KEGG   Homo sapiens (human): 84679
Entry
84679             CDS       T01001                                 
Symbol
SLC9A7, MRX108, NHE-7, NHE7, SLC9A6
Name
(RefSeq) solute carrier family 9 member A7
  KO
K12041  solute carrier family 9 (sodium/hydrogen exchanger), member 6/7
Organism
hsa  Homo sapiens (human)
Pathway
hsa04260  Cardiac muscle contraction
Disease
H00480  X-linked intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09153 Circulatory system
   04260 Cardiac muscle contraction
    84679 (SLC9A7)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    84679 (SLC9A7)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC9: Na+/H+ exchanger
   84679 (SLC9A7)
SSDB
Motif
Pfam: Na_H_Exchanger
Other DBs
NCBI-GeneID: 84679
NCBI-ProteinID: NP_115980
OMIM: 300368
HGNC: 17123
Ensembl: ENSG00000065923
UniProt: Q96T83
Position
X:complement(46599251..46759118)
AA seq 725 aa
MEPGDAARPGSGRATGAPPPRLLLLPLLLGWGLRVAAAASASSSGAAAEDSSAMEELATE
KEAEESHRQDSVSLLTFILLLTLTILTIWLFKHRRVRFLHETGLAMIYGLIVGVILRYGT
PATSGRDKSLSCTQEDRAFSTLLVNVSGKFFEYTLKGEISPGKINSVEQNDMLRKVTFDP
EVFFNILLPPIIFHAGYSLKKRHFFRNLGSILAYAFLGTAVSCFIIGNLMYGVVKLMKIM
GQLSDKFYYTDCLFFGAIISATDPVTVLAIFNELHADVDLYALLFGESVLNDAVAIVLSS
SIVAYQPAGLNTHAFDAAAFFKSVGIFLGIFSGSFTMGAVTGVNANVTKFTKLHCFPLLE
TALFFLMSWSTFLLAEACGFTGVVAVLFCGITQAHYTYNNLSVESRSRTKQLFEVLHFLA
ENFIFSYMGLALFTFQKHVFSPIFIIGAFVAIFLGRAAHIYPLSFFLNLGRRHKIGWNFQ
HMMMFSGLRGAMAFALAIRDTASYARQMMFTTTLLIVFFTVWIIGGGTTPMLSWLNIRVG
VEEPSEEDQNEHHWQYFRVGVDPDQDPPPNNDSFQVLQGDGPDSARGNRTKQESAWIFRL
WYSFDHNYLKPILTHSGPPLTTTLPAWCGLLARCLTSPQVYDNQEPLREEDSDFILTEGD
LTLTYGDSTVTANGSSSSHTASTSLEGSRRTKSSSEEVLERDLGMGDQKVSSRGTRLVFP
LEDNA
NT seq 2178 nt   +upstreamnt  +downstreamnt
atggagcctggtgacgcggcgcgccctggctcgggtcgggctaccggggcgccgccgccg
cggctgctgctgctgccgctgctgctgggttgggggctgcgagtcgcggccgcggcctcg
gcctcctcctctggggcggcggcggaggacagcagcgccatggaggagctcgctactgag
aaggaggcggaggagagccaccggcaagacagcgtgagcctgctcaccttcatcctgctg
ctcacgctcaccatcctcaccatctggctcttcaagcaccgccgggtgcgctttctgcac
gagaccgggctggccatgatctatgggctcatcgttggggtgatcctgaggtatggtacc
cctgctaccagtggccgtgacaaatcactcagctgcactcaggaagacagggccttcagt
accttattagtgaatgtcagcggaaagttcttcgaatacactctgaaaggagaaatcagt
cctggcaagatcaacagcgtagagcagaatgatatgctacggaaggtaacattcgatcca
gaagtatttttcaacattcttctgcctccaattatttttcatgctggatacagcttaaag
aagagacactttttcagaaatcttggatctatactggcctatgccttcttggggactgct
gtttcatgcttcattattggaaatctcatgtatggtgtggtgaagctcatgaagattatg
ggacagctctcagataaattttactacacagattgtctcttttttggagcaatcatctct
gccactgacccagtgactgtgctggcgatatttaatgaattgcatgcagacgtggatctt
tacgcacttctttttggagagagcgtcctaaatgatgctgttgccattgtactgtcctcg
tctattgttgcctaccagccagcgggactgaacactcacgcctttgatgctgctgccttt
tttaagtcagttggcatttttctaggtatatttagtggctcttttaccatgggagctgtg
actggtgttaatgccaacgtgactaagtttaccaaactgcactgcttccccctgctggag
acggcgctgttcttcctcatgtcctggagcacgtttctcttggcagaagcctgcggattt
acaggtgttgtagctgtccttttctgtggaatcacacaagctcattacacctacaacaat
ctgtcggtggaatcaagaagtcgaaccaagcagctctttgaggtgttacatttcctggca
gagaacttcatcttctcctacatgggcctggcactgtttaccttccagaagcacgttttc
agccccattttcatcatcggagcttttgttgccatcttcctgggcagagccgcgcacatc
tacccgctctccttcttcctcaacttgggcagaaggcataagattggctggaattttcaa
cacatgatgatgttttcaggcctcaggggagcaatggcatttgcgttggccatccgtgac
acggcatcctatgctcgccagatgatgttcacgaccacccttctcattgtgttcttcact
gtctggatcattggaggaggcacgacacccatgttgtcatggcttaacatcagagttggc
gtcgaggagccctccgaagaggaccagaatgaacaccactggcagtacttcagagttggt
gttgaccccgatcaagacccaccacccaacaacgacagctttcaagtcttacaaggggac
ggcccagattctgccagaggaaaccggacaaaacaggagagcgcatggatattcaggctg
tggtacagctttgatcacaattacctgaagcccatcctcacacacagtggtcccccacta
accaccacgctccccgcctggtgtggcttactagctcgatgtctgaccagtccccaggtg
tacgataaccaagagccactgagagaggaagactctgatttcatcctgaccgaaggcgac
ctgacattgacctacggggacagcacagtgactgcaaatggctcctcaagttcgcacacc
gcctccacgagtctggagggcagccggagaacgaagagcagctcggaggaagtgctggag
cgagacctgggaatgggagaccagaaggtttcgagccggggcacccgcctagtgtttccc
ctggaagataatgcttga

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (18)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (16)   
DNA sequence (32)   
   RefSeq(nuc) (18)   
   GenBank (7)   
   EMBL (7)   
Protein domain (1)   
   Pfam (1)   
All databases (68)   

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