Type | Description |
---|---|
Definition | hemoglobin subunit gamma 2 |
Date | Results | Publications |
---|---|---|
2021-04-17 13:37:00 | Multi-Locus Models to Address Hb F Variability in Portuguese beta-Thalassemia Carriers. | 32319326 |
2020-10-03 12:59:00 | Association between BCL11A, HSB1L-MYB, and XmnI gammaG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients. | 32772141 |
2019-08-10 11:19:00 | Prx2 interacts with hemoglobin A (Alpha2Beta2) and hemoglobin F (Alpha2Gamma2) but not with hemoglobin A2 (Alpha2Delta2) | 30844732 |
2019-05-11 10:18:00 | Some forms of hereditary persistence of fetal hemoglobin, a rare benign condition where individuals express the gamma-globin gene throughout adulthood, are caused by point mutations in the gamma-globin gene promoter at regions residing ~115 and 200 bp upstream of the transcription start site. We found that the major fetal globin gene repressors BCL11A and ZBTB7A directly bound to the sites at -115 and -200 bp, respecti... | 29610478 |
2018-10-27 12:02:00 | Data suggest that studying genotype frequency of the Xmn1 gammaG globin polymorphism (-158C>T ) in Siwa Oasis, Egypt can be considered as a starting point for further research targeting this community sector. | 29932071 |
Type | IDs |
---|---|
Synonymous | HBG-T1, TNCY |
Gene |
UniProtKB-ID:
HBG2_HUMAN,
D9YZU9_HUMAN
UniprotKB:
P69892,
D9YZU9
UniParc:
UPI00000012DA
EMBL:
BC130457,
V00515,
M15386,
M11427,
AK290492,
BC130459,
BC029387,
U01317,
M91037,
GU324926,
BC010914,
LT548099,
AY662983,
M91036
Ensembl:
ENSG00000196565
KO:
hsa:3048
|
Nucleutide sequences |
EMBL-CDS:
AAB50159.1,
CAA23773.1,
AAT98611.1,
AAI30458.1,
BAF83181.1,
AAB59428.1,
AAI30460.1,
AAH29387.1,
AAH10914.1,
AAA58492.1,
AAA35957.1,
AAA16331.1,
ADL14497.1,
SAI82133.1
Ensembl_TRS:
ENST00000336906
|
Protein sequencees |
Ensembl_PRO:
ENSP00000338082
RefSeq:
NP_000175.1
|
Others |
UniRef100:
UniRef100_P69892
UniRef90:
UniRef90_P69892
UniRef50:
UniRef50_P69892
UniGene:
Hs.302145
CCDS:
CCDS7755.1
|
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Refseq |
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