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NM_030775.2 - NP_110402.2
NM_032642.3 - NP_116031.1 (MANE)
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
12
Location
Chr12:1,616,556-1,647,712
LOEUF
0.494
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ClinVar
Pathogenic/ Likely pa...
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Drug response
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VUS
Benign/Likely benign
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GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
Others
Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
81029
Ensembl
ENSG00000111186
GeneCards
WNT5B
UniProt
Q9H1J7
KEGG
hsa:81029
gnomAD
ENSG00000111186
ICGC
ENSG00000111186
RefDIC
81029
RefEx
81029
DTX
WNT5B
AS-ALPS
WNT5B
WNT5B
Wnt family member 5B
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