Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam20 |
A |
T |
8: 41,248,801 (GRCm39) |
I304F |
probably damaging |
Het |
Adamts5 |
A |
G |
16: 85,666,800 (GRCm39) |
|
probably benign |
Het |
Akr1c6 |
A |
G |
13: 4,504,544 (GRCm39) |
R132G |
probably benign |
Het |
Ash1l |
T |
A |
3: 88,892,183 (GRCm39) |
M1354K |
possibly damaging |
Het |
C6 |
T |
C |
15: 4,844,311 (GRCm39) |
I911T |
possibly damaging |
Het |
Calm2 |
T |
C |
17: 87,743,150 (GRCm39) |
|
probably null |
Het |
Ccdc80 |
G |
A |
16: 44,938,528 (GRCm39) |
R745Q |
probably damaging |
Het |
Celsr3 |
T |
C |
9: 108,721,233 (GRCm39) |
I2685T |
possibly damaging |
Het |
Chkb |
T |
C |
15: 89,313,788 (GRCm39) |
|
probably benign |
Het |
Dennd5b |
T |
A |
6: 148,943,011 (GRCm39) |
|
probably null |
Het |
Dnah2 |
T |
C |
11: 69,415,209 (GRCm39) |
Y175C |
probably damaging |
Het |
Dnajc13 |
A |
G |
9: 104,069,313 (GRCm39) |
S1154P |
probably benign |
Het |
Ephb4 |
T |
C |
5: 137,359,404 (GRCm39) |
S325P |
probably damaging |
Het |
Fzd9 |
C |
T |
5: 135,279,714 (GRCm39) |
R57H |
probably damaging |
Het |
Gemin6 |
T |
G |
17: 80,535,178 (GRCm39) |
V46G |
probably damaging |
Het |
Gm9949 |
A |
G |
18: 62,313,587 (GRCm39) |
|
probably benign |
Het |
Gnb4 |
A |
T |
3: 32,643,994 (GRCm39) |
M188K |
probably benign |
Het |
Hr |
G |
T |
14: 70,794,067 (GRCm39) |
G109V |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 40,812,328 (GRCm39) |
S2426P |
probably damaging |
Het |
Map2k4 |
A |
G |
11: 65,610,413 (GRCm39) |
W88R |
probably damaging |
Het |
Map4 |
C |
T |
9: 109,866,851 (GRCm39) |
|
probably benign |
Het |
Moxd2 |
C |
T |
6: 40,859,048 (GRCm39) |
|
probably null |
Het |
Mtrex |
T |
C |
13: 113,049,715 (GRCm39) |
S232G |
probably null |
Het |
Or5p68 |
A |
C |
7: 107,945,312 (GRCm39) |
I292S |
probably damaging |
Het |
Padi2 |
T |
C |
4: 140,659,382 (GRCm39) |
F229S |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,666,172 (GRCm39) |
N1136S |
probably benign |
Het |
Pcdhb1 |
A |
T |
18: 37,398,811 (GRCm39) |
N254I |
possibly damaging |
Het |
Plcb2 |
A |
G |
2: 118,548,727 (GRCm39) |
Y400H |
probably damaging |
Het |
Plce1 |
A |
C |
19: 38,608,926 (GRCm39) |
T412P |
probably benign |
Het |
Prg4 |
T |
C |
1: 150,331,519 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,586,501 (GRCm39) |
N2510S |
possibly damaging |
Het |
Psme4 |
T |
A |
11: 30,741,168 (GRCm39) |
S107T |
probably benign |
Het |
Resf1 |
C |
A |
6: 149,230,611 (GRCm39) |
S1219* |
probably null |
Het |
Rint1 |
G |
T |
5: 23,999,363 (GRCm39) |
A51S |
probably benign |
Het |
Rsad1 |
T |
A |
11: 94,434,515 (GRCm39) |
R306S |
probably damaging |
Het |
Sema3c |
T |
G |
5: 17,922,068 (GRCm39) |
|
probably null |
Het |
Sirt3 |
G |
A |
7: 140,444,928 (GRCm39) |
T290I |
probably damaging |
Het |
Spam1 |
G |
A |
6: 24,800,731 (GRCm39) |
G490D |
probably benign |
Het |
Speer4f2 |
C |
T |
5: 17,581,498 (GRCm39) |
R147W |
possibly damaging |
Het |
Sppl2c |
A |
T |
11: 104,078,126 (GRCm39) |
I309L |
probably benign |
Het |
Srxn1 |
G |
A |
2: 151,947,799 (GRCm39) |
V66M |
probably damaging |
Het |
St3gal4 |
C |
T |
9: 34,964,752 (GRCm39) |
