Type | Description |
---|---|
Definition | betaine--homocysteine S-methyltransferase 2 |
Date | Results | Publications |
---|---|---|
2018-11-10 11:21:00 | Our study suggested markers in BHMT/BHMT2 and DMGDH might affect the risk of NSCL/P through pairwise interaction. | 29356306 |
2016-06-04 10:48:00 | A three-way interaction among maternal and fetal variants in BHMT2, GSTP1 and GPX3 contribute to congenital heart defects | 26612412 |
2016-05-07 11:25:00 | The faster evolutionary rate of BHMT2 overall suggests that selective constraints were reduced relative to BHMT. | 26213999 |
2016-02-20 11:05:00 | Multiple SNPs in BHMT and BHMT2 were identified to be associated with the occurrence of infant obstructive heart defects and interaction effects with maternal use of folic acid supplements. | 25846410 |
2011-10-15 11:29:00 | No significant level of association was found with cleft lip with or without cleft palate and BHMT2 variants. | 21564312 |
Type | IDs |
---|---|
Gene |
UniProtKB-ID:
BHMT2_HUMAN,
A0A024RAQ0_HUMAN
UniprotKB:
Q9H2M3,
A0A024RAQ0
UniParc:
UPI0001914DF0,
UPI00000701B9
EMBL:
AK298298,
AK000008,
AC008502,
AF257473,
BC020665,
CH471084
Ensembl:
ENSG00000132840
KO:
hsa:23743
|
Nucleutide sequences |
EMBL-CDS:
AAG41356.1,
BAA90880.1,
BAH12752.1,
AAH20665.1,
EAW95830.1,
EAW95829.1
Gene_ORFName:
hCG_2016006
Ensembl_TRS:
ENST00000255192,
ENST00000521567
|
Protein sequencees |
Ensembl_PRO:
ENSP00000255192,
ENSP00000430278
RefSeq:
NP_001171476.1,
NP_060084.2
|
Others |
UniRef100:
UniRef100_Q9H2M3
UniRef90:
UniRef90_Q9H2M3
UniRef50:
UniRef50_Q9H2M3
UniGene:
Hs.114172
CCDS:
CCDS4045.1,
CCDS54871.1
|
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Refseq |
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