Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030468B19Rik |
A |
G |
11: 117,693,739 (GRCm39) |
K69E |
probably damaging |
Het |
Abcb5 |
C |
T |
12: 118,865,087 (GRCm39) |
|
probably null |
Het |
Acot1 |
G |
T |
12: 84,061,194 (GRCm39) |
G167* |
probably null |
Het |
Agbl1 |
C |
T |
7: 76,069,715 (GRCm39) |
H164Y |
probably damaging |
Het |
Atp4b |
T |
C |
8: 13,443,549 (GRCm39) |
Y43C |
probably damaging |
Het |
Bsn |
T |
C |
9: 107,984,055 (GRCm39) |
D3333G |
unknown |
Het |
Ccdc27 |
A |
C |
4: 154,120,742 (GRCm39) |
D351E |
unknown |
Het |
Cd200r4 |
T |
C |
16: 44,641,313 (GRCm39) |
F19L |
probably benign |
Het |
Dbndd1 |
T |
A |
8: 124,236,731 (GRCm39) |
I75F |
probably damaging |
Het |
Dennd5b |
T |
C |
6: 148,946,334 (GRCm39) |
K426E |
probably benign |
Het |
Drg2 |
A |
G |
11: 60,350,334 (GRCm39) |
T98A |
possibly damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,245 (GRCm39) |
|
probably null |
Het |
Fmo1 |
T |
C |
1: 162,678,916 (GRCm39) |
|
probably benign |
Het |
Foxn2 |
A |
T |
17: 88,791,837 (GRCm39) |
I236F |
probably damaging |
Het |
Glmp |
G |
A |
3: 88,233,718 (GRCm39) |
V107I |
probably damaging |
Het |
Gpr15 |
A |
G |
16: 58,538,723 (GRCm39) |
F122S |
probably damaging |
Het |
Gvin-ps3 |
T |
C |
7: 105,682,780 (GRCm39) |
I158M |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,462,716 (GRCm39) |
D5140E |
probably benign |
Het |
Hspa1a |
C |
T |
17: 35,190,703 (GRCm39) |
V67M |
probably damaging |
Het |
Igfbp4 |
A |
G |
11: 98,939,061 (GRCm39) |
E27G |
probably damaging |
Het |
Il7 |
A |
G |
3: 7,642,226 (GRCm39) |
|
probably benign |
Het |
Kat6a |
G |
T |
8: 23,352,380 (GRCm39) |
V55F |
probably damaging |
Het |
Kynu |
A |
G |
2: 43,571,451 (GRCm39) |
T456A |
probably benign |
Het |
Lcorl |
A |
G |
5: 45,932,729 (GRCm39) |
|
probably benign |
Het |
Lrp5 |
G |
A |
19: 3,655,290 (GRCm39) |
R1077* |
probably null |
Het |
Mab21l2 |
T |
C |
3: 86,454,211 (GRCm39) |
E263G |
possibly damaging |
Het |
Macf1 |
T |
A |
4: 123,338,744 (GRCm39) |
D1436V |
probably benign |
Het |
Map4k2 |
C |
A |
19: 6,394,081 (GRCm39) |
T252N |
probably benign |
Het |
Muc5ac |
C |
A |
7: 141,368,460 (GRCm39) |
T3063K |
possibly damaging |
Het |
Myo18a |
T |
A |
11: 77,668,292 (GRCm39) |
S51T |
possibly damaging |
Het |
Ncoa3 |
G |
T |
2: 165,896,718 (GRCm39) |
G503V |
possibly damaging |
Het |
Ncor1 |
A |
T |
11: 62,264,183 (GRCm39) |
H406Q |
probably benign |
Het |
Nectin2 |
T |
C |
7: 19,458,510 (GRCm39) |
K434E |
possibly damaging |
Het |
Nipal2 |
A |
T |
15: 34,578,852 (GRCm39) |
|
probably null |
Het |
Nub1 |
G |
C |
5: 24,912,851 (GRCm39) |
S517T |
probably benign |
Het |
Or10a4 |
T |
C |
7: 106,696,816 (GRCm39) |
L48P |
possibly damaging |
Het |
Or4d10c |
A |
G |
19: 12,065,391 (GRCm39) |
V255A |
probably damaging |
Het |
Or8b101 |
A |
T |
9: 38,020,134 (GRCm39) |
I51F |
possibly damaging |
Het |
Or8c17 |
T |
G |
9: 38,179,814 (GRCm39) |
S2A |
probably benign |
Het |
Plscr3 |
G |
A |
11: 69,740,964 (GRCm39) |
V267M |
probably benign |
Het |
Plxnb2 |
G |
T |
15: 89,050,602 (GRCm39) |
N451K |
probably benign |
