Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930595M18Rik |
A |
G |
X: 81,420,817 |
V428A |
probably benign |
Het |
Aanat |
T |
C |
11: 116,596,231 |
L88P |
probably damaging |
Het |
Arhgap5 |
A |
T |
12: 52,519,888 |
N1214I |
probably benign |
Het |
BC034090 |
A |
T |
1: 155,241,797 |
S192T |
probably damaging |
Het |
Bco1 |
G |
A |
8: 117,130,676 |
V461I |
possibly damaging |
Het |
Cass4 |
C |
T |
2: 172,432,558 |
P753L |
probably damaging |
Het |
Cubn |
G |
A |
2: 13,427,914 |
R1199C |
probably damaging |
Het |
Dcaf12l1 |
T |
C |
X: 44,788,436 |
N495S |
possibly damaging |
Het |
Dopey2 |
C |
A |
16: 93,771,846 |
Q1599K |
possibly damaging |
Het |
Dyrk1a |
C |
A |
16: 94,685,074 |
L427I |
probably benign |
Het |
Esp16 |
T |
C |
17: 39,537,848 |
I11T |
possibly damaging |
Het |
Esyt3 |
A |
T |
9: 99,315,281 |
F832Y |
possibly damaging |
Het |
F8 |
A |
T |
X: 75,285,365 |
|
probably null |
Het |
Fam135a |
T |
C |
1: 24,028,311 |
Y259C |
probably benign |
Het |
Fbxo38 |
T |
C |
18: 62,533,462 |
|
probably null |
Het |
Fbxo43 |
T |
C |
15: 36,162,859 |
I67M |
probably benign |
Het |
Gcfc2 |
G |
T |
6: 81,930,767 |
C154F |
probably benign |
Het |
Gm21731 |
G |
T |
13: 120,240,931 |
V88F |
probably damaging |
Het |
Hipk2 |
C |
T |
6: 38,698,556 |
R1029H |
probably damaging |
Het |
Ilk |
G |
A |
7: 105,742,087 |
W73* |
probably null |
Het |
Ism1 |
T |
C |
2: 139,740,253 |
S162P |
probably damaging |
Het |
Itpkb |
T |
A |
1: 180,333,173 |
L288Q |
possibly damaging |
Het |
Itpr2 |
C |
A |
6: 146,415,354 |
K306N |
probably damaging |
Het |
Kdm2a |
C |
T |
19: 4,324,512 |
E864K |
possibly damaging |
Het |
Kdm4b |
G |
A |
17: 56,355,944 |
V172M |
probably damaging |
Het |
Kyat3 |
A |
T |
3: 142,737,844 |
K406M |
probably null |
Het |
Lipe |
T |
A |
7: 25,397,620 |
K299N |
possibly damaging |
Het |
Lrrc2 |
T |
A |
9: 110,966,517 |
C123* |
probably null |
Het |
Mptx2 |
T |
A |
1: 173,274,673 |
I150F |
probably damaging |
Het |
Mucl2 |
T |
C |
15: 103,898,426 |
T27A |
possibly damaging |
Het |
Nfx1 |
T |
A |
4: 41,004,357 |
C709* |
probably null |
Het |
Olfr164 |
A |
G |
16: 19,285,946 |
S266P |
possibly damaging |
Het |
Olfr624 |
A |
T |
7: 103,670,146 |
I295N |
probably damaging |
Het |
Oprm1 |
T |
C |
10: 6,839,544 |
S390P |
probably benign |
Het |
Pcdhb14 |
T |
C |
18: 37,449,662 |
L607P |
probably damaging |
Het |
Rap1gds1 |
A |
T |
3: 138,965,960 |
I133N |
probably damaging |
Het |
Rasl10a |
T |
C |
11: 5,059,461 |
L83S |
probably damaging |
Het |
Satb2 |
C |
T |
1: 56,845,620 |
V382M |
probably damaging |
Het |
Sh3gl1 |
T |
C |
17: 56,018,949 |
K160R |
probably damaging |
Het |
Sirt4 |
T |
C |
5: 115,480,292 |
D241G |
probably benign |
Het |
Sla2 |
G |
A |
2: 156,875,942 |
R137C |
probably damaging |
Het |
Spef2 |
A |
G |
15: 9,704,536 |
I454T |
probably damaging |
Het |
Stag3 |
A |
G |
5: 138,298,349 |
K490E |
probably benign |
Het |
Tctn3 |
T |
C |
19: 40,611,711 |
K95R |
probably benign |
Het |
Tdgf1 |
C |
T |
9: 110,943,190 |
R46Q |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,200,329 |
I1784V |
probably damaging |
Het |
Ttc21a |
A |
T |
9: 119,954,165 |
E511V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,711,888 |
F25258L |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,808,946 |
C13828G |
probably damaging |
Het |
Vmn1r210 |
T |
A |
13: 22,827,403 |
M238L |
probably damaging |
Het |
Vmn1r38 |
A |
G |
6: 66,776,907 |
I75T |
probably benign |
Het |
Vmn2r84 |
T |
A |
10: 130,385,800 |
*850C |
probably null |
Het |
Vwa7 |
T |
C |
17: 35,025,159 |
|
probably null |
Het |
Zfp128 |
T |
A |
7: 12,884,732 |
D52E |
probably damaging |
Het |
Zfp618 |
T |
C |
4: 63,115,491 |
|
probably benign |
Het |
Zkscan2 |
T |
A |
7: 123,485,002 |
E633V |
possibly damaging |
Het |
|