Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef39 |
A |
G |
4: 43,497,590 (GRCm39) |
L222P |
probably damaging |
Het |
Art3 |
T |
A |
5: 92,551,473 (GRCm39) |
Y17* |
probably null |
Het |
Cadps2 |
A |
G |
6: 23,355,851 (GRCm39) |
L859P |
probably damaging |
Het |
Celsr2 |
A |
G |
3: 108,322,159 (GRCm39) |
Y218H |
probably damaging |
Het |
Ces5a |
A |
G |
8: 94,228,847 (GRCm39) |
V461A |
probably damaging |
Het |
Clic4 |
C |
A |
4: 134,966,204 (GRCm39) |
V51L |
probably benign |
Het |
Col6a3 |
A |
G |
1: 90,730,236 (GRCm39) |
L1083P |
probably damaging |
Het |
Cul5 |
T |
C |
9: 53,546,307 (GRCm39) |
E328G |
probably damaging |
Het |
Erap1 |
T |
C |
13: 74,812,350 (GRCm39) |
|
probably benign |
Het |
Fn1 |
G |
A |
1: 71,645,900 (GRCm39) |
P1527L |
probably damaging |
Het |
Gm20547 |
T |
A |
17: 35,100,631 (GRCm39) |
Q63L |
probably benign |
Het |
Gm5089 |
T |
C |
14: 122,673,575 (GRCm39) |
T49A |
unknown |
Het |
Ippk |
T |
C |
13: 49,602,740 (GRCm39) |
L362S |
probably damaging |
Het |
Krt23 |
T |
C |
11: 99,377,593 (GRCm39) |
M138V |
probably benign |
Het |
Magi3 |
A |
G |
3: 104,013,037 (GRCm39) |
|
probably benign |
Het |
Mcc |
T |
A |
18: 44,624,223 (GRCm39) |
I266F |
probably benign |
Het |
Mcph1 |
A |
G |
8: 18,681,535 (GRCm39) |
E224G |
probably damaging |
Het |
Neurod4 |
A |
T |
10: 130,106,887 (GRCm39) |
L129H |
probably damaging |
Het |
Or14j5 |
T |
A |
17: 37,920,853 (GRCm39) |
D263V |
probably damaging |
Het |
Or4c123 |
T |
A |
2: 89,127,014 (GRCm39) |
N200I |
probably damaging |
Het |
Or5b24 |
T |
C |
19: 12,912,926 (GRCm39) |
S275P |
probably damaging |
Het |
Or8h7 |
T |
C |
2: 86,721,093 (GRCm39) |
Y142C |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,160,630 (GRCm39) |
I2342N |
probably damaging |
Het |
Pnpt1 |
A |
G |
11: 29,105,787 (GRCm39) |
Q632R |
probably benign |
Het |
Ppp2r2c |
T |
C |
5: 37,097,570 (GRCm39) |
M252T |
possibly damaging |
Het |
Ppp4r2 |
A |
G |
6: 100,841,644 (GRCm39) |
N142D |
possibly damaging |
Het |
Prex2 |
G |
T |
1: 11,240,965 (GRCm39) |
K1024N |
probably damaging |
Het |
Rimklb |
T |
A |
6: 122,436,129 (GRCm39) |
I150F |
probably damaging |
Het |
Slco4c1 |
T |
C |
1: 96,770,218 (GRCm39) |
Q282R |
probably damaging |
Het |
Tmem92 |
T |
C |
11: 94,669,519 (GRCm39) |
E148G |
probably damaging |
Het |
Traf7 |
T |
C |
17: 24,729,349 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
G |
A |
15: 37,998,623 (GRCm39) |
T1622M |
probably damaging |
Het |
Vmn1r5 |
T |
A |
6: 56,962,911 (GRCm39) |
S195R |
probably damaging |
Het |
Vmn2r67 |
C |
T |
7: 84,785,651 (GRCm39) |
V785I |
probably damaging |
Het |
Zfp184 |
T |
C |
13: 22,134,395 (GRCm39) |
|
probably benign |
Het |
Zfp654 |
T |
C |
16: 64,605,004 (GRCm39) |
N525S |
probably benign |
Het |
|
Other mutations in Ythdc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Ythdc2
|
APN |
18 |
44,993,040 (GRCm39) |
missense |
probably benign |
|
IGL00341:Ythdc2
|
APN |
18 |
44,983,464 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00502:Ythdc2
|
APN |
18 |
44,980,879 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00585:Ythdc2
|
APN |
18 |
44,997,428 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01081:Ythdc2
|
APN |
18 |
44,983,726 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01569:Ythdc2
|
APN |
18 |
45,020,718 (GRCm39) |
missense |
probably benign |
|
IGL01577:Ythdc2
|
APN |
18 |
44,991,349 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01617:Ythdc2
|
APN |
18 |
44,974,482 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01736:Ythdc2
|
APN |
18 |
44,983,735 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02095:Ythdc2
|
APN |
18 |
45,006,207 (GRCm39) |
splice site |
probably benign |
|
IGL02245:Ythdc2
|
APN |
18 |
44,995,751 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02524:Ythdc2
|
APN |
18 |
44,980,921 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02542:Ythdc2
|
APN |
18 |
44,973,308 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02622:Ythdc2
|
APN |
18 |
44,993,001 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02795:Ythdc2
|
APN |
18 |
44,970,505 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02935:Ythdc2
|
APN |
18 |
44,988,112 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4618001:Ythdc2
|
UTSW |
18 |
44,967,665 (GRCm39) |
missense |
probably benign |
0.19 |
R0115:Ythdc2
|
UTSW |
18 |
44,974,490 (GRCm39) |
splice site |
