Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr1b |
A |
T |
1: 36,740,588 (GRCm39) |
C222S |
probably benign |
Het |
Actrt3 |
T |
G |
3: 30,651,992 (GRCm39) |
R367S |
probably damaging |
Het |
Alg1 |
T |
C |
16: 5,060,416 (GRCm39) |
V379A |
probably damaging |
Het |
Ankrd36 |
A |
G |
11: 5,593,763 (GRCm39) |
E456G |
probably benign |
Het |
Arhgef33 |
G |
T |
17: 80,681,148 (GRCm39) |
A763S |
possibly damaging |
Het |
Armc5 |
T |
G |
7: 127,841,783 (GRCm39) |
V597G |
probably benign |
Het |
Asb10 |
G |
T |
5: 24,738,690 (GRCm39) |
R456S |
probably damaging |
Het |
Asph |
A |
G |
4: 9,453,417 (GRCm39) |
F702L |
probably damaging |
Het |
Atf7 |
T |
A |
15: 102,449,324 (GRCm39) |
T326S |
probably benign |
Het |
Atxn7l2 |
T |
C |
3: 108,114,250 (GRCm39) |
N171D |
probably benign |
Het |
BC049715 |
T |
A |
6: 136,816,979 (GRCm39) |
M73K |
possibly damaging |
Het |
C2cd6 |
A |
G |
1: 59,105,312 (GRCm39) |
V322A |
probably benign |
Het |
Cadps2 |
A |
C |
6: 23,382,938 (GRCm39) |
C807W |
probably damaging |
Het |
Ccdc57 |
C |
T |
11: 120,788,788 (GRCm39) |
R353H |
probably benign |
Het |
Ccdc89 |
T |
C |
7: 90,075,793 (GRCm39) |
M1T |
probably null |
Het |
Cntn1 |
G |
A |
15: 92,132,347 (GRCm39) |
V148M |
probably damaging |
Het |
Csmd3 |
T |
A |
15: 47,561,572 (GRCm39) |
I1335F |
|
Het |
Dap3 |
A |
G |
3: 88,834,334 (GRCm39) |
M294T |
probably damaging |
Het |
Dbh |
A |
G |
2: 27,060,328 (GRCm39) |
D168G |
probably benign |
Het |
Dchs2 |
C |
A |
3: 83,253,592 (GRCm39) |
A2334E |
probably benign |
Het |
Dcun1d4 |
T |
A |
5: 73,678,310 (GRCm39) |
Y102N |
probably benign |
Het |
Dhtkd1 |
T |
C |
2: 5,903,533 (GRCm39) |
T918A |
probably benign |
Het |
Dmgdh |
C |
T |
13: 93,825,118 (GRCm39) |
T147I |
possibly damaging |
Het |
Dmxl2 |
T |
G |
9: 54,301,105 (GRCm39) |
K2335N |
possibly damaging |
Het |
Efna5 |
T |
C |
17: 63,188,125 (GRCm39) |
M1V |
probably null |
Het |
Fpr-rs3 |
T |
C |
17: 20,844,944 (GRCm39) |
N66D |
probably damaging |
Het |
Gas2l2 |
C |
A |
11: 83,313,999 (GRCm39) |
A438S |
probably benign |
Het |
Hivep3 |
T |
C |
4: 119,989,521 (GRCm39) |
S1991P |
probably damaging |
Het |
Hsp90b1 |
A |
T |
10: 86,541,169 (GRCm39) |
|
probably null |
Het |
Iars1 |
T |
A |
13: 49,878,102 (GRCm39) |
N875K |
probably damaging |
Het |
Jag1 |
A |
C |
2: 136,943,521 (GRCm39) |
M225R |
possibly damaging |
Het |
Jag1 |
T |
C |
2: 136,932,708 (GRCm39) |
|
probably benign |
Het |
Kcnn2 |
C |
T |
18: 45,692,502 (GRCm39) |
S26L |
possibly damaging |
Het |
Kctd2 |
T |
C |
11: 115,311,279 (GRCm39) |
S96P |
probably damaging |
Het |
Klhl25 |
A |
G |
7: 75,516,359 (GRCm39) |
N422D |
probably damaging |
Het |
Lhx8 |
A |
T |
3: 154,027,886 (GRCm39) |
V222E |
possibly damaging |
Het |
Lrig1 |
A |
T |
6: 94,631,840 (GRCm39) |
V120D |
possibly damaging |
Het |
Manba |
T |
A |
3: 135,256,995 (GRCm39) |
S553T |
