Homo sapiens (human): 10479 Help Entry 10479             CDS       T01001                                  Gene name SLC9A6, MRSA, NHE6 Definition (RefSeq) solute carrier family 9 member A6   KO K12041   solute carrier family 9 (sodium/hydrogen exchanger), member 6/7 Organism hsa  Homo sapiens (human) Pathway hsa04260   Cardiac muscle contraction Disease H01914   Christianson syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     10479 (SLC9A6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     10479 (SLC9A6) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC9: Na+/H+ exchanger    10479 (SLC9A6) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Na_H_Exchanger Reo_sigmaC Stevor Motif Other DBs NCBI-GeneID:  10479 NCBI-ProteinID:  NP_006350 OMIM:  300231 HGNC:  11079 Ensembl:  ENSG00000198689 Vega:  OTTHUMG00000022498 Pharos:  Q92581(Tbio) UniProt:  Q92581 LinkDB All DBs Position Xq26.3 AA seq 669 aa AA seqDB search MARRGWRRAPLRRGVGSSPRARRLMRPLWLLLAVGVFDWAGASDGGGGEARAMDEEIVSE KQAEESHRQDSANLLIFILLLTLTILTIWLFKHRRARFLHETGLAMIYGLLVGLVLRYGI HVPSDVNNVTLSCEVQSSPTTLLVTFDPEVFFNILLPPIIFYAGYSLKRRHFFRNLGSIL AYAFLGTAISCFVIGSIMYGCVTLMKVTGQLAGDFYFTDCLLFGAIVSATDPVTVLAIFH ELQVDVELYALLFGESVLNDAVAIVLSSSIVAYQPAGDNSHTFDVTAMFKSIGIFLGIFS GSFAMGAATGVVTALVTKFTKLREFQLLETGLFFLMSWSTFLLAEAWGFTGVVAVLFCGI TQAHYTYNNLSTESQHRTKQLFELLNFLAENFIFSYMGLTLFTFQNHVFNPTFVVGAFVA IFLGRAANIYPLSLLLNLGRRSKIGSNFQHMMMFAGLRGAMAFALAIRDTATYARQMMFS TTLLIVFFTVWVFGGGTTAMLSCLHIRVGVDSDQEHLGVPENERRTTKAESAWLFRMWYN FDHNYLKPLLTHSGPPLTTTLPACCGPIARCLTSPQAYENQEQLKDDDSDLILNDGDISL TYGDSTVNTEPATSSAPRRFMGNSSEDALDRELAFGDHELVIRGTRLVLPMDDSEPPLNL LDNTRHGPA NT seq 2010 nt NT seq  +upstreamnt  +downstreamnt atggctcggcgcggctggcggcgggcacccctccgccgtggcgtcggcagcagtccccga gcccgcaggctcatgcggcccctttggttgctcctcgcagtgggcgtctttgactgggca ggggcttcggacggcggcggcggagaggctagagccatggacgaggagatcgtgtccgag aagcaagccgaggagagccaccggcaggacagcgccaacctgctcatcttcatcctgctg ctcaccctcaccattctcacaatctggctcttcaagcaccgccgggcccgcttcctgcac gaaaccggcctggctatgatttatggtcttttggtgggccttgtgcttcggtatggcatt catgttccgagtgatgtaaataatgtgaccctgagctgtgaagtgcagtcaagtccaact accttactggttacttttgatccagaagtatttttcaacatattacttcctcctatcata ttttatgcaggttatagcctgaaaaggagacatttttttcgaaatcttgggtctatccta gcatacgcttttcttggaacagcaatttcttgtttcgttattgggtcaataatgtatggc tgtgtaacgctgatgaaggtaacgggacaacttgcaggagatttttactttacagattgc ctactgtttggtgccattgtatcagcaactgatccagtgactgttcttgctatattccac gagcttcaagttgatgttgaactctatgcacttctttttggtgaaagtgtcctcaatgat gctgttgccatagtgctgtcctcctcaatagtggcataccagccagctggagacaacagt cacacctttgatgtcacagcgatgttcaagtctattgggatcttccttggaatcttcagt