Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933409G03Rik |
A |
G |
2: 68,446,591 (GRCm39) |
|
probably benign |
Het |
Aass |
G |
A |
6: 23,109,519 (GRCm39) |
P317L |
probably damaging |
Het |
Abca12 |
T |
A |
1: 71,298,972 (GRCm39) |
N2313I |
possibly damaging |
Het |
Adamts12 |
T |
C |
15: 11,071,594 (GRCm39) |
I46T |
probably benign |
Het |
Adipoq |
T |
G |
16: 22,965,393 (GRCm39) |
|
probably null |
Het |
Amy1 |
A |
T |
3: 113,363,070 (GRCm39) |
D92E |
probably benign |
Het |
Asb15 |
G |
A |
6: 24,564,392 (GRCm39) |
R282Q |
probably damaging |
Het |
Bag6 |
G |
C |
17: 35,363,239 (GRCm39) |
G693A |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,887,282 (GRCm39) |
I870T |
possibly damaging |
Het |
Cand2 |
A |
G |
6: 115,766,463 (GRCm39) |
K356R |
probably damaging |
Het |
Cbfa2t3 |
T |
C |
8: 123,360,076 (GRCm39) |
Q525R |
possibly damaging |
Het |
Cd4 |
T |
C |
6: 124,844,769 (GRCm39) |
R339G |
probably damaging |
Het |
Cdh8 |
A |
G |
8: 99,917,066 (GRCm39) |
S350P |
probably damaging |
Het |
Cep295 |
A |
T |
9: 15,249,509 (GRCm39) |
S469T |
probably damaging |
Het |
Ckap2l |
A |
T |
2: 129,127,342 (GRCm39) |
S279T |
probably benign |
Het |
Clnk |
T |
A |
5: 38,927,282 (GRCm39) |
N66Y |
probably damaging |
Het |
Col27a1 |
A |
T |
4: 63,142,503 (GRCm39) |
T64S |
probably benign |
Het |
Crtc1 |
T |
C |
8: 70,838,871 (GRCm39) |
D599G |
probably damaging |
Het |
Cyp2c23 |
A |
C |
19: 44,000,795 (GRCm39) |
I363S |
probably damaging |
Het |
Dnah10 |
A |
T |
5: 124,911,139 (GRCm39) |
I4519F |
possibly damaging |
Het |
Dner |
T |
A |
1: 84,348,553 (GRCm39) |
I716F |
probably damaging |
Het |
Dsel |
T |
G |
1: 111,789,333 (GRCm39) |
T401P |
possibly damaging |
Het |
Egfr |
A |
G |
11: 16,861,746 (GRCm39) |
D1175G |
probably benign |
Het |
Ephb3 |
A |
T |
16: 21,036,804 (GRCm39) |
N343I |
probably damaging |
Het |
Fbxw10 |
T |
A |
11: 62,768,070 (GRCm39) |
F974I |
probably benign |
Het |
Gfi1b |
T |
C |
2: 28,503,786 (GRCm39) |
Y138C |
probably damaging |
Het |
Gm11168 |
T |
A |
9: 3,005,175 (GRCm39) |
L6H |
probably benign |
Het |
Grb10 |
A |
C |
11: 11,895,583 (GRCm39) |
V247G |
probably damaging |
Het |
Gstp2 |
A |
T |
19: 4,090,514 (GRCm39) |
|
probably null |
Het |
Hars2 |
C |
T |
18: 36,922,257 (GRCm39) |
Q291* |
probably null |
Het |
Hyal4 |
G |
T |
6: 24,756,220 (GRCm39) |
W146L |
probably damaging |
Het |
Il22ra1 |
C |
T |
4: 135,461,556 (GRCm39) |
T107I |
possibly damaging |
Het |
Itga8 |
A |
G |
2: 12,209,540 (GRCm39) |
|
probably null |
Het |
Klhl25 |
T |
C |
7: 75,515,450 (GRCm39) |
S119P |
probably damaging |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Lrrc8c |
T |
C |
5: 105,754,636 (GRCm39) |
V137A |
probably benign |
Het |
Macrod2 |
A |
T |
2: 142,018,545 (GRCm39) |
E226V |
probably damaging |
Het |
Mcemp1 |
A |
T |
8: 3,718,201 (GRCm39) |
Q165L |
probably benign |
Het |
Mcpt9 |
T |
A |
14: 56,265,453 (GRCm39) |
K82M |
probably benign |
Het |
Mpzl3 |
A |
G |
9: 44,973,458 (GRCm39) |
T66A |
probably damaging |
Het |
Msh6 |
G |
A |
17: 88,287,788 (GRCm39) |
V143I |
possibly damaging |
Het |
Mug1 |
G |
A |
6: 121,815,684 (GRCm39) |
|
probably null |
Het |
Ncr1 |
G |
T |
7: 4,343,972 (GRCm39) |
C153F |
probably damaging |
Het |
Nf1 |
T |
A |
11: 79,359,595 (GRCm39) |
M1411K |
possibly damaging |
Het |
Nf1 |
T |
A |
11: 79,469,098 (GRCm39) |
V786D |
probably damaging |
Het |
Nisch |
T |
C |
14: 30,925,351 (GRCm39) |
|
probably benign |
Het |
Nwd2 |
T |
A |
5: 63,963,694 (GRCm39) |
Y1093N |
probably benign |
Het |
Oas3 |
G |
A |
5: 120,894,210 (GRCm39) |
R39C |
probably damaging |
Het |
Or1e32 |
A |
T |
11: 73,705,731 (GRCm39) |
M59K |
probably damaging |
Het |
Or7a36 |
C |
T |
10: 78,820,023 (GRCm39) |
T133I |
possibly damaging |
Het |
P3h3 |
T |
