Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra2 |
A |
T |
8: 27,601,268 (GRCm39) |
I303F |
possibly damaging |
Het |
Cldn9 |
A |
G |
17: 23,902,023 (GRCm39) |
S201P |
probably benign |
Het |
Clstn2 |
G |
T |
9: 97,343,584 (GRCm39) |
P621Q |
probably damaging |
Het |
Ctdspl2 |
A |
G |
2: 121,837,445 (GRCm39) |
N403S |
probably damaging |
Het |
Cyp2j5 |
T |
C |
4: 96,524,045 (GRCm39) |
Y329C |
possibly damaging |
Het |
Elapor1 |
A |
G |
3: 108,377,231 (GRCm39) |
L461P |
probably damaging |
Het |
Elovl1 |
A |
G |
4: 118,287,700 (GRCm39) |
|
probably benign |
Het |
Fam83a |
A |
G |
15: 57,856,439 (GRCm39) |
D206G |
possibly damaging |
Het |
Fhl2 |
T |
C |
1: 43,170,970 (GRCm39) |
M115V |
possibly damaging |
Het |
Fry |
T |
A |
5: 150,304,387 (GRCm39) |
D592E |
probably benign |
Het |
Lrp1 |
G |
A |
10: 127,396,005 (GRCm39) |
H2422Y |
probably damaging |
Het |
Mamdc2 |
T |
A |
19: 23,280,997 (GRCm39) |
I684F |
probably damaging |
Het |
Mia2 |
T |
C |
12: 59,155,156 (GRCm39) |
Y290H |
probably damaging |
Het |
Mup12 |
C |
T |
4: 60,696,642 (GRCm39) |
|
probably null |
Het |
Olr1 |
T |
A |
6: 129,477,040 (GRCm39) |
|
probably null |
Het |
Or51a24 |
T |
C |
7: 103,733,661 (GRCm39) |
T209A |
probably benign |
Het |
Pcdhb15 |
T |
C |
18: 37,607,860 (GRCm39) |
V364A |
possibly damaging |
Het |
Pfkp |
A |
G |
13: 6,636,575 (GRCm39) |
S654P |
possibly damaging |
Het |
Rab3gap2 |
T |
G |
1: 185,015,607 (GRCm39) |
V1275G |
probably damaging |
Het |
Rbbp4 |
A |
G |
4: 129,222,414 (GRCm39) |
F93L |
probably benign |
Het |
Ripk1 |
T |
C |
13: 34,194,587 (GRCm39) |
V75A |
probably damaging |
Het |
Scg2 |
T |
A |
1: 79,413,499 (GRCm39) |
Q368L |
possibly damaging |
Het |
Tmprss9 |
A |
G |
10: 80,734,145 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Fancd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00401:Fancd2
|
APN |
6 |
113,541,357 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00475:Fancd2
|
APN |
6 |
113,545,571 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01319:Fancd2
|
APN |
6 |
113,561,860 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01339:Fancd2
|
APN |
6 |
113,530,713 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01373:Fancd2
|
APN |
6 |
113,530,713 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01393:Fancd2
|
APN |
6 |
113,554,321 (GRCm39) |
splice site |
probably benign |
|
IGL01630:Fancd2
|
APN |
6 |
113,540,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01769:Fancd2
|
APN |
6 |
113,522,072 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01882:Fancd2
|
APN |
6 |
113,523,601 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02029:Fancd2
|
APN |
6 |
113,547,936 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02224:Fancd2
|
APN |
6 |
113,545,281 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02271:Fancd2
|
APN |
6 |
113,512,720 (GRCm39) |
splice site |
probably benign |
|
IGL02352:Fancd2
|
APN |
6 |
113,540,073 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02359:Fancd2
|
APN |
6 |
113,540,073 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02427:Fancd2
|
APN |
6 |
113,526,313 (GRCm39) |
splice site |
probably null |
|
IGL02512:Fancd2
|
APN |
6 |
113,547,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02530:Fancd2
|
APN |
6 |
113,539,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Fancd2
|
APN |
6 |
113,570,278 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03090:Fancd2
|
APN |
6 |
113,514,558 (GRCm39) |
splice site |
probably null |
|
IGL03247:Fancd2
|
APN |
6 |
113,545,169 (GRCm39) |
missense |
probably benign |
0.03 |
R0278:Fancd2
|
UTSW |
6 |
113,525,409 (GRCm39) |
critical splice donor site |
probably null |
|
R0401:Fancd2
|
UTSW |
6 |
113,525,304 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0420:Fancd2
|
UTSW |
6 |
113,513,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R0496:Fancd2
|
UTSW |
6 |
113,532,091 (GRCm39) |
splice site |
probably benign |
|
R0762:Fancd2
|
UTSW |
6 |
113,551,619 (GRCm39) |
missense |
probably benign |
0.20 |
R0827:Fancd2
|
UTSW |
6 |
113,563,210 (GRCm39) |
critical splice donor site |
probably null |
|
R1225:Fancd2
|
UTSW |
6 |
113,512,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R1576:Fancd2
|
UTSW |
6 |
113,555,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R2010:Fancd2
|
UTSW |
6 |
113,570,252 (GRCm39) |
missense |
probably damaging |
0.96 |
R2079:Fancd2
|
UTSW |
6 |
113,532,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Fancd2
