Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932416K20Rik |
G |
A |
8: 105,524,271 (GRCm39) |
|
noncoding transcript |
Het |
Abcg8 |
A |
T |
17: 84,994,127 (GRCm39) |
E48V |
probably damaging |
Het |
Afap1l2 |
T |
C |
19: 56,911,406 (GRCm39) |
T289A |
probably benign |
Het |
Atf6 |
T |
A |
1: 170,574,758 (GRCm39) |
D560V |
probably damaging |
Het |
Bcl2l14 |
A |
T |
6: 134,404,362 (GRCm39) |
K183N |
probably damaging |
Het |
Carmil3 |
T |
C |
14: 55,730,696 (GRCm39) |
L52P |
probably damaging |
Het |
Cct3 |
T |
A |
3: 88,208,274 (GRCm39) |
N61K |
probably damaging |
Het |
Col18a1 |
A |
G |
10: 77,002,177 (GRCm39) |
V10A |
unknown |
Het |
Col26a1 |
G |
A |
5: 136,876,420 (GRCm39) |
Q67* |
probably null |
Het |
Cyp2d34 |
T |
C |
15: 82,501,341 (GRCm39) |
D329G |
probably null |
Het |
Dchs1 |
T |
A |
7: 105,422,247 (GRCm39) |
I58F |
probably damaging |
Het |
Ddx60 |
T |
C |
8: 62,401,931 (GRCm39) |
L269P |
probably damaging |
Het |
Dis3l2 |
G |
A |
1: 86,806,154 (GRCm39) |
G325D |
probably damaging |
Het |
Dync1h1 |
A |
T |
12: 110,612,707 (GRCm39) |
K2861* |
probably null |
Het |
Ednra |
A |
G |
8: 78,401,696 (GRCm39) |
I198T |
possibly damaging |
Het |
Ep300 |
T |
C |
15: 81,524,115 (GRCm39) |
|
probably benign |
Het |
Fam120a |
G |
A |
13: 49,034,409 (GRCm39) |
P1068S |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,815,084 (GRCm39) |
M3606L |
probably benign |
Het |
Garre1 |
A |
T |
7: 33,953,413 (GRCm39) |
W238R |
probably damaging |
Het |
Gm7713 |
T |
C |
15: 59,866,492 (GRCm39) |
|
noncoding transcript |
Het |
Gprin3 |
A |
T |
6: 59,331,398 (GRCm39) |
V303D |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,570,629 (GRCm39) |
V2178D |
possibly damaging |
Het |
Hoxa11 |
A |
G |
6: 52,222,380 (GRCm39) |
V107A |
possibly damaging |
Het |
Iqub |
C |
A |
6: 24,454,250 (GRCm39) |
M544I |
possibly damaging |
Het |
Itgb4 |
A |
T |
11: 115,879,258 (GRCm39) |
|
probably benign |
Het |
Itpkb |
A |
G |
1: 180,161,818 (GRCm39) |
|
probably benign |
Het |
Kalrn |
A |
T |
16: 33,796,190 (GRCm39) |
V1195E |
probably damaging |
Het |
Kif12 |
C |
A |
4: 63,084,178 (GRCm39) |
R608M |
probably damaging |
Het |
Lcorl |
A |
T |
5: 45,952,709 (GRCm39) |
|
probably null |
Het |
Lrrc24 |
T |
C |
15: 76,606,910 (GRCm39) |
E162G |
probably damaging |
Het |
Med6 |
A |
G |
12: 81,626,418 (GRCm39) |
S119P |
probably damaging |
Het |
Mmab |
A |
C |
5: 114,574,775 (GRCm39) |
L166R |
probably damaging |
Het |
Myef2l |
A |
G |
3: 10,153,566 (GRCm39) |
R112G |
probably damaging |
Het |
Nom1 |
A |
G |
5: 29,651,873 (GRCm39) |
K737R |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,946,970 (GRCm39) |
S4352G |
probably damaging |
Het |
Or10ag60 |
A |
T |
2: 87,438,517 (GRCm39) |
T262S |
probably benign |
Het |
Or2w25 |
T |
A |
11: 59,504,712 (GRCm39) |
D307E |
probably benign |
Het |
Or4k35 |
A |
T |
2: 111,100,057 (GRCm39) |
Y218* |
probably null |
Het |
Or6d12 |
A |
C |
6: 116,492,912 (GRCm39) |
D58A |
possibly damaging |
Het |
Pdzrn3 |
G |
A |
6: 101,149,275 (GRCm39) |
S351L |
probably benign |
Het |
Pdzrn4 |
A |
T |
15: 92,655,562 (GRCm39) |
E485V |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,597,252 (GRCm39) |
I2804K |
possibly damaging |
Het |
Psg28 |
A |
G |
7: 18,164,640 (GRCm39) |
L24P |
probably damaging |
Het |
Resp18 |
A |
G |
1: 75,250,644 (GRCm39) |
V145A |
possibly damaging |
Het |
Rgl3 |
T |
C |
9: 21,892,908 (GRCm39) |
M259V |
probably benign |
Het |
Rhot2 |
A |
T |
17: 26,058,781 (GRCm39) |
S540T |
probably benign |
Het |
Ring1 |
T |
C |
17: 34,241,282 (GRCm39) |
Y278C |
possibly damaging |
Het |
Rpn2 |
A |
