Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
T |
A |
4: 62,457,109 (GRCm39) |
L143M |
possibly damaging |
Het |
Actbl2 |
G |
A |
13: 111,391,694 (GRCm39) |
V10I |
probably benign |
Het |
Adamts12 |
C |
T |
15: 11,310,665 (GRCm39) |
T974I |
probably damaging |
Het |
Aifm2 |
G |
A |
10: 61,571,383 (GRCm39) |
V306M |
possibly damaging |
Het |
Arhgef38 |
T |
C |
3: 132,866,514 (GRCm39) |
K208E |
probably benign |
Het |
Atxn7l3 |
C |
A |
11: 102,182,807 (GRCm39) |
R278L |
possibly damaging |
Het |
Bcl9 |
A |
G |
3: 97,116,231 (GRCm39) |
L821P |
probably benign |
Het |
Cdh19 |
C |
T |
1: 110,847,320 (GRCm39) |
V430I |
probably benign |
Het |
Clns1a |
T |
A |
7: 97,363,111 (GRCm39) |
|
probably null |
Het |
Col3a1 |
T |
A |
1: 45,385,281 (GRCm39) |
C133S |
probably damaging |
Het |
Csmd1 |
G |
A |
8: 17,266,749 (GRCm39) |
T59I |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,736,071 (GRCm39) |
*493W |
probably null |
Het |
Cyp2j8 |
A |
T |
4: 96,395,438 (GRCm39) |
D62E |
probably benign |
Het |
Dcbld1 |
A |
T |
10: 52,196,075 (GRCm39) |
M428L |
probably benign |
Het |
Dhx32 |
A |
T |
7: 133,323,976 (GRCm39) |
Y523* |
probably null |
Het |
Dlgap2 |
C |
T |
8: 14,828,206 (GRCm39) |
A538V |
possibly damaging |
Het |
Dlgap3 |
T |
C |
4: 127,129,982 (GRCm39) |
S919P |
probably benign |
Het |
Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
Dsc1 |
A |
T |
18: 20,243,209 (GRCm39) |
H81Q |
probably benign |
Het |
Dusp8 |
A |
T |
7: 141,636,298 (GRCm39) |
S431T |
possibly damaging |
Het |
Dync1i1 |
A |
T |
6: 5,767,096 (GRCm39) |
T59S |
probably damaging |
Het |
Ecel1 |
A |
G |
1: 87,075,997 (GRCm39) |
S727P |
probably damaging |
Het |
Ednrb |
T |
A |
14: 104,059,204 (GRCm39) |
D274V |
probably benign |
Het |
Eef1d |
G |
T |
15: 75,775,062 (GRCm39) |
A199E |
probably benign |
Het |
Eml3 |
T |
A |
19: 8,911,718 (GRCm39) |
|
probably null |
Het |
Enah |
G |
T |
1: 181,749,318 (GRCm39) |
A138E |
probably damaging |
Het |
Fgf18 |
A |
C |
11: 33,068,003 (GRCm39) |
F129C |
probably damaging |
Het |
Gba1 |
A |
T |
3: 89,112,868 (GRCm39) |
E170V |
probably benign |
Het |
Hdac1 |
C |
T |
4: 129,416,157 (GRCm39) |
R212Q |
probably benign |
Het |
Heatr1 |
T |
A |
13: 12,447,527 (GRCm39) |
L1740Q |
probably null |
Het |
Inhbb |
T |
A |
1: 119,348,431 (GRCm39) |
H129L |
probably benign |
Het |
Inpp5b |
T |
A |
4: 124,691,662 (GRCm39) |
H862Q |
probably benign |
Het |
Itsn2 |
C |
A |
12: 4,757,025 (GRCm39) |
R1372S |
probably benign |
Het |
Klk1b21 |
A |
T |
7: 43,755,193 (GRCm39) |
T163S |
probably benign |
Het |
Lmo3 |
A |
T |
6: 138,393,492 (GRCm39) |
C43S |
probably damaging |
Het |
Metrn |
C |
T |
17: 26,014,197 (GRCm39) |
V210I |
probably benign |
Het |
Ndufaf7 |
A |
T |
17: 79,252,442 (GRCm39) |
I284F |
possibly damaging |
Het |
Nlrp6 |
T |
C |
7: 140,506,357 (GRCm39) |
V766A |
probably benign |
Het |
Or10a5 |
A |
G |
7: 106,635,938 (GRCm39) |
D192G |
probably damaging |
Het |
Osbpl7 |
T |
C |
11: 96,946,905 (GRCm39) |
S403P |
probably benign |
Het |
Pabpc4l |
T |
C |
3: 46,401,276 (GRCm39) |
T123A |
probably benign |
Het |
Pde6d |
A |
G |
1: 86,473,524 (GRCm39) |
F91L |
probably benign |
Het |
Psg20 |
T |
A |
7: 18,414,947 (GRCm39) |
Y316F |
probably benign |
Het |
Psmd1 |
T |
A |
1: 86,006,422 (GRCm39) |
S263T |
possibly damaging |
Het |
Pum1 |
C |
A |
4: 130,396,581 (GRCm39) |
T112K |
possibly damaging |
Het |
Rasgrp2 |
T |
A |
19: 6,454,425 (GRCm39) |
M156K |
probably benign |
Het |
Reln |
T |
A |
5: 22,223,998 (GRCm39) |
E917V |
probably damaging |
Het |
Rfc4 |
A |
T |
16: 22,943,314 (GRCm39) |
V61E |
probably damaging |
Het |
Rnf112 |
C |
T |
11: 61,341,854 (GRCm39) |
V317I |
possibly damaging |
Het |
Rpe |
T |
C |
1: 66,754,387 (GRCm39) |
M153T |
