Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap13 |
T |
C |
7: 75,327,157 (GRCm39) |
S719P |
probably damaging |
Het |
Atxn2l |
A |
T |
7: 126,096,466 (GRCm39) |
N425K |
probably benign |
Het |
B3galt4 |
G |
A |
17: 34,169,813 (GRCm39) |
R142C |
probably damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,404,249 (GRCm39) |
|
probably null |
Het |
Ccar2 |
A |
G |
14: 70,377,964 (GRCm39) |
S674P |
probably damaging |
Het |
Ccm2 |
T |
A |
11: 6,520,119 (GRCm39) |
Y56* |
probably null |
Het |
Cdc14b |
A |
T |
13: 64,363,490 (GRCm39) |
V257E |
probably damaging |
Het |
Cdca8 |
A |
C |
4: 124,815,798 (GRCm39) |
S171R |
probably benign |
Het |
Cep192 |
C |
T |
18: 67,971,125 (GRCm39) |
T1042I |
probably benign |
Het |
Cfap100 |
T |
A |
6: 90,389,986 (GRCm39) |
T101S |
possibly damaging |
Het |
Cfap46 |
T |
A |
7: 139,222,513 (GRCm39) |
M1155L |
probably benign |
Het |
Cyp3a13 |
T |
A |
5: 137,892,626 (GRCm39) |
I473F |
possibly damaging |
Het |
Dclk3 |
A |
G |
9: 111,298,138 (GRCm39) |
I561V |
possibly damaging |
Het |
Dock6 |
A |
T |
9: 21,744,908 (GRCm39) |
L556H |
probably damaging |
Het |
Dqx1 |
G |
A |
6: 83,038,070 (GRCm39) |
C486Y |
probably damaging |
Het |
Drd1 |
T |
A |
13: 54,207,333 (GRCm39) |
M294L |
probably benign |
Het |
Dsel |
A |
G |
1: 111,788,403 (GRCm39) |
S711P |
probably damaging |
Het |
Fcho2 |
A |
T |
13: 98,869,167 (GRCm39) |
I568N |
probably damaging |
Het |
Folr1 |
A |
G |
7: 101,507,810 (GRCm39) |
M210T |
probably damaging |
Het |
Gatc |
T |
A |
5: 115,478,904 (GRCm39) |
|
probably null |
Het |
Gja8 |
A |
T |
3: 96,826,740 (GRCm39) |
F307L |
probably benign |
Het |
H1f7 |
G |
A |
15: 98,154,636 (GRCm39) |
T171I |
unknown |
Het |
Hnrnpd |
C |
A |
5: 100,114,016 (GRCm39) |
*87L |
probably null |
Het |
Hpd |
C |
T |
5: 123,312,532 (GRCm39) |
R279H |
possibly damaging |
Het |
Igfals |
G |
A |
17: 25,099,457 (GRCm39) |
V183M |
probably damaging |
Het |
Izumo1 |
A |
G |
7: 45,276,598 (GRCm39) |
Y387C |
probably benign |
Het |
Kdm5a |
A |
G |
6: 120,375,999 (GRCm39) |
N585S |
probably null |
Het |
Marchf2 |
C |
A |
17: 33,928,762 (GRCm39) |
G45C |
probably damaging |
Het |
Myo15a |
A |
T |
11: 60,370,442 (GRCm39) |
R1067S |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Nell1 |
A |
G |
7: 49,770,411 (GRCm39) |
S157G |
probably damaging |
Het |
Nf1 |
A |
T |
11: 79,437,859 (GRCm39) |
E2072D |
probably damaging |
Het |
Nipal1 |
CGGG |
CGG |
5: 72,825,334 (GRCm39) |
|
probably null |
Het |
Nop2 |
T |
A |
6: 125,114,149 (GRCm39) |
V205E |
probably benign |
Het |
Nphs1 |
G |
T |
7: 30,173,702 (GRCm39) |
S939I |
probably damaging |
Het |
Nudt8 |
T |
A |
19: 4,051,925 (GRCm39) |
W179R |
probably damaging |
Het |
Nutm1 |
A |
T |
2: 112,080,274 (GRCm39) |
I547N |
probably benign |
Het |
Oog2 |
A |
C |
4: 143,922,856 (GRCm39) |
T374P |
probably damaging |
Het |
Or4k5 |
A |
T |
14: 50,385,384 (GRCm39) |
F316I |
probably benign |
Het |
Or8b54 |
C |
A |
9: 38,686,631 (GRCm39) |
L27I |
probably damaging |
Het |
Otud4 |
T |
A |
8: 80,390,722 (GRCm39) |
M413K |
probably benign |
Het |
Pear1 |
A |
G |
3: 87,667,606 (GRCm39) |
|
probably benign |
Het |
Pla2g3 |
G |
A |
11: 3,438,551 (GRCm39) |
C67Y |
probably damaging |
Het |
Plxdc2 |
A |
G |
2: 16,716,917 (GRCm39) |
T334A |
probably benign |
Het |
Ppl |
G |
A |
16: 4,917,864 (GRCm39) |
R543W |
probably damaging |
Het |
Prl5a1 |
G |
A |
13: 28,333,880 (GRCm39) |
V128I |
probably damaging |
Het |
Pth1r |
A |
T |
9: 110,571,295 (GRCm39) |
L25Q |
probably damaging |
Het |
Pth1r |
T |
C |
9: 110,558,689 (GRCm39) |
D96G |
probably benign |
Het |
Rfpl4 |
G |
T |
7: 5,113,517 (GRCm39) |
D215E |
probably damaging |
Het |
Rnf146 |
T |
A |
