Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
T |
C |
3: 36,128,525 (GRCm39) |
Y129H |
probably damaging |
Het |
Adcy4 |
C |
T |
14: 56,016,486 (GRCm39) |
D322N |
probably damaging |
Het |
Adgre1 |
G |
A |
17: 57,748,321 (GRCm39) |
G507E |
probably damaging |
Het |
Aif1 |
T |
C |
17: 35,390,074 (GRCm39) |
|
probably null |
Het |
Akr1c6 |
A |
T |
13: 4,488,608 (GRCm39) |
|
probably null |
Het |
Akt2 |
T |
A |
7: 27,337,597 (GRCm39) |
|
probably null |
Het |
Ankrd35 |
T |
A |
3: 96,590,989 (GRCm39) |
L425Q |
possibly damaging |
Het |
Arhgap40 |
A |
G |
2: 158,385,326 (GRCm39) |
T520A |
possibly damaging |
Het |
Arhgef28 |
T |
A |
13: 98,066,062 (GRCm39) |
D1597V |
possibly damaging |
Het |
Aspm |
A |
G |
1: 139,399,472 (GRCm39) |
D1079G |
probably benign |
Het |
Atp1a2 |
A |
T |
1: 172,119,009 (GRCm39) |
|
probably benign |
Het |
Cage1 |
C |
A |
13: 38,207,406 (GRCm39) |
E252D |
possibly damaging |
Het |
Ccdc185 |
A |
G |
1: 182,576,582 (GRCm39) |
S36P |
possibly damaging |
Het |
Cd300a |
T |
C |
11: 114,784,247 (GRCm39) |
V85A |
probably damaging |
Het |
Cd38 |
A |
C |
5: 44,064,887 (GRCm39) |
D235A |
possibly damaging |
Het |
Cdcp1 |
T |
C |
9: 123,009,088 (GRCm39) |
K530R |
probably benign |
Het |
Ceacam20 |
T |
A |
7: 19,705,651 (GRCm39) |
L214Q |
probably damaging |
Het |
Cntn4 |
G |
A |
6: 106,502,379 (GRCm39) |
A379T |
probably benign |
Het |
Col4a2 |
A |
T |
8: 11,479,505 (GRCm39) |
E796V |
probably benign |
Het |
Copa |
A |
G |
1: 171,910,453 (GRCm39) |
|
probably benign |
Het |
Cpa5 |
A |
G |
6: 30,631,363 (GRCm39) |
T426A |
possibly damaging |
Het |
Csmd1 |
A |
G |
8: 16,249,931 (GRCm39) |
F1016L |
probably damaging |
Het |
Cyb5r3 |
A |
T |
15: 83,042,822 (GRCm39) |
L290* |
probably null |
Het |
Ddx42 |
A |
G |
11: 106,133,766 (GRCm39) |
T581A |
probably damaging |
Het |
Deaf1 |
C |
T |
7: 140,902,381 (GRCm39) |
G221S |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,165,366 (GRCm39) |
S580P |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,754,017 (GRCm39) |
E1598G |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,350,262 (GRCm39) |
|
probably benign |
Het |
Eif3f |
C |
A |
7: 108,533,847 (GRCm39) |
|
probably benign |
Het |
Fam184a |
G |
T |
10: 53,574,901 (GRCm39) |
T236K |
probably benign |
Het |
Gas7 |
C |
T |
11: 67,550,876 (GRCm39) |
T126M |
possibly damaging |
Het |
Gckr |
T |
G |
5: 31,465,608 (GRCm39) |
F408C |
probably damaging |
Het |
Gm17472 |
A |
G |
6: 42,958,004 (GRCm39) |
D91G |
probably damaging |
Het |
Gm5117 |
G |
A |
8: 32,228,608 (GRCm39) |
|
noncoding transcript |
Het |
Gsto1 |
T |
A |
19: 47,843,759 (GRCm39) |
I47N |
probably damaging |
Het |
Hck |
C |
T |
2: 152,976,597 (GRCm39) |
P244S |
probably damaging |
Het |
Hif3a |
T |
C |
7: 16,784,490 (GRCm39) |
T250A |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,752,111 (GRCm39) |
|
probably benign |
Het |
Impa1 |
G |
A |
3: 10,380,340 (GRCm39) |
S247F |
probably damaging |
Het |
Ints14 |
G |
C |
9: 64,889,340 (GRCm39) |
R397P |
probably damaging |
Het |
Iqgap1 |
T |
C |
7: 80,373,524 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
C |
15: 101,722,377 (GRCm39) |
K436R |
probably damaging |
Het |
Lama3 |
G |
A |
18: 12,581,362 (GRCm39) |
C607Y |
probably damaging |
Het |
Loxl4 |
G |
T |
19: 42,599,133 (GRCm39) |
|
probably benign |
Het |
Lrrc8d |
C |
T |
5: 105,961,234 (GRCm39) |
T548M |
probably damaging |
Het |
Man1b1 |
T |
A |
2: 25,228,196 (GRCm39) |
D155E |
probably damaging |
Het |
Mapk8ip2 |
C |
T |
15: 89,341,431 (GRCm39) |
P214L |
probably benign |
Het |
Mast1 |
G |
A |
8: 85,645,357 (GRCm39) |
T696I |
probably damaging |
Het |
Muc15 |
C |
T |
