Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp6v0e2 |
A |
G |
6: 48,517,045 (GRCm39) |
Y75C |
probably benign |
Het |
Bltp3a |
T |
C |
17: 28,096,393 (GRCm39) |
|
probably benign |
Het |
Cacna1g |
A |
G |
11: 94,324,582 (GRCm39) |
L1190P |
probably damaging |
Het |
Ccdc190 |
A |
G |
1: 169,757,586 (GRCm39) |
D15G |
probably damaging |
Het |
Cep126 |
G |
T |
9: 8,099,777 (GRCm39) |
P919Q |
possibly damaging |
Het |
Cfhr4 |
T |
A |
1: 139,660,131 (GRCm39) |
T665S |
probably damaging |
Het |
Chchd6 |
A |
G |
6: 89,361,623 (GRCm39) |
V260A |
probably benign |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cramp1 |
T |
C |
17: 25,196,514 (GRCm39) |
K867E |
probably damaging |
Het |
Dnah6 |
A |
T |
6: 73,168,602 (GRCm39) |
N440K |
probably benign |
Het |
Fbxw15 |
G |
A |
9: 109,387,314 (GRCm39) |
S227F |
probably damaging |
Het |
Gjb3 |
G |
A |
4: 127,220,224 (GRCm39) |
R103W |
probably damaging |
Het |
Gm17421 |
A |
T |
12: 113,333,334 (GRCm39) |
|
noncoding transcript |
Het |
H2bc13 |
T |
C |
13: 21,900,280 (GRCm39) |
K12E |
probably benign |
Het |
Hdac3 |
A |
G |
18: 38,087,766 (GRCm39) |
V36A |
probably damaging |
Het |
Hoxa13 |
CCG |
CCGCG |
6: 52,237,618 (GRCm39) |
|
probably null |
Het |
Itga10 |
G |
A |
3: 96,559,811 (GRCm39) |
E489K |
probably damaging |
Het |
Mgat5b |
A |
C |
11: 116,869,223 (GRCm39) |
I589L |
probably benign |
Het |
Mindy4 |
A |
G |
6: 55,232,601 (GRCm39) |
N348S |
probably benign |
Het |
Mmp15 |
A |
G |
8: 96,098,931 (GRCm39) |
D586G |
probably benign |
Het |
Mmp9 |
A |
G |
2: 164,791,247 (GRCm39) |
D139G |
probably damaging |
Het |
Morc2a |
C |
A |
11: 3,630,216 (GRCm39) |
L471I |
possibly damaging |
Het |
Mycbp2 |
T |
A |
14: 103,536,303 (GRCm39) |
|
probably benign |
Het |
Mylip |
T |
A |
13: 45,559,412 (GRCm39) |
S105T |
probably damaging |
Het |
Nat8f4 |
A |
T |
6: 85,878,406 (GRCm39) |
L39Q |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,403,157 (GRCm39) |
I210N |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,920,198 (GRCm39) |
|
probably benign |
Het |
Or10ak13 |
T |
C |
4: 118,639,579 (GRCm39) |
T68A |
probably benign |
Het |
Or11m3 |
G |
A |
15: 98,396,135 (GRCm39) |
V261M |
possibly damaging |
Het |
Or51k2 |
T |
A |
7: 103,596,589 (GRCm39) |
V272D |
possibly damaging |
Het |
Or5t7 |
T |
C |
2: 86,507,507 (GRCm39) |
M57V |
possibly damaging |
Het |
Or9k2 |
G |
T |
10: 129,999,185 (GRCm39) |
D3E |
probably benign |
Het |
Pramel29 |
T |
C |
4: 143,934,129 (GRCm39) |
D326G |
probably damaging |
Het |
Prl2c2 |
G |
C |
13: 13,176,786 (GRCm39) |
T47R |
probably damaging |
Het |
Rab11fip1 |
G |
T |
8: 27,633,388 (GRCm39) |
A1106E |
probably damaging |
Het |
Rfc1 |
A |
G |
5: 65,448,537 (GRCm39) |
S363P |
probably damaging |
Het |
Skint10 |
A |
G |
4: 112,622,228 (GRCm39) |
|
probably benign |
Het |
Spen |
T |
C |
4: 141,196,711 (GRCm39) |
