Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
29888
Gene name Gene Name - the full gene name approved by the HGNC.
Striatin 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STRN4
Synonyms (NCBI Gene) Gene synonyms aliases
PPP2R6C, ZIN, zinedin
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.32
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT040848 hsa-miR-18a-3p CLASH 23622248
MIRT490922 hsa-miR-4688 PAR-CLIP 23592263
MIRT490921 hsa-miR-6743-5p PAR-CLIP 23592263
MIRT490920 hsa-miR-6784-5p PAR-CLIP 23592263
MIRT490919 hsa-miR-4508 PAR-CLIP 23592263
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 20195357, 32814053
GO:0005516 Function Calmodulin binding IBA 21873635
GO:0005516 Function Calmodulin binding NAS 10748158
GO:0005737 Component Cytoplasm IEA
GO:0008150 Process Biological_process ND
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614767 15721 ENSG00000090372
Protein
UniProt ID Q9NRL3
Protein name Striatin-4 (Zinedin)
Protein function Calmodulin-binding scaffolding protein which is the center of the striatin-interacting phosphatase and kinase (STRIPAK) complexes (PubMed:18782753, PubMed:32640226). STRIPAK complexes have critical roles in protein (de)phosphorylation and are re
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08232 Striatin 64 193 Striatin family Family
PF00400 WD40 428 466 WD domain, G-beta repeat Repeat
PF00400 WD40 534 572 WD domain, G-beta repeat Repeat
PF00400 WD40 669 707 WD domain, G-beta repeat Repeat
PF00400 WD40 711 752 WD domain, G-beta repeat Repeat
Sequence
MMEERAAAAVAAAASSCRPLGSGAGPGPTGAAPVSAPAPGPGPAGKGGGGGGSPGPTAGP
EPLSLPGILHFIQHEWARFEAEKARWEAERAELQAQVAFLQGERKGQENLKTDLVRRIKM
LEYALKQERAKYHKLKFGTDLNQGEKKADVSEQVSNGPVESVTLENSPLVWKEGRQLLRQ
YLEEVGYTDTILD
MRSKRVRSLLGRSLELNGAVEPSEGAPRAPPGPAGLSGGESLLVKQI
EEQIKRNAAGKDGKERLGGSVLGQIPFLQNCEDEDSDEDDELDSVQHKKQRVKLPSKALV
PEMEDEDEEDDSEDAINEFDFLGSGEDGEGAPDPRRCTVDGSPHELESRRVKLQGILADL
RDVDGLPPKVTGPPPGTPQPRPHEDVFIMDTIGGGEVSLGDLADLTVTNDNDLSCDLSDS
KDAFKKTWNPKFTLRSHYDGIRSLAFHHSQSALLTASEDGTLKLWNLQKAVTAKKNAALD
VEPIHAFRAHRGPVLAVAMGSNSEYCYSGGADACIHSWKIPDLSMDPYDGYDPSVLSHVL
EGHGDAVWGLAFSPTSQRLASCSADGTVRIWD
PSSSSPACLCTFPTASEHGVPTSVAFTS
TEPAHIVASFRSGDTVLYDMEVGSALLTLESRGSSGPTQINQVVSHPNQPLTITAHDDRG
IRFLDNRTGKPVHSMVAHLDAVTCLAVDPNGAFLMSGSHDCSLRLWSLDNKTCVQEITAH
RKKHEEAIHAVACHPSKALIASAGADALAKVF
V
Sequence length 753
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Limb-girdle muscular dystrophy MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I rs2137534216, rs104894422, rs762777463, rs104894423, rs137854524, rs137854521, rs137854523, rs137854529, rs398123555, rs119463996, rs587777814, rs119463992, rs267606971, rs267606967, rs28941782
View all (762 more)
Myopia Myopia rs387907109, rs146936371, rs587776903, rs786205127, rs398122836, rs199624584, rs587777625, rs786205216, rs758872875, rs764211125, rs1135402746, rs765658563, rs1555941129, rs1555941116, rs199923805
View all (6 more)
Scoliosis Scoliosis, unspecified rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085
Associations from Text Mining
Disease Name Relationship Type References
Asthma Associate 36835202
Carcinoma Hepatocellular Associate 34375307
Endometrial Neoplasms Associate 32640226
Glioma Associate 19544381
Neoplasms Associate 19544381