probably damaging |
Het |
Mllt10 |
T |
A |
2: 18,167,583 (GRCm39) |
S503T |
probably damaging |
Het |
Nxpe4 |
A |
G |
9: 48,304,050 (GRCm39) |
N46D |
probably benign |
Het |
Or1l4b |
C |
T |
2: 37,037,016 (GRCm39) |
S264L |
probably benign |
Het |
Or8b50 |
A |
C |
9: 38,518,441 (GRCm39) |
K227Q |
probably benign |
Het |
Pdzd2 |
C |
T |
15: 12,437,252 (GRCm39) |
E450K |
probably damaging |
Het |
Phrf1 |
T |
A |
7: 140,838,651 (GRCm39) |
F615L |
unknown |
Het |
Plch2 |
C |
A |
4: 155,083,324 (GRCm39) |
G538V |
probably damaging |
Het |
Ppp2r2d |
T |
A |
7: 138,475,897 (GRCm39) |
I235N |
probably damaging |
Het |
Prdm15 |
A |
T |
16: 97,638,888 (GRCm39) |
D57E |
probably benign |
Het |
Psd3 |
T |
C |
8: 68,417,003 (GRCm39) |
D45G |
probably damaging |
Het |
Ptger4 |
T |
A |
15: 5,272,138 (GRCm39) |
R185S |
probably benign |
Het |
Ptp4a2 |
T |
A |
4: 129,740,299 (GRCm39) |
M121K |
probably damaging |
Het |
Ptpre |
T |
G |
7: 135,283,306 (GRCm39) |
F659V |
possibly damaging |
Het |
Rad54l2 |
T |
G |
9: 106,596,809 (GRCm39) |
D199A |
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,647,521 (GRCm39) |
M556V |
probably benign |
Het |
Scaf8 |
T |
C |
17: 3,243,349 (GRCm39) |
V711A |
probably benign |
Het |
Sesn3 |
G |
A |
9: 14,225,964 (GRCm39) |
C233Y |
probably damaging |
Het |
Slc45a1 |
T |
A |
4: 150,714,206 (GRCm39) |
I680F |
probably damaging |
Het |
Slco1a6 |
C |
T |
6: 142,078,897 (GRCm39) |
V133M |
probably benign |
Het |
Syt6 |
T |
C |
3: 103,492,850 (GRCm39) |
L119P |
probably benign |
Het |
Szt2 |
A |
C |
4: 118,226,613 (GRCm39) |
S2974R |
unknown |
Het |
Taok1 |
A |
T |
11: 77,444,712 (GRCm39) |
H454Q |
probably damaging |
Het |
Tbx10 |
G |
A |
19: 4,047,303 (GRCm39) |
V136M |
probably damaging |
Het |
Tespa1 |
A |
G |
10: 130,198,027 (GRCm39) |
T350A |
probably benign |
Het |
Tnks1bp1 |
T |
A |
2: 84,900,980 (GRCm39) |
Y1562* |
probably null |
Het |
Trank1 |
T |
A |
9: 111,218,344 (GRCm39) |
F1908Y |
probably benign |
Het |
Tspoap1 |
T |
C |
11: 87,669,197 (GRCm39) |
I1490T |
probably benign |
Het |
Ttc21a |
T |
C |
9: 119,770,286 (GRCm39) |
F119S |
probably damaging |
Het |
Ttll3 |
T |
G |
6: 113,385,949 (GRCm39) |
M594R |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,798,790 (GRCm39) |
R495* |
probably null |
Het |
Twf1 |
A |
C |
15: 94,479,110 (GRCm39) |
L250V |
probably damaging |
Het |
Ubr4 |
A |
T |
4: 139,149,076 (GRCm39) |
E458D |
|
Het |
Unc50 |
T |
C |
1: 37,476,244 (GRCm39) |
F135L |
probably benign |
Het |
Vwa3a |
T |
A |
7: 120,375,299 (GRCm39) |
I371N |
probably damaging |
Het |
Zfp180 |
T |
C |
7: 23,805,161 (GRCm39) |
S527P |
probably damaging |
Het |
Zfp512 |
T |
A |
5: 31,630,882 (GRCm39) |
I408N |
probably damaging |
Het |
Zfp57 |
A |
G |
17: 37,317,077 (GRCm39) |
T52A |
probably benign |
Het |
Zranb2 |
A |
G |
3: 157,247,327 (GRCm39) |
|
probably benign |
Het |
|