KEGG   Homo sapiens (human): 283375
Entry
283375            CDS       T01001                                 
Symbol
SLC39A5, LZT-Hs7, MYP24, ZIP5
Name
(RefSeq) solute carrier family 39 member 5
  KO
K14711  solute carrier family 39 (zinc transporter), member 5
Organism
hsa  Homo sapiens (human)
Pathway
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
Disease
H02041  Myopia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    283375 (SLC39A5)
   05012 Parkinson disease
    283375 (SLC39A5)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    283375 (SLC39A5)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC39: Metal ion transporter
   283375 (SLC39A5)
SSDB
Motif
Pfam: Zip EF-hand_Zip
Other DBs
NCBI-GeneID: 283375
NCBI-ProteinID: NP_001128667
OMIM: 608730
HGNC: 20502
Ensembl: ENSG00000139540
UniProt: Q6ZMH5
Structure
Position
12:56230051..56237846
AA seq 540 aa
MMGSPVSHLLAGFCVWVVLGWVGGSVPNLGPAEQEQNHYLAQLFGLYGENGTLTAGGLAR
LLHSLGLGRVQGLRLGQHGPLTGRAASPAADNSTHRPQNPELSVDVWAGMPLGPSGWGDL
EESKAPHLPRGPAPSGLDLLHRLLLLDHSLADHLNEDCLNGSQLLVNFGLSPAAPLTPRQ
FALLCPALLYQIDSRVCIGAPAPAPPGDLLSALLQSALAVLLLSLPSPLSLLLLRLLGPR
LLRPLLGFLGALAVGTLCGDALLHLLPHAQEGRHAGPGGLPEKDLGPGLSVLGGLFLLFV
LENMLGLLRHRGLRPRCCRRKRRNLETRNLDPENGSGMALQPLQAAPEPGAQGQREKNSQ
HPPALAPPGHQGHSHGHQGGTDITWMVLLGDGLHNLTDGLAIGAAFSDGFSSGLSTTLAV
FCHELPHELGDFAMLLQSGLSFRRLLLLSLVSGALGLGGAVLGVGLSLGPVPLTPWVFGV
TAGVFLYVALVDMLPALLRPPEPLPTPHVLLQGLGLLLGGGLMLAITLLEERLLPVTTEG
NT seq 1623 nt   +upstreamnt  +downstreamnt
atgatggggtccccagtgagtcatctgctggccggcttctgtgtgtgggtcgtcttgggc
tgggtagggggctcagtccccaacctgggccctgctgagcaggagcagaaccattacctg
gcccagctgtttggcctgtacggcgagaatgggacgctgactgcagggggcttggcgcgg
cttctccacagcctggggctaggccgagttcaggggcttcgcctgggacagcatgggcct
ctgactggacgggctgcatccccagctgcagacaattccacacacaggccacagaaccct
gagctgagtgtggatgtctgggcagggatgcctctgggtccctcagggtggggtgacctg
gaagagtcaaaggcccctcacctaccccgtgggccagccccctcgggcctggacctcctt
cacaggcttctgttgctggaccactcattggctgaccacctgaatgaggattgtctgaac
ggctcccagctgctggtcaattttggcttgagccccgctgctcctctgacccctcgtcag
tttgctctgctgtgcccagccctgctttatcagatcgacagccgcgtctgcatcggcgct
ccggcccctgcacccccaggggatctactatctgccctgcttcagagtgccctggcagtc
ctgttgctcagcctcccttctcccctatccctgctgctgctgcggctcctgggacctcgt
ctactacggcccttgctgggcttcctgggggccctggcggtgggcactctttgtggggat
gcactgctacatctgctaccgcatgcacaagaagggcggcacgcaggacctggcggacta
ccagagaaggacctgggcccggggctgtcagtgctcggaggcctcttcctgctctttgtg
ctggagaacatgctggggcttttgcggcaccgagggctcaggccaagatgctgcaggcga
aaacgaaggaatctcgaaacacgcaacttggatccggagaatggcagtgggatggccctt
cagcccctacaggcagctccagagccaggggctcagggccagagggagaagaacagccag
cacccaccagctctggcccctcctgggcaccaaggccacagtcatgggcaccagggtggc
actgatatcacgtggatggtcctcctgggagatggtctacacaacctcactgatgggctg
gccataggtgctgccttctctgatggcttctccagcggcctcagtaccaccttagcggtc
ttctgccatgagctgccccacgaactgggtgactttgccatgctgctccagtcagggctg
tcctttcggcggctgctgctgctgagcctcgtgtctggagccctgggattggggggtgca
gtcctgggggtggggctcagcctgggccctgtccccctcactccctgggtgtttggggtc
actgctggggtcttcctctatgtggcccttgtggacatgctaccagccctgcttcgtcct
ccggagcccctgcctacgccccatgtgctcctgcaggggctggggctgctgctggggggc
ggcctcatgcttgccataaccctgctggaggagcggctactgcccgtgaccactgagggc
tga

  All links  
Disease (2)   
   OMIM (2)   
Gene (14)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (20)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (18)   
DNA sequence (32)   
   RefSeq(nuc) (20)   
   GenBank (6)   
   EMBL (6)   
3D Structure (3)   
   PDB (3)   
Protein domain (2)   
   Pfam (2)   
All databases (73)   

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