N3595D |
possibly damaging |
Het |
Swsap1 |
A |
G |
9: 21,868,450 (GRCm39) |
K241E |
probably benign |
Het |
Tab1 |
A |
G |
15: 80,044,315 (GRCm39) |
T448A |
possibly damaging |
Het |
Tktl1 |
G |
T |
X: 73,241,289 (GRCm39) |
G302V |
probably damaging |
Het |
Usp25 |
A |
G |
16: 76,912,331 (GRCm39) |
T1017A |
probably benign |
Het |
Vmn2r78 |
T |
A |
7: 86,571,477 (GRCm39) |
M429K |
possibly damaging |
Het |
Wdr49 |
A |
T |
3: 75,336,640 (GRCm39) |
F356I |
probably damaging |
Het |
Wnt1 |
T |
C |
15: 98,689,764 (GRCm39) |
F184L |
probably damaging |
Het |
Zbtb39 |
A |
G |
10: 127,579,369 (GRCm39) |
I648V |
possibly damaging |
Het |
|
Other mutations in Yy1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Yy1
|
APN |
12 |
108,781,463 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02158:Yy1
|
APN |
12 |
108,780,525 (GRCm39) |
splice site |
probably benign |
|
IGL02223:Yy1
|
APN |
12 |
108,759,466 (GRCm39) |
missense |
unknown |
|
IGL02412:Yy1
|
APN |
12 |
108,760,023 (GRCm39) |
splice site |
probably benign |
|
IGL02718:Yy1
|
APN |
12 |
108,781,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Yy1
|
UTSW |
12 |
108,759,457 (GRCm39) |
missense |
unknown |
|
R1855:Yy1
|
UTSW |
12 |
108,759,916 (GRCm39) |
small insertion |
probably benign |
|
R1989:Yy1
|
UTSW |
12 |
108,772,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Yy1
|
UTSW |
12 |
108,759,916 (GRCm39) |
small insertion |
probably benign |
|
R4566:Yy1
|
UTSW |
12 |
108,778,889 (GRCm39) |
missense |
probably damaging |
0.98 |
R4717:Yy1
|
UTSW |
12 |
108,759,972 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5041:Yy1
|
UTSW |
12 |
108,759,557 (GRCm39) |
small insertion |
probably benign |
|
R5089:Yy1
|
UTSW |
12 |
108,759,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R5597:Yy1
|
UTSW |
12 |
108,781,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5907:Yy1
|
UTSW |
12 |
108,772,354 (GRCm39) |
intron |
probably benign |
|
R6876:Yy1
|
UTSW |
12 |
108,772,518 (GRCm39) |
missense |
probably benign |
0.13 |
R6878:Yy1
|
UTSW |
12 |
108,780,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R6923:Yy1
|
UTSW |
12 |
108,759,594 (GRCm39) |
missense |
probably benign |
0.28 |
R8218:Yy1
|
UTSW |
12 |
108,759,619 (GRCm39) |
missense |
probably benign |
0.00 |
R8378:Yy1
|
UTSW |
12 |
108,759,562 (GRCm39) |
missense |
unknown |
|
R8808:Yy1
|
UTSW |
12 |
108,759,506 (GRCm39) |
small deletion |
probably benign |
|
R8809:Yy1
|
UTSW |
12 |
108,759,506 (GRCm39) |
small deletion |
probably benign |
|
R9072:Yy1
|
UTSW |
12 |
108,759,921 (GRCm39) |
missense |
probably benign |
0.19 |
R9073:Yy1
|
UTSW |
12 |
108,759,921 (GRCm39) |
missense |
probably benign |
0.19 |
R9672:Yy1
|
UTSW |
12 |
108,759,584 (GRCm39) |
missense |
unknown |
|
R9749:Yy1
|
UTSW |
12 |
108,772,417 (GRCm39) |
missense |
possibly damaging |
0.95 |
|