KEGG   Homo sapiens (human): 7780
Entry
7780              CDS       T01001                                 
Symbol
SLC30A2, PP12488, TNZD, ZNT2, ZnT-2
Name
(RefSeq) solute carrier family 30 member 2
  KO
K14689  solute carrier family 30 (zinc transporter), member 2
Organism
hsa  Homo sapiens (human)
Disease
H01925  Transient neonatal zinc deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    7780 (SLC30A2)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC30: Zinc efflux transporter
   7780 (SLC30A2)
SSDB
Motif
Pfam: Cation_efflux
Other DBs
NCBI-GeneID: 7780
NCBI-ProteinID: NP_001004434
OMIM: 609617
HGNC: 11013
Ensembl: ENSG00000158014
UniProt: Q9BRI3
Position
1:complement(26037252..26046118)
AA seq 372 aa
MEAKEKQHLLDARPAIRSYTGSLWQEGAGWIPLPRPGLDLQAIELAAQSNHHCHAQKGPD
SHCDPKKGKAQRQLYVASAICLLFMIGEVVGGYLAHSLAVMTDAAHLLTDFASMLISLFS
LWMSSRPATKTMNFGWQRAEILGALVSVLSIWVVTGVLVYLAVERLISGDYEIDGGTMLI
TSGCAVAVNIIMGLTLHQSGHGHSHGTTNQQEENPSVRAAFIHVIGDFMQSMGVLVAAYI
LYFKPEYKYVDPICTFVFSILVLGTTLTILRDVILVLMEGTPKGVDFTAVRDLLLSVEGV
EALHSLHIWALTVAQPVLSVHIAIAQNTDAQAVLKTASSRLQGKFHFHTVTIQIEDYSED
MKDCQACQGPSD
NT seq 1119 nt   +upstreamnt  +downstreamnt
atggaggccaaggagaagcagcatctgttggacgccaggccggcaatccggtcatacacg
ggatctctgtggcaggaaggggctggctggattcctctgccccgacctggcctggacttg
caggccattgagctggctgcccagagcaaccatcactgccatgctcagaagggtcctgac
agtcactgtgaccccaagaaggggaaggcccagcgccagctgtatgtagcctctgccatc
tgcctgttgttcatgatcggagaagtcgttggtgggtacctggcacacagcttggctgtc
atgactgacgcagcacacctgctcactgactttgccagcatgctcatcagcctcttctcc
ctctggatgtcctcccggccagccaccaagaccatgaactttggctggcagagagctgag
atcttgggagccctggtctctgtactgtccatctgggtcgtgacgggggtactggtgtac
ctggctgtggagcggctgatctctggggactatgaaattgacggggggaccatgctgatc
acgtcgggctgcgctgtggctgtgaacatcataatggggttgacccttcaccagtctggc
catgggcacagccacggcaccaccaaccagcaggaggagaaccccagcgtccgagctgcc
ttcatccatgtgatcggcgactttatgcagagcatgggtgtcctagtggcagcctatatt
ttatacttcaagccagaatacaagtatgtagaccccatctgcaccttcgtcttctccatc
ctggtcctggggacaaccttgaccatcctgagagatgtgatcctggtgttgatggaaggg
acccccaagggcgttgacttcacagctgttcgtgatctgctgctgtcggtggagggggta
gaagccctgcacagcctgcatatctgggcactgacggtggcccagcctgttctgtctgtc
cacatcgccattgctcagaatacagacgcccaggctgtgctgaagacagccagcagccgc
ctccaagggaagttccacttccacaccgtgaccatccagatcgaggactactcggaggac
atgaaggactgtcaggcatgccagggcccctcagactga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (16)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (9)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (18)   
   RefSeq(nuc) (2)   
   GenBank (8)   
   EMBL (8)   
Protein domain (1)   
   Pfam (1)   
All databases (45)   

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