probably benign |
|
R0329:Ythdc2
|
UTSW |
18 |
44,998,127 (GRCm39) |
splice site |
probably benign |
|
R0472:Ythdc2
|
UTSW |
18 |
44,997,424 (GRCm39) |
missense |
probably benign |
0.02 |
R0530:Ythdc2
|
UTSW |
18 |
44,983,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R0547:Ythdc2
|
UTSW |
18 |
44,973,331 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0563:Ythdc2
|
UTSW |
18 |
44,997,915 (GRCm39) |
splice site |
probably benign |
|
R0609:Ythdc2
|
UTSW |
18 |
44,997,424 (GRCm39) |
missense |
probably benign |
0.02 |
R1291:Ythdc2
|
UTSW |
18 |
44,988,276 (GRCm39) |
missense |
probably benign |
0.33 |
R1469:Ythdc2
|
UTSW |
18 |
44,997,529 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Ythdc2
|
UTSW |
18 |
44,997,529 (GRCm39) |
missense |
probably benign |
0.00 |
R1724:Ythdc2
|
UTSW |
18 |
44,961,757 (GRCm39) |
missense |
probably benign |
0.04 |
R1860:Ythdc2
|
UTSW |
18 |
45,006,023 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2040:Ythdc2
|
UTSW |
18 |
44,988,241 (GRCm39) |
nonsense |
probably null |
|
R2308:Ythdc2
|
UTSW |
18 |
44,980,815 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3711:Ythdc2
|
UTSW |
18 |
44,966,240 (GRCm39) |
missense |
probably damaging |
0.98 |
R4005:Ythdc2
|
UTSW |
18 |
44,966,195 (GRCm39) |
missense |
probably benign |
0.00 |
R4580:Ythdc2
|
UTSW |
18 |
44,991,265 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4631:Ythdc2
|
UTSW |
18 |
45,020,698 (GRCm39) |
missense |
probably benign |
0.03 |
R4815:Ythdc2
|
UTSW |
18 |
45,018,307 (GRCm39) |
missense |
probably benign |
0.40 |
R4924:Ythdc2
|
UTSW |
18 |
44,980,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Ythdc2
|
UTSW |
18 |
45,004,532 (GRCm39) |
missense |
probably benign |
0.01 |
R5011:Ythdc2
|
UTSW |
18 |
44,987,809 (GRCm39) |
missense |
probably benign |
0.38 |
R5141:Ythdc2
|
UTSW |
18 |
44,998,114 (GRCm39) |
missense |
probably benign |
0.01 |
R5147:Ythdc2
|
UTSW |
18 |
44,977,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R5280:Ythdc2
|
UTSW |
18 |
44,993,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5388:Ythdc2
|
UTSW |
18 |
44,990,092 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5928:Ythdc2
|
UTSW |
18 |
44,966,272 (GRCm39) |
missense |
probably benign |
|
R5931:Ythdc2
|
UTSW |
18 |
45,006,023 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5995:Ythdc2
|
UTSW |
18 |
45,019,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Ythdc2
|
UTSW |
18 |
44,993,503 (GRCm39) |
missense |
probably benign |
0.02 |
R6056:Ythdc2
|
UTSW |
18 |
44,973,277 (GRCm39) |
missense |
probably damaging |
0.98 |
R6318:Ythdc2
|
UTSW |
18 |
44,993,444 (GRCm39) |
missense |
probably benign |
0.04 |
R6399:Ythdc2
|
UTSW |
18 |
45,019,469 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6586:Ythdc2
|
UTSW |
18 |
44,978,855 (GRCm39) |
missense |
probably benign |
0.00 |
R6684:Ythdc2
|
UTSW |
18 |
45,006,136 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7040:Ythdc2
|
UTSW |
18 |
44,967,529 (GRCm39) |
missense |
probably benign |
0.02 |
R7071:Ythdc2
|
UTSW |
18 |
44,978,855 (GRCm39) |
missense |
probably benign |
0.00 |
R7105:Ythdc2
|
UTSW |
18 |
44,967,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R7148:Ythdc2
|
UTSW |
18 |
44,966,189 (GRCm39) |
missense |
probably benign |
0.42 |
R7290:Ythdc2
|
UTSW |
18 |
44,970,558 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7806:Ythdc2
|
UTSW |
18 |
44,983,491 (GRCm39) |
missense |
probably benign |
0.05 |
R7806:Ythdc2
|
UTSW |
18 |
44,977,353 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8114:Ythdc2
|
UTSW |
18 |
45,010,807 (GRCm39) |
missense |
probably benign |
0.15 |
R8820:Ythdc2
|
UTSW |
18 |
44,967,531 (GRCm39) |
nonsense |
probably null |
|
R8840:Ythdc2
|
UTSW |
18 |
44,993,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R8998:Ythdc2
|
UTSW |
18 |
44,997,371 (GRCm39) |
missense |
probably benign |
0.31 |
R9065:Ythdc2
|
UTSW |
18 |
44,977,418 (GRCm39) |
missense |
probably benign |
0.00 |
R9196:Ythdc2
|
UTSW |
18 |
44,988,464 (GRCm39) |
missense |
probably damaging |
0.96 |
R9251:Ythdc2
|
UTSW |
18 |
44,974,442 (GRCm39) |
missense |
probably benign |
0.00 |
R9331:Ythdc2
|
UTSW |
18 |
44,970,499 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9469:Ythdc2
|
UTSW |
18 |
45,019,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R9634:Ythdc2
|
UTSW |
18 |
45,006,037 (GRCm39) |
missense |
probably benign |
|
|