Homo sapiens (human): 4891
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Entry
4891 CDS
T01001
Symbol
SLC11A2, AHMIO1, DCT1, DMT1, NRAMP2
Name
(RefSeq) solute carrier family 11 member 2
KO
K21398
natural resistance-associated macrophage protein 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04142
Lysosome
hsa04216
Ferroptosis
hsa04978
Mineral absorption
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
Network
nt06525
Ferroptosis
Element
N01587
Fe-TF transport
Disease
H01196
Hypochromic microcytic anemia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04142 Lysosome
4891 (SLC11A2)
09143 Cell growth and death
04216 Ferroptosis
4891 (SLC11A2)
09150 Organismal Systems
09154 Digestive system
04978 Mineral absorption
4891 (SLC11A2)
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
4891 (SLC11A2)
05012 Parkinson disease
4891 (SLC11A2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
4891 (SLC11A2)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC11: Proton-coupled metal ion transporter
4891 (SLC11A2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Nramp
Motif
Other DBs
NCBI-GeneID:
4891
NCBI-ProteinID:
NP_001167597
OMIM:
600523
HGNC:
10908
Ensembl:
ENSG00000110911
UniProt:
P49281
A0A0X8GKR4
Structure
PDB
PDBj
LinkDB
All DBs
Position
12:complement(50952263..51028886)
Genome browser
AA seq
568 aa
AA seq
DB search
MVLGPEQKMSDDSVSGDHGESASLGNINPAYSNPSLSQSPGDSEEYFATYFNEKISIPEE
EYSCFSFRKLWAFTGPGFLMSIAYLDPGNIESDLQSGAVAGFKLLWILLLATLVGLLLQR
LAARLGVVTGLHLAEVCHRQYPKVPRVILWLMVELAIIGSDMQEVIGSAIAINLLSVGRI
PLWGGVLITIADTFVFLFLDKYGLRKLEAFFGFLITIMALTFGYEYVTVKPSQSQVLKGM
FVPSCSGCRTPQIEQAVGIVGAVIMPHNMYLHSALVKSRQVNRNNKQEVREANKYFFIES
CIALFVSFIINVFVVSVFAEAFFGKTNEQVVEVCTNTSSPHAGLFPKDNSTLAVDIYKGG
VVLGCYFGPAALYIWAVGILAAGQSSTMTGTYSGQFVMEGFLNLKWSRFARVVLTRSIAI
IPTLLVAVFQDVEHLTGMNDFLNVLQSLQLPFALIPILTFTSLRPVMSDFANGLGWRIAG
GILVLIICSINMYFVVVYVRDLGHVALYVVAAVVSVAYLGFVFYLGWQCLIALGMSFLDC
GHTCHLGLTAQPELYLLNTMDADSLVSR
NT seq
1707 nt
NT seq
+upstream
nt +downstream
nt
atggtgctgggtcctgaacagaagatgtcagatgacagtgtttctggagatcatggggag
tctgccagtcttggtaacatcaaccctgcctatagtaatccctctctttcacagtcccct
ggggactcagaggagtacttcgccacttactttaatgagaagatctccattcctgaggag
gagtactcttgttttagctttcgtaaactctgggctttcaccggaccaggttttcttatg
agcattgcctacctggatccaggaaatattgaatccgatttgcagtctggagcagtggct
ggatttaagttgctctggatccttctgttggccacccttgtggggctgctgctccagcgg
cttgcagctagactgggagtggttactgggctgcatcttgctgaagtatgtcaccgtcag
tatcccaaggtcccacgagtcatcctgtggctgatggtggagttggctatcatcggctca
gacatgcaagaagtcattggctcagccattgctatcaatcttctgtctgtaggaagaatt
cctctgtggggtggcgttctcatcaccattgcagatacttttgtatttctcttcttggac
aaatatggcttgcggaagctagaagcattttttggctttctcatcactattatggccctc
acatttggatatgagtatgttacagtgaaacccagccagagccaggtactcaagggcatg
ttcgtaccatcctgttcaggctgtcgcactccacagattgaacaggctgtgggcatcgtg
ggagctgtcatcatgccacacaacatgtacctgcattctgccttagtcaagtctagacag
gtaaaccggaacaataagcaggaagttcgagaagccaataagtactttttcattgaatcc
tgcattgcactctttgtttccttcatcatcaatgtctttgttgtctcagtctttgctgaa
gcattttttgggaaaaccaacgagcaggtggttgaagtctgtacaaataccagcagtcct
catgctggcctctttcctaaagataactcgacactggctgtggacatctacaaagggggt
gttgtgctgggatgttactttgggcctgctgcactctacatttgggcagtggggatcctg
gctgcaggacagagctccaccatgacaggaacctattctggccagtttgtcatggaggga
ttcctgaacctaaagtggtcacgctttgcccgagtggttctgactcgctctattgccatc
atccccactctgcttgttgctgtcttccaagatgtagagcatctaacagggatgaatgac
tttctgaatgttctacagagcttacagcttccctttgctctcatacccatcctcacattt
acgagcttgcggccagtaatgagtgactttgccaatggactaggctggcggattgcagga
ggaatcttggtccttatcatctgttccatcaatatgtactttgtagtggtttatgtccgg
gacctagggcatgtggcattatatgtggtggctgctgtggtcagcgtggcttatctgggc
tttgtgttctacttgggttggcaatgtttgattgcactgggcatgtccttcctggactgt
gggcatacgtgccatctgggattgacagctcagcctgaactctatcttctgaacaccatg
gacgctgactcacttgtgtctagatga
DBGET
integrated database retrieval system
