Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310007B03Rik |
T |
C |
1: 93,154,515 |
N294S |
probably benign |
Het |
Aass |
A |
G |
6: 23,094,220 |
S500P |
possibly damaging |
Het |
Aldh9a1 |
T |
A |
1: 167,357,396 |
N292K |
probably benign |
Het |
Art2b |
A |
T |
7: 101,580,451 |
S80R |
probably benign |
Het |
Atp6v1b2 |
G |
T |
8: 69,102,567 |
A194S |
possibly damaging |
Het |
Bsnd |
T |
C |
4: 106,491,912 |
M44V |
probably damaging |
Het |
Cadps2 |
A |
T |
6: 23,583,429 |
V383E |
probably benign |
Het |
Cd93 |
T |
C |
2: 148,442,539 |
T296A |
possibly damaging |
Het |
Cdk15 |
G |
T |
1: 59,265,655 |
E138D |
probably benign |
Het |
Cdon |
A |
G |
9: 35,463,895 |
I406V |
probably benign |
Het |
Cyp3a41a |
A |
G |
5: 145,705,853 |
V232A |
probably benign |
Het |
Dbndd1 |
T |
A |
8: 123,509,121 |
D130V |
probably damaging |
Het |
Eddm3b |
A |
G |
14: 51,116,930 |
Y125C |
probably damaging |
Het |
Enah |
A |
T |
1: 181,922,392 |
V294E |
probably damaging |
Het |
Farp2 |
A |
G |
1: 93,603,415 |
E545G |
probably damaging |
Het |
Farsb |
T |
C |
1: 78,482,357 |
E22G |
possibly damaging |
Het |
Fezf1 |
A |
G |
6: 23,247,836 |
V80A |
probably benign |
Het |
Fpr2 |
T |
C |
17: 17,893,271 |
Y39H |
unknown |
Het |
Fsd1l |
C |
A |
4: 53,694,054 |
R344S |
probably damaging |
Het |
Fuk |
G |
A |
8: 110,887,156 |
P758S |
probably damaging |
Het |
Fxyd1 |
G |
T |
7: 31,051,976 |
R90S |
unknown |
Het |
Galnt4 |
T |
A |
10: 99,108,604 |
Y64N |
probably damaging |
Het |
Gatb |
C |
T |
3: 85,636,951 |
Q409* |
probably null |
Het |
Glipr2 |
A |
C |
4: 43,968,667 |
D73A |
possibly damaging |
Het |
Gm2035 |
G |
A |
12: 87,919,722 |
R46W |
possibly damaging |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 142,240,713 |
|
probably benign |
Het |
Gm4788 |
A |
G |
1: 139,733,084 |
V622A |
possibly damaging |
Het |
Gpr88 |
C |
T |
3: 116,251,994 |
V223I |
possibly damaging |
Het |
Gtf2h3 |
A |
G |
5: 124,584,004 |
N55S |
probably benign |
Het |
Htr4 |
T |
A |
18: 62,437,427 |
C184* |
probably null |
Het |
Ighv6-3 |
T |
A |
12: 114,391,855 |
R71S |
probably benign |
Het |
Itpr2 |
G |
C |
6: 146,311,087 |
I1510M |
possibly damaging |
Het |
Keap1 |
T |
C |
9: 21,233,838 |
Q292R |
probably benign |
Het |
Malt1 |
A |
C |
18: 65,447,693 |
E219D |
probably benign |
Het |
Manba |
T |
C |
3: 135,523,154 |
V279A |
possibly damaging |
Het |
Map4k5 |
T |
A |
12: 69,874,321 |
H41L |
probably benign |
Het |
Mcm2 |
T |
G |
6: 88,891,794 |
Y327S |
probably damaging |
Het |
Nectin3 |
A |
G |
16: 46,395,121 |
I503T |
possibly damaging |
Het |
Nqo1 |
T |
C |
8: 107,392,647 |
I99M |
probably damaging |
Het |
Nrxn2 |
A |
G |
19: 6,490,552 |
H845R |
probably damaging |
Het |
Otogl |
C |
T |
10: 107,763,200 |
C2254Y |
probably damaging |
Het |
Pmm1 |
T |
C |
15: 81,956,214 |
N110S |
probably damaging |
Het |
Poc1b |
G |
T |
10: 99,134,337 |
C68F |
probably benign |
Het |
Polr1b |
A |
G |
2: 129,123,922 |
Y828C |
possibly damaging |
Het |
Prl3d1 |
A |
G |
13: 27,098,636 |
H119R |
probably damaging |
Het |
Pum3 |
A |
G |
19: 27,426,012 |
S30P |
probably benign |
Het |
Rgl2 |
T |
C |
17: 33,934,990 |
F457L |
possibly damaging |
Het |
Rusc1 |
T |
C |
3: 89,091,887 |
E196G |
possibly damaging |
Het |
Sf3a3 |
A |
G |
4: 124,714,979 |
K29E |
probably benign |
Het |
Slc13a1 |
A |
T |
6: 24,092,312 |
I475K |
probably damaging |
Het |
Slc26a5 |
G |
T |
5: 21,837,246 |
Y237* |
probably null |
Het |
Slc7a14 |
C |
T |
3: 31,227,063 |
G366D |
probably damaging |
Het |
Tbc1d5 |
A |
G |
17: 50,800,082 |
V482A |
probably benign |
Het |
Tdrd5 |
G |
T |
1: 156,259,935 |
Q883K |
probably benign |
Het |
Tet2 |
T |
C |
3: 133,473,630 |
Y1258C |
probably damaging |
Het |
Upf2 |
A |
G |
2: 6,023,320 |
D739G |
unknown |
Het |
Vmn1r122 |
A |
T |
7: 21,133,895 |
F78L |
probably benign |
Het |
Vmn1r75 |
A |
T |
7: 11,880,988 |
K216* |
probably null |
Het |
Vmn2r11 |
A |
T |
5: 109,053,415 |
Y408N |
probably damaging |
Het |
Wscd1 |
T |
A |
11: 71,788,717 |
V472D |
probably damaging |
Het |
Zdbf2 |
G |
T |
1: 63,306,505 |
V1348F |
possibly damaging |
Het |
Zfp442 |
G |
T |
2: 150,408,136 |
H615Q |
possibly damaging |
Het |
Zfp457 |
C |
A |
13: 67,294,001 |
C170F |
possibly damaging |
Het |
Zscan10 |
A |
G |
17: 23,607,029 |
|
probably null |
Het |
|