Homo sapiens Protein: CHD7
Summary
InnateDB Protein IDBP-594593.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CHD7
Protein Name chromodomain helicase DNA binding protein 7
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000437061
InnateDB Gene IDBG-22967 (CHD7)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 36 experimentally validated interaction(s) in this database.
They are also associated with 11 interaction(s) predicted by orthology.
Experimentally validated
Total 36 [view]
Protein-Protein 36 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 11 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003682 chromatin binding
GO:0004386 helicase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016817 hydrolase activity, acting on acid anhydrides
Biological Process
GO:0001501 skeletal system development
GO:0001701 in utero embryonic development
GO:0003007 heart morphogenesis
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006364 rRNA processing
GO:0007417 central nervous system development
GO:0016568 chromatin modification
GO:0021545 cranial nerve development
GO:0030217 T cell differentiation
GO:0042472 inner ear morphogenesis
GO:0043584 nose development
GO:0048806 genitalia development
GO:0050890 cognition
GO:0060021 palate development
GO:0060041 retina development in camera-type eye
GO:0060123 regulation of growth hormone secretion
GO:0060173 limb development
GO:0060324 face development
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR006576 BRK domain
PFAM PF07533
PRINTS
PIRSF
SMART SM00592
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9P2D1
PhosphoSite PhosphoSite-Q9P2D1
TrEMBL H0YDC1
UniProt Splice Variant
Entrez Gene 55636
UniGene Hs.733236
RefSeq
HUGO HGNC:20626
OMIM 608892
CCDS
HPRD 10595
IMGT
EMBL AB037837 AC023102 AC113143 AK000364 AK000368 BC014681 BC051264 BC053890 BC068000 BC080627 BC110818 GU060498
GenPept AAH14681 AAH51264 AAH53890 AAH68000 AAH80627 AAI10819 ACY35999 BAA91113 BAA91116 BAA92654