Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd8 |
A |
T |
8: 71,911,085 (GRCm39) |
I282N |
probably benign |
Het |
Akr1c18 |
T |
C |
13: 4,186,654 (GRCm39) |
I265V |
probably benign |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Arfgef1 |
T |
C |
1: 10,210,706 (GRCm39) |
I1788V |
probably benign |
Het |
Cacng7 |
T |
A |
7: 3,415,445 (GRCm39) |
I270N |
possibly damaging |
Het |
Ccdc81 |
C |
T |
7: 89,515,769 (GRCm39) |
E637K |
probably benign |
Het |
Cnbd2 |
A |
G |
2: 156,170,328 (GRCm39) |
I138V |
possibly damaging |
Het |
Cntnap5b |
A |
G |
1: 100,311,342 (GRCm39) |
K983E |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,383,331 (GRCm39) |
S1770P |
probably benign |
Het |
Cpsf6 |
A |
T |
10: 117,201,973 (GRCm39) |
|
probably benign |
Het |
Ctsc |
G |
A |
7: 87,959,037 (GRCm39) |
R439H |
probably damaging |
Het |
Dcun1d1 |
A |
G |
3: 35,951,930 (GRCm39) |
|
probably benign |
Het |
Flg2 |
A |
G |
3: 93,108,514 (GRCm39) |
I181V |
probably benign |
Het |
Gbp2 |
A |
T |
3: 142,343,183 (GRCm39) |
S567C |
probably damaging |
Het |
Gm5114 |
A |
G |
7: 39,058,510 (GRCm39) |
S370P |
probably damaging |
Het |
Kcnh7 |
A |
G |
2: 62,546,527 (GRCm39) |
V1018A |
probably benign |
Het |
Kmt2a |
G |
A |
9: 44,758,993 (GRCm39) |
A952V |
probably damaging |
Het |
Krt1 |
C |
T |
15: 101,756,326 (GRCm39) |
E340K |
possibly damaging |
Het |
Lim2 |
T |
A |
7: 43,084,826 (GRCm39) |
I141N |
probably damaging |
Het |
Nlrp4a |
T |
C |
7: 26,152,892 (GRCm39) |
V654A |
probably benign |
Het |
Or5b24 |
T |
A |
19: 12,912,638 (GRCm39) |
C179S |
probably damaging |
Het |
Prr14l |
T |
C |
5: 32,986,826 (GRCm39) |
S890G |
probably benign |
Het |
Psmd14 |
T |
A |
2: 61,627,726 (GRCm39) |
|
probably null |
Het |
Ptpn13 |
A |
G |
5: 103,734,655 (GRCm39) |
D2129G |
probably benign |
Het |
Pum1 |
C |
T |
4: 130,499,199 (GRCm39) |
T760M |
probably damaging |
Het |
Rif1 |
A |
G |
2: 51,975,041 (GRCm39) |
I317V |
probably damaging |
Het |
Sh3bgrl2 |
C |
T |
9: 83,459,684 (GRCm39) |
|
probably benign |
Het |
Slfn8 |
A |
T |
11: 82,894,337 (GRCm39) |
H767Q |
possibly damaging |
Het |
Sned1 |
G |
A |
1: 93,184,114 (GRCm39) |
G114D |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Tenm3 |
A |
T |
8: 48,681,577 (GRCm39) |
D2684E |
probably damaging |
Het |
Tet2 |
T |
C |
3: 133,182,362 (GRCm39) |
T1201A |
possibly damaging |
Het |
Vax2 |
T |
C |
6: 83,714,759 (GRCm39) |
S225P |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,833,196 (GRCm39) |
|
probably null |
Het |
Zc3h13 |
A |
G |
14: 75,567,989 (GRCm39) |
D1094G |
probably damaging |
Het |
Zmiz1 |
A |
G |
14: 25,663,404 (GRCm39) |
Y1051C |
unknown |
Het |
Zswim2 |
G |
A |
2: 83,745,737 (GRCm39) |
S567L |
probably damaging |
Het |
|
Other mutations in Washc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00861:Washc5
|
APN |
15 |
59,209,125 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01096:Washc5
|
APN |
15 |
59,222,060 (GRCm39) |
splice site |
probably benign |
|
IGL01305:Washc5
|
APN |
15 |
59,227,688 (GRCm39) |
nonsense |
probably null |
|
IGL01707:Washc5
|
APN |
15 |
59,213,864 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01921:Washc5
|
APN |
15 |
59,213,958 (GRCm39) |
splice site |
probably null |
|
IGL02056:Washc5
|
APN |
15 |
59,222,185 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02145:Washc5
|
APN |
15 |
59,241,060 (GRCm39) |
missense |
probably benign |
|
IGL02430:Washc5
|
APN |
15 |
59,238,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02450:Washc5
|
APN |
15 |
59,204,166 (GRCm39) |
nonsense |
probably null |
|
IGL03238:Washc5
|
APN |
15 |
59,218,691 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Washc5
|
APN |
15 |
59,235,199 (GRCm39) |
splice site |
probably benign |
|
ANU22:Washc5
|
UTSW |
15 |
59,227,688 (GRCm39) |
nonsense |
probably null |
|
R0004:Washc5
|
UTSW |
15 |
59,239,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Washc5
|
UTSW |
15 |
59,239,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R0100:Washc5
|
UTSW |
15 |
59,215,947 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0100:Washc5
|
UTSW |
15 |
59,215,947 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0179:Washc5
|
UTSW |
15 |
59,224,379 (GRCm39) |
missense |
probably benign |
0.01 |
R0265:Washc5
|
UTSW |
15 |
59,210,809 (GRCm39) |
missense |
probably benign |
0.43 |
R0315:Washc5
|
UTSW |
15 |
