Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
T |
A |
4: 103,127,964 (GRCm39) |
I54F |
possibly damaging |
Het |
Ackr1 |
A |
T |
1: 173,159,916 (GRCm39) |
H134Q |
probably benign |
Het |
Agtr1b |
A |
T |
3: 20,370,473 (GRCm39) |
F44L |
probably benign |
Het |
Ahnak |
G |
A |
19: 8,989,173 (GRCm39) |
D3486N |
possibly damaging |
Het |
Akap9 |
T |
C |
5: 4,089,345 (GRCm39) |
|
probably null |
Het |
Anks6 |
T |
A |
4: 47,039,726 (GRCm39) |
Q495L |
probably benign |
Het |
Arpp21 |
A |
G |
9: 111,896,237 (GRCm39) |
S684P |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,983,531 (GRCm39) |
E2911G |
probably damaging |
Het |
Avpi1 |
C |
T |
19: 42,113,248 (GRCm39) |
E70K |
probably damaging |
Het |
Btbd17 |
G |
T |
11: 114,686,650 (GRCm39) |
P9T |
probably benign |
Het |
C4b |
A |
G |
17: 34,948,245 (GRCm39) |
|
probably benign |
Het |
Carm1 |
T |
C |
9: 21,497,785 (GRCm39) |
V385A |
probably damaging |
Het |
Casd1 |
A |
G |
6: 4,624,104 (GRCm39) |
D299G |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,730,307 (GRCm39) |
K179N |
probably benign |
Het |
Col1a2 |
T |
C |
6: 4,538,691 (GRCm39) |
S1204P |
unknown |
Het |
Col24a1 |
C |
T |
3: 145,072,624 (GRCm39) |
Q780* |
probably null |
Het |
Cxadr |
C |
A |
16: 78,131,133 (GRCm39) |
N216K |
probably damaging |
Het |
Daam1 |
C |
T |
12: 71,942,656 (GRCm39) |
T40I |
unknown |
Het |
Dab2 |
C |
T |
15: 6,459,182 (GRCm39) |
P365S |
possibly damaging |
Het |
Dnah1 |
A |
T |
14: 31,001,139 (GRCm39) |
I2402N |
probably damaging |
Het |
Dscaml1 |
T |
A |
9: 45,663,988 (GRCm39) |
S1954R |
possibly damaging |
Het |
Dync2h1 |
T |
C |
9: 7,131,891 (GRCm39) |
T1639A |
probably benign |
Het |
Ebf1 |
A |
T |
11: 44,815,393 (GRCm39) |
I336F |
probably damaging |
Het |
Ebna1bp2 |
A |
G |
4: 118,482,881 (GRCm39) |
N290S |
possibly damaging |
Het |
Gabra2 |
A |
G |
5: 71,171,906 (GRCm39) |
I110T |
probably benign |
Het |
Galk2 |
A |
G |
2: 125,773,210 (GRCm39) |
N203S |
probably benign |
Het |
Gria4 |
T |
C |
9: 4,424,448 (GRCm39) |
T806A |
probably benign |
Het |
Impg2 |
A |
G |
16: 56,080,889 (GRCm39) |
T789A |
probably benign |
Het |
Itga6 |
A |
G |
2: 71,617,546 (GRCm39) |
T22A |
probably benign |
Het |
Itgb4 |
T |
A |
11: 115,894,315 (GRCm39) |
I1312N |
probably damaging |
Het |
Kdm4c |
A |
G |
4: 74,216,721 (GRCm39) |
D160G |
probably benign |
Het |
Kdr |
A |
G |
5: 76,129,127 (GRCm39) |
V173A |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,455,202 (GRCm39) |
S1575P |
probably benign |
Het |
Lcp1 |
G |
A |
14: 75,436,884 (GRCm39) |
|
probably null |
Het |
Lipe |
C |
A |
7: 25,084,750 (GRCm39) |
S516I |
probably damaging |
Het |
Lrrc61 |
G |
A |
6: 48,545,708 (GRCm39) |
R177Q |
possibly damaging |
Het |
Macf1 |
A |
G |
4: 123,272,487 (GRCm39) |
I6429T |
probably damaging |
Het |
Map3k4 |
C |
T |
17: 12,468,458 (GRCm39) |
E1012K |
probably benign |
Het |
Map3k5 |
T |
C |
10: 19,986,593 (GRCm39) |
F936L |
possibly damaging |
Het |
Mllt3 |
A |
T |
4: 87,701,901 (GRCm39) |
N497K |
probably damaging |
Het |
Moxd1 |
G |
A |
10: 24,157,394 (GRCm39) |
G342D |
probably damaging |
Het |
Mtdh |
A |
C |
15: 34,114,985 (GRCm39) |
Q202H |
possibly damaging |
