Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
T |
6: 83,138,893 (GRCm39) |
M273L |
probably benign |
Het |
Abi3bp |
A |
T |
16: 56,452,241 (GRCm39) |
K912N |
unknown |
Het |
Arfgap2 |
T |
C |
2: 91,096,028 (GRCm39) |
F62L |
probably benign |
Het |
Arhgap45 |
A |
G |
10: 79,853,909 (GRCm39) |
E141G |
probably damaging |
Het |
Atraid |
G |
A |
5: 31,211,642 (GRCm39) |
|
probably null |
Het |
Cd101 |
G |
A |
3: 100,927,898 (GRCm39) |
A65V |
probably damaging |
Het |
Cd177 |
A |
G |
7: 24,459,067 (GRCm39) |
V114A |
probably benign |
Het |
Cdh6 |
T |
C |
15: 13,044,757 (GRCm39) |
N455S |
probably damaging |
Het |
Cdk14 |
A |
T |
5: 5,277,195 (GRCm39) |
S145T |
possibly damaging |
Het |
Cfap58 |
A |
G |
19: 48,017,543 (GRCm39) |
Y801C |
probably benign |
Het |
Clec2d |
C |
T |
6: 129,161,847 (GRCm39) |
T160M |
probably benign |
Het |
Cryz |
A |
G |
3: 154,327,382 (GRCm39) |
I269V |
probably benign |
Het |
Ctdp1 |
A |
T |
18: 80,499,223 (GRCm39) |
Y240N |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,909,212 (GRCm39) |
Y1275C |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,908,201 (GRCm39) |
I2385T |
probably benign |
Het |
Dpp8 |
A |
G |
9: 64,985,362 (GRCm39) |
M807V |
probably benign |
Het |
Entpd3 |
T |
A |
9: 120,384,720 (GRCm39) |
I99N |
probably damaging |
Het |
Fbxw11 |
A |
G |
11: 32,670,646 (GRCm39) |
E204G |
possibly damaging |
Het |
Fscn1 |
T |
C |
5: 142,946,616 (GRCm39) |
M138T |
probably damaging |
Het |
Gm5114 |
T |
A |
7: 39,057,552 (GRCm39) |
Q689L |
probably benign |
Het |
Iqgap2 |
T |
C |
13: 95,861,076 (GRCm39) |
N350S |
probably benign |
Het |
Kcnj10 |
T |
A |
1: 172,196,809 (GRCm39) |
C108S |
probably damaging |
Het |
Krtap10-4 |
G |
A |
10: 77,662,840 (GRCm39) |
R13C |
unknown |
Het |
Lmo7 |
T |
C |
14: 102,163,736 (GRCm39) |
I1527T |
unknown |
Het |
Lrrc17 |
A |
G |
5: 21,775,329 (GRCm39) |
K297R |
probably benign |
Het |
Ltb4r1 |
G |
A |
14: 56,005,579 (GRCm39) |
R294H |
probably damaging |
Het |
Macc1 |
A |
G |
12: 119,410,324 (GRCm39) |
D364G |
probably damaging |
Het |
Mavs |
A |
C |
2: 131,087,395 (GRCm39) |
T298P |
probably damaging |
Het |
Myh8 |
G |
T |
11: 67,180,647 (GRCm39) |
A628S |
probably benign |
Het |
Neurl4 |
A |
T |
11: 69,799,056 (GRCm39) |
|
probably null |
Het |
Nicn1 |
C |
A |
9: 108,172,304 (GRCm39) |
T213K |
probably damaging |
Het |
Nptx1 |
G |
A |
11: 119,433,492 (GRCm39) |
T369I |
probably damaging |
Het |
Nt5c1a |
T |
C |
4: 123,102,235 (GRCm39) |
S54P |
probably damaging |
Het |
Nup210l |
G |
A |
3: 90,022,428 (GRCm39) |
R132Q |
probably damaging |
Het |
Or2b11 |
A |
T |
11: 59,461,870 (GRCm39) |
I232N |
probably damaging |
Het |
Or4k41 |
A |
G |
2: 111,279,505 (GRCm39) |
T7A |
probably benign |
Het |
Or4p18 |
A |
T |
2: 88,233,040 (GRCm39) |
F79L |
probably benign |
Het |
Or7g22 |
G |
A |
9: 19,048,988 (GRCm39) |
G233E |
probably damaging |
Het |
Pip5k1b |
A |
T |
19: 24,337,355 (GRCm39) |
I311N |
probably damaging |
Het |
Pkdrej |
C |
T |
15: 85,699,655 (GRCm39) |
V2094I |
probably benign |
Het |
Pla2g2f |
A |
G |
4: 138,479,621 (GRCm39) |
Y179H |
probably damaging |
Het |
Plekha3 |
A |
T |
2: 76,516,992 (GRCm39) |
T115S |
probably damaging |
Het |
Ppp4c |
A |
G |
7: 126,386,496 (GRCm39) |
L167P |
probably damaging |
Het |
Pramel28 |
T |
A |
4: 143,691,611 (GRCm39) |
S371C |
probably benign |
Het |
Rarg |
