Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
T |
G |
8: 60,979,657 (GRCm39) |
I173S |
probably damaging |
Het |
Actrt2 |
T |
A |
4: 154,751,920 (GRCm39) |
H72L |
probably benign |
Het |
Adgrf1 |
A |
G |
17: 43,621,164 (GRCm39) |
D467G |
probably benign |
Het |
Axdnd1 |
A |
G |
1: 156,215,616 (GRCm39) |
L226P |
|
Het |
Begain |
T |
C |
12: 108,999,250 (GRCm39) |
D507G |
probably damaging |
Het |
Bsdc1 |
A |
G |
4: 129,362,830 (GRCm39) |
N134S |
probably benign |
Het |
Ccdc39 |
C |
A |
3: 33,886,706 (GRCm39) |
E301* |
probably null |
Het |
Cdh23 |
A |
G |
10: 60,243,210 (GRCm39) |
V1055A |
probably damaging |
Het |
Efcab8 |
A |
G |
2: 153,656,339 (GRCm39) |
D591G |
unknown |
Het |
Frem3 |
T |
G |
8: 81,340,071 (GRCm39) |
V788G |
possibly damaging |
Het |
Ftcd |
A |
T |
10: 76,422,973 (GRCm39) |
I423L |
probably benign |
Het |
Gad1 |
G |
A |
2: 70,409,546 (GRCm39) |
|
probably null |
Het |
Gm8229 |
T |
C |
14: 44,606,238 (GRCm39) |
L156P |
|
Het |
Grm7 |
T |
C |
6: 111,335,874 (GRCm39) |
Y762H |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,433,496 (GRCm39) |
V937D |
possibly damaging |
Het |
Ifnz |
T |
C |
4: 88,701,525 (GRCm39) |
V168A |
probably benign |
Het |
Irx4 |
C |
G |
13: 73,416,649 (GRCm39) |
C348W |
probably damaging |
Het |
Itgb4 |
G |
T |
11: 115,897,923 (GRCm39) |
G1603V |
probably damaging |
Het |
Krt32 |
A |
G |
11: 99,977,580 (GRCm39) |
V162A |
possibly damaging |
Het |
Mpped2 |
A |
G |
2: 106,697,319 (GRCm39) |
T265A |
probably benign |
Het |
Npas3 |
T |
C |
12: 54,114,818 (GRCm39) |
L580P |
possibly damaging |
Het |
Or4f47 |
G |
A |
2: 111,972,397 (GRCm39) |
V36M |
probably benign |
Het |
Or5b109 |
A |
T |
19: 13,212,400 (GRCm39) |
Q262L |
possibly damaging |
Het |
Or8b54 |
G |
A |
9: 38,686,960 (GRCm39) |
M136I |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,058,117 (GRCm39) |
L3940P |
probably damaging |
Het |
Pum2 |
T |
C |
12: 8,763,904 (GRCm39) |
Y283H |
probably damaging |
Het |
Rad54l |
T |
C |
4: 115,967,215 (GRCm39) |
H281R |
probably damaging |
Het |
Rftn2 |
T |
A |
1: 55,224,149 (GRCm39) |
Q397L |
probably damaging |
Het |
Rnf166 |
C |
T |
8: 123,195,068 (GRCm39) |
A151T |
probably benign |
Het |
Setdb1 |
A |
T |
3: 95,246,113 (GRCm39) |
I604N |
possibly damaging |
Het |
Smr2 |
A |
G |
5: 88,256,726 (GRCm39) |
T135A |
unknown |
Het |
Snai2 |
C |
A |
16: 14,524,946 (GRCm39) |
H151N |
possibly damaging |
Het |
Spag6l |
A |
T |
16: 16,598,492 (GRCm39) |
I333N |
probably benign |
Het |
Spta1 |
A |
G |
1: 174,039,139 (GRCm39) |
T1161A |
probably benign |
Het |
Sult2a1 |
G |
T |
7: 13,566,627 (GRCm39) |
A116E |
probably benign |
Het |
Tas2r120 |
T |
A |
6: 132,634,626 (GRCm39) |
L236* |
probably null |
Het |
Tchhl1 |
T |
A |
3: 93,377,819 (GRCm39) |
N174K |
possibly damaging |
Het |
Tex15 |
T |
C |
8: 34,065,784 (GRCm39) |
L1738P |
probably damaging |
Het |
Timp4 |
T |
C |
6: 115,224,270 (GRCm39) |
Y133C |
probably damaging |
Het |
Tmem25 |
A |
G |
9: 44,710,476 (GRCm39) |
|
probably null |
Het |
Tubd1 |
A |
T |
11: 86,456,537 (GRCm39) |
T399S |
probably benign |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Zfp110 |
A |
T |
7: 12,582,485 (GRCm39) |
I378L |
probably benign |
Het |
|
Other mutations in Fibcd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Fibcd1
|
APN |
2 |
31,723,886 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01069:Fibcd1
|
APN |
2 |
31,711,531 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01606:Fibcd1
|
APN |
2 |
31,723,865 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02345:Fibcd1
|
APN |
2 |
31,706,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02639:Fibcd1
|
APN |
2 |
31,707,162 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02682:Fibcd1
|
APN |
2 |
31,728,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R0006:Fibcd1
|
UTSW |
2 |
31,728,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Fibcd1
|
UTSW |
2 |
31,711,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Fibcd1
|
UTSW |
2 |
31,706,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R2397:Fibcd1
|
UTSW |
2 |
31,724,435 (GRCm39) |
missense |
probably benign |
0.37 |
R2877:Fibcd1
|
UTSW |
2 |
31,728,678 (GRCm39) |
missense |
probably benign |
0.12 |
R2878:Fibcd1
|
UTSW |
2 |
31,728,678 (GRCm39) |
missense |
probably benign |
0.12 |
R2940:Fibcd1
|
UTSW |
2 |
31,707,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R4518:Fibcd1
|
UTSW |
2 |
31,707,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5272:Fibcd1
|
UTSW |
2 |
31,706,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R5272:Fibcd1
|
UTSW |
2 |
31,706,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Fibcd1
|
UTSW |
2 |
31,728,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7263:Fibcd1
|
UTSW |
2 |
31,707,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Fibcd1
|
UTSW |
2 |
31,723,880 (GRCm39) |
missense |
probably damaging |
0.99 |
R8316:Fibcd1
|
UTSW |
2 |
31,723,791 (GRCm39) |
splice site |
probably benign |
|
R8536:Fibcd1
|
UTSW |
2 |
31,706,643 (GRCm39) |
missense |
probably damaging |
0.98 |
R9184:Fibcd1
|
UTSW |
2 |
31,706,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R9490:Fibcd1
|
UTSW |
2 |
31,723,815 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9609:Fibcd1
|
UTSW |
2 |
31,728,653 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Fibcd1
|
UTSW |
2 |
31,728,551 (GRCm39) |
missense |
probably benign |
0.17 |
|