Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
C |
T |
14: 