Homo sapiens Gene: FRMD7
Summary
InnateDB Gene IDBG-86486.5
Last Modified 2012-02-14 [Report errors or provide feedback]
Gene Symbol FRMD7
Gene Name FERM domain containing 7
Synonyms NYS; NYS1; XIPAN;
Species Homo sapiens
Ensembl Gene ENSG00000165694
Encoded Proteins
FERM domain containing 7
FERM domain containing 7
FERM domain containing 7
Protein Structure
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:131211021-131262048
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: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
Method
Confidence
Comments
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Not yet available
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Cross-References
SwissProt Q6ZUT3
TrEMBL
UniProt Splice Variant
Entrez Gene 90167
UniGene Hs.170776
RefSeq NM_194277
HUGO 8079
OMIM 300628
CCDS CCDS35397
HPRD 06624
IMGT
EMBL AK125336 AL049792 AL109749 BC114371 FJ717411
GenPept AAI14372 ACN56448 BAC86135 CAI42080
ImmGen FRMD7 (murine)
RNA Seq Atlas 90167