Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,771,419 (GRCm39) |
R203* |
probably null |
Het |
Acp6 |
T |
C |
3: 97,083,054 (GRCm39) |
L355P |
probably damaging |
Het |
Aebp2 |
T |
C |
6: 140,579,464 (GRCm39) |
S234P |
probably damaging |
Het |
Anapc7 |
A |
G |
5: 122,577,567 (GRCm39) |
D374G |
probably benign |
Het |
Apob |
A |
T |
12: 8,051,039 (GRCm39) |
I1088F |
probably damaging |
Het |
Arid4b |
T |
C |
13: 14,307,021 (GRCm39) |
V92A |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Asxl2 |
G |
T |
12: 3,534,558 (GRCm39) |
G252* |
probably null |
Het |
Atl1 |
A |
T |
12: 70,010,102 (GRCm39) |
K556M |
probably damaging |
Het |
AU018091 |
A |
G |
7: 3,212,104 (GRCm39) |
V206A |
probably benign |
Het |
Bcas1 |
A |
T |
2: 170,212,397 (GRCm39) |
D383E |
possibly damaging |
Het |
Bmx |
A |
G |
X: 163,015,192 (GRCm39) |
W257R |
probably benign |
Het |
Bpifb6 |
T |
C |
2: 153,747,270 (GRCm39) |
|
probably null |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Cand1 |
A |
G |
10: 119,045,972 (GRCm39) |
S978P |
probably damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Caps2 |
G |
A |
10: 112,036,591 (GRCm39) |
A384T |
probably benign |
Het |
Catsperg2 |
A |
T |
7: 29,420,470 (GRCm39) |
Y223* |
probably null |
Het |
Cd81 |
G |
T |
7: 142,620,938 (GRCm39) |
G206* |
probably null |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cdkn2aip |
G |
T |
8: 48,165,211 (GRCm39) |
N167K |
probably benign |
Het |
Ceacam14 |
T |
A |
7: 17,549,290 (GRCm39) |
L227* |
probably null |
Het |
Ceacam5 |
A |
T |
7: 17,491,805 (GRCm39) |
D725V |
probably damaging |
Het |
Cldn34a |
A |
T |
X: 151,346,841 (GRCm39) |
H171L |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cp |
A |
G |
3: 20,033,177 (GRCm39) |
D667G |
probably damaging |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Crat |
A |
G |
2: 30,295,060 (GRCm39) |
Y452H |
possibly damaging |
Het |
Cyp4f13 |
T |
A |
17: 33,144,542 (GRCm39) |
H318L |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dmbt1 |
A |
G |
7: 130,660,018 (GRCm39) |
N527S |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,853,785 (GRCm39) |
D1583V |
probably damaging |
Het |
Fgb |
G |
T |
3: 82,951,560 (GRCm39) |
Y256* |
probably null |
Het |
Frmd3 |
T |
A |
4: 74,105,676 (GRCm39) |
S441T |
probably damaging |
Het |
Glp1r |
T |
A |
17: 31,149,722 (GRCm39) |
C329S |
possibly damaging |
Het |
Gm14190 |
G |
T |
11: 99,581,431 (GRCm39) |
Q46K |
unknown |
Het |
Golt1b |
T |
A |
6: 142,338,080 (GRCm39) |
F17Y |
probably damaging |
Het |
Gsdmc |
A |
G |
15: 63,673,748 (GRCm39) |
I179T |
probably benign |
Het |
Gsdmc2 |
T |
A |
15: 63,700,086 (GRCm39) |
M229L |
probably benign |
Het |
Gulp1 |
A |
C |
1: 44,805,274 (GRCm39) |
N121T |
possibly damaging |
Het |
Ift122 |
T |
A |
6: 115,901,328 (GRCm39) |
F1037I |
probably damaging |
Het |
Ildr1 |
A |
T |
16: 36,536,568 (GRCm39) |
Y199F |
probably damaging |
Het |
Ints2 |
T |
A |
11: 86,139,760 (GRCm39) |
H278L |
possibly damaging |
Het |
Invs |
T |
C |
4: 48,392,599 (GRCm39) |
V271A |
possibly damaging |
Het |
Kcnj2 |
T |
C |
11: 110,963,709 (GRCm39) |
I367T |
probably benign |
Het |
Kif21b |
T |
C |
1: 136,089,508 (GRCm39) |
S1115P |
probably damaging |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Lcmt2 |
