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
IDBP-86488 FERM domain containing 7
IDBP-86490 FERM domain containing 7
IDBP-475038 FERM domain containing 7
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
Accession GO Term
Molecular Function
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
ENSMUSG00000036131 Ortholuge Non-SSD Ortholog Possible paralog/unusual divergence/ gene prediction error
ENSBTAG00000007344 Not yet available Ortholuge Non-SSD Ortholog Possible paralog/unusual divergence/ gene prediction error
Pathways
NETPATH
REACTOME
KEGG
INOH
PID BIOCARTA
PID NCI
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