Homo sapiens Gene: CXXC4
Summary
InnateDB Gene IDBG-32662.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CXXC4
Gene Name CXXC finger protein 4
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000168772
Encoded Proteins
CXXC finger protein 4
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 4:104468312-104494901
Strand Reverse strand
Band q24
Transcripts
ENST00000394767 ENSP00000378248
ENST00000466963
ENST00000515509
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0030165 PDZ domain binding
Biological Process
GO:0007352 zygotic specification of dorsal/ventral axis
GO:0016055 Wnt signaling pathway
GO:0030178 negative regulation of Wnt signaling pathway
Cellular Component
GO:0005737 cytoplasm
GO:0016023 cytoplasmic membrane-bounded vesicle
GO:0031410 cytoplasmic vesicle
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
negative regulation of TCF-dependent signaling by DVL-interacting proteins pathway
misspliced LRP5 mutants have enhanced beta-catenin-dependent signaling pathway
Signaling by WNT in cancer pathway
Signaling by Wnt pathway
Signal Transduction pathway
TCF dependent signaling in response to WNT pathway
RNF mutants show enhanced WNT signaling and proliferation pathway
XAV939 inhibits tankyrase, stabilizing AXIN pathway
Disease pathway
KEGG
Wnt signaling pathway pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.12248 Hs.624057
RefSeq NM_025212
HUGO
OMIM
CCDS CCDS3665
HPRD 16773
IMGT
EMBL
GenPept
RNA Seq Atlas