Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
114815
Gene name Gene Name - the full gene name approved by the HGNC.
Sortilin related VPS10 domain containing receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SORCS1
Synonyms (NCBI Gene) Gene synonyms aliases
hSorCS
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q25.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes one family member of vacuolar protein sorting 10 (VPS10) domain-containing receptor proteins. The VPS10 domain name comes from the yeast carboxypeptidase Y sorting receptor Vps10 protein. Members of this gene family are large with many e
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT622145 hsa-miR-5582-3p HITS-CLIP 23824327
MIRT622145 hsa-miR-5582-3p HITS-CLIP 23824327
MIRT1379523 hsa-miR-1253 CLIP-seq
MIRT1379524 hsa-miR-1290 CLIP-seq
MIRT1379525 hsa-miR-1303 CLIP-seq
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 12482870, 24128306
GO:0005794 Component Golgi apparatus IBA 21873635
GO:0006892 Process Post-Golgi vesicle-mediated transport IBA 21873635
GO:0007218 Process Neuropeptide signaling pathway NAS 11499680
GO:0008188 Function Neuropeptide receptor activity NAS 11499680
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606283 16697 ENSG00000108018
Protein
UniProt ID Q8WY21
Protein name VPS10 domain-containing receptor SorCS1 (hSorCS)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15902 Sortilin-Vps10 205 635 Sortilin, neurotensin receptor 3, Domain
PF15901 Sortilin_C 637 792 Sortilin, neurotensin receptor 3, C-terminal Domain
PF00801 PKD 803 880 PKD domain Domain
Tissue specificity TISSUE SPECIFICITY: Detected in fetal and infant brain and in fetal retina.
Sequence
MGKVGAGGGSQARLSALLAGAGLLILCAPGVCGGGSCCPSPHPSSAPRSASTPRGFSHQG
RPGRAPATPLPLVVRPLFSVAPGDRALSLERARGTGASMAVAARSGRRRRSGADQEKAER
GEGASRSPRGVLRDGGQQEPGTRERDPDKATRFRMEELRLTSTTFALTGDSAHNQAMVHW
SGHNSSVILILTKLYDYNLGSITESSLWRSTDYGTTYEKLNDKVGLKTILSYLYVCPTNK
RKIMLLTDPEIESSLLISSDEGATYQKYRLNFYIQSLLFHPKQEDWILAYSQDQKLYSSA
EFGRRWQLIQEGVVPNRFYWSVMGSNKEPDLVHLEARTVDGHSHYLTCRMQNCTEANRNQ
PFPGYIDPDSLIVQDHYVFVQLTSGGRPHYYVSYRRNAFAQMKLPKYALPKDMHVISTDE
NQVFAAVQEWNQNDTYNLYISDTRGVYFTLALENVQSSRGPEGNIMIDLYEVAGIKGMFL
ANKKIDNQVKTFITYNKGRDWRLLQAPDTDLRGDPVHCLLPYCSLHLHLKVSENPYTSGI
IASKDTAPSIIVASGNIGSELSDTDISMFVSSDAGNTWRQIFEEEHSVLYLDQGGVLVAM
KHTSLPIRHLWLSFDEGRSWSKYSFTSIPLFVDGV
LGEPGEETLIMTVFGHFSHRSEWQL
VKVDYKSIFDRRCAEEDYRPWQLHSQGEACIMGAKRIYKKRKSERKCMQGKYAGAMESEP
CVCTEADFDCDYGYERHSNGQCLPAFWFNPSSLSKDCSLGQSYLNSTGYRKVVSNNCTDG
VREQYTAKPQKC
PGKAPRGLRIVTADGKLTAEQGHNVTLMVQLEEGDVQRTLIQVDFGDG
IAVSYVNLSSMEDGIKHVYQNVGIFRVTVQVDNSLGSDSA
VLYLHVTCPLEHVHLSLPFV
TTKNKEVNATAVLWPSQVGTLTYVWWYGNNTEPLITLEGSISFRFTSEGMNTITVQVSAG
NAILQDTKTIAVYEEFRSLRLSFSPNLDDYNPDIPEWRRDIGRVIKKSLVEATGVPGQHI
LVAVLPGLPTTAELFVLPYQDPAGENKRSTDDLEQISELLIHTLNQNSVHFELKPGVRVL
VHAAHLTAAPLVDLTPTHSGSAMLMLLSVVFVGLAVFVIYKFKRRVALPSPPSPSTQPGD
SSLRLQRARHATPPSTPKRGSAGAQYAI
Sequence length 1168
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism Autistic Disorder rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
22843504
Breast cancer Malignant neoplasm of breast rs587776547, rs1137887, rs137853007, rs587776650, rs80359351, rs80359714, rs121917783, rs104886456, rs121964878, rs80359874, rs80357868, rs80357508, rs387906843, rs80357569, rs80358158
View all (309 more)
Unknown
Disease term Disease name Evidence References Source
Uterine Fibroids Uterine Fibroids GWAS
Oligodendroglioma Oligodendroglioma GWAS
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 28350845
Alzheimer Disease Associate 18830724, 19241460, 21280075, 23279143, 23595767, 23673467, 23700427, 24731980, 26166206, 36697254
Arteriolosclerosis Associate 35156446
Carcinogenesis Associate 28350845
Cognition Disorders Associate 23673467
Colorectal Neoplasms Associate 33858496
Diabetes Complications Associate 19875614
Diabetes Mellitus Associate 19875614
Diabetes Mellitus Type 2 Associate 23279143
Down Syndrome Associate 26166206