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Gene : FANCB Homo sapiens

Name  ? FA complementation group B Cytological Location  Xp22.2
Brief Description  FA complementation group B
Description  This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
  • synonyms:
  • OTTHUMG00000021168,
  • FA2,
  • FAAP90,
  • FAB,
  • FLJ34064,
  • FAAP95,
  • FAB,
  • FACB,
  • uc004cwh.2,
  • Fanconi anemia complementation group B,
  • FAAP95,
  • NM_152633,
  • FANCB,
  • HGNC:3583,
  • AK091383
  • identifiers:
  • 2187,
  • ENSG00000181544,
  • FANCB

Genome feature

Region: gene ? Length: 182393  
Location: X:14690863-14873255 reverse strand Cyto location: Xp22.2


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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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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 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

322 SN Ps

5 Cross References

18 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results