Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox4 |
C |
A |
1: 58,274,366 (GRCm39) |
S384Y |
probably damaging |
Het |
Arhgef15 |
T |
C |
11: 68,844,673 (GRCm39) |
E308G |
probably damaging |
Het |
Asb15 |
A |
G |
6: 24,559,281 (GRCm39) |
D142G |
probably benign |
Het |
Atg13 |
A |
G |
2: 91,509,711 (GRCm39) |
S394P |
probably damaging |
Het |
Atp10a |
G |
C |
7: 58,308,597 (GRCm39) |
W132S |
probably damaging |
Het |
Bltp1 |
G |
T |
3: 36,974,436 (GRCm39) |
|
probably null |
Het |
Bod1l |
T |
A |
5: 41,974,099 (GRCm39) |
N2405I |
probably benign |
Het |
Capsl |
C |
T |
15: 9,462,770 (GRCm39) |
R137C |
probably damaging |
Het |
Cd109 |
T |
A |
9: 78,617,441 (GRCm39) |
M1313K |
probably damaging |
Het |
Chst13 |
G |
A |
6: 90,286,566 (GRCm39) |
A132V |
possibly damaging |
Het |
Cobl |
T |
C |
11: 12,362,117 (GRCm39) |
|
probably benign |
Het |
Coq9 |
A |
T |
8: 95,577,214 (GRCm39) |
E193V |
probably benign |
Het |
Cpd |
T |
A |
11: 76,704,385 (GRCm39) |
I410F |
probably benign |
Het |
Cyth3 |
T |
G |
5: 143,693,229 (GRCm39) |
V351G |
probably damaging |
Het |
Dcp1a |
T |
C |
14: 30,201,775 (GRCm39) |
|
probably null |
Het |
Dennd3 |
A |
G |
15: 73,394,079 (GRCm39) |
I35V |
probably benign |
Het |
Dlgap4 |
C |
T |
2: 156,587,973 (GRCm39) |
R606W |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,343,817 (GRCm39) |
I1720M |
probably benign |
Het |
Erbin |
A |
G |
13: 103,995,907 (GRCm39) |
L265P |
probably damaging |
Het |
Ern1 |
T |
C |
11: 106,291,134 (GRCm39) |
D847G |
probably damaging |
Het |
Esyt3 |
T |
G |
9: 99,207,024 (GRCm39) |
S342R |
probably benign |
Het |
Exoc2 |
A |
T |
13: 31,060,752 (GRCm39) |
I584K |
probably benign |
Het |
Fam240a |
T |
C |
9: 110,744,090 (GRCm39) |
R50G |
probably damaging |
Het |
Glis3 |
A |
T |
19: 28,241,360 (GRCm39) |
M858K |
probably benign |
Het |
Gls2 |
C |
T |
10: 128,030,998 (GRCm39) |
R86C |
unknown |
Het |
Gm10972 |
C |
A |
3: 94,550,901 (GRCm39) |
Y25* |
probably null |
Het |
H2-T10 |
A |
T |
17: 36,428,622 (GRCm39) |
M350K |
probably benign |
Het |
Has1 |
A |
T |
17: 18,070,792 (GRCm39) |
V43D |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,878,275 (GRCm39) |
S4609R |
probably benign |
Het |
Hmgcs2 |
A |
C |
3: 98,198,582 (GRCm39) |
T162P |
probably damaging |
Het |
Hspg2 |
G |
T |
4: 137,239,177 (GRCm39) |
C368F |
probably damaging |
Het |
Ighv11-1 |
A |
G |
12: 113,945,722 (GRCm39) |
S44P |
probably damaging |
Het |
Inppl1 |
A |
G |
7: 101,473,545 (GRCm39) |
V1035A |
probably benign |
Het |
Kmt2a |
C |
T |
9: 44,730,295 (GRCm39) |
V3341I |
unknown |
Het |
Lrp1b |
T |
C |
2: 40,691,517 (GRCm39) |
N3434S |
|
Het |
Lrriq1 |
G |
C |
10: 103,051,815 (GRCm39) |
S312R |
probably damaging |
Het |
Map1a |
G |
A |
2: 121,132,517 (GRCm39) |
S1111N |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,392,922 (GRCm39) |
V1029A |
|
Het |
Nol11 |
T |
C |
11: 107,069,908 (GRCm39) |
H314R |
possibly damaging |
Het |
Nphs1 |
A |
T |
7: 30,162,733 (GRCm39) |
D404V |
probably damaging |
Het |
Odr4 |
A |
G |
1: 150,247,788 (GRCm39) |
V387A |
probably benign |
Het |
Or51r1 |
A |
T |
7: 102,220,971 (GRCm39) |
|
probably benign |
Het |
Pabpc2 |
T |
C |
18: 39,907,607 (GRCm39) |
Y291H |
possibly damaging |
Het |
Pcdh15 |
G |
A |
10: 74,322,088 (GRCm39) |
A1020T |
probably benign |
Het |
Pla2g4f |
A |
C |
2: 120,135,490 (GRCm39) |
S395A |
possibly damaging |
Het |
Ppp1r18 |
A |
G |
17: 36,178,176 (GRCm39) |
Q17R |
probably damaging |
Het |
Prokr2 |
A |
T |
2: 132,215,996 (GRCm39) |
V155D |
probably damaging |
Het |
Pwwp2a |
T |
G |
11: 43,596,696 (GRCm39) |
C620W |
probably damaging |
Het |
Rabepk |
T |
C |
2: 34,675,605 (GRCm39) |
D175G |
probably damaging |
Het |
Rad54l |
T |
C |
4: 115,956,866 (GRCm39) |
Y485C |
