Human (GRCh38.p14)
Description

complement factor properdin [Source:HGNC Symbol;Acc:HGNC:8864]

Gene Synonyms

PFC

Location

Chromosome X: 47,623,172-47,630,305 reverse strand.

GRCh38:CM000685.2

About this gene

This gene has 8 transcripts (splice variants), 123 orthologues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000396992.8CFP-2032489469aaENSP00000380189.3
 
Protein coding
CCDS14282A0A0S2Z4I5 P27918 NM_001145252.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000247153.7CFP-2011713469aaENSP00000247153.3
 
Protein coding
CCDS14282A0A0S2Z4I5 P27918 -GENCODE basicAPPRIS P1TSL:5
ENST00000377005.6CFP-2021435415aaENSP00000366204.2
 
Protein coding
E9PAQ1 -GENCODE basicTSL:1
ENST00000469388.1CFP-204928167aaENSP00000418258.1
 
Protein coding
C9J7V5 -TSL:5CDS 3' incomplete
ENST00000480317.1CFP-206569No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000485991.5CFP-2074040No protein-
 
Retained intron
--TSL:2
ENST00000640573.1CFP-2082751No protein-
 
Retained intron
--TSL:5
ENST00000478222.1CFP-205593No protein-
 
Retained intron
--TSL:2