Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adss1 |
A |
C |
12: 112,602,831 (GRCm39) |
I341L |
probably benign |
Het |
Aldh1b1 |
T |
A |
4: 45,803,092 (GRCm39) |
M210K |
possibly damaging |
Het |
Ankrd17 |
G |
A |
5: 90,431,451 (GRCm39) |
Q778* |
probably null |
Het |
Bmper |
T |
C |
9: 23,318,106 (GRCm39) |
V575A |
probably damaging |
Het |
Brinp2 |
A |
G |
1: 158,073,913 (GRCm39) |
V736A |
probably benign |
Het |
Ccdc81 |
A |
T |
7: 89,515,723 (GRCm39) |
L652* |
probably null |
Het |
Cdt1 |
C |
T |
8: 123,298,585 (GRCm39) |
R437W |
probably damaging |
Het |
Ckb |
A |
C |
12: 111,637,466 (GRCm39) |
L165R |
possibly damaging |
Het |
Col25a1 |
G |
T |
3: 130,290,075 (GRCm39) |
G255V |
probably damaging |
Het |
Ddx17 |
A |
G |
15: 79,420,156 (GRCm39) |
|
probably null |
Het |
Dennd4a |
G |
T |
9: 64,759,794 (GRCm39) |
G300W |
possibly damaging |
Het |
Dlg4 |
T |
A |
11: 69,930,008 (GRCm39) |
I316N |
probably damaging |
Het |
Dlgap2 |
C |
T |
8: 14,793,410 (GRCm39) |
P467L |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,732,227 (GRCm39) |
I4226M |
possibly damaging |
Het |
Drc1 |
G |
A |
5: 30,521,829 (GRCm39) |
A734T |
probably benign |
Het |
Entpd1 |
A |
G |
19: 40,600,865 (GRCm39) |
M1V |
probably null |
Het |
Exph5 |
T |
G |
9: 53,287,935 (GRCm39) |
I1672S |
possibly damaging |
Het |
Fam149b |
T |
A |
14: 20,427,852 (GRCm39) |
D379E |
probably damaging |
Het |
Fgfr2 |
T |
C |
7: 129,787,074 (GRCm39) |
T461A |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,919,946 (GRCm39) |
V469A |
probably damaging |
Het |
Frem3 |
A |
T |
8: 81,338,231 (GRCm39) |
K175* |
probably null |
Het |
Fsd2 |
C |
T |
7: 81,209,629 (GRCm39) |
G71E |
probably benign |
Het |
Gcat |
T |
C |
15: 78,919,188 (GRCm39) |
I116T |
probably damaging |
Het |
Gigyf2 |
G |
A |
1: 87,331,458 (GRCm39) |
S202N |
unknown |
Het |
Glra3 |
T |
G |
8: 56,565,911 (GRCm39) |
|
probably null |
Het |
Golga4 |
C |
T |
9: 118,365,836 (GRCm39) |
T296I |
possibly damaging |
Het |
Herc1 |
C |
T |
9: 66,341,552 (GRCm39) |
T1816I |
possibly damaging |
Het |
Igfbpl1 |
C |
A |
4: 45,826,786 (GRCm39) |
R3L |
unknown |
Het |
Ighv15-2 |
A |
T |
12: 114,528,470 (GRCm39) |
S28T |
probably benign |
Het |
Kat2b |
T |
A |
17: 53,955,835 (GRCm39) |
M427K |
probably benign |
Het |
Kdm4c |
A |
G |
4: 74,295,906 (GRCm39) |
T882A |
probably damaging |
Het |
Kif1a |
G |
T |
1: 92,967,496 (GRCm39) |
F1138L |
probably damaging |
Het |
Klhl20 |
A |
T |
1: 160,934,307 (GRCm39) |
S237R |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,123,014 (GRCm39) |
N725K |
probably damaging |
Het |
Lmtk3 |
A |
G |
7: 45,444,890 (GRCm39) |
D1191G |
unknown |
Het |
Ltbp1 |
C |
A |
17: 75,670,358 (GRCm39) |
N1466K |
possibly damaging |
Het |
Ly75 |
T |
C |
2: 60,195,432 (GRCm39) |
E242G |
probably damaging |
Het |
Lyrm1 |
T |
C |
7: 119,515,449 (GRCm39) |
V113A |
probably benign |
Het |
Mfsd13a |
G |
T |
19: 46,360,446 (GRCm39) |
A333S |
probably benign |
Het |
Mllt10 |
T |
C |
2: 18,167,214 (GRCm39) |
S380P |
possibly damaging |
Het |
Muc5ac |
A |
T |
7: 141,363,528 (GRCm39) |
I2280F |
unknown |
Het |
Neurod2 |
A |
C |
11: 98,218,023 (GRCm39) |
F380L |
probably damaging |
Het |
Ntrk3 |
G |
A |
7: 78,005,954 (GRCm39) |
A469V |
probably damaging |
Het |
Nup205 |
T |
C |
6: 35,175,888 (GRCm39) |
F584L |
probably damaging |
Het |
Oas1d |
A |
T |
5: 121,057,210 (GRCm39) |
Y272F |
probably damaging |
Het |
Olfm3 |
T |
C |
3: 114,874,794 (GRCm39) |
V30A |
probably benign |
Het |
Or4c110 |
T |
A |
2: 88,831,973 (GRCm39) |
I220F |
probably damaging |
Het |
Or5b117 |
A |
G |
19: 13,431,563 (GRCm39) |
I106T |
probably benign |
Het |
Or8k22 |
A |
G |
2: 86,163,064 (GRCm39) |
V212A |
probably benign |
Het |
Pcdhga12 |
A |
G |
18: 37,901,427 (GRCm39) |
Y753C |
