KEGG   Homo sapiens (human): 55630
Entry
55630             CDS       T01001                                 
Symbol
SLC39A4, AEZ, AWMS2, ZIP4
Name
(RefSeq) solute carrier family 39 member 4
  KO
K14710  solute carrier family 39 (zinc transporter), member 4
Organism
hsa  Homo sapiens (human)
Pathway
hsa04978  Mineral absorption
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
Disease
H00212  Acrodermatitis enteropathica
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04978 Mineral absorption
    55630 (SLC39A4)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    55630 (SLC39A4)
   05012 Parkinson disease
    55630 (SLC39A4)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    55630 (SLC39A4)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC39: Metal ion transporter
   55630 (SLC39A4)
SSDB
Motif
Pfam: Zip EF-hand_Zip ZIP4_domain
Other DBs
NCBI-GeneID: 55630
NCBI-ProteinID: NP_570901
OMIM: 607059
HGNC: 17129
Ensembl: ENSG00000147804
UniProt: Q6P5W5
Position
8:complement(144412414..144416844)
AA seq 647 aa
MASLVSLELGLLLAVLVVTATASPPAGLLSLLTSGQGALDQEALGGLLNTLADRVHCANG
PCGKCLSVEDALGLGEPEGSGLPPGPVLEARYVARLSAAAVLYLSNPEGTCEDARAGLWA
SHADHLLALLESPKALTPGLSWLLQRMQARAAGQTPKMACVDIPQLLEEAVGAGAPGSAG
GVLAALLDHVRSGSCFHALPSPQYFVDFVFQQHSSEVPMTLAELSALMQRLGVGREAHSD
HSHRHRGASSRDPVPLISSSNSSSVWDTVCLSARDVMAAYGLSEQAGVTPEAWAQLSPAL
LQQQLSGACTSQSRPPVQDQLSQSERYLYGSLATLLICLCAVFGLLLLTCTGCRGVTHYI
LQTFLSLAVGAVTGDAVLHLTPKVLGLHTHSEEGLSPQPTWRLLAMLAGLYAFFLFENLF
NLLLPRDPEDLEDGPCGHSSHSHGGHSHGVSLQLAPSELRQPKPPHEGSRADLVAEESPE
LLNPEPRRLSPELRLLPYMITLGDAVHNFADGLAVGAAFASSWKTGLATSLAVFCHELPH
ELGDFAALLHAGLSVRQALLLNLASALTAFAGLYVALAVGVSEESEAWILAVATGLFLYV
ALCDMLPAMLKVRDPRPWLLFLLHNVGLLGGWTVLLLLSLYEDDITF
NT seq 1944 nt   +upstreamnt  +downstreamnt
atggcgtccctggtctcgctggagctggggctgcttctggctgtgctggtggtgacggcg
acggcgtccccgcctgctggtctgctgagcctgctcacctctggccagggcgctctggat
caagaggctctgggcggcctgttaaatacgctggcggaccgtgtgcactgcgccaacggg
ccgtgtggaaagtgcctgtctgtggaggacgccctgggcctgggcgagcctgaggggtca
gggctgcccccgggcccggtcctggaggccaggtacgtcgcccgcctcagtgccgccgcc
gtcctgtacctcagcaaccccgagggcacctgtgaggacgctcgggctggcctctgggcc
tctcatgcagaccacctcctggccctgctcgagagccccaaggccctgaccccgggcctg
agctggctgctgcagaggatgcaggcccgggctgccggccagacccccaagatggcctgc
gtagatatccctcagctgctggaggaggcggtgggggcgggggctccgggcagtgctggc
ggcgtcctggctgccctgctggaccatgtcaggagcgggtcttgcttccacgccttgccg
agccctcagtacttcgtggactttgtgttccagcagcacagcagcgaggtccctatgacg
ctggccgagctgtcagccttgatgcagcgcctgggggtgggcagggaggcccacagtgac
cacagtcatcggcacaggggagccagcagccgggaccctgtgcccctcatcagctccagc
aacagctccagtgtgtgggacacggtatgcctgagtgccagggacgtgatggctgcatat
ggactgtcggaacaggctggggtgaccccggaggcctgggcccaactgagccctgccctg
ctccaacagcagctgagtggagcctgcacctcccagtccaggccccccgtccaggaccag
ctcagccagtcagagaggtatctgtacggctccctggccacgctgctcatctgcctctgc
gcggtctttggcctcctgctgctgacctgcactggctgcaggggggtcacccactacatc
ctgcagaccttcctgagcctggcagtgggtgcagtcactggggacgctgtcctgcatctg
acgcccaaggtgctggggctgcatacacacagcgaagagggcctcagcccacagcccacc
tggcgcctcctggctatgctggccgggctctacgccttcttcctgtttgagaacctcttc
aatctcctgctgcccagggacccggaggacctggaggacgggccctgcggccacagcagc
catagccacgggggccacagccacggtgtgtccctgcagctggcacccagcgagctccgg
cagcccaagcccccccacgagggctcccgcgcagacctggtggcggaggagagcccggag
ctgctgaaccctgagcccaggagactgagcccagagttgaggctactgccctatatgatc
actctgggcgacgccgtgcacaacttcgccgacgggctggccgtgggcgccgccttcgcg
tcctcctggaagaccgggctggccacctcgctggccgtgttctgccacgagttgccacac
gagctgggggacttcgccgccttgctgcacgcggggctgtccgtgcgccaagcactgctg
ctgaacctggcctccgcgctcacggccttcgctggtctctacgtggcactcgcggttgga
gtcagcgaggagagcgaggcctggatcctggcagtggccaccggcctgttcctctacgta
gcactctgcgacatgctcccggcgatgttgaaagtacgggacccgcggccctggctcctc
ttcctgctgcacaacgtgggcctgctgggcggctggaccgtcctgctgctgctgtccctg
tacgaggatgacatcaccttctga

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