Other mutations in this stock |
Total: 124 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
A |
T |
11: 72,057,581 (GRCm39) |
H739Q |
probably benign |
Het |
Abca3 |
C |
T |
17: 24,593,274 (GRCm39) |
R224C |
probably damaging |
Het |
Abca8b |
A |
G |
11: 109,865,814 (GRCm39) |
|
probably null |
Het |
Adam1b |
C |
T |
5: 121,639,222 (GRCm39) |
V608M |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,735,520 (GRCm39) |
|
probably benign |
Het |
Ankrd17 |
A |
C |
5: 90,430,727 (GRCm39) |
L1019R |
probably damaging |
Het |
Arih1 |
T |
C |
9: 59,393,515 (GRCm39) |
N39S |
unknown |
Het |
Best3 |
G |
A |
10: 116,824,647 (GRCm39) |
V38I |
probably benign |
Het |
Bicc1 |
A |
G |
10: 70,783,713 (GRCm39) |
S393P |
possibly damaging |
Het |
C1d |
T |
A |
11: 17,216,674 (GRCm39) |
N135K |
probably benign |
Het |
Cage1 |
G |
T |
13: 38,195,387 (GRCm39) |
S778* |
probably null |
Het |
Capn7 |
T |
A |
14: 31,074,383 (GRCm39) |
V262E |
probably damaging |
Het |
Ccdc190 |
A |
G |
1: 169,760,656 (GRCm39) |
R95G |
probably damaging |
Het |
Cd163 |
C |
T |
6: 124,302,247 (GRCm39) |
T937I |
probably damaging |
Het |
Cdh18 |
G |
A |
15: 23,259,752 (GRCm39) |
S194N |
probably damaging |
Het |
Ceacam23 |
A |
T |
7: 17,636,631 (GRCm39) |
D236V |
probably damaging |
Het |
Clec4b2 |
A |
T |
6: 123,177,915 (GRCm39) |
S77C |
probably null |
Het |
Ctsw |
T |
A |
19: 5,516,077 (GRCm39) |
D237V |
probably damaging |
Het |
Cyp2c68 |
G |
A |
19: 39,700,951 (GRCm39) |
T289I |
probably benign |
Het |
Cyp4f39 |
A |
G |
17: 32,700,078 (GRCm39) |
Y133C |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,186,690 (GRCm39) |
E1847G |
probably damaging |
Het |
Dnah7a |
C |
A |
1: 53,686,407 (GRCm39) |
E248* |
probably null |
Het |
Eef2kmt |
T |
A |
16: 5,065,463 (GRCm39) |
D248V |
probably damaging |
Het |
Ewsr1 |
T |
C |
11: 5,038,054 (GRCm39) |
T113A |
possibly damaging |
Het |
Fbxo4 |
A |
G |
15: 4,007,238 (GRCm39) |
|
probably null |
Het |
Fbxo43 |
A |
T |
15: 36,163,075 (GRCm39) |
M44K |
probably benign |
Het |
Fchsd1 |
A |
G |
18: 38,097,863 (GRCm39) |
I340T |
possibly damaging |
Het |
Fgf5 |
C |
A |
5: 98,409,874 (GRCm39) |
A141E |
probably damaging |
Het |
Gfm1 |
T |
C |
3: 67,380,877 (GRCm39) |
V664A |
probably damaging |
Het |
Glp2r |
T |
C |
11: 67,631,858 (GRCm39) |
T121A |
possibly damaging |
Het |
Gm10803 |
A |
C |
2: 93,394,517 (GRCm39) |
L96F |
probably damaging |
Het |
Gm14569 |
T |
C |
X: 35,694,470 (GRCm39) |
D1413G |
probably benign |
Het |
Gm15455 |
T |
C |
1: 33,876,432 (GRCm39) |
|
noncoding transcript |
Het |
Gm1818 |
G |
C |
12: 48,602,318 (GRCm39) |
|
noncoding transcript |
Het |
Gnb2 |
G |
A |
5: 137,528,202 (GRCm39) |
|
probably null |
Het |
Gpc4 |
G |
A |
X: 51,163,440 (GRCm39) |
R148C |
probably damaging |
Het |
Gpx5 |
C |
T |
13: 21,472,915 (GRCm39) |
V140I |
probably damaging |
Het |
Gtpbp1 |
A |
T |
15: 79,603,422 (GRCm39) |
Q637L |
possibly damaging |
Het |
H2-T9 |
A |
G |
17: 36,420,307 (GRCm39) |
|
probably benign |
Het |
Herc1 |
A |
T |
9: 66,377,608 (GRCm39) |
K3458M |
possibly damaging |
Het |
Hhat |
A |
T |