C |
A |
2: 120,970,762 (GRCm39) |
R107L |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lrrc9 |
A |
C |
12: 72,544,635 (GRCm39) |
R71S |
probably damaging |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mis18bp1 |
T |
C |
12: 65,205,468 (GRCm39) |
T235A |
probably benign |
Het |
Mta2 |
C |
T |
19: 8,919,696 (GRCm39) |
|
probably benign |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,860,764 (GRCm38) |
T467A |
probably benign |
Het |
Nexn |
A |
T |
3: 151,958,576 (GRCm39) |
F106I |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,896,972 (GRCm39) |
Y282* |
probably null |
Het |
Nxf3 |
G |
A |
X: 134,976,583 (GRCm39) |
P380S |
possibly damaging |
Het |
Oma1 |
C |
T |
4: 103,178,971 (GRCm39) |
T208I |
probably damaging |
Het |
Or1a1 |
T |
C |
11: 74,086,989 (GRCm39) |
V220A |
probably damaging |
Het |
Or4c31 |
A |
G |
2: 88,291,686 (GRCm39) |
M1V |
probably null |
Het |
Or4d10c |
C |
A |
19: 12,065,620 (GRCm39) |
V179F |
probably damaging |
Het |
Or4p21 |
A |
G |
2: 88,277,033 (GRCm39) |
L83P |
probably damaging |
Het |
Or51a42 |
A |
T |
7: 103,708,335 (GRCm39) |
I158N |
possibly damaging |
Het |
Or52l1 |
A |
T |
7: 104,830,221 (GRCm39) |
C115S |
probably damaging |
Het |
Or5p66 |
C |
A |
7: 107,885,566 (GRCm39) |
G256* |
probably null |
Het |
Or5p70 |
A |
G |
7: 107,995,041 (GRCm39) |
Y238C |
probably benign |
Het |
Panx2 |
A |
T |
15: 88,953,941 (GRCm39) |
Y632F |
possibly damaging |
Het |
Pdia4 |
T |
C |
6: 47,773,589 (GRCm39) |
T587A |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pigk |
T |
A |
3: 152,450,131 (GRCm39) |
Y212N |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,380,838 (GRCm39) |
Y395F |
probably damaging |
Het |
Prl3b1 |
C |
T |
13: 27,429,775 (GRCm39) |
T71I |
possibly damaging |
Het |
Rab3gap1 |
A |
G |
1: 127,870,166 (GRCm39) |
E929G |
possibly damaging |
Het |
Rabl3 |
T |
C |
16: 37,384,079 (GRCm39) |
I162T |
probably benign |
Het |
Rasgrf2 |
T |
A |
13: 92,172,473 (GRCm39) |
T188S |
probably damaging |
Het |
Slc12a2 |
A |
G |
18: 58,043,358 (GRCm39) |
I601V |
possibly damaging |
Het |
Slc25a42 |
A |
T |
8: 70,644,519 (GRCm39) |
I60N |
probably benign |
Het |
Slc2a3 |
C |
T |
6: 122,713,694 (GRCm39) |
G173S |
probably damaging |
Het |
Slc46a3 |
G |
A |
5: 147,823,404 (GRCm39) |
T146M |
probably damaging |
Het |
Specc1 |
C |
A |
11: 61,920,120 (GRCm39) |
P7T |
possibly damaging |
Het |
Sptbn4 |
T |
C |
7: 27,123,235 (GRCm39) |
D229G |
probably benign |
Het |
Sspo |
T |
C |
6: 48,427,984 (GRCm39) |
I154T |
probably benign |
Het |
Stx5a |
T |
C |
19: 8,726,254 (GRCm39) |
|
probably null |
Het |
Stxbp6 |
A |
T |
12: 44,902,640 (GRCm39) |
C210* |
probably null |
Het |
Tagap1 |
C |
T |
17: 7,224,285 (GRCm39) |
R137Q |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,997,932 (GRCm39) |
Y1163C |
probably damaging |
Het |
Tnnt3 |
C |
T |
7: 142,065,262 (GRCm39) |
R131C |
possibly damaging |
Het |
Tpx2 |
T |
A |
2: 152,732,544 (GRCm39) |
M606K |
probably benign |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,424,188 (GRCm39) |
S1485L |
probably benign |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Unc80 |
T |
C |
1: 66,731,708 (GRCm39) |
L3053P |
probably damaging |
