Other mutations in this stock |
Total: 127 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
C |
A |
12: 84,655,790 (GRCm39) |
G295* |
probably null |
Het |
Acad9 |
T |
C |
3: 36,128,525 (GRCm39) |
Y129H |
probably damaging |
Het |
Actn4 |
C |
T |
7: 28,597,549 (GRCm39) |
G608D |
probably benign |
Het |
Adcyap1r1 |
T |
A |
6: 55,458,100 (GRCm39) |
N300K |
probably damaging |
Het |
Adh5 |
A |
G |
3: 138,157,245 (GRCm39) |
I269V |
probably benign |
Het |
Afap1l2 |
G |
A |
19: 56,901,821 (GRCm39) |
A842V |
possibly damaging |
Het |
AI429214 |
A |
T |
8: 37,461,154 (GRCm39) |
K101* |
probably null |
Het |
Alg10b |
T |
A |
15: 90,109,860 (GRCm39) |
W58R |
probably damaging |
Het |
Alpk2 |
C |
T |
18: 65,438,754 (GRCm39) |
E1347K |
probably benign |
Het |
Amotl2 |
G |
T |
9: 102,601,922 (GRCm39) |
E389* |
probably null |
Het |
Ap5m1 |
G |
A |
14: 49,323,705 (GRCm39) |
R465Q |
probably damaging |
Het |
Apoa1 |
A |
C |
9: 46,140,512 (GRCm39) |
S48R |
probably damaging |
Het |
Asb1 |
T |
C |
1: 91,471,950 (GRCm39) |
L34P |
probably damaging |
Het |
Atg14 |
C |
T |
14: 47,788,781 (GRCm39) |
A191T |
probably damaging |
Het |
Atp13a4 |
C |
T |
16: 29,260,102 (GRCm39) |
V235I |
possibly damaging |
Het |
Atrnl1 |
C |
T |
19: 57,744,048 (GRCm39) |
Q1217* |
probably null |
Het |
Bltp2 |
T |
C |
11: 78,159,598 (GRCm39) |
V549A |
probably benign |
Het |
Bsn |
A |
T |
9: 107,992,085 (GRCm39) |
H1222Q |
probably benign |
Het |
Catsper4 |
A |
T |
4: 133,945,552 (GRCm39) |
V169E |
probably damaging |
Het |
Cbx4 |
C |
T |
11: 118,972,718 (GRCm39) |
G219E |
probably damaging |
Het |
Ccdc136 |
C |
T |
6: 29,413,031 (GRCm39) |
T406I |
possibly damaging |
Het |
Celsr3 |
A |
T |
9: 108,715,669 (GRCm39) |
Y2117F |
probably damaging |
Het |
Cenpf |
T |
A |
1: 189,411,299 (GRCm39) |
Q295L |
probably damaging |
Het |
Ces1b |
A |
G |
8: 93,794,783 (GRCm39) |
V272A |
probably benign |
Het |
Cgn |
A |
T |
3: 94,687,116 (GRCm39) |
V62D |
probably damaging |
Het |
Ckap4 |
T |
G |
10: 84,369,387 (GRCm39) |
Q115P |
possibly damaging |
Het |
Clec10a |
T |
C |
11: 70,060,650 (GRCm39) |
|
probably null |
Het |
Clmn |
A |
T |
12: 104,747,067 (GRCm39) |
S827T |
probably benign |
Het |
Cntn4 |
T |
C |
6: 106,466,658 (GRCm39) |
S187P |
probably damaging |
Het |
Cntnap5a |
A |
T |
1: 116,116,095 (GRCm39) |
I526F |
probably damaging |
Het |
Cntnap5b |
A |
G |
1: 100,202,140 (GRCm39) |
Q329R |
probably benign |
Het |
Col1a1 |
T |
A |
11: 94,839,188 (GRCm39) |
S979T |
unknown |
Het |
Crat |
T |
A |
2: 30,292,654 (GRCm39) |
Y606F |
probably benign |
Het |
Cyp2c29 |
G |
T |
19: 39,318,708 (GRCm39) |
C396F |
probably damaging |
Het |
Cyp2d34 |
G |
T |
15: 82,501,817 (GRCm39) |
P231Q |
probably damaging |
Het |
Ddi2 |
A |
T |
4: 141,430,591 (GRCm39) |
|
probably null |
Het |
Dicer1 |
A |
T |
12: 104,679,473 (GRCm39) |
H501Q |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,488,098 (GRCm39) |
I1001V |
probably damaging |
Het |
Dnase2a |
T |
A |
8: 85,637,500 (GRCm39) |
C301S |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,584,280 (GRCm39) |
D142V |
probably damaging |
Het |
Dpp8 |
G |
A |
9: 64,971,150 (GRCm39) |
C590Y |
probably benign |
Het |
Dst |
T |
A |
1: 34,314,317 (GRCm39) |
