Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
T |
11: 109,999,479 (GRCm39) |
W1459R |
probably damaging |
Het |
Abca9 |
A |
T |
11: 110,032,488 (GRCm39) |
|
probably benign |
Het |
Adam25 |
T |
A |
8: 41,208,467 (GRCm39) |
C578S |
probably damaging |
Het |
Adam32 |
T |
A |
8: 25,412,353 (GRCm39) |
|
probably null |
Het |
Add1 |
T |
C |
5: 34,773,992 (GRCm39) |
V67A |
probably benign |
Het |
Aggf1 |
A |
T |
13: 95,492,988 (GRCm39) |
|
probably benign |
Het |
Ahcyl2 |
A |
T |
6: 29,891,242 (GRCm39) |
I449F |
probably benign |
Het |
Ak6 |
A |
G |
13: 100,791,650 (GRCm39) |
Y31C |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,188,037 (GRCm39) |
V1817A |
probably benign |
Het |
Arhgef17 |
G |
T |
7: 100,578,057 (GRCm39) |
P964T |
probably damaging |
Het |
Atxn7l3b |
A |
T |
10: 112,764,485 (GRCm39) |
L48Q |
possibly damaging |
Het |
Bbs10 |
T |
G |
10: 111,136,926 (GRCm39) |
S680A |
probably damaging |
Het |
Bcl7c |
G |
A |
7: 127,304,936 (GRCm39) |
T164I |
probably damaging |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
Ccdc110 |
T |
A |
8: 46,388,119 (GRCm39) |
D25E |
probably damaging |
Het |
Ccdc83 |
T |
A |
7: 89,875,891 (GRCm39) |
T327S |
possibly damaging |
Het |
Coro1b |
T |
C |
19: 4,203,250 (GRCm39) |
Y364H |
probably damaging |
Het |
Cstf3 |
A |
G |
2: 104,482,791 (GRCm39) |
D313G |
probably damaging |
Het |
Dlgap5 |
T |
A |
14: 47,650,432 (GRCm39) |
|
probably null |
Het |
Dusp3 |
A |
T |
11: 101,872,547 (GRCm39) |
I83N |
probably damaging |
Het |
Eea1 |
A |
T |
10: 95,831,444 (GRCm39) |
K178N |
possibly damaging |
Het |
Efr3b |
T |
A |
12: 4,032,925 (GRCm39) |
D144V |
probably damaging |
Het |
Gfus |
C |
A |
15: 75,798,827 (GRCm39) |
D127Y |
probably damaging |
Het |
Gm1110 |
T |
A |
9: 26,794,514 (GRCm39) |
E504V |
probably null |
Het |
Got2 |
T |
C |
8: 96,614,881 (GRCm39) |
H18R |
probably benign |
Het |
Gprc5b |
T |
C |
7: 118,582,856 (GRCm39) |
M338V |
probably benign |
Het |
Has2 |
A |
T |
15: 56,531,831 (GRCm39) |
F295I |
probably damaging |
Het |
Hcn3 |
T |
C |
3: 89,056,107 (GRCm39) |
D519G |
probably damaging |
Het |
Ino80 |
T |
A |
2: 119,210,160 (GRCm39) |
D1377V |
probably benign |
Het |
Iqsec3 |
A |
T |
6: 121,390,521 (GRCm39) |
|
probably benign |
Het |
Kif3c |
T |
A |
12: 3,415,989 (GRCm39) |
S3R |
probably benign |
Het |
Krt17 |
A |
G |
11: 100,151,445 (GRCm39) |
I116T |
possibly damaging |
Het |
Lrba |
T |
C |
3: 86,275,816 (GRCm39) |
V1728A |
probably damaging |
Het |
Map3k6 |
G |
T |
4: 132,974,252 (GRCm39) |
V550L |
possibly damaging |
Het |
Mcph1 |
T |
C |
8: 18,838,487 (GRCm39) |
V803A |
probably damaging |
Het |
Med13 |
A |
G |
11: 86,210,702 (GRCm39) |
V480A |
probably benign |
Het |
Ms4a20 |
A |
G |
19: 11,074,311 (GRCm39) |
V207A |
possibly damaging |
Het |
Msh5 |
T |
C |
17: 35,248,630 (GRCm39) |
E772G |
probably null |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Ndfip2 |
T |
C |
14: 105,542,174 (GRCm39) |
L308P |
probably damaging |
Het |
Ndufb10 |
T |
C |
17: 24,943,209 (GRCm39) |
T34A |