2: 110,561,617 (GRCm39) |
P18S |
probably damaging |
Het |
Mybl2 |
T |
C |
2: 162,922,716 (GRCm39) |
S205P |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,809,331 (GRCm39) |
S1763P |
probably damaging |
Het |
Nek10 |
T |
A |
14: 14,860,986 (GRCm38) |
L513M |
possibly damaging |
Het |
Nfib |
A |
G |
4: 82,271,808 (GRCm39) |
M252T |
probably benign |
Het |
Nid2 |
C |
A |
14: 19,828,146 (GRCm39) |
Y261* |
probably null |
Het |
Nmd3 |
C |
T |
3: 69,638,970 (GRCm39) |
R187C |
possibly damaging |
Het |
Nomo1 |
G |
T |
7: 45,700,155 (GRCm39) |
|
probably benign |
Het |
Npy4r |
A |
G |
14: 33,868,437 (GRCm39) |
F284L |
probably damaging |
Het |
Nt5dc2 |
T |
C |
14: 30,860,878 (GRCm39) |
V351A |
possibly damaging |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or5b121 |
T |
A |
19: 13,507,178 (GRCm39) |
L91Q |
probably null |
Het |
Or5g27 |
T |
A |
2: 85,410,069 (GRCm39) |
L162* |
probably null |
Het |
Pcdhb12 |
T |
A |
18: 37,569,209 (GRCm39) |
D118E |
probably damaging |
Het |
Pdcd11 |
C |
T |
19: 47,116,404 (GRCm39) |
T1518I |
probably benign |
Het |
Pde6a |
T |
A |
18: 61,364,434 (GRCm39) |
C163* |
probably null |
Het |
Pign |
A |
T |
1: 105,572,227 (GRCm39) |
W314R |
probably benign |
Het |
Pip5k1b |
T |
A |
19: 24,367,799 (GRCm39) |
H76L |
probably damaging |
Het |
Plcz1 |
T |
C |
6: 139,974,277 (GRCm39) |
N55S |
possibly damaging |
Het |
Pou5f1 |
A |
T |
17: 35,821,438 (GRCm39) |
H350L |
possibly damaging |
Het |
Rchy1 |
A |
T |
5: 92,110,487 (GRCm39) |
|
probably null |
Het |
Ric8b |
A |
G |
10: 84,793,946 (GRCm39) |
T270A |
possibly damaging |
Het |
Rprml |
A |
G |
11: 103,540,644 (GRCm39) |
E13G |
probably benign |
Het |
Secisbp2 |
T |
A |
13: 51,836,063 (GRCm39) |
I719N |
probably damaging |
Het |
Sergef |
C |
T |
7: 46,283,259 (GRCm39) |
R148H |
probably benign |
Het |
Serpina6 |
T |
A |
12: 103,618,221 (GRCm39) |
|
probably null |
Het |
Sirpb1b |
C |
A |
3: 15,613,887 (GRCm39) |
W65L |
probably damaging |
Het |
Slc32a1 |
A |
T |
2: 158,455,977 (GRCm39) |
I211F |
possibly damaging |
Het |
Slc5a9 |
C |
A |
4: 111,748,941 (GRCm39) |
|
probably null |
Het |
Smarce1 |
A |
G |
11: 99,105,977 (GRCm39) |
V226A |
probably benign |
Het |
Spata31d1b |
A |
T |
13: 59,864,097 (GRCm39) |
E415V |
probably damaging |
Het |
Speg |
G |
A |
1: 75,400,508 (GRCm39) |
R2556H |
possibly damaging |
Het |
Suclg2 |
A |
C |
6: 95,543,417 (GRCm39) |
V338G |
probably damaging |
Het |
Tarbp1 |
T |
C |
8: 127,174,184 (GRCm39) |
E874G |
possibly damaging |
Het |
Tex14 |
G |
T |
11: 87,427,727 (GRCm39) |
|
probably null |
Het |
Trim36 |
T |
A |
18: 46,329,245 (GRCm39) |
D53V |
possibly damaging |
Het |
Tsga10ip |
T |
A |
19: 5,444,368 (GRCm39) |
Y21F |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,620,289 (GRCm39) |
V15849M |
probably damaging |
Het |
Ube3b |
T |
C |
5: 114,539,471 (GRCm39) |
S421P |
probably benign |
Het |
Unc5a |
A |
T |
13: 55,147,683 (GRCm39) |
M498L |
probably benign |
Het |
Vipr2 |
A |
G |
12: 116,107,876 (GRCm39) |
I420M |
probably benign |
Het |
Vmn1r179 |
T |
A |
7: 23,628,515 (GRCm39) |
H235Q |
probably damaging |
Het |
Vps35 |
T |
A |
8: 86,008,475 (GRCm39) |
I267F |
probably damaging |
Het |
Wdr26 |
G |
A |
1: 181,025,216 (GRCm39) |
R279W |
probably damaging |
Het |
Xpo6 |
C |
A |
7: 125,768,443 (GRCm39) |
R88L |
probably damaging |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 106,210,376 (GRCm39) |
|
probably null |
Het |
Zfp105 |
T |
A |
9: 122,758,880 (GRCm39) |
S184T |
probably benign |
Het |
Zfp574 |
G |
A |
7: 24,780,388 (GRCm39) |
R470H |
probably damaging |
Het |
Zswim9 |
T |
A |
7: 13,003,484 (GRCm39) |
H122L |
probably damaging |
Het |
|