Human (GRCh38.p14)
Description

WD repeat domain 13 [Source:HGNC Symbol;Acc:HGNC:14352]

Location

Chromosome X: 48,590,042-48,608,869 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 12 transcripts (splice variants), 195 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000376729.10WDR13-2025457485aaENSP00000365919.5
 
Protein coding
CCDS14302Q9H1Z4 NM_001347217.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000218056.9WDR13-2012124485aaENSP00000218056.5
 
Protein coding
CCDS14302Q9H1Z4 -GENCODE basicAPPRIS P1TSL:1
ENST00000482760.3WDR13-207562187aaENSP00000483191.1
 
Protein coding
A0A087X091 -TSL:3CDS 5' and 3' incomplete
ENST00000470124.1WDR13-204437107aaENSP00000480532.1
 
Protein coding
A0A087WWV5 -TSL:3CDS 3' incomplete
ENST00000486125.5WDR13-20893643aaENSP00000482667.1
 
Nonsense mediated decay
A0A087X2H9 -TSL:2
ENST00000498631.5WDR13-21285943aaENSP00000484996.1
 
Nonsense mediated decay
A0A087X2H9 -TSL:2
ENST00000492715.1WDR13-2092612No protein-
 
Retained intron
--TSL:5
ENST00000479279.5WDR13-2062486No protein-
 
Retained intron
--TSL:1
ENST00000466962.1WDR13-203684No protein-
 
Retained intron
--TSL:3
ENST00000495575.1WDR13-211547No protein-
 
Retained intron
--TSL:2
ENST00000492873.1WDR13-210470No protein-
 
Retained intron
--TSL:2
ENST00000472440.1WDR13-205430No protein-
 
Retained intron
--TSL:2