probably benign |
Het |
Nipal3 |
A |
T |
4: 135,195,829 (GRCm39) |
I258N |
possibly damaging |
Het |
Nup54 |
A |
G |
5: 92,570,423 (GRCm39) |
V328A |
probably damaging |
Het |
Oprm1 |
T |
C |
10: 6,739,071 (GRCm39) |
V66A |
possibly damaging |
Het |
Or10p21 |
T |
A |
10: 128,847,191 (GRCm39) |
F12L |
possibly damaging |
Het |
Or51ah3 |
G |
T |
7: 103,210,289 (GRCm39) |
V202F |
probably benign |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Or8b56 |
T |
A |
9: 38,739,111 (GRCm39) |
Y41* |
probably null |
Het |
Or9s14 |
T |
C |
1: 92,535,615 (GRCm39) |
F19L |
probably damaging |
Het |
Peg12 |
G |
A |
7: 62,113,296 (GRCm39) |
T267I |
unknown |
Het |
Phf20 |
A |
G |
2: 156,145,061 (GRCm39) |
S890G |
probably benign |
Het |
Plk2 |
C |
T |
13: 110,535,997 (GRCm39) |
T567M |
probably damaging |
Het |
Pola2 |
A |
T |
19: 5,992,370 (GRCm39) |
|
probably benign |
Het |
Ppp1r12b |
A |
G |
1: 134,793,514 (GRCm39) |
|
probably null |
Het |
Prickle1 |
A |
T |
15: 93,400,900 (GRCm39) |
L528* |
probably null |
Het |
Prpf6 |
T |
A |
2: 181,297,250 (GRCm39) |
N903K |
probably benign |
Het |
Ptprc |
G |
A |
1: 138,010,453 (GRCm39) |
A601V |
probably benign |
Het |
Ranbp1 |
A |
T |
16: 18,059,607 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
C |
T |
11: 54,582,075 (GRCm39) |
S1334L |
probably benign |
Het |
Rgs2 |
T |
C |
1: 143,878,022 (GRCm39) |
|
probably null |
Het |
Ripk2 |
A |
T |
4: 16,129,125 (GRCm39) |
|
probably null |
Het |
Rnf17 |
A |
G |
14: 56,719,650 (GRCm39) |
S967G |
probably null |
Het |
Rock2 |
T |
A |
12: 17,009,517 (GRCm39) |
|
probably benign |
Het |
Rpusd3 |
C |
T |
6: 113,392,514 (GRCm39) |
|
probably null |
Het |
Scgb1b20 |
G |
T |
7: 33,072,935 (GRCm39) |
V48L |
probably benign |
Het |
Sec16a |
T |
A |
2: 26,314,426 (GRCm39) |
|
probably null |
Het |
Serpina5 |
T |
A |
12: 104,069,589 (GRCm39) |
L267H |
probably damaging |
Het |
Slc12a3 |
C |
T |
8: 95,082,986 (GRCm39) |
H875Y |
probably benign |
Het |
Slc45a4 |
A |
G |
15: 73,453,763 (GRCm39) |
S745P |
probably benign |
Het |
Sun2 |
C |
A |
15: 79,621,277 (GRCm39) |
V213F |
probably damaging |
Het |
Taar2 |
G |
A |
10: 23,817,393 (GRCm39) |
R311H |
probably benign |
Het |
Tac1 |
C |
T |
6: 7,562,424 (GRCm39) |
R129C |
probably damaging |
Het |
Taf6 |
T |
C |
5: 138,180,975 (GRCm39) |
E202G |
probably benign |
Het |
Tex21 |
T |
A |
12: 76,286,307 (GRCm39) |
H64L |
probably benign |
Het |
Tgs1 |
A |
G |
4: 3,593,620 (GRCm39) |
S503G |
probably benign |
Het |
Tmem184c |
C |
T |
8: 78,324,441 (GRCm39) |
V350I |
possibly damaging |
Het |
Tnks1bp1 |
A |
G |
2: 84,901,273 (GRCm39) |
S960G |
possibly damaging |
Het |
Trbc2 |
T |
C |
6: 41,525,083 (GRCm39) |
|
probably benign |
Het |
Tubgcp2 |
A |
T |
7: 139,581,518 (GRCm39) |
|
probably benign |
Het |
Vmn1r39 |
T |
A |
6: 66,782,181 (GRCm39) |
T46S |
probably benign |
Het |
Vmn1r61 |
T |
C |
7: 5,613,699 (GRCm39) |
H205R |
probably benign |
Het |
Zdhhc14 |
T |
C |
17: 5,775,539 (GRCm39) |
S264P |
possibly damaging |
Het |
Zfp101 |
T |
