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  
Disease (3)   
   OMIM (3)   
Gene (40)   
   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 (182)   

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