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Gene : USH1C Homo sapiens

Name  ? USH1 protein network component harmonin Brief Description  Usher syndrome 1C (autosomal recessive, severe)
  • synonyms:
  • PDZ73,
  • PDZ-45,
  • DFNB18,
  • harmonin,
  • AIE-75,
  • AB006955,
  • NY-CO-37,
  • NY-CO-38,
  • Usher syndrome 1C (autosomal recessive, severe),
  • DFNB18,
  • PDZD7C,
  • PDZ-73/NY-CO-38,
  • AIE-75,
  • PDZ-73,
  • deafness, autosomal recessive 18,
  • PDZ-73,
  • USH1C,
  • NY-CO-37,
  • PDZD7C,
  • NY-CO-38,
  • HGNC:12597,
  • NM_005709,
  • OTTHUMG00000166323,
  • uc001mne.3,
  • PDZ73,
  • Usher syndrome 1C,
  • DFNB18A,
  • ush1cpst
  • identifiers:
  • 10083,
  • ENSG00000006611,
  • USH1C

Genome feature

Region: gene ? Length: 50522  
Location: 11:17493895-17544416 reverse strand


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Function

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0 Pathways

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

3 Diseases

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

Gene --> Alleles and Disease

Gene --> Disease (OMIM)

Mouse Gene --> Allele [Phenotype]

Homology

Homologue Displayer

Gene --> Orthologues

Interactions

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Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

64 Child Features

7 Cross References

14 Data Sets

6 Homologues

0 Located Features