Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam21 |
G |
A |
12: 81,607,247 (GRCm39) |
Q172* |
probably null |
Het |
Ankib1 |
A |
G |
5: 3,752,890 (GRCm39) |
|
probably null |
Het |
Avpr1b |
C |
T |
1: 131,527,674 (GRCm39) |
R66C |
probably damaging |
Het |
Bbs7 |
A |
T |
3: 36,661,744 (GRCm39) |
C152S |
possibly damaging |
Het |
Cacna1a |
C |
A |
8: 85,285,784 (GRCm39) |
R810S |
probably damaging |
Het |
Ccdc17 |
G |
A |
4: 116,457,129 (GRCm39) |
A538T |
possibly damaging |
Het |
Cd93 |
T |
C |
2: 148,285,080 (GRCm39) |
M89V |
probably benign |
Het |
Clec11a |
G |
T |
7: 43,955,323 (GRCm39) |
D157E |
probably benign |
Het |
Crtam |
A |
C |
9: 40,895,641 (GRCm39) |
D228E |
probably benign |
Het |
Cyp2a4 |
A |
G |
7: 26,012,209 (GRCm39) |
I331V |
probably benign |
Het |
Cysltr2 |
T |
C |
14: 73,267,078 (GRCm39) |
I211V |
probably benign |
Het |
Dcaf13 |
T |
C |
15: 38,982,836 (GRCm39) |
S123P |
probably damaging |
Het |
Dctn1 |
T |
G |
6: 83,160,108 (GRCm39) |
V116G |
possibly damaging |
Het |
Dmrt3 |
G |
A |
19: 25,588,550 (GRCm39) |
A130T |
probably benign |
Het |
Dnah1 |
A |
T |
14: 31,026,924 (GRCm39) |
L700Q |
probably benign |
Het |
Dnajc1 |
T |
C |
2: 18,313,645 (GRCm39) |
T159A |
probably damaging |
Het |
Dpyd |
C |
T |
3: 118,935,585 (GRCm39) |
S670L |
probably damaging |
Het |
Dsg2 |
A |
T |
18: 20,708,069 (GRCm39) |
I57F |
possibly damaging |
Het |
Dzip3 |
A |
C |
16: 48,801,338 (GRCm39) |
I62S |
probably damaging |
Het |
Ern1 |
A |
T |
11: 106,312,776 (GRCm39) |
S202T |
probably damaging |
Het |
Foxm1 |
T |
A |
6: 128,350,206 (GRCm39) |
C517* |
probably null |
Het |
Galnt16 |
G |
A |
12: 80,644,879 (GRCm39) |
V501I |
probably benign |
Het |
Gmip |
A |
T |
8: 70,273,134 (GRCm39) |
R840S |
probably benign |
Het |
Gna14 |
A |
C |
19: 16,585,458 (GRCm39) |
I279L |
|
Het |
Irak2 |
T |
C |
6: 113,663,783 (GRCm39) |
M444T |
probably benign |
Het |
Itfg2 |
T |
C |
6: 128,389,755 (GRCm39) |
|
probably null |
Het |
Kif5a |
T |
A |
10: 127,083,909 (GRCm39) |
H94L |
probably damaging |
Het |
Kmt2e |
A |
G |
5: 23,698,215 (GRCm39) |
T636A |
probably benign |
Het |
Krba1 |
T |
C |
6: 48,382,212 (GRCm39) |
S152P |
probably damaging |
Het |
Mad1l1 |
T |
A |
5: 140,300,822 (GRCm39) |
M25L |
probably benign |
Het |
Map7d1 |
T |
C |
4: 126,132,315 (GRCm39) |
N286D |
probably benign |
Het |
Mfrp |
A |
G |
9: 44,014,802 (GRCm39) |
K280E |
probably benign |
Het |
Mlh3 |
G |
T |
12: 85,308,488 (GRCm39) |
L1100I |
probably damaging |
Het |
Mtnr1b |
A |
T |
9: 15,785,724 (GRCm39) |
C11* |
probably null |
Het |
Mx1 |
T |
C |
16: 97,252,917 (GRCm39) |
E401G |
probably damaging |
Het |
Mypn |
T |
C |
10: 63,003,036 (GRCm39) |
