Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
G |
7: 131,357,660 (GRCm38) |
S150P |
probably damaging |
Het |
5530400C23Rik |
T |
G |
6: 133,293,211 (GRCm38) |
|
probably benign |
Het |
Ahctf1 |
A |
C |
1: 179,763,468 (GRCm38) |
|
probably null |
Het |
Ang5 |
T |
C |
14: 43,962,749 (GRCm38) |
V90A |
probably benign |
Het |
Ano9 |
C |
T |
7: 141,104,710 (GRCm38) |
G442R |
probably damaging |
Het |
Apaf1 |
G |
A |
10: 91,060,052 (GRCm38) |
T386I |
probably damaging |
Het |
Apob |
C |
A |
12: 8,006,440 (GRCm38) |
H1608N |
probably damaging |
Het |
Arhgap12 |
C |
A |
18: 6,064,433 (GRCm38) |
|
probably benign |
Het |
Asxl1 |
T |
A |
2: 153,399,904 (GRCm38) |
D791E |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,736,906 (GRCm38) |
V383A |
probably benign |
Het |
Btbd1 |
A |
C |
7: 81,816,006 (GRCm38) |
D197E |
probably damaging |
Het |
Camta2 |
T |
C |
11: 70,673,959 (GRCm38) |
I938V |
possibly damaging |
Het |
Ccn5 |
G |
A |
2: 163,825,313 (GRCm38) |
C78Y |
probably damaging |
Het |
Cdca7 |
C |
A |
2: 72,483,467 (GRCm38) |
A200D |
possibly damaging |
Het |
Cep104 |
A |
T |
4: 154,006,792 (GRCm38) |
Y923F |
possibly damaging |
Het |
Cep135 |
G |
C |
5: 76,621,305 (GRCm38) |
V601L |
probably benign |
Het |
Ces2b |
G |
A |
8: 104,835,910 (GRCm38) |
G291S |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,761,440 (GRCm38) |
G1400D |
probably damaging |
Het |
Cyth2 |
T |
C |
7: 45,813,117 (GRCm38) |
E1G |
probably damaging |
Het |
Dand5 |
A |
T |
8: 84,816,292 (GRCm38) |
L185Q |
probably damaging |
Het |
Dck |
T |
C |
5: 88,781,221 (GRCm38) |
V253A |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,679,080 (GRCm38) |
S650P |
probably damaging |
Het |
Dicer1 |
G |
A |
12: 104,706,864 (GRCm38) |
P799S |
probably damaging |
Het |
Dst |
C |
T |
1: 34,189,119 (GRCm38) |
P1606L |
probably damaging |
Het |
Eya2 |
G |
A |
2: 165,769,237 (GRCm38) |
C477Y |
probably damaging |
Het |
Fip1l1 |
T |
A |
5: 74,595,842 (GRCm38) |
N498K |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,636,339 (GRCm38) |
|
probably benign |
Het |
Galntl6 |
T |
C |
8: 57,837,183 (GRCm38) |
|
probably null |
Het |
Gda |
A |
T |
19: 21,434,303 (GRCm38) |
F44I |
possibly damaging |
Het |
Gli2 |
G |
A |
1: 118,840,389 (GRCm38) |
R703C |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,916,271 (GRCm38) |
L1960Q |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,308,355 (GRCm38) |
D341G |
probably damaging |
Het |
Grid2 |
G |
T |
6: 63,503,435 (GRCm38) |
A78S |
probably benign |
Het |
Hao2 |
A |
T |
3: 98,883,560 (GRCm38) |
|
probably benign |
Het |
Hook3 |
A |
G |
8: 26,118,986 (GRCm38) |
V10A |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,629,209 (GRCm38) |
E425G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,567,383 (GRCm38) |
D2107G |
probably benign |
Het |
Lrriq3 |
T |
C |
3: 155,187,736 (GRCm38) |
I358T |
possibly damaging |
Het |
Mad2l2 |
A |
G |
4: 148,140,924 (GRCm38) |
D17G |
possibly damaging |
Het |
Mastl |
G |
T |
2: 23,133,346 (GRCm38) |
T455K |
probably benign |
Het |
Mkln1 |
G |
T |
6: 31,432,927 (GRCm38) |
|
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,387,947 (GRCm38) |
Y16N |
possibly damaging |
Het |
Mmp24 |
C |
T |
2: 155,792,597 (GRCm38) |
A79V |
probably benign |
Het |
Mrps35 |
T |
A |
6: 147,070,734 (GRCm38) |
C292S |
possibly damaging |
Het |
Myom1 |
T |
C |
17: 71,120,648 (GRCm38) |
F1435L |
possibly damaging |
Het |
Nars2 |
C |
T |
7: 97,039,923 (GRCm38) |
H351Y |
probably damaging |