ggatcttttgcaatgggtgctgctactggagtggtgacagctttagtgacaaagttcacc aaattacgggagttccagttgttggagacaggcctgttcttcttgatgtcctggagtacc ttcctcttggctgaagcatggggcttcacaggtgtagttgcagtattgttttgtggcatc acacaagcacattatacgtataataatttgtccacggagtctcagcatagaactaaacag ttgtttgagcttctcaatttcttggcagagaatttcatcttctcctacatggggctgaca ctgttcaccttccagaaccatgtctttaacccaacatttgtagtaggagcatttgttgct attttcttgggaagagctgccaatatttaccccttgtccctcttacttaatttgggtaga agaagtaagattggatcaaattttcaacacatgatgatgtttgctggccttcgtggtgca atggcatttgccttggccattcgagatactgccacttatgcacggcaaatgatgttcagc accacgcttctgattgtgttttttaccgtgtgggtatttggtggtggcaccactgcaatg ctgtcatgcttgcatatcagggttggtgttgattcagaccaagaacacttgggtgttcct gaaaatgaaaggagaactaccaaagcagagagtgcttggcttttccggatgtggtacaac tttgatcataactatctgaagcctctgctgacccacagcgggcctccgctgacaacaaca ctccctgcctgctgtggacccatcgccaggtgcctcaccagcccccaggcttacgaaaac caggaacagttgaaagatgatgattctgatcttattctcaatgatggtgacatcagtttg acatatggagattctactgtgaacactgaaccggccacatccagcgccccaaggagattt atgggaaacagttctgaagatgccttggatcgggagcttgcatttggggaccatgaactg gtcattcgaggaacacgcctggttcttccaatggatgattctgaacccccgctaaatttg ttagataatacgagacatggtccagcctaa

Homo sapiens (human): 84679 Help Entry 84679             CDS       T01001                                  Gene name SLC9A7, MRX108, NHE-7, NHE7, SLC9A6 Definition (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 mental retardation 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) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Na_H_Exchanger Motif Other DBs NCBI-GeneID:  84679 NCBI-ProteinID:  NP_115980 OMIM:  300368 HGNC:  17123 Ensembl:  ENSG00000065923 Vega:  OTTHUMG00000021428 Pharos:  Q96T83(Tbio) UniProt:  Q96T83 A0A024R176 LinkDB All DBs Position Xp11.3 AA seq 725 aa AA seqDB search MEPGDAARPGSGRATGAPPPRLLLLPLLLGWGLRVAAAASASSSGAAAEDSSAMEELATE KEAEESHRQDSVSLLTFILLLTLTILTIWLFKHRRVRFLHETGLAMIYGLIVGVILRYGT PATSGRDKSLSCTQEDRAFSTLLVNVSGKFFEYTLKGEISPGKINSVEQNDMLRKVTFDP EVFFNILLPPIIFHAGYSLKKRHFFRNLGSILAYAFLGTAVSCFIIGNLMYGVVKLMKIM GQLSDKFYYTDCLFFGAIISATDPVTVLAIFNELHADVDLYALLFGESVLNDAVAIVLSS SIVAYQPAGLNTHAFDAAAFFKSVGIFLGIFSGSFTMGAVTGVNANVTKFTKLHCFPLLE TALFFLMSWSTFLLAEACGFTGVVAVLFCGITQAHYTYNNLSVESRSRTKQLFEVLHFLA ENFIFSYMGLALFTFQKHVFSPIFIIGAFVAIFLGRAAHIYPLSFFLNLGRRHKIGWNFQ HMMMFSGLRGAMAFALAIRDTASYARQMMFTTTLLIVFFTVWIIGGGTTPMLSWLNIRVG VEEPSEEDQNEHHWQYFRVGVDPDQDPPPNNDSFQVLQGDGPDSARGNRTKQESAWIFRL WYSFDHNYLKPILTHSGPPLTTTLPAWCGLLARCLTSPQVYDNQEPLREEDSDFILTEGD LTLTYGDSTVTANGSSSSHTASTSLEGSRRTKSSSEEVLERDLGMGDQKVSSRGTRLVFP LEDNA NT seq 2178 nt NT seq  +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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