Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,969,808 |
|
probably benign |
Het |
Abi3 |
T |
C |
11: 95,833,634 |
|
probably benign |
Het |
Adam2 |
T |
C |
14: 66,057,646 |
N250S |
probably damaging |
Het |
Agbl4 |
T |
A |
4: 111,657,388 |
I532K |
probably benign |
Het |
Agrn |
T |
G |
4: 156,174,453 |
E905A |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,970,843 |
|
probably benign |
Het |
Aifm2 |
A |
G |
10: 61,726,452 |
N89S |
probably benign |
Het |
Arsj |
C |
T |
3: 126,438,184 |
T193I |
probably damaging |
Het |
Ascc2 |
T |
A |
11: 4,682,933 |
V702E |
probably damaging |
Het |
Avpr1b |
T |
C |
1: 131,600,281 |
S181P |
probably damaging |
Het |
Bcl7a |
G |
A |
5: 123,351,940 |
V56I |
possibly damaging |
Het |
Cd160 |
T |
A |
3: 96,805,786 |
D54V |
probably damaging |
Het |
Celsr2 |
C |
A |
3: 108,414,977 |
R173M |
probably damaging |
Het |
Cfap57 |
A |
G |
4: 118,569,727 |
|
probably benign |
Het |
Cfap69 |
G |
A |
5: 5,663,951 |
T27I |
probably damaging |
Het |
Chaf1b |
T |
C |
16: 93,900,017 |
|
probably benign |
Het |
Cldn8 |
C |
T |
16: 88,562,639 |
V133M |
probably damaging |
Het |
Col2a1 |
A |
T |
15: 97,980,192 |
V954E |
unknown |
Het |
Col6a4 |
T |
C |
9: 106,028,187 |
|
probably benign |
Het |
Col6a6 |
T |
C |
9: 105,709,486 |
M1779V |
probably benign |
Het |
Coq8b |
A |
G |
7: 27,242,249 |
E253G |
probably benign |
Het |
Ctse |
T |
C |
1: 131,674,778 |
|
probably benign |
Het |
Cyp2c29 |
T |
A |
19: 39,309,726 |
N238K |
probably benign |
Het |
Dcaf1 |
T |
A |
9: 106,846,649 |
|
probably benign |
Het |
Dcc |
A |
T |
18: 71,809,204 |
|
probably benign |
Het |
Dkk1 |
A |
G |
19: 30,549,345 |
F12S |
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,129,474 |
V1760A |
probably benign |
Het |
Fam117b |
G |
A |
1: 59,958,353 |
S288N |
possibly damaging |
Het |
Fam216a |
A |
T |
5: 122,367,646 |
M110K |
probably damaging |
Het |
Frem3 |
T |
A |
8: 80,613,952 |
I958N |
possibly damaging |
Het |
Gab1 |
T |
A |
8: 80,800,116 |
N118Y |
probably damaging |
Het |
Gda |
T |
A |
19: 21,409,887 |
I251L |
probably benign |
Het |
Gli2 |
C |
A |
1: 118,844,460 |
R505L |
probably damaging |
Het |
Gpnmb |
C |
T |
6: 49,048,015 |
S327L |
probably benign |
Het |
Gpr156 |
T |
A |
16: 37,992,141 |
Y280N |
probably damaging |
Het |
Gria4 |
A |
G |
9: 4,427,071 |
Y790H |
probably damaging |
Het |
Guf1 |
C |
A |
5: 69,566,352 |
|
probably null |
Het |
H6pd |
T |
C |
4: 149,982,573 |
E452G |
possibly damaging |
Het |
Herc1 |
T |
A |
9: 66,386,838 |
Y487* |
probably null |
Het |
Ifi30 |
T |
A |
8: 70,764,949 |
|
probably benign |
Het |
Klf13 |
G |
A |
7: 63,938,071 |
A159V |
possibly damaging |
Het |
Med11 |
T |
A |
11: 70,453,226 |
M124K |
possibly damaging |
Het |
Myom3 |
A |
G |
4: 135,788,426 |
|
