Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
T |
C |
5: 138,562,936 |
S155G |
probably benign |
Het |
Abcc4 |
T |
C |
14: 118,627,654 |
N320S |
probably damaging |
Het |
Akr1c19 |
G |
A |
13: 4,237,070 |
R96H |
probably benign |
Het |
Ankrd17 |
T |
C |
5: 90,291,151 |
D451G |
possibly damaging |
Het |
Ano8 |
T |
A |
8: 71,485,110 |
D36V |
probably damaging |
Het |
Aqp3 |
A |
G |
4: 41,098,003 |
V36A |
probably benign |
Het |
Atf7ip |
A |
G |
6: 136,560,710 |
T314A |
probably benign |
Het |
Atp2c1 |
A |
T |
9: 105,422,999 |
D700E |
probably damaging |
Het |
Axin2 |
G |
A |
11: 108,939,376 |
V341M |
possibly damaging |
Het |
Bin3 |
A |
G |
14: 70,134,527 |
Q139R |
probably damaging |
Het |
Brca2 |
A |
G |
5: 150,532,337 |
D181G |
probably damaging |
Het |
C330027C09Rik |
T |
A |
16: 49,001,653 |
S215T |
probably benign |
Het |
Capn3 |
A |
G |
2: 120,494,814 |
E466G |
probably damaging |
Het |
Ccdc14 |
T |
A |
16: 34,723,619 |
Y830* |
probably null |
Het |
Cdk12 |
T |
C |
11: 98,221,084 |
F723L |
unknown |
Het |
Cep89 |
G |
A |
7: 35,429,928 |
R630H |
probably damaging |
Het |
Clca2 |
T |
A |
3: 145,098,784 |
I61F |
probably damaging |
Het |
Clca4b |
T |
C |
3: 144,922,768 |
T393A |
not run |
Het |
Cldn5 |
G |
A |
16: 18,777,095 |
A34T |
probably damaging |
Het |
Cobll1 |
A |
T |
2: 65,098,373 |
S870T |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,706,360 |
K68E |
probably damaging |
Het |
Crnn |
A |
T |
3: 93,148,534 |
Q209L |
probably damaging |
Het |
Cwf19l1 |
A |
T |
19: 44,132,140 |
F45I |
probably damaging |
Het |
Cyfip2 |
T |
A |
11: 46,207,440 |
K1052* |
probably null |
Het |
D930020B18Rik |
G |
A |
10: 121,667,811 |
|
probably null |
Het |
Dcc |
G |
A |
18: 71,826,123 |
P193S |
probably damaging |
Het |
Dda1 |
T |
A |
8: 71,474,493 |
C48S |
probably benign |
Het |
Disc1 |
A |
G |
8: 125,155,041 |
R572G |
probably damaging |
Het |
Dsel |
C |
T |
1: 111,861,573 |
G411S |
probably damaging |
Het |
Dynlrb2 |
T |
C |
8: 116,514,957 |
V80A |
probably benign |
Het |
Eif3a |
A |
T |
19: 60,766,644 |
D1033E |
unknown |
Het |
Enam |
C |
A |
5: 88,501,488 |
H285Q |
possibly damaging |
Het |
Ep400 |
T |
C |
5: 110,719,614 |
D980G |
unknown |
Het |
Epha7 |
C |
T |
4: 28,871,937 |
S422L |
probably benign |
Het |
Erc2 |
A |
C |
14: 28,040,389 |
D703A |
probably damaging |
Het |
Ezh2 |
G |
T |
6: 47,533,758 |
S639* |
probably null |
Het |
Fbn1 |
G |
A |
2: 125,352,049 |
H1333Y |
probably damaging |
Het |
Flad1 |
A |
G |
3: 89,408,665 |
S197P |
possibly damaging |
Het |
Gfm2 |
G |
T |
13: 97,143,021 |
C26F |
probably benign |
Het |
Gm5294 |
A |
G |
5: 138,820,981 |
H82R |
probably damaging |
Het |
Gm597 |
A |
T |
1: 28,780,152 |
M16K |
probably benign |
Het |
Golga2 |
C |
T |
2: 32,303,001 |
Q444* |
probably null |
Het |
Gp5 |
A |
T |
16: 30,308,608 |
V416D |
probably damaging |
Het |
Gpat2 |
A |
G |
2: 127,426,981 |
|
probably null |
Het |
Gpr137c |
A |
G |
14: 45,279,014 |
D353G |
probably damaging |
Het |
Hoxa13 |
A |
C |
6: 52,259,882 |
W133G |
probably damaging |
Het |
Hydin |
A |
T |
8: 110,557,662 |
I3189F |
probably damaging |
Het |
Hydin |
A |
T |
8: 110,601,273 |
K4804M |
probably damaging |
Het |