probably damaging |
Het |
Rtn4ip1 |
A |
G |
10: 43,811,993 (GRCm39) |
|
probably null |
Het |
Sap18 |
T |
A |
14: 58,036,011 (GRCm39) |
S66T |
probably damaging |
Het |
Scamp5 |
C |
A |
9: 57,354,508 (GRCm39) |
V49F |
possibly damaging |
Het |
Serhl |
A |
G |
15: 82,999,776 (GRCm39) |
Q252R |
probably benign |
Het |
Sestd1 |
T |
C |
2: 77,042,867 (GRCm39) |
D229G |
probably benign |
Het |
Slc35g1 |
T |
C |
19: 38,391,735 (GRCm39) |
V339A |
probably benign |
Het |
Slc9b2 |
T |
A |
3: 135,034,743 (GRCm39) |
|
probably null |
Het |
Stk40 |
C |
T |
4: 126,022,640 (GRCm39) |
T138I |
probably benign |
Het |
Syt10 |
C |
T |
15: 89,674,979 (GRCm39) |
D456N |
probably damaging |
Het |
Tep1 |
T |
G |
14: 51,076,443 (GRCm39) |
K1664Q |
probably benign |
Het |
Tmod2 |
T |
C |
9: 75,493,377 (GRCm39) |
K193E |
possibly damaging |
Het |
Trak1 |
T |
A |
9: 121,302,063 (GRCm39) |
*940R |
probably null |
Het |
Ttc5 |
A |
T |
14: 51,012,822 (GRCm39) |
Y189N |
probably damaging |
Het |
Ugt2a3 |
A |
T |
5: 87,484,430 (GRCm39) |
M198K |
probably damaging |
Het |
Uox |
A |
G |
3: 146,318,297 (GRCm39) |
H66R |
probably benign |
Het |
Usp9y |
A |
T |
Y: 1,303,451 (GRCm39) |
D2487E |
probably benign |
Het |
Vnn3 |
G |
A |
10: 23,740,311 (GRCm39) |
G205R |
probably damaging |
Het |
Vps11 |
T |
C |
9: 44,260,294 (GRCm39) |
D856G |
probably benign |
Het |
Zdhhc17 |
T |
C |
10: 110,817,909 (GRCm39) |
N90D |
possibly damaging |
Het |
Zfp105 |
T |
A |
9: 122,758,743 (GRCm39) |
L138* |
probably null |
Het |
Zfp28 |
A |
G |
7: 6,397,875 (GRCm39) |
Y770C |
probably benign |
Het |
Zfp655 |
T |
A |
5: 145,181,594 (GRCm39) |
L484Q |
probably damaging |
Het |
Zfp868 |
C |
A |
8: 70,064,646 (GRCm39) |
E230* |
probably null |
Het |
Zfpm2 |
A |
G |
15: 40,966,419 (GRCm39) |
Y836C |
probably damaging |
Het |
|
Other mutations in Jaml |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Jaml
|
APN |
9 |
45,012,287 (GRCm39) |
unclassified |
probably benign |
|
IGL00771:Jaml
|
APN |
9 |
45,005,105 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01139:Jaml
|
APN |
9 |
45,012,317 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02669:Jaml
|
APN |
9 |
45,015,489 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03405:Jaml
|
APN |
9 |
45,005,107 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0207:Jaml
|
UTSW |
9 |
45,005,065 (GRCm39) |
missense |
probably benign |
0.01 |
R1962:Jaml
|
UTSW |
9 |
45,015,495 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2120:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R2358:Jaml
|
UTSW |
9 |
45,012,361 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3917:Jaml
|
UTSW |
9 |
45,012,449 (GRCm39) |
unclassified |
probably benign |
|
R4801:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4802:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5224:Jaml
|
UTSW |
9 |
45,015,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R5739:Jaml
|
UTSW |
9 |
45,000,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5760:Jaml
|
UTSW |
9 |
45,009,052 (GRCm39) |
missense |
probably benign |
0.02 |
R6033:Jaml
|
UTSW |
9 |
45,000,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Jaml
|
UTSW |
9 |
45,000,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Jaml
|
UTSW |
9 |
45,000,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6245:Jaml
|
UTSW |
9 |
45,009,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R6753:Jaml
|
UTSW |
9 |
45,018,677 (GRCm39) |
missense |
probably benign |
0.43 |
R6797:Jaml
|
UTSW |
9 |
45,000,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8184:Jaml
|
UTSW |
9 |
45,000,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Jaml
|
UTSW |
9 |
45,000,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|