A |
G |
15: 102,148,393 (GRCm39) |
I238T |
probably damaging |
Het |
Scn7a |
A |
T |
2: 66,531,203 (GRCm39) |
I558N |
probably damaging |
Het |
Sema3a |
C |
A |
5: 13,649,215 (GRCm39) |
H655N |
probably damaging |
Het |
Serpinb6c |
T |
C |
13: 34,064,201 (GRCm39) |
M285V |
probably benign |
Het |
Setx |
T |
A |
2: 29,035,046 (GRCm39) |
S510R |
possibly damaging |
Het |
Sgcz |
A |
G |
8: 37,990,457 (GRCm39) |
S299P |
probably damaging |
Het |
Slc12a2 |
T |
A |
18: 58,032,403 (GRCm39) |
F368I |
probably benign |
Het |
Slc7a9 |
C |
A |
7: 35,153,542 (GRCm39) |
T181K |
probably damaging |
Het |
Slco2b1 |
G |
A |
7: 99,334,760 (GRCm39) |
T237M |
probably benign |
Het |
Spg11 |
A |
G |
2: 121,900,348 (GRCm39) |
|
probably null |
Het |
Tbc1d22b |
G |
T |
17: 29,791,945 (GRCm39) |
G225V |
probably damaging |
Het |
Tbcd |
A |
G |
11: 121,487,969 (GRCm39) |
|
probably null |
Het |
Unc93a |
T |
C |
17: 13,328,560 (GRCm39) |
Y431C |
probably benign |
Het |
Vmn1r65 |
C |
T |
7: 6,011,464 (GRCm39) |
V257I |
possibly damaging |
Het |
Vmn2r124 |
A |
T |
17: 18,282,433 (GRCm39) |
T154S |
probably benign |
Het |
Wnk2 |
A |
T |
13: 49,214,415 (GRCm39) |
L1487* |
probably null |
Het |
Zfp853 |
G |
A |
5: 143,274,018 (GRCm39) |
A549V |
probably damaging |
Het |
Zfp936 |
C |
T |
7: 42,839,547 (GRCm39) |
T338I |
possibly damaging |
Het |
|
Other mutations in Ces1h |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Ces1h
|
APN |
8 |
94,084,091 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00227:Ces1h
|
APN |
8 |
94,079,098 (GRCm39) |
missense |
unknown |
|
IGL02343:Ces1h
|
APN |
8 |
94,078,654 (GRCm39) |
makesense |
probably null |
|
IGL02490:Ces1h
|
APN |
8 |
94,083,627 (GRCm39) |
critical splice donor site |
probably null |
|
H8786:Ces1h
|
UTSW |
8 |
94,089,550 (GRCm39) |
missense |
probably damaging |
0.99 |
P0012:Ces1h
|
UTSW |
8 |
94,080,138 (GRCm39) |
missense |
unknown |
|
R0395:Ces1h
|
UTSW |
8 |
94,083,706 (GRCm39) |
missense |
unknown |
|
R0538:Ces1h
|
UTSW |
8 |
94,083,628 (GRCm39) |
critical splice donor site |
probably null |
|
R0562:Ces1h
|
UTSW |
8 |
94,083,771 (GRCm39) |
missense |
unknown |
|
R0569:Ces1h
|
UTSW |
8 |
94,078,774 (GRCm39) |
missense |
unknown |
|
R1854:Ces1h
|
UTSW |
8 |
94,085,450 (GRCm39) |
missense |
probably benign |
0.13 |
R5945:Ces1h
|
UTSW |
8 |
94,090,254 (GRCm39) |
missense |
probably benign |
0.04 |
R5950:Ces1h
|
UTSW |
8 |
94,089,587 (GRCm39) |
missense |
probably benign |
|
R6015:Ces1h
|
UTSW |
8 |
94,083,691 (GRCm39) |
missense |
unknown |
|
R6275:Ces1h
|
UTSW |
8 |
94,099,274 (GRCm39) |
missense |
probably benign |
0.23 |
R6317:Ces1h
|
UTSW |
8 |
94,084,046 (GRCm39) |
missense |
unknown |
|
R6647:Ces1h
|
UTSW |
8 |
94,078,654 (GRCm39) |
makesense |
probably null |
|
R6981:Ces1h
|
UTSW |
8 |
94,080,123 (GRCm39) |
missense |
unknown |
|
R7800:Ces1h
|
UTSW |
8 |
94,106,322 (GRCm39) |
missense |
|
|
R7861:Ces1h
|
UTSW |
8 |
94,084,053 (GRCm39) |
missense |
unknown |
|
R8897:Ces1h
|
UTSW |
8 |
94,080,093 (GRCm39) |
missense |
unknown |
|
R9355:Ces1h
|
UTSW |
8 |
94,101,149 (GRCm39) |
missense |
|
|
X0027:Ces1h
|
UTSW |
8 |
94,089,506 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Ces1h
|
UTSW |
8 |
94,078,662 (GRCm39) |
missense |
unknown |
|
Z1177:Ces1h
|
UTSW |
8 |
94,093,468 (GRCm39) |
critical splice acceptor site |
probably null |
|
|