Het |
Nav1 |
A |
G |
1: 135,522,972 (GRCm39) |
|
probably benign |
Het |
Nop56 |
T |
C |
2: 130,119,886 (GRCm39) |
V109A |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,970,712 (GRCm39) |
D2540G |
probably damaging |
Het |
Omg |
T |
C |
11: 79,393,679 (GRCm39) |
I60V |
probably benign |
Het |
Or10q12 |
A |
T |
19: 13,746,659 (GRCm39) |
T318S |
probably benign |
Het |
Or12e9 |
A |
T |
2: 87,202,290 (GRCm39) |
Y138F |
probably damaging |
Het |
Osbpl5 |
G |
A |
7: 143,248,110 (GRCm39) |
H652Y |
probably damaging |
Het |
Parvb |
T |
C |
15: 84,182,192 (GRCm39) |
|
probably benign |
Het |
Pcdhb3 |
A |
C |
18: 37,436,375 (GRCm39) |
E780D |
probably benign |
Het |
Pik3c3 |
A |
G |
18: 30,456,639 (GRCm39) |
D723G |
possibly damaging |
Het |
Prkdc |
T |
C |
16: 15,612,958 (GRCm39) |
V3172A |
probably benign |
Het |
Psme4 |
G |
T |
11: 30,756,310 (GRCm39) |
W272L |
probably damaging |
Het |
Rem1 |
G |
A |
2: 152,476,455 (GRCm39) |
V238M |
probably damaging |
Het |
Rhobtb1 |
A |
C |
10: 69,108,601 (GRCm39) |
S434R |
probably benign |
Het |
Rhobtb1 |
G |
C |
10: 69,108,602 (GRCm39) |
S434T |
possibly damaging |
Het |
Rnf8 |
T |
C |
17: 29,853,735 (GRCm39) |
F413S |
probably damaging |
Het |
Rpn2 |
A |
G |
2: 157,156,888 (GRCm39) |
N497S |
probably damaging |
Het |
Rsbn1l |
G |
T |
5: 21,156,488 (GRCm39) |
P99Q |
probably benign |
Het |
Serpinb3b |
A |
T |
1: 107,083,164 (GRCm39) |
M246K |
probably benign |
Het |
Sgsm2 |
T |
C |
11: 74,787,652 (GRCm39) |
E19G |
probably null |
Het |
Shank1 |
A |
G |
7: 43,969,161 (GRCm39) |
H352R |
unknown |
Het |
Slc17a7 |
A |
G |
7: 44,819,728 (GRCm39) |
I177V |
probably benign |
Het |
Slc28a2 |
T |
A |
2: 122,281,494 (GRCm39) |
F228I |
probably damaging |
Het |
Slc35b4 |
C |
T |
6: 34,147,484 (GRCm39) |
V35I |
probably benign |
Het |
Slc38a1 |
T |
C |
15: 96,476,641 (GRCm39) |
I407V |
probably damaging |
Het |
Slc39a13 |
A |
G |
2: 90,893,442 (GRCm39) |
V326A |
probably damaging |
Het |
Slc44a5 |
T |
C |
3: 153,944,743 (GRCm39) |
L120P |
probably damaging |
Het |
Slfn3 |
T |
C |
11: 83,104,140 (GRCm39) |
I214T |
probably damaging |
Het |
Snx14 |
T |
C |
9: 88,297,728 (GRCm39) |
Y180C |
probably damaging |
Het |
Sorl1 |
T |
A |
9: 41,907,538 (GRCm39) |
K1483I |
probably benign |
Het |
Ssrp1 |
C |
A |
2: 84,871,104 (GRCm39) |
H247N |
probably damaging |
Het |
Stk39 |
A |
T |
2: 68,137,460 (GRCm39) |
|
probably benign |
Het |
Syde1 |
C |
T |
10: 78,421,530 (GRCm39) |
G674R |
probably damaging |
Het |
Tent4a |
A |
T |
13: 69,651,170 (GRCm39) |
I565N |
probably benign |
Het |
Themis3 |
G |
A |
17: 66,862,848 (GRCm39) |
S370L |
probably benign |
Het |
Tll1 |
T |
A |
8: 64,554,907 (GRCm39) |
N259Y |
probably damaging |
Het |
Tnip2 |
T |
G |
5: 34,661,175 (GRCm39) |
|
probably benign |
Het |
Top2b |
T |
C |
14: 16,409,823 (GRCm38) |
V830A |
probably benign |
Het |
Trpm8 |
T |
A |
1: 88,292,802 (GRCm39) |
N934K |
probably damaging |
Het |
Ttc14 |
A |
G |
3: 33,857,069 (GRCm39) |
Y179C |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,573,965 (GRCm39) |
I17316L |
possibly damaging |
Het |
Tufm |
T |
C |
7: 126,086,871 (GRCm39) |
V52A |
probably benign |
Het |
