Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
221935
Gene name Gene Name - the full gene name approved by the HGNC.
Sidekick cell adhesion molecule 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SDK1
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p22.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the immunoglobulin superfamily. The protein contains six immunoglobulin-like domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellula
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT040164 hsa-miR-615-3p CLASH 23622248
MIRT492410 hsa-miR-3173-3p PAR-CLIP 23592263
MIRT492408 hsa-miR-6891-5p PAR-CLIP 23592263
MIRT492409 hsa-miR-6783-5p PAR-CLIP 23592263
MIRT492407 hsa-miR-6892-3p 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:0005886 Component Plasma membrane TAS
GO:0007156 Process Homophilic cell adhesion via plasma membrane adhesion molecules IBA 21873635
GO:0007156 Process Homophilic cell adhesion via plasma membrane adhesion molecules ISS
GO:0007416 Process Synapse assembly IBA 21873635
GO:0007416 Process Synapse assembly ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607216 19307 ENSG00000146555
Protein
UniProt ID Q7Z5N4
Protein name Protein sidekick-1
Protein function Adhesion molecule that promotes lamina-specific synaptic connections in the retina. Expressed in specific subsets of interneurons and retinal ganglion cells (RGCs) and promotes synaptic connectivity via homophilic interactions. {ECO:0000250|UniP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13927 Ig_3 104 173 Domain
PF07679 I-set 192 278 Immunoglobulin I-set domain Domain
PF13927 Ig_3 292 365 Domain
PF07679 I-set 386 475 Immunoglobulin I-set domain Domain
PF07679 I-set 480 570 Immunoglobulin I-set domain Domain
PF13927 Ig_3 575 650 Domain
PF00041 fn3 669 755 Fibronectin type III domain Domain
PF00041 fn3 770 857 Fibronectin type III domain Domain
PF00041 fn3 871 960 Fibronectin type III domain Domain
PF00041 fn3 973 1057 Fibronectin type III domain Domain
PF00041 fn3 1071 1160 Fibronectin type III domain Domain
PF00041 fn3 1175 1264 Fibronectin type III domain Domain
PF00041 fn3 1278 1365 Fibronectin type III domain Domain
PF00041 fn3 1379 1463 Fibronectin type III domain Domain
PF00041 fn3 1478 1565 Fibronectin type III domain Domain
PF00041 fn3 1580 1689 Fibronectin type III domain Domain
PF00041 fn3 1703 1790 Fibronectin type III domain Domain
PF00041 fn3 1803 1889 Fibronectin type III domain Domain
PF00041 fn3 1904 1990 Fibronectin type III domain Domain
Tissue specificity TISSUE SPECIFICITY: Up-regulated in glomeruli in HIV-associated nephropathy. In diseased glomeruli, significantly overexpressed and the expression is no longer restricted to mesangial cells but includes podocytes and parietal epithelial cells (PubMed:1521
Sequence
MARGARPSAAGGGGGGAEPPERAGPGRPRGSPPGRARPSLAPRPGPEPSRPRAAPETSGG
DTAGAGRCGGRRAAKLGPGRRGWWALLALQLHLLRALAQDDVAPYFKTEPGLPQIHLEGN