10: 29,223,092 (GRCm39) |
R265* |
probably null |
Het |
Rpe65 |
T |
C |
3: 159,312,122 (GRCm39) |
I207T |
probably benign |
Het |
Rptn |
A |
G |
3: 93,305,532 (GRCm39) |
E955G |
possibly damaging |
Het |
Rwdd2b |
A |
T |
16: 87,233,738 (GRCm39) |
C121S |
probably damaging |
Het |
Scn10a |
A |
G |
9: 119,438,340 (GRCm39) |
I1843T |
probably damaging |
Het |
Sirt5 |
A |
G |
13: 43,524,245 (GRCm39) |
I6V |
probably benign |
Het |
Slc5a3 |
G |
A |
16: 91,874,383 (GRCm39) |
A147T |
probably damaging |
Het |
Stk39 |
T |
C |
2: 68,240,390 (GRCm39) |
S114G |
probably damaging |
Het |
Stxbp1 |
T |
C |
2: 32,704,979 (GRCm39) |
|
probably null |
Het |
Syt3 |
G |
T |
7: 44,040,106 (GRCm39) |
G113V |
probably damaging |
Het |
Tatdn2 |
A |
G |
6: 113,686,506 (GRCm39) |
T644A |
probably damaging |
Het |
Trim9 |
T |
A |
12: 70,298,791 (GRCm39) |
|
probably null |
Het |
Tut1 |
A |
G |
19: 8,936,719 (GRCm39) |
N181S |
probably benign |
Het |
Vill |
T |
C |
9: 118,895,892 (GRCm39) |
S151P |
probably damaging |
Het |
Vmn2r90 |
A |
T |
17: 17,948,400 (GRCm39) |
I549F |
probably damaging |
Het |
Wdfy4 |
T |
C |
14: 32,801,923 (GRCm39) |
T1912A |
possibly damaging |
Het |
|
Other mutations in Slc25a36 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01552:Slc25a36
|
APN |
9 |
96,961,286 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01634:Slc25a36
|
APN |
9 |
96,962,534 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02149:Slc25a36
|
APN |
9 |
96,975,122 (GRCm39) |
splice site |
probably benign |
|
R0394:Slc25a36
|
UTSW |
9 |
96,962,257 (GRCm39) |
missense |
probably benign |
0.36 |
R0518:Slc25a36
|
UTSW |
9 |
96,979,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1208:Slc25a36
|
UTSW |
9 |
96,967,188 (GRCm39) |
splice site |
probably benign |
|
R1439:Slc25a36
|
UTSW |
9 |
96,975,126 (GRCm39) |
splice site |
probably benign |
|
R1466:Slc25a36
|
UTSW |
9 |
96,962,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Slc25a36
|
UTSW |
9 |
96,962,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Slc25a36
|
UTSW |
9 |
96,975,135 (GRCm39) |
missense |
probably benign |
0.00 |
R2247:Slc25a36
|
UTSW |
9 |
96,982,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2317:Slc25a36
|
UTSW |
9 |
96,961,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R2518:Slc25a36
|
UTSW |
9 |
96,961,124 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3756:Slc25a36
|
UTSW |
9 |
96,982,208 (GRCm39) |
nonsense |
probably null |
|
R4405:Slc25a36
|
UTSW |
9 |
96,967,171 (GRCm39) |
missense |
probably benign |
0.00 |
R4624:Slc25a36
|
UTSW |
9 |
96,961,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R4719:Slc25a36
|
UTSW |
9 |
96,972,172 (GRCm39) |
utr 3 prime |
probably benign |
|
R5492:Slc25a36
|
UTSW |
9 |
96,982,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R6152:Slc25a36
|
UTSW |
9 |
96,982,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Slc25a36
|
UTSW |
9 |
96,966,444 (GRCm39) |
critical splice donor site |
probably null |
|
R8139:Slc25a36
|
UTSW |
9 |
96,962,505 (GRCm39) |
missense |
probably benign |
|
R8925:Slc25a36
|
UTSW |
9 |
96,982,126 (GRCm39) |
critical splice donor site |
probably null |
|
R8927:Slc25a36
|
UTSW |
9 |
96,982,126 (GRCm39) |
critical splice donor site |
probably null |
|
R8984:Slc25a36
|
UTSW |
9 |
96,961,259 (GRCm39) |
missense |
probably benign |
0.36 |
R9280:Slc25a36
|
UTSW |
9 |
96,982,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R9485:Slc25a36
|
UTSW |
9 |
96,962,522 (GRCm39) |
missense |
probably benign |
|
R9631:Slc25a36
|
UTSW |
9 |
96,982,153 (GRCm39) |
missense |
probably benign |
0.00 |
R9712:Slc25a36
|
UTSW |
9 |
96,961,230 (GRCm39) |
missense |
probably benign |
0.03 |
|