Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12b |
T |
A |
12: 70,206,221 (GRCm39) |
N67K |
probably benign |
Het |
Amotl1 |
C |
A |
9: 14,556,216 (GRCm39) |
E37* |
probably null |
Het |
Ap4b1 |
C |
A |
3: 103,720,601 (GRCm39) |
Y90* |
probably null |
Het |
Apc |
A |
G |
18: 34,431,480 (GRCm39) |
E277G |
possibly damaging |
Het |
Atl1 |
T |
A |
12: 69,972,813 (GRCm39) |
H44Q |
probably damaging |
Het |
Atp6v0b |
G |
A |
4: 117,742,864 (GRCm39) |
T74M |
probably benign |
Het |
Auts2 |
T |
C |
5: 131,469,437 (GRCm39) |
T627A |
probably benign |
Het |
B4galnt4 |
T |
A |
7: 140,647,449 (GRCm39) |
I372N |
possibly damaging |
Het |
B4galt2 |
A |
G |
4: 117,731,148 (GRCm39) |
S338P |
probably damaging |
Het |
Cfap43 |
A |
C |
19: 47,773,717 (GRCm39) |
|
probably null |
Het |
Col4a1 |
T |
C |
8: 11,362,538 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
A |
C |
9: 108,798,494 (GRCm39) |
I1741L |
possibly damaging |
Het |
Coprs |
A |
T |
8: 13,935,750 (GRCm39) |
S90T |
probably benign |
Het |
Csrnp3 |
T |
C |
2: 65,779,408 (GRCm39) |
V40A |
possibly damaging |
Het |
Ephx1 |
C |
A |
1: 180,827,287 (GRCm39) |
|
probably null |
Het |
Erich6 |
C |
A |
3: 58,526,220 (GRCm39) |
R594L |
probably benign |
Het |
F2rl2 |
A |
T |
13: 95,837,038 (GRCm39) |
N28Y |
probably damaging |
Het |
Fbxo38 |
A |
T |
18: 62,639,740 (GRCm39) |
N1041K |
possibly damaging |
Het |
Fcgr2b |
C |
T |
1: 170,790,977 (GRCm39) |
|
probably null |
Het |
Fsip2 |
T |
A |
2: 82,809,061 (GRCm39) |
N1793K |
probably damaging |
Het |
Gatad1 |
T |
C |
5: 3,693,540 (GRCm39) |
R210G |
probably benign |
Het |
Gcnt3 |
A |
G |
9: 69,942,169 (GRCm39) |
I133T |
probably damaging |
Het |
Gm57859 |
A |
G |
11: 113,578,818 (GRCm39) |
D71G |
probably benign |
Het |
Hoxa1 |
T |
A |
6: 52,135,021 (GRCm39) |
I61F |
probably damaging |
Het |
Impact |
C |
T |
18: 13,115,169 (GRCm39) |
L102F |
probably damaging |
Het |
Ist1 |
A |
T |
8: 110,404,284 (GRCm39) |
I196N |
probably damaging |
Het |
Kcnv2 |
T |
A |
19: 27,311,282 (GRCm39) |
S550T |
probably benign |
Het |
Krt1c |
A |
T |
15: 101,726,314 (GRCm39) |
S75T |
unknown |
Het |
Krtap21-1 |
A |
G |
16: 89,200,466 (GRCm39) |
S59P |
unknown |
Het |
Lef1 |
A |
T |
3: 130,905,223 (GRCm39) |
I35F |
probably damaging |
Het |
Lpcat2 |
A |
C |
8: 93,599,707 (GRCm39) |
N225T |
probably damaging |
Het |
Lztfl1 |
A |
T |
9: 123,538,649 (GRCm39) |
N142K |
probably benign |
Het |
Mettl26 |
A |
G |
17: 26,095,658 (GRCm39) |
D171G |
probably damaging |
Het |
Mrps24 |
A |
T |
11: 5,654,663 (GRCm39) |
M97K |
probably benign |
Het |
Ms4a14 |
A |
T |
19: 11,279,499 (GRCm39) |
C1020S |
probably benign |
Het |
Mterf1a |
A |
T |
5: 3,940,854 (GRCm39) |
I338K |
probably benign |
Het |
Odad2 |
A |
T |
18: 7,294,479 (GRCm39) |
Y45N |
probably benign |
Het |
Or1e22 |
A |
G |
11: 73,377,299 (GRCm39) |
I117T |
probably benign |
Het |
Or4p20 |
T |
C |
2: 88,254,156 (GRCm39) |
Y71C |
possibly damaging |
Het |