Het |
Wars1 |
G |
T |
12: 108,854,359 (GRCm39) |
N18K |
possibly damaging |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Xndc1 |
T |
A |
7: 101,722,398 (GRCm39) |
V21E |
probably damaging |
Het |
Zfp493 |
T |
A |
13: 67,934,388 (GRCm39) |
C114S |
probably damaging |
Het |
|
Other mutations in Tex14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Tex14
|
APN |
11 |
87,426,469 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00494:Tex14
|
APN |
11 |
87,446,310 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01604:Tex14
|
APN |
11 |
87,400,524 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02690:Tex14
|
APN |
11 |
87,377,100 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02888:Tex14
|
APN |
11 |
87,418,738 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03073:Tex14
|
APN |
11 |
87,426,435 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03109:Tex14
|
APN |
11 |
87,434,191 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03047:Tex14
|
UTSW |
11 |
87,427,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R0141:Tex14
|
UTSW |
11 |
87,383,857 (GRCm39) |
splice site |
probably null |
|
R0455:Tex14
|
UTSW |
11 |
87,405,131 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0624:Tex14
|
UTSW |
11 |
87,411,525 (GRCm39) |
missense |
probably benign |
0.19 |
R0718:Tex14
|
UTSW |
11 |
87,390,439 (GRCm39) |
missense |
probably benign |
0.20 |
R1077:Tex14
|
UTSW |
11 |
87,410,571 (GRCm39) |
splice site |
probably benign |
|
R1118:Tex14
|
UTSW |
11 |
87,413,343 (GRCm39) |
missense |
probably benign |
0.07 |
R1120:Tex14
|
UTSW |
11 |
87,429,502 (GRCm39) |
splice site |
probably benign |
|
R1168:Tex14
|
UTSW |
11 |
87,427,568 (GRCm39) |
missense |
probably benign |
0.11 |
R1190:Tex14
|
UTSW |
11 |
87,385,934 (GRCm39) |
splice site |
probably null |
|
R1470:Tex14
|
UTSW |
11 |
87,440,355 (GRCm39) |
splice site |
probably benign |
|
R1563:Tex14
|
UTSW |
11 |
87,427,634 (GRCm39) |
missense |
probably damaging |
0.99 |
R1607:Tex14
|
UTSW |
11 |
87,445,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1696:Tex14
|
UTSW |
11 |
87,402,371 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1873:Tex14
|
UTSW |
11 |
87,390,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R1894:Tex14
|
UTSW |
11 |
87,365,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Tex14
|
UTSW |
11 |
87,385,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Tex14
|
UTSW |
11 |
87,400,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Tex14
|
UTSW |
11 |
87,402,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Tex14
|
UTSW |
11 |
87,440,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Tex14
|
UTSW |
11 |
87,427,581 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2106:Tex14
|
UTSW |
11 |
87,377,076 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2118:Tex14
|
UTSW |
11 |
87,410,569 (GRCm39) |
splice site |
probably benign |
|
R2860:Tex14
|
UTSW |
11 |
87,365,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:Tex14
|
UTSW |
11 |
87,365,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R4016:Tex14
|
UTSW |
11 |
87,429,449 (GRCm39) |
splice site |
probably null |
|
R4089:Tex14
|
UTSW |
11 |
87,403,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R4158:Tex14
