Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
A |
3: 137,770,909 (GRCm39) |
Q33K |
possibly damaging |
Het |
Acap2 |
A |
G |
16: 30,925,906 (GRCm39) |
L550P |
probably damaging |
Het |
Acsm3 |
A |
T |
7: 119,373,845 (GRCm39) |
S244C |
probably benign |
Het |
Adam28 |
T |
A |
14: 68,846,593 (GRCm39) |
D740V |
probably benign |
Het |
Adcy4 |
C |
A |
14: 56,016,426 (GRCm39) |
V342L |
probably damaging |
Het |
Adcyap1r1 |
A |
G |
6: 55,458,107 (GRCm39) |
T303A |
probably benign |
Het |
Agr2 |
T |
C |
12: 36,046,091 (GRCm39) |
V74A |
probably benign |
Het |
Akp3 |
A |
T |
1: 87,054,786 (GRCm39) |
T374S |
possibly damaging |
Het |
Ankrd36 |
A |
T |
11: 5,610,696 (GRCm39) |
I1181L |
probably benign |
Het |
Arhgap11a |
A |
T |
2: 113,664,411 (GRCm39) |
V624E |
probably benign |
Het |
Arhgap30 |
A |
T |
1: 171,228,258 (GRCm39) |
D112V |
probably damaging |
Het |
Atp8b4 |
A |
G |
2: 126,184,883 (GRCm39) |
F927L |
probably benign |
Het |
Bend4 |
C |
A |
5: 67,584,475 (GRCm39) |
G150C |
unknown |
Het |
Cd300lg |
T |
A |
11: 101,944,998 (GRCm39) |
S403T |
probably damaging |
Het |
Cep57l1 |
T |
A |
10: 41,607,086 (GRCm39) |
Q159L |
probably damaging |
Het |
Cipc |
C |
T |
12: 86,999,634 (GRCm39) |
T57M |
probably damaging |
Het |
Def8 |
T |
C |
8: 124,186,391 (GRCm39) |
C377R |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,720,746 (GRCm39) |
D1285G |
probably damaging |
Het |
Efcab10 |
A |
G |
12: 33,448,398 (GRCm39) |
D77G |
probably damaging |
Het |
Eml4 |
C |
T |
17: 83,764,479 (GRCm39) |
T663M |
probably damaging |
Het |
Ercc8 |
A |
G |
13: 108,320,389 (GRCm39) |
E325G |
possibly damaging |
Het |
Ermap |
C |
A |
4: 119,035,240 (GRCm39) |
A583S |
probably damaging |
Het |
F13a1 |
C |
T |
13: 37,102,506 (GRCm39) |
G406S |
probably null |
Het |
Faap20 |
T |
A |
4: 155,335,426 (GRCm39) |
C141S |
probably benign |
Het |
Fam193a |
A |
G |
5: 34,616,536 (GRCm39) |
T904A |
possibly damaging |
Het |
Garin2 |
T |
C |
12: 78,757,097 (GRCm39) |
F18S |
probably benign |
Het |
Gas8 |
A |
G |
8: 124,260,134 (GRCm39) |
D455G |
probably benign |
Het |
Gm21863 |
T |
C |
12: 20,004,521 (GRCm39) |
S6P |
probably damaging |
Het |
Gm4841 |
A |
T |
18: 60,403,988 (GRCm39) |
I35N |
probably damaging |
Het |
Grk4 |
T |
A |
5: 34,877,084 (GRCm39) |
C260S |
probably damaging |
Het |
Huwe1 |
G |
A |
X: 150,716,084 (GRCm39) |
R4331Q |
unknown |
Het |
Ighv5-6 |
A |
G |
12: 113,589,247 (GRCm39) |
Y78H |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kl |
T |
A |
5: 150,876,491 (GRCm39) |
S104T |
probably benign |
Het |
Lyve1 |
C |
A |
7: 110,453,182 (GRCm39) |
C138F |
probably damaging |
Het |
Med27 |
G |
A |
2: 29,399,446 (GRCm39) |
W92* |
probably null |
Het |
Mical3 |
A |
T |
6: 120,986,848 (GRCm39) |
|
probably benign |
Het |
Mrgpra4 |
C |
A |
7: 47,631,208 (GRCm39) |
R131L |
possibly damaging |
Het |
Myf5 |
T |
C |
10: 107,321,308 (GRCm39) |
N162S |
probably benign |
Het |
Myh15 |
G |
A |
16: 49,007,433 (GRCm39) |
E1835K |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,716,757 (GRCm39) |
Y486N |
probably damaging |
Het |
Ncapg |
T |
A |
5: 45,853,115 (GRCm39) |
N860K |
probably benign |
Het |
Nr4a3 |
T |
C |
4: 48,052,194 (GRCm39) |
F316S |
possibly damaging |
Het |