M6707K |
probably damaging |
Het |
Duox1 |
T |
C |
2: 122,167,735 (GRCm39) |
V1006A |
probably benign |
Het |
Dync1h1 |
T |
C |
12: 110,596,420 (GRCm39) |
S1623P |
probably damaging |
Het |
Ehmt1 |
A |
T |
2: 24,694,015 (GRCm39) |
D1011E |
probably damaging |
Het |
Epc2 |
T |
A |
2: 49,422,235 (GRCm39) |
D376E |
probably benign |
Het |
Eps8 |
C |
A |
6: 137,514,633 (GRCm39) |
|
probably null |
Het |
F11 |
T |
C |
8: 45,699,869 (GRCm39) |
T406A |
probably benign |
Het |
Fat3 |
T |
G |
9: 15,911,082 (GRCm39) |
D1640A |
probably damaging |
Het |
Fbxo15 |
A |
T |
18: 84,977,230 (GRCm39) |
R47S |
probably benign |
Het |
Fbxo28 |
A |
T |
1: 182,157,490 (GRCm39) |
V109E |
probably damaging |
Het |
Fn1 |
A |
T |
1: 71,665,323 (GRCm39) |
S931R |
probably damaging |
Het |
Fndc3b |
T |
C |
3: 27,697,185 (GRCm39) |
D9G |
probably damaging |
Het |
Frem2 |
G |
A |
3: 53,560,343 (GRCm39) |
T1388I |
probably damaging |
Het |
Fstl3 |
C |
A |
10: 79,617,012 (GRCm39) |
T185N |
probably damaging |
Het |
Glo1 |
A |
T |
17: 30,823,014 (GRCm39) |
Y49* |
probably null |
Het |
Gtsf2 |
T |
C |
15: 103,348,100 (GRCm39) |
M137V |
probably benign |
Het |
Gzmk |
C |
T |
13: 113,310,489 (GRCm39) |
G110S |
probably benign |
Het |
Hdac9 |
G |
T |
12: 34,439,331 (GRCm39) |
S428R |
probably damaging |
Het |
Hnrnpul1 |
G |
A |
7: 25,432,694 (GRCm39) |
T456I |
possibly damaging |
Het |
Ino80 |
T |
A |
2: 119,284,565 (GRCm39) |
H172L |
probably damaging |
Het |
Itgb8 |
A |
C |
12: 119,154,347 (GRCm39) |
L230R |
probably damaging |
Het |
Klf9 |
C |
T |
19: 23,142,052 (GRCm39) |
R171W |
probably damaging |
Het |
Kmt2b |
G |
T |
7: 30,282,812 (GRCm39) |
P1050Q |
probably damaging |
Het |
Krt15 |
A |
T |
11: 100,026,484 (GRCm39) |
F67L |
unknown |
Het |
Maml3 |
T |
A |
3: 51,598,077 (GRCm39) |
Y223F |
probably damaging |
Het |
Mcm9 |
C |
T |
10: 53,491,943 (GRCm39) |
|
probably null |
Het |
Mettl3 |
A |
G |
14: 52,532,441 (GRCm39) |
*104Q |
probably null |
Het |
Msrb3 |
T |
A |
10: 120,687,985 (GRCm39) |
D30V |
possibly damaging |
Het |
Mycbp2 |
T |
C |
14: 103,457,512 (GRCm39) |
T1562A |
probably damaging |
Het |
Nat14 |
T |
C |
7: 4,927,038 (GRCm39) |
V70A |
possibly damaging |
Het |
Nbeal2 |
T |
C |
9: 110,454,474 (GRCm39) |
T2685A |
probably damaging |
Het |
Nek1 |
A |
G |
8: 61,469,327 (GRCm39) |
D128G |
probably damaging |
Het |
Nfam1 |
T |
A |
15: 82,899,202 (GRCm39) |
K155* |
probably null |
Het |
Noc4l |
A |
T |
5: 110,798,425 (GRCm39) |
M255K |
possibly damaging |
Het |
Nolc1 |
GCA |
GCAACA |
19: 46,069,800 (GRCm39) |
|
probably benign |
Het |
Nolc1 |
CAG |
CAGGAG |
19: 46,069,798 (GRCm39) |
|
probably benign |
Het |
Nprl2 |
T |
C |
9: 107,422,511 (GRCm39) |
S334P |
probably benign |
Het |
Nsrp1 |
A |
G |
11: 76,937,396 (GRCm39) |
S267P |
probably benign |
Het |
Ntn4 |
A |
T |
10: 93,480,701 (GRCm39) |
M142L |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,194,113 (GRCm39) |
C139* |
probably null |
Het |
Nup210l |
A |
T |
3: 90,098,281 (GRCm39) |
N1411I |
possibly damaging |
Het |
Or10g1 |
A |
G |
14: 52,647,753 (GRCm39) |
L192P |
probably damaging |
Het |
Or5ak24 |
T |
G |
2: 85,260,430 (GRCm39) |
T248P |
probably damaging |
Het |
Pard3 |
A |
T |