|
UTSW |
11 |
87,407,595 (GRCm39) |
missense |
probably benign |
0.06 |
R4533:Tex14
|
UTSW |
11 |
87,427,655 (GRCm39) |
nonsense |
probably null |
|
R4713:Tex14
|
UTSW |
11 |
87,427,691 (GRCm39) |
missense |
probably damaging |
0.99 |
R4758:Tex14
|
UTSW |
11 |
87,405,311 (GRCm39) |
missense |
probably benign |
0.00 |
R4880:Tex14
|
UTSW |
11 |
87,377,121 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4953:Tex14
|
UTSW |
11 |
87,427,727 (GRCm39) |
critical splice donor site |
probably null |
|
R5092:Tex14
|
UTSW |
11 |
87,405,668 (GRCm39) |
missense |
probably benign |
0.03 |
R5119:Tex14
|
UTSW |
11 |
87,324,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5322:Tex14
|
UTSW |
11 |
87,402,298 (GRCm39) |
missense |
probably benign |
0.04 |
R5470:Tex14
|
UTSW |
11 |
87,442,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R5607:Tex14
|
UTSW |
11 |
87,413,404 (GRCm39) |
missense |
probably benign |
0.00 |
R5642:Tex14
|
UTSW |
11 |
87,405,046 (GRCm39) |
missense |
probably benign |
|
R5643:Tex14
|
UTSW |
11 |
87,426,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:Tex14
|
UTSW |
11 |
87,405,121 (GRCm39) |
missense |
probably damaging |
0.97 |
R6478:Tex14
|
UTSW |
11 |
87,405,199 (GRCm39) |
missense |
probably benign |
|
R6560:Tex14
|
UTSW |
11 |
87,388,688 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6661:Tex14
|
UTSW |
11 |
87,385,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:Tex14
|
UTSW |
11 |
87,388,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R7156:Tex14
|
UTSW |
11 |
87,375,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R7465:Tex14
|
UTSW |
11 |
87,405,256 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7675:Tex14
|
UTSW |
11 |
87,400,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Tex14
|
UTSW |
11 |
87,385,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Tex14
|
UTSW |
11 |
87,424,428 (GRCm39) |
critical splice donor site |
probably null |
|
R8015:Tex14
|
UTSW |
11 |
87,400,426 (GRCm39) |
missense |
probably benign |
0.13 |
R8226:Tex14
|
UTSW |
11 |
87,375,585 (GRCm39) |
missense |
probably damaging |
0.96 |
R8283:Tex14
|
UTSW |
11 |
87,365,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8292:Tex14
|
UTSW |
11 |
87,388,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Tex14
|
UTSW |
11 |
87,383,878 (GRCm39) |
missense |
probably benign |
0.22 |
R8932:Tex14
|
UTSW |
11 |
87,324,675 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9023:Tex14
|
UTSW |
11 |
87,365,239 (GRCm39) |
missense |
|
|
R9144:Tex14
|
UTSW |
11 |
87,413,423 (GRCm39) |
critical splice donor site |
probably null |
|
R9610:Tex14
|
UTSW |
11 |
87,377,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Tex14
|
UTSW |
11 |
87,377,084 (GRCm39) |
missense |
probably damaging |
1.00 |
RF018:Tex14
|
UTSW |
11 |
87,405,572 (GRCm39) |
missense |
probably benign |
0.01 |
X0017:Tex14
|
UTSW |
11 |
87,426,375 (GRCm39) |
nonsense |
probably null |
|
Z1176:Tex14
|
UTSW |
11 |
87,390,419 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Tex14
|
UTSW |
11 |
87,375,633 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Tex14
|
UTSW |
11 |
87,404,981 (GRCm39) |
missense |
probably damaging |
0.96 |
|