Incidental Mutation 'IGL00903:Mrgpra1'
ID |
27774 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Mrgpra1
|
Ensembl Gene |
ENSMUSG00000050650 |
Gene Name |
MAS-related GPR, member A1 |
Synonyms |
MrgA1 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.070)
|
Stock # |
IGL00903
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
46984623-47003988 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 46985326 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Valine
at position 118
(M118V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129978
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098438]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000098438
AA Change: M118V
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000129978 Gene: ENSMUSG00000050650 AA Change: M118V
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
27 |
N/A |
INTRINSIC |
low complexity region
|
36 |
49 |
N/A |
INTRINSIC |
Pfam:7tm_1
|
57 |
225 |
2.1e-8 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arsk |
A |
G |
13: 76,246,487 (GRCm39) |
|
probably null |
Het |
As3mt |
A |
G |
19: 46,700,673 (GRCm39) |
I159V |
probably benign |
Het |
Atpsckmt |
T |
C |
15: 31,606,261 (GRCm39) |
V73A |
possibly damaging |
Het |
Ctsll3 |
C |
A |
13: 60,948,075 (GRCm39) |
V201L |
probably benign |
Het |
Dapk1 |
T |
C |
13: 60,909,211 (GRCm39) |
Y1275H |
probably damaging |
Het |
Erap1 |
G |
A |
13: 74,821,826 (GRCm39) |
R727H |
probably benign |
Het |
Fcrl6 |
T |
A |
1: 172,426,674 (GRCm39) |
T91S |
probably benign |
Het |
Gvin1 |
T |
C |
7: 105,757,377 (GRCm39) |
E2364G |
probably benign |
Het |
Hacd3 |
T |
C |
9: 64,911,535 (GRCm39) |
|
probably benign |
Het |
Hcls1 |
T |
A |
16: 36,776,383 (GRCm39) |
|
probably null |
Het |
Igf2r |
C |
T |
17: 12,902,754 (GRCm39) |
R2432H |
possibly damaging |
Het |
Kif27 |
C |
A |
13: 58,492,486 (GRCm39) |
V218F |
possibly damaging |
Het |
Klhl20 |
T |
C |
1: 160,918,076 (GRCm39) |
Y70C |
probably benign |
Het |
Krt86 |
C |
T |
15: 101,371,741 (GRCm39) |
H104Y |
probably benign |
Het |
Lcn12 |
G |
T |
2: 25,383,332 (GRCm39) |
N15K |
possibly damaging |
Het |
Nacad |
G |
T |
11: 6,550,632 (GRCm39) |
T853K |
probably damaging |
Het |
Nos3 |
A |
T |
5: 24,574,860 (GRCm39) |
Q293L |
probably damaging |
Het |
Prkca |
C |
T |
11: 107,874,800 (GRCm39) |
V381M |
probably damaging |
Het |
Ptcd3 |
A |
G |
6: 71,884,828 (GRCm39) |
F37S |
possibly damaging |
Het |
Ptgs2 |
A |
G |
1: 149,980,175 (GRCm39) |
Y371C |
probably damaging |
Het |
Pygl |
T |
C |
12: 70,254,516 (GRCm39) |
Y143C |
probably damaging |
Het |
Samhd1 |
A |
G |
2: 156,949,343 (GRCm39) |
|
probably benign |
Het |
Scube1 |
T |
A |
15: 83,587,702 (GRCm39) |
H89L |
probably damaging |
Het |
Tmem59l |
G |
A |
8: 70,938,315 (GRCm39) |
|
probably benign |
Het |
Vmn2r108 |
A |
G |
17: 20,682,774 (GRCm39) |
V810A |
probably damaging |
Het |
Vmn2r61 |
T |
G |
7: 41,949,935 (GRCm39) |
F785C |
probably damaging |
Het |
Zfas1 |
G |
T |
2: 166,907,406 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Mrgpra1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01317:Mrgpra1
|
APN |
7 |
46,985,372 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01718:Mrgpra1
|
APN |
7 |
46,985,675 (GRCm39) |
splice site |
probably null |
|
IGL02252:Mrgpra1
|
APN |
7 |
46,984,912 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03301:Mrgpra1
|
APN |
7 |
46,985,164 (GRCm39) |
missense |
probably benign |
|
R0012:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R1019:Mrgpra1
|
UTSW |
7 |
46,984,833 (GRCm39) |
missense |
probably benign |
0.00 |
R2224:Mrgpra1
|
UTSW |
7 |
46,984,854 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2520:Mrgpra1
|
UTSW |
7 |
46,985,020 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2924:Mrgpra1
|
UTSW |
7 |
46,984,618 (GRCm39) |
splice site |
probably null |
|
R3038:Mrgpra1
|
UTSW |
7 |
46,984,744 (GRCm39) |
nonsense |
probably null |
|
R3900:Mrgpra1
|
UTSW |
7 |
46,985,275 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4692:Mrgpra1
|
UTSW |
7 |
46,985,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R4784:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R4785:Mrgpra1
|
UTSW |
7 |
46,985,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R4981:Mrgpra1
|
UTSW |
7 |
46,984,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R5031:Mrgpra1
|
UTSW |
7 |
46,984,985 (GRCm39) |
nonsense |
probably null |
|
R6760:Mrgpra1
|
UTSW |
7 |
46,984,789 (GRCm39) |
missense |
probably benign |
0.03 |
R7305:Mrgpra1
|
UTSW |
7 |
46,985,203 (GRCm39) |
missense |
probably benign |
0.38 |
R7348:Mrgpra1
|
UTSW |
7 |
46,985,157 (GRCm39) |
missense |
probably benign |
0.09 |
R7837:Mrgpra1
|
UTSW |
7 |
46,985,076 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8158:Mrgpra1
|
UTSW |
7 |
46,985,204 (GRCm39) |
nonsense |
probably null |
|
R8856:Mrgpra1
|
UTSW |
7 |
46,985,583 (GRCm39) |
missense |
probably benign |
0.30 |
R9100:Mrgpra1
|
UTSW |
7 |
46,984,732 (GRCm39) |
missense |
probably damaging |
0.97 |
R9694:Mrgpra1
|
UTSW |
7 |
46,985,268 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Mrgpra1
|
UTSW |
7 |
46,985,623 (GRCm39) |
missense |
probably benign |
|
|
Posted On |
2013-04-17 |