Homo sapiens (human): 91252
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Zip
Motif
Other DBs
NCBI-GeneID:
91252
NCBI-ProteinID:
NP_001121697
OMIM:
608735
HGNC:
20859
Ensembl:
ENSG00000165915
UniProt:
Q96H72
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All DBs
Position
11:47407276..47416500
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AA seq
371 aa
AA seq
DB search
MPGCPCPGCGMAGPRLLFLTALALELLERAGGSQPALRSRGTATACRLDNKESESWGALL
SGERLDTWICSLLGSLMVGLSGVFPLLVIPLEMGTMLRSEAGAWRLKQLLSFALGGLLGN
VFLHLLPEAWAYTCSASPGGEGQSLQQQQQLGLWVIAGILTFLALEKMFLDSKEEGTSQA
PNKDPTAAAAALNGGHCLAQPAAEPGLGAVVRSIKVSGYLNLLANTIDNFTHGLAVAASF
LVSKKIGLLTTMAILLHEIPHEVGDFAILLRAGFDRWSAAKLQLSTALGGLLGAGFAICT
QSPKGVVGCSPAAEETAAWVLPFTSGGFLYIALVNVLPDLLEEEDPWRSLQQLLLLCAGI
VVMVLFSLFVD
NT seq
1116 nt
NT seq
+upstream
nt +downstream
nt
atgcctggatgtccctgccctggctgtggcatggcgggcccaaggctcctcttcctcact
gcccttgccctggagctcttggaaagggctgggggttcccagccggccctccggagccgg
gggactgcgacggcctgtcgcctggacaacaaggaaagcgagtcctggggggctctgctg
agcggagagcggctggacacctggatctgctccctcctgggttccctcatggtggggctc
agtggggtcttcccgttgcttgtcattcccctagagatggggaccatgctgcgctcagaa
gctggggcctggcgcctgaagcagctgctcagcttcgccctggggggactcttgggcaat
gtgtttctgcatctgctgcccgaagcctgggcctacacgtgcagcgccagccctggtggt
gaggggcagagcctgcagcagcagcaacagctggggctgtgggtcattgctggcatcctg
accttcctggcgttggagaagatgttcctggacagcaaggaggaggggaccagccaggcc
cccaacaaagaccccactgctgctgccgccgcgctcaatggaggccactgtctggcccag
ccggctgcagagcccggcctcggtgccgtggtccggagcatcaaagtcagcggctacctc
aacctgctggccaacaccatcgataacttcacccacgggctggctgtggctgccagcttc
cttgtgagcaagaagatcgggctcctgacaaccatggccatcctcctgcatgagatcccc
catgaggtgggcgactttgccatcctgctccgggccggctttgaccgatggagcgcagcc
aagctgcaactctcaacagcgctggggggcctactgggcgctggcttcgccatctgtacc
cagtcccccaagggagtagttgggtgttctcccgctgcagaggagacggcagcctgggtc
ctgcccttcacctctggcggctttctctacatcgccttggtgaacgtgctccctgacctc
ttggaagaagaggacccgtggcgctccctgcagcagctgcttctgctctgtgcgggcatc
gtggtaatggtgctgttctcgctcttcgtggattaa
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