D367G |
probably benign |
Het |
Nherf2 |
T |
C |
17: 24,861,233 (GRCm39) |
I176V |
probably damaging |
Het |
Or52a33 |
T |
A |
7: 103,289,059 (GRCm39) |
D96V |
probably damaging |
Het |
Or6c5b |
T |
C |
10: 129,245,649 (GRCm39) |
V138A |
probably benign |
Het |
Or8s8 |
T |
G |
15: 98,354,929 (GRCm39) |
I246R |
probably damaging |
Het |
Or9g19 |
T |
A |
2: 85,600,307 (GRCm39) |
L54H |
probably damaging |
Het |
Plcb1 |
T |
G |
2: 135,177,369 (GRCm39) |
M567R |
probably damaging |
Het |
Plekhd1 |
A |
T |
12: 80,752,861 (GRCm39) |
D109V |
probably damaging |
Het |
Polr2e |
A |
G |
10: 79,875,424 (GRCm39) |
I17T |
probably benign |
Het |
Pot1b |
T |
C |
17: 55,973,537 (GRCm39) |
D421G |
probably benign |
Het |
Prkar1b |
A |
T |
5: 139,036,451 (GRCm39) |
W224R |
probably damaging |
Het |
Psmd1 |
C |
A |
1: 86,016,585 (GRCm39) |
R490S |
probably damaging |
Het |
Pwp2 |
A |
G |
10: 78,013,659 (GRCm39) |
W521R |
probably damaging |
Het |
Rhpn2 |
C |
A |
7: 35,075,680 (GRCm39) |
Q286K |
probably benign |
Het |
Rnf103 |
T |
A |
6: 71,486,602 (GRCm39) |
M411K |
probably benign |
Het |
Scpep1 |
A |
C |
11: 88,835,298 (GRCm39) |
V125G |
probably damaging |
Het |
Serpinb9c |
C |
T |
13: 33,335,793 (GRCm39) |
V248M |
probably null |
Het |
Snx15 |
T |
A |
19: 6,170,593 (GRCm39) |
N282I |
probably benign |
Het |
Spaca3 |
A |
T |
11: 80,758,514 (GRCm39) |
D159V |
probably benign |
Het |
Srrm4 |
A |
G |
5: 116,605,567 (GRCm39) |
V230A |
unknown |
Het |
Ssu2 |
T |
A |
6: 112,359,312 (GRCm39) |
I103F |
possibly damaging |
Het |
Strip2 |
T |
A |
6: 29,931,815 (GRCm39) |
F453I |
probably damaging |
Het |
Tac2 |
C |
T |
10: 127,564,319 (GRCm39) |
P72L |
possibly damaging |
Het |
Tiparp |
T |
G |
3: 65,460,125 (GRCm39) |
S473R |
probably damaging |
Het |
Tmem135 |
C |
T |
7: 88,956,456 (GRCm39) |
R53Q |
probably damaging |
Het |
Tmem200b |
T |
A |
4: 131,649,406 (GRCm39) |
F109I |
probably damaging |
Het |
Tmem245 |
A |
T |
4: 56,886,141 (GRCm39) |
I825N |
probably damaging |
Het |
Tmem63c |
G |
T |
12: 87,103,306 (GRCm39) |
V27F |
probably damaging |
Het |
Tshz1 |
T |
C |
18: 84,033,162 (GRCm39) |
I415M |
probably damaging |
Het |
Tut4 |
C |
G |
4: 108,407,940 (GRCm39) |
A1403G |
probably damaging |
Het |
Wfdc2 |
T |
A |
2: 164,407,818 (GRCm39) |
N162K |
probably damaging |
Het |
Zeb2 |
T |
A |
2: 44,887,939 (GRCm39) |
I373F |
probably damaging |
Het |
Zfp27 |
T |
C |
7: 29,594,804 (GRCm39) |
N387S |
possibly damaging |
Het |
Zfp760 |
A |
T |
17: 21,941,356 (GRCm39) |
H177L |
possibly damaging |
Het |
Zg16 |
A |
G |
7: 126,649,518 (GRCm39) |
S148P |
possibly damaging |
Het |
Zic2 |
A |
G |
14: 122,714,129 (GRCm39) |
N348D |
probably benign |