R152H |
probably damaging |
Het |
Sv2c |
A |
T |
13: 96,114,591 (GRCm39) |
F532I |
probably damaging |
Het |
Tacc1 |
C |
A |
8: 25,654,431 (GRCm39) |
K705N |
probably null |
Het |
Tekt3 |
G |
T |
11: 62,985,619 (GRCm39) |
S475I |
probably damaging |
Het |
Tjap1 |
T |
C |
17: 46,571,101 (GRCm39) |
T139A |
probably damaging |
Het |
Tnfrsf8 |
T |
A |
4: 145,019,214 (GRCm39) |
K207M |
possibly damaging |
Het |
Tnn |
T |
C |
1: 159,937,831 (GRCm39) |
T965A |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trmt2a |
A |
G |
16: 18,068,814 (GRCm39) |
H270R |
probably damaging |
Het |
Ttc21a |
T |
C |
9: 119,780,037 (GRCm39) |
L448P |
probably benign |
Het |
Ttll4 |
C |
A |
1: 74,718,480 (GRCm39) |
N110K |
probably benign |
Het |
Ttn |
T |
A |
2: 76,585,168 (GRCm39) |
I22042F |
probably damaging |
Het |
Tut7 |
A |
G |
13: 59,948,471 (GRCm39) |
Y215H |
probably damaging |
Het |
Ubr1 |
A |
G |
2: 120,698,783 (GRCm39) |
Y1595H |
possibly damaging |
Het |
Unc45a |
G |
A |
7: 79,978,787 (GRCm39) |
P621S |
probably damaging |
Het |
Xrn2 |
A |
T |
2: 146,866,633 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Mrgprx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01152:Mrgprx1
|
APN |
7 |
47,671,234 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01326:Mrgprx1
|
APN |
7 |
47,671,517 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02117:Mrgprx1
|
APN |
7 |
47,671,371 (GRCm39) |
nonsense |
probably null |
|
IGL02219:Mrgprx1
|
APN |
7 |
47,671,477 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02431:Mrgprx1
|
APN |
7 |
47,670,875 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02441:Mrgprx1
|
APN |
7 |
47,671,336 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02682:Mrgprx1
|
APN |
7 |
47,671,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Mrgprx1
|
UTSW |
7 |
47,671,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R4366:Mrgprx1
|
UTSW |
7 |
47,670,941 (GRCm39) |
missense |
probably damaging |
0.98 |
R4521:Mrgprx1
|
UTSW |
7 |
47,671,447 (GRCm39) |
missense |
probably benign |
|
R4801:Mrgprx1
|
UTSW |
7 |
47,670,959 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4802:Mrgprx1
|
UTSW |
7 |
47,670,959 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5537:Mrgprx1
|
UTSW |
7 |
47,670,898 (GRCm39) |
missense |
probably benign |
|
R6444:Mrgprx1
|
UTSW |
7 |
47,671,562 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6834:Mrgprx1
|
UTSW |
7 |
47,671,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R7406:Mrgprx1
|
UTSW |
7 |
47,671,733 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9664:Mrgprx1
|
UTSW |
7 |
47,671,273 (GRCm39) |
missense |
probably benign |
0.38 |
RF020:Mrgprx1
|
UTSW |
7 |
47,671,259 (GRCm39) |
small insertion |
probably benign |
|
RF024:Mrgprx1
|
UTSW |
7 |
47,671,259 (GRCm39) |
small insertion |
probably benign |
|
RF026:Mrgprx1
|
UTSW |
7 |
47,671,257 (GRCm39) |
small insertion |
probably benign |
|
RF043:Mrgprx1
|
UTSW |
7 |
47,671,257 (GRCm39) |
small insertion |
probably benign |
|
Z1088:Mrgprx1
|
UTSW |
7 |
47,670,877 (GRCm39) |
missense |
probably damaging |
0.98 |
|