KEGG   Homo sapiens (human): 148867
Entry
148867            CDS       T01001                                 
Symbol
SLC30A7, ZHS, ZNT7, ZnT-7, ZnTL2
Name
(RefSeq) solute carrier family 30 member 7
  KO
K14692  solute carrier family 30 (zinc transporter), member 5/7
Organism
hsa  Homo sapiens (human)
Disease
H02529  Bone marrow failure syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    148867 (SLC30A7)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC30: Zinc efflux transporter
   148867 (SLC30A7)
SSDB
Motif
Pfam: Cation_efflux
Other DBs
NCBI-GeneID: 148867
NCBI-ProteinID: NP_001138356
OMIM: 611149
HGNC: 19306
Ensembl: ENSG00000162695
UniProt: Q8NEW0
Structure
Position
1:100896090..100996078
AA seq 376 aa
MLPLSIKDDEYKPPKFNLFGKISGWFRSILSDKTSRNLFFFLCLNLSFAFVELLYGIWSN
CLGLISDSFHMFFDSTAILAGLAASVISKWRDNDAFSYGYVRAEVLAGFVNGLFLIFTAF
FIFSEGVERALAPPDVHHERLLLVSILGFVVNLIGIFVFKHGGHGHSHGSGHGHSHSLFN
GALDQAHGHVDHCHSHEVKHGAAHSHDHAHGHGHFHSHDGPSLKETTGPSRQILQGVFLH
ILADTLGSIGVIASAIMMQNFGLMIADPICSILIAILIVVSVIPLLRESVGILMQRTPPL
LENSLPQCYQRVQQLQGVYSLQEQHFWTLCSDVYVGTLKLIVAPDADARWILSQTHNIFT
QAGVRQLYVQIDFAAM
NT seq 1131 nt   +upstreamnt  +downstreamnt
atgttgcccctgtccatcaaagacgatgaatacaaaccacccaagttcaatttgttcggc
aagatctcgggctggtttaggtctatactgtccgacaagacttcccggaacctgtttttc
ttcctgtgcctgaacctctctttcgcttttgtggaactactctacggcatctggagcaac
tgcttaggcttgatttccgactcttttcacatgtttttcgatagcactgccattttggct
ggactggcagcttctgttatttcaaaatggagagataatgatgctttctcctatgggtat
gttagagcggaagttctggctggctttgtcaatggcctatttttgatcttcactgctttt
tttattttctcagaaggagttgagagagcattagcccctccagatgtccaccatgagaga
ctgcttcttgtttccattcttgggtttgtggtaaacctaataggaatatttgttttcaaa
catggaggtcatggacattctcatggctctggccacggacacagtcattccctctttaat
ggtgctctagatcaggcacatggccatgtcgatcattgccatagccatgaagtgaaacat
ggtgctgcacatagccatgatcatgctcatggacatggacactttcattctcatgatggc
ccgtccttaaaagaaacaacaggacccagcagacagattttacaaggtgtatttttacat
atcctagcagatacacttggaagtattggtgtaattgcttctgccatcatgatgcaaaat
tttggtctgatgatagcagatcctatctgttcaattcttatagccattcttatagttgta
agtgttattcctcttttaagagaatctgttggaatattaatgcagagaactcctccccta
ttagaaaatagtctgcctcagtgctatcagagggtacagcagttgcaaggagtttacagt
ttacaggaacagcacttctggactttatgttctgacgtttatgttgggaccttgaaatta
atagtagcacctgatgctgatgctaggtggattttaagccaaacacataatatttttact
caggctggagtgagacagctctacgtacagattgactttgcagccatgtag

  All links  
Disease (2)   
   OMIM (2)   
Gene (12)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (8)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (6)   
DNA sequence (28)   
   RefSeq(nuc) (8)   
   GenBank (10)   
   EMBL (10)   
3D Structure (7)   
   PDB (7)   
Protein domain (1)   
   Pfam (1)   
All databases (58)   

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