Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700009N14Rik |
A |
T |
4: 39,451,201 (GRCm39) |
I136F |
possibly damaging |
Het |
Abca13 |
A |
T |
11: 9,247,915 (GRCm39) |
K2554M |
probably damaging |
Het |
Ankrd12 |
C |
T |
17: 66,291,225 (GRCm39) |
D1403N |
possibly damaging |
Het |
Ankrd17 |
A |
G |
5: 90,408,011 (GRCm39) |
V1402A |
possibly damaging |
Het |
Ankrd36 |
A |
T |
11: 5,585,176 (GRCm39) |
N329I |
possibly damaging |
Het |
Atr |
A |
T |
9: 95,756,233 (GRCm39) |
D815V |
probably damaging |
Het |
C9orf72 |
T |
C |
4: 35,192,997 (GRCm39) |
D444G |
unknown |
Het |
Ceacam1 |
T |
C |
7: 25,173,375 (GRCm39) |
Y271C |
probably damaging |
Het |
Cenpo |
T |
C |
12: 4,264,597 (GRCm39) |
H265R |
probably benign |
Het |
Chd8 |
G |
A |
14: 52,463,539 (GRCm39) |
R702W |
probably damaging |
Het |
Ckap5 |
A |
G |
2: 91,389,455 (GRCm39) |
N309S |
probably benign |
Het |
Cxxc1 |
C |
T |
18: 74,350,855 (GRCm39) |
R83C |
probably damaging |
Het |
Dcaf6 |
T |
C |
1: 165,227,284 (GRCm39) |
D281G |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,717,754 (GRCm39) |
T584A |
probably damaging |
Het |
Drgx |
T |
A |
14: 32,350,845 (GRCm39) |
L227Q |
probably damaging |
Het |
Dync2h1 |
G |
T |
9: 7,114,914 (GRCm39) |
H2415N |
probably damaging |
Het |
Dzip1l |
A |
G |
9: 99,543,015 (GRCm39) |
E490G |
possibly damaging |
Het |
Fam124a |
T |
C |
14: 62,843,526 (GRCm39) |
S345P |
probably benign |
Het |
Fam83b |
G |
A |
9: 76,399,330 (GRCm39) |
T591I |
probably benign |
Het |
Frem1 |
T |
C |
4: 82,907,401 (GRCm39) |
S838G |
probably benign |
Het |
Fsip2 |
G |
T |
2: 82,818,723 (GRCm39) |
D4819Y |
probably benign |
Het |
Gm43302 |
T |
G |
5: 105,425,691 (GRCm39) |
K246T |
probably benign |
Het |
Gml |
T |
C |
15: 74,685,462 (GRCm39) |
|
probably benign |
Het |
Gpc1 |
A |
T |
1: 92,781,171 (GRCm39) |
H90L |
probably benign |
Het |
Grik3 |
T |
C |
4: 125,579,812 (GRCm39) |
L519P |
probably damaging |
Het |
Grwd1 |
A |
G |
7: 45,475,438 (GRCm39) |
V368A |
probably damaging |
Het |
Gstm3 |
G |
A |
3: 107,876,555 (GRCm39) |
|
probably benign |
Het |
Gtpbp6 |
A |
G |
5: 110,252,252 (GRCm39) |
S427P |
probably damaging |
Het |
Heatr5b |
C |
T |
17: 79,126,252 (GRCm39) |
G560E |
probably damaging |
Het |
Heatr9 |
A |
G |
11: 83,409,019 (GRCm39) |
V176A |
probably damaging |
Het |
Ints3 |
G |
T |
3: 90,307,720 (GRCm39) |
Q660K |
probably benign |
Het |
Itpr2 |
A |
T |
6: 146,126,274 (GRCm39) |
L2048Q |
probably damaging |
Het |
Kcnq1 |
G |
A |
7: 142,660,342 (GRCm39) |
|
probably null |
Het |
Lsm12 |
A |
T |
11: 102,055,995 (GRCm39) |
|
probably null |
Het |
Mcoln3 |
A |
G |
3: 145,845,247 (GRCm39) |
Y481C |