Nsd3 |
T |
A |
8: 26,172,576 (GRCm39) |
S778R |
probably benign |
Het |
Or2r2 |
A |
G |
6: 42,463,795 (GRCm39) |
F111L |
probably damaging |
Het |
Or4c119 |
A |
T |
2: 88,986,988 (GRCm39) |
V177E |
probably benign |
Het |
Or4c31 |
A |
G |
2: 88,292,196 (GRCm39) |
I190V |
probably damaging |
Het |
Or5p6 |
A |
G |
7: 107,631,286 (GRCm39) |
F88S |
probably damaging |
Het |
Or7e173 |
T |
C |
9: 19,938,344 (GRCm39) |
N297D |
|
Het |
Or8b37 |
T |
A |
9: 37,958,885 (GRCm39) |
Y122* |
probably null |
Het |
Or8w1 |
A |
T |
2: 87,465,369 (GRCm39) |
C241S |
probably damaging |
Het |
Or9m2 |
A |
G |
2: 87,820,568 (GRCm39) |
T38A |
probably damaging |
Het |
Pdlim4 |
C |
T |
11: 53,946,280 (GRCm39) |
G231S |
probably benign |
Het |
Pknox2 |
C |
T |
9: 36,821,044 (GRCm39) |
V273I |
possibly damaging |
Het |
Pm20d1 |
A |
G |
1: 131,739,822 (GRCm39) |
H390R |
probably benign |
Het |
Prkg2 |
A |
T |
5: 99,114,386 (GRCm39) |
D587E |
probably benign |
Het |
Prps1l1 |
T |
A |
12: 35,035,546 (GRCm39) |
D220E |
possibly damaging |
Het |
Prss3l |
A |
G |
6: 41,422,990 (GRCm39) |
F4L |
probably benign |
Het |
Ptchd3 |
T |
C |
11: 121,721,682 (GRCm39) |
V185A |
possibly damaging |
Het |
Rag2 |
A |
T |
2: 101,460,494 (GRCm39) |
N268I |
possibly damaging |
Het |
Rarres2 |
A |
G |
6: 48,549,020 (GRCm39) |
|
probably null |
Het |
Rrp12 |
T |
C |
19: 41,860,223 (GRCm39) |
H1000R |
probably benign |
Het |
S100a2 |
A |
T |
3: 90,498,811 (GRCm39) |
Y104F |
unknown |
Het |
Sell |
A |
G |
1: 163,893,042 (GRCm39) |
Y86C |
probably damaging |
Het |
Serpinb6d |
A |
T |
13: 33,851,656 (GRCm39) |
T138S |
possibly damaging |
Het |
Slamf7 |
T |
A |
1: 171,466,312 (GRCm39) |
I228F |
probably benign |
Het |
Slc11a1 |
G |
A |
1: 74,416,325 (GRCm39) |
V92M |
probably damaging |
Het |
Spi1 |
A |
G |
2: 90,912,862 (GRCm39) |
N5S |
unknown |
Het |
Stard9 |
G |
T |
2: 120,536,283 (GRCm39) |
D4151Y |
probably damaging |
Het |
Stmnd1 |
A |
G |
13: 46,452,983 (GRCm39) |
T220A |
probably benign |
Het |
Tmc5 |
A |
G |
7: 118,241,594 (GRCm39) |
N429S |
possibly damaging |
Het |
Tmem201 |
A |
C |
4: 149,812,627 (GRCm39) |
L230V |
probably benign |
Het |
Tmem222 |
T |
C |
4: 132,997,119 (GRCm39) |
E94G |
possibly damaging |
Het |
Trappc4 |
A |
G |
9: 44,315,655 (GRCm39) |
F186S |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,862,273 (GRCm39) |
N435S |
probably benign |
Het |
Trim68 |
A |
T |
7: 102,329,447 (GRCm39) |
L227Q |
probably damaging |
Het |
Tuba3b |
T |
G |
6: 145,563,996 (GRCm39) |
V14G |
possibly damaging |
Het |
Ubr2 |
G |
T |
17: 47,245,041 (GRCm39) |
H1662N |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,861,863 (GRCm39) |
V2915E |
probably damaging |
Het |
Vsig10 |
C |
T |
5: 117,476,323 (GRCm39) |
T259I |
probably benign |
Het |
Zfp267 |
A |
G |
3: 36,219,066 (GRCm39) |
Y363C |
possibly damaging |
Het |
|
Other mutations in Tacc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00836:Tacc2
|
APN |
7 |
130,360,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01396:Tacc2
|
APN |
7 |
130,360,919 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01621:Tacc2
|
APN |
7 |
130,331,498 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02000:Tacc2
|
APN |
7 |
130,330,898 (GRCm39) |
