Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asap2 |
G |
T |
12: 21,235,188 (GRCm39) |
A97S |
probably damaging |
Het |
Brd10 |
T |
C |
19: 29,712,545 (GRCm39) |
K785E |
probably damaging |
Het |
C1qtnf1 |
A |
T |
11: 118,334,616 (GRCm39) |
E32V |
possibly damaging |
Het |
Ccdc81 |
A |
G |
7: 89,525,081 (GRCm39) |
L500P |
probably damaging |
Het |
Cdo1 |
T |
C |
18: 46,861,130 (GRCm39) |
E27G |
probably benign |
Het |
Ceacam5 |
G |
A |
7: 17,484,620 (GRCm39) |
G454D |
probably damaging |
Het |
Cemip |
T |
C |
7: 83,600,648 (GRCm39) |
D991G |
probably damaging |
Het |
Cep170 |
A |
C |
1: 176,616,071 (GRCm39) |
I79S |
probably damaging |
Het |
Cep19 |
A |
G |
16: 31,926,039 (GRCm39) |
Q149R |
possibly damaging |
Het |
Cideb |
A |
T |
14: 55,992,619 (GRCm39) |
L99* |
probably null |
Het |
Cntnap5a |
A |
G |
1: 116,356,207 (GRCm39) |
N746S |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,564,080 (GRCm39) |
N1715S |
probably benign |
Het |
Col3a1 |
T |
C |
1: 45,360,848 (GRCm39) |
S93P |
unknown |
Het |
Csmd3 |
C |
A |
15: 47,449,028 (GRCm39) |
|
probably null |
Het |
Disp3 |
T |
C |
4: 148,344,373 (GRCm39) |
I510V |
probably benign |
Het |
Drosha |
T |
A |
15: 12,914,070 (GRCm39) |
V1115E |
probably damaging |
Het |
Dzip3 |
A |
C |
16: 48,757,369 (GRCm39) |
L888R |
probably damaging |
Het |
Emx2 |
C |
A |
19: 59,452,442 (GRCm39) |
A242E |
probably benign |
Het |
Fto |
G |
A |
8: 92,168,314 (GRCm39) |
E256K |
possibly damaging |
Het |
Gabrb2 |
A |
C |
11: 42,482,715 (GRCm39) |
Y191S |
possibly damaging |
Het |
Gm6526 |
A |
T |
14: 43,987,394 (GRCm39) |
H110L |
probably damaging |
Het |
Grin3b |
T |
A |
10: 79,810,436 (GRCm39) |
N647K |
probably damaging |
Het |
Ifit2 |
T |
G |
19: 34,550,602 (GRCm39) |
S47R |
probably benign |
Het |
Il5ra |
A |
T |
6: 106,712,781 (GRCm39) |
V244E |
possibly damaging |
Het |
Inppl1 |
A |
G |
7: 101,482,153 (GRCm39) |
L141P |
probably benign |
Het |
Iws1 |
A |
G |
18: 32,213,178 (GRCm39) |
D202G |
probably benign |
Het |
Kctd4 |
A |
C |
14: 76,200,523 (GRCm39) |
I165L |
probably benign |
Het |
Lrch3 |
G |
A |
16: 32,770,746 (GRCm39) |
C116Y |
probably damaging |
Het |
Mettl25 |
T |
C |
10: 105,668,844 (GRCm39) |
T93A |
possibly damaging |
Het |
Mgat4d |
A |
G |
8: 84,095,666 (GRCm39) |
I314V |
probably benign |
Het |
Mrgprb4 |
A |
T |
7: 47,848,159 (GRCm39) |
Y256* |
probably null |
Het |
Myo9b |
G |
T |
8: 71,808,408 (GRCm39) |
V1672L |
probably damaging |
Het |
Nek1 |
C |
T |
8: 61,502,975 (GRCm39) |
P449L |
probably benign |
Het |
Nucb2 |
G |
A |
7: 116,123,642 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 58,919,412 (GRCm39) |
Y6864C |
probably damaging |
Het |
Omt2b |
A |
T |
9: 78,235,420 (GRCm39) |
|
probably benign |
Het |
Or2y3 |
T |
A |
17: 38,393,486 (GRCm39) |
I128F |
probably damaging |
Het |
Or4p18 |
C |
T |
2: 88,232,777 (GRCm39) |
C167Y |
probably damaging |
Het |
Or5ac15 |
G |
A |
16: 58,940,293 (GRCm39) |
L47F |
probably damaging |
Het |
Or6c208 |
A |
G |
10: 129,224,176 (GRCm39) |
K225E |
probably benign |
Het |
Otogl |
G |
T |
10: 107,705,387 (GRCm39) |
P647T |
probably damaging |
Het |
Oxnad1 |
A |
G |
14: 31,824,244 (GRCm39) |
D271G |
probably benign |
Het |
Pbx3 |
T |
C |
2: 34,261,776 (GRCm39) |
I53V |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,639,865 (GRCm39) |
|
probably null |
Het |
Ppp4r3a |
A |
T |
12: 101,007,000 (GRCm39) |
D810E |
probably damaging |
Het |
Ptpro |
A |
T |
6: 137,438,724 (GRCm39) |
D1189V |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,492,002 (GRCm39) |
N3758S |
probably damaging |
