Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921528I07Rik |
G |
A |
9: 114,129,077 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl2 |
T |
A |
3: 59,932,143 (GRCm39) |
Y219* |
probably null |
Het |
Adamts13 |
C |
A |
2: 26,895,198 (GRCm39) |
D1096E |
probably benign |
Het |
Adamts16 |
T |
G |
13: 70,927,671 (GRCm39) |
K523Q |
possibly damaging |
Het |
Adcy2 |
A |
G |
13: 68,820,019 (GRCm39) |
F740S |
probably benign |
Het |
Carmil1 |
T |
A |
13: 24,266,003 (GRCm39) |
N253I |
probably damaging |
Het |
Ccdc97 |
T |
C |
7: 25,413,833 (GRCm39) |
T283A |
probably damaging |
Het |
Cmpk2 |
G |
T |
12: 26,527,150 (GRCm39) |
E380* |
probably null |
Het |
Csmd3 |
A |
G |
15: 47,833,543 (GRCm39) |
I911T |
probably damaging |
Het |
Cyp2c39 |
T |
C |
19: 39,502,079 (GRCm39) |
L156P |
probably damaging |
Het |
D7Ertd443e |
T |
C |
7: 133,899,866 (GRCm39) |
I499V |
possibly damaging |
Het |
Dhx58 |
A |
C |
11: 100,592,374 (GRCm39) |
|
probably null |
Het |
Dip2a |
C |
T |
10: 76,134,621 (GRCm39) |
G390S |
probably damaging |
Het |
Dusp10 |
A |
G |
1: 183,801,253 (GRCm39) |
D340G |
probably damaging |
Het |
Epha1 |
A |
T |
6: 42,342,407 (GRCm39) |
C314S |
probably damaging |
Het |
Exph5 |
A |
T |
9: 53,284,602 (GRCm39) |
H561L |
probably benign |
Het |
Fbxw26 |
A |
G |
9: 109,552,780 (GRCm39) |
|
probably null |
Het |
Foxc1 |
A |
C |
13: 31,991,495 (GRCm39) |
N102T |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,814,908 (GRCm39) |
I3547T |
probably benign |
Het |
Gm5464 |
G |
T |
14: 67,106,774 (GRCm39) |
|
probably benign |
Het |
Gnptab |
C |
T |
10: 88,269,456 (GRCm39) |
R720C |
possibly damaging |
Het |
Greb1l |
T |
C |
18: 10,469,375 (GRCm39) |
V130A |
possibly damaging |
Het |
Hmg20a |
A |
T |
9: 56,394,934 (GRCm39) |
D216V |
probably damaging |
Het |
Hnrnpul2 |
C |
A |
19: 8,801,777 (GRCm39) |
D328E |
probably damaging |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Ift172 |
T |
C |
5: 31,410,985 (GRCm39) |
Y1691C |
probably damaging |
Het |
Kremen2 |
T |
C |
17: 23,961,784 (GRCm39) |
D241G |
probably benign |
Het |
Meis2 |
T |
C |
2: 115,893,897 (GRCm39) |
D5G |
possibly damaging |
Het |
Mrps5 |
G |
A |
2: 127,433,749 (GRCm39) |
R46K |
probably benign |
Het |
Myh14 |
C |
T |
7: 44,310,374 (GRCm39) |
V170M |
probably damaging |
Het |
Nexn |
T |
C |
3: 151,953,894 (GRCm39) |
N123D |
probably benign |
Het |
Or11g26 |
T |
A |
14: 50,753,282 (GRCm39) |
M207K |
probably benign |
Het |
Or4d11 |
A |
T |
19: 12,013,765 (GRCm39) |
S114T |
probably benign |
Het |
Or51l14 |
T |
A |
7: 103,101,423 (GRCm39) |
I293N |
probably damaging |
Het |
Pacs1 |
C |
T |
19: 5,191,726 (GRCm39) |
V704M |
probably damaging |
Het |
Pdlim3 |
T |
C |
8: 46,370,543 (GRCm39) |
V281A |
probably benign |
Het |
Plpp4 |
T |
G |
7: 128,925,190 (GRCm39) |
F142V |
probably damaging |
Het |
Prb1a |
G |
A |
6: 132,184,620 (GRCm39) |
Q338* |
probably null |
Het |
Psg26 |
G |
T |
7: 18,216,481 (GRCm39) |
Y119* |
probably null |
Het |
Ptger4 |
A |
G |
15: 5,272,491 (GRCm39) |
C68R |
probably benign |
Het |
Ptpre |
T |
A |
7: 135,272,444 (GRCm39) |
I399N |
probably damaging |
Het |
Ripply2 |
A |
G |
9: 86,898,372 (GRCm39) |
Y72C |
probably damaging |
Het |
Rp1l1 |
T |
A |
14: 64,266,837 (GRCm39) |
S808T |
possibly damaging |
Het |
Scn5a |
G |
A |
9: 119,362,838 (GRCm39) |
T594I |
probably damaging |
Het |
Sf3b1 |
T |
C |
1: 55,037,267 (GRCm39) |
D883G |
probably benign |
Het |
Skint5 |
A |
T |
4: 113,369,220 (GRCm39) |
|
probably null |
Het |
Terf1 |
A |
G |
1: 15,889,207 (GRCm39) |
H212R |
probably damaging |
Het |
Tmco5 |
T |
G |
2: 116,711,269 (GRCm39) |
|
probably null |
Het |
Tnfaip3 |
A |
T |
10: 18,882,660 (GRCm39) |
Y252* |
