Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
G |
12: 71,211,189 (GRCm39) |
D641G |
possibly damaging |
Het |
4921539E11Rik |
T |
C |
4: 103,092,666 (GRCm39) |
E272G |
unknown |
Het |
Abca16 |
C |
T |
7: 120,065,023 (GRCm39) |
T560I |
possibly damaging |
Het |
Adcy3 |
A |
G |
12: 4,259,455 (GRCm39) |
R911G |
probably damaging |
Het |
Adgra2 |
A |
G |
8: 27,612,031 (GRCm39) |
T1327A |
possibly damaging |
Het |
Aldh9a1 |
T |
C |
1: 167,184,904 (GRCm39) |
V272A |
possibly damaging |
Het |
Ankfn1 |
T |
A |
11: 89,396,167 (GRCm39) |
H193L |
probably benign |
Het |
Asb1 |
A |
G |
1: 91,480,116 (GRCm39) |
R280G |
probably benign |
Het |
Atg14 |
G |
T |
14: 47,788,780 (GRCm39) |
A191E |
probably damaging |
Het |
Bcl9 |
G |
T |
3: 97,112,960 (GRCm39) |
P1165Q |
possibly damaging |
Het |
Cdk8 |
G |
A |
5: 146,235,664 (GRCm39) |
A264T |
probably damaging |
Het |
Cep152 |
G |
A |
2: 125,406,150 (GRCm39) |
Q1461* |
probably null |
Het |
Cep170b |
G |
T |
12: 112,704,045 (GRCm39) |
W659L |
probably damaging |
Het |
Cep57l1 |
T |
C |
10: 41,597,626 (GRCm39) |
E335G |
probably damaging |
Het |
Cpt1b |
T |
A |
15: 89,303,229 (GRCm39) |
T609S |
possibly damaging |
Het |
Cyp2c50 |
A |
T |
19: 40,086,512 (GRCm39) |
I359F |
probably damaging |
Het |
Dpf1 |
T |
A |
7: 29,013,742 (GRCm39) |
N272K |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,821,984 (GRCm39) |
T5906A |
possibly damaging |
Het |
Gin1 |
A |
T |
1: 97,712,498 (GRCm39) |
R220S |
probably benign |
Het |
Gm30083 |
T |
C |
14: 33,736,861 (GRCm39) |
Y32C |
probably benign |
Het |
Gm45861 |
A |
G |
8: 27,994,083 (GRCm39) |
E445G |
unknown |
Het |
Golga2 |
T |
C |
2: 32,193,874 (GRCm39) |
S567P |
probably damaging |
Het |
Gpr89 |
A |
G |
3: 96,780,813 (GRCm39) |
V353A |
probably damaging |
Het |
Grin2d |
T |
C |
7: 45,506,948 (GRCm39) |
K509R |
possibly damaging |
Het |
Hip1r |
T |
C |
5: 124,139,319 (GRCm39) |
I904T |
probably damaging |
Het |
Ikbke |
T |
A |
1: 131,187,022 (GRCm39) |
|
probably null |
Het |
Il1r1 |
T |
A |
1: 40,341,532 (GRCm39) |
C315S |
probably damaging |
Het |
Ireb2 |
T |
A |
9: 54,789,730 (GRCm39) |
F135I |
possibly damaging |
Het |
Jakmip3 |
C |
T |
7: 138,621,915 (GRCm39) |
L272F |
probably damaging |
Het |
Kntc1 |
T |
A |
5: 123,949,440 (GRCm39) |
F1937Y |
probably damaging |
Het |
Krtap4-16 |
G |
A |
11: 99,742,271 (GRCm39) |
T43I |
unknown |
Het |
Lats2 |
A |
G |
14: 57,936,875 (GRCm39) |
V538A |
possibly damaging |
Het |
Megf8 |
T |
A |
7: 25,046,907 (GRCm39) |
W1597R |
probably damaging |
Het |
Mideas |
A |
T |
12: 84,219,885 (GRCm39) |
D356E |
probably benign |
Het |
Mtus2 |
A |
T |
5: 148,014,025 (GRCm39) |
T273S |
probably benign |
Het |
Nsun6 |
T |
A |
2: 15,047,106 (GRCm39) |
E81D |
probably benign |
Het |
Or13c7 |
G |
A |
4: 43,855,183 (GRCm39) |
M291I |
probably benign |
Het |
Or4c125 |
A |
T |
2: 89,170,517 (GRCm39) |
I43K |
probably damaging |
Het |
Or56a41 |
A |
G |
7: 104,740,445 (GRCm39) |
F134L |
probably benign |
Het |
Or8c10 |
A |
G |
9: 38,278,912 (GRCm39) |
I13M |
probably damaging |
Het |
Or8k23 |
A |
G |
2: 86,186,408 (GRCm39) |
F106S |
probably benign |
Het |
Oxsm |
T |
C |
14: 16,241,000 (GRCm38) |
T350A |
probably damaging |
Het |
Pard3 |
G |
A |
8: 128,115,900 (GRCm39) |
R663Q |
possibly damaging |
Het |
Pcdh15 |
T |
A |
10: 74,479,335 (GRCm39) |
I482N |
probably benign |
Het |
Pcsk2 |
G |
A |
2: 143,655,501 (GRCm39) |
D562N |
probably damaging |
Het |
Pdzk1ip1 |
T |
C |
4: 114,950,177 (GRCm39) |
M146T |
probably benign |
Het |
Plch1 |
T |
A |
3: 63,660,747 (GRCm39) |
T279S |
|
Het |
Plec |
C |
T |
15: 76,058,177 (GRCm39) |
R3920Q |
probably damaging |
Het |
Polr2g |
A |
T |
