Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310079G19Rik |
A |
G |
16: 88,424,108 (GRCm39) |
S128P |
probably damaging |
Het |
Abcc1 |
G |
C |
16: 14,231,247 (GRCm39) |
|
probably null |
Het |
Atg2a |
G |
A |
19: 6,300,249 (GRCm39) |
G686S |
possibly damaging |
Het |
Atrnl1 |
A |
T |
19: 57,626,882 (GRCm39) |
|
probably null |
Het |
Brd4 |
T |
C |
17: 32,440,884 (GRCm39) |
|
probably benign |
Het |
Camsap3 |
A |
G |
8: 3,658,242 (GRCm39) |
E688G |
probably damaging |
Het |
Cc2d2a |
T |
A |
5: 43,891,271 (GRCm39) |
S1402R |
probably benign |
Het |
Ccnb1 |
A |
G |
13: 100,922,888 (GRCm39) |
|
probably null |
Het |
Cdc42bpb |
G |
A |
12: 111,292,519 (GRCm39) |
H339Y |
probably damaging |
Het |
Ciart |
T |
A |
3: 95,786,392 (GRCm39) |
T94S |
probably benign |
Het |
Col6a5 |
T |
A |
9: 105,789,674 (GRCm39) |
K1540* |
probably null |
Het |
Csmd3 |
A |
T |
15: 47,574,387 (GRCm39) |
V1969E |
probably damaging |
Het |
Dgka |
T |
G |
10: 128,556,356 (GRCm39) |
N710T |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,731,666 (GRCm39) |
V1212A |
probably benign |
Het |
Dync2i2 |
A |
G |
2: 29,928,278 (GRCm39) |
V116A |
possibly damaging |
Het |
En1 |
C |
T |
1: 120,531,051 (GRCm39) |
P97L |
unknown |
Het |
Esd |
T |
A |
14: 74,982,102 (GRCm39) |
F172L |
probably damaging |
Het |
Gfer |
C |
A |
17: 24,914,942 (GRCm39) |
D34Y |
probably damaging |
Het |
Gm2832 |
G |
A |
14: 41,001,696 (GRCm39) |
M68I |
|
Het |
Hmgcr |
A |
G |
13: 96,795,418 (GRCm39) |
S384P |
probably benign |
Het |
Hsp90aa1 |
T |
C |
12: 110,660,546 (GRCm39) |
T299A |
possibly damaging |
Het |
Igsf10 |
A |
G |
3: 59,239,122 (GRCm39) |
M353T |
probably benign |
Het |
Ino80b |
T |
C |
6: 83,099,306 (GRCm39) |
T211A |
probably benign |
Het |
Lamb2 |
C |
A |
9: 108,366,687 (GRCm39) |
T1607K |
probably benign |
Het |
Lhfpl5 |
A |
G |
17: 28,801,957 (GRCm39) |
E218G |
probably benign |
Het |
Lpo |
C |
A |
11: 87,707,269 (GRCm39) |
C248F |
probably damaging |
Het |
Lrrc3 |
C |
T |
10: 77,736,825 (GRCm39) |
D204N |
probably damaging |
Het |
Mavs |
C |
A |
2: 131,085,051 (GRCm39) |
L160I |
probably benign |
Het |
Morn4 |
C |
T |
19: 42,066,483 (GRCm39) |
D35N |
possibly damaging |
Het |
Mroh8 |
G |
A |
2: 157,063,183 (GRCm39) |
H813Y |
probably benign |
Het |
Myf6 |
T |
C |
10: 107,330,390 (GRCm39) |
E59G |
probably damaging |
Het |
Nhsl3 |
T |
A |
4: 129,119,201 (GRCm39) |
E173V |
probably null |
Het |
Nlrp10 |
T |
A |
7: 108,524,405 (GRCm39) |
E358D |
possibly damaging |
Het |
Odad2 |
A |
C |
18: 7,211,593 (GRCm39) |
D760E |
probably benign |
Het |
Or12e8 |
A |
G |
2: 87,188,066 (GRCm39) |
T93A |
probably benign |
Het |
Or13a19 |
T |
C |
7: 139,902,759 (GRCm39) |
I49T |
possibly damaging |
Het |
Or1e1d-ps1 |
T |
A |
11: 73,819,332 (GRCm39) |
L94* |
probably null |
Het |
Or1o1 |
T |
C |
17: 37,717,095 (GRCm39) |
F219L |
probably benign |
Het |
Or5g9 |
T |
A |
2: 85,551,952 (GRCm39) |
F68I |
probably damaging |
Het |
Or7g28 |
T |
C |
9: 19,272,579 (GRCm39) |
E24G |
possibly damaging |
Het |
Plxna4 |
T |
A |
6: 32,169,204 (GRCm39) |
H1331L |
probably damaging |
Het |
Poli |
A |
T |
18: 70,649,920 (GRCm39) |
M357K |
possibly damaging |
Het |
Psd4 |
T |
G |
2: 24,284,555 (GRCm39) |
C140G |
possibly damaging |
Het |
Rab3gap1 |
T |
A |
1: 127,818,835 (GRCm39) |
|
probably null |
Het |
Rasa3 |
T |
C |
8: 13,681,826 (GRCm39) |
N41S |
probably benign |
Het |
Rps6kc1 |
A |
G |
1: 190,532,407 (GRCm39) |
S532P |
probably benign |
Het |
S100a3 |
T |
A |
3: 90,509,747 (GRCm39) |
|
probably null |
Het |
Sfrp5 |
T |
C |
19: 42,190,204 (GRCm39) |
K83E |
possibly damaging |
Het |
Slco1a4 |
T |
C |
6: 141,780,434 (GRCm39) |
I119V |
probably benign |
Het |
Snx15 |
T |
A |
19: 6,170,626 (GRCm39) |
Q271L |
probably damaging |
Het |
Sorcs2 |
C |
A |
5: 36,178,605 (GRCm39) |
S1128I |
probably damaging |
Het |
Tbc1d7 |
A |
T |
13: 43,308,211 (GRCm39) |
F85I |
probably damaging |
Het |
Thoc7 |
A |
G |
14: 13,953,528 (GRCm38) |
Y46H |
probably damaging |
Het |
Top1mt |
T |
A |
15: 75,539,297 (GRCm39) |
Y366F |
probably damaging |
Het |
Trpv2 |
C |
A |
11: 62,475,287 (GRCm39) |
S233R |
probably benign |
Het |
Vav1 |
C |
A |
17: 57,586,268 (GRCm39) |
T24N |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Wdfy4 |
G |
T |
14: 32,686,583 (GRCm39) |
|
probably null |
Het |
Wdr3 |
A |
G |
3: 100,062,313 (GRCm39) |
S201P |
probably benign |
Het |
Wfs1 |
C |
T |
5: 37,124,294 (GRCm39) |
D866N |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,942,687 (GRCm39) |
|
probably benign |
Het |
Xpot |
G |
T |
10: 121,438,304 (GRCm39) |
Q762K |
probably benign |
Het |
Zfp287 |
A |
T |
11: 62,605,764 (GRCm39) |
L370H |
possibly damaging |
Het |
|
Other mutations in Optn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01295:Optn
|
APN |
2 |
5,037,967 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01433:Optn
|
APN |
2 |
5,031,955 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01480:Optn
|
APN |
2 |
5,050,829 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01863:Optn
|
APN |
2 |
5,026,298 (GRCm39) |
splice site |
probably benign |
|
IGL02108:Optn
|
APN |
2 |
5,036,084 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02150:Optn
|
APN |
2 |
5,037,963 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02623:Optn
|
APN |
2 |
5,039,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Optn
|
UTSW |
2 |
5,028,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0121:Optn
|
UTSW |
2 |
5,028,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Optn
|
UTSW |
2 |
5,039,066 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0332:Optn
|
UTSW |
2 |
5,028,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0335:Optn
|
UTSW |
2 |
5,028,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Optn
|
UTSW |
2 |
5,051,006 (GRCm39) |
missense |
probably benign |
|
R0437:Optn
|
UTSW |
2 |
5,028,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Optn
|
UTSW |
2 |
5,057,941 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2229:Optn
|
UTSW |
2 |
5,028,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R3237:Optn
|
UTSW |
2 |
5,039,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R3740:Optn
|
UTSW |
2 |
5,039,009 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3741:Optn
|
UTSW |
2 |
5,039,009 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4667:Optn
|
UTSW |
2 |
5,037,950 (GRCm39) |
missense |
probably benign |
0.20 |
R4783:Optn
|
UTSW |
2 |
5,059,438 (GRCm39) |
missense |
probably benign |
|
R4965:Optn
|
UTSW |
2 |
5,026,190 (GRCm39) |
missense |
probably benign |
0.14 |
R5121:Optn
|
UTSW |
2 |
5,050,917 (GRCm39) |
missense |
probably benign |
0.25 |
R6119:Optn
|
UTSW |
2 |
5,026,134 (GRCm39) |
splice site |
probably null |
|
R7167:Optn
|
UTSW |
2 |
5,047,294 (GRCm39) |
missense |
probably benign |
0.00 |
R7685:Optn
|
UTSW |
2 |
5,059,461 (GRCm39) |
missense |
probably benign |
0.01 |
R8103:Optn
|
UTSW |
2 |
5,045,013 (GRCm39) |
missense |
probably damaging |
0.97 |
R8267:Optn
|
UTSW |
2 |
5,059,462 (GRCm39) |
missense |
probably benign |
0.00 |
R8844:Optn
|
UTSW |
2 |
5,031,923 (GRCm39) |
critical splice donor site |
probably null |
|
R9082:Optn
|
UTSW |
2 |
5,059,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R9141:Optn
|
UTSW |
2 |
5,059,485 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9238:Optn
|
UTSW |
2 |
5,057,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9260:Optn
|
UTSW |
2 |
5,045,076 (GRCm39) |
missense |
probably benign |
|
R9287:Optn
|
UTSW |
2 |
5,036,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R9426:Optn
|
UTSW |
2 |
5,059,485 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9787:Optn
|
UTSW |
2 |
5,036,150 (GRCm39) |
missense |
probably damaging |
1.00 |
|