Mus musculus Gene: Chd7
Summary
InnateDB Gene IDBG-128871.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Chd7
Gene Name chromodomain helicase DNA binding protein 7
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000041235
Encoded Proteins
chromodomain helicase DNA binding protein 7
chromodomain helicase DNA binding protein 7
chromodomain helicase DNA binding protein 7
chromodomain helicase DNA binding protein 7
chromodomain helicase DNA binding protein 7
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a protein containing two chromodomains and an ATP-binding helicase domain that functions as a regulator of transcription. Mutations in this gene result in an array of development defects, including inner ear problems. The related gene in humans has been implicated in CHARGE syndrome. [provided by RefSeq, Mar 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:8690406-8867659
Strand Forward strand
Band A1
Transcripts
ENSMUST00000051558 ENSMUSP00000059079
ENSMUST00000039267 ENSMUSP00000043903
ENSMUST00000127476 ENSMUSP00000118711
ENSMUST00000129655 ENSMUSP00000123241
ENSMUST00000130709
ENSMUST00000170457
ENSMUST00000170391 ENSMUSP00000127007
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 15 experimentally validated interaction(s) in this database.
They are also associated with 36 interaction(s) predicted by orthology.
Experimentally validated
Total 15 [view]
Protein-Protein 7 [view]
Protein-DNA 8 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 36 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003676 nucleic acid binding
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:0001568 blood vessel 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:0007512 adult heart development
GO:0007605 sensory perception of sound
GO:0007626 locomotory behavior
GO:0007628 adult walking behavior
GO:0008015 blood circulation
GO:0008152 metabolic process
GO:0016568 chromatin modification
GO:0021545 cranial nerve development
GO:0021553 olfactory nerve development
GO:0021772 olfactory bulb development
GO:0030217 T cell differentiation
GO:0030540 female genitalia development
GO:0035116 embryonic hindlimb morphogenesis
GO:0040018 positive regulation of multicellular organism growth
GO:0042048 olfactory behavior
GO:0042471 ear morphogenesis
GO:0042472 inner ear morphogenesis
GO:0043010 camera-type eye development
GO:0043584 nose development
GO:0048752 semicircular canal morphogenesis
GO:0048806 genitalia development
GO:0048844 artery morphogenesis
GO:0050767 regulation of neurogenesis
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
GO:0060429 epithelium development
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathway Predictions based on Human Orthology Data
NETPATH
Wnt pathway
REACTOME
KEGG
INOH
PID NCI
Noncanonical Wnt signaling pathway
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.138792 Mm.435033 Mm.475509
RefSeq NM_001081417 NM_001277149 XM_006538004 XM_006538005 XM_006538006
OMIM
CCDS CCDS38689
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas