Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110051M20Rik |
A |
G |
2: 91,421,953 |
L21P |
probably damaging |
Het |
4833420G17Rik |
G |
A |
13: 119,470,095 |
R291K |
probably benign |
Het |
4932438A13Rik |
A |
T |
3: 36,989,804 |
H2820L |
possibly damaging |
Het |
Abca2 |
T |
C |
2: 25,442,845 |
S1519P |
probably damaging |
Het |
Abcb11 |
G |
A |
2: 69,257,295 |
A1042V |
probably damaging |
Het |
Abcc10 |
G |
T |
17: 46,312,920 |
|
probably benign |
Het |
Abcc10 |
A |
T |
17: 46,312,919 |
|
probably null |
Het |
Alkbh3 |
A |
C |
2: 93,981,569 |
L240V |
probably damaging |
Het |
Apol10b |
T |
C |
15: 77,585,408 |
S190G |
probably benign |
Het |
Atp1a3 |
C |
A |
7: 24,998,967 |
C135F |
probably benign |
Het |
Atp4a |
C |
G |
7: 30,720,101 |
R659G |
probably benign |
Het |
BC030499 |
T |
C |
11: 78,291,536 |
L57P |
probably benign |
Het |
Bicra |
A |
G |
7: 15,988,762 |
S277P |
possibly damaging |
Het |
Bmp8a |
T |
C |
4: 123,316,897 |
E275G |
probably benign |
Het |
Ccdc102a |
T |
C |
8: 94,913,426 |
E80G |
probably damaging |
Het |
Cdh23 |
T |
C |
10: 60,410,797 |
D954G |
probably damaging |
Het |
Chrm4 |
A |
G |
2: 91,928,443 |
T399A |
possibly damaging |
Het |
Clcn3 |
A |
G |
8: 60,934,537 |
V199A |
possibly damaging |
Het |
Crlf1 |
T |
C |
8: 70,499,514 |
|
probably null |
Het |
Crx |
G |
T |
7: 15,871,146 |
S57* |
probably null |
Het |
Cyp4f16 |
A |
G |
17: 32,537,098 |
I34V |
possibly damaging |
Het |
Daxx |
T |
C |
17: 33,913,624 |
V576A |
probably benign |
Het |
Ddx17 |
C |
T |
15: 79,537,471 |
R351H |
probably damaging |
Het |
Dhx38 |
T |
C |
8: 109,558,629 |
|
probably benign |
Het |
Dnd1 |
T |
C |
18: 36,764,499 |
|
probably benign |
Het |
Dync1i2 |
A |
T |
2: 71,227,825 |
|
probably null |
Het |
E2f6 |
T |
C |
12: 16,816,445 |
S52P |
probably benign |
Het |
Epb41l4a |
A |
G |
18: 33,880,273 |
F116S |
probably damaging |
Het |
Ext1 |
T |
C |
15: 53,106,106 |
N362S |
probably damaging |
Het |
Fam227a |
C |
A |
15: 79,643,988 |
K79N |
possibly damaging |
Het |
Fam228a |
T |
A |
12: 4,732,759 |
L111F |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,282,799 |
T2363A |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,996,932 |
N2591K |
probably damaging |
Het |
Frem2 |
A |
G |
3: 53,653,015 |
M1357T |
possibly damaging |
Het |
Frmd4b |
A |
T |
6: 97,423,463 |
V29D |
probably damaging |
Het |
G930045G22Rik |
A |
G |
6: 50,846,938 |
|
noncoding transcript |
Het |
Galnt3 |
A |
G |
2: 66,107,229 |
S46P |
possibly damaging |
Het |
Gmeb2 |
A |
G |
2: 181,253,973 |
V468A |
possibly damaging |
Het |
Herc2 |
C |
T |
7: 56,219,815 |
R4271* |
probably null |
Het |
Il5 |
C |
A |
11: 53,723,906 |
|
probably benign |
Het |
Ints9 |
G |
A |
14: 64,986,369 |
|
probably benign |
Het |
Itga10 |
T |
C |
3: 96,649,137 |
F196S |
probably damaging |
Het |
Itgb3bp |
T |
C |
4: 99,781,889 |
T138A |
probably damaging |
Het |
Kcnd1 |
G |
A |
X: 7,824,683 |
V281M |
probably benign |
Het |
Lcp2 |
T |
C |
11: 34,087,229 |
L391P |
probably benign |
Het |
Lrrc66 |
T |
C |
5: 73,607,687 |
Y671C |
probably benign |
Het |
Mettl23 |
T |
C |
11: 116,849,294 |
V197A |
possibly damaging |
Het |
Mmp15 |
C |
A |
8: 95,370,772 |
D456E |
probably benign |
Het |
Mospd4 |
T |
C |
18: 46,465,781 |
|
noncoding transcript |
Het |
Mov10l1 |
C |
A |
15: 89,005,312 |
H484N |
probably damaging |
Het |
Mphosph9 |
T |
C |
5: 124,315,568 |
Q197R |
probably benign |
Het |
Ms4a1 |
T |
A |
19: 11,256,569 |
|
probably null |
Het |
Mybbp1a |
T |
C |
11: 72,448,848 |
V919A |
possibly damaging |
Het |
Mycbpap |
A |
T |
11: 94,513,512 |
|
probably benign |
Het |
Naip6 |
G |
A |
13: 100,296,924 |
S1135F |
possibly damaging |
Het |
Ndufc2 |
T |
A |
7: 97,400,337 |
M50K |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,648,082 |
V842A |
probably damaging |
Het |
Ntsr2 |
G |
T |
12: 16,653,695 |
G66W |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,995,088 |
|
probably benign |
Het |
Olfr1206 |
T |
A |
2: 88,864,885 |
N93K |
probably benign |
Het |
Olfr1219 |
T |
A |
2: 89,074,612 |
I160F |
probably benign |
Het |
Olfr427 |
G |
A |
1: 174,100,399 |
G314R |
probably benign |
Het |
Olfr820 |
T |
C |
10: 130,018,096 |
V245A |
probably damaging |
Het |
Otud4 |
T |
A |
8: 79,669,997 |
H628Q |
probably benign |
Het |
Padi6 |
T |
C |
4: 140,728,929 |
T585A |
probably benign |
Het |
Pex16 |
G |
T |
2: 92,375,592 |
R10L |
probably damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,131,089 |
|
probably benign |
Het |
Pom121l2 |
A |
G |
13: 21,983,205 |
T549A |
possibly damaging |
Het |
Prdm15 |
A |
T |
16: 97,812,559 |
M470K |
probably benign |
Het |
Prkag2 |
T |
A |
5: 25,028,505 |
D49V |
possibly damaging |
Het |
Prl3c1 |
A |
G |
13: 27,199,464 |
M38V |
probably benign |
Het |
Prpf18 |
T |
A |
2: 4,643,761 |
I85F |
possibly damaging |
Het |
Psg27 |
A |
G |
7: 18,560,711 |
|
probably benign |
Het |
Relt |
A |
G |
7: 100,848,784 |
|
probably benign |
Het |
Serpina3b |
A |
T |
12: 104,130,670 |
N70I |
probably damaging |
Het |
Slc19a3 |
T |
C |
1: 83,022,565 |
S244G |
probably benign |
Het |
Slc39a5 |
T |
C |
10: 128,399,847 |
T81A |
possibly damaging |
Het |
Slc7a2 |
G |
A |
8: 40,904,526 |
G277D |
probably damaging |
Het |
Slc9c1 |
C |
T |
16: 45,599,887 |
|
probably benign |
Het |
Slx1b |
A |
G |
7: 126,692,581 |
F104L |
probably benign |
Het |
Smg6 |
G |
A |
11: 74,929,701 |
S266N |
probably damaging |
Het |
Spata9 |
T |
C |
13: 75,998,495 |
V162A |
possibly damaging |
Het |
Szrd1 |
T |
C |
4: 141,118,744 |
I47V |
probably benign |
Het |
Tha1 |
G |
T |
11: 117,868,575 |
L363M |
probably benign |
Het |
Tmc6 |
G |
A |
11: 117,778,261 |
T89I |
possibly damaging |
Het |
Tmem132d |
C |
T |
5: 127,789,785 |
G684R |
probably damaging |
Het |
Trim55 |
G |
A |
3: 19,670,978 |
G220S |
probably benign |
Het |
Ttn |
A |
G |
2: 76,770,530 |
L18836P |
probably damaging |
Het |
Ubn1 |
G |
T |
16: 5,072,184 |
|
probably benign |
Het |
Ush2a |
T |
G |
1: 188,911,031 |
W4197G |
probably benign |
Het |
Vmn1r189 |
A |
T |
13: 22,102,061 |
V202E |
probably damaging |
Het |
Vmn1r209 |
T |
C |
13: 22,806,356 |
I55V |
probably benign |
Het |
Vmn2r86 |
A |
T |
10: 130,446,543 |
C735S |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,566,318 |
D174V |
probably damaging |
Het |
Zfp438 |
T |
C |
18: 5,214,910 |
N16S |
probably damaging |
Het |
Zfp444 |
C |
T |
7: 6,189,409 |
T142I |
probably benign |
Het |
Zfp804a |
A |
G |
2: 82,053,791 |
M1V |
probably null |
Het |
Zfp936 |
T |
G |
7: 43,189,310 |
I67S |
probably benign |
Het |
Zfp948 |
A |
T |
17: 21,586,998 |
N151Y |
unknown |
Het |
|
Other mutations in Optn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01295:Optn
|
APN |
2 |
5,033,156 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL01433:Optn
|
APN |
2 |
5,027,144 (GRCm38) |
missense |
probably benign |
0.07 |
IGL01480:Optn
|
APN |
2 |
5,046,018 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01863:Optn
|
APN |
2 |
5,021,487 (GRCm38) |
splice site |
probably benign |
|
IGL02108:Optn
|
APN |
2 |
5,031,273 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL02150:Optn
|
APN |
2 |
5,033,152 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02623:Optn
|
APN |
2 |
5,035,022 (GRCm38) |
missense |
probably damaging |
1.00 |
R0119:Optn
|
UTSW |
2 |
5,024,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R0121:Optn
|
UTSW |
2 |
5,024,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R0330:Optn
|
UTSW |
2 |
5,034,255 (GRCm38) |
missense |
possibly damaging |
0.53 |
R0332:Optn
|
UTSW |
2 |
5,024,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R0335:Optn
|
UTSW |
2 |
5,024,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R0390:Optn
|
UTSW |
2 |
5,046,195 (GRCm38) |
missense |
probably benign |
|
R1710:Optn
|
UTSW |
2 |
5,053,130 (GRCm38) |
missense |
possibly damaging |
0.90 |
R2229:Optn
|
UTSW |
2 |
5,024,117 (GRCm38) |
missense |
probably damaging |
1.00 |
R3237:Optn
|
UTSW |
2 |
5,034,203 (GRCm38) |
missense |
probably damaging |
1.00 |
R3740:Optn
|
UTSW |
2 |
5,034,198 (GRCm38) |
missense |
possibly damaging |
0.51 |
R3741:Optn
|
UTSW |
2 |
5,034,198 (GRCm38) |
missense |
possibly damaging |
0.51 |
R4667:Optn
|
UTSW |
2 |
5,033,139 (GRCm38) |
missense |
probably benign |
0.20 |
R4783:Optn
|
UTSW |
2 |
5,054,627 (GRCm38) |
missense |
probably benign |
|
R4965:Optn
|
UTSW |
2 |
5,021,379 (GRCm38) |
missense |
probably benign |
0.14 |
R5121:Optn
|
UTSW |
2 |
5,046,106 (GRCm38) |
missense |
probably benign |
0.25 |
R6119:Optn
|
UTSW |
2 |
5,021,323 (GRCm38) |
splice site |
probably null |
|
R7024:Optn
|
UTSW |
2 |
5,052,837 (GRCm38) |
splice site |
probably null |
|
R7167:Optn
|
UTSW |
2 |
5,042,483 (GRCm38) |
missense |
probably benign |
0.00 |
R7685:Optn
|
UTSW |
2 |
5,054,650 (GRCm38) |
missense |
probably benign |
0.01 |
R8103:Optn
|
UTSW |
2 |
5,040,202 (GRCm38) |
missense |
probably damaging |
0.97 |
R8267:Optn
|
UTSW |
2 |
5,054,651 (GRCm38) |
missense |
probably benign |
0.00 |
R8844:Optn
|
UTSW |
2 |
5,027,112 (GRCm38) |
critical splice donor site |
probably null |
|
R9082:Optn
|
UTSW |
2 |
5,054,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R9141:Optn
|
UTSW |
2 |
5,054,674 (GRCm38) |
missense |
possibly damaging |
0.93 |
R9238:Optn
|
UTSW |
2 |
5,053,140 (GRCm38) |
missense |
probably damaging |
1.00 |
R9260:Optn
|
UTSW |
2 |
5,040,265 (GRCm38) |
missense |
probably benign |
|
R9287:Optn
|
UTSW |
2 |
5,031,315 (GRCm38) |
missense |
probably damaging |
0.98 |
R9426:Optn
|
UTSW |
2 |
5,054,674 (GRCm38) |
missense |
possibly damaging |
0.93 |
R9787:Optn
|
UTSW |
2 |
5,031,339 (GRCm38) |
missense |
probably damaging |
1.00 |
|