Homo sapiens Gene: FRMD7
Summary
InnateDB Gene IDBG-86486.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FRMD7
Gene Name FERM domain containing 7
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000165694
Encoded Proteins
FERM domain containing 7
FERM domain containing 7
FERM domain containing 7
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Mutations in this gene are associated with X-linked congenital nystagmus. [provided by RefSeq, Dec 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome X:132076993-132128020
Strand Reverse strand
Band q26.2
Transcripts
ENST00000370879 ENSP00000359916
ENST00000298542 ENSP00000298542
ENST00000464296 ENSP00000417996
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0010975 regulation of neuron projection development
Cellular Component
GO:0005615 extracellular space
GO:0005856 cytoskeleton
GO:0030426 growth cone
GO:0043005 neuron projection
GO:0043025 neuronal cell body
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.170776
RefSeq NM_194277 XM_005262493
HUGO
OMIM
CCDS CCDS35397
HPRD 06624
IMGT
EMBL
GenPept
RNA Seq Atlas