probably damaging |
Het |
Phox2b |
A |
G |
5: 67,253,514 (GRCm39) |
V294A |
unknown |
Het |
Prdm2 |
A |
T |
4: 142,859,812 (GRCm39) |
C1159* |
probably null |
Het |
Ptpn12 |
G |
T |
5: 21,207,631 (GRCm39) |
S275* |
probably null |
Het |
Rigi |
T |
C |
4: 40,209,894 (GRCm39) |
M725V |
probably damaging |
Het |
Rnf223 |
A |
T |
4: 156,216,776 (GRCm39) |
E50D |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,879,548 (GRCm39) |
Y169N |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,757,736 (GRCm39) |
|
probably null |
Het |
Shank2 |
T |
C |
7: 143,964,798 (GRCm39) |
I802T |
probably damaging |
Het |
Skint2 |
A |
T |
4: 112,481,329 (GRCm39) |
N64I |
probably damaging |
Het |
Smpd3 |
A |
C |
8: 106,982,254 (GRCm39) |
C617G |
probably benign |
Het |
Tmem106c |
G |
C |
15: 97,865,985 (GRCm39) |
G192R |
probably damaging |
Het |
Tmem72 |
T |
C |
6: 116,673,800 (GRCm39) |
H106R |
probably damaging |
Het |
Upf2 |
G |
C |
2: 6,030,926 (GRCm39) |
V789L |
unknown |
Het |
Vash1 |
A |
G |
12: 86,726,758 (GRCm39) |
|
probably benign |
Het |
Vmn1r201 |
T |
A |
13: 22,658,875 (GRCm39) |
Y30N |
probably benign |
Het |
Xpr1 |
A |
G |
1: 155,166,035 (GRCm39) |
F571L |
possibly damaging |
Het |
Yif1a |
T |
C |
19: 5,139,815 (GRCm39) |
S87P |
probably damaging |
Het |
Zer1 |
T |
C |
2: 29,997,520 (GRCm39) |
Y462C |
probably damaging |
Het |
Zfp597 |
G |
A |
16: 3,684,375 (GRCm39) |
P127L |
possibly damaging |
Het |
Zxdc |
T |
C |
6: 90,375,749 (GRCm39) |
S742P |
probably benign |
Het |
|
Other mutations in Mrc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01105:Mrc2
|
APN |
11 |
105,219,567 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01374:Mrc2
|
APN |
11 |
105,238,469 (GRCm39) |
nonsense |
probably null |
|
IGL01751:Mrc2
|
APN |
11 |
105,216,560 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01780:Mrc2
|
APN |
11 |
105,216,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01835:Mrc2
|
APN |
11 |
105,227,503 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02350:Mrc2
|
APN |
11 |
105,216,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02357:Mrc2
|
APN |
11 |
105,216,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02829:Mrc2
|
APN |
11 |
105,227,533 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02863:Mrc2
|
APN |
11 |
105,224,446 (GRCm39) |
splice site |
probably benign |
|
IGL02940:Mrc2
|
APN |
11 |
105,231,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02988:Mrc2
|
UTSW |
11 |
105,216,397 (GRCm39) |
missense |
probably benign |
0.04 |
R0254:Mrc2
|
UTSW |
11 |
105,238,692 (GRCm39) |
missense |
probably benign |
0.00 |
R0634:Mrc2
|
UTSW |
11 |
105,238,518 (GRCm39) |
missense |
probably benign |
0.01 |
R1102:Mrc2
|
UTSW |
11 |
105,231,647 (GRCm39) |
missense |
probably benign |
|
R1233:Mrc2
|
UTSW |
11 |
105,239,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R1244:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R1458:Mrc2
|
UTSW |
11 |
105,228,598 (GRCm39) |
missense |
probably benign |
0.01 |
R1500:Mrc2
|
UTSW |
11 |
105,238,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1573:Mrc2
|
UTSW |
11 |
105,227,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Mrc2
|
UTSW |
11 |
105,229,619 (GRCm39) |
missense |
probably damaging |
0.99 |
R1842:Mrc2
|
UTSW |
11 |
105,228,546 (GRCm39) |
missense |
probably damaging |
0.98 |
R2156:Mrc2
|
UTSW |
11 |
105,238,682 (GRCm39) |
splice site |
probably null |
|