probably damaging |
Het |
Meis3 |
A |
G |
7: 15,916,322 (GRCm39) |
N266D |
probably benign |
Het |
Mgat5 |
G |
A |
1: 127,339,941 (GRCm39) |
E441K |
probably benign |
Het |
Mroh6 |
C |
T |
15: 75,756,089 (GRCm39) |
R689H |
probably benign |
Het |
Mtg1 |
T |
C |
7: 139,729,662 (GRCm39) |
Y251H |
probably damaging |
Het |
Mtus2 |
A |
T |
5: 148,014,998 (GRCm39) |
Q597L |
probably benign |
Het |
Myt1 |
A |
G |
2: 181,439,390 (GRCm39) |
E346G |
probably benign |
Het |
Nat8f4 |
A |
G |
6: 85,877,873 (GRCm39) |
S217P |
probably benign |
Het |
Ngf |
G |
A |
3: 102,417,140 (GRCm39) |
G17R |
unknown |
Het |
Or7e171-ps1 |
A |
T |
9: 19,852,980 (GRCm39) |
M252K |
unknown |
Het |
Pam |
T |
C |
1: 97,749,572 (GRCm39) |
Y968C |
probably damaging |
Het |
Pcdhga7 |
T |
A |
18: 37,847,996 (GRCm39) |
M1K |
probably null |
Het |
Pde8b |
G |
T |
13: 95,170,679 (GRCm39) |
D554E |
probably benign |
Het |
Pdzd7 |
G |
A |
19: 45,033,962 (GRCm39) |
R41* |
probably null |
Het |
Pkhd1l1 |
C |
T |
15: 44,441,977 (GRCm39) |
P3639S |
probably damaging |
Het |
Plce1 |
A |
T |
19: 38,769,140 (GRCm39) |
E2280V |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,804,257 (GRCm39) |
I538V |
probably benign |
Het |
Scaf11 |
A |
G |
15: 96,316,942 (GRCm39) |
L874P |
possibly damaging |
Het |
Scpep1 |
G |
T |
11: 88,824,347 (GRCm39) |
D307E |
possibly damaging |
Het |
Septin4 |
A |
G |
11: 87,480,065 (GRCm39) |
E327G |
probably damaging |
Het |
Skint2 |
T |
G |
4: 112,473,751 (GRCm39) |
V11G |
possibly damaging |
Het |
Slc26a4 |
T |
C |
12: 31,594,482 (GRCm39) |
N289D |
probably damaging |
Het |
Slc35f3 |
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CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
8: 127,115,777 (GRCm39) |
|
probably benign |
Het |
Slx4 |
T |
C |
16: 3,804,846 (GRCm39) |
E656G |
probably benign |
Het |
Socs5 |
T |
C |
17: 87,441,791 (GRCm39) |
S244P |
probably benign |
Het |
Spata31h1 |
C |
T |
10: 82,123,329 (GRCm39) |
C3227Y |
probably benign |
Het |
Speer1e |
C |
A |
5: 11,234,185 (GRCm39) |
H30Q |
probably benign |
Het |
Stt3b |
A |
C |
9: 115,105,887 (GRCm39) |
L196R |
probably damaging |
Het |
Syne2 |
T |
A |
12: 75,975,877 (GRCm39) |
|
probably null |
Het |
Tab2 |
T |
A |
10: 7,796,188 (GRCm39) |
N24I |
probably damaging |
Het |
Taf4b |
T |
C |
18: 14,946,331 (GRCm39) |
S385P |
probably damaging |
Het |
Tg |
T |
C |
15: 66,721,453 (GRCm39) |
Y2720H |
probably damaging |
Het |
Tjap1 |
C |
T |
17: 46,569,616 (GRCm39) |
G448E |
probably benign |
Het |
Tll1 |
A |
T |
8: 64,478,271 (GRCm39) |
C827* |
probably null |
Het |
Tlr11 |
T |
A |
14: 50,599,382 (GRCm39) |
I456K |
probably benign |
Het |