A |
17: 33,601,213 (GRCm39) |
H181L |
possibly damaging |
Het |
|
Other mutations in Sucla2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00973:Sucla2
|
APN |
14 |
73,828,347 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01539:Sucla2
|
APN |
14 |
73,828,561 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02064:Sucla2
|
APN |
14 |
73,816,913 (GRCm39) |
nonsense |
probably null |
|
IGL02240:Sucla2
|
APN |
14 |
73,828,287 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02640:Sucla2
|
APN |
14 |
73,819,246 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02965:Sucla2
|
APN |
14 |
73,816,871 (GRCm39) |
missense |
probably benign |
0.00 |
3-1:Sucla2
|
UTSW |
14 |
73,806,397 (GRCm39) |
nonsense |
probably null |
|
PIT4812001:Sucla2
|
UTSW |
14 |
73,816,889 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0764:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R0765:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R0844:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1065:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1067:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1136:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1162:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1311:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1312:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1345:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1416:Sucla2
|
UTSW |
14 |
73,798,074 (GRCm39) |
unclassified |
probably benign |
|
R1677:Sucla2
|
UTSW |
14 |
73,830,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Sucla2
|
UTSW |
14 |
73,831,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R2126:Sucla2
|
UTSW |
14 |
73,830,108 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2484:Sucla2
|
UTSW |
14 |
73,819,149 (GRCm39) |
missense |
probably benign |
0.12 |
R2566:Sucla2
|
UTSW |
14 |
73,790,244 (GRCm39) |
intron |
probably benign |
|
R3706:Sucla2
|
UTSW |
14 |
73,828,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Sucla2
|
UTSW |
14 |
73,806,429 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5620:Sucla2
|
UTSW |
14 |
73,832,836 (GRCm39) |
missense |
probably damaging |
0.99 |
R5650:Sucla2
|
UTSW |
14 |
73,828,569 (GRCm39) |
missense |
probably benign |
0.38 |
R5947:Sucla2
|
UTSW |
14 |
73,830,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R6045:Sucla2
|
UTSW |
14 |
73,806,404 (GRCm39) |
nonsense |
probably null |
|
R6236:Sucla2
|
UTSW |
14 |
73,831,190 (GRCm39) |
missense |
probably benign |
0.39 |
R6693:Sucla2
|
UTSW |
14 |
73,806,107 (GRCm39) |
nonsense |
probably null |
|
R7706:Sucla2
|
UTSW |
14 |
73,806,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R8786:Sucla2
|
UTSW |
14 |
73,797,905 (GRCm39) |
missense |
probably benign |
0.13 |
R9055:Sucla2
|
UTSW |
14 |
73,819,068 (GRCm39) |
intron |
probably benign |
|
R9064:Sucla2
|
UTSW |
14 |
73,828,303 (GRCm39) |
missense |
probably benign |
|
R9380:Sucla2
|
UTSW |
14 |
73,828,312 (GRCm39) |
missense |
probably benign |
|
|