Homo sapiens Gene: WISP3 | |||||||
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Summary | |||||||
InnateDB Gene | IDBG-95510.6 | ||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
Gene Symbol | WISP3 | ||||||
Gene Name | WNT1 inducible signaling pathway protein 3 | ||||||
Synonyms | CCN6; LIBC; PPAC; PPD | ||||||
Species | Homo sapiens | ||||||
Ensembl Gene | ENSG00000112761 | ||||||
Encoded Proteins |
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
WNT1 inducible signaling pathway protein 3
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Protein Structure | |||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||
Entrez Gene | |||||||
Summary |
This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like domain. This gene is overexpressed in colon tumors. It may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. Mutations of this gene are associated with progressive pseudorheumatoid dysplasia, an autosomal recessive skeletal disorder, indicating that the gene is essential for normal postnatal skeletal growth and cartilage homeostasis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||||
Type | Protein coding | ||||||
Genomic Location | Chromosome 6:112054072-112070969 | ||||||
Strand | Forward strand | ||||||
Band | q21 | ||||||
Transcripts | |||||||
Interactions | |||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||
SwissProt | |||||||
TrEMBL | |||||||
UniProt Splice Variant | |||||||
Entrez Gene | |||||||
UniGene | Hs.558428 Hs.672389 | ||||||
RefSeq | NM_003880 NM_198239 XM_006715590 | ||||||
HUGO | |||||||
OMIM | |||||||
CCDS | CCDS5097 CCDS5098 | ||||||
HPRD | 04550 | ||||||
IMGT | |||||||
EMBL | |||||||
GenPept | |||||||
RNA Seq Atlas | |||||||