R2165:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2265:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2266:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2267:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2268:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2269:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2270:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2271:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2272:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2296:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2298:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2300:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2326:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2518:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2519:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2520:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R2895:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3029:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3030:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3079:Mrc2
|
UTSW |
11 |
105,227,539 (GRCm39) |
missense |
probably damaging |
0.97 |
R3122:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3149:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3150:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3420:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3422:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3441:Mrc2
|
UTSW |
11 |
105,238,542 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3726:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3731:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3800:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3820:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3821:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3837:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3838:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3849:Mrc2
|
UTSW |
11 |
105,183,729 (GRCm39) |
critical splice donor site |
probably null |
|
R3850:Mrc2
|
UTSW |
11 |
105,183,729 (GRCm39) |
critical splice donor site |
probably null |
|
R3914:Mrc2
|
UTSW |
11 |
105,238,058 (GRCm39) |
splice site |
probably benign |
|
R3932:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3933:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R3971:Mrc2
|
UTSW |
11 |
105,218,857 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4105:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4107:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4113:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4274:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4399:Mrc2
|
UTSW |
11 |
105,227,484 (GRCm39) |
nonsense |
probably null |
|
R4477:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4478:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4493:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4494:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4495:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4547:Mrc2
|
UTSW |
11 |
105,227,467 (GRCm39) |
missense |
probably benign |
0.04 |
R4600:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4601:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4602:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4603:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4610:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4611:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4637:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4672:Mrc2
|
UTSW |
11 |
105,233,923 (GRCm39) |
missense |
probably benign |
0.22 |
R4674:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4675:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4693:Mrc2
|
UTSW |
11 |
105,234,528 (GRCm39) |
missense |
probably benign |
0.00 |
R4706:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4707:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4791:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4792:Mrc2
|
UTSW |
11 |
105,239,257 (GRCm39) |
splice site |
probably null |
|
R4888:Mrc2
|
