KEGG   Homo sapiens (human): 9187
Entry
9187              CDS       T01001                                 
Symbol
SLC24A1, CSNB1D, HsT17412, NCKX, NCKX1, RODX
Name
(RefSeq) solute carrier family 24 member 1
  KO
K13749  solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04744  Phototransduction
Disease
H00787  Congenital stationary night blindness
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09157 Sensory system
   04744 Phototransduction
    9187 (SLC24A1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    9187 (SLC24A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC24: Na+/(Ca2+-K+) exchanger
   9187 (SLC24A1)
SSDB
Motif
Pfam: Na_Ca_ex
Other DBs
NCBI-GeneID: 9187
NCBI-ProteinID: NP_004718
OMIM: 603617
HGNC: 10975
Ensembl: ENSG00000074621
UniProt: O60721
Position
15:65611350..65661002
AA seq 1099 aa
MGKLIRMGPQERWLLRTKRLHWSRLLFLLGMLIIGSTYQHLRRPRGLSSLWAAVSSHQPI
KLASRDLSSEEMMMMSSSPSKPSSEMGGKMLVPQASVGSDEATLSMTVENIPSMPKRTAK
MIPTTTKNNYSPTAAGTERRKEDTPTSSRTLTYYTSTSSRQIVKKYTPTPRGEMKSYSPT
QVREKVKYTPSPRGRRVGTYVPSTFMTMETSHAITPRTTVKDSDITATYKILETNSLKRI
MEETTPTTLKGMFDSTPTFLTHEVEANVLTSPRSVMEKNNLFPPRRVESNSSAHPWGLVG
KSNPKTPQGTVLLHTPATSEGQVTISTMTGSSPAETKAFTAAWSLRNPSPRTSVSAIKTA
PAIVWRLAKKPSTAPSTSTTPTVRAKLTMQVHHCVVVKPTPAMLTTPSPSLTTALLPEEL
SPSPSVLPPSLPDLHPKGEYPPDLFSVEERRQGWVVLHVFGMMYVFVALAIVCDEYFVPA
LGVITDKLQISEDVAGATFMAAGGSAPELFTSLIGVFISHSNVGIGTIVGSAVFNILFVI
GTCSLFSREILNLTWWPLFRDVSFYILDLIMLILFFLDSLIAWWESLLLLLAYAFYVFTM
KWNKHIEVWVKEQLSRRPVAKVMALEDLSKPGDGAIAVDELQDNKKLKLPSLLTRGSSST
SLHNSTIRSTIYQLMLHSLDPLREVRLAKEKEEESLNQGARAQPQAKAESKPEEEEPAKL
PAVTVTPAPVPDIKGDQKENPGGQEDVAEAESTGEMPGEEGETAGEGETEEKSGGETQPE
GEGETETQGKGEECEDENEAEGKGDNEGEDEGEIHAEDGEMKGNEGETESQELSAENHGE
AKNDEKGVEDGGGSDGGDSEEEEEEEEEQEEEEEEEEQEEEEEEEEEEEEKGNEEPLSLD
WPETRQKQAIYLFLLPIVFPLWLTVPDVRRQESRKFFVFTFLGSIMWIAMFSYLMVWWAH
QVGETIGISEEIMGLTILAAGTSIPDLITSVIVARKGLGDMAVSSSVGSNIFDITVGLPV
PWLLFSLINGLQPVPVSSNGLFCAIVLLFLMLLFVISSIASCKWRMNKILGFTMFLLYFV
FLIISVMLEDRIISCPVSV
NT seq 3300 nt   +upstreamnt  +downstreamnt
atggggaaattgatcaggatggggccgcaagagaggtggttactccggacaaagcggctt
cattggagtcgcctcctcttcttactgggaatgttgatcatcggttctacttatcagcac
cttaggagaccccggggcctttcctcattgtgggcagcagtctcttctcatcagcctata
aaactggccagtcgggacctctccagtgaagagatgatgatgatgagcagcagcccttca
aaacctagctccgaaatggggggtaagatgctggtaccccaagcctcagtgggcagtgat
gaagcaacactgagcatgacagtggagaatatccccagtatgcctaaaagaacagccaag
atgatcccaacaacaaccaagaataattacagcccaacagcagcaggtacagaaagaagg
aaggaagacaccccaacatccagtagaacactgacttactacacctcaacttcaagcaga
caaatagtaaaaaagtataccccaacacccaggggagaaatgaagagctacagcccaact
caagtgagggaaaaggtgaagtatactccttccccacgtggtagaagagtaggcacttac
gtgccgtccacattcatgacaatggaaacaagccatgcgatcacccccaggacaacagtg
aaagacagtgacattacagcaacctataaaatactcgaaaccaactctcttaagagaata
atggaggaaaccaccccaaccactctcaagggaatgtttgatagcaccccaacttttctg
acacatgaggtagaagcaaacgtcttgacttctccaaggagcgtcatggaaaaaaacaac
