Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl11 |
T |
C |
9: 107,808,409 (GRCm39) |
Y911H |
possibly damaging |
Het |
Arhgef26 |
A |
C |
3: 62,288,331 (GRCm39) |
K467T |
possibly damaging |
Het |
Armcx6 |
A |
T |
X: 133,650,625 (GRCm39) |
W69R |
probably damaging |
Het |
Asl |
T |
C |
5: 130,042,245 (GRCm39) |
Y277C |
probably damaging |
Het |
Atm |
T |
C |
9: 53,406,011 (GRCm39) |
Y1219C |
probably damaging |
Het |
Azin2 |
C |
T |
4: 128,828,397 (GRCm39) |
C270Y |
probably benign |
Het |
Brsk1 |
A |
T |
7: 4,711,139 (GRCm39) |
I545F |
possibly damaging |
Het |
Carm1 |
C |
A |
9: 21,490,692 (GRCm39) |
|
probably null |
Het |
Cfap410 |
A |
G |
10: 77,817,507 (GRCm39) |
N78S |
probably benign |
Het |
Cfap69 |
G |
A |
5: 5,694,432 (GRCm39) |
A143V |
probably damaging |
Het |
Cldn14 |
T |
C |
16: 93,716,192 (GRCm39) |
K218R |
probably damaging |
Het |
Col5a3 |
T |
C |
9: 20,706,954 (GRCm39) |
K714R |
unknown |
Het |
Crybg2 |
A |
G |
4: 133,809,745 (GRCm39) |
H1517R |
possibly damaging |
Het |
Dagla |
A |
C |
19: 10,233,728 (GRCm39) |
F382C |
probably damaging |
Het |
Dixdc1 |
G |
A |
9: 50,622,259 (GRCm39) |
A25V |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,750,496 (GRCm39) |
F473L |
possibly damaging |
Het |
Eif5 |
T |
C |
12: 111,506,713 (GRCm39) |
C102R |
probably damaging |
Het |
Faiml |
A |
G |
9: 99,114,527 (GRCm39) |
C121R |
probably damaging |
Het |
Fhdc1 |
A |
G |
3: 84,364,577 (GRCm39) |
V223A |
possibly damaging |
Het |
Gpatch8 |
A |
G |
11: 102,399,010 (GRCm39) |
V74A |
unknown |
Het |
Haghl |
A |
G |
17: 26,004,060 (GRCm39) |
V8A |
possibly damaging |
Het |
Ksr1 |
A |
G |
11: 78,936,007 (GRCm39) |
|
probably null |
Het |
Lama5 |
A |
C |
2: 179,840,747 (GRCm39) |
Y584D |
probably damaging |
Het |
Lgi4 |
C |
T |
7: 30,767,253 (GRCm39) |
R427* |
probably null |
Het |
Lrriq1 |
T |
A |
10: 102,980,750 (GRCm39) |
S1462C |
probably damaging |
Het |
Map3k4 |
C |
T |
17: 12,480,157 (GRCm39) |
E682K |
probably damaging |
Het |
Myo9b |
G |
A |
8: 71,786,981 (GRCm39) |
R721Q |
probably benign |
Het |
Nherf1 |
C |
T |
11: 115,071,270 (GRCm39) |
R335C |
probably damaging |
Het |
Nmnat2 |
C |
A |
1: 152,950,474 (GRCm39) |
S53Y |
probably damaging |
Het |
Or8b12i |
C |
A |
9: 20,082,061 (GRCm39) |
G269W |
probably benign |
Het |
Or8g34 |
G |
A |
9: 39,373,226 (GRCm39) |
M166I |
probably benign |
Het |
Pcsk7 |
C |
T |
9: 45,827,322 (GRCm39) |
A363V |
probably damaging |
Het |
Pdrg1 |
C |
T |
2: 152,854,355 (GRCm39) |
G62R |
probably damaging |
Het |
Pdzd7 |
A |
G |
19: 45,033,862 (GRCm39) |
I74T |
possibly damaging |
Het |
Plcb4 |
T |
C |
2: 135,781,123 (GRCm39) |
|
probably benign |
Het |
Pramel28 |
A |
G |
4: 143,693,247 (GRCm39) |
V77A |
probably benign |
Het |
Rnf25 |
A |
G |
1: 74,635,047 (GRCm39) |
V135A |
possibly damaging |
Het |
Rph3a |
A |
G |
5: 121,118,212 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Senp6 |
G |
A |
9: 80,051,124 (GRCm39) |
A1134T |
probably benign |
Het |
Slc1a6 |
G |
T |
10: 78,650,448 (GRCm39) |
*562L |
probably null |
Het |
Slc26a6 |
G |
A |
9: 108,734,236 (GRCm39) |
V206I |
probably benign |
Het |
Slc45a3 |
A |
G |
1: 131,905,637 (GRCm39) |
E206G |
probably damaging |
Het |
Smc1a |
T |
A |
X: 150,816,695 (GRCm39) |
Y516N |
probably damaging |
Het |
Smpd3 |
A |
G |
8: 106,984,039 (GRCm39) |
V560A |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,972,946 (GRCm39) |
K760E |
probably benign |
Het |
Ssc4d |
T |
C |
5: 135,994,578 (GRCm39) |
T51A |
possibly damaging |
Het |
Suco |
A |
G |
1: 161,676,220 (GRCm39) |
I386T |
probably damaging |
Het |
Tecta |
A |
T |
9: 42,289,290 (GRCm39) |
M425K |
possibly damaging |
Het |
Tmprss11e |
G |
A |
5: 86,869,266 (GRCm39) |
R96W |
probably damaging |
Het |
Trim63 |
T |
C |
4: 134,050,308 (GRCm39) |
|
probably benign |
