Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
A |
T |
10: 28,862,092 (GRCm39) |
I66N |
probably damaging |
Het |
Adgrg3 |
A |
T |
8: 95,760,071 (GRCm39) |
I97F |
probably benign |
Het |
AI987944 |
T |
A |
7: 41,023,937 (GRCm39) |
R350S |
probably benign |
Het |
Arap3 |
T |
C |
18: 38,109,096 (GRCm39) |
T1214A |
probably damaging |
Het |
Arid5a |
A |
G |
1: 36,356,739 (GRCm39) |
E127G |
possibly damaging |
Het |
Bbx |
T |
C |
16: 50,044,920 (GRCm39) |
E547G |
possibly damaging |
Het |
Ceacam16 |
T |
C |
7: 19,587,803 (GRCm39) |
I322V |
probably damaging |
Het |
Chd2 |
G |
T |
7: 73,130,230 (GRCm39) |
N808K |
probably damaging |
Het |
Copg2 |
A |
C |
6: 30,787,399 (GRCm39) |
L615* |
probably null |
Het |
Cyp21a1 |
A |
G |
17: 35,022,017 (GRCm39) |
L221P |
probably damaging |
Het |
Dnah9 |
C |
A |
11: 65,856,507 (GRCm39) |
V2885L |
probably damaging |
Het |
Dnajb13 |
A |
G |
7: 100,152,446 (GRCm39) |
L290P |
probably damaging |
Het |
Eif3e |
A |
G |
15: 43,128,957 (GRCm39) |
V221A |
probably damaging |
Het |
Evc |
G |
A |
5: 37,473,701 (GRCm39) |
R511* |
probably null |
Het |
Far2 |
C |
T |
6: 148,059,434 (GRCm39) |
P250S |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,686,996 (GRCm39) |
T44S |
|
Het |
Grid1 |
A |
G |
14: 35,302,492 (GRCm39) |
E919G |
possibly damaging |
Het |
Grip1 |
G |
A |
10: 119,874,569 (GRCm39) |
E778K |
possibly damaging |
Het |
Hoxb2 |
A |
G |
11: 96,242,725 (GRCm39) |
E30G |
probably damaging |
Het |
Il5ra |
G |
A |
6: 106,689,331 (GRCm39) |
P75L |
unknown |
Het |
Il5ra |
T |
A |
6: 106,721,297 (GRCm39) |
M1L |
possibly damaging |
Het |
Inpp4b |
T |
C |
8: 82,497,555 (GRCm39) |
|
probably null |
Het |
Itgb8 |
T |
A |
12: 119,153,708 (GRCm39) |
H269L |
possibly damaging |
Het |
Jrk |
G |
A |
15: 74,578,403 (GRCm39) |
A294V |
probably damaging |
Het |
Knl1 |
A |
T |
2: 118,887,782 (GRCm39) |
D2V |
probably damaging |
Het |
Lrrc71 |
T |
C |
3: 87,650,258 (GRCm39) |
I272V |
possibly damaging |
Het |
Mdn1 |
T |
C |
4: 32,741,372 (GRCm39) |
S3825P |
probably damaging |
Het |
Mex3d |
C |
A |
10: 80,218,129 (GRCm39) |
V363L |
|
Het |
Mfsd13b |
C |
A |
7: 120,598,134 (GRCm39) |
H347N |
possibly damaging |
Het |
Mllt1 |
G |
T |
17: 57,209,572 (GRCm39) |
H179Q |
probably benign |
Het |
Mmp14 |
A |
T |
14: 54,678,069 (GRCm39) |
R563S |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,549,973 (GRCm39) |
D5440G |
probably benign |
Het |
Muc2 |
A |
T |
7: 141,300,559 (GRCm39) |
E294V |
|
Het |
Myh7b |
A |
G |
2: 155,459,641 (GRCm39) |
N241S |
probably damaging |
Het |
Myo1b |
T |
C |
1: 51,796,404 (GRCm39) |
I1007V |
possibly damaging |
Het |
Or10j5 |
T |
C |
1: 172,784,893 (GRCm39) |
F177S |
probably damaging |
Het |
Or4a77 |
A |
G |
2: 89,487,005 (GRCm39) |
V260A |
possibly damaging |
Het |
Or8g33 |
T |
A |
9: 39,337,851 (GRCm39) |
D172V |
possibly damaging |
Het |
Pan2 |
T |
