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Gene : FAM126A Homo sapiens

Name  ? family with sequence similarity 126 member A Cytological Location  7p15.3
Brief Description  family with sequence similarity 126 member A
Description  The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC). [provided by RefSeq, Oct 2008]
  • synonyms:
  • HYCC1,
  • HYCC1,
  • OTTHUMG00000128435,
  • NM_032581,
  • hyccin,
  • family with sequence similarity 126, member A,
  • HLD5,
  • DRCTNNB1A,
  • down regulated by Ctnnb1, a,
  • DRCTNNB1A,
  • HGNC:24587,
  • BC018710,
  • HCC,
  • HCC,
  • FAM126A,
  • uc003svm.5
  • identifiers:
  • 84668,
  • ENSG00000122591,
  • FAM126A

Genome feature

Region: gene ? Length: 118286  
Location: 7:22895848-23014133 reverse strand Cyto location: 7p15.3


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

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

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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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results