KEGG   Homo sapiens (human): 375611
Entry
375611            CDS       T01001                                 
Symbol
SLC26A5, DFNB61, PRES
Name
(RefSeq) solute carrier family 26 member 5
  KO
K14703  solute carrier family 26, member 5
Organism
hsa  Homo sapiens (human)
Disease
H00605  Deafness, autosomal recessive
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    375611 (SLC26A5)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC26: Multifunctional anion exchanger
   375611 (SLC26A5)
SSDB
Motif
Pfam: Sulfate_transp STAS
Other DBs
NCBI-GeneID: 375611
NCBI-ProteinID: NP_945350
OMIM: 604943
HGNC: 9359
Ensembl: ENSG00000170615
UniProt: P58743
Structure
Position
7:complement(103352730..103446207)
AA seq 744 aa
MDHAEENEILAATQRYYVERPIFSHPVLQERLHTKDKVPDSIADKLKQAFTCTPKKIRNI
IYMFLPITKWLPAYKFKEYVLGDLVSGISTGVLQLPQGLAFAMLAAVPPIFGLYSSFYPV
IMYCFLGTSRHISIGPFAVISLMIGGVAVRLVPDDIVIPGGVNATNGTEARDALRVKVAM
SVTLLSGIIQFCLGVCRFGFVAIYLTEPLVRGFTTAAAVHVFTSMLKYLFGVKTKRYSGI
FSVVYSTVAVLQNVKNLNVCSLGVGLMVFGLLLGGKEFNERFKEKLPAPIPLEFFAVVMG
TGISAGFNLKESYNVDVVGTLPLGLLPPANPDTSLFHLVYVDAIAIAIVGFSVTISMAKT
LANKHGYQVDGNQELIALGLCNSIGSLFQTFSISCSLSRSLVQEGTGGKTQLAGCLASLM
ILLVILATGFLFESLPQAVLSAIVIVNLKGMFMQFSDLPFFWRTSKIELTIWLTTFVSSL
FLGLDYGLITAVIIALLTVIYRTQSPSYKVLGKLPETDVYIDIDAYEEVKEIPGIKIFQI
NAPIYYANSDLYSNALKRKTGVNPAVIMGARRKAMRKYAKEVGNANMANATVVKADAEVD
GEDATKPEEEDGEVKYPPIVIKSTFPEEMQRFMPPGDNVHTVILDFTQVNFIDSVGVKTL
AGIVKEYGDVGIYVYLAGCSAQVVNDLTRNRFFENPALWELLFHSIHDAVLGSQLREALA
EQEASAPPSQEDLEPNATPATPEA
NT seq 2235 nt   +upstreamnt  +downstreamnt
atggatcatgctgaagaaaatgaaatccttgcagcaacccagaggtactatgtggaaagg
cctatctttagtcatccggtcctccaggaaagactacacacaaaggacaaggttcctgat
tccattgcggataagctgaaacaggcattcacatgtactcctaaaaaaataagaaatatc
atttatatgttcctacccataactaaatggctgccagcatacaaattcaaggaatatgtg
ttgggtgacttggtctcaggcataagcacaggggtgcttcagcttcctcaaggcttagcc
tttgcaatgctggcagctgtgcctccaatatttggcctgtactcttcattttaccctgtt
atcatgtattgttttcttggaacctccagacacatatccataggtccttttgctgttatt
agcctgatgattggtggtgtagctgttcgattagtaccagatgatatagtcattccagga
ggagtaaatgcaaccaatggcacagaggccagagatgccttgagagtgaaagtcgccatg
tctgtgaccttactttcaggaatcattcagttttgcctaggtgtctgtaggtttggattt
gtggccatatatctcacagagcctctggtccgtgggtttaccaccgcagcagctgtgcat
gtcttcacctccatgttaaaatatctgtttggagttaaaacaaagcggtacagtggaatc
ttttccgtggtgtatagtacagttgctgtgttgcagaatgttaaaaacctcaacgtgtgt
tccctaggcgtcgggctgatggtttttggtttgctgttgggtggcaaggagtttaatgag
agatttaaagagaaattgccggcgcctattcctttagagttctttgcggtcgtaatggga
actggcatttcagctgggtttaacttgaaagaatcatacaatgtggatgtcgttggaaca
cttcctctagggctgctacctccagccaatccggacaccagcctcttccaccttgtgtac
gtagatgccattgccatagccatcgttggattttcagtgaccatctccatggccaagacc
ttagcaaataaacatggctaccaggttgacggcaatcaggagctcattgccctgggactg
tgcaattccattggctcactcttccagaccttttcaatttcatgctccttgtctcgaagc
cttgttcaggagggaaccggtgggaagacacagcttgcaggttgtttggcctcattaatg
attctgctggtcatattagcaactggattcctctttgaatcattgccccaggctgtgctg
tcggccattgtgattgtcaacctgaagggaatgtttatgcagttctcagatctccccttt
ttctggagaaccagcaaaatagagctgaccatctggcttaccacttttgtgtcctccttg
ttcctgggattggactatggtttgatcactgctgtgatcattgctctgctgactgtgatt
tacagaacacagagtccaagctacaaagtccttggaaagcttcctgaaactgatgtgtat
attgatatagacgcatatgaggaggtgaaagaaattcctggaataaaaatatttcaaata
aatgcaccaatttactatgcaaatagcgacttgtatagcaatgcattaaaacgaaagact
ggagtgaacccagcagtcatcatgggagcaaggagaaaggccatgcggaagtacgctaag
gaagtcggaaatgcaaatatggccaacgcaactgttgtcaaagcagatgcagaagtagat
ggagaggatgctaccaagcctgaagaagaggatggtgaagtaaaatatcccccaatagtg
atcaaaagcacatttcctgaggaaatgcaaagatttatgcccccaggggataacgtccac
actgtcattttggatttcactcaagtcaattttattgattctgttggagtgaaaactctg
gcagggattgtaaaagaatatggagacgtcggtatatatgtatacttagcaggatgcagt
gcacaagttgtgaatgacctcactcggaatagattttttgaaaatcctgccctatgggag
ctgctgttccacagcattcatgatgcagttttaggcagccaacttagagaggcacttgct
gaacaggaagcctcggctcccccttcccaggaggacttggagcccaatgccactcctgcc
actcctgaggcatag

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (11)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (9)   
DNA sequence (40)   
   RefSeq(nuc) (16)   
   GenBank (12)   
   EMBL (12)   
3D Structure (4)   
   PDB (4)   
Protein domain (2)   
   Pfam (2)   
All databases (77)   

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