Het |
Trpv1 |
A |
G |
11: 73,145,675 (GRCm39) |
K403R |
probably damaging |
Het |
Ttc39d |
A |
G |
17: 80,524,982 (GRCm39) |
Y547C |
probably damaging |
Het |
Unc79 |
C |
T |
12: 102,957,684 (GRCm39) |
T33I |
probably damaging |
Het |
Usp47 |
G |
A |
7: 111,681,743 (GRCm39) |
S518N |
probably damaging |
Het |
Vmn2r22 |
T |
A |
6: 123,614,594 (GRCm39) |
D332V |
probably damaging |
Het |
Vmn2r55 |
A |
G |
7: 12,385,832 (GRCm39) |
L716P |
probably damaging |
Het |
Zfp558 |
T |
C |
9: 18,367,924 (GRCm39) |
N288S |
possibly damaging |
Het |
|
Other mutations in Garin4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Garin4
|
APN |
1 |
190,895,224 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01541:Garin4
|
APN |
1 |
190,896,606 (GRCm39) |
nonsense |
probably null |
|
IGL02364:Garin4
|
APN |
1 |
190,895,713 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02573:Garin4
|
APN |
1 |
190,896,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02705:Garin4
|
APN |
1 |
190,896,499 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03057:Garin4
|
APN |
1 |
190,895,141 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03283:Garin4
|
APN |
1 |
190,895,029 (GRCm39) |
missense |
probably benign |
0.08 |
R0234:Garin4
|
UTSW |
1 |
190,895,105 (GRCm39) |
missense |
probably benign |
0.00 |
R0234:Garin4
|
UTSW |
1 |
190,895,105 (GRCm39) |
missense |
probably benign |
0.00 |
R0402:Garin4
|
UTSW |
1 |
190,896,637 (GRCm39) |
missense |
probably benign |
0.03 |
R0635:Garin4
|
UTSW |
1 |
190,895,924 (GRCm39) |
missense |
probably benign |
|
R0750:Garin4
|
UTSW |
1 |
190,896,682 (GRCm39) |
start gained |
probably benign |
|
R1118:Garin4
|
UTSW |
1 |
190,896,682 (GRCm39) |
start gained |
probably benign |
|
R1521:Garin4
|
UTSW |
1 |
190,896,219 (GRCm39) |
missense |
probably benign |
0.00 |
R1573:Garin4
|
UTSW |
1 |
190,896,682 (GRCm39) |
start gained |
probably benign |
|
R1654:Garin4
|
UTSW |
1 |
190,895,678 (GRCm39) |
missense |
probably benign |
0.00 |
R1699:Garin4
|
UTSW |
1 |
190,896,018 (GRCm39) |
missense |
probably benign |
0.01 |
R1900:Garin4
|
UTSW |
1 |
190,896,631 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2912:Garin4
|
UTSW |
1 |
190,895,425 (GRCm39) |
missense |
probably benign |
0.00 |
R3747:Garin4
|
UTSW |
1 |
190,896,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Garin4
|
UTSW |
1 |
190,895,205 (GRCm39) |
missense |
probably benign |
0.05 |
R6038:Garin4
|
UTSW |
1 |
190,894,919 (GRCm39) |
missense |
probably damaging |
0.98 |
R6038:Garin4
|
UTSW |
1 |
190,894,919 (GRCm39) |
missense |
probably damaging |
0.98 |
R7179:Garin4
|
UTSW |
1 |
190,896,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R7182:Garin4
|
UTSW |
1 |
190,895,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R7261:Garin4
|
UTSW |
1 |
190,896,308 (GRCm39) |
missense |
unknown |
|
R7326:Garin4
|
UTSW |
1 |
190,896,550 (GRCm39) |
missense |
probably benign |
0.00 |
R7363:Garin4
|
UTSW |
1 |
190,895,910 (GRCm39) |
missense |
probably damaging |
0.99 |
R7960:Garin4
|
UTSW |
1 |
190,895,645 (GRCm39) |
missense |
probably benign |
0.02 |
R8120:Garin4
|
UTSW |
1 |
190,895,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R8916:Garin4
|
UTSW |
1 |
190,895,857 (GRCm39) |
missense |
probably benign |
0.00 |
R9011:Garin4
|
UTSW |
1 |
190,895,258 (GRCm39) |
missense |
probably benign |
0.08 |
R9090:Garin4
|
UTSW |
1 |
190,895,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R9165:Garin4
|
UTSW |
1 |
190,895,258 (GRCm39) |
missense |
probably benign |
0.04 |
R9189:Garin4
|
UTSW |
1 |
190,894,900 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9271:Garin4
|
UTSW |
1 |
190,895,153 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Garin4
|
UTSW |
1 |
190,895,942 (GRCm39) |
missense |
probably benign |
0.03 |
|