Homo sapiens Gene: CFDP1
Summary
InnateDB Gene IDBG-42521.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CFDP1
Gene Name craniofacial development protein 1
Synonyms BCNT; BUCENTAUR; CENP-29; CP27; p97; SWC5; Yeti;
Species Homo sapiens
Ensembl Gene ENSG00000153774
Encoded Proteins
craniofacial development protein 1
craniofacial development protein 1
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 16:75293698-75433485
Strand Reverse strand
Band q23.1
Transcripts
ENST00000283882 ENSP00000283882
ENST00000565646
ENST00000562602
ENST00000564793
ENST00000570279
ENST00000570103
ENST00000569341 ENSP00000462862
ENST00000566254 ENSP00000455564
ENST00000566901
ENST00000564286
ENST00000612761 ENSP00000481200
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 7 [view]
Protein-Protein 7 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0007155 cell adhesion
GO:0007275 multicellular organismal development
GO:0008150 biological_process
GO:0008360 regulation of cell shape
GO:0042127 regulation of cell proliferation
GO:2000270 negative regulation of fibroblast apoptotic process
Cellular Component
GO:0005575 cellular_component
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL H3BQ17
UniProt Splice Variant
Entrez Gene 10428
UniGene Hs.461361
RefSeq NM_006324
HUGO HGNC:1873
OMIM 608108
CCDS CCDS10916
HPRD 16282
IMGT
EMBL AC009054 AC009163
GenPept
RNA Seq Atlas 10428