Human (GRCh38.p14)
Description

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

Gene Synonyms

PFC

Location

Chromosome X: 47,621,537-47,630,305 reverse strand.

GRCh38:CM000685.2

About this gene

This gene has 12 transcripts (splice variants), 122 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 PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000862734.1CFP-2094274469aaENSP00000532793.1
 
Protein coding
CCDS14282A0A0S2Z4I5 -GENCODE BasicAPPRIS P1
ENST00000247153.7CFP-2011713469aaENSP00000247153.3
 
Protein coding
CCDS14282A0A0S2Z4I5 P27918 -GENCODE BasicAPPRIS P1TSL:5
ENST00000377005.6CFP-2021435415aaENSP00000366204.2
 
Protein coding
E9PAQ1 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000862735.1CFP-2101343411aaENSP00000532794.1
 
Protein coding
--GENCODE Basic
ENST00000862736.1CFP-2111314412aaENSP00000532795.1
 
Protein coding
--GENCODE Basic
ENST00000952425.1CFP-2121157347aaENSP00000622484.1
 
Protein coding
--GENCODE Basic
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