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Gene : CFHR2 Homo sapiens

Name  ? complement factor H related 2 Cytological Location  1q31.3
Brief Description  complement factor H related 2
Description  This gene belongs to a family of complement factor H-related genes (CFHR), which are clustered together with complement factor H gene on chromosome 1, and are involved in regulation of complement. Mutations in CFHR genes have been associated with dense deposit disease and atypical haemolytic-uraemic syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]
  • synonyms:
  • X64877,
  • CFHR2,
  • HFL3,
  • H factor (complement)-like 3,
  • FHR2,
  • CFHL2,
  • HFL3,
  • FHR2,
  • CFHL2,
  • OTTHUMG00000036518,
  • complement factor H-related 2,
  • HGNC:4890,
  • uc001gtq.2,
  • NM_005666
  • identifiers:
  • 3080,
  • ENSG00000080910,
  • CFHR2

Genome feature

Region: gene ? Length: 15885  
Location: 1:196943738-196959622 Cyto location: 1q31.3

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Gene -> HPO annotation (Human Phenotype Ontology)

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0 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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

Gene Ontology

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0 SN Ps

5 Cross References

13 Data Sets

0 Homologues

0 Located Features

97 Rna Seq Results