A |
6: 124,822,235 (GRCm39) |
N583Y |
probably damaging |
Het |
Pcdh18 |
A |
T |
3: 49,711,147 (GRCm39) |
|
probably null |
Het |
Pcnp |
C |
T |
16: 55,844,896 (GRCm39) |
|
probably benign |
Het |
Pdzd8 |
G |
T |
19: 59,289,563 (GRCm39) |
D612E |
probably benign |
Het |
Pi4kb |
T |
C |
3: 94,906,261 (GRCm39) |
S8P |
probably damaging |
Het |
Pikfyve |
T |
G |
1: 65,295,231 (GRCm39) |
V1454G |
possibly damaging |
Het |
Podn |
T |
C |
4: 107,878,695 (GRCm39) |
N246D |
probably damaging |
Het |
Prg4 |
T |
C |
1: 150,330,243 (GRCm39) |
|
probably benign |
Het |
R3hdm2 |
T |
C |
10: 127,320,390 (GRCm39) |
Y523H |
probably damaging |
Het |
Rpf1 |
T |
A |
3: 146,213,904 (GRCm39) |
E231V |
possibly damaging |
Het |
Slc16a10 |
C |
T |
10: 39,932,611 (GRCm39) |
E317K |
probably benign |
Het |
Slc34a1 |
A |
T |
13: 55,560,078 (GRCm39) |
I435F |
probably damaging |
Het |
Snx19 |
A |
G |
9: 30,344,683 (GRCm39) |
D629G |
probably damaging |
Het |
Tomm70a |
T |
C |
16: 56,966,463 (GRCm39) |
I472T |
probably benign |
Het |
Trp53 |
A |
G |
11: 69,479,506 (GRCm39) |
Y202C |
probably damaging |
Het |
Ttc14 |
T |
A |
3: 33,863,403 (GRCm39) |
|
probably benign |
Het |
Ugt1a1 |
C |
T |
1: 88,140,277 (GRCm39) |
A185V |
possibly damaging |
Het |
Usp28 |
A |
G |
9: 48,939,578 (GRCm39) |
D655G |
probably damaging |
Het |
Vmn1r215 |
C |
T |
13: 23,260,254 (GRCm39) |
T98I |
probably damaging |
Het |
Vmn2r121 |
G |
T |
X: 123,041,879 (GRCm39) |
T426N |
probably benign |
Het |
Vmn2r99 |
A |
G |
17: 19,614,835 (GRCm39) |
N852D |
probably benign |
Het |
Xrn2 |
T |
A |
2: 146,889,580 (GRCm39) |
D654E |
probably damaging |
Het |
Yju2 |
C |
A |
17: 56,271,653 (GRCm39) |
D191E |
probably damaging |
Het |
Zfp335 |
C |
G |
2: 164,738,065 (GRCm39) |
A849P |
possibly damaging |
Het |
Zfp954 |
C |
T |
7: 7,118,390 (GRCm39) |
V385M |
probably damaging |
Het |
Zmynd15 |
A |
G |
11: 70,355,052 (GRCm39) |
T350A |
probably damaging |
Het |
|
Other mutations in Oxa1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Oxa1l
|
APN |
14 |
54,600,802 (GRCm39) |
nonsense |
probably null |
|
R0541:Oxa1l
|
UTSW |
14 |
54,605,646 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1773:Oxa1l
|
UTSW |
14 |
54,600,909 (GRCm39) |
missense |
probably benign |
0.01 |
R2197:Oxa1l
|
UTSW |
14 |
54,598,924 (GRCm39) |
missense |
probably benign |
0.29 |
R5652:Oxa1l
|
UTSW |
14 |
54,604,289 (GRCm39) |
nonsense |
probably null |
|
R5850:Oxa1l
|
UTSW |
14 |
54,605,121 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5898:Oxa1l
|
UTSW |
14 |
54,600,758 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6088:Oxa1l
|
UTSW |
14 |
54,605,151 (GRCm39) |
critical splice donor site |
probably null |
|
R6162:Oxa1l
|
UTSW |
14 |
54,605,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R6869:Oxa1l
|
UTSW |
14 |
54,604,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R7244:Oxa1l
|
UTSW |
14 |
54,598,312 (GRCm39) |
start codon destroyed |
probably benign |
0.33 |
R7247:Oxa1l
|
UTSW |
14 |
54,598,312 (GRCm39) |
start codon destroyed |
probably benign |
0.33 |
R7317:Oxa1l
|
UTSW |
14 |
54,598,312 (GRCm39) |
start codon destroyed |
probably benign |
0.33 |
R7562:Oxa1l
|
UTSW |
14 |
54,600,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7939:Oxa1l
|
UTSW |
14 |
54,604,876 (GRCm39) |
missense |
probably benign |
0.00 |
R8018:Oxa1l
|
UTSW |
14 |
54,600,757 (GRCm39) |
missense |
not run |
|
R8245:Oxa1l
|
UTSW |
14 |
54,605,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R8275:Oxa1l
|
UTSW |
14 |
54,600,758 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8483:Oxa1l
|
UTSW |
14 |
54,606,001 (GRCm39) |
splice site |
probably null |
|
R8679:Oxa1l
|
UTSW |
14 |
54,605,248 (GRCm39) |
critical splice acceptor site |
probably null |
|
|