59,213,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R0545:Washc5
|
UTSW |
15 |
59,213,942 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0611:Washc5
|
UTSW |
15 |
59,213,007 (GRCm39) |
missense |
probably damaging |
0.99 |
R0636:Washc5
|
UTSW |
15 |
59,231,258 (GRCm39) |
missense |
probably benign |
0.01 |
R1006:Washc5
|
UTSW |
15 |
59,241,036 (GRCm39) |
missense |
probably benign |
0.06 |
R1237:Washc5
|
UTSW |
15 |
59,210,757 (GRCm39) |
splice site |
probably benign |
|
R1835:Washc5
|
UTSW |
15 |
59,231,189 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1888:Washc5
|
UTSW |
15 |
59,231,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R1888:Washc5
|
UTSW |
15 |
59,231,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R2005:Washc5
|
UTSW |
15 |
59,213,004 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2006:Washc5
|
UTSW |
15 |
59,213,004 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2060:Washc5
|
UTSW |
15 |
59,222,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Washc5
|
UTSW |
15 |
59,241,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Washc5
|
UTSW |
15 |
59,221,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R2177:Washc5
|
UTSW |
15 |
59,235,118 (GRCm39) |
nonsense |
probably null |
|
R2975:Washc5
|
UTSW |
15 |
59,217,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Washc5
|
UTSW |
15 |
59,211,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R4824:Washc5
|
UTSW |
15 |
59,205,485 (GRCm39) |
nonsense |
probably null |
|
R4843:Washc5
|
UTSW |
15 |
59,222,220 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4991:Washc5
|
UTSW |
15 |
59,215,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4996:Washc5
|
UTSW |
15 |
59,205,484 (GRCm39) |
missense |
probably benign |
|
R5103:Washc5
|
UTSW |
15 |
59,222,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Washc5
|
UTSW |
15 |
59,217,377 (GRCm39) |
splice site |
probably null |
|
R5591:Washc5
|
UTSW |
15 |
59,241,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R6073:Washc5
|
UTSW |
15 |
59,207,019 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6123:Washc5
|
UTSW |
15 |
59,206,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Washc5
|
UTSW |
15 |
59,217,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Washc5
|
UTSW |
15 |
59,227,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R6297:Washc5
|
UTSW |
15 |
59,215,895 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6374:Washc5
|
UTSW |
15 |
59,209,044 (GRCm39) |
missense |
probably benign |
0.14 |
R6659:Washc5
|
UTSW |
15 |
59,212,739 (GRCm39) |
critical splice donor site |
probably null |
|
R6880:Washc5
|
UTSW |
15 |
59,222,021 (GRCm39) |
missense |
probably benign |
0.00 |
R7146:Washc5
|
UTSW |
15 |
59,224,350 (GRCm39) |
nonsense |
probably null |
|
R7330:Washc5
|
UTSW |
15 |
59,205,516 (GRCm39) |
missense |
probably benign |
0.02 |
R7430:Washc5
|
UTSW |
15 |
59,241,762 (GRCm39) |
nonsense |
probably null |
|
R7490:Washc5
|
UTSW |
15 |
59,209,053 (GRCm39) |
missense |
probably benign |
0.18 |
R7532:Washc5
|
UTSW |
15 |
59,239,260 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7560:Washc5
|
UTSW |
15 |
59,238,041 (GRCm39) |
missense |
probably damaging |
0.97 |
R7803:Washc5
|
UTSW |
15 |
59,240,308 (GRCm39) |
missense |
probably damaging |
0.98 |
R8242:Washc5
|
UTSW |
15 |
59,215,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8841:Washc5
|
UTSW |
15 |
59,206,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Washc5
|
UTSW |
15 |
59,233,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Washc5
|
UTSW |
15 |
59,217,233 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9123:Washc5
|
UTSW |
15 |
59,209,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Washc5
|
UTSW |
15 |
59,209,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9310:Washc5
|
UTSW |
15 |
59,218,067 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9423:Washc5
|
UTSW |
15 |
59,227,735 (GRCm39) |
missense |
probably benign |
|
R9556:Washc5
|
UTSW |
15 |
59,218,716 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9569:Washc5
|
UTSW |
15 |
59,215,980 (GRCm39) |
missense |
probably benign |
|
R9668:Washc5
|
UTSW |
15 |
59,218,062 (GRCm39) |
critical splice donor site |
probably null |
|
R9691:Washc5
|
UTSW |
15 |
59,218,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R9718:Washc5
|
UTSW |
15 |
59,217,192 (GRCm39) |
missense |
probably benign |
0.19 |
|