Het |
Zswim4 |
A |
T |
8: 84,939,313 (GRCm39) |
D856E |
possibly damaging |
Het |
|
Other mutations in Mrgprx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01603:Mrgprx2
|
APN |
7 |
48,132,374 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01655:Mrgprx2
|
APN |
7 |
48,132,439 (GRCm39) |
nonsense |
probably null |
|
IGL02052:Mrgprx2
|
APN |
7 |
48,132,042 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02254:Mrgprx2
|
APN |
7 |
48,132,686 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02985:Mrgprx2
|
APN |
7 |
48,132,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R0026:Mrgprx2
|
UTSW |
7 |
48,131,771 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0387:Mrgprx2
|
UTSW |
7 |
48,148,908 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R0514:Mrgprx2
|
UTSW |
7 |
48,132,712 (GRCm39) |
start codon destroyed |
probably null |
|
R0650:Mrgprx2
|
UTSW |
7 |
48,132,666 (GRCm39) |
missense |
probably damaging |
0.96 |
R1014:Mrgprx2
|
UTSW |
7 |
48,132,306 (GRCm39) |
splice site |
probably null |
|
R2011:Mrgprx2
|
UTSW |
7 |
48,132,282 (GRCm39) |
missense |
probably damaging |
0.96 |
R2224:Mrgprx2
|
UTSW |
7 |
48,132,608 (GRCm39) |
missense |
probably benign |
0.43 |
R4238:Mrgprx2
|
UTSW |
7 |
48,132,738 (GRCm39) |
missense |
probably benign |
|
R4846:Mrgprx2
|
UTSW |
7 |
48,132,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R5385:Mrgprx2
|
UTSW |
7 |
48,132,753 (GRCm39) |
missense |
probably benign |
0.11 |
R5891:Mrgprx2
|
UTSW |
7 |
48,131,994 (GRCm39) |
missense |
probably benign |
|
R6490:Mrgprx2
|
UTSW |
7 |
48,132,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6576:Mrgprx2
|
UTSW |
7 |
48,132,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R6934:Mrgprx2
|
UTSW |
7 |
48,131,813 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6948:Mrgprx2
|
UTSW |
7 |
48,132,464 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7938:Mrgprx2
|
UTSW |
7 |
48,132,240 (GRCm39) |
missense |
probably benign |
0.01 |
R7944:Mrgprx2
|
UTSW |
7 |
48,132,753 (GRCm39) |
missense |
probably benign |
0.11 |
R7945:Mrgprx2
|
UTSW |
7 |
48,132,753 (GRCm39) |
missense |
probably benign |
0.11 |
R8221:Mrgprx2
|
UTSW |
7 |
48,132,527 (GRCm39) |
missense |
probably benign |
0.00 |
R8782:Mrgprx2
|
UTSW |
7 |
48,132,299 (GRCm39) |
missense |
probably damaging |
0.98 |
R9015:Mrgprx2
|
UTSW |
7 |
48,148,938 (GRCm39) |
unclassified |
probably benign |
|
X0027:Mrgprx2
|
UTSW |
7 |
48,132,246 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Mrgprx2
|
UTSW |
7 |
48,132,546 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Mrgprx2
|
UTSW |
7 |
48,132,090 (GRCm39) |
missense |
probably damaging |
0.98 |
|