Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actbl2 |
T |
A |
13: 111,392,238 (GRCm39) |
M191K |
probably benign |
Het |
Actn1 |
T |
C |
12: 80,230,342 (GRCm39) |
N304S |
probably benign |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adamtsl2 |
T |
A |
2: 26,985,410 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,572,377 (GRCm39) |
E4928G |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,673,713 (GRCm39) |
C3103S |
probably benign |
Het |
Appl2 |
T |
A |
10: 83,438,696 (GRCm39) |
I578F |
probably benign |
Het |
Atp10b |
T |
C |
11: 43,121,282 (GRCm39) |
S982P |
probably benign |
Het |
Brd10 |
G |
T |
19: 29,732,250 (GRCm39) |
P254Q |
probably damaging |
Het |
Capn7 |
T |
C |
14: 31,090,160 (GRCm39) |
|
probably null |
Het |
Cd200r3 |
A |
G |
16: 44,778,093 (GRCm39) |
T166A |
possibly damaging |
Het |
Dctn6 |
C |
T |
8: 34,572,135 (GRCm39) |
|
probably null |
Het |
Duxf4 |
G |
A |
10: 58,071,717 (GRCm39) |
H166Y |
possibly damaging |
Het |
Fam114a1 |
T |
A |
5: 65,185,776 (GRCm39) |
F366I |
probably damaging |
Het |
Fam98b |
A |
T |
2: 117,089,737 (GRCm39) |
S85C |
probably damaging |
Het |
Fat3 |
T |
A |
9: 15,830,463 (GRCm39) |
N4344Y |
probably damaging |
Het |
Fhl3 |
T |
G |
4: 124,599,796 (GRCm39) |
C92W |
probably damaging |
Het |
Flrt1 |
T |
C |
19: 7,073,105 (GRCm39) |
T481A |
probably damaging |
Het |
Gng2 |
G |
T |
14: 19,941,426 (GRCm39) |
N5K |
probably benign |
Het |
Iqcm |
A |
T |
8: 76,441,417 (GRCm39) |
D230V |
probably benign |
Het |
Limk2 |
T |
C |
11: 3,302,332 (GRCm39) |
I176V |
probably benign |
Het |
Lrrk2 |
T |
A |
15: 91,698,847 (GRCm39) |
|
probably null |
Het |
Maml1 |
T |
C |
11: 50,157,180 (GRCm39) |
T332A |
probably benign |
Het |
Mbd1 |
T |
C |
18: 74,402,581 (GRCm39) |
F28L |
probably benign |
Het |
Morf4l1 |
G |
A |
9: 89,977,183 (GRCm39) |
T246I |
probably benign |
Het |
Mtres1 |
T |
C |
10: 43,408,861 (GRCm39) |
K94R |
probably benign |
Het |
Naa12 |
C |
T |
18: 80,255,138 (GRCm39) |
A144V |
probably damaging |
Het |
Ndufaf1 |
T |
G |
2: 119,490,958 (GRCm39) |
D34A |
probably benign |
Het |
Or4a77 |
T |
A |
2: 89,487,414 (GRCm39) |
I124F |
probably damaging |
Het |
Or4c114 |
C |
T |
2: 88,905,208 (GRCm39) |
V76I |
probably benign |
Het |
Patl1 |
C |
T |
19: 11,913,082 (GRCm39) |
R542C |
possibly damaging |
Het |
Pcdha2 |
T |
C |
18: 37,072,474 (GRCm39) |
V35A |
probably damaging |
Het |
Phf11b |
G |
A |
14: 59,568,713 (GRCm39) |
P67S |
probably benign |
Het |
Plxnd1 |
T |
C |
6: 115,934,609 (GRCm39) |
I1775V |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,771,386 (GRCm39) |
T2552S |
probably damaging |
Het |
Scai |
A |
T |
2: 38,973,585 (GRCm39) |
L52H |
probably damaging |
Het |
Scai |
G |
C |
2: 38,973,586 (GRCm39) |
L52V |
probably damaging |
Het |
Stag1 |
A |
T |
9: 100,838,506 (GRCm39) |
|
probably null |
Het |
Tgs1 |
A |
G |
4: 3,586,170 (GRCm39) |
K349R |
probably benign |
Het |
Tpbgl |
T |
C |
7: 99,274,961 (GRCm39) |
I299V |
probably benign |
Het |
Ttc3 |
A |
G |
16: 94,258,241 (GRCm39) |
T1325A |
probably benign |
Het |
Ubxn11 |
A |
T |
4: 133,852,396 (GRCm39) |
E210D |
probably damaging |
Het |
Unc13c |
T |
C |
9: 73,453,271 (GRCm39) |
I1840V |
probably benign |
Het |
Zfp74 |
A |
T |
7: 29,635,316 (GRCm39) |
F131I |
probably benign |
Het |
|
Other mutations in Matcap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01152:Matcap2
|
APN |
9 |
22,346,460 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01574:Matcap2
|
APN |
9 |
22,355,426 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01666:Matcap2
|
APN |
9 |
22,342,994 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02111:Matcap2
|
APN |
9 |
22,335,475 (GRCm39) |
missense |
probably benign |
|
IGL02310:Matcap2
|
APN |
9 |
22,335,724 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02638:Matcap2
|
APN |
9 |
22,341,775 (GRCm39) |
nonsense |
probably null |
|
LCD18:Matcap2
|
UTSW |
9 |
22,442,083 (GRCm38) |
intron |
probably benign |
|
R1239:Matcap2
|
UTSW |
9 |
22,335,995 (GRCm39) |
intron |
probably benign |
|
R1519:Matcap2
|
UTSW |
9 |
22,341,671 (GRCm39) |
missense |
probably benign |
0.01 |
R2248:Matcap2
|
UTSW |
9 |
22,355,410 (GRCm39) |
missense |
probably benign |
0.36 |
R2438:Matcap2
|
UTSW |
9 |
22,342,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R4838:Matcap2
|
UTSW |
9 |
22,335,673 (GRCm39) |
missense |
probably damaging |
0.98 |
R5304:Matcap2
|
UTSW |
9 |
22,335,528 (GRCm39) |
missense |
probably benign |
0.28 |
R5418:Matcap2
|
UTSW |
9 |
22,343,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Matcap2
|
UTSW |
9 |
22,335,786 (GRCm39) |
missense |
probably benign |
0.00 |
R6008:Matcap2
|
UTSW |
9 |
22,335,422 (GRCm39) |
nonsense |
probably null |
|
R8334:Matcap2
|
UTSW |
9 |
22,355,414 (GRCm39) |
missense |
probably benign |
0.26 |
R9474:Matcap2
|
UTSW |
9 |
22,343,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R9640:Matcap2
|
UTSW |
9 |
22,351,228 (GRCm39) |
missense |
possibly damaging |
0.62 |
|