Or52s1b |
T |
A |
7: 102,822,442 (GRCm39) |
H134L |
probably damaging |
Het |
Or7g12 |
T |
A |
9: 18,899,689 (GRCm39) |
I135N |
probably damaging |
Het |
Paqr3 |
T |
A |
5: 97,256,146 (GRCm39) |
H76L |
probably damaging |
Het |
Parp1 |
T |
A |
1: 180,417,071 (GRCm39) |
Y618* |
probably null |
Het |
Pilrb2 |
C |
T |
5: 137,870,049 (GRCm39) |
|
probably benign |
Het |
Pkm |
A |
G |
9: 59,575,853 (GRCm39) |
N90D |
probably damaging |
Het |
Pla2g4c |
T |
G |
7: 13,078,459 (GRCm39) |
|
probably null |
Het |
Plppr4 |
C |
T |
3: 117,116,667 (GRCm39) |
V339I |
probably damaging |
Het |
Pnkp |
T |
A |
7: 44,510,462 (GRCm39) |
D304E |
probably damaging |
Het |
Pnlip |
T |
C |
19: 58,668,067 (GRCm39) |
|
probably null |
Het |
Polr2a |
A |
G |
11: 69,638,026 (GRCm39) |
C148R |
probably damaging |
Het |
Ppp1r10 |
G |
A |
17: 36,240,443 (GRCm39) |
G578S |
probably benign |
Het |
Ptges2 |
C |
T |
2: 32,287,683 (GRCm39) |
T137I |
possibly damaging |
Het |
Ptpre |
T |
C |
7: 135,270,877 (GRCm39) |
V344A |
possibly damaging |
Het |
Rag1 |
A |
G |
2: 101,472,137 (GRCm39) |
F1002L |
probably damaging |
Het |
Rcn2 |
T |
A |
9: 55,960,298 (GRCm39) |
Y188* |
probably null |
Het |
Rest |
A |
G |
5: 77,416,046 (GRCm39) |
S87G |
probably damaging |
Het |
Rgsl1 |
C |
T |
1: 153,675,568 (GRCm39) |
D913N |
probably damaging |
Het |
Scp2 |
A |
G |
4: 107,928,475 (GRCm39) |
M1T |
probably null |
Het |
Slamf8 |
T |
A |
1: 172,415,590 (GRCm39) |
N83Y |
probably damaging |
Het |
Slc26a11 |
T |
A |
11: 119,248,844 (GRCm39) |
F75Y |
possibly damaging |
Het |
Slc26a5 |
A |
G |
5: 22,045,570 (GRCm39) |
S133P |
probably damaging |
Het |
Sncb |
A |
T |
13: 54,910,487 (GRCm39) |
V83E |
probably damaging |
Het |
Tmem243 |
A |
G |
5: 9,151,348 (GRCm39) |
T11A |
probably damaging |
Het |
Trim38 |
A |
G |
13: 23,973,502 (GRCm39) |
N277D |
probably benign |
Het |
Vmn1r189 |
C |
T |
13: 22,286,628 (GRCm39) |
G70S |
probably damaging |
Het |
Vmn2r-ps117 |
A |
G |
17: 19,058,495 (GRCm39) |
R684G |
probably benign |
Het |
Wdr59 |
T |
C |
8: 112,187,420 (GRCm39) |
N792D |
possibly damaging |
Het |
Wnt5a |
A |
G |
14: 28,244,527 (GRCm39) |
D238G |
possibly damaging |
Het |
Zbtb42 |
C |
A |
12: 112,646,824 (GRCm39) |
T333K |
probably damaging |
Het |
Zfp119b |
A |
G |
17: 56,245,564 (GRCm39) |
S509P |
probably benign |
Het |
Zfp365 |
T |
A |
10: 67,745,594 (GRCm39) |
K61N |
probably damaging |
Het |
Zfp553 |
T |
C |
7: 126,835,825 (GRCm39) |
F460S |
probably damaging |
Het |
Zfp788 |
C |
T |
7: 41,299,301 (GRCm39) |
Q594* |
probably null |
Het |
Zfp984 |
T |
A |
4: 147,845,707 (GRCm39) |
M1L |
possibly damaging |
Het |
Zmiz2 |
T |
A |
11: 6,347,566 (GRCm39) |
Y291* |
probably null |
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 |
IGL02582:Mdh1b
|
APN |
1 |
63,758,756 (GRCm39) |
missense |
probably benign |
0.08 |
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 |
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 |
|