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Gene: WNT9B (Wnt family member 9B) Homo sapiens
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Symbol: WNT9B
Name: Wnt family member 9B
Description: The WNT gene family consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. Study of its expression in the teratocarcinoma cell line NT2 suggests that it may be implicated in the early process of neuronal differentiation of NT2 cells induced by retinoic acid. This gene is clustered with WNT3, another family member, in the chromosome 17q21 region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: protein Wnt-14b; protein Wnt-9b; wingless-type MMTV integration site family member 9B; wingless-type MMTV integration site family, member 15; wingless-type MMTV integration site family, member 9B; WNT14B; WNT15
Orthologs:
Mus musculus (house mouse) : Wnt9b (wingless-type MMTV integration site family, member 9B)  MGI  Alliance
Rattus norvegicus (Norway rat) : Wnt9b (Wnt family member 9B)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Wnt9b (Wnt family member 9B)
Pan paniscus (bonobo/pygmy chimpanzee) : WNT9B (Wnt family member 9B)
Canis lupus familiaris (dog) : WNT9B (Wnt family member 9B)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Wnt9b (Wnt family member 9B)
Sus scrofa (pig) : WNT9B (Wnt family member 9B)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381746,833,201 - 46,886,738 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371744,928,952 - 44,964,096 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361742,283,967 - 42,309,436 (+)NCBINCBI36hg18NCBI36
Build 341742,283,966 - 42,309,436NCBI
Celera1741,378,455 - 41,403,922 (+)NCBI
Cytogenetic Map17q21.32NCBI
HuRef1740,307,364 - 40,332,821 (+)NCBIHuRef
CHM1_11744,993,079 - 45,028,223 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on WNT9B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1319983
Created: 2005-01-12
Species: Homo sapiens
Last Modified: 2019-09-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.