Homo sapiens Gene: CNNM4
Summary
InnateDB Gene IDBG-61884.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CNNM4
Gene Name cyclin M4
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000158158
Encoded Proteins
cyclin M4
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq, Feb 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:96760902-96811891
Strand Forward strand
Band q11.2
Transcripts
ENST00000377075 ENSP00000366275
ENST00000482716
ENST00000496186
ENST00000493384
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:0030554 adenyl nucleotide binding
Biological Process
GO:0006811 ion transport
GO:0007601 visual perception
GO:0031214 biomineral tissue development
GO:0050896 response to stimulus
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.175043
RefSeq NM_020184
HUGO
OMIM
CCDS CCDS2024
HPRD 07420
IMGT
EMBL
GenPept
RNA Seq Atlas