probably null |
Het |
Tnrc6a |
T |
A |
7: 122,770,083 (GRCm39) |
N624K |
probably damaging |
Het |
Top3a |
C |
A |
11: 60,633,615 (GRCm39) |
R827L |
probably damaging |
Het |
Unc79 |
G |
A |
12: 103,055,031 (GRCm39) |
|
probably null |
Het |
Usp20 |
T |
C |
2: 30,901,116 (GRCm39) |
S422P |
probably benign |
Het |
Utrn |
T |
C |
10: 12,509,766 (GRCm39) |
E2402G |
probably benign |
Het |
Wdr3 |
G |
A |
3: 100,063,734 (GRCm39) |
Q181* |
probably null |
Het |
Zfp536 |
T |
C |
7: 37,267,373 (GRCm39) |
E681G |
probably damaging |
Het |
Zfp91 |
C |
T |
19: 12,747,438 (GRCm39) |
V562I |
possibly damaging |
Het |
Zfp942 |
A |
T |
17: 22,148,017 (GRCm39) |
I204N |
probably benign |
Het |
|
Other mutations in Papolg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00987:Papolg
|
APN |
11 |
23,826,377 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01016:Papolg
|
APN |
11 |
23,835,570 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01394:Papolg
|
APN |
11 |
23,817,235 (GRCm39) |
missense |
probably benign |
|
IGL01710:Papolg
|
APN |
11 |
23,814,026 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01786:Papolg
|
APN |
11 |
23,824,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02008:Papolg
|
APN |
11 |
23,829,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02127:Papolg
|
APN |
11 |
23,820,870 (GRCm39) |
unclassified |
probably benign |
|
IGL02329:Papolg
|
APN |
11 |
23,841,869 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02535:Papolg
|
APN |
11 |
23,840,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02588:Papolg
|
APN |
11 |
23,840,252 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03058:Papolg
|
APN |
11 |
23,845,029 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03301:Papolg
|
APN |
11 |
23,824,503 (GRCm39) |
missense |
probably benign |
0.05 |
Runningback
|
UTSW |
11 |
23,823,919 (GRCm39) |
splice site |
probably null |
|
R0124:Papolg
|
UTSW |
11 |
23,817,535 (GRCm39) |
missense |
probably benign |
0.21 |
R0454:Papolg
|
UTSW |
11 |
23,829,868 (GRCm39) |
splice site |
probably null |
|
R0743:Papolg
|
UTSW |
11 |
23,820,818 (GRCm39) |
splice site |
probably null |
|
R0931:Papolg
|
UTSW |
11 |
23,832,257 (GRCm39) |
missense |
probably damaging |
0.96 |
R1856:Papolg
|
UTSW |
11 |
23,817,379 (GRCm39) |
missense |
probably benign |
0.06 |
R1940:Papolg
|
UTSW |
11 |
23,817,279 (GRCm39) |
missense |
probably benign |
0.00 |
R2239:Papolg
|
UTSW |
11 |
23,826,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R3802:Papolg
|
UTSW |
11 |
23,826,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R4275:Papolg
|
UTSW |
11 |
23,818,378 (GRCm39) |
missense |
probably benign |
|
R4989:Papolg
|
UTSW |
11 |
23,823,919 (GRCm39) |
splice site |
probably null |
|
R5074:Papolg
|
UTSW |
11 |
23,817,331 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5122:Papolg
|
UTSW |
11 |
23,817,501 (GRCm39) |
critical splice donor site |
probably null |
|
R6048:Papolg
|
UTSW |
11 |
23,841,815 (GRCm39) |
missense |
probably benign |
0.04 |
R6365:Papolg
|
UTSW |
11 |
23,832,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R6577:Papolg
|
UTSW |
11 |
23,829,857 (GRCm39) |
critical splice donor site |
probably benign |
|
R7117:Papolg
|
UTSW |
11 |
23,845,207 (GRCm39) |
start gained |
probably benign |
|
R7283:Papolg
|
UTSW |
11 |
23,817,394 (GRCm39) |
missense |
not run |
|
R7372:Papolg
|
UTSW |
11 |
23,816,439 (GRCm39) |
missense |
probably benign |
0.16 |
R7761:Papolg
|
UTSW |
11 |
23,841,884 (GRCm39) |
missense |
probably benign |
0.05 |
R8503:Papolg
|
UTSW |
11 |
23,820,292 (GRCm39) |
missense |
probably benign |
0.01 |
R9212:Papolg
|
UTSW |
11 |
23,823,817 (GRCm39) |
missense |
probably benign |
|
|