Ice2 |
T |
C |
9: 69,400,512 |
F26S |
probably damaging |
Het |
Ints11 |
T |
C |
4: 155,872,230 |
|
probably null |
Het |
Ipo5 |
A |
G |
14: 120,920,085 |
I112V |
probably benign |
Het |
Itgax |
T |
A |
7: 128,135,309 |
S346R |
probably damaging |
Het |
Kcnj13 |
T |
A |
1: 87,389,017 |
M125L |
probably damaging |
Het |
Lmbrd1 |
T |
A |
1: 24,744,867 |
V359E |
possibly damaging |
Het |
Lrrc7 |
T |
G |
3: 158,198,161 |
K287N |
probably damaging |
Het |
Mau2 |
C |
T |
8: 70,029,234 |
A191T |
possibly damaging |
Het |
Mkx |
C |
A |
18: 7,000,747 |
R65L |
possibly damaging |
Het |
Mroh4 |
T |
A |
15: 74,610,371 |
K746* |
probably null |
Het |
Myh4 |
A |
G |
11: 67,242,848 |
T238A |
probably damaging |
Het |
Nlrp9c |
T |
A |
7: 26,371,397 |
N920Y |
possibly damaging |
Het |
Nr4a3 |
T |
G |
4: 48,051,290 |
S15A |
possibly damaging |
Het |
Ntn4 |
T |
C |
10: 93,644,804 |
L130P |
probably damaging |
Het |
Olfr1240 |
A |
G |
2: 89,440,198 |
V27A |
probably benign |
Het |
Olfr1312 |
A |
T |
2: 112,043,014 |
V6E |
possibly damaging |
Het |
Olfr682-ps1 |
T |
A |
7: 105,128,345 |
I21F |
probably benign |
Het |
Olfr695 |
A |
G |
7: 106,713,964 |
V239A |
probably benign |
Het |
Olfr930 |
A |
T |
9: 38,930,776 |
I202F |
probably damaging |
Het |
Otog |
T |
C |
7: 46,298,308 |
L110P |
probably damaging |
Het |
Platr25 |
G |
A |
13: 62,700,905 |
H48Y |
probably benign |
Het |
Plcxd2 |
T |
C |
16: 45,980,426 |
E145G |
probably damaging |
Het |
Pltp |
A |
T |
2: 164,854,322 |
N143K |
probably damaging |
Het |
Pnpt1 |
T |
C |
11: 29,161,334 |
Y735H |
probably damaging |
Het |
Prom1 |
A |
G |
5: 44,020,831 |
Y520H |
probably damaging |
Het |
Rag2 |
A |
G |
2: 101,630,773 |
Y476C |
probably damaging |
Het |
Rdh16f2 |
A |
G |
10: 127,877,024 |
Y297C |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 29,085,755 |
E1844G |
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,640,275 |
C3679R |
probably damaging |
Het |
Sirt1 |
A |
G |
10: 63,322,003 |
I544T |
probably benign |
Het |
Slc26a10 |
A |
T |
10: 127,176,847 |
I382N |
possibly damaging |
Het |
Sox2 |
C |
A |
3: 34,650,972 |
P186Q |
possibly damaging |
Het |
Tnpo3 |
A |
G |
6: 29,556,996 |
L752P |
probably damaging |
Het |
Top2b |
T |
A |
14: 16,416,649 |
N1136K |
probably benign |
Het |
Tpsg1 |
G |
T |
17: 25,373,210 |
G86V |
probably damaging |
Het |
Ttf2 |
C |
A |
3: 100,963,302 |
D152Y |
possibly damaging |
Het |
Txndc15 |
T |
C |
13: 55,714,788 |
L4P |
unknown |
Het |
Unc5a |
T |
C |
13: 54,996,573 |
V237A |
possibly damaging |
Het |
Urb1 |
CACTTAC |
CAC |
16: 90,772,573 |
|
probably benign |
Het |
Vav3 |
C |
A |
3: 109,628,099 |
P616T |
possibly damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,293,239 |
D251V |
probably benign |
Het |
Vmn2r15 |
A |
G |
5: 109,297,522 |
L12S |
probably benign |
Het |
Wfs1 |
A |
C |
5: 36,967,732 |
I605S |
probably benign |
Het |
Wif1 |
G |
A |
10: 121,083,909 |
R187Q |
possibly damaging |
Het |
Yipf1 |
A |
G |
4: 107,350,541 |
|
probably null |
Het |
Zdhhc20 |
G |
T |
14: 57,873,920 |
F74L |
possibly damaging |
Het |
Zfp507 |
T |
C |
7: 35,776,418 |
T303A |
unknown |
Het |
Zfp763 |
A |
T |
17: 33,033,378 |
|
probably benign |
Het |
|