Het |
Ppp2r2a |
A |
G |
14: 67,259,892 (GRCm39) |
L268P |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,186,694 (GRCm39) |
I1743F |
probably benign |
Het |
Rack1 |
A |
G |
11: 48,693,131 (GRCm39) |
T105A |
probably benign |
Het |
Rhot1 |
G |
A |
11: 80,116,907 (GRCm39) |
V94I |
probably damaging |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
Smc6 |
T |
A |
12: 11,351,517 (GRCm39) |
|
probably benign |
Het |
Spink8 |
T |
A |
9: 109,645,861 (GRCm39) |
V11D |
probably damaging |
Het |
Ss18l1 |
A |
T |
2: 179,705,103 (GRCm39) |
Q365L |
unknown |
Het |
Tbc1d31 |
T |
A |
15: 57,779,474 (GRCm39) |
H62Q |
probably benign |
Het |
Tbc1d9b |
T |
C |
11: 50,061,954 (GRCm39) |
V1171A |
possibly damaging |
Het |
Tln1 |
G |
A |
4: 43,536,413 (GRCm39) |
|
probably benign |
Het |
Tmem220 |
G |
A |
11: 66,916,077 (GRCm39) |
A25T |
possibly damaging |
Het |
Tmem259 |
T |
C |
10: 79,814,282 (GRCm39) |
N334S |
possibly damaging |
Het |
Tmod3 |
A |
T |
9: 75,414,809 (GRCm39) |
|
probably benign |
Het |
Tmprss2 |
A |
T |
16: 97,398,021 (GRCm39) |
Y52N |
probably damaging |
Het |
Tsga10 |
A |
T |
1: 37,873,278 (GRCm39) |
N200K |
possibly damaging |
Het |
Ube2frt |
T |
C |
12: 36,141,036 (GRCm39) |
|
probably benign |
Het |
Vmn1r189 |
T |
A |
13: 22,286,382 (GRCm39) |
T152S |
probably benign |
Het |
Vmn2r76 |
C |
T |
7: 85,880,415 (GRCm39) |
M90I |
probably benign |
Het |
Zfr |
C |
T |
15: 12,166,277 (GRCm39) |
A849V |
probably damaging |
Het |
Znhit6 |
T |
C |
3: 145,284,099 (GRCm39) |
M95T |
probably benign |
Het |
|
Other mutations in Mterf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01097:Mterf2
|
APN |
10 |
84,955,677 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02553:Mterf2
|
APN |
10 |
84,956,331 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02851:Mterf2
|
APN |
10 |
84,955,878 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02861:Mterf2
|
APN |
10 |
84,956,195 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03111:Mterf2
|
APN |
10 |
84,955,786 (GRCm39) |
nonsense |
probably null |
|
IGL03169:Mterf2
|
APN |
10 |
84,956,324 (GRCm39) |
missense |
probably benign |
0.02 |
R0941:Mterf2
|
UTSW |
10 |
84,955,934 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2241:Mterf2
|
UTSW |
10 |
84,956,180 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4964:Mterf2
|
UTSW |
10 |
84,955,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Mterf2
|
UTSW |
10 |
84,955,596 (GRCm39) |
missense |
probably benign |
0.00 |
R6586:Mterf2
|
UTSW |
10 |
84,955,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R7032:Mterf2
|
UTSW |
10 |
84,956,527 (GRCm39) |
nonsense |
probably null |
|
R7405:Mterf2
|
UTSW |
10 |
84,956,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R7705:Mterf2
|
UTSW |
10 |
84,956,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Mterf2
|
UTSW |
10 |
84,956,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9375:Mterf2
|
UTSW |
10 |
84,956,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R9626:Mterf2
|
UTSW |
10 |
84,956,295 (GRCm39) |
missense |
probably benign |
0.00 |
|