G |
2: 157,137,265 (GRCm39) |
Y216C |
probably damaging |
Het |
Scgb2b18 |
G |
A |
7: 32,873,255 (GRCm39) |
L5F |
unknown |
Het |
Slamf7 |
T |
C |
1: 171,466,838 (GRCm39) |
|
probably null |
Het |
Spen |
A |
T |
4: 141,205,495 (GRCm39) |
V1044D |
unknown |
Het |
Sqor |
A |
T |
2: 122,651,261 (GRCm39) |
M175L |
probably benign |
Het |
Stx16 |
G |
A |
2: 173,935,292 (GRCm39) |
G156R |
probably damaging |
Het |
Tars3 |
T |
G |
7: 65,333,873 (GRCm39) |
F632V |
probably damaging |
Het |
Tln1 |
A |
G |
4: 43,545,191 (GRCm39) |
V1008A |
probably benign |
Het |
Tmem145 |
A |
G |
7: 25,015,039 (GRCm39) |
H554R |
probably benign |
Het |
Trank1 |
A |
T |
9: 111,195,744 (GRCm39) |
D1256V |
possibly damaging |
Het |
Trbv19 |
A |
G |
6: 41,155,794 (GRCm39) |
Y55C |
possibly damaging |
Het |
Ttc23l |
C |
T |
15: 10,551,555 (GRCm39) |
C57Y |
probably benign |
Het |
Uap1 |
A |
T |
1: 169,988,949 (GRCm39) |
C158S |
probably benign |
Het |
Zfp353-ps |
T |
A |
8: 42,535,647 (GRCm39) |
|
noncoding transcript |
Het |
Zfp629 |
T |
A |
7: 127,210,307 (GRCm39) |
I501F |
probably damaging |
Het |
Zfp820 |
T |
C |
17: 22,037,702 (GRCm39) |
Y542C |
probably damaging |
Het |
|
Other mutations in Slc22a12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02033:Slc22a12
|
APN |
19 |
6,587,844 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02586:Slc22a12
|
APN |
19 |
6,590,487 (GRCm39) |
missense |
probably benign |
0.03 |
mutual
|
UTSW |
19 |
6,592,683 (GRCm39) |
nonsense |
probably null |
|
reinforcement
|
UTSW |
19 |
6,587,199 (GRCm39) |
missense |
probably benign |
0.03 |
R1353:Slc22a12
|
UTSW |
19 |
6,587,812 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1757:Slc22a12
|
UTSW |
19 |
6,586,761 (GRCm39) |
splice site |
probably null |
|
R1816:Slc22a12
|
UTSW |
19 |
6,592,683 (GRCm39) |
nonsense |
probably null |
|
R2254:Slc22a12
|
UTSW |
19 |
6,592,571 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4110:Slc22a12
|
UTSW |
19 |
6,590,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R4125:Slc22a12
|
UTSW |
19 |
6,588,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R4342:Slc22a12
|
UTSW |
19 |
6,591,129 (GRCm39) |
missense |
probably benign |
0.15 |
R4762:Slc22a12
|
UTSW |
19 |
6,588,474 (GRCm39) |
missense |
probably benign |
0.02 |
R4927:Slc22a12
|
UTSW |
19 |
6,587,791 (GRCm39) |
missense |
probably benign |
0.23 |
R5690:Slc22a12
|
UTSW |
19 |
6,586,878 (GRCm39) |
missense |
probably benign |
0.00 |
R5946:Slc22a12
|
UTSW |
19 |
6,587,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R6137:Slc22a12
|
UTSW |
19 |
6,592,754 (GRCm39) |
missense |
probably benign |
0.07 |
R7740:Slc22a12
|
UTSW |
19 |
6,587,199 (GRCm39) |
missense |
probably benign |
0.03 |
R7978:Slc22a12
|
UTSW |
19 |
6,586,938 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8028:Slc22a12
|
UTSW |
19 |
6,588,469 (GRCm39) |
missense |
probably benign |
0.15 |
R8508:Slc22a12
|
UTSW |
19 |
6,592,467 (GRCm39) |
missense |
probably benign |
0.03 |
R8992:Slc22a12
|
UTSW |
19 |
6,592,514 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9559:Slc22a12
|
UTSW |
19 |
6,587,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R9644:Slc22a12
|
UTSW |
19 |
6,587,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R9716:Slc22a12
|
UTSW |
19 |
6,586,765 (GRCm39) |
critical splice donor site |
probably null |
|
X0062:Slc22a12
|
UTSW |
19 |
6,587,157 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Slc22a12
|
UTSW |
19 |
6,588,493 (GRCm39) |
missense |
possibly damaging |
0.54 |
Z1177:Slc22a12
|
UTSW |
19 |
6,590,431 (GRCm39) |
missense |
probably benign |
0.01 |
|