Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
G |
5: 76,882,681 |
S691P |
probably benign |
Het |
Adgrb3 |
T |
C |
1: 25,226,831 |
|
probably null |
Het |
Aplf |
A |
T |
6: 87,646,033 |
Y355N |
probably damaging |
Het |
Bms1 |
A |
G |
6: 118,389,389 |
|
probably benign |
Het |
Catsperb |
T |
C |
12: 101,463,114 |
I182T |
probably damaging |
Het |
Cd300ld2 |
T |
C |
11: 115,013,777 |
D88G |
probably benign |
Het |
Cebpz |
T |
C |
17: 78,934,752 |
N491S |
probably damaging |
Het |
Crybg2 |
T |
C |
4: 134,081,459 |
S1415P |
probably damaging |
Het |
Ddc |
A |
G |
11: 11,829,131 |
V331A |
probably benign |
Het |
Decr2 |
T |
C |
17: 26,083,024 |
E244G |
probably damaging |
Het |
Dhrs11 |
A |
G |
11: 84,823,117 |
M136T |
probably damaging |
Het |
Eapp |
G |
A |
12: 54,685,948 |
Q126* |
probably null |
Het |
Fam111a |
T |
A |
19: 12,587,778 |
V297D |
probably damaging |
Het |
Fam84a |
G |
A |
12: 14,150,408 |
A106V |
probably benign |
Het |
Fbxo10 |
A |
C |
4: 45,062,118 |
L136R |
probably damaging |
Het |
Fbxo30 |
T |
A |
10: 11,291,374 |
H613Q |
possibly damaging |
Het |
Frk |
A |
T |
10: 34,591,810 |
|
probably null |
Het |
Gm10392 |
T |
A |
11: 77,517,481 |
D104V |
probably benign |
Het |
Gm960 |
T |
A |
19: 4,652,171 |
K282N |
probably damaging |
Het |
Gpn1 |
A |
G |
5: 31,497,338 |
E78G |
possibly damaging |
Het |
Hhip |
T |
C |
8: 79,990,276 |
Y506C |
probably damaging |
Het |
Hid1 |
G |
A |
11: 115,356,750 |
S274L |
possibly damaging |
Het |
Immp2l |
G |
T |
12: 41,703,765 |
|
probably benign |
Het |
Klhl21 |
T |
C |
4: 152,009,624 |
F228L |
possibly damaging |
Het |
Lamc1 |
T |
A |
1: 153,243,478 |
|
probably null |
Het |
Lars |
G |
A |
18: 42,210,050 |
R1101C |
probably damaging |
Het |
Magi2 |
T |
C |
5: 19,227,332 |
V15A |
probably benign |
Het |
Map2k7 |
T |
C |
8: 4,243,621 |
|
probably null |
Het |
Mga |
T |
A |
2: 119,963,960 |
H2590Q |
possibly damaging |
Het |
Mlxip |
T |
C |
5: 123,450,223 |
I238T |
possibly damaging |
Het |
Mylk |
T |
A |
16: 34,875,586 |
D230E |
probably benign |
Het |
Nacad |
T |
A |
11: 6,601,185 |
T669S |
probably benign |
Het |
Nin |
C |
T |
12: 70,031,738 |
M1691I |
probably benign |
Het |
Nlrp4d |
C |
T |
7: 10,382,237 |
A203T |
probably damaging |
Het |
Olfr1204 |
T |
G |
2: 88,852,262 |
F104C |
probably damaging |
Het |
Olfr1301 |
A |
T |
2: 111,754,425 |
M59L |
probably damaging |
Het |
Olfr1495 |
A |
T |
19: 13,768,510 |
H56L |
probably benign |
Het |
Olfr201 |
A |
G |
16: 59,269,031 |
V212A |
probably benign |
Het |
Olfr433 |
T |
C |
1: 174,042,480 |
F177L |
probably benign |
Het |
Olfr729 |
C |
A |
14: 50,148,774 |
M33I |
probably benign |
Het |
Osbp |
C |
A |
19: 11,977,829 |
Q282K |
probably benign |
Het |
Osbpl2 |
A |
G |
2: 180,148,463 |
S177G |
probably damaging |
Het |
Pax1 |
A |
G |
2: 147,366,255 |
H261R |
possibly damaging |
Het |
Pcif1 |
A |
T |
2: 164,886,727 |
L274F |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,117,825 |
S3420P |
probably benign |
Het |
Prss3 |
A |
C |
6: 41,377,627 |
|
probably benign |
Het |
Ptk2b |
T |
C |
14: 66,163,114 |
T751A |
possibly damaging |
Het |
Pus10 |
T |
C |
11: 23,673,239 |
V126A |
probably damaging |
Het |
Rai14 |
A |
C |
15: 10,587,916 |
D258E |
probably damaging |
Het |
Rbp3 |
T |
C |
14: 33,954,524 |
V143A |
possibly damaging |
Het |
Sarm1 |
G |
A |
11: 78,483,327 |
Q625* |
probably null |
Het |
Scgb1b21 |
T |
G |
7: 33,527,667 |
|
noncoding transcript |
Het |
Scrn1 |
A |
T |
6: 54,520,769 |
V279E |
probably damaging |
Het |
Sipa1l2 |
T |
C |
8: 125,421,895 |
T1670A |
probably damaging |
Het |
Slc9a4 |
A |
T |
1: 40,600,962 |
I305F |
probably benign |
Het |
Smarcc1 |
A |
G |
9: 110,213,617 |
T918A |
probably damaging |
Het |
Tas2r109 |
A |
T |
6: 132,980,426 |
H180Q |
probably benign |
Het |
Tas2r121 |
G |
A |
6: 132,700,230 |
R260* |
probably null |
Het |
Tenm3 |
T |
C |
8: 48,279,074 |
D1249G |
probably benign |
Het |
Tgtp1 |
C |
G |
11: 48,987,530 |
G116A |
probably damaging |
Het |
Tial1 |
A |
G |
7: 128,443,910 |
Y317H |
probably damaging |
Het |
Trim66 |
A |
T |
7: 109,455,080 |
W1308R |
probably damaging |
Het |
Ulk2 |
T |
G |
11: 61,783,545 |
K878N |
possibly damaging |
Het |
Zfp41 |
T |
A |
15: 75,618,291 |
S31T |
possibly damaging |
Het |
|