Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
A |
T |
16: 56,507,455 (GRCm39) |
Y1091F |
probably damaging |
Het |
Arl8b |
A |
G |
6: 108,792,250 (GRCm39) |
I104V |
probably benign |
Het |
Asb2 |
C |
A |
12: 103,304,457 (GRCm39) |
G16C |
probably benign |
Het |
Bptf |
T |
C |
11: 106,945,836 (GRCm39) |
S2468G |
probably damaging |
Het |
Capns1 |
T |
A |
7: 29,889,963 (GRCm39) |
D182V |
probably damaging |
Het |
Cct5 |
T |
C |
15: 31,594,658 (GRCm39) |
H182R |
possibly damaging |
Het |
Cd200 |
G |
A |
16: 45,215,157 (GRCm39) |
R165C |
probably benign |
Het |
Chd3 |
C |
T |
11: 69,247,097 (GRCm39) |
V1024I |
probably damaging |
Het |
Chd8 |
CAGGGTCTGCCCTCATGGTATTGTATTTCTCATAGCCTAAAAGAACAAGGG |
C |
14: 52,448,037 (GRCm39) |
|
probably null |
Het |
Csmd1 |
T |
C |
8: 16,048,794 (GRCm39) |
S2303G |
probably benign |
Het |
Ctsl |
A |
G |
13: 64,514,314 (GRCm39) |
S255P |
probably damaging |
Het |
Dclre1c |
T |
G |
2: 3,444,714 (GRCm39) |
N268K |
possibly damaging |
Het |
Dock10 |
T |
C |
1: 80,521,134 (GRCm39) |
D1158G |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,757,797 (GRCm39) |
D102E |
probably benign |
Het |
Dvl3 |
T |
A |
16: 20,344,495 (GRCm39) |
D290E |
probably damaging |
Het |
Fam72a |
T |
A |
1: 131,458,461 (GRCm39) |
C74* |
probably null |
Het |
Gnrh1 |
T |
A |
14: 67,985,334 (GRCm39) |
L73Q |
probably damaging |
Het |
Grina |
T |
A |
15: 76,132,497 (GRCm39) |
S115T |
probably damaging |
Het |
Grm3 |
A |
T |
5: 9,554,725 (GRCm39) |
S856T |
probably benign |
Het |
Hars1 |
C |
A |
18: 36,899,996 (GRCm39) |
R490L |
possibly damaging |
Het |
Ide |
T |
A |
19: 37,292,241 (GRCm39) |
K318I |
|
Het |
Immt |
C |
A |
6: 71,829,762 (GRCm39) |
S156* |
probably null |
Het |
Iqcd |
A |
G |
5: 120,738,232 (GRCm39) |
I17V |
possibly damaging |
Het |
Klhdc1 |
T |
C |
12: 69,298,808 (GRCm39) |
V131A |
probably damaging |
Het |
Klk6 |
C |
A |
7: 43,478,061 (GRCm39) |
N144K |
|
Het |
Klk6 |
T |
C |
7: 43,478,062 (GRCm39) |
C145R |
probably damaging |
Het |
Lrfn2 |
A |
T |
17: 49,404,132 (GRCm39) |
T752S |
probably damaging |
Het |
Lrguk |
A |
C |
6: 34,080,572 (GRCm39) |
Q1269P |
unknown |
Het |
Lrwd1 |
G |
T |
5: 136,164,787 (GRCm39) |
Q7K |
probably benign |
Het |
Macf1 |
A |
T |
4: 123,302,204 (GRCm39) |
M766K |
probably benign |
Het |
Myo3a |
A |
T |
2: 22,245,864 (GRCm39) |
T4S |
probably benign |
Het |
Neb |
T |
C |
2: 52,084,438 (GRCm39) |
Y5587C |
probably damaging |
Het |
Nf1 |
A |
T |
11: 79,286,679 (GRCm39) |
|
probably null |
Het |
Npepps |
G |
T |
11: 97,131,823 (GRCm39) |
R344S |
probably damaging |
Het |
Nudt16l2 |
C |
T |
9: 105,021,648 (GRCm39) |
D133N |
probably damaging |
Het |
Or52p1 |
A |
T |
7: 104,267,486 (GRCm39) |
Y200F |
probably damaging |
Het |
Or5v1b |
A |
G |
17: 37,841,333 (GRCm39) |
N155S |
probably damaging |
Het |
Pcnx1 |
T |
A |
12: 82,042,597 (GRCm39) |
W2286R |
probably damaging |
Het |
Ppm1g |
A |
T |
5: 31,365,768 (GRCm39) |
N51K |
probably benign |
Het |
Ppp1r13b |
T |
C |
12: 111,799,981 (GRCm39) |
K722E |
probably damaging |
Het |
Prim1 |
A |
G |
10: 127,859,761 (GRCm39) |
S318G |
probably damaging |
Het |
Prl4a1 |
T |
C |
13: 28,207,307 (GRCm39) |
Y194H |
probably damaging |
Het |
