Human (GRCh38.p14)
Description

Wnt family member 3 [Source:HGNC Symbol;Acc:HGNC:12782]

Gene Synonyms

INT4, MGC131950, MGC138321, MGC138323

Location

Chromosome 17: 46,762,506-46,833,154 reverse strand.

GRCh38:CM000679.2

View alleles of this gene on alternative sequences

About this gene

This gene has 8 transcripts (splice variants), 1 gene allele, 202 orthologues, 18 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000225512.6WNT3-2013287355aaENSP00000225512.5
 
Protein coding
CCDS11505P56703 NM_030753.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000706495.1WNT3-2083411290aaENSP00000516418.1
 
Protein coding
--GENCODE basic
ENST00000706483.1WNT3-2052909170aaENSP00000516407.1
 
Protein coding
--GENCODE basic
ENST00000706485.1WNT3-2071785170aaENSP00000516409.1
 
Protein coding
--GENCODE basic
ENST00000706484.1WNT3-206304367aaENSP00000516408.1
 
Nonsense mediated decay
---
ENST00000572508.1WNT3-202734No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000573788.5WNT3-203559No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000576471.2WNT3-2041236No protein-
 
Retained intron
--TSL:4