1: 192,409,647 (GRCm39) |
L138Q |
probably damaging |
Het |
Hipk1 |
G |
T |
3: 103,684,823 (GRCm39) |
T264N |
probably damaging |
Het |
Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
Hnf4g |
G |
T |
3: 3,709,647 (GRCm39) |
A144S |
probably damaging |
Het |
Hook3 |
TAGAG |
TAG |
8: 26,522,047 (GRCm39) |
|
probably null |
Het |
Ifi204 |
G |
A |
1: 173,579,306 (GRCm39) |
T513I |
possibly damaging |
Het |
Ino80b |
G |
T |
6: 83,102,023 (GRCm39) |
S26R |
probably damaging |
Het |
Ints9 |
T |
A |
14: 65,217,677 (GRCm39) |
L68H |
probably damaging |
Het |
Kel |
A |
G |
6: 41,665,045 (GRCm39) |
L255P |
probably damaging |
Het |
Klf11 |
T |
A |
12: 24,705,358 (GRCm39) |
S271T |
probably benign |
Het |
Klhl20 |
A |
C |
1: 160,936,790 (GRCm39) |
|
probably null |
Het |
Lama2 |
G |
A |
10: 27,066,500 (GRCm39) |
T1127I |
probably damaging |
Het |
Larp1b |
T |
A |
3: 40,988,420 (GRCm39) |
N81K |
possibly damaging |
Het |
Lsm11 |
T |
C |
11: 45,835,666 (GRCm39) |
D25G |
probably damaging |
Het |
Map3k20 |
T |
A |
2: 72,232,689 (GRCm39) |
|
probably benign |
Het |
Mbd6 |
C |
T |
10: 127,122,310 (GRCm39) |
V173I |
probably benign |
Het |
Milr1 |
A |
G |
11: 106,657,791 (GRCm39) |
D131G |
possibly damaging |
Het |
Mybpc1 |
T |
G |
10: 88,379,636 (GRCm39) |
D635A |
probably damaging |
Het |
Myh7b |
G |
C |
2: 155,474,293 (GRCm39) |
R1669S |
possibly damaging |
Het |
Ndufa7 |
A |
G |
17: 34,043,577 (GRCm39) |
|
probably benign |
Het |
Ndufs3 |
C |
A |
2: 90,729,004 (GRCm39) |
A161S |
probably benign |
Het |
Neo1 |
T |
C |
9: 58,897,554 (GRCm39) |
D134G |
probably damaging |
Het |
Nme4 |
G |
A |
17: 26,312,642 (GRCm39) |
T129I |
probably benign |
Het |
Npffr2 |
A |
T |
5: 89,730,546 (GRCm39) |
T159S |
probably benign |
Het |
Nup153 |
A |
T |
13: 46,834,585 (GRCm39) |
|
probably benign |
Het |
Or3a10 |
T |
A |
11: 73,935,881 (GRCm39) |
D73V |
probably damaging |
Het |
Or51ac3 |
A |
C |
7: 103,214,378 (GRCm39) |
M36R |
possibly damaging |
Het |
Pate2 |
T |
C |
9: 35,597,407 (GRCm39) |
|
probably benign |
Het |
Pcca |
A |
G |
14: 123,027,810 (GRCm39) |
N73D |
probably damaging |
Het |
Pip5k1c |
G |
A |
10: 81,146,723 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
A |
T |
15: 44,391,587 (GRCm39) |
H1551L |
probably benign |
Het |
Pkhd1l1 |
G |
A |
15: 44,445,623 (GRCm39) |
M3768I |
probably benign |
Het |
Ppa2 |
A |
G |
3: 133,076,195 (GRCm39) |
M275V |
probably benign |
Het |
Ptpn23 |
G |
A |
9: 110,217,624 (GRCm39) |
T744I |
probably benign |
Het |
Ptprv |
A |
T |
1: 135,052,244 (GRCm39) |
|
noncoding transcript |
Het |
Rad17 |
A |
T |
13: 100,781,571 (GRCm39) |
H75Q |
possibly damaging |
Het |
Rbm44 |
T |
C |
1: 91,096,820 (GRCm39) |
|
probably null |
Het |
Rbpj |
C |
T |
5: 53,806,757 (GRCm39) |
R201W |
probably damaging |
Het |
Rbpjl |
C |
A |
2: 164,252,209 (GRCm39) |
L215I |
probably damaging |
Het |
Ror1 |
A |
G |
4: 100,283,129 (GRCm39) |
E398G |
probably benign |
Het |
Scamp3 |
T |
A |
3: 89,089,600 (GRCm39) |
|
probably benign |
Het |
Selenot |
CATGTATG |
CATGTATGTATG |
3: 58,495,874 (GRCm39) |
|
probably null |
Het |
Siglec15 |
A |
G |