splice site |
probably null |
|
IGL02075:Tacc2
|
APN |
7 |
130,330,582 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02201:Tacc2
|
APN |
7 |
130,227,942 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02205:Tacc2
|
APN |
7 |
130,228,412 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02399:Tacc2
|
APN |
7 |
130,225,129 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02456:Tacc2
|
APN |
7 |
130,227,991 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02559:Tacc2
|
APN |
7 |
130,360,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02734:Tacc2
|
APN |
7 |
130,227,829 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02800:Tacc2
|
APN |
7 |
130,225,809 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02938:Tacc2
|
APN |
7 |
130,330,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03031:Tacc2
|
APN |
7 |
130,225,585 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03278:Tacc2
|
APN |
7 |
130,335,298 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03283:Tacc2
|
APN |
7 |
130,343,996 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03371:Tacc2
|
APN |
7 |
130,227,791 (GRCm39) |
missense |
possibly damaging |
0.90 |
aces
|
UTSW |
7 |
130,335,258 (GRCm39) |
missense |
probably damaging |
1.00 |
Jacks
|
UTSW |
7 |
130,227,494 (GRCm39) |
missense |
probably damaging |
0.98 |
kings
|
UTSW |
7 |
130,225,213 (GRCm39) |
missense |
probably damaging |
0.96 |
R0002:Tacc2
|
UTSW |
7 |
130,223,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R0119:Tacc2
|
UTSW |
7 |
130,223,605 (GRCm39) |
missense |
probably damaging |
0.98 |
R0244:Tacc2
|
UTSW |
7 |
130,353,555 (GRCm39) |
splice site |
probably benign |
|
R0619:Tacc2
|
UTSW |
7 |
130,318,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Tacc2
|
UTSW |
7 |
130,179,239 (GRCm39) |
missense |
probably damaging |
0.99 |
R0632:Tacc2
|
UTSW |
7 |
130,227,325 (GRCm39) |
nonsense |
probably null |
|
R1015:Tacc2
|
UTSW |
7 |
130,225,795 (GRCm39) |
missense |
probably benign |
|
R1081:Tacc2
|
UTSW |
7 |
130,330,304 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1086:Tacc2
|
UTSW |
7 |
130,228,227 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1351:Tacc2
|
UTSW |
7 |
130,264,733 (GRCm39) |
intron |
probably benign |
|
R1538:Tacc2
|
UTSW |
7 |
130,227,149 (GRCm39) |
missense |
probably benign |
0.03 |
R1743:Tacc2
|
UTSW |
7 |
130,228,328 (GRCm39) |
nonsense |
probably null |
|
R1771:Tacc2
|
UTSW |
7 |
130,343,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R1876:Tacc2
|
UTSW |
7 |
130,225,475 (GRCm39) |
missense |
probably benign |
0.38 |
R1893:Tacc2
|
UTSW |
7 |
130,227,055 (GRCm39) |
missense |
probably benign |
0.01 |
R1899:Tacc2
|
UTSW |
7 |
130,225,932 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2005:Tacc2
|
UTSW |
7 |
130,333,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Tacc2
|
UTSW |
7 |
130,223,587 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2338:Tacc2
|
UTSW |
7 |
130,335,299 (GRCm39) |
splice site |
probably null |
|
R2407:Tacc2
|
UTSW |
7 |
130,223,770 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3051:Tacc2
|
UTSW |
7 |
130,227,226 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3052:Tacc2
|
UTSW |
7 |