ctgtttccccccagaagagtggaaagtaacagctcagcccatccctgggggttagtggga
aagagcaacccgaagactccccagggaacagtcctgttgcataccccagccacctctgag
gggcaggtgacaataagcaccatgacaggcagcagcccagcagaaaccaaagccttcact
gctgcctggagtcttaggaatccttcacccaggaccagtgtatcagccatcaaaacagcc
ccagccatagtctggaggctggcaaagaaaccttccacagcacccagcacctcaacaacc
cctacggtcagggcaaagctgaccatgcaggtccatcactgtgtggttgtgaagccaacc
ccagccatgctcaccactccctccccaagcctcacaacagccctgctcccagaggagctc
agtcctagtccctcagtgctgcctcccagcttgccagacctccaccccaagggagagtac
cccccagatctgttcagtgtggaggagcggcggcagggctgggtggtcctgcacgttttt
ggcatgatgtatgtgtttgtggccttggccattgtttgcgacgagtacttcgttccagcc
ctgggtgtcatcacagacaagctgcagatctccgaggatgtggcaggcgccacattcatg
gctgctggaggctctgctcctgagctcttcacctccctcatcggtgtcttcatttcccac
agcaacgtgggcattggtaccattgtgggctctgctgtgttcaacattctctttgtcatt
ggcacttgttccctcttctcccgagagatcctcaacctcacctggtggcccttattccgt
gatgtctccttctacatccttgacctgataatgctcatcctcttcttcctggacagcctc
attgcctggtgggagagcctgctgctgctgctggcctatgccttctatgtgttcaccatg
aagtggaacaagcatatcgaggtctgggtgaaggagcagctcagcaggaggccagtggcc
aaggtcatggccttagaagacctcagcaagccgggcgatggggccattgcggtggatgag
ctacaggataacaagaagctgaagctcccgtccttgctgacccgagggagcagctcgacc
tctctgcacaacagcaccatccgcagcaccatctaccagctcatgctccacagcctggac
cccctgagggaagttcgccttgccaaggagaaggaggaggagagcttgaatcaaggggcc
agagcccaaccccaggccaaagcagaaagcaaaccagaagaggaggagccagccaagctc
cctgcggtcacggtcacaccagcccctgttccagacatcaagggagatcagaaggagaat
ccaggcggtcaggaagatgtggctgaggccgagagcacaggtgaaatgccaggcgaagag
ggcgaaactgctggtgaaggtgaaactgaagagaaaagtggaggtgaaactcaaccagaa
ggtgaaggtgaaactgaaacacaaggaaaaggagaagaatgtgaagatgaaaatgaagca
gaaggaaaaggagacaatgaaggtgaagatgagggtgaaatccacgcagaagatggtgaa
atgaaaggtaatgaaggtgaaactgaaagccaggaactcagtgctgaaaatcacggtgaa
gccaaaaatgatgagaaaggtgtagaagatggagggggaagtgatggaggggatagcgaa
gaggaggaagaggaggaggaagagcaggaggaagaggaggaggaggaagagcaggaggaa
gaggaggaggaggaggaggaagaggaggagaagggaaatgaagagcctctgtccctggac
tggcctgaaaccaggcagaagcaggccatttacctcttccttctgcccatcgtgttccca
ctgtggctgacagtccccgacgtccgaaggcaggagtctaggaagttttttgttttcacc
ttcctgggatctatcatgtggatagccatgttctcatacctcatggtgtggtgggctcac
caggttggtgaaacaatagggatttctgaagagatcatgggcctgacaatccttgcagca
ggcacatcaattcctgacctcatcaccagtgtgattgtcgctcgaaaaggcctgggagac
atggctgtgtcaagctctgtgggcagtaacatatttgatatcactgtgggcttgcctgtt
ccttggttgcttttctctcttatcaatggattacagccagttccagtcagcagcaatggc
ttgttttgtgcaattgttttgctttttctcatgcttctgtttgtgatctcttcaattgcg
tcatgtaaatggagaatgaacaagatcctgggcttcacaatgttcctcctttactttgta
ttcctgataatcagtgtgatgttagaagatcgaatcatatcctgtcctgtatctgtctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (41)   
   KEGG ORTHOLOGY (1)   
   RefGene (33)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (54)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (52)   
DNA sequence (84)   
   RefSeq(nuc) (54)   
   GenBank (15)   
   EMBL (15)   
Protein domain (1)   
   Pfam (1)   
All databases (187)   

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