|
UTSW |
6 |
113,537,035 (GRCm39) |
splice site |
probably benign |
|
R2141:Fancd2
|
UTSW |
6 |
113,526,282 (GRCm39) |
missense |
probably benign |
0.00 |
R2168:Fancd2
|
UTSW |
6 |
113,568,120 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2180:Fancd2
|
UTSW |
6 |
113,551,598 (GRCm39) |
missense |
probably benign |
0.33 |
R3016:Fancd2
|
UTSW |
6 |
113,513,687 (GRCm39) |
missense |
probably benign |
0.00 |
R3153:Fancd2
|
UTSW |
6 |
113,570,230 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3154:Fancd2
|
UTSW |
6 |
113,570,230 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3783:Fancd2
|
UTSW |
6 |
113,542,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R3786:Fancd2
|
UTSW |
6 |
113,542,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Fancd2
|
UTSW |
6 |
113,542,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Fancd2
|
UTSW |
6 |
113,538,677 (GRCm39) |
missense |
probably benign |
0.00 |
R4388:Fancd2
|
UTSW |
6 |
113,533,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R4544:Fancd2
|
UTSW |
6 |
113,549,603 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4598:Fancd2
|
UTSW |
6 |
113,562,438 (GRCm39) |
missense |
probably benign |
0.06 |
R4832:Fancd2
|
UTSW |
6 |
113,530,683 (GRCm39) |
missense |
probably benign |
0.16 |
R4841:Fancd2
|
UTSW |
6 |
113,539,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Fancd2
|
UTSW |
6 |
113,562,434 (GRCm39) |
missense |
probably benign |
0.03 |
R5375:Fancd2
|
UTSW |
6 |
113,545,673 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5579:Fancd2
|
UTSW |
6 |
113,537,012 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5782:Fancd2
|
UTSW |
6 |
113,525,833 (GRCm39) |
missense |
probably benign |
0.00 |
R5871:Fancd2
|
UTSW |
6 |
113,533,243 (GRCm39) |
missense |
probably benign |
0.30 |
R5901:Fancd2
|
UTSW |
6 |
113,526,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Fancd2
|
UTSW |
6 |
113,538,672 (GRCm39) |
missense |
probably benign |
|
R6026:Fancd2
|
UTSW |
6 |
113,528,731 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6166:Fancd2
|
UTSW |
6 |
113,532,212 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6393:Fancd2
|
UTSW |
6 |
113,555,374 (GRCm39) |
missense |
probably benign |
0.01 |
R6666:Fancd2
|
UTSW |
6 |
113,562,470 (GRCm39) |
missense |
probably damaging |
0.96 |
R6669:Fancd2
|
UTSW |
6 |
113,570,288 (GRCm39) |
missense |
probably benign |
0.00 |
R6762:Fancd2
|
UTSW |
6 |
113,562,977 (GRCm39) |
splice site |
probably null |
|
R6911:Fancd2
|
UTSW |
6 |
113,525,346 (GRCm39) |
missense |
probably damaging |
0.98 |
R6992:Fancd2
|
UTSW |
6 |
113,547,979 (GRCm39) |
critical splice donor site |
probably null |
|
R7091:Fancd2
|
UTSW |
6 |
113,522,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R7252:Fancd2
|
UTSW |
6 |
113,533,246 (GRCm39) |
missense |
probably damaging |
0.98 |
R7343:Fancd2
|
UTSW |
6 |
113,513,900 (GRCm39) |
missense |
probably benign |
0.01 |
R7344:Fancd2
|
UTSW |
6 |
113,545,670 (GRCm39) |
missense |
probably benign |
0.09 |
R7354:Fancd2
|
UTSW |
6 |
113,572,907 (GRCm39) |
missense |
unknown |
|
R7489:Fancd2
|
UTSW |
6 |
113,541,265 (GRCm39) |
missense |
probably benign |
|
R7501:Fancd2
|
UTSW |
6 |
113,525,364 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7504:Fancd2
|
UTSW |
6 |
113,521,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R7992:Fancd2
|
UTSW |
6 |
113,542,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8027:Fancd2
|
UTSW |
6 |
113,523,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R8487:Fancd2
|
UTSW |
6 |
113,545,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8509:Fancd2
|
UTSW |
6 |
113,549,531 (GRCm39) |
missense |
probably benign |
0.00 |
R8757:Fancd2
|
UTSW |
6 |
113,537,054 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8960:Fancd2
|
UTSW |
6 |
113,540,129 (GRCm39) |
critical splice donor site |
probably null |
|
R8978:Fancd2
|
UTSW |
6 |
113,562,507 (GRCm39) |
splice site |
probably benign |
|
R9110:Fancd2
|
UTSW |
6 |
113,512,762 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9116:Fancd2
|
UTSW |
6 |
113,532,180 (GRCm39) |
missense |
probably benign |
0.00 |
R9490:Fancd2
|
UTSW |
6 |
113,555,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R9667:Fancd2
|
UTSW |
6 |
113,530,717 (GRCm39) |
nonsense |
probably null |
|
Z1088:Fancd2
|
UTSW |
6 |
113,558,383 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Fancd2
|
UTSW |
6 |
113,521,986 (GRCm39) |
missense |
probably benign |
0.00 |
|