Synonyms:CFHL2, CFHR2, ENTREZ:3080, FHR2, HFL3, HGNC:4890, MIM:600889, NM_001312672, NM_005666, NP_001299601, NP_005657, XM_005245113, XM_011509458, XM_011509459, XM_011509460, XM_017001109, XP_005245170, XP_011507760, XP_011507761, XP_011507762, XP_016856598, complement factor H related 2
Omim:OMIM:600889
Id:edb81ecc-5f56-5b3d-93c4-024839827b90
Hgnc:HGNC:4890
Description:complement factor H related 2
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]