19: 8,774,631 (GRCm39) |
V84E |
probably damaging |
Het |
Ppp2r2c |
G |
T |
5: 37,080,383 (GRCm39) |
V48L |
probably damaging |
Het |
Pramel25 |
T |
A |
4: 143,521,855 (GRCm39) |
C490* |
probably null |
Het |
Prcp |
A |
T |
7: 92,524,598 (GRCm39) |
T18S |
probably benign |
Het |
Rapsn |
A |
G |
2: 90,872,268 (GRCm39) |
S201G |
probably damaging |
Het |
Rragd |
A |
G |
4: 33,012,998 (GRCm39) |
T332A |
probably benign |
Het |
Scrn2 |
A |
G |
11: 96,921,342 (GRCm39) |
D34G |
probably damaging |
Het |
Serpinb6c |
T |
C |
13: 34,079,303 (GRCm39) |
T130A |
probably benign |
Het |
Setd1b |
G |
A |
5: 123,298,401 (GRCm39) |
G1479D |
probably damaging |
Het |
Shd |
T |
A |
17: 56,283,268 (GRCm39) |
L299Q |
probably damaging |
Het |
Slc5a4b |
C |
T |
10: 75,945,896 (GRCm39) |
V55I |
probably benign |
Het |
Smg1 |
C |
A |
7: 117,755,933 (GRCm39) |
R2405L |
unknown |
Het |
Stxbp2 |
A |
T |
8: 3,686,392 (GRCm39) |
M332L |
|
Het |
Tedc2 |
A |
G |
17: 24,435,328 (GRCm39) |
C354R |
probably benign |
Het |
Tek |
A |
T |
4: 94,692,523 (GRCm39) |
R210S |
possibly damaging |
Het |
Tnk2 |
T |
A |
16: 32,489,018 (GRCm39) |
M286K |
probably damaging |
Het |
Ttc21a |
G |
A |
9: 119,771,686 (GRCm39) |
V162I |
probably benign |
Het |
Usf3 |
T |
A |
16: 44,042,170 (GRCm39) |
C2217S |
possibly damaging |
Het |
Wdr72 |
C |
T |
9: 74,118,041 (GRCm39) |
P930S |
probably damaging |
Het |
Zan |
A |
G |
5: 137,456,812 (GRCm39) |
V1308A |
unknown |
Het |
Zfp521 |
C |
T |
18: 13,978,922 (GRCm39) |
R497Q |
probably damaging |
Het |
Zfp799 |
T |
A |
17: 33,039,435 (GRCm39) |
K277M |
probably damaging |
Het |
Zfp949 |
C |
T |
9: 88,436,500 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ppm1m |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02003:Ppm1m
|
APN |
9 |
106,076,356 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02090:Ppm1m
|
APN |
9 |
106,074,001 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02644:Ppm1m
|
APN |
9 |
106,074,082 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02691:Ppm1m
|
APN |
9 |
106,072,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03094:Ppm1m
|
APN |
9 |
106,073,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Ppm1m
|
UTSW |
9 |
106,073,895 (GRCm39) |
nonsense |
probably null |
|
R0047:Ppm1m
|
UTSW |
9 |
106,073,895 (GRCm39) |
nonsense |
probably null |
|
R0361:Ppm1m
|
UTSW |
9 |
106,075,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R0452:Ppm1m
|
UTSW |
9 |
106,074,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3053:Ppm1m
|
UTSW |
9 |
106,075,874 (GRCm39) |
missense |
probably benign |
|
R4654:Ppm1m
|
UTSW |
9 |
106,073,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5121:Ppm1m
|
UTSW |
9 |
106,073,004 (GRCm39) |
missense |
probably benign |
0.03 |
R5450:Ppm1m
|
UTSW |
9 |
106,074,041 (GRCm39) |
missense |
probably benign |
0.02 |
R5516:Ppm1m
|
UTSW |
9 |
106,075,138 (GRCm39) |
missense |
probably damaging |
0.98 |
R6278:Ppm1m
|
UTSW |
9 |
106,074,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R6533:Ppm1m
|
UTSW |
9 |
106,074,069 (GRCm39) |
unclassified |
probably benign |
|
R6746:Ppm1m
|
UTSW |
9 |
106,075,351 (GRCm39) |
nonsense |
probably null |
|
R7466:Ppm1m
|
UTSW |
9 |
106,073,356 (GRCm39) |
missense |
probably damaging |
0.99 |
R7486:Ppm1m
|
UTSW |
9 |
106,073,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Ppm1m
|
UTSW |
9 |
106,075,895 (GRCm39) |
missense |
probably benign |
|
R7936:Ppm1m
|
UTSW |
9 |
106,075,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R8815:Ppm1m
|
UTSW |
9 |
106,076,237 (GRCm39) |
unclassified |
probably benign |
|
X0022:Ppm1m
|
UTSW |
9 |
106,075,321 (GRCm39) |
nonsense |
probably null |
|
|