Het |
Nfix |
G |
A |
8: 84,726,526 (GRCm38) |
R300C |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 104,153,869 (GRCm38) |
Y462* |
probably null |
Het |
Or13p5 |
C |
T |
4: 118,734,789 (GRCm38) |
H87Y |
probably damaging |
Het |
Or1j12 |
C |
A |
2: 36,452,648 (GRCm38) |
A21E |
probably benign |
Het |
Or2w3 |
C |
A |
11: 58,666,160 (GRCm38) |
F200L |
probably damaging |
Het |
Or4c122 |
C |
A |
2: 89,249,398 (GRCm38) |
E87* |
probably null |
Het |
Or4e1 |
T |
C |
14: 52,463,509 (GRCm38) |
I167V |
probably benign |
Het |
Or5p70 |
T |
A |
7: 108,395,231 (GRCm38) |
I37N |
probably damaging |
Het |
Or7g35 |
T |
C |
9: 19,585,304 (GRCm38) |
S256P |
possibly damaging |
Het |
Or8d2b |
T |
A |
9: 38,877,815 (GRCm38) |
I213N |
probably damaging |
Het |
Or8g20 |
A |
T |
9: 39,484,988 (GRCm38) |
F85L |
probably benign |
Het |
Otog |
A |
T |
7: 46,251,395 (GRCm38) |
|
probably benign |
Het |
Pdcd2l |
A |
T |
7: 34,192,807 (GRCm38) |
D212E |
possibly damaging |
Het |
Pex5 |
T |
C |
6: 124,404,637 (GRCm38) |
N213S |
probably benign |
Het |
Pkn3 |
C |
T |
2: 30,081,134 (GRCm38) |
P238S |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,629,299 (GRCm38) |
I45K |
probably damaging |
Het |
Prl2b1 |
A |
T |
13: 27,390,740 (GRCm38) |
|
probably null |
Het |
Ptprb |
A |
T |
10: 116,368,807 (GRCm38) |
I1849L |
possibly damaging |
Het |
Rasal3 |
G |
T |
17: 32,393,526 (GRCm38) |
S787Y |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,701,833 (GRCm38) |
D596E |
possibly damaging |
Het |
Sdhd |
A |
T |
9: 50,603,764 (GRCm38) |
V9D |
possibly damaging |
Het |
Serinc5 |
T |
C |
13: 92,708,057 (GRCm38) |
S436P |
probably damaging |
Het |
Slc27a1 |
C |
T |
8: 71,584,164 (GRCm38) |
P348L |
probably damaging |
Het |
Slc28a2b |
A |
T |
2: 122,514,398 (GRCm38) |
I162F |
probably damaging |
Het |
Smg1 |
G |
A |
7: 118,160,383 (GRCm38) |
|
probably benign |
Het |
Sorl1 |
A |
T |
9: 42,043,900 (GRCm38) |
|
probably benign |
Het |
Sprtn |
T |
A |
8: 124,900,218 (GRCm38) |
H112Q |
probably damaging |
Het |
Tasor2 |
A |
T |
13: 3,576,054 (GRCm38) |
F1299I |
probably benign |
Het |
Tet2 |
A |
G |
3: 133,467,602 (GRCm38) |
M1633T |
probably benign |
Het |
Tet2 |
T |
A |
3: 133,467,725 (GRCm38) |
D1592V |
probably benign |
Het |
Tmem68 |
A |
T |
4: 3,569,667 (GRCm38) |
C8S |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 123,171,816 (GRCm38) |
I943N |
probably benign |
Het |
Trib2 |
A |
T |
12: 15,794,068 (GRCm38) |
V191D |
probably damaging |
Het |
Tsc22d4 |
T |
C |
5: 137,762,655 (GRCm38) |
S113P |
probably damaging |
Het |
Ttc21b |
T |
C |
2: 66,239,570 (GRCm38) |
R250G |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 46,967,248 (GRCm38) |
Y721C |
probably damaging |
Het |
Ubtfl1 |
A |
T |
9: 18,409,364 (GRCm38) |
I63F |
probably damaging |
Het |
Ush1c |
G |
A |
7: 46,224,908 (GRCm38) |
P171S |
probably benign |
Het |
Utp20 |
A |
T |
10: 88,767,461 (GRCm38) |
N1843K |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,166,937 (GRCm38) |
Y285H |
probably damaging |
Het |
Virma |
A |
G |
4: 11,498,769 (GRCm38) |
D70G |
probably damaging |
Het |
Vmn2r102 |
T |
C |
17: 19,678,015 (GRCm38) |
F431L |
probably benign |
Het |
Wdr17 |
A |
G |
8: 54,661,495 (GRCm38) |
I662T |
probably damaging |
Het |
Wdr87-ps |
T |
A |
7: 29,533,265 (GRCm38) |
|
noncoding transcript |
Het |
Zfp160 |
G |
A |
17: 21,027,006 (GRCm38) |
R606H |
probably benign |
Het |
Zfp369 |
C |
T |
13: 65,296,434 (GRCm38) |
R464C |
probably damaging |
Het |
|