8: 128,115,018 (GRCm39) |
T579S |
probably damaging |
Het |
Pcnx3 |
G |
T |
19: 5,721,584 (GRCm39) |
D1071E |
possibly damaging |
Het |
Pi4k2a |
T |
A |
19: 42,103,510 (GRCm39) |
I340N |
possibly damaging |
Het |
Pkdrej |
T |
A |
15: 85,703,185 (GRCm39) |
D917V |
probably damaging |
Het |
Plekhg4 |
T |
A |
8: 106,106,066 (GRCm39) |
F821Y |
probably damaging |
Het |
Ptgfrn |
C |
T |
3: 100,984,625 (GRCm39) |
R189H |
probably benign |
Het |
Ptpn18 |
T |
A |
1: 34,510,742 (GRCm39) |
S235R |
probably damaging |
Het |
Rabep2 |
A |
G |
7: 126,044,460 (GRCm39) |
|
probably null |
Het |
Rbp3 |
T |
G |
14: 33,678,014 (GRCm39) |
I654S |
probably benign |
Het |
Rimbp3 |
T |
C |
16: 17,027,539 (GRCm39) |
L321P |
probably benign |
Het |
Rims2 |
T |
A |
15: 39,374,722 (GRCm39) |
M1028K |
probably benign |
Het |
Ruvbl1 |
T |
A |
6: 88,460,003 (GRCm39) |
V221D |
probably damaging |
Het |
Ruvbl2 |
A |
T |
7: 45,073,527 (GRCm39) |
|
probably null |
Het |
Scn7a |
C |
T |
2: 66,506,312 (GRCm39) |
D1526N |
probably damaging |
Het |
Scnn1a |
T |
C |
6: 125,314,774 (GRCm39) |
F218S |
possibly damaging |
Het |
Sh3tc2 |
T |
A |
18: 62,146,176 (GRCm39) |
M1185K |
probably damaging |
Het |
Slain1 |
C |
A |
14: 103,888,282 (GRCm39) |
D67E |
possibly damaging |
Het |
Snx33 |
T |
C |
9: 56,833,724 (GRCm39) |
D115G |
probably benign |
Het |
Sowaha |
G |
A |
11: 53,369,789 (GRCm39) |
R316C |
probably damaging |
Het |
Spata17 |
A |
T |
1: 186,830,108 (GRCm39) |
F309I |
possibly damaging |
Het |
Spmip7 |
G |
A |
11: 11,440,293 (GRCm39) |
|
probably null |
Het |
Ssrp1 |
G |
T |
2: 84,873,350 (GRCm39) |
|
probably null |
Het |
St6gal1 |
C |
G |
16: 23,147,167 (GRCm39) |
T225S |
probably damaging |
Het |
Sulf1 |
C |
G |
1: 12,918,398 (GRCm39) |
F38L |
probably damaging |
Het |
Tbc1d7 |
G |
A |
13: 43,306,562 (GRCm39) |
T138M |
probably damaging |
Het |
Tdpoz4 |
T |
A |
3: 93,704,351 (GRCm39) |
M216K |
probably damaging |
Het |
Tmem200a |
A |
G |
10: 25,869,220 (GRCm39) |
S350P |
probably damaging |
Het |
Tnpo3 |
A |
T |
6: 29,551,871 (GRCm39) |
D903E |
probably benign |
Het |
Trpc4ap |
A |
T |
2: 155,499,856 (GRCm39) |
I222N |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,781,021 (GRCm39) |
Y3261N |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,542,954 (GRCm39) |
V33344A |
possibly damaging |
Het |
Uxs1 |
A |
G |
1: 43,810,933 (GRCm39) |
Y97H |
probably damaging |
Het |
Vmn1r192 |
A |
T |
13: 22,371,800 (GRCm39) |
V140D |
possibly damaging |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
Vmn2r7 |
A |
G |
3: 64,599,025 (GRCm39) |
S511P |
possibly damaging |
Het |
Vmn2r88 |
T |
C |
14: 51,655,651 (GRCm39) |
L621P |
probably damaging |
Het |
Vps45 |
A |
T |
3: 95,954,365 (GRCm39) |
M174K |
probably benign |
Het |
Wdr72 |
A |
T |
9: 74,052,454 (GRCm39) |
M162L |
probably benign |
Het |
Wdr81 |
T |
A |
11: 75,344,461 (GRCm39) |
M269L |
probably benign |
Het |
Zfp53 |
A |
G |
17: 21,728,713 (GRCm39) |
T249A |
probably benign |
Het |
Zfp758 |
T |
C |
17: 22,580,626 (GRCm39) |
S22P |
probably benign |
Het |
Zfp780b |
T |
C |
7: 27,663,298 (GRCm39) |
D419G |
possibly damaging |
Het |
Zfp934 |
A |
T |
13: 62,666,507 (GRCm39) |
Y45N |
probably damaging |
Het |
|