Tmem209 |
T |
C |
6: 30,497,854 (GRCm39) |
D305G |
probably damaging |
Het |
Tmem82 |
A |
T |
4: 141,345,035 (GRCm39) |
|
probably null |
Het |
Tnfrsf14 |
A |
G |
4: 155,007,750 (GRCm39) |
V207A |
probably benign |
Het |
Tnks |
A |
T |
8: 35,328,694 (GRCm39) |
N625K |
probably benign |
Het |
Tomm20 |
G |
A |
8: 127,666,700 (GRCm39) |
P58S |
possibly damaging |
Het |
Ttc9b |
A |
G |
7: 27,353,761 (GRCm39) |
D137G |
probably benign |
Het |
Ulk4 |
C |
T |
9: 121,092,734 (GRCm39) |
E168K |
possibly damaging |
Het |
Usp9y |
T |
A |
Y: 1,444,573 (GRCm39) |
D122V |
probably damaging |
Het |
Vps41 |
C |
A |
13: 19,026,438 (GRCm39) |
T512K |
possibly damaging |
Het |
Wdr49 |
T |
A |
3: 75,182,335 (GRCm39) |
N698I |
probably benign |
Het |
Zfp568 |
G |
A |
7: 29,722,150 (GRCm39) |
C365Y |
probably damaging |
Het |
Zfp663 |
A |
T |
2: 165,194,453 (GRCm39) |
C589S |
probably damaging |
Het |
Zfp971 |
A |
G |
2: 177,675,292 (GRCm39) |
K297R |
probably damaging |
Het |
Zkscan16 |
G |
T |
4: 58,951,843 (GRCm39) |
E173* |
probably null |
Het |
|
Other mutations in Hsf2bp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01134:Hsf2bp
|
APN |
17 |
32,206,378 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03274:Hsf2bp
|
APN |
17 |
32,226,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R0563:Hsf2bp
|
UTSW |
17 |
32,226,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Hsf2bp
|
UTSW |
17 |
32,232,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R0960:Hsf2bp
|
UTSW |
17 |
32,226,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Hsf2bp
|
UTSW |
17 |
32,206,378 (GRCm39) |
nonsense |
probably null |
|
R4375:Hsf2bp
|
UTSW |
17 |
32,206,322 (GRCm39) |
missense |
probably null |
1.00 |
R4567:Hsf2bp
|
UTSW |
17 |
32,165,708 (GRCm39) |
missense |
probably benign |
0.01 |
R5510:Hsf2bp
|
UTSW |
17 |
32,165,721 (GRCm39) |
missense |
unknown |
|
R5546:Hsf2bp
|
UTSW |
17 |
32,165,669 (GRCm39) |
missense |
probably damaging |
0.98 |
R5988:Hsf2bp
|
UTSW |
17 |
32,230,149 (GRCm39) |
critical splice donor site |
probably null |
|
R7026:Hsf2bp
|
UTSW |
17 |
32,252,254 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7459:Hsf2bp
|
UTSW |
17 |
32,165,708 (GRCm39) |
missense |
probably benign |
0.01 |
R7944:Hsf2bp
|
UTSW |
17 |
32,226,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R8781:Hsf2bp
|
UTSW |
17 |
32,252,241 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9130:Hsf2bp
|
UTSW |
17 |
32,230,082 (GRCm39) |
intron |
probably benign |
|
R9275:Hsf2bp
|
UTSW |
17 |
32,206,336 (GRCm39) |
nonsense |
probably null |
|
R9588:Hsf2bp
|
UTSW |
17 |
32,241,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|