KEGG   Homo sapiens (human): 23516
Entry
23516             CDS       T01001                                 
Symbol
SLC39A14, HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19
Name
(RefSeq) solute carrier family 39 member 14
  KO
K14720  solute carrier family 39 (zinc transporter), member 14
Organism
hsa  Homo sapiens (human)
Pathway
hsa04216  Ferroptosis
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
Network
nt06525  Ferroptosis
  Element
N01587  Fe-TF transport
Disease
H01938  Hypermanganesemia with dystonia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    23516 (SLC39A14)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    23516 (SLC39A14)
   05012 Parkinson disease
    23516 (SLC39A14)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    23516 (SLC39A14)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC39: Metal ion transporter
   23516 (SLC39A14)
SSDB
Motif
Pfam: Zip
Other DBs
NCBI-GeneID: 23516
NCBI-ProteinID: NP_001121903
OMIM: 608736
HGNC: 20858
Ensembl: ENSG00000104635
UniProt: Q15043
Position
8:22367278..22434129
AA seq 492 aa
MKLLLLHPAFQSCLLLTLLGLWRTTPEAHASSLGAPAISAASFLQDLIHRYGEGDSLTLQ
QLKALLNHLDVGVGRGNVTQHVQGHRNLSTCFSSGDLFTAHNFSEQSRIGSSELQEFCPT
ILQQLDSRACTSENQENEENEQTEEGRPSAVEVWGYGLLCVTVISLCSLLGASVVPFMKK
TFYKRLLLYFIALAIGTLYSNALFQLIPEAFGFNPLEDYYVSKSAVVFGGFYLFFFTEKI
LKILLKQKNEHHHGHSHYASESLPSKKDQEEGVMEKLQNGDLDHMIPQHCSSELDGKAPM
VDEKVIVGSLSVQDLQASQSACYWLKGVRYSDIGTLAWMITLSDGLHNFIDGLAIGASFT
VSVFQGISTSVAILCEEFPHELGDFVILLNAGMSIQQALFFNFLSACCCYLGLAFGILAG
SHFSANWIFALAGGMFLYISLADMFPEMNEVCQEDERKGSILIPFIIQNLGLLTGFTIMV
VLTMYSGQIQIG
NT seq 1479 nt   +upstreamnt  +downstreamnt
atgaagctgctgctgctgcacccggccttccagagctgcctcctgctgaccctgcttggc
ttatggagaaccacccctgaggctcacgcttcatccctgggtgcaccagctatcagcgct
gcctccttcctgcaggatctaatacatcggtatggcgagggtgacagcctcactctgcag
cagctgaaggccctactcaaccacctggatgtgggagtgggccggggtaatgtcacccag
cacgtgcaaggacacaggaacctctccacgtgctttagttctggagacctcttcactgcc
cacaatttcagcgagcagtcgcggattgggagcagcgagctccaggagttctgccccacc
atcctccagcagctggattcccgggcctgcacctcggagaaccaggaaaacgaggagaat
gagcagacggaggaggggcggccaagcgctgttgaagtgtggggatacggtctcctctgt
gtgaccgtcatctccctctgctccctcctgggggccagcgtggtgcccttcatgaagaag
accttttacaagaggctgctgctctacttcatagctctggcgattggaaccctctactcc
aacgccctcttccagctcatcccggaggcatttggtttcaaccctctggaagattattat
gtctccaagtctgcagtggtgtttgggggcttttatcttttctttttcacagagaagatc
ttgaagattcttcttaagcagaaaaatgagcatcatcatggacacagccattatgcctct
gagtcgcttccctccaagaaggaccaggaggagggggtgatggagaagctgcagaacggg
gacctggaccacatgattcctcagcactgcagcagtgagctggacggcaaggcgcccatg
gtggacgagaaggtcattgtgggctcgctctctgtgcaggacctgcaggcttcccagagt
gcttgctactggctgaaaggtgtccgctactctgatatcggcactctggcctggatgatc
actctgagcgacggcctccataatttcatcgatggcctggccatcggtgcttccttcact
gtgtcagttttccaaggcatcagcacctcggtggccatcctctgtgaggagttcccacat
gagctaggagactttgtcatcctgctcaacgctgggatgagcatccaacaagctctcttc
ttcaacttcctttctgcctgctgctgctacctgggtctggcctttggcatcctggccggc
agccacttctctgccaactggatttttgcgctagctggaggaatgttcttgtatatttct
ctggctgatatgttccctgagatgaatgaggtctgtcaagaggatgaaaggaagggcagc
atcttgattccatttatcatccagaacctgggcctcctgactggattcaccatcatggtg
gtcctcaccatgtattcaggacagatccagattgggtag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (3)   
   KEGG PATHWAY (3)   
Network (2)   
   KEGG NETWORK (2)   
Disease (4)   
   KEGG DISEASE (1)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (20)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (18)   
DNA sequence (48)   
   RefSeq(nuc) (18)   
   GenBank (15)   
   EMBL (15)   
Protein domain (1)   
   Pfam (1)   
All databases (95)   

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