Human (GRCh38.p14)
Description

WD repeat domain 81 [Source:HGNC Symbol;Acc:HGNC:26600]

Gene Synonyms

CAMRQ2, FLJ33817, PPP1R166, SORF-2

Location

Chromosome 17: 1,716,523-1,738,599 forward strand.

GRCh38:CM000679.2

View alleles of this gene on alternative sequences

About this gene

This gene has 14 transcripts (splice variants), 1 gene allele, 203 orthologues, 26 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000409644.6WDR81-20269821941aaENSP00000386609.1
 
Protein coding
CCDS54062Q562E7-1 NM_001163809.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000309182.9WDR81-2013808890aaENSP00000312074.5
 
Protein coding
Q562E7-3 -GENCODE basicTSL:2
ENST00000419248.5WDR81-2043315714aaENSP00000407845.1
 
Protein coding
CCDS54063Q562E7-6 -GENCODE basicTSL:2
ENST00000437219.6WDR81-2053184738aaENSP00000391074.2
 
Protein coding
CCDS54061Q562E7-5 -GENCODE basicTSL:2
ENST00000446363.5WDR81-2062968580aaENSP00000401560.1
 
Protein coding
E9PDG3 -GENCODE basicTSL:1
ENST00000575206.1WDR81-214590197aaENSP00000458811.1
 
Protein coding
I3L1G2 -TSL:3CDS 5' and 3' incomplete
ENST00000418841.5WDR81-203582132aaENSP00000395198.1
 
Protein coding
C9JD20 -TSL:3CDS 3' incomplete
ENST00000455636.5WDR81-207570172aaENSP00000395226.1
 
Protein coding
C9JCF9 -TSL:3CDS 3' incomplete
ENST00000468539.5WDR81-209562171aaENSP00000460742.1
 
Protein coding
I3L3U7 -TSL:4CDS 3' incomplete
ENST00000474958.2WDR81-210561123aaENSP00000466240.1
 
Nonsense mediated decay
K7ELV8 -TSL:5CDS 5' incomplete
ENST00000464528.5WDR81-2084432No protein-
 
Retained intron
--TSL:2
ENST00000479966.1WDR81-211621No protein-
 
Retained intron
--TSL:2
ENST00000495411.1WDR81-213553No protein-
 
Retained intron
--TSL:4
ENST00000492901.1WDR81-212545No protein-
 
Retained intron
--TSL:4