Homo sapiens (human): 3039
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Entry
3039 CDS
T01001
Symbol
HBA1, ECYT7, HBA-T3, HBH, METHBA
Name
(RefSeq) hemoglobin subunit alpha 1
KO
K13822
hemoglobin subunit alpha
Organism
hsa
Homo sapiens (human)
Pathway
hsa05143
African trypanosomiasis
hsa05144
Malaria
Disease
H00228
Thalassemia
H00235
Methemoglobinemia
H00236
Congenital polycythemia
H02868
Heinz body anemia
Drug target
Oxidized cellulose (
DG00168
):
D03436
D06456
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09174 Infectious disease: parasitic
05144 Malaria
3039 (HBA1)
05143 African trypanosomiasis
3039 (HBA1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
hsa04147
]
3039 (HBA1)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of hepatic cells
3039 (HBA1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Globin
Motif
Other DBs
NCBI-GeneID:
3039
NCBI-ProteinID:
NP_000549
OMIM:
141800
HGNC:
4823
Ensembl:
ENSG00000206172
UniProt:
P69905
D1MGQ2
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:176680..177522
Genome browser
AA seq
142 aa
AA seq
DB search
MVLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHG
KKVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTP
AVHASLDKFLASVSTVLTSKYR
NT seq
429 nt
NT seq
+upstream
nt +downstream
nt
atggtgctgtctcctgccgacaagaccaacgtcaaggccgcctggggtaaggtcggcgcg
cacgctggcgagtatggtgcggaggccctggagaggatgttcctgtccttccccaccacc
aagacctacttcccgcacttcgacctgagccacggctctgcccaggttaagggccacggc
aagaaggtggccgacgcgctgaccaacgccgtggcgcacgtggacgacatgcccaacgcg
ctgtccgccctgagcgacctgcacgcgcacaagcttcgggtggacccggtcaacttcaag
ctcctaagccactgcctgctggtgaccctggccgcccacctccccgccgagttcacccct
gcggtgcacgcctccctggacaagttcctggcttctgtgagcaccgtgctgacctccaaa
taccgttaa
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integrated database retrieval system