probably benign |
Het |
Nat2 |
A |
T |
8: 67,501,804 |
I189F |
probably damaging |
Het |
Nhlrc4 |
C |
G |
17: 25,943,684 |
G30R |
probably damaging |
Het |
Nkx3-2 |
G |
A |
5: 41,762,127 |
R173C |
probably damaging |
Het |
Nox3 |
T |
C |
17: 3,695,564 |
N23S |
probably damaging |
Het |
Npr2 |
A |
T |
4: 43,646,991 |
Y708F |
probably damaging |
Het |
Nsun2 |
A |
G |
13: 69,629,542 |
N409S |
probably benign |
Het |
Nucb2 |
T |
C |
7: 116,535,851 |
|
probably benign |
Het |
Olfr1105 |
A |
G |
2: 87,033,882 |
F113S |
probably damaging |
Het |
Olfr541 |
T |
C |
7: 140,704,787 |
F179L |
possibly damaging |
Het |
Olfr874 |
T |
C |
9: 37,746,217 |
F28L |
probably benign |
Het |
Orai2 |
A |
T |
5: 136,161,599 |
V52D |
probably damaging |
Het |
Pcyox1 |
A |
T |
6: 86,394,442 |
M154K |
probably damaging |
Het |
Pik3r4 |
C |
A |
9: 105,653,976 |
T492K |
possibly damaging |
Het |
Pmpca |
T |
A |
2: 26,391,097 |
Y150N |
probably damaging |
Het |
Ppp1r12b |
G |
T |
1: 134,876,082 |
S446R |
probably damaging |
Het |
Ptpdc1 |
A |
G |
13: 48,586,905 |
I289T |
probably benign |
Het |
Pyroxd2 |
A |
G |
19: 42,727,642 |
|
probably benign |
Het |
Qrfpr |
G |
A |
3: 36,189,559 |
T131M |
probably damaging |
Het |
Rab33b |
A |
G |
3: 51,493,417 |
Y104C |
probably damaging |
Het |
Rad54l |
G |
T |
4: 116,099,750 |
|
probably benign |
Het |
Rad9a |
A |
T |
19: 4,197,360 |
|
probably null |
Het |
Slc1a5 |
A |
T |
7: 16,786,904 |
M233L |
probably benign |
Het |
Slc47a2 |
C |
T |
11: 61,342,504 |
V67I |
possibly damaging |
Het |
Slco1a5 |
T |
A |
6: 142,268,278 |
Y39F |
probably benign |
Het |
Slfn5 |
T |
C |
11: 82,961,403 |
V785A |
probably damaging |
Het |
Sp6 |
C |
T |
11: 97,021,544 |
P28S |
possibly damaging |
Het |
Sptbn5 |
A |
G |
2: 120,062,675 |
|
probably null |
Het |
Sry |
ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
Y: 2,662,944 |
|
probably benign |
Het |
St8sia1 |
A |
G |
6: 142,829,254 |
W200R |
probably damaging |
Het |
Stxbp1 |
C |
A |
2: 32,800,695 |
|
probably benign |
Het |
Syne1 |
A |
G |
10: 5,033,138 |
|
probably benign |
Het |
Thbs3 |
T |
A |
3: 89,220,165 |
I371N |
possibly damaging |
Het |
Tll1 |
C |
T |
8: 64,074,290 |
S399N |
probably damaging |
Het |
Tmem209 |
A |
C |
6: 30,505,834 |
C114G |
probably null |
Het |
Tmem25 |
C |
T |
9: 44,795,514 |
|
probably benign |
Het |
Tmem8b |
T |
C |
4: 43,674,562 |
I282T |
possibly damaging |
Het |
Trdmt1 |
T |
A |
2: 13,544,580 |
H18L |
probably benign |
Het |
Trim63 |
A |
G |
4: 134,316,405 |
T60A |
probably benign |
Het |
Trpv2 |
T |
C |
11: 62,584,676 |
|
probably null |
Het |
Ubr2 |
A |
T |
17: 46,938,653 |
I1591K |
probably damaging |
Het |
Use1 |
A |
T |
8: 71,367,065 |
|
probably benign |
Het |
Zfp850 |
A |
T |
7: 27,985,217 |
C35S |
possibly damaging |
Het |
|