RLVLTCLAEGSWPLEFKWMRDDSELTTYSSEYKYIIPSLQKLDAGFYRCVVRN
RMGALLQ
RKSEVQVAYMGSFMDTDQRKTVSQGRAAILNLLPITSYPRPQVTWFREGHKIIPSNRIAI
TLENQLVILATTTSDAGAYYVQAVNEKNGENKTSPFIH
LSIARDVGTPETMAPTIVVPPG
NRSVVAGSSETTLECIASARPVEDLSVTWKRNGVRITSGLHSFGRRLTISNPTSADTGPY
VCEAA
LPGSAFEPARATAFLFIIEPPYFTAEPESRISAEVEETVDIGCQAMGVPLPTLQW
YKDAISISRLQNPRYKVLASGGLRIQKLRPEDSGIFQCFASNEGGEIQTHTYLDV
TNIAP
VFTQRPVDTTVTDGMTAILRCEVSGAPKPAITWKRENHILASGSVRIPRFMLLESGGLQI
APVFIQDAGNYTCYAANTEGSLNASATLTV
WNRTSIVHPPEDHVVIKGTTATLHCGATHD
PRVSLRYVWKKDNVALTPSSTSRIVVEKDGSLLISQTWSGDIGDYSCEIV
SEGGNDSRMA
RLEVIELPHSPQNLLVSPNSSHSHAVVLSWVRPFDGNSPILYYIVELSENNSPWKVHLSN
VGPEMTGVTVSGLTPARTYQFRVCAVNEVGRGQYS
AETSRLMLPEEPPSAPPKNIVASGR
TNQSIMVQWQPPPETEHNGVLRGYILRYRLAGLPGEYQQRNITSPEVNYCLVTDLIIWTQ
YEIQVAAYNGAGLGVFS
RAVTEYTLQGVPTAPPQNVQTEAVNSTTIQFLWNPPPQQFING
INQGYKLLAWPADAPEAVTVVTIAPDFHGVHHGHITNLKKFTAYFTSVLCFTTPGDGPPS

TPQLVWTQEDKPGAVGHLSFTEILDTSLKVSWQEPLEKNGIITGYQISWEVYGRNDSRLT
HTLNSTTHEYKIQGLSSLTTYTIDVAAVTAVGTGLVT
SSTISSGVPPDLPGAPSNLVISN
ISPRSATLQFRPGYDGKTSISRWIVEGQVGAIGDEEEWVTLYEEENEPDAQMLEIPNLTP
YTHYRFRMKQVNIVGPSPYS
PSSRVIQTLQAPPDVAPTSVTVRTASETSLRLRWVPLPDS
QYNGNPESVGYRIKYWRSDLQSSAVAQVVSDRLEREFTIEELEEWMEYELQMQAFNAVGA
GPWS
EVVRGRTRESVPSAAPENVSAEAVSSTQILLTWTSVPEQDQNGLILGYKILFRAKD
LDPEPRSHIVRGNHTQSALLAGLRKFVLYELQVLAFTRIGNGVPS
TPLILERTKDDAPGP
PVRLVFPEVRLTSVRIVWQPPEEPNGIILGYQIAYRLASSSPHTFTTVEVGATVRQFTAT
DLAPESAYIFRLSAKTRQGWGEP
LEATVITTEKRERPAPPRELLVPQAEVTARSLRLQWV
PGSDGASPIRYFTMQVRELPRGEWQTYSSSISHEATACVVDRLRPFTSYKLRLKATNDIG
DSDFS
SETEAVTTLQDVPGEPPGSVSATPHTTSSVLIQWQPPRDESLNGLLQGYRIYYRE
LEYEAGSGTEAKTLKNPIALHAELTAQSSFKTVNSSSTSTMCELTHLKKYRRYEVIMTAY
NIIGESPAS
APVEVFVGEAAPAMAPQNVQVTPLTASQLEVTWDPPPPESQNGNIQGYKIY
YWEADSQNETEKMKVLFLPEPVVRLKNLTSHTKYLVSISAFNAAGDGPKS
DPQQGRTHQA
APGAPSFLAFSEITSTTLNVSWGEPAAANGILQGYRVVYEPLAPVQGVSKVVTVEVRGNW
QRWLKVRDLTKGVTYFFRVQARTITYGPE
LQANITAGPAEGSPGSPRDVLVTKSASELTL
QWTEGHSGDTPTTGYVIEARPSDEGLWDMFVKDIPRSATSYTLSLDKLRQGVTYEFRVVA
VNEAGYGEPS
NPSTAVSAQVEAPFYEEWWFLLVMALSSLIVILLVVFALVLHGQNKKYKN
CSTGKGISTMEESVTLDNGGFAALELSSRHLNVKSTFSKKNGTRSPPRPSPGGLHYSDED
ICNKYNGAVLTESVSLKEKSADASESEATDSDYEDALPKHSFVNHYMSDPTYYNSWKRRA
QGRAPAPHRYEAVAGSEAGAQLHPVITTQSAGGVYTPAGPGARTPLTGFSSFV
Sequence length 2213
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    SDK 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)
22935194
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Eczema Eczema GWAS
Dermatitis Dermatitis GWAS
Asthma Asthma GWAS
Gastroesophageal Reflux Disease Gastroesophageal Reflux Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 35441736, 35733175
Adrenocortical Carcinoma Associate 25490274
Alzheimer Disease Associate 36928034
Autism Spectrum Disorder Associate 32807774
Autistic Disorder Associate 24204716
Bipolar Disorder Associate 34341362
Cap Myopathy Associate 23576568
Carcinogenesis Associate 25490274
Carcinoma Hepatocellular Associate 28514750
Cardiovascular Diseases Associate 34895303