UTSW |
11 |
105,232,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R5523:Mrc2
|
UTSW |
11 |
105,234,408 (GRCm39) |
missense |
probably benign |
|
R5600:Mrc2
|
UTSW |
11 |
105,224,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Mrc2
|
UTSW |
11 |
105,227,040 (GRCm39) |
nonsense |
probably null |
|
R5692:Mrc2
|
UTSW |
11 |
105,227,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R5706:Mrc2
|
UTSW |
11 |
105,223,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Mrc2
|
UTSW |
11 |
105,228,639 (GRCm39) |
missense |
probably benign |
0.00 |
R6140:Mrc2
|
UTSW |
11 |
105,237,615 (GRCm39) |
missense |
probably benign |
|
R6146:Mrc2
|
UTSW |
11 |
105,216,470 (GRCm39) |
missense |
probably damaging |
0.98 |
R6225:Mrc2
|
UTSW |
11 |
105,237,646 (GRCm39) |
missense |
probably benign |
0.01 |
R6437:Mrc2
|
UTSW |
11 |
105,240,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R6618:Mrc2
|
UTSW |
11 |
105,240,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R6675:Mrc2
|
UTSW |
11 |
105,233,906 (GRCm39) |
splice site |
probably null |
|
R6680:Mrc2
|
UTSW |
11 |
105,216,579 (GRCm39) |
missense |
probably damaging |
0.98 |
R6868:Mrc2
|
UTSW |
11 |
105,219,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R6979:Mrc2
|
UTSW |
11 |
105,239,461 (GRCm39) |
missense |
probably damaging |
0.96 |
R7038:Mrc2
|
UTSW |
11 |
105,223,062 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7303:Mrc2
|
UTSW |
11 |
105,216,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Mrc2
|
UTSW |
11 |
105,220,061 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7422:Mrc2
|
UTSW |
11 |
105,183,609 (GRCm39) |
start gained |
probably benign |
|
R7537:Mrc2
|
UTSW |
11 |
105,183,623 (GRCm39) |
missense |
probably benign |
|
R7640:Mrc2
|
UTSW |
11 |
105,223,121 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7709:Mrc2
|
UTSW |
11 |
105,237,285 (GRCm39) |
missense |
probably benign |
0.10 |
R7885:Mrc2
|
UTSW |
11 |
105,223,092 (GRCm39) |
missense |
probably damaging |
0.98 |
R8042:Mrc2
|
UTSW |
11 |
105,239,181 (GRCm39) |
missense |
probably damaging |
0.98 |
R8096:Mrc2
|
UTSW |
11 |
105,234,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Mrc2
|
UTSW |
11 |
105,223,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R8453:Mrc2
|
UTSW |
11 |
105,223,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R8519:Mrc2
|
UTSW |
11 |
105,238,132 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8771:Mrc2
|
UTSW |
11 |
105,240,596 (GRCm39) |
missense |
probably benign |
|
R8787:Mrc2
|
UTSW |
11 |
105,238,465 (GRCm39) |
missense |
probably benign |
|
R8925:Mrc2
|
UTSW |
11 |
105,216,334 (GRCm39) |
missense |
probably benign |
0.00 |
R8927:Mrc2
|
UTSW |
11 |
105,216,334 (GRCm39) |
missense |
probably benign |
0.00 |
R8991:Mrc2
|
UTSW |
11 |
105,229,740 (GRCm39) |
missense |
probably benign |
|
R9017:Mrc2
|
UTSW |
11 |
105,216,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R9096:Mrc2
|
UTSW |
11 |
105,231,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R9097:Mrc2
|
UTSW |
11 |
105,231,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Mrc2
|
UTSW |
11 |
105,220,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R9471:Mrc2
|
UTSW |
11 |
105,234,559 (GRCm39) |
missense |
probably benign |
0.03 |
R9531:Mrc2
|
UTSW |
11 |
105,240,731 (GRCm39) |
missense |
possibly damaging |
0.82 |
T0970:Mrc2
|
UTSW |
11 |
105,238,453 (GRCm39) |
missense |
probably benign |
0.41 |
X0004:Mrc2
|
UTSW |
11 |
105,238,453 (GRCm39) |
missense |
probably benign |
0.41 |
X0062:Mrc2
|
UTSW |
11 |
105,238,301 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Mrc2
|
UTSW |
11 |
105,238,186 (GRCm39) |
nonsense |
probably null |
|
Z1176:Mrc2
|
UTSW |
11 |
105,232,202 (GRCm39) |
missense |
possibly damaging |
0.94 |
|