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Gene : HCCS Homo sapiens

Name  ? holocytochrome c synthase Brief Description  holocytochrome c synthase
  • synonyms:
  • NM_001122608,
  • uc004cuj.3,
  • CCHL,
  • LSDMCA1,
  • HGNC:4837,
  • MLS,
  • MLS,
  • MCOPS7,
  • microphthalamia with linear skin defects,
  • HCCS,
  • holocytochrome c synthase (cytochrome c heme-lyase),
  • cytochrome c heme-lyase,
  • CCHL,
  • OTTHUMG00000021128
  • identifiers:
  • 3052,
  • ENSG00000004961,
  • HCCS

Genome feature

Region: gene ? Length: 11801  
Location: X:11111286-11123086


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Function

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Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease

Gene --> Disease (OMIM)

Mouse Gene --> Allele [Phenotype]

Homology

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Gene --> Orthologues

Interactions

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Gene Ontology

Gene --> GO terms.

 

Other

0 Child Features

7 Cross References

16 Data Sets

7 Homologues

0 Located Features