembl Release 99. wikidata.org.
  22. [23] ↑ . Ensembl Release 99. wikidata.org.
  23. [24] ↑ . Ensembl Release 99. wikidata.org.
  24. [25] ↑ . Ensembl Release 99. wikidata.org.
  25. [26] ↑ . Ensembl Release 99. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). Chromosome 12 open reading frame 57. Retrieved May 3, 2026, from https://4ort.xyz/entity/chromosome-12-open-reading-frame-57
MLA “Chromosome 12 open reading frame 57.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/chromosome-12-open-reading-frame-57.
BibTeX @misc{4ortxyz_chromosome-12-open-reading-frame-57_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Chromosome 12 open reading frame 57}}, year = {2026}, url = {https://4ort.xyz/entity/chromosome-12-open-reading-frame-57}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Chromosome 12 open reading frame 57 — https://4ort.xyz/entity/chromosome-12-open-reading-frame-57 (retrieved 2026-05-03)

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