KEGG   Homo sapiens (human): 91252
Entry
91252             CDS       T01001                                 
Symbol
SLC39A13, EDSSPD3, LZT-Hs9, SCDEDS, ZIP13
Name
(RefSeq) solute carrier family 39 member 13
  KO
K14719  solute carrier family 39 (zinc transporter), member 13
Organism
hsa  Homo sapiens (human)
Pathway
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
Disease
H02239  Ehlers-Danlos syndrome, spondylodysplastic type
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    91252 (SLC39A13)
   05012 Parkinson disease
    91252 (SLC39A13)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    91252 (SLC39A13)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC39: Metal ion transporter
   91252 (SLC39A13)
SSDB
Motif
Pfam: Zip
Other DBs
NCBI-GeneID: 91252
NCBI-ProteinID: NP_001121697
OMIM: 608735
HGNC: 20859
Ensembl: ENSG00000165915
UniProt: Q96H72
Position
11:47407276..47416500
AA seq 371 aa
MPGCPCPGCGMAGPRLLFLTALALELLERAGGSQPALRSRGTATACRLDNKESESWGALL
SGERLDTWICSLLGSLMVGLSGVFPLLVIPLEMGTMLRSEAGAWRLKQLLSFALGGLLGN
VFLHLLPEAWAYTCSASPGGEGQSLQQQQQLGLWVIAGILTFLALEKMFLDSKEEGTSQA
PNKDPTAAAAALNGGHCLAQPAAEPGLGAVVRSIKVSGYLNLLANTIDNFTHGLAVAASF
LVSKKIGLLTTMAILLHEIPHEVGDFAILLRAGFDRWSAAKLQLSTALGGLLGAGFAICT
QSPKGVVGCSPAAEETAAWVLPFTSGGFLYIALVNVLPDLLEEEDPWRSLQQLLLLCAGI
VVMVLFSLFVD
NT seq 1116 nt   +upstreamnt  +downstreamnt
atgcctggatgtccctgccctggctgtggcatggcgggcccaaggctcctcttcctcact
gcccttgccctggagctcttggaaagggctgggggttcccagccggccctccggagccgg
gggactgcgacggcctgtcgcctggacaacaaggaaagcgagtcctggggggctctgctg
agcggagagcggctggacacctggatctgctccctcctgggttccctcatggtggggctc
agtggggtcttcccgttgcttgtcattcccctagagatggggaccatgctgcgctcagaa
gctggggcctggcgcctgaagcagctgctcagcttcgccctggggggactcttgggcaat
gtgtttctgcatctgctgcccgaagcctgggcctacacgtgcagcgccagccctggtggt
gaggggcagagcctgcagcagcagcaacagctggggctgtgggtcattgctggcatcctg
accttcctggcgttggagaagatgttcctggacagcaaggaggaggggaccagccaggcc
cccaacaaagaccccactgctgctgccgccgcgctcaatggaggccactgtctggcccag
ccggctgcagagcccggcctcggtgccgtggtccggagcatcaaagtcagcggctacctc
aacctgctggccaacaccatcgataacttcacccacgggctggctgtggctgccagcttc
cttgtgagcaagaagatcgggctcctgacaaccatggccatcctcctgcatgagatcccc
catgaggtgggcgactttgccatcctgctccgggccggctttgaccgatggagcgcagcc
aagctgcaactctcaacagcgctggggggcctactgggcgctggcttcgccatctgtacc
cagtcccccaagggagtagttgggtgttctcccgctgcagaggagacggcagcctgggtc
ctgcccttcacctctggcggctttctctacatcgccttggtgaacgtgctccctgacctc
ttggaagaagaggacccgtggcgctccctgcagcagctgcttctgctctgtgcgggcatc
gtggtaatggtgctgttctcgctcttcgtggattaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (2)   
   KEGG PATHWAY (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (13)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (31)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (29)   
DNA sequence (82)   
   RefSeq(nuc) (42)   
   GenBank (20)   
   EMBL (20)   
Protein domain (1)   
   Pfam (1)   
All databases (135)   

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