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
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
BLTP1_N
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
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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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