Prl7c1 |
A |
T |
13: 27,957,854 (GRCm39) |
D195E |
probably benign |
Het |
Psmb2 |
A |
G |
4: 126,603,330 (GRCm39) |
D186G |
probably benign |
Het |
Ptprq |
A |
G |
10: 107,482,513 (GRCm39) |
V1020A |
probably benign |
Het |
Scgb2b20 |
T |
C |
7: 33,065,689 (GRCm39) |
T13A |
unknown |
Het |
Sdccag8 |
G |
A |
1: 176,783,473 (GRCm39) |
E661K |
probably damaging |
Het |
Sema4f |
G |
A |
6: 82,894,873 (GRCm39) |
L441F |
probably benign |
Het |
Sema4f |
A |
C |
6: 82,894,874 (GRCm39) |
Y440* |
probably null |
Het |
Tmem262 |
C |
T |
19: 6,130,118 (GRCm39) |
|
probably benign |
Het |
Trim33 |
A |
G |
3: 103,236,392 (GRCm39) |
T501A |
probably damaging |
Het |
Trio |
C |
A |
15: 27,741,150 (GRCm39) |
V2692F |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,772,774 (GRCm39) |
V2453E |
unknown |
Het |
Ttn |
G |
T |
2: 76,541,956 (GRCm39) |
R33677S |
probably benign |
Het |
Uaca |
T |
A |
9: 60,778,852 (GRCm39) |
S1080T |
probably benign |
Het |
Vav3 |
T |
A |
3: 109,555,051 (GRCm39) |
C660S |
probably benign |
Het |
Vmn1r229 |
T |
A |
17: 21,034,990 (GRCm39) |
D78E |
probably damaging |
Het |
Vmn2r73 |
A |
G |
7: 85,521,179 (GRCm39) |
V263A |
probably damaging |
Het |
Yeats2 |
A |
T |
16: 19,969,260 (GRCm39) |
D17V |
probably benign |
Het |
Zfp658 |
T |
A |
7: 43,222,240 (GRCm39) |
W172R |
probably benign |
Het |
Zfp804a |
A |
C |
2: 82,089,459 (GRCm39) |
H1096P |
possibly damaging |
Het |
Zkscan14 |
C |
T |
5: 145,138,375 (GRCm39) |
W37* |
probably null |
Het |
Zmynd15 |
A |
T |
11: 70,355,017 (GRCm39) |
D468V |
probably damaging |
Het |
Zmynd8 |
A |
T |
2: 165,654,466 (GRCm39) |
V682E |
probably benign |
Het |
|
Other mutations in Scly |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02314:Scly
|
APN |
1 |
91,246,763 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02690:Scly
|
APN |
1 |
91,233,047 (GRCm39) |
missense |
probably benign |
|
R0597:Scly
|
UTSW |
1 |
91,237,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Scly
|
UTSW |
1 |
91,236,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Scly
|
UTSW |
1 |
91,233,116 (GRCm39) |
missense |
probably benign |
0.08 |
R1978:Scly
|
UTSW |
1 |
91,247,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R2290:Scly
|
UTSW |
1 |
91,226,172 (GRCm39) |
critical splice donor site |
probably null |
|
R3861:Scly
|
UTSW |
1 |
91,230,573 (GRCm39) |
utr 3 prime |
probably benign |
|
R4508:Scly
|
UTSW |
1 |
91,236,047 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4876:Scly
|
UTSW |
1 |
91,247,850 (GRCm39) |
missense |
probably damaging |
0.98 |
R7035:Scly
|
UTSW |
1 |
91,236,125 (GRCm39) |
missense |
probably damaging |
0.98 |
R7701:Scly
|
UTSW |
1 |
91,236,030 (GRCm39) |
missense |
|
|
R7887:Scly
|
UTSW |
1 |
91,228,363 (GRCm39) |
critical splice donor site |
probably null |
|
R8079:Scly
|
UTSW |
1 |
91,236,089 (GRCm39) |
missense |
probably damaging |
0.99 |
R8501:Scly
|
UTSW |
1 |
91,246,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R9533:Scly
|
UTSW |
1 |
91,228,413 (GRCm39) |
intron |
probably benign |
|
X0021:Scly
|
UTSW |
1 |
91,247,828 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Scly
|
UTSW |
1 |
91,233,035 (GRCm39) |
missense |
probably benign |
0.00 |
|