KEGG   Homo sapiens (human): 64116
Entry
64116             CDS       T01001                                 
Symbol
SLC39A8, BIGM103, CDG2N, LZT-Hs6, PP3105, ZIP8
Name
(RefSeq) solute carrier family 39 member 8
  KO
K14714  solute carrier family 39 (zinc transporter), member 8
Organism
hsa  Homo sapiens (human)
Pathway
hsa04216  Ferroptosis
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
Network
nt06525  Ferroptosis
  Element
N01587  Fe-TF transport
Disease
H00119  Congenital disorders of glycosylation type II
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    64116 (SLC39A8)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    64116 (SLC39A8)
   05012 Parkinson disease
    64116 (SLC39A8)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    64116 (SLC39A8)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC39: Metal ion transporter
   64116 (SLC39A8)
SSDB
Motif
Pfam: Zip EF-hand_Zip DUF4271
Other DBs
NCBI-GeneID: 64116
NCBI-ProteinID: NP_001128618
OMIM: 608732
HGNC: 20862
Ensembl: ENSG00000138821
UniProt: Q9C0K1
Position
4:complement(102251041..102345482)
AA seq 460 aa
MAPGRAVAGLLLLAAAGLGGVAEGPGLAFSEDVLSVFGANLSLSAAQLQHLLEQMGAASR
VGVPEPGQLHFNQCLTAEEIFSLHGFSNATQITSSKFSVICPAVLQQLNFHPCEDRPKHK
TRPSHSEVWGYGFLSVTIINLASLLGLILTPLIKKSYFPKILTFFVGLAIGTLFSNAIFQ
LIPEAFGFDPKVDSYVEKAVAVFGGFYLLFFFERMLKMLLKTYGQNGHTHFGNDNFGPQE
KTHQPKALPAINGVTCYANPAVTEANGHIHFDNVSVVSLQDGKKEPSSCTCLKGPKLSEI
GTIAWMITLCDALHNFIDGLAIGASCTLSLLQGLSTSIAILCEEFPHELGDFVILLNAGM
STRQALLFNFLSACSCYVGLAFGILVGNNFAPNIIFALAGGMFLYISLADMFPEMNDMLR
EKVTGRKTDFTFFMIQNAGMLTGFTAILLITLYAGEIELE
NT seq 1383 nt   +upstreamnt  +downstreamnt
atggccccgggtcgcgcggtggccgggctcctgttgctggcggccgccggcctcggagga
gtggcggaggggccagggctagccttcagcgaggatgtgctgagcgtgttcggcgcgaat
ctgagcctgtcggcggcgcagctccagcacttgctggagcagatgggagccgcctcccgc
gtgggcgtcccggagcctggccagctgcacttcaaccagtgtttaactgctgaagagatc
ttttcccttcatggcttttcaaatgctacccaaataaccagctccaaattctctgtcatc
tgtccagcagtcttacagcaattgaactttcacccatgtgaggatcggcccaagcacaaa
acaagaccaagtcattcagaagtttggggatatggattcctgtcagtgacgattattaat
ctggcatctctcctcggattgattttgactccactgataaagaaatcttatttcccaaag
attttgaccttttttgtggggctggctattgggactcttttttcaaatgcaattttccaa
cttattccagaggcatttggatttgatcccaaagtcgacagttatgttgagaaggcagtt
gctgtgtttggtggattttacctacttttcttttttgaaagaatgctaaagatgttatta
aagacatatggtcagaatggtcatacccactttggaaatgataactttggtcctcaagaa
aaaactcatcaacctaaagcattacctgccatcaatggtgtgacatgctatgcaaatcct
gctgtcacagaagctaatggacatatccattttgataatgtcagtgtggtatctctacag
gatggaaaaaaagagccaagttcatgtacctgtttgaaggggcccaaactgtcagaaata
gggacgattgcctggatgataacgctctgcgatgccctccacaatttcatcgatggcctg
gcgattggggcttcctgcaccttgtctctccttcagggactcagtacttccatagcaatc
ctatgtgaggagtttccccacgagttaggagactttgtgatcctactcaatgcagggatg
agcactcgacaagccttgctattcaacttcctttctgcatgttcctgctatgttgggcta
gcttttggcattttggtgggcaacaatttcgctccaaatattatatttgcacttgctgga
ggcatgttcctctatatttctctggcagatatgtttccagagatgaatgatatgctgaga
gaaaaggtaactggaagaaaaaccgatttcaccttcttcatgattcagaatgctggaatg
ttaactggattcacagccattctactcattaccttgtatgcaggagaaatcgaattggag
taa

  All links  
Disease (2)   
   OMIM (2)   
Gene (15)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (16)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (14)   
DNA sequence (40)   
   RefSeq(nuc) (14)   
   GenBank (13)   
   EMBL (13)   
Protein domain (3)   
   Pfam (3)   
All databases (76)   

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