Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,297,384 (GRCm39) |
T2369A |
probably benign |
Het |
Abhd6 |
T |
G |
14: 8,042,828 (GRCm38) |
|
probably null |
Het |
Abhd6 |
G |
T |
14: 8,042,826 (GRCm38) |
G128C |
probably damaging |
Het |
Acsm3 |
A |
G |
7: 119,378,896 (GRCm39) |
E426G |
probably benign |
Het |
Ankrd11 |
T |
C |
8: 123,618,368 (GRCm39) |
D1828G |
probably benign |
Het |
Asmt |
T |
A |
X: 169,108,766 (GRCm39) |
|
probably null |
Het |
Casp4 |
A |
G |
9: 5,324,884 (GRCm39) |
Q232R |
probably benign |
Het |
Cenpt |
A |
T |
8: 106,575,833 (GRCm39) |
L171* |
probably null |
Het |
Chd3 |
AGCGGCGGCGGCGGCGGCGG |
AGCGGCGGCGGCGGCGG |
11: 69,259,982 (GRCm39) |
|
probably benign |
Het |
Col5a2 |
G |
T |
1: 45,429,275 (GRCm39) |
H948N |
possibly damaging |
Het |
Dnah9 |
G |
T |
11: 65,951,923 (GRCm39) |
H1859N |
probably damaging |
Het |
Dscaml1 |
G |
A |
9: 45,664,104 (GRCm39) |
R1993Q |
probably benign |
Het |
Fbxw8 |
C |
A |
5: 118,263,028 (GRCm39) |
R217L |
probably benign |
Het |
Flnb |
T |
G |
14: 7,892,275 (GRCm38) |
|
probably null |
Het |
Fyb2 |
A |
G |
4: 104,802,739 (GRCm39) |
N214D |
probably benign |
Het |
Gbp2b |
A |
G |
3: 142,316,801 (GRCm39) |
E484G |
possibly damaging |
Het |
Gzmk |
A |
G |
13: 113,317,045 (GRCm39) |
Y45H |
probably damaging |
Het |
Ivl |
CCTGCTGCTGCTGCT |
CCTGCTGCTGCT |
3: 92,479,217 (GRCm39) |
|
probably benign |
Het |
Kcnj6 |
A |
G |
16: 94,633,685 (GRCm39) |
V142A |
possibly damaging |
Het |
Lama3 |
T |
A |
18: 12,710,897 (GRCm39) |
V3144E |
probably damaging |
Het |
Mark1 |
G |
A |
1: 184,644,786 (GRCm39) |
S390L |
possibly damaging |
Het |
Mbd3l1 |
T |
C |
9: 18,396,024 (GRCm39) |
Y50H |
probably benign |
Het |
Mcat |
T |
C |
15: 83,433,383 (GRCm39) |
N220S |
probably benign |
Het |
Muc2 |
A |
G |
7: 141,282,941 (GRCm39) |
E81G |
probably benign |
Het |
Neto1 |
A |
T |
18: 86,512,985 (GRCm39) |
K327* |
probably null |
Het |
Or10j3 |
G |
T |
1: 173,031,847 (GRCm39) |
R308L |
probably benign |
Het |
Or4a67 |
A |
T |
2: 88,598,587 (GRCm39) |
L24Q |
probably damaging |
Het |
Or52p1 |
A |
T |
7: 104,267,648 (GRCm39) |
Y254F |
probably damaging |
Het |
Or52u1 |
T |
C |
7: 104,237,218 (GRCm39) |
L69P |
probably damaging |
Het |
Pidd1 |
A |
T |
7: 141,019,494 (GRCm39) |
V722D |
probably damaging |
Het |
Ppp2r2a |
G |
T |
14: 67,257,253 (GRCm39) |
H326N |
probably damaging |
Het |
Smarca5 |
G |
A |
8: 81,446,281 (GRCm39) |
T473I |
probably damaging |
Het |
Spg11 |
C |
A |
2: 121,922,773 (GRCm39) |
W892L |
probably damaging |
Het |
Tas2r110 |
T |
A |
6: 132,845,248 (GRCm39) |
I93N |
possibly damaging |
Het |
Tiam2 |
CGGG |
CGGGG |
17: 3,464,897 (GRCm39) |
|
probably null |
Het |
Vmn1r71 |
T |
A |
7: 10,482,608 (GRCm39) |
I27F |
probably benign |
Het |
Vsnl1 |
A |
G |
12: 11,376,489 (GRCm39) |
V132A |
probably benign |
Het |
Wdsub1 |
T |
C |
2: 59,708,652 (GRCm39) |
T74A |
probably damaging |
Het |
Ywhaz |
T |
C |
15: 36,791,166 (GRCm39) |
Y19C |
probably damaging |
Het |
|
Other mutations in Klri2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00672:Klri2
|
APN |
6 |
129,710,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R0137:Klri2
|
UTSW |
6 |
129,709,171 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0371:Klri2
|
UTSW |
6 |
129,709,106 (GRCm39) |
makesense |
probably null |
|
R0396:Klri2
|
UTSW |
6 |
129,717,251 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0671:Klri2
|
UTSW |
6 |
129,717,171 (GRCm39) |
missense |
probably benign |
|
R0903:Klri2
|
UTSW |
6 |
129,710,739 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1353:Klri2
|
UTSW |
6 |
129,716,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R1557:Klri2
|
UTSW |
6 |
129,709,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R1642:Klri2
|
UTSW |
6 |
129,715,837 (GRCm39) |
missense |
probably benign |
0.00 |
R2221:Klri2
|
UTSW |
6 |
129,717,272 (GRCm39) |
missense |
probably damaging |
0.99 |
R6044:Klri2
|
UTSW |
6 |
129,717,247 (GRCm39) |
missense |
probably damaging |
0.98 |
R6236:Klri2
|
UTSW |
6 |
129,715,858 (GRCm39) |
missense |
probably benign |
|
R6640:Klri2
|
UTSW |
6 |
129,709,158 (GRCm39) |
missense |
probably benign |
0.01 |
R6883:Klri2
|
UTSW |
6 |
129,709,985 (GRCm39) |
missense |
probably benign |
|
R8330:Klri2
|
UTSW |
6 |
129,710,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R8947:Klri2
|
UTSW |
6 |
129,710,742 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9268:Klri2
|
UTSW |
6 |
129,710,037 (GRCm39) |
missense |
probably damaging |
1.00 |
RF009:Klri2
|
UTSW |
6 |
129,710,737 (GRCm39) |
frame shift |
probably null |
|
|