Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
G |
T |
12: 72,950,060 (GRCm39) |
S271R |
possibly damaging |
Het |
Adrb2 |
A |
G |
18: 62,312,345 (GRCm39) |
V160A |
possibly damaging |
Het |
Atp13a5 |
T |
C |
16: 29,167,820 (GRCm39) |
D113G |
possibly damaging |
Het |
B4galt7 |
T |
A |
13: 55,757,138 (GRCm39) |
V312D |
possibly damaging |
Het |
Bccip |
A |
G |
7: 133,311,220 (GRCm39) |
D45G |
probably benign |
Het |
Bcl2l2 |
A |
G |
14: 55,122,860 (GRCm39) |
Y151C |
probably damaging |
Het |
Ccdc146 |
T |
C |
5: 21,604,790 (GRCm39) |
E16G |
unknown |
Het |
Cdr2l |
C |
A |
11: 115,284,865 (GRCm39) |
D400E |
probably damaging |
Het |
Celsr2 |
A |
C |
3: 108,299,949 (GRCm39) |
*2920E |
probably null |
Het |
Cib1 |
A |
G |
7: 79,877,749 (GRCm39) |
F183L |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 96,460,952 (GRCm39) |
Y1716H |
probably benign |
Het |
Copb1 |
A |
G |
7: 113,825,989 (GRCm39) |
V665A |
probably benign |
Het |
Crmp1 |
C |
T |
5: 37,448,539 (GRCm39) |
T683I |
probably damaging |
Het |
Cubn |
G |
C |
2: 13,433,567 (GRCm39) |
F1114L |
probably benign |
Het |
Dab2 |
A |
T |
15: 6,458,840 (GRCm39) |
R251* |
probably null |
Het |
Ddx28 |
A |
G |
8: 106,736,912 (GRCm39) |
V382A |
probably benign |
Het |
Eml1 |
C |
A |
12: 108,496,580 (GRCm39) |
T612K |
probably damaging |
Het |
Hoxb3 |
CGGCGGTGGCGG |
CGGCGGTGGCGGTGGCGG |
11: 96,236,415 (GRCm39) |
|
probably benign |
Het |
Hoxb3 |
TGGCGG |
TGGCGGAGGCGG |
11: 96,236,421 (GRCm39) |
|
probably benign |
Het |
Iapp |
T |
A |
6: 142,244,612 (GRCm39) |
I13N |
probably damaging |
Het |
Ifit1bl1 |
A |
T |
19: 34,576,666 (GRCm39) |
|
probably null |
Het |
Itgb4 |
T |
A |
11: 115,882,544 (GRCm39) |
|
probably null |
Het |
Kcnh3 |
T |
C |
15: 99,124,934 (GRCm39) |
V128A |
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,756,720 (GRCm39) |
F1176L |
probably damaging |
Het |
Lifr |
A |
G |
15: 7,220,462 (GRCm39) |
T1031A |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,281,641 (GRCm39) |
D3910G |
probably damaging |
Het |
Man1a2 |
A |
T |
3: 100,592,001 (GRCm39) |
S60T |
probably benign |
Het |
Mdh1 |
C |
T |
11: 21,514,138 (GRCm39) |
R93K |
probably benign |
Het |
Mical1 |
G |
T |
10: 41,354,591 (GRCm39) |
K142N |
probably damaging |
Het |
Nf2 |
T |
A |
11: 4,741,118 (GRCm39) |
E365D |
probably benign |
Het |
Nfrkb |
A |
G |
9: 31,330,323 (GRCm39) |
M1192V |
probably benign |
Het |
Npas4 |
A |
C |
19: 5,036,108 (GRCm39) |
D685E |
probably benign |
Het |
Or11h4b |
T |
A |
14: 50,918,606 (GRCm39) |
I162F |
probably damaging |
Het |
Or12k5 |
G |
T |
2: 36,894,794 (GRCm39) |
Y277* |
probably null |
Het |
Or4f4-ps1 |
A |
G |
2: 111,330,310 (GRCm39) |
T238A |
probably damaging |
Het |
Plat |
G |
T |
8: 23,262,248 (GRCm39) |
G91W |
probably damaging |
Het |
Pld1 |
A |
T |
3: 28,142,795 (GRCm39) |
I668F |
probably damaging |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Ppa1 |
A |
G |
10: 61,496,704 (GRCm39) |
D64G |
possibly damaging |
Het |
Rnf133 |
T |
C |
6: 23,649,405 (GRCm39) |
I175V |
probably benign |
Het |
Rpp30 |
A |
G |
19: 36,071,812 (GRCm39) |
I127V |
probably benign |
Het |
Scube2 |
T |
A |
7: 109,399,797 (GRCm39) |
H913L |
probably damaging |
Het |
Sema6d |
T |
A |
2: 124,507,197 (GRCm39) |
S1045T |
probably benign |
Het |
Skida1 |
A |
T |
2: 18,051,402 (GRCm39) |
N496K |
unknown |
Het |
Slc29a2 |
A |
T |
19: 5,080,448 (GRCm39) |
I397F |
probably benign |
Het |
Slc38a2 |
G |
T |
15: 96,590,294 (GRCm39) |
R316S |
probably damaging |
Het |
Slc40a1 |
A |
C |
1: 45,951,498 (GRCm39) |
Y220D |
probably damaging |
Het |
Strc |
T |
G |
2: 121,208,012 (GRCm39) |
H453P |
probably damaging |
Het |
Tmprss3 |
T |
A |
17: 31,407,358 (GRCm39) |
I312F |
probably damaging |
Het |
Tnn |
G |
A |
1: 159,958,256 (GRCm39) |
T529I |
probably damaging |
Het |
Tnr |
A |
T |
1: 159,713,801 (GRCm39) |
D743V |
possibly damaging |
Het |
Trim42 |
A |
T |
9: 97,245,174 (GRCm39) |
F542Y |
probably benign |
Het |
Trpm2 |
A |
T |
10: 77,747,236 (GRCm39) |
Y1421N |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,576,901 (GRCm39) |
E24664G |
probably damaging |
Het |
Ube2q2 |
T |
C |
9: 55,092,250 (GRCm39) |
|
probably null |
Het |
Unc79 |
A |
T |
12: 103,045,297 (GRCm39) |
R824S |
probably benign |
Het |
V1ra8 |
A |
G |
6: 90,180,559 (GRCm39) |
D254G |
probably damaging |
Het |
Vmn1r173 |
A |
T |
7: 23,401,959 (GRCm39) |
I65F |
probably damaging |
Het |
Vmn2r16 |
T |
A |
5: 109,488,138 (GRCm39) |
