Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adora2b |
T |
A |
11: 62,140,141 (GRCm39) |
C72S |
probably damaging |
Het |
Atcay |
T |
C |
10: 81,048,782 (GRCm39) |
Y183C |
probably damaging |
Het |
Atp1a1 |
A |
T |
3: 101,494,220 (GRCm39) |
I460N |
probably damaging |
Het |
Bhmt1b |
C |
T |
18: 87,775,575 (GRCm39) |
S366F |
probably damaging |
Het |
Celf4 |
T |
C |
18: 25,637,327 (GRCm39) |
S223G |
possibly damaging |
Het |
Ces2c |
T |
A |
8: 105,574,714 (GRCm39) |
V57D |
probably damaging |
Het |
Ces2f |
T |
C |
8: 105,674,808 (GRCm39) |
V70A |
possibly damaging |
Het |
Cntnap1 |
C |
T |
11: 101,068,416 (GRCm39) |
P114S |
probably damaging |
Het |
Cpsf1 |
A |
G |
15: 76,484,483 (GRCm39) |
F666S |
probably damaging |
Het |
Cuzd1 |
T |
A |
7: 130,913,297 (GRCm39) |
D440V |
probably damaging |
Het |
Dhx57 |
T |
C |
17: 80,585,718 (GRCm39) |
E107G |
probably damaging |
Het |
Dop1a |
G |
T |
9: 86,382,925 (GRCm39) |
R286L |
probably damaging |
Het |
Fam135a |
G |
A |
1: 24,067,908 (GRCm39) |
T987I |
probably benign |
Het |
Fastkd1 |
G |
T |
2: 69,517,425 (GRCm39) |
Y818* |
probably null |
Het |
Fer1l4 |
A |
C |
2: 155,894,163 (GRCm39) |
F47V |
possibly damaging |
Het |
Fryl |
A |
G |
5: 73,275,790 (GRCm39) |
*125R |
probably null |
Het |
Herc6 |
A |
G |
6: 57,560,191 (GRCm39) |
D77G |
probably benign |
Het |
Hmox1 |
T |
C |
8: 75,823,959 (GRCm39) |
L209P |
probably damaging |
Het |
Kcns3 |
A |
T |
12: 11,141,654 (GRCm39) |
D348E |
probably benign |
Het |
Lama1 |
T |
A |
17: 68,052,918 (GRCm39) |
I417N |
|
Het |
Lmo7 |
T |
C |
14: 102,139,800 (GRCm39) |
S1028P |
probably benign |
Het |
Lrrc37a |
C |
G |
11: 103,392,411 (GRCm39) |
E1005Q |
probably benign |
Het |
Mis18bp1 |
A |
T |
12: 65,201,585 (GRCm39) |
I372K |
possibly damaging |
Het |
Nr4a3 |
A |
G |
4: 48,051,348 (GRCm39) |
D34G |
probably damaging |
Het |
Or4c113 |
A |
T |
2: 88,884,948 (GRCm39) |
V274D |
probably benign |
Het |
Parp12 |
T |
C |
6: 39,068,279 (GRCm39) |
D496G |
probably benign |
Het |
Rom1 |
A |
G |
19: 8,905,244 (GRCm39) |
V282A |
probably benign |
Het |
Rp1l1 |
G |
A |
14: 64,266,258 (GRCm39) |
V615I |
probably benign |
Het |
Rpgrip1 |
A |
G |
14: 52,389,658 (GRCm39) |
|
probably null |
Het |
Ryr2 |
A |
G |
13: 11,699,364 (GRCm39) |
I2959T |
possibly damaging |
Het |
Sema4a |
T |
G |
3: 88,359,341 (GRCm39) |
K117Q |
probably damaging |
Het |
Slc22a29 |
A |
G |
19: 8,139,004 (GRCm39) |
M486T |
possibly damaging |
Het |
Sntb2 |
T |
A |
8: 107,728,166 (GRCm39) |
C371* |
probably null |
Het |
Spata31d1c |
A |
G |
13: 65,184,044 (GRCm39) |
T529A |
probably benign |
Het |
Tchp |
G |
T |
5: 114,846,827 (GRCm39) |
R38L |
possibly damaging |
Het |
Tnpo2 |
T |
C |
8: 85,773,926 (GRCm39) |
V320A |
probably benign |
Het |
Trim50 |
A |
T |
5: 135,392,646 (GRCm39) |
D187V |
probably damaging |
Het |
Ttl |
A |
G |
2: 128,923,163 (GRCm39) |
E168G |
possibly damaging |
Het |
Tyr |
C |
T |
7: 87,087,175 (GRCm39) |
G446R |
probably damaging |
Het |
Vps35 |
C |
T |
8: 86,001,487 (GRCm39) |
V444I |
probably benign |
Het |
Vstm2b |
T |
C |
7: 40,551,899 (GRCm39) |
S76P |
probably damaging |
Het |
|
Other mutations in Tuba1c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02190:Tuba1c
|
APN |
15 |
98,935,870 (GRCm39) |
missense |
unknown |
|
R2261:Tuba1c
|
UTSW |
15 |
98,935,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R2262:Tuba1c
|
UTSW |
15 |
98,935,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4939:Tuba1c
|
UTSW |
15 |
98,935,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R6367:Tuba1c
|
UTSW |
15 |
98,935,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R6397:Tuba1c
|
UTSW |
15 |
98,935,738 (GRCm39) |
missense |
probably benign |
0.29 |
R6999:Tuba1c
|
UTSW |
15 |
98,935,193 (GRCm39) |
missense |
probably benign |
0.00 |
R8146:Tuba1c
|
UTSW |
15 |
98,935,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R8186:Tuba1c
|
UTSW |
15 |
98,935,396 (GRCm39) |
missense |
probably benign |
|
R9192:Tuba1c
|
UTSW |
15 |
98,935,737 (GRCm39) |
nonsense |
probably null |
|
|