Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010003K11Rik |
A |
G |
19: 4,498,264 |
W86R |
probably damaging |
Het |
Als2cr11b |
T |
A |
1: 59,004,234 |
|
noncoding transcript |
Het |
Ankrd6 |
T |
C |
4: 32,818,651 |
E225G |
probably damaging |
Het |
Armc4 |
A |
T |
18: 7,294,566 |
Y16N |
probably benign |
Het |
Atxn10 |
A |
G |
15: 85,336,584 |
|
probably null |
Het |
Bcas2 |
A |
G |
3: 103,175,635 |
I146V |
probably damaging |
Het |
Cachd1 |
G |
A |
4: 100,968,085 |
V579I |
possibly damaging |
Het |
Col11a1 |
A |
G |
3: 114,095,240 |
T311A |
unknown |
Het |
Cyp2c50 |
A |
T |
19: 40,090,616 |
L134F |
probably benign |
Het |
Cyp2j11 |
T |
C |
4: 96,307,352 |
H369R |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,097,653 |
V171A |
possibly damaging |
Het |
Dnah12 |
A |
G |
14: 26,879,738 |
N3718D |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 118,112,514 |
I541V |
probably damaging |
Het |
Eif3i |
T |
C |
4: 129,595,186 |
D86G |
probably benign |
Het |
Epc1 |
C |
T |
18: 6,490,689 |
|
probably benign |
Het |
Epc2 |
A |
G |
2: 49,513,230 |
N110S |
probably benign |
Het |
Epha8 |
A |
T |
4: 136,931,935 |
L831Q |
probably damaging |
Het |
Esd |
G |
T |
14: 74,742,113 |
R119I |
probably damaging |
Het |
F2 |
T |
C |
2: 91,634,932 |
K96E |
possibly damaging |
Het |
Fcgbp |
T |
C |
7: 28,089,734 |
V575A |
probably damaging |
Het |
Gemin6 |
T |
C |
17: 80,225,755 |
V39A |
probably damaging |
Het |
Glmp |
G |
T |
3: 88,326,655 |
|
probably benign |
Het |
Gm10306 |
C |
A |
4: 94,556,807 |
|
probably benign |
Het |
Gm4846 |
A |
T |
1: 166,497,453 |
L23* |
probably null |
Het |
Gm7102 |
C |
T |
19: 61,175,926 |
G24R |
unknown |
Het |
Grik1 |
CGG |
CGGG |
16: 87,923,194 |
|
probably null |
Het |
Ifi203 |
T |
C |
1: 173,926,919 |
T749A |
possibly damaging |
Het |
Kcnip2 |
C |
A |
19: 45,794,246 |
A133S |
probably benign |
Het |
Limch1 |
A |
T |
5: 66,881,957 |
I76F |
probably damaging |
Het |
Mcph1 |
T |
A |
8: 18,689,061 |
|
probably null |
Het |
Myh7 |
A |
G |
14: 54,986,563 |
|
probably benign |
Het |
Olfr11 |
A |
C |
13: 21,638,779 |
V248G |
probably damaging |
Het |
Olfr1106 |
T |
G |
2: 87,049,165 |
K24Q |
probably damaging |
Het |
Olfr346 |
A |
T |
2: 36,688,094 |
I31F |
probably benign |
Het |
Olfr54 |
A |
C |
11: 51,027,334 |
N111H |
probably benign |
Het |
Olfr583 |
A |
C |
7: 103,051,535 |
D79A |
probably damaging |
Het |
Olfr601 |
A |
C |
7: 103,358,522 |
L224R |
probably damaging |
Het |
Olfr700 |
A |
C |
7: 106,805,734 |
S243A |
probably damaging |
Het |
Opcml |
A |
G |
9: 28,675,325 |
D113G |
possibly damaging |
Het |
Pcdhb1 |
G |
T |
18: 37,267,255 |
C753F |
probably benign |
Het |
Phip |
T |
C |
9: 82,900,756 |
S879G |
possibly damaging |
Het |
Pi4k2b |
A |
G |
5: 52,741,756 |
D13G |
possibly damaging |
Het |
Ptpn18 |
A |
T |
1: 34,463,178 |
I68F |
probably damaging |
Het |
Rnf168 |
C |
T |
16: 32,298,584 |
T321I |
possibly damaging |
Het |
Soga3 |
A |
T |
10: 29,147,106 |
I150L |
probably benign |
Het |
Sp110 |
C |
G |
1: 85,589,118 |
E219D |
probably damaging |
Het |
Srgap1 |
C |
T |
10: 121,785,377 |
|
probably benign |
Het |
Sry |
A |
T |
Y: 2,663,647 |
H4Q |
probably benign |
Het |
Taf2 |
G |
A |
15: 55,045,740 |
A703V |
probably benign |
Het |
Taf5l |
A |
G |
8: 124,003,651 |
F65L |
probably damaging |
Het |
Tcp10b |
T |
C |
17: 13,063,067 |
|
probably null |
Het |
Timm44 |
A |
T |
8: 4,266,814 |
I273N |
probably damaging |
Het |
Tspan4 |
A |
G |
7: 141,489,615 |
T43A |
probably damaging |
Het |
Ube2r2 |
T |
C |
4: 41,190,846 |
|
probably benign |
Het |
Urgcp |
T |
C |
11: 5,717,754 |
T195A |
possibly damaging |
Het |
Vmn1r197 |
T |
C |
13: 22,328,191 |
I94T |
probably damaging |
Het |
Vmn2r15 |
A |
T |
5: 109,286,807 |
I677K |
probably damaging |
Het |
Zfp853 |
T |
A |
5: 143,288,563 |
H434L |
unknown |
Het |
|