Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl3 |
T |
A |
6: 34,834,606 (GRCm39) |
L930H |
possibly damaging |
Het |
Albfm1 |
T |
C |
5: 90,727,531 (GRCm39) |
L383S |
probably damaging |
Het |
Alcam |
C |
T |
16: 52,109,276 (GRCm39) |
|
probably null |
Het |
Ankrd31 |
A |
G |
13: 97,015,462 (GRCm39) |
H1577R |
probably benign |
Het |
Arfgef1 |
T |
C |
1: 10,302,694 (GRCm39) |
N9S |
probably benign |
Het |
Cpne9 |
T |
C |
6: 113,279,079 (GRCm39) |
V491A |
possibly damaging |
Het |
Cyb5d1 |
A |
T |
11: 69,285,865 (GRCm39) |
L57Q |
possibly damaging |
Het |
Cyp7a1 |
T |
A |
4: 6,272,763 (GRCm39) |
Q150L |
possibly damaging |
Het |
D430041D05Rik |
A |
C |
2: 103,979,363 (GRCm39) |
Y1336* |
probably null |
Het |
Dcaf7 |
T |
C |
11: 105,944,579 (GRCm39) |
V254A |
probably benign |
Het |
Dchs1 |
T |
C |
7: 105,408,445 (GRCm39) |
T1796A |
probably benign |
Het |
Defa27 |
T |
A |
8: 21,805,657 (GRCm39) |
D32E |
probably benign |
Het |
Eno2 |
T |
C |
6: 124,744,019 (GRCm39) |
E96G |
probably benign |
Het |
Fbxw19 |
T |
A |
9: 109,311,069 (GRCm39) |
Y380F |
probably damaging |
Het |
Fer1l4 |
A |
T |
2: 155,890,195 (GRCm39) |
N243K |
probably damaging |
Het |
Fndc7 |
G |
A |
3: 108,776,568 (GRCm39) |
A491V |
probably damaging |
Het |
Gm14305 |
A |
G |
2: 176,410,790 (GRCm39) |
Q15R |
probably benign |
Het |
Gpr155 |
T |
C |
2: 73,213,291 (GRCm39) |
|
probably benign |
Het |
Grm5 |
A |
G |
7: 87,624,513 (GRCm39) |
H360R |
probably damaging |
Het |
Ifi203 |
G |
A |
1: 173,754,688 (GRCm39) |
T681I |
unknown |
Het |
Klc2 |
A |
G |
19: 5,158,647 (GRCm39) |
S616P |
probably benign |
Het |
Lifr |
A |
G |
15: 7,214,258 (GRCm39) |
Y704C |
probably damaging |
Het |
Lingo4 |
A |
C |
3: 94,306,767 (GRCm39) |
D15A |
possibly damaging |
Het |
Mcm8 |
A |
G |
2: 132,669,963 (GRCm39) |
T374A |
not run |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Naa25 |
A |
G |
5: 121,576,791 (GRCm39) |
T847A |
possibly damaging |
Het |
Nrxn2 |
T |
A |
19: 6,531,825 (GRCm39) |
M763K |
possibly damaging |
Het |
Onecut2 |
T |
A |
18: 64,474,046 (GRCm39) |
M180K |
possibly damaging |
Het |
Or1p4-ps1 |
A |
C |
11: 74,208,357 (GRCm39) |
T169P |
unknown |
Het |
Or2r3 |
T |
A |
6: 42,448,870 (GRCm39) |
M81L |
probably benign |
Het |
Or5m11 |
A |
T |
2: 85,782,218 (GRCm39) |
E270D |
probably benign |
Het |
Or8c13 |
A |
T |
9: 38,092,002 (GRCm39) |
V39E |
probably damaging |
Het |
Otx1 |
G |
A |
11: 21,949,458 (GRCm39) |
Q7* |
probably null |
Het |
Pabpc4 |
T |
G |
4: 123,182,763 (GRCm39) |
D133E |
probably damaging |
Het |
Pcsk5 |
A |
T |
19: 17,542,144 (GRCm39) |
C816S |
probably damaging |
Het |
Pgm2 |
A |
G |
5: 64,265,522 (GRCm39) |
T408A |
possibly damaging |
Het |
Polr2m |
G |
C |
9: 71,390,757 (GRCm39) |
Y148* |
probably null |
Het |
Reln |
T |
C |
5: 22,176,933 (GRCm39) |
N1911S |
probably damaging |
Het |
Scaf4 |
T |
C |
16: 90,026,445 (GRCm39) |
D1124G |
unknown |
Het |
Scgb1b19 |
C |
T |
7: 32,986,784 (GRCm39) |
T18I |
probably damaging |
Het |
Septin12 |
T |
A |
16: 4,814,320 (GRCm39) |
I50F |
probably damaging |
Het |
Slc25a20 |
T |
A |
9: 108,539,491 (GRCm39) |
M22K |
probably benign |
Het |
Sltm |
C |
G |
9: 70,493,955 (GRCm39) |
P802R |
possibly damaging |
Het |
Smchd1 |
A |
G |
17: 71,705,684 (GRCm39) |
F972L |
probably benign |
Het |
Spem1 |
T |
C |
11: 69,712,409 (GRCm39) |