Het |
Scarb2 |
G |
A |
5: 92,594,200 (GRCm39) |
T454M |
possibly damaging |
Het |
Sec23a |
A |
C |
12: 59,032,972 (GRCm39) |
|
probably null |
Het |
Spire2 |
C |
T |
8: 124,095,502 (GRCm39) |
A535V |
probably benign |
Het |
Svopl |
A |
T |
6: 38,006,570 (GRCm39) |
F142L |
probably benign |
Het |
Tas2r144 |
T |
C |
6: 42,192,674 (GRCm39) |
I138T |
probably benign |
Het |
Tnfaip1 |
C |
T |
11: 78,420,971 (GRCm39) |
V30M |
possibly damaging |
Het |
Topaz1 |
T |
A |
9: 122,625,108 (GRCm39) |
W1398R |
probably damaging |
Het |
Tpo |
A |
G |
12: 30,134,694 (GRCm39) |
S755P |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,606,460 (GRCm39) |
S18116R |
probably damaging |
Het |
Vmn2r78 |
A |
G |
7: 86,571,465 (GRCm39) |
|
probably null |
Het |
Wdr49 |
T |
A |
3: 75,304,227 (GRCm39) |
K494M |
probably benign |
Het |
Yeats2 |
A |
G |
16: 20,024,836 (GRCm39) |
M697V |
probably damaging |
Het |
Zfp407 |
G |
A |
18: 84,579,158 (GRCm39) |
P652S |
possibly damaging |
Het |
Zfp462 |
A |
G |
4: 55,009,002 (GRCm39) |
M323V |
probably benign |
Het |
Zfp629 |
G |
T |
7: 127,209,931 (GRCm39) |
P626Q |
possibly damaging |
Het |
Zfp804a |
A |
T |
2: 82,088,532 (GRCm39) |
Y787F |
probably benign |
Het |
|
Other mutations in Tbc1d15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Tbc1d15
|
APN |
10 |
115,045,546 (GRCm39) |
nonsense |
probably null |
|
IGL01161:Tbc1d15
|
APN |
10 |
115,038,435 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02458:Tbc1d15
|
APN |
10 |
115,065,111 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03145:Tbc1d15
|
APN |
10 |
115,038,421 (GRCm39) |
missense |
probably benign |
0.03 |
R0140:Tbc1d15
|
UTSW |
10 |
115,056,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R0466:Tbc1d15
|
UTSW |
10 |
115,055,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Tbc1d15
|
UTSW |
10 |
115,075,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R0633:Tbc1d15
|
UTSW |
10 |
115,056,215 (GRCm39) |
missense |
probably benign |
0.00 |
R1699:Tbc1d15
|
UTSW |
10 |
115,056,219 (GRCm39) |
missense |
probably benign |
0.05 |
R1727:Tbc1d15
|
UTSW |
10 |
115,046,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R2063:Tbc1d15
|
UTSW |
10 |
115,065,078 (GRCm39) |
missense |
probably benign |
|
R2111:Tbc1d15
|
UTSW |
10 |
115,076,819 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4751:Tbc1d15
|
UTSW |
10 |
115,038,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Tbc1d15
|
UTSW |
10 |
115,044,874 (GRCm39) |
nonsense |
probably null |
|
R5480:Tbc1d15
|
UTSW |
10 |
115,069,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R5746:Tbc1d15
|
UTSW |
10 |
115,046,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R5891:Tbc1d15
|
UTSW |
10 |
115,056,213 (GRCm39) |
missense |
probably benign |
0.20 |
R6012:Tbc1d15
|
UTSW |
10 |
115,055,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Tbc1d15
|
UTSW |
10 |
115,069,148 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6989:Tbc1d15
|
UTSW |
10 |
115,045,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Tbc1d15
|
UTSW |
10 |
115,057,492 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8134:Tbc1d15
|
UTSW |
10 |
115,045,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R8231:Tbc1d15
|
UTSW |
10 |
115,065,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Tbc1d15
|
UTSW |
10 |
115,038,407 (GRCm39) |
critical splice donor site |
probably null |
|
R8682:Tbc1d15
|
UTSW |
10 |
115,046,195 (GRCm39) |
missense |
probably benign |
0.04 |
R9336:Tbc1d15
|
UTSW |
10 |
115,044,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|