C |
10: 128,140,135 (GRCm39) |
S19P |
probably benign |
Het |
Pkn3 |
A |
G |
2: 29,976,723 (GRCm39) |
D588G |
probably null |
Het |
Pkp4 |
A |
G |
2: 59,178,104 (GRCm39) |
N988D |
possibly damaging |
Het |
Plxdc1 |
T |
C |
11: 97,824,844 (GRCm39) |
D344G |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,192,169 (GRCm39) |
R807H |
possibly damaging |
Het |
Potefam3b |
T |
A |
8: 21,174,962 (GRCm39) |
F285I |
possibly damaging |
Het |
Prdm15 |
A |
T |
16: 97,623,142 (GRCm39) |
S237T |
probably benign |
Het |
Sanbr |
A |
C |
11: 23,531,642 (GRCm39) |
M661R |
possibly damaging |
Het |
Slc9a2 |
G |
A |
1: 40,721,061 (GRCm39) |
V10M |
probably benign |
Het |
Sytl2 |
T |
C |
7: 90,024,800 (GRCm39) |
S263P |
probably benign |
Het |
Taf7l2 |
A |
T |
10: 115,948,931 (GRCm39) |
D198E |
probably benign |
Het |
Trrap |
G |
A |
5: 144,777,330 (GRCm39) |
V3043M |
probably damaging |
Het |
Tshz3 |
C |
T |
7: 36,470,492 (GRCm39) |
T827I |
possibly damaging |
Het |
Ttll1 |
T |
C |
15: 83,384,226 (GRCm39) |
T134A |
possibly damaging |
Het |
Vmn1r196 |
G |
T |
13: 22,477,920 (GRCm39) |
M186I |
probably damaging |
Het |
Vrk2 |
C |
T |
11: 26,433,157 (GRCm39) |
|
probably null |
Het |
Zfp59 |
T |
A |
7: 27,554,483 (GRCm39) |
V645E |
probably benign |
Het |
|
Other mutations in Ms4a18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0556:Ms4a18
|
UTSW |
19 |
10,991,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R1987:Ms4a18
|
UTSW |
19 |
10,991,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2031:Ms4a18
|
UTSW |
19 |
10,991,014 (GRCm39) |
missense |
probably benign |
0.06 |
R2137:Ms4a18
|
UTSW |
19 |
10,974,695 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2138:Ms4a18
|
UTSW |
19 |
10,974,695 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2139:Ms4a18
|
UTSW |
19 |
10,974,695 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2192:Ms4a18
|
UTSW |
19 |
10,991,029 (GRCm39) |
missense |
probably benign |
0.09 |
R2211:Ms4a18
|
UTSW |
19 |
10,974,669 (GRCm39) |
missense |
probably benign |
0.33 |
R3739:Ms4a18
|
UTSW |
19 |
10,988,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Ms4a18
|
UTSW |
19 |
10,991,038 (GRCm39) |
missense |
probably benign |
0.00 |
R6102:Ms4a18
|
UTSW |
19 |
10,990,887 (GRCm39) |
missense |
probably benign |
|
R7091:Ms4a18
|
UTSW |
19 |
10,986,092 (GRCm39) |
missense |
probably damaging |
0.98 |
R7316:Ms4a18
|
UTSW |
19 |
10,979,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Ms4a18
|
UTSW |
19 |
10,991,071 (GRCm39) |
missense |
probably benign |
0.00 |
R8854:Ms4a18
|
UTSW |
19 |
10,990,887 (GRCm39) |
missense |
probably benign |
|
R9098:Ms4a18
|
UTSW |
19 |
10,990,741 (GRCm39) |
missense |
|
|
R9157:Ms4a18
|
UTSW |
19 |
10,988,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R9313:Ms4a18
|
UTSW |
19 |
10,988,804 (GRCm39) |
missense |
probably damaging |
0.98 |
|