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Gene : FAH Homo sapiens

Name  ? fumarylacetoacetate hydrolase Cytological Location  15q25.1
Brief Description  fumarylacetoacetate hydrolase
Description  This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT). [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000144187,
  • FAH,
  • NM_000137,
  • HGNC:3579,
  • M55150,
  • uc021srz.2,
  • fumarylacetoacetase
  • identifiers:
  • 2184,
  • ENSG00000103876,
  • FAH

Genome feature

Region: gene ? Length: 34161  
Location: 15:80152789-80186949 Cyto location: 15q25.1


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

3753 SN Ps

5 Cross References

20 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results