Vamp8 |
T |
A |
6: 72,365,270 (GRCm39) |
N20I |
probably benign |
Het |
Vmn1r170 |
A |
T |
7: 23,306,288 (GRCm39) |
H230L |
probably benign |
Het |
Vmn2r50 |
T |
G |
7: 9,771,731 (GRCm39) |
T657P |
probably damaging |
Het |
Xirp2 |
G |
A |
2: 67,342,762 (GRCm39) |
G1668R |
probably benign |
Het |
Zik1 |
C |
A |
7: 10,224,311 (GRCm39) |
R262L |
possibly damaging |
Het |
Zscan25 |
T |
G |
5: 145,220,501 (GRCm39) |
Y99D |
probably damaging |
Het |
|
Other mutations in Slitrk3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Slitrk3
|
APN |
3 |
72,958,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00857:Slitrk3
|
APN |
3 |
72,957,174 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Slitrk3
|
APN |
3 |
72,957,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01010:Slitrk3
|
APN |
3 |
72,956,606 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01299:Slitrk3
|
APN |
3 |
72,956,349 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01609:Slitrk3
|
APN |
3 |
72,957,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01881:Slitrk3
|
APN |
3 |
72,956,639 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01941:Slitrk3
|
APN |
3 |
72,958,404 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02183:Slitrk3
|
APN |
3 |
72,957,312 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02187:Slitrk3
|
APN |
3 |
72,957,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02478:Slitrk3
|
APN |
3 |
72,958,046 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02512:Slitrk3
|
APN |
3 |
72,957,735 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02720:Slitrk3
|
APN |
3 |
72,958,101 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03113:Slitrk3
|
APN |
3 |
72,957,723 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03224:Slitrk3
|
APN |
3 |
72,957,263 (GRCm39) |
missense |
possibly damaging |
0.72 |
wee
|
UTSW |
3 |
72,958,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Slitrk3
|
UTSW |
3 |
72,955,910 (GRCm39) |
missense |
probably benign |
0.00 |
R0233:Slitrk3
|
UTSW |
3 |
72,955,910 (GRCm39) |
missense |
probably benign |
0.00 |
R0639:Slitrk3
|
UTSW |
3 |
72,956,982 (GRCm39) |
missense |
probably benign |
0.02 |
R1448:Slitrk3
|
UTSW |
3 |
72,957,674 (GRCm39) |
missense |
probably damaging |
0.99 |
R1656:Slitrk3
|
UTSW |
3 |
72,957,672 (GRCm39) |
missense |
probably damaging |
0.98 |
R1992:Slitrk3
|
UTSW |
3 |
72,957,104 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1999:Slitrk3
|
UTSW |
3 |
72,957,297 (GRCm39) |
missense |
probably benign |
0.13 |
R2359:Slitrk3
|
UTSW |
3 |
72,956,678 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3083:Slitrk3
|
UTSW |
3 |
72,955,928 (GRCm39) |
missense |
probably benign |
0.00 |
R3153:Slitrk3
|
UTSW |
3 |
72,956,315 (GRCm39) |
nonsense |
probably null |
|
R3821:Slitrk3
|
UTSW |
3 |
72,956,549 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4208:Slitrk3
|
UTSW |
3 |
72,958,490 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4323:Slitrk3
|
UTSW |
3 |
72,958,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Slitrk3
|
UTSW |
3 |
72,958,539 (GRCm39) |
missense |
probably damaging |
0.96 |
R4730:Slitrk3
|
UTSW |
3 |
72,956,852 (GRCm39) |
missense |
probably benign |
0.08 |
R4742:Slitrk3
|
UTSW |
3 |
72,955,898 (GRCm39) |
missense |
probably benign |
0.00 |
R4979:Slitrk3
|
UTSW |
3 |
72,957,129 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5018:Slitrk3
|
UTSW |
3 |
72,957,845 (GRCm39) |
missense |
probably benign |
0.31 |
R5023:Slitrk3
|
UTSW |
3 |
72,957,981 (GRCm39) |
missense |
probably benign |
0.24 |
R5057:Slitrk3
|
UTSW |
3 |
72,957,981 (GRCm39) |
missense |
probably benign |
0.24 |
R5156:Slitrk3
|
UTSW |
3 |
72,956,592 (GRCm39) |
missense |
probably benign |
|
R5500:Slitrk3
|
UTSW |
3 |
72,957,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R5582:Slitrk3
|
UTSW |
3 |
72,957,737 (GRCm39) |
missense |
probably benign |
0.09 |
R5797:Slitrk3
|
UTSW |
3 |
72,955,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R5963:Slitrk3
|
UTSW |
3 |
72,958,046 (GRCm39) |
missense |
probably benign |
0.30 |
R5985:Slitrk3
|
UTSW |
3 |
72,958,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R6123:Slitrk3
|
UTSW |
3 |
72,957,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Slitrk3
|
UTSW |
3 |
72,957,247 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6529:Slitrk3
|
UTSW |
3 |
72,958,551 (GRCm39) |
missense |
probably benign |
0.02 |
R6584:Slitrk3
|
UTSW |
3 |
72,956,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R6645:Slitrk3
|
UTSW |
3 |
72,957,194 (GRCm39) |
missense |
probably benign |
0.13 |
R7001:Slitrk3
|
UTSW |
3 |
72,957,942 (GRCm39) |
nonsense |
probably null |
|
R7282:Slitrk3
|
UTSW |
3 |
72,957,798 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7534:Slitrk3
|
UTSW |
3 |
72,957,440 (GRCm39) |
missense |
probably damaging |
0.98 |
R7577:Slitrk3
|
UTSW |
3 |
72,958,448 (GRCm39) |
missense |
probably damaging |
0.99 |
R7757:Slitrk3
|
UTSW |
3 |
72,958,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Slitrk3
|
UTSW |
3 |
72,956,729 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8354:Slitrk3
|
UTSW |
3 |
72,956,513 (GRCm39) |
missense |
probably benign |
0.08 |
R8454:Slitrk3
|
UTSW |
3 |
72,956,513 (GRCm39) |
missense |
probably benign |
0.08 |
R8488:Slitrk3
|
UTSW |
3 |
72,958,520 (GRCm39) |
missense |
probably benign |
0.02 |
R8491:Slitrk3
|
UTSW |
3 |
72,958,592 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8843:Slitrk3
|
UTSW |
3 |
72,956,164 (GRCm39) |
missense |
probably benign |
0.04 |
R9140:Slitrk3
|
UTSW |
3 |
72,957,792 (GRCm39) |
missense |
probably benign |
0.02 |
R9451:Slitrk3
|
UTSW |
3 |
72,958,616 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9511:Slitrk3
|
UTSW |
3 |
72,958,272 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9575:Slitrk3
|
UTSW |
3 |
72,956,127 (GRCm39) |
missense |
probably benign |
0.00 |
R9589:Slitrk3
|
UTSW |
3 |
72,957,981 (GRCm39) |
missense |
probably benign |
0.24 |
R9603:Slitrk3
|
UTSW |
3 |
72,958,649 (GRCm39) |
missense |
probably benign |
0.00 |
X0022:Slitrk3
|
UTSW |
3 |
72,957,599 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Slitrk3
|
UTSW |
3 |
72,956,103 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:Slitrk3
|
UTSW |
3 |
72,956,475 (GRCm39) |
missense |
probably benign |
0.00 |
|