Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
T |
13: 81,545,322 (GRCm39) |
D5654E |
probably benign |
Het |
Alg6 |
A |
G |
4: 99,630,598 (GRCm39) |
S146G |
probably null |
Het |
Anks1 |
T |
C |
17: 28,278,367 (GRCm39) |
|
probably null |
Het |
Bcor |
T |
C |
X: 11,904,059 (GRCm39) |
I1662V |
probably damaging |
Het |
Bzw1 |
T |
C |
1: 58,438,213 (GRCm39) |
F98L |
probably damaging |
Het |
Cdc14b |
A |
G |
13: 64,353,217 (GRCm39) |
V453A |
probably benign |
Het |
Copg1 |
G |
T |
6: 87,870,880 (GRCm39) |
A228S |
possibly damaging |
Het |
D1Pas1 |
A |
G |
1: 186,701,609 (GRCm39) |
I513V |
possibly damaging |
Het |
Efemp1 |
G |
A |
11: 28,876,223 (GRCm39) |
V463M |
probably benign |
Het |
Ep400 |
T |
A |
5: 110,883,356 (GRCm39) |
|
probably benign |
Het |
Faim |
G |
A |
9: 98,874,218 (GRCm39) |
G15R |
probably damaging |
Het |
Fgd3 |
A |
G |
13: 49,418,262 (GRCm39) |
|
probably benign |
Het |
Furin |
C |
A |
7: 80,042,315 (GRCm39) |
G427W |
probably damaging |
Het |
Glycam1 |
T |
G |
15: 103,472,659 (GRCm39) |
D25A |
probably damaging |
Het |
Gpr119 |
A |
G |
X: 47,763,047 (GRCm39) |
L30P |
probably damaging |
Het |
Gria1 |
T |
A |
11: 57,208,568 (GRCm39) |
M752K |
possibly damaging |
Het |
Mcph1 |
C |
T |
8: 18,682,413 (GRCm39) |
P517S |
possibly damaging |
Het |
Mug1 |
T |
A |
6: 121,859,597 (GRCm39) |
Y1199N |
probably damaging |
Het |
Myt1 |
A |
G |
2: 181,449,308 (GRCm39) |
D663G |
probably damaging |
Het |
Ppp1r1c |
A |
T |
2: 79,540,241 (GRCm39) |
|
probably null |
Het |
Rab1a |
C |
T |
11: 20,174,727 (GRCm39) |
T100M |
possibly damaging |
Het |
Rfx6 |
A |
G |
10: 51,554,501 (GRCm39) |
K114R |
probably benign |
Het |
Rmdn1 |
T |
C |
4: 19,595,119 (GRCm39) |
V177A |
probably benign |
Het |
Setd5 |
T |
G |
6: 113,088,375 (GRCm39) |
L168V |
probably damaging |
Het |
Slc25a10 |
A |
T |
11: 120,385,976 (GRCm39) |
|
probably benign |
Het |
Slc38a7 |
A |
T |
8: 96,570,748 (GRCm39) |
I252N |
probably damaging |
Het |
Slit2 |
G |
A |
5: 48,146,493 (GRCm39) |
E95K |
possibly damaging |
Het |
Taar8c |
A |
T |
10: 23,977,173 (GRCm39) |
I213N |
probably damaging |
Het |
Tmcc2 |
C |
A |
1: 132,308,436 (GRCm39) |
A153S |
probably benign |
Het |
Tuft1 |
A |
T |
3: 94,523,138 (GRCm39) |
I291N |
probably damaging |
Het |
Vmn2r10 |
T |
A |
5: 109,150,451 (GRCm39) |
M198L |
possibly damaging |
Het |
Vps13d |
T |
A |
4: 144,882,564 (GRCm39) |
M1004L |
probably benign |
Het |
Wfdc3 |
T |
C |
2: 164,584,945 (GRCm39) |
|
probably benign |
Het |
Wfikkn2 |
G |
A |
11: 94,128,921 (GRCm39) |
Q407* |
probably null |
Het |
Zfp106 |
T |
C |
2: 120,357,329 (GRCm39) |
I1189V |
probably benign |
Het |
Zic2 |
T |
A |
14: 122,715,971 (GRCm39) |
C364* |
probably null |
Het |
|
Other mutations in Tagln3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02640:Tagln3
|
APN |
16 |
45,544,596 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02715:Tagln3
|
APN |
16 |
45,544,588 (GRCm39) |
missense |
probably benign |
|
R0619:Tagln3
|
UTSW |
16 |
45,544,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R1118:Tagln3
|
UTSW |
16 |
45,544,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R1119:Tagln3
|
UTSW |
16 |
45,544,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R1865:Tagln3
|
UTSW |
16 |
45,532,013 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2111:Tagln3
|
UTSW |
16 |
45,531,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Tagln3
|
UTSW |
16 |
45,544,701 (GRCm39) |
start gained |
probably benign |
|
R6329:Tagln3
|
UTSW |
16 |
45,533,365 (GRCm39) |
missense |
probably benign |
0.03 |
R6857:Tagln3
|
UTSW |
16 |
45,544,599 (GRCm39) |
missense |
probably benign |
|
R6995:Tagln3
|
UTSW |
16 |
45,543,321 (GRCm39) |
missense |
probably benign |
0.01 |
R7398:Tagln3
|
UTSW |
16 |
45,543,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R8144:Tagln3
|
UTSW |
16 |
45,544,554 (GRCm39) |
missense |
probably benign |
0.00 |
R9678:Tagln3
|
UTSW |
16 |
45,544,605 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Tagln3
|
UTSW |
16 |
45,543,460 (GRCm39) |
missense |
probably benign |
|
|