Y85C |
probably benign |
Het |
Strip1 |
C |
T |
3: 107,524,247 (GRCm39) |
V557I |
possibly damaging |
Het |
Tcirg1 |
G |
T |
19: 3,947,160 (GRCm39) |
Q634K |
probably damaging |
Het |
Tma7 |
T |
A |
9: 108,911,507 (GRCm39) |
|
probably benign |
Het |
Tmem204 |
A |
G |
17: 25,299,414 (GRCm39) |
L35P |
probably damaging |
Het |
Trpc6 |
A |
G |
9: 8,626,702 (GRCm39) |
T351A |
probably benign |
Het |
Tubb2a |
A |
G |
13: 34,259,227 (GRCm39) |
S188P |
probably damaging |
Het |
Ubr5 |
C |
A |
15: 38,029,751 (GRCm39) |
L485F |
|
Het |
Vmn1r71 |
A |
T |
7: 10,482,378 (GRCm39) |
S103R |
probably damaging |
Het |
Vmn2r40 |
C |
T |
7: 8,911,119 (GRCm39) |
D725N |
|
Het |
Zfp473 |
T |
C |
7: 44,383,128 (GRCm39) |
R402G |
possibly damaging |
Het |
Zfp82 |
A |
T |
7: 29,755,851 (GRCm39) |
S410R |
probably damaging |
Het |
|
Other mutations in Lrrc74a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01370:Lrrc74a
|
APN |
12 |
86,801,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01380:Lrrc74a
|
APN |
12 |
86,808,496 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01715:Lrrc74a
|
APN |
12 |
86,801,189 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01832:Lrrc74a
|
APN |
12 |
86,808,488 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01953:Lrrc74a
|
APN |
12 |
86,788,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Lrrc74a
|
APN |
12 |
86,795,822 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02637:Lrrc74a
|
APN |
12 |
86,788,521 (GRCm39) |
nonsense |
probably null |
|
IGL03397:Lrrc74a
|
APN |
12 |
86,805,312 (GRCm39) |
missense |
probably benign |
0.39 |
R0201:Lrrc74a
|
UTSW |
12 |
86,808,547 (GRCm39) |
splice site |
probably benign |
|
R0360:Lrrc74a
|
UTSW |
12 |
86,784,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R0403:Lrrc74a
|
UTSW |
12 |
86,787,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Lrrc74a
|
UTSW |
12 |
86,792,353 (GRCm39) |
nonsense |
probably null |
|
R1675:Lrrc74a
|
UTSW |
12 |
86,787,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Lrrc74a
|
UTSW |
12 |
86,795,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Lrrc74a
|
UTSW |
12 |
86,784,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Lrrc74a
|
UTSW |
12 |
86,784,472 (GRCm39) |
nonsense |
probably null |
|
R6023:Lrrc74a
|
UTSW |
12 |
86,805,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Lrrc74a
|
UTSW |
12 |
86,783,263 (GRCm39) |
missense |
probably benign |
0.01 |
R6226:Lrrc74a
|
UTSW |
12 |
86,795,231 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6247:Lrrc74a
|
UTSW |
12 |
86,805,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R7275:Lrrc74a
|
UTSW |
12 |
86,787,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R7857:Lrrc74a
|
UTSW |
12 |
86,788,485 (GRCm39) |
missense |
probably benign |
0.00 |
R8172:Lrrc74a
|
UTSW |
12 |
86,788,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R8715:Lrrc74a
|
UTSW |
12 |
86,805,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R8717:Lrrc74a
|
UTSW |
12 |
86,783,253 (GRCm39) |
missense |
probably damaging |
0.99 |
R9080:Lrrc74a
|
UTSW |
12 |
86,795,908 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9612:Lrrc74a
|
UTSW |
12 |
86,805,345 (GRCm39) |
missense |
possibly damaging |
0.84 |
X0024:Lrrc74a
|
UTSW |
12 |
86,795,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|