Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
A |
10: 79,842,733 (GRCm39) |
V1164E |
probably damaging |
Het |
Acnat2 |
A |
G |
4: 49,380,262 (GRCm39) |
V372A |
probably benign |
Het |
Adam17 |
A |
T |
12: 21,392,883 (GRCm39) |
D313E |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,735,709 (GRCm39) |
R200* |
probably null |
Het |
Akr1d1 |
G |
A |
6: 37,527,150 (GRCm39) |
E129K |
probably benign |
Het |
Arhgap29 |
T |
A |
3: 121,787,230 (GRCm39) |
V382E |
probably damaging |
Het |
Arhgef40 |
G |
A |
14: 52,238,456 (GRCm39) |
V1312I |
probably damaging |
Het |
Bbs9 |
A |
G |
9: 22,479,060 (GRCm39) |
S168G |
probably damaging |
Het |
Carmil1 |
T |
A |
13: 24,276,541 (GRCm39) |
K202* |
probably null |
Het |
Cnep1r1 |
A |
G |
8: 88,846,438 (GRCm39) |
E19G |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 31,022,765 (GRCm39) |
Q1124L |
probably benign |
Het |
Dph1 |
G |
T |
11: 75,072,143 (GRCm39) |
A242D |
probably damaging |
Het |
Efcab7 |
T |
A |
4: 99,719,738 (GRCm39) |
Y73* |
probably null |
Het |
Esp18 |
G |
T |
17: 39,720,853 (GRCm39) |
E33* |
probably null |
Het |
Fbln2 |
T |
A |
6: 91,211,241 (GRCm39) |
I395K |
probably benign |
Het |
Grin3a |
C |
T |
4: 49,844,969 (GRCm39) |
C38Y |
probably damaging |
Het |
Hivep3 |
T |
A |
4: 119,956,105 (GRCm39) |
S1474T |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,868,670 (GRCm39) |
V45M |
probably damaging |
Het |
Intu |
T |
A |
3: 40,655,723 (GRCm39) |
F937I |
possibly damaging |
Het |
Llgl2 |
G |
A |
11: 115,735,767 (GRCm39) |
G121D |
probably damaging |
Het |
Myo7a |
C |
T |
7: 97,722,374 (GRCm39) |
V1184M |
probably benign |
Het |
Nsmce4a |
G |
T |
7: 130,144,479 (GRCm39) |
|
|
Het |
Or5w20 |
T |
C |
2: 87,726,935 (GRCm39) |
Y131H |
probably damaging |
Het |
Or6c69c |
A |
T |
10: 129,911,007 (GRCm39) |
M243L |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,286,469 (GRCm39) |
V590E |
probably damaging |
Het |
Pigo |
G |
A |
4: 43,021,412 (GRCm39) |
S510L |
probably benign |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Rnf19a |
A |
G |
15: 36,253,205 (GRCm39) |
I378T |
possibly damaging |
Het |
Rnf216 |
G |
T |
5: 142,978,589 (GRCm39) |
P793T |
possibly damaging |
Het |
Samd8 |
T |
C |
14: 21,833,866 (GRCm39) |
|
probably null |
Het |
Son |
T |
A |
16: 91,454,490 (GRCm39) |
M1079K |
probably damaging |
Het |
Spata7 |
T |
A |
12: 98,624,596 (GRCm39) |
M166K |
probably benign |
Het |
Spta1 |
G |
A |
1: 174,044,767 (GRCm39) |
E1468K |
probably damaging |
Het |
Taar3 |
A |
T |
10: 23,825,705 (GRCm39) |
I84F |
possibly damaging |
Het |
Tas2r107 |
T |
A |
6: 131,636,977 (GRCm39) |
D24V |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,106,123 (GRCm39) |
R885G |
probably damaging |
Het |
Tox3 |
C |
A |
8: 90,984,687 (GRCm39) |
R164L |
probably benign |
Het |
Vmn1r179 |
A |
G |
7: 23,628,076 (GRCm39) |
N89S |
possibly damaging |
Het |
Zfp944 |
T |
C |
17: 22,557,846 (GRCm39) |
E467G |
probably benign |
Het |
Zzef1 |
A |
T |
11: 72,813,982 (GRCm39) |
D2857V |
possibly damaging |
Het |
|
Other mutations in Ttc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03398:Ttc5
|
APN |
14 |
51,018,964 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0665:Ttc5
|
UTSW |
14 |
51,003,415 (GRCm39) |
missense |
probably benign |
0.17 |
R0667:Ttc5
|
UTSW |
14 |
51,003,415 (GRCm39) |
missense |
probably benign |
0.17 |
R1125:Ttc5
|
UTSW |
14 |
51,015,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1186:Ttc5
|
UTSW |
14 |
51,004,683 (GRCm39) |
nonsense |
probably null |
|
R2011:Ttc5
|
UTSW |
14 |
51,019,007 (GRCm39) |
nonsense |
probably null |
|
R2119:Ttc5
|
UTSW |
14 |
51,012,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Ttc5
|
UTSW |
14 |
51,018,962 (GRCm39) |
missense |
probably benign |
0.01 |
R6050:Ttc5
|
UTSW |
14 |
51,010,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R6059:Ttc5
|
UTSW |
14 |
51,015,303 (GRCm39) |
missense |
probably damaging |
0.97 |
R6329:Ttc5
|
UTSW |
14 |
51,003,385 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6612:Ttc5
|
UTSW |
14 |
51,022,926 (GRCm39) |
splice site |
probably null |
|
R7311:Ttc5
|
UTSW |
14 |
51,003,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7669:Ttc5
|
UTSW |
14 |
51,014,787 (GRCm39) |
missense |
probably benign |
0.00 |
R7712:Ttc5
|
UTSW |
14 |
51,010,769 (GRCm39) |
missense |
probably benign |
0.00 |
|