Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700009N14Rik |
A |
G |
4: 39,451,391 |
H199R |
not run |
Het |
Ak9 |
A |
G |
10: 41,432,484 |
N1804S |
unknown |
Het |
Akr1c21 |
C |
A |
13: 4,577,140 |
T147N |
probably damaging |
Het |
Aldh1a2 |
A |
G |
9: 71,215,934 |
T30A |
probably benign |
Het |
Alox15 |
T |
C |
11: 70,345,898 |
D447G |
probably damaging |
Het |
Amigo2 |
T |
C |
15: 97,245,075 |
I489V |
probably benign |
Het |
Ano9 |
A |
T |
7: 141,107,437 |
Y322N |
probably damaging |
Het |
Arhgap40 |
G |
T |
2: 158,547,656 |
W583L |
probably benign |
Het |
Atxn2 |
A |
G |
5: 121,778,021 |
E430G |
probably damaging |
Het |
B020004J07Rik |
A |
T |
4: 101,835,528 |
V425E |
probably benign |
Het |
Brip1 |
T |
C |
11: 86,143,278 |
Y539C |
possibly damaging |
Het |
C87436 |
T |
A |
6: 86,465,808 |
L454Q |
probably damaging |
Het |
Casp4 |
T |
G |
9: 5,324,868 |
Y227D |
probably benign |
Het |
Ccdc151 |
T |
C |
9: 22,002,471 |
T2A |
probably damaging |
Het |
Chd4 |
T |
A |
6: 125,106,592 |
|
probably null |
Het |
Chrna10 |
A |
G |
7: 102,112,086 |
C433R |
probably benign |
Het |
Cntln |
A |
T |
4: 85,118,473 |
N214I |
probably damaging |
Het |
Colec12 |
G |
A |
18: 9,848,922 |
V367I |
probably damaging |
Het |
Cyp46a1 |
T |
C |
12: 108,351,996 |
I222T |
probably benign |
Het |
Dagla |
A |
T |
19: 10,262,581 |
|
probably null |
Het |
Dcaf7 |
C |
A |
11: 106,047,843 |
|
probably null |
Het |
Dclk2 |
C |
T |
3: 86,793,259 |
R638H |
probably damaging |
Het |
E2f7 |
A |
G |
10: 110,766,303 |
|
probably null |
Het |
Fam184a |
G |
T |
10: 53,698,805 |
T236K |
probably benign |
Het |
Fam46a |
C |
A |
9: 85,326,717 |
G18C |
probably benign |
Het |
Glyctk |
T |
C |
9: 106,155,462 |
T451A |
probably damaging |
Het |
Hspbap1 |
G |
T |
16: 35,817,230 |
C243F |
unknown |
Het |
Hspg2 |
A |
C |
4: 137,519,946 |
N1160T |
probably benign |
Het |
Ighv5-8 |
C |
T |
12: 113,655,108 |
L48F |
probably benign |
Het |
Jazf1 |
C |
A |
6: 52,777,652 |
E146D |
probably benign |
Het |
Katnb1 |
C |
T |
8: 95,095,497 |
Q284* |
probably null |
Het |
Kctd18 |
G |
T |
1: 57,961,956 |
Y213* |
probably null |
Het |
Klk1b26 |
T |
C |
7: 44,014,789 |
S23P |
possibly damaging |
Het |
Krt88 |
T |
C |
15: 101,450,511 |
L26P |
probably damaging |
Het |
Lrrc8b |
G |
A |
5: 105,481,656 |
V623I |
probably benign |
Het |
Map3k4 |
T |
A |
17: 12,272,068 |
M159L |
probably benign |
Het |
Mast3 |
C |
A |
8: 70,789,682 |
|
probably null |
Het |
Mier1 |
G |
A |
4: 103,139,347 |
|
probably null |
Het |
Mrpl46 |
T |
C |
7: 78,781,459 |
D117G |
probably damaging |
Het |
Ms4a6b |
A |
G |
19: 11,520,396 |
S20G |
probably benign |
Het |
Mup10 |
A |
T |
4: 60,582,078 |
M4K |
unknown |
Het |
Nlrp5 |
C |
T |
7: 23,417,391 |
A180V |
possibly damaging |
Het |
Nlrx1 |
T |
A |
9: 44,264,704 |
|
probably null |
Het |
Olfr1195 |
T |
C |
2: 88,683,625 |
T36A |
possibly damaging |
Het |
Olfr313 |
T |
A |
11: 58,817,540 |
C177* |
probably null |
Het |
Olfr315 |
T |
C |
11: 58,778,996 |
Y290H |
probably damaging |
Het |
Olfr437 |
T |
C |
6: 43,167,810 |
F251L |
probably damaging |
Het |
Olfr612 |
C |
T |
7: 103,538,788 |
A149T |
probably benign |
Het |
Olfr992 |
A |
G |
2: 85,399,639 |
I298T |
probably benign |
Het |
Otud1 |
C |
A |
2: 19,658,931 |
D290E |
probably damaging |
Het |
Pank4 |
A |
G |
4: 154,970,920 |
N249S |
probably benign |
Het |
Pccb |
G |
T |
9: 101,031,913 |
S84R |
probably benign |
Het |
Pemt |
A |
T |
11: 59,971,255 |
H194Q |
possibly damaging |
Het |
Phtf2 |
A |
G |
5: 20,765,858 |
I634T |
possibly damaging |
Het |
Pias2 |
T |
G |
18: 77,120,115 |
I232R |
probably damaging |
Het |
Plce1 |
A |
G |
19: 38,698,508 |
E620G |
probably damaging |
Het |
Ptpn13 |
G |
A |
5: 103,565,284 |
E1758K |
possibly damaging |
Het |
Ptprq |
T |
A |
10: 107,608,273 |
Q1490L |
probably benign |
Het |
Ptx3 |
G |
T |
3: 66,224,947 |
M296I |
probably benign |
Het |
R3hdm2 |
C |
T |
10: 127,481,775 |
P464L |
probably damaging |
Het |
Rapgef1 |
A |
G |
2: 29,699,721 |
E258G |
possibly damaging |
Het |
Rgl2 |
T |
C |
17: 33,934,990 |
F457L |
possibly damaging |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCCGCGGCGGC |
7: 97,579,915 |
|
probably benign |
Het |
Senp8 |
T |
C |
9: 59,737,195 |
N226S |
probably benign |
Het |
Six5 |
C |
T |
7: 19,094,976 |
R114C |
probably damaging |
Het |
Slc10a1 |
T |
C |
12: 80,958,184 |
T195A |
probably benign |
Het |
Slpi |
G |
T |
2: 164,355,547 |
Q51K |
probably benign |
Het |
Smarca4 |
T |
C |
9: 21,658,960 |
V753A |
probably benign |
Het |
Tbc1d32 |
C |
A |
10: 56,198,441 |
M225I |
probably benign |
Het |
Tnfrsf21 |
G |
A |
17: 43,037,667 |
V57I |
probably benign |
Het |
Trim44 |
G |
T |
2: 102,346,968 |
P336T |
possibly damaging |
Het |
Txlnb |
A |
G |
10: 17,827,885 |
I264V |
probably damaging |
Het |
Wisp3 |
T |
G |
10: 39,155,035 |
N164T |
probably benign |
Het |
Xirp2 |
A |
C |
2: 67,513,482 |
E2022D |
probably benign |
Het |
Zfp975 |
A |
G |
7: 42,661,612 |
*526R |
probably null |
Het |
Zp1 |
A |
G |
19: 10,916,569 |
L424P |
probably damaging |
Het |
|