Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak1 |
A |
T |
2: 32,520,391 (GRCm39) |
K79M |
probably benign |
Het |
Amy1 |
T |
C |
3: 113,356,278 (GRCm39) |
K293E |
probably benign |
Het |
Bcl2l10 |
A |
G |
9: 75,255,333 (GRCm39) |
Q50R |
probably benign |
Het |
Bpifa6 |
G |
A |
2: 153,826,740 (GRCm39) |
G35D |
probably benign |
Het |
Cachd1 |
C |
A |
4: 100,634,339 (GRCm39) |
P5Q |
unknown |
Het |
Capn13 |
A |
T |
17: 73,652,191 (GRCm39) |
I266N |
probably damaging |
Het |
Chil3 |
A |
G |
3: 106,063,081 (GRCm39) |
S170P |
possibly damaging |
Het |
Ckap4 |
A |
G |
10: 84,363,350 (GRCm39) |
I571T |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,242,964 (GRCm39) |
M371V |
unknown |
Het |
Dag1 |
A |
G |
9: 108,085,467 (GRCm39) |
L558P |
possibly damaging |
Het |
Edem3 |
G |
A |
1: 151,694,270 (GRCm39) |
E868K |
probably benign |
Het |
Eif3k |
T |
C |
7: 28,673,624 (GRCm39) |
Y150C |
probably damaging |
Het |
Farp1 |
T |
C |
14: 121,518,281 (GRCm39) |
I988T |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,910,248 (GRCm39) |
M1918T |
probably benign |
Het |
Gba2 |
A |
G |
4: 43,578,112 (GRCm39) |
I79T |
probably benign |
Het |
Gbp8 |
T |
C |
5: 105,179,169 (GRCm39) |
D110G |
probably damaging |
Het |
Gm57858 |
G |
T |
3: 36,089,428 (GRCm39) |
N165K |
probably benign |
Het |
H2-M2 |
T |
A |
17: 37,793,428 (GRCm39) |
M193L |
probably benign |
Het |
H2-T13 |
A |
G |
17: 36,391,956 (GRCm39) |
V39A |
possibly damaging |
Het |
Ighv7-1 |
T |
A |
12: 113,860,110 (GRCm39) |
D94V |
probably damaging |
Het |
Il2ra |
T |
C |
2: 11,689,202 (GRCm39) |
F244L |
possibly damaging |
Het |
Jag1 |
A |
T |
2: 136,931,764 (GRCm39) |
H602Q |
probably null |
Het |
Kidins220 |
A |
T |
12: 25,036,966 (GRCm39) |
I16F |
possibly damaging |
Het |
Klb |
A |
G |
5: 65,529,368 (GRCm39) |
T299A |
possibly damaging |
Het |
Lama4 |
A |
G |
10: 38,951,444 (GRCm39) |
K1063R |
probably benign |
Het |
Lrit2 |
A |
G |
14: 36,794,550 (GRCm39) |
E538G |
possibly damaging |
Het |
Lrrc7 |
A |
T |
3: 158,059,011 (GRCm39) |
L32* |
probably null |
Het |
Lrrtm3 |
A |
T |
10: 63,765,883 (GRCm39) |
I568N |
probably damaging |
Het |
Myom1 |
A |
G |
17: 71,343,295 (GRCm39) |
D164G |
probably damaging |
Het |
Naaladl2 |
T |
C |
3: 23,900,742 (GRCm39) |
D696G |
probably damaging |
Het |
Nalcn |
A |
T |
14: 123,545,792 (GRCm39) |
L1073* |
probably null |
Het |
Nid2 |
T |
C |
14: 19,853,278 (GRCm39) |
S1166P |
probably damaging |
Het |
Nlrp4c |
T |
C |
7: 6,095,621 (GRCm39) |
V833A |
probably benign |
Het |
Nyap2 |
T |
C |
1: 81,275,712 (GRCm39) |
S619P |
probably damaging |
Het |
Or10d5j |
T |
C |
9: 39,867,878 (GRCm39) |
M118V |
probably damaging |
Het |
Or2a20 |
A |
T |
6: 43,194,086 (GRCm39) |
T80S |
probably benign |
Het |
Or4a71 |
A |
G |
2: 89,357,987 (GRCm39) |
Y256H |
probably damaging |
Het |
Or8k16 |
C |
A |
2: 85,520,644 (GRCm39) |
Y290* |
probably null |
Het |
P3h2 |
T |
C |
16: 25,923,991 (GRCm39) |
N148S |
probably benign |
Het |
P4htm |
A |
G |
9: 108,460,081 (GRCm39) |
M231T |
probably damaging |
Het |
Pank1 |
T |
A |
19: 34,804,634 (GRCm39) |
K349I |
possibly damaging |
Het |
Pgam5 |
A |
G |
5: 110,413,466 (GRCm39) |
Y210H |
probably benign |
Het |
Prb1b |
T |
C |
6: 132,288,996 (GRCm39) |
H276R |
unknown |
Het |
Prl2a1 |
T |
A |
13: 27,992,535 (GRCm39) |
C220S |
probably damaging |
Het |
Psca |
C |
T |
15: 74,587,932 (GRCm39) |
Q39* |
probably null |
Het |
Rgs20 |
A |
T |
1: 5,091,067 (GRCm39) |
M121K |
possibly damaging |
Het |
S100z |
C |
T |
13: 95,613,883 (GRCm39) |
V76M |
possibly damaging |
Het |
Slc30a10 |
T |
C |
1: 185,195,034 (GRCm39) |
I282T |
probably damaging |
Het |
Slc30a3 |
T |
C |
5: 31,246,088 (GRCm39) |
Y214C |
probably damaging |
Het |
Sox5 |
C |
T |
6: 143,790,570 (GRCm39) |
E497K |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,971,519 (GRCm39) |
D284G |
probably benign |
Het |
Sptbn1 |
C |
T |
11: 30,087,551 (GRCm39) |
E963K |
possibly damaging |
Het |
Srl |
T |
C |
16: 4,311,723 (GRCm39) |
E465G |
possibly damaging |
Het |
Tas2r119 |
T |
G |
15: 32,177,932 (GRCm39) |
V166G |
probably benign |
Het |
Tcf7l1 |
A |
G |
6: 72,611,205 (GRCm39) |
V191A |
probably damaging |
Het |
Thap7 |
A |
T |
16: 17,346,901 (GRCm39) |
I92K |
probably damaging |
Het |
Tnfsf10 |
A |
G |
3: 27,371,407 (GRCm39) |
T38A |
possibly damaging |
Het |
Trav7-5 |
C |
G |
14: 53,768,615 (GRCm39) |
A61G |
probably benign |
Het |
Trim30c |
C |
T |
7: 104,031,553 (GRCm39) |
V421I |
probably benign |
Het |
Ugt2b38 |
A |
T |
5: 87,571,729 (GRCm39) |
M101K |
probably benign |
Het |
Vmn1r44 |
T |
A |
6: 89,870,565 (GRCm39) |
C104S |
probably damaging |
Het |
Wdr74 |
T |
A |
19: 8,715,240 (GRCm39) |
V133E |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,580,600 (GRCm39) |
Y33F |
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 |
R9026:Tacc2
|
UTSW |
7 |
130,225,266 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|