Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat1 |
T |
A |
9: 53,506,045 (GRCm39) |
I92F |
probably benign |
Het |
Actr3b |
A |
G |
5: 26,037,411 (GRCm39) |
I208V |
probably benign |
Het |
Car12 |
T |
C |
9: 66,621,159 (GRCm39) |
V10A |
probably benign |
Het |
Ccdc171 |
C |
A |
4: 83,661,255 (GRCm39) |
R1122S |
probably damaging |
Het |
Cep97 |
A |
G |
16: 55,742,539 (GRCm39) |
V136A |
probably damaging |
Het |
Cilp2 |
G |
T |
8: 70,333,936 (GRCm39) |
Q1021K |
probably damaging |
Het |
Col24a1 |
C |
A |
3: 145,020,247 (GRCm39) |
T206N |
probably damaging |
Het |
Crebbp |
A |
T |
16: 3,902,141 (GRCm39) |
I2328K |
possibly damaging |
Het |
Ctns |
A |
G |
11: 73,087,478 (GRCm39) |
F16S |
probably benign |
Het |
Dbf4 |
T |
C |
5: 8,453,172 (GRCm39) |
K276E |
probably benign |
Het |
Dnase2b |
T |
A |
3: 146,294,840 (GRCm39) |
Q118L |
probably benign |
Het |
Elf1 |
T |
C |
14: 79,773,819 (GRCm39) |
L10P |
probably damaging |
Het |
Exosc5 |
T |
C |
7: 25,364,988 (GRCm39) |
|
probably null |
Het |
Fam163b |
C |
T |
2: 27,003,570 (GRCm39) |
C28Y |
probably damaging |
Het |
Fam180a |
G |
T |
6: 35,290,647 (GRCm39) |
A112E |
possibly damaging |
Het |
Fam3b |
A |
T |
16: 97,272,391 (GRCm39) |
Y89* |
probably null |
Het |
Gcg |
C |
T |
2: 62,308,922 (GRCm39) |
W77* |
probably null |
Het |
Gm17472 |
G |
A |
6: 42,957,832 (GRCm39) |
V34I |
possibly damaging |
Het |
Klhl23 |
T |
A |
2: 69,654,582 (GRCm39) |
C151S |
probably damaging |
Het |
Mfsd11 |
T |
A |
11: 116,764,701 (GRCm39) |
I375N |
probably damaging |
Het |
Mroh2b |
T |
A |
15: 4,937,997 (GRCm39) |
I206N |
probably damaging |
Het |
Myo1b |
T |
C |
1: 51,821,133 (GRCm39) |
E456G |
possibly damaging |
Het |
Nat8 |
G |
A |
6: 85,807,783 (GRCm39) |
Q117* |
probably null |
Het |
Nlrp4g |
A |
C |
9: 124,349,764 (GRCm38) |
|
noncoding transcript |
Het |
Nmt1 |
G |
T |
11: 102,955,625 (GRCm39) |
G468C |
possibly damaging |
Het |
Nobox |
G |
T |
6: 43,281,973 (GRCm39) |
Q367K |
possibly damaging |
Het |
Nusap1 |
A |
G |
2: 119,479,470 (GRCm39) |
*428W |
probably null |
Het |
Or12j4 |
T |
C |
7: 140,046,560 (GRCm39) |
F149L |
probably benign |
Het |
Or4c126 |
G |
A |
2: 89,824,656 (GRCm39) |
M306I |
probably benign |
Het |
Pbp2 |
T |
C |
6: 135,287,147 (GRCm39) |
I67V |
probably benign |
Het |
Pcdhb8 |
T |
G |
18: 37,488,427 (GRCm39) |
M35R |
possibly damaging |
Het |
Pkp1 |
T |
C |
1: 135,817,664 (GRCm39) |
E157G |
probably damaging |
Het |
Pomgnt1 |
C |
T |
4: 116,015,747 (GRCm39) |
L560F |
probably damaging |
Het |
Prkcz |
T |
C |
4: 155,355,713 (GRCm39) |
T227A |
probably damaging |
Het |
Ptprd |
T |
A |
4: 75,865,361 (GRCm39) |
R1446S |
probably damaging |
Het |
Ptprq |
T |
C |
10: 107,479,860 (GRCm39) |
T1137A |
probably benign |
Het |
Sec22c |
T |
C |
9: 121,514,630 (GRCm39) |
I153V |
probably benign |
Het |
Slc30a5 |
C |
T |
13: 100,949,155 (GRCm39) |
|
probably null |
Het |
Smcr8 |
T |
C |
11: 60,669,721 (GRCm39) |
S290P |
probably benign |
Het |
Stambpl1 |
T |
G |
19: 34,212,612 (GRCm39) |
L261V |
probably benign |
Het |
Stk38l |