130,227,226 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3053:Tacc2
|
UTSW |
7 |
130,227,226 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3116:Tacc2
|
UTSW |
7 |
130,360,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R3412:Tacc2
|
UTSW |
7 |
130,336,724 (GRCm39) |
missense |
probably benign |
0.02 |
R3683:Tacc2
|
UTSW |
7 |
130,226,800 (GRCm39) |
missense |
probably benign |
0.40 |
R3685:Tacc2
|
UTSW |
7 |
130,226,800 (GRCm39) |
missense |
probably benign |
0.40 |
R3872:Tacc2
|
UTSW |
7 |
130,224,152 (GRCm39) |
missense |
probably benign |
0.02 |
R4063:Tacc2
|
UTSW |
7 |
130,330,852 (GRCm39) |
missense |
probably damaging |
0.97 |
R4410:Tacc2
|
UTSW |
7 |
130,343,941 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4434:Tacc2
|
UTSW |
7 |
130,225,271 (GRCm39) |
missense |
probably damaging |
0.96 |
R4438:Tacc2
|
UTSW |
7 |
130,225,271 (GRCm39) |
missense |
probably damaging |
0.96 |
R4618:Tacc2
|
UTSW |
7 |
130,227,946 (GRCm39) |
missense |
probably benign |
0.10 |
R4674:Tacc2
|
UTSW |
7 |
130,226,591 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4742:Tacc2
|
UTSW |
7 |
130,227,697 (GRCm39) |
missense |
probably benign |
0.00 |
R4934:Tacc2
|
UTSW |
7 |
130,330,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Tacc2
|
UTSW |
7 |
130,227,629 (GRCm39) |
missense |
probably damaging |
0.98 |
R4964:Tacc2
|
UTSW |
7 |
130,330,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R4966:Tacc2
|
UTSW |
7 |
130,330,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Tacc2
|
UTSW |
7 |
130,225,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R5052:Tacc2
|
UTSW |
7 |
130,336,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R5276:Tacc2
|
UTSW |
7 |
130,331,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Tacc2
|
UTSW |
7 |
130,335,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R5331:Tacc2
|
UTSW |
7 |
130,335,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Tacc2
|
UTSW |
7 |
130,224,990 (GRCm39) |
missense |
probably benign |
0.09 |
R5556:Tacc2
|
UTSW |
7 |
130,276,336 (GRCm39) |
missense |
probably damaging |
0.97 |
R5645:Tacc2
|
UTSW |
7 |
130,225,781 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5886:Tacc2
|
UTSW |
7 |
130,330,850 (GRCm39) |
missense |
probably benign |
0.18 |
R5996:Tacc2
|
UTSW |
7 |
130,225,213 (GRCm39) |
missense |
probably damaging |
0.96 |
R6074:Tacc2
|
UTSW |
7 |
130,227,165 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6127:Tacc2
|
UTSW |
7 |
130,227,845 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6156:Tacc2
|
UTSW |
7 |
130,227,494 (GRCm39) |
missense |
probably damaging |
0.98 |
R6298:Tacc2
|
UTSW |
7 |
130,228,255 (GRCm39) |
missense |
probably benign |
0.26 |
R6444:Tacc2
|
UTSW |
7 |
130,225,142 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6533:Tacc2
|
UTSW |
7 |
130,224,567 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6724:Tacc2
|
UTSW |
7 |
130,330,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Tacc2
|
UTSW |
7 |
130,330,618 (GRCm39) |
missense |
probably benign |
0.16 |
R7150:Tacc2
|
UTSW |
7 |
130,330,807 (GRCm39) |
missense |
probably benign |
|
R7290:Tacc2
|
UTSW |
7 |
130,331,103 (GRCm39) |
missense |
probably benign |
0.07 |
R7404:Tacc2
|
UTSW |
