Gene Gene information from NCBI Gene database.
Entrez ID 85369
Gene name Striatin interacting protein 1
Gene symbol STRIP1
Synonyms (NCBI Gene)
FAM40AFAR11A
Chromosome 1
Chromosome location 1p13.3
Summary This gene encodes a member of the striatin-interacting phosphatase and kinase complex, which is involved in localization of the Golgi body. The encoded protein participates in cytosketelal organization. Alternative splicing results in multiple transcript
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT041414 hsa-miR-193b-3p CLASH 23622248
MIRT128241 hsa-miR-30a-5p HITS-CLIP 22473208
MIRT128245 hsa-miR-30b-5p HITS-CLIP 22473208
MIRT128242 hsa-miR-30c-5p HITS-CLIP 22473208
MIRT128243 hsa-miR-30d-5p HITS-CLIP 22473208
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 18782753, 19156129, 24255178, 25531779, 26496610, 28330616, 28514442, 32707033, 33961781, 35271311
GO:0005634 Component Nucleus IDA 15302935
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol IBA
GO:0005829 Component Cytosol IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617918 25916 ENSG00000143093
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5VSL9
Protein name Striatin-interacting protein 1 (Protein FAM40A)
Protein function Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the cortical actin filament dynamics and cell shape. Part of the striatin-interacting phosphatase and kinase (STRIPAK) complexes. STRIPAK complexes have
PDB 7K36
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07923 N1221 66 337 N1221-like protein Family
PF11882 DUF3402 437 632 Domain of unknown function (DUF3402) Family
PF11882 DUF3402 626 796 Domain of unknown function (DUF3402) Family
Sequence
MEPAVGGPGPLIVNNKQPQPPPPPPPAAAQPPPGAPRAAAGLLPGGKAREFNRNQRKDSE
GYSESPDLEFEYADTDKWAAELSELYSYTEGPEFLMNRKCFEEDFRIHVTDKKWTELDTN
QHRTHAMRLLDGLEVTAREKRLKVARAILYVAQGTFGECSSEAEVQSWMRYNIFLLLEVG
TFNALVELLNMEIDNSAACSSAVRKPAISLADSTDLRVLLNIMYLIVETVHQECEGDKAE
WRTMRQTFRAELGSPLYNNEPFAIMLFGMVTKFCSGHAPHFPMKKVLLLLWKTVLCTLGG
FEELQSMKAEKRSILGLPPLPEDSIKVIRNMRAASPP
ASASDLIEQQQKRGRREHKALIK
QDNLDAFNERDPYKADDSREEEEENDDDNSLEGETFPLERDEVMPPPLQHPQTDRLTCPK
GLPWAPKVREKDIEMFLESSRSKFIGYTLGSDTNTVVGLPRPIHESIKTLKQHKYTSIAE
VQAQMEEEYLRSPLSGGEEEVEQVPAETLYQGLLPSLPQYMIALLKILLAAAPTSKAKTD
SINILADVLPEEMPTTVLQSMKLGVDVNRHKEVIVKAISAVLLLLLKHFKLNHVYQFEYM
AQHLVFANCIPLILKFFNQNIMSYI
TAKNSISVLDYPHCVVHELPELTAESLEAGDSNQF
CWRNLFSCINLLRILNKLTKWKHSRTMMLVVFKSAPILKRALKVKQAMMQLYVLKLLKVQ
TKYLGRQWRKSNMKTMSAIYQKVRHRLNDDWAYGNDLDARPWDFQAEECALRANIERFNA
RRYDRAHSNPDFLPVD
NCLQSVLGQRVDLPEDFQMNYDLWLEREVFSKPISWEELLQ
Sequence length 837
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
See cases Uncertain significance rs72687299 RCV001197005
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Cerebral Cavernous Malformations 3 Associate 18782753