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SDK1 (sidekick cell adhesion molecule 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
221935
Gene nameGene Name - the full gene name approved by the HGNC.
Sidekick cell adhesion molecule 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
SDK1
SynonymsGene synonyms aliases
-
ChromosomeChromosome number
7
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p22.2
SummarySummary 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
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
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
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
Reactome
    SDK interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Autism Autistic Disorder rs121964908, rs121912597, rs2710102, rs7794745, rs142990298, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699, rs1553510219, rs1684182454, rs1559060428, rs1553510677, rs1576352885, rs1574152522, rs1574152672, rs1696658542, rs1751123722, rs1750373491, rs1751075634 22935194
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease name Disease term dbSNP ID References
Anxiety disorder Anxiety Disorders 31116379
Gastroesophageal reflux disease Gastroesophageal reflux disease 31527586
Motion sickness Motion Sickness 25628336
Biliary cirrhosis Primary biliary cirrhosis 23000144

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