KEGG   Homo sapiens (human): 55532
Entry
55532             CDS       T01001                                 
Symbol
SLC30A10, HMDPC, HMNDYT1, ZNT10, ZNT8, ZRC1, ZnT-10
Name
(RefSeq) solute carrier family 30 member 10
  KO
K14697  solute carrier family 30 (zinc transporter), member 10
Organism
hsa  Homo sapiens (human)
Disease
H01938  Hypermanganesemia with dystonia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    55532 (SLC30A10)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC30: Zinc efflux transporter
   55532 (SLC30A10)
SSDB
Motif
Pfam: Cation_efflux DUF2530 Dicty_CAR
Other DBs
NCBI-GeneID: 55532
NCBI-ProteinID: NP_061183
OMIM: 611146
HGNC: 25355
Ensembl: ENSG00000196660
UniProt: Q6XR72 B3KR19
Position
1:complement(219910445..219959098)
AA seq 485 aa
MGRYSGKTCRLLFMLVLTVAFFVAELVSGYLGNSIALLSDSFNMLSDLISLCVGLSAGYI
ARRPTRGFSATYGYARAEVVGALSNAVFLTALCFTIFVEAVLRLARPERIDDPELVLIVG
VLGLLVNVVGLLIFQDCAAWFACCLRGRSRRLQQRQQLAEGCVPGAFGGPQGAEDPRRAA
DPTAPGSDSAVTLRGTSVERKREKGATVFANVAGDSFNTQNEPEDMMKKEKKSEALNIRG
VLLHVMGDALGSVVVVITAIIFYVLPLKSEDPCNWQCYIDPSLTVLMVIIILSSAFPLIK
ETAAILLQMVPKGVNMEELMSKLSAVPGISSVHEVHIWELVSGKIIATLHIKYPKDRGYQ
DASTKIREIFHHAGIHNVTIQFENVDLKEPLEQKDLLLLCNSPCISKGCAKQLCCPPGAL
PLAHVNGCAEHNGGPSLDTYGSDGLSRRDAREVAIEVSLDSCLSDHGQSLNKTQEDQCYV
NRTHF
NT seq 1458 nt   +upstreamnt  +downstreamnt
atgggccgctactctggcaagacgtgccggctgctcttcatgctggtgctcaccgtcgcc
ttcttcgtggcggagctggtctccggctacctgggcaactccatcgcgctgctctccgac
tccttcaacatgctctccgacctgatctcgctgtgcgtgggcctgagcgccggctacatc
gcccggcgccccacccggggcttcagcgccacctacggctacgcccgcgccgaggtggtg
ggcgcgctgagcaacgcggtcttcctcaccgcgctctgcttcaccatcttcgtggaggcc
gtgctgcgcctggcccggcccgagcgcatcgatgaccccgagctggtgctcatcgtcggc
gtcctggggctgttggtcaacgtggtggggctgctcatcttccaggactgcgccgcctgg
ttcgcgtgctgcctccggggacgcagtcgccgcctgcagcagcggcagcagctggcggag
ggctgtgtccccggcgctttcggggggcctcagggcgcggaggacccgcggcgcgcggcg
gacccgacagccccaggctcggactcggccgtaaccctccgggggacctcggtggaaagg
aagcgggagaagggggcgaccgtgttcgcaaacgtagcaggtgattccttcaacacccag
aatgagccagaagacatgatgaaaaaagagaaaaagtctgaagctctgaatatcagaggt
gtacttttgcatgtgatgggagatgccctggggtccgtggttgtggtcatcacggccatc
atattctatgtgcttcccctgaagagtgaggacccgtgtaactggcagtgttacattgac
cccagcctgactgtcctcatggtcatcatcattttgtcatctgccttcccgcttatcaag
gagaccgctgccattctgctacagatggtcccaaaaggagtcaacatggaagagctgatg
agtaaactctctgctgtgcctggaattagcagtgtacatgaagtgcacatctgggaactt
gtaagtggaaagattattgccaccctgcacatcaagtatcctaaggacaggggatatcaa
gatgccagcacaaaaattcgagaaatcttccaccatgcgggaatccacaatgtgaccatc
cagtttgaaaatgtggacttgaaggaacccctggagcagaaggacttactgttgctctgc
aactcaccctgcatctccaagggctgtgctaagcagctgtgttgtccccccggggcactg
cctctggctcacgtcaatggctgtgctgagcacaatggtgggccctctctagacacatac
ggaagtgatggcctcagtagaagagacgcaagagaagtggctattgaagtgtctttggat
agctgtctgagtgaccacggacaaagtcttaacaaaactcaggaggaccaatgttatgtc
aacagaacgcatttttaa

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (13)   
   KEGG ORTHOLOGY (1)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (7)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (17)   
   RefSeq(nuc) (5)   
   GenBank (6)   
   EMBL (6)   
Protein domain (3)   
   Pfam (3)   
All databases (46)   

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