probably damaging |
Het |
Rasef |
A |
G |
4: 73,652,771 (GRCm39) |
S577P |
probably damaging |
Het |
Rgma |
C |
A |
7: 73,067,752 (GRCm39) |
L446I |
unknown |
Het |
Rnf212b |
T |
C |
14: 55,079,825 (GRCm39) |
S182P |
probably damaging |
Het |
Rnf6 |
C |
A |
5: 146,147,986 (GRCm39) |
R344I |
probably damaging |
Het |
Rnf6 |
T |
A |
5: 146,147,987 (GRCm39) |
R344* |
probably null |
Het |
Sgo1 |
A |
G |
17: 53,986,639 (GRCm39) |
I184T |
possibly damaging |
Het |
Sgpl1 |
A |
T |
10: 60,953,502 (GRCm39) |
I78N |
possibly damaging |
Het |
Snx13 |
T |
A |
12: 35,157,483 (GRCm39) |
Y510N |
probably damaging |
Het |
Sptbn2 |
G |
A |
19: 4,784,171 (GRCm39) |
E638K |
possibly damaging |
Het |
Sspo |
A |
G |
6: 48,428,316 (GRCm39) |
T349A |
probably damaging |
Het |
Sv2c |
C |
T |
13: 96,126,223 (GRCm39) |
S343N |
probably damaging |
Het |
Syne1 |
C |
A |
10: 5,283,560 (GRCm39) |
V1502F |
possibly damaging |
Het |
Syne1 |
T |
A |
10: 5,283,632 (GRCm39) |
I1478F |
possibly damaging |
Het |
Tmem121 |
C |
T |
12: 113,151,992 (GRCm39) |
A70V |
probably damaging |
Het |
Tmem215 |
A |
G |
4: 40,474,042 (GRCm39) |
I40V |
possibly damaging |
Het |
Trim25 |
A |
G |
11: 88,899,943 (GRCm39) |
|
probably null |
Het |
Trio |
A |
G |
15: 27,889,504 (GRCm39) |
V534A |
unknown |
Het |
Tyr |
T |
A |
7: 87,142,218 (GRCm39) |
E114V |
probably benign |
Het |
Ush2a |
A |
T |
1: 188,285,457 (GRCm39) |
T1998S |
probably benign |
Het |
Usp40 |
G |
T |
1: 87,909,900 (GRCm39) |
A518E |
probably benign |
Het |
Usp48 |
T |
A |
4: 137,331,956 (GRCm39) |
|
probably null |
Het |
Vash1 |
T |
A |
12: 86,733,767 (GRCm39) |
F152L |
probably damaging |
Het |
Vsig10l |
C |
A |
7: 43,113,141 (GRCm39) |
P31Q |
probably damaging |
Het |
Xab2 |
C |
T |
8: 3,669,018 (GRCm39) |
E43K |
probably benign |
Het |
Zfp423 |
G |
A |
8: 88,507,512 (GRCm39) |
S944F |
probably damaging |
Het |
Zp2 |
A |
T |
7: 119,736,392 (GRCm39) |
D350E |
probably benign |
Het |
Zscan4e |
T |
G |
7: 11,041,461 (GRCm39) |
Q165P |
probably damaging |
Het |
|
Other mutations in Dcdc2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02892:Dcdc2c
|
APN |
12 |
28,585,544 (GRCm39) |
missense |
probably benign |
0.03 |
R1214:Dcdc2c
|
UTSW |
12 |
28,580,429 (GRCm39) |
nonsense |
probably null |
|
R3040:Dcdc2c
|
UTSW |
12 |
28,602,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R4937:Dcdc2c
|
UTSW |
12 |
28,580,472 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5268:Dcdc2c
|
UTSW |
12 |
28,566,656 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5920:Dcdc2c
|
UTSW |
12 |
28,585,536 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5921:Dcdc2c
|
UTSW |
12 |
28,574,774 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6444:Dcdc2c
|
UTSW |
12 |
28,585,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6939:Dcdc2c
|
UTSW |
12 |
28,591,496 (GRCm39) |
missense |
probably benign |
0.09 |
R7044:Dcdc2c
|
UTSW |
12 |
28,520,493 (GRCm39) |
utr 3 prime |
probably benign |
|
R7235:Dcdc2c
|
UTSW |
12 |
28,520,718 (GRCm39) |
missense |
|
|
R7287:Dcdc2c
|
UTSW |
12 |
28,566,685 (GRCm39) |
missense |
probably benign |
|
R7896:Dcdc2c
|
UTSW |
12 |
28,520,619 (GRCm39) |
nonsense |
probably null |
|
R7964:Dcdc2c
|
UTSW |
12 |
28,520,318 (GRCm39) |
missense |
|
|
R8802:Dcdc2c
|
UTSW |
12 |
28,576,720 (GRCm39) |
missense |
probably benign |
|
R9111:Dcdc2c
|
UTSW |
12 |
28,585,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R9545:Dcdc2c
|
UTSW |
12 |
28,602,295 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9578:Dcdc2c
|
UTSW |
12 |
28,602,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Dcdc2c
|
UTSW |
12 |
28,585,553 (GRCm39) |
missense |
|
|
Z1176:Dcdc2c
|
UTSW |
12 |
28,574,706 (GRCm39) |
missense |
probably benign |
0.09 |
|