T |
C |
6: 146,668,321 (GRCm39) |
|
probably null |
Het |
Themis |
T |
C |
10: 28,637,543 (GRCm39) |
F216L |
probably benign |
Het |
Trmt1l |
T |
C |
1: 151,309,536 (GRCm39) |
|
probably benign |
Het |
Usp17lb |
C |
A |
7: 104,489,937 (GRCm39) |
C330F |
probably damaging |
Het |
Vmn2r120 |
A |
T |
17: 57,831,724 (GRCm39) |
L355H |
probably damaging |
Het |
Zc3h7b |
T |
A |
15: 81,653,341 (GRCm39) |
C82S |
probably benign |
Het |
|
Other mutations in Mdh1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01694:Mdh1b
|
APN |
1 |
63,750,265 (GRCm39) |
splice site |
probably benign |
|
IGL02314:Mdh1b
|
APN |
1 |
63,750,273 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02390:Mdh1b
|
APN |
1 |
63,760,716 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02864:Mdh1b
|
APN |
1 |
63,760,762 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02887:Mdh1b
|
APN |
1 |
63,754,523 (GRCm39) |
splice site |
probably benign |
|
IGL03073:Mdh1b
|
APN |
1 |
63,760,646 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03372:Mdh1b
|
APN |
1 |
63,759,154 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02835:Mdh1b
|
UTSW |
1 |
63,757,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Mdh1b
|
UTSW |
1 |
63,760,959 (GRCm39) |
splice site |
probably benign |
|
R0015:Mdh1b
|
UTSW |
1 |
63,760,959 (GRCm39) |
splice site |
probably benign |
|
R0255:Mdh1b
|
UTSW |
1 |
63,758,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Mdh1b
|
UTSW |
1 |
63,758,681 (GRCm39) |
missense |
probably benign |
|
R2057:Mdh1b
|
UTSW |
1 |
63,760,741 (GRCm39) |
missense |
probably benign |
0.11 |
R3177:Mdh1b
|
UTSW |
1 |
63,750,690 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3277:Mdh1b
|
UTSW |
1 |
63,750,690 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3522:Mdh1b
|
UTSW |
1 |
63,758,927 (GRCm39) |
missense |
probably damaging |
0.97 |
R4938:Mdh1b
|
UTSW |
1 |
63,750,663 (GRCm39) |
missense |
probably benign |
0.00 |
R4967:Mdh1b
|
UTSW |
1 |
63,759,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R5093:Mdh1b
|
UTSW |
1 |
63,750,620 (GRCm39) |
missense |
probably benign |
0.08 |
R5160:Mdh1b
|
UTSW |
1 |
63,764,804 (GRCm39) |
missense |
probably null |
0.01 |
R5311:Mdh1b
|
UTSW |
1 |
63,759,163 (GRCm39) |
missense |
probably benign |
0.00 |
R6345:Mdh1b
|
UTSW |
1 |
63,754,398 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6974:Mdh1b
|
UTSW |
1 |
63,760,975 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Mdh1b
|
UTSW |
1 |
63,760,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R7728:Mdh1b
|
UTSW |
1 |
63,754,429 (GRCm39) |
missense |
probably benign |
0.23 |
R7780:Mdh1b
|
UTSW |
1 |
63,759,133 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8271:Mdh1b
|
UTSW |
1 |
63,759,164 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8556:Mdh1b
|
UTSW |
1 |
63,750,141 (GRCm39) |
splice site |
probably null |
|
R8681:Mdh1b
|
UTSW |
1 |
63,754,360 (GRCm39) |
missense |
probably benign |
|
Z1176:Mdh1b
|
UTSW |
1 |
63,750,690 (GRCm39) |
missense |
probably benign |
0.00 |
|