| Type | Description |
|---|---|
| Definition | muscle RAS oncogene homolog |
| Date | Results | Publications |
|---|---|---|
| 2021-03-27 14:43:00 | Correlation between MRAS gene polymorphism and atherosclerosis. | 32495899 |
| 2020-08-01 15:06:00 | We confirmed that the MRAS gene represents a causative gene for RASopathy. | 31173466 |
| 2019-12-28 12:44:00 | In Chinese Han population, no association of MRAS single nucleotide polymorphisms with Ischemic Stroke risk was observed, while G allele of rs40593 was associated with increased risk of cerebral infarction. rs40593, rs751357, rs6782181 were associated with increased total cholesterol levels. | 31770223 |
| 2019-06-29 12:41:00 | In human dorsal root ganglia and blood indicated this variant is an expression quantitative trait locus, with the minor allele associated with decreased expression of the nearby muscle RAS oncogene homolog (MRAS) gene. | 30431558 |
| 2018-03-17 11:28:00 | acute coronary syndrome in Czechs (30.4% vs 29.4% carriers of the minor T allele of MRAS[recessive model], p = 0.54; OR 1.05; 95% CI 0.89-1.24 for males and 32.1% vs 29.7% carriers of the minor T allele, p = 0.28; OR 1.12; 95% CI 0.91-1.37 for females) | 29264877 |
| Type | IDs |
|---|---|
| Synonymous | M-RAs, R-RAS3, RRAS3 |
| Gene |
UniProtKB-ID:
RASM_HUMAN,
Q6FGP0_HUMAN,
Q8WVM9_HUMAN
UniprotKB:
O14807,
Q6FGP0,
Q8WVM9
UniParc:
UPI0000001253,
UPI0000072A63,
UPI000000DC31
EMBL:
CR542067,
AK124954,
CH471052,
AK295640,
BC017733,
BT020057,
AC022337,
AF022080,
AF493918,
AC022497,
BC047690,
AK316071,
AF043938
Ensembl:
ENSG00000158186
KO:
hsa:22808
|
| Nucleutide sequences |
EMBL-CDS:
AAD02287.1,
AAM12632.1,
AAC52085.1,
AAV38860.1,
BAG58512.1,
BAH14442.1,
BAG54117.1,
EAW79070.1,
CAG46864.1,
EAW79068.1,
EAW79071.1,
AAH17733.1
Gene_ORFName:
hCG_17104
Ensembl_TRS:
ENST00000423968,
ENST00000464896,
ENST00000621127,
ENST00000289104,
ENST00000614350,
ENST00000474559
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000481637,
ENSP00000389682,
ENSP00000418356,
ENSP00000484586,
ENSP00000289104,
ENSP00000419582
RefSeq:
XP_016861376.1,
NP_036351.3,
XP_005247286.1,
XP_024309166.1,
NP_001239022.1,
NP_001239021.1,
XP_024309165.1,
NP_001239020.1,
NP_001239019.1,
XP_005247285.1,
XP_024309164.1,
NP_001078518.1
|
| Others |
UniRef100:
UniRef100_O14807,
UniRef100_Q8WVM9
UniRef90:
UniRef90_O14807,
UniRef90_Q8WVM9
UniRef50:
UniRef50_Q8WVM9,
UniRef50_O14807
UniGene:
Hs.527021,
Hs.735125
CCDS:
CCDS3100.1,
CCDS58855.1
|
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|---|---|---|---|---|---|---|---|---|
| Refseq |
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