M337K |
probably benign |
Het |
Wfs1 |
C |
A |
5: 37,125,431 (GRCm39) |
G487C |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,242,926 (GRCm39) |
Y127C |
probably damaging |
Het |
Zfp229 |
T |
C |
17: 21,965,815 (GRCm39) |
S682P |
probably damaging |
Het |
Zscan4-ps1 |
A |
T |
7: 10,802,447 (GRCm39) |
D117E |
possibly damaging |
Het |
|
Other mutations in Ovch2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00568:Ovch2
|
APN |
7 |
107,388,297 (GRCm39) |
missense |
probably null |
1.00 |
IGL02198:Ovch2
|
APN |
7 |
107,394,041 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02200:Ovch2
|
APN |
7 |
107,394,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02442:Ovch2
|
APN |
7 |
107,395,755 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02531:Ovch2
|
APN |
7 |
107,389,405 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02862:Ovch2
|
APN |
7 |
107,394,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Ovch2
|
UTSW |
7 |
107,400,343 (GRCm39) |
missense |
probably damaging |
0.98 |
R0413:Ovch2
|
UTSW |
7 |
107,381,243 (GRCm39) |
missense |
probably benign |
|
R0631:Ovch2
|
UTSW |
7 |
107,381,228 (GRCm39) |
missense |
probably benign |
0.01 |
R1028:Ovch2
|
UTSW |
7 |
107,395,755 (GRCm39) |
missense |
probably benign |
0.37 |
R1329:Ovch2
|
UTSW |
7 |
107,384,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Ovch2
|
UTSW |
7 |
107,389,412 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2254:Ovch2
|
UTSW |
7 |
107,389,402 (GRCm39) |
missense |
probably benign |
0.02 |
R2265:Ovch2
|
UTSW |
7 |
107,383,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R2358:Ovch2
|
UTSW |
7 |
107,394,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R2922:Ovch2
|
UTSW |
7 |
107,389,596 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2923:Ovch2
|
UTSW |
7 |
107,389,596 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3034:Ovch2
|
UTSW |
7 |
107,384,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R3885:Ovch2
|
UTSW |
7 |
107,395,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R3957:Ovch2
|
UTSW |
7 |
107,388,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R4687:Ovch2
|
UTSW |
7 |
107,395,755 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5307:Ovch2
|
UTSW |
7 |
107,391,341 (GRCm39) |
missense |
probably benign |
0.26 |
R5353:Ovch2
|
UTSW |
7 |
107,393,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R5688:Ovch2
|
UTSW |
7 |
107,393,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R5730:Ovch2
|
UTSW |
7 |
107,392,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R5767:Ovch2
|
UTSW |
7 |
107,381,185 (GRCm39) |
missense |
probably benign |
|
R5979:Ovch2
|
UTSW |
7 |
107,393,595 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6039:Ovch2
|
UTSW |
7 |
107,388,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R6039:Ovch2
|
UTSW |
7 |
107,388,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R6064:Ovch2
|
UTSW |
7 |
107,395,779 (GRCm39) |
missense |
probably damaging |
0.98 |
R6247:Ovch2
|
UTSW |
7 |
107,384,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R6638:Ovch2
|
UTSW |
7 |
107,388,301 (GRCm39) |
missense |
probably benign |
0.17 |
R6877:Ovch2
|
UTSW |
7 |
107,389,315 (GRCm39) |
missense |
probably benign |
0.25 |
R7040:Ovch2
|
UTSW |
7 |
107,395,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Ovch2
|
UTSW |
7 |
107,393,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Ovch2
|
UTSW |
7 |
107,393,577 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7824:Ovch2
|
UTSW |
7 |
107,388,295 (GRCm39) |
critical splice donor site |
probably null |
|
R7841:Ovch2
|
UTSW |
7 |
107,393,298 (GRCm39) |
missense |
probably benign |
0.01 |
R7908:Ovch2
|
UTSW |
7 |
107,388,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R8745:Ovch2
|
UTSW |
7 |
107,389,584 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8812:Ovch2
|
UTSW |
7 |
107,393,251 (GRCm39) |
nonsense |
probably null |
|
R8812:Ovch2
|
UTSW |
7 |
107,392,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:Ovch2
|
UTSW |
7 |
107,392,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Ovch2
|
UTSW |
7 |
107,395,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R9308:Ovch2
|
UTSW |
7 |
107,389,560 (GRCm39) |
missense |
probably benign |
0.03 |
R9703:Ovch2
|
UTSW |
7 |
107,383,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R9717:Ovch2
|
UTSW |
7 |
107,393,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|