18: 78,091,890 (GRCm39) |
C104R |
probably damaging |
Het |
Sis |
T |
C |
3: 72,841,455 (GRCm39) |
I787V |
probably benign |
Het |
Slc17a8 |
T |
C |
10: 89,412,422 (GRCm39) |
D521G |
probably benign |
Het |
Slc7a10 |
T |
A |
7: 34,896,780 (GRCm39) |
M172K |
possibly damaging |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Slitrk3 |
T |
C |
3: 72,957,981 (GRCm39) |
T264A |
probably benign |
Het |
Smg8 |
A |
C |
11: 86,976,963 (GRCm39) |
V206G |
probably damaging |
Het |
Smg9 |
A |
G |
7: 24,105,297 (GRCm39) |
K137R |
possibly damaging |
Het |
Srrm2 |
C |
A |
17: 24,038,291 (GRCm39) |
|
probably benign |
Het |
Sult2a2 |
T |
A |
7: 13,468,785 (GRCm39) |
Y84N |
possibly damaging |
Het |
Syngr2 |
A |
T |
11: 117,703,336 (GRCm39) |
I34F |
probably benign |
Het |
Tank |
G |
A |
2: 61,408,979 (GRCm39) |
|
probably benign |
Het |
Tead4 |
T |
C |
6: 128,271,134 (GRCm39) |
|
probably benign |
Het |
Tesl1 |
G |
A |
X: 23,773,480 (GRCm39) |
G327E |
probably damaging |
Het |
Tex36 |
A |
T |
7: 133,197,019 (GRCm39) |
C33S |
probably benign |
Het |
Timd5 |
T |
A |
11: 46,419,359 (GRCm39) |
D58E |
probably damaging |
Het |
Timm21 |
C |
A |
18: 84,967,539 (GRCm39) |
V112L |
possibly damaging |
Het |
Tmem240 |
T |
A |
4: 155,824,131 (GRCm39) |
L92Q |
probably damaging |
Het |
Tmem268 |
C |
G |
4: 63,486,777 (GRCm39) |
S100C |
probably damaging |
Het |
Tmod3 |
G |
A |
9: 75,418,488 (GRCm39) |
P183S |
probably damaging |
Het |
Trappc10 |
G |
T |
10: 78,052,994 (GRCm39) |
F260L |
possibly damaging |
Het |
Trim16 |
A |
T |
11: 62,727,638 (GRCm39) |
Y233F |
probably benign |
Het |
Trmt112 |
T |
C |
19: 6,888,121 (GRCm39) |
V91A |
probably benign |
Het |
Ttc3 |
A |
G |
16: 94,230,218 (GRCm39) |
E450G |
probably benign |
Het |
Ttk |
A |
G |
9: 83,745,594 (GRCm39) |
D647G |
probably damaging |
Het |
Ubash3b |
A |
G |
9: 40,948,755 (GRCm39) |
C187R |
possibly damaging |
Het |
Vmn1r29 |
T |
A |
6: 58,285,052 (GRCm39) |
Y257* |
probably null |
Het |
Vmn1r33 |
T |
C |
6: 66,589,089 (GRCm39) |
N155S |
probably benign |
Het |
Vmn2r28 |
T |
A |
7: 5,489,463 (GRCm39) |
I459L |
probably benign |
Het |
Vps16 |
A |
G |
2: 130,281,372 (GRCm39) |
S235G |
probably benign |
Het |
Vwde |
T |
C |
6: 13,192,641 (GRCm39) |
I421V |
possibly damaging |
Het |
Xiap |
T |
C |
X: 41,183,342 (GRCm39) |
F23L |
probably benign |
Het |
Xkr7 |
A |
G |
2: 152,896,300 (GRCm39) |
T385A |
probably benign |
Het |
Zbtb11 |
A |
G |
16: 55,826,428 (GRCm39) |
Y819C |
probably damaging |
Het |
Zfp112 |
A |
G |
7: 23,825,909 (GRCm39) |
T624A |
probably damaging |
Het |
Zfp592 |
A |
G |
7: 80,674,095 (GRCm39) |
D353G |
probably damaging |
Het |
Zfp62 |
T |
A |
11: 49,106,556 (GRCm39) |
S216T |
probably damaging |
Het |
Zfp677 |
A |
T |
17: 21,618,056 (GRCm39) |
H371L |
probably damaging |
Het |
Zfp780b |
T |
C |
7: 27,662,873 (GRCm39) |
K561E |
possibly damaging |
Het |
Zfp936 |
G |
A |
7: 42,836,681 (GRCm39) |
D31N |
probably damaging |
Het |
Znfx1 |
T |
C |
2: 166,881,746 (GRCm39) |
Y217C |
probably damaging |
Het |
Zpbp |
C |
T |
11: 11,365,248 (GRCm39) |
E200K |
probably benign |
Het |
|