Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap3 |
G |
T |
4: 155,990,371 (GRCm39) |
R819L |
possibly damaging |
Het |
App |
A |
G |
16: 84,876,767 (GRCm39) |
V208A |
unknown |
Het |
C1qtnf7 |
G |
A |
5: 43,773,204 (GRCm39) |
E168K |
probably damaging |
Het |
Cacna1e |
C |
T |
1: 154,349,632 (GRCm39) |
M757I |
probably benign |
Het |
Casp1 |
A |
G |
9: 5,299,333 (GRCm39) |
T21A |
probably benign |
Het |
Ccdc92 |
C |
T |
5: 124,912,705 (GRCm39) |
A275T |
possibly damaging |
Het |
Ccr4 |
T |
A |
9: 114,325,620 (GRCm39) |
|
probably benign |
Het |
Cct8l1 |
C |
T |
5: 25,722,908 (GRCm39) |
T541I |
probably benign |
Het |
Chrng |
G |
T |
1: 87,138,397 (GRCm39) |
R396L |
possibly damaging |
Het |
Cmip |
A |
G |
8: 118,103,925 (GRCm39) |
T50A |
probably damaging |
Het |
Ddx21 |
C |
A |
10: 62,434,486 (GRCm39) |
S91I |
probably benign |
Het |
Dnmbp |
A |
G |
19: 43,890,225 (GRCm39) |
L514P |
probably benign |
Het |
Echs1 |
A |
T |
7: 139,690,499 (GRCm39) |
M191K |
probably damaging |
Het |
Eps8 |
A |
G |
6: 137,489,175 (GRCm39) |
S408P |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,200,896 (GRCm39) |
E726G |
probably damaging |
Het |
Fpr2 |
T |
C |
17: 18,113,190 (GRCm39) |
I62T |
probably benign |
Het |
Gemin4 |
G |
A |
11: 76,102,848 (GRCm39) |
Q638* |
probably null |
Het |
Glrb |
A |
T |
3: 80,769,285 (GRCm39) |
N147K |
probably damaging |
Het |
Gm10800 |
CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA |
CAAGAAAACTGAAAATCA |
2: 98,497,361 (GRCm39) |
|
probably null |
Het |
Gtf2i |
T |
C |
5: 134,278,720 (GRCm39) |
N637S |
probably benign |
Het |
Hivep3 |
A |
G |
4: 119,953,937 (GRCm39) |
E751G |
possibly damaging |
Het |
Ifnb1 |
G |
T |
4: 88,440,547 (GRCm39) |
N155K |
probably damaging |
Het |
Igf2bp3 |
G |
T |
6: 49,065,365 (GRCm39) |
T509K |
probably damaging |
Het |
Igsf10 |
T |
C |
3: 59,243,633 (GRCm39) |
M234V |
probably benign |
Het |
Iqgap2 |
C |
T |
13: 95,818,711 (GRCm39) |
A682T |
probably benign |
Het |
Ireb2 |
T |
G |
9: 54,799,786 (GRCm39) |
M409R |
probably benign |
Het |
Kat6b |
C |
T |
14: 21,719,629 (GRCm39) |
T1327I |
probably benign |
Het |
Krtap5-5 |
A |
G |
7: 141,783,630 (GRCm39) |
S7P |
unknown |
Het |
Lelp1 |
A |
T |
3: 92,042,978 (GRCm39) |
C24S |
unknown |
Het |
Malrd1 |
A |
T |
2: 16,260,145 (GRCm39) |
K2122* |
probably null |
Het |
Mei1 |
C |
A |
15: 81,954,212 (GRCm39) |
R6S |
unknown |
Het |
Meis3 |
T |
A |
7: 15,911,887 (GRCm39) |
I119N |
probably benign |
Het |
Mmp20 |
T |
C |
9: 7,639,288 (GRCm39) |
V152A |
probably benign |
Het |
Muc6 |
T |
A |
7: 141,233,791 (GRCm39) |
I797F |
possibly damaging |
Het |
Myo7a |
C |
T |
7: 97,741,820 (GRCm39) |
E439K |
probably damaging |
Het |
Neb |
C |
A |
2: 52,133,222 (GRCm39) |
A3439S |
probably damaging |
Het |
Nfe2l1 |
T |
A |
11: 96,708,620 (GRCm39) |
D715V |
unknown |
Het |
Obscn |
C |
A |
11: 59,026,762 (GRCm39) |
R147L |
probably benign |
Het |
Or14j5 |
T |
A |
17: 38,162,101 (GRCm39) |
M206K |
probably benign |
Het |
Or2m12 |
T |
A |
16: 19,105,383 (GRCm39) |
I37F |
probably damaging |
Het |
Or2y1b |
A |
T |
11: 49,209,206 (GRCm39) |
T278S |
probably benign |
Het |
Or4e5 |
G |
A |
14: 52,728,010 (GRCm39) |
T137I |
probably benign |
Het |
Or5d38 |
A |
G |
2: 87,954,778 (GRCm39) |
S184P |
probably damaging |
Het |
Plg |
T |
A |
17: 12,629,790 (GRCm39) |
F608Y |
probably benign |
Het |
Plppr1 |
C |
A |
4: 49,319,836 (GRCm39) |
P154Q |
probably damaging |
Het |
Ppp2r5e |
T |
C |
12: 75,500,570 (GRCm39) |
K441R |
probably benign |
Het |
Prkaca |
T |
C |
8: 84,703,714 (GRCm39) |
S5P |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,041,420 (GRCm39) |
K69R |
probably benign |
Het |
Rbpms2 |
T |
C |
9: 65,558,351 (GRCm39) |
I129T |
probably benign |
Het |
Serpina1c |
A |
T |
12: 103,865,117 (GRCm39) |
N176K |
probably damaging |
Het |
Sgsm3 |
C |
T |
15: 80,890,796 (GRCm39) |
H117Y |
probably damaging |
Het |
Sphkap |
A |
T |
1: 83,256,685 (GRCm39) |
C355S |
probably benign |
Het |
Stpg2 |
T |
A |
3: 139,004,170 (GRCm39) |
V249E |
probably damaging |
Het |
Syt2 |
T |
C |
1: 134,675,391 (GRCm39) |
V414A |
possibly damaging |
Het |
Tiam2 |
T |
C |
17: 3,527,471 (GRCm39) |
I1050T |
probably benign |
Het |
Tmem131 |
A |
T |
1: 36,848,046 (GRCm39) |
I1134N |
probably damaging |
Het |
Ttc41 |
C |
A |
10: 86,548,865 (GRCm39) |
R20S |
probably benign |
Het |
Ttn |
C |
T |
2: 76,571,133 (GRCm39) |
V26587M |
probably damaging |
Het |
Ugt2a2 |
T |
C |
5: 87,608,270 (GRCm39) |
K523R |
possibly damaging |
Het |
Unc13c |
A |
G |
9: 73,656,830 (GRCm39) |
C1124R |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,175,281 (GRCm39) |
N1126K |
probably damaging |
Het |
Usp36 |
A |
T |
11: 118,165,840 (GRCm39) |
L326Q |
probably damaging |
Het |
Zfp568 |
T |
C |
7: 29,713,307 (GRCm39) |
M120T |
probably benign |
Het |
Zfp944 |
T |
C |
17: 22,558,761 (GRCm39) |
D162G |
probably benign |
Het |
|
Other mutations in Ttc23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02852:Ttc23
|
APN |
7 |
67,316,903 (GRCm39) |
unclassified |
probably benign |
|
IGL03257:Ttc23
|
APN |
7 |
67,361,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03365:Ttc23
|
APN |
7 |
67,312,085 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03404:Ttc23
|
APN |
7 |
67,328,645 (GRCm39) |
missense |
probably damaging |
0.99 |
F5770:Ttc23
|
UTSW |
7 |
67,359,063 (GRCm39) |
splice site |
probably benign |
|
PIT4445001:Ttc23
|
UTSW |
7 |
67,316,961 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4791001:Ttc23
|
UTSW |
7 |
67,312,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Ttc23
|
UTSW |
7 |
67,319,600 (GRCm39) |
unclassified |
probably benign |
|
R0316:Ttc23
|
UTSW |
7 |
67,328,821 (GRCm39) |
critical splice donor site |
probably null |
|
R0336:Ttc23
|
UTSW |
7 |
67,312,231 (GRCm39) |
missense |
probably benign |
0.01 |
R1456:Ttc23
|
UTSW |
7 |
67,316,902 (GRCm39) |
unclassified |
probably benign |
|
R1543:Ttc23
|
UTSW |
7 |
67,328,743 (GRCm39) |
missense |
probably benign |
0.01 |
R1662:Ttc23
|
UTSW |
7 |
67,375,069 (GRCm39) |
splice site |
probably null |
|
R1708:Ttc23
|
UTSW |
7 |
67,316,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R1857:Ttc23
|
UTSW |
7 |
67,328,821 (GRCm39) |
critical splice donor site |
probably null |
|
R2292:Ttc23
|
UTSW |
7 |
67,319,535 (GRCm39) |
missense |
probably benign |
0.08 |
R4471:Ttc23
|
UTSW |
7 |
67,319,904 (GRCm39) |
missense |
probably benign |
0.37 |
R6036:Ttc23
|
UTSW |
7 |
67,361,114 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6036:Ttc23
|
UTSW |
7 |
67,361,114 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6841:Ttc23
|
UTSW |
7 |
67,319,476 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7690:Ttc23
|
UTSW |
7 |
67,319,918 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8305:Ttc23
|
UTSW |
7 |
67,312,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R8837:Ttc23
|
UTSW |
7 |
67,319,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9052:Ttc23
|
UTSW |
7 |
67,342,687 (GRCm39) |
nonsense |
probably null |
|
R9150:Ttc23
|
UTSW |
7 |
67,375,850 (GRCm39) |
missense |
probably damaging |
0.99 |
RF009:Ttc23
|
UTSW |
7 |
67,375,777 (GRCm39) |
missense |
possibly damaging |
0.61 |
X0021:Ttc23
|
UTSW |
7 |
67,319,879 (GRCm39) |
missense |
probably damaging |
1.00 |
|