7 |
130,225,066 (GRCm39) |
missense |
probably benign |
0.22 |
R7460:Tacc2
|
UTSW |
7 |
130,226,363 (GRCm39) |
missense |
probably benign |
0.39 |
R7651:Tacc2
|
UTSW |
7 |
130,224,884 (GRCm39) |
missense |
probably benign |
0.25 |
R7666:Tacc2
|
UTSW |
7 |
130,318,544 (GRCm39) |
start gained |
probably benign |
|
R7695:Tacc2
|
UTSW |
7 |
130,330,633 (GRCm39) |
missense |
probably benign |
0.08 |
R7766:Tacc2
|
UTSW |
7 |
130,345,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R7793:Tacc2
|
UTSW |
7 |
130,224,843 (GRCm39) |
missense |
probably benign |
0.34 |
R7861:Tacc2
|
UTSW |
7 |
130,227,161 (GRCm39) |
missense |
probably benign |
0.00 |
R8204:Tacc2
|
UTSW |
7 |
130,226,159 (GRCm39) |
missense |
probably damaging |
0.97 |
R8244:Tacc2
|
UTSW |
7 |
130,330,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R8245:Tacc2
|
UTSW |
7 |
130,331,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R8283:Tacc2
|
UTSW |
7 |
130,227,034 (GRCm39) |
missense |
probably benign |
0.02 |
R8348:Tacc2
|
UTSW |
7 |
130,225,019 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8369:Tacc2
|
UTSW |
7 |
130,223,888 (GRCm39) |
missense |
probably damaging |
0.98 |
R8381:Tacc2
|
UTSW |
7 |
130,225,972 (GRCm39) |
missense |
probably benign |
0.00 |
R8804:Tacc2
|
UTSW |
7 |
130,294,693 (GRCm39) |
missense |
probably benign |
|
R8809:Tacc2
|
UTSW |
7 |
130,276,421 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8835:Tacc2
|
UTSW |
7 |
130,228,258 (GRCm39) |
missense |
probably benign |
0.00 |
R8880:Tacc2
|
UTSW |
7 |
130,318,564 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8918:Tacc2
|
UTSW |
7 |
130,227,823 (GRCm39) |
missense |
probably benign |
0.00 |
R8936:Tacc2
|
UTSW |
7 |
130,228,367 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8953:Tacc2
|
UTSW |
7 |
130,227,487 (GRCm39) |
missense |
probably benign |
0.00 |
R9193:Tacc2
|
UTSW |
7 |
130,228,304 (GRCm39) |
missense |
probably benign |
0.04 |
R9221:Tacc2
|
UTSW |
7 |
130,226,209 (GRCm39) |
missense |
probably benign |
0.00 |
R9221:Tacc2
|
UTSW |
7 |
130,226,058 (GRCm39) |
missense |
probably damaging |
0.98 |
R9222:Tacc2
|
UTSW |
7 |
130,227,985 (GRCm39) |
missense |
probably benign |
0.00 |
R9264:Tacc2
|
UTSW |
7 |
130,228,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R9312:Tacc2
|
UTSW |
7 |
130,223,978 (GRCm39) |
missense |
probably benign |
0.00 |
R9380:Tacc2
|
UTSW |
7 |
130,226,771 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9515:Tacc2
|
UTSW |
7 |
130,366,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R9705:Tacc2
|
UTSW |
7 |
130,361,018 (GRCm39) |
missense |
probably damaging |
1.00 |
X0010:Tacc2
|
UTSW |
7 |
130,336,787 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tacc2
|
UTSW |
7 |
130,346,327 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tacc2
|
UTSW |
7 |
130,226,000 (GRCm39) |
missense |
possibly damaging |
0.59 |
Z1176:Tacc2
|
UTSW |
7 |
130,225,100 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Tacc2
|
UTSW |
7 |
130,336,679 (GRCm39) |
missense |
possibly damaging |
0.96 |
Z1177:Tacc2
|
UTSW |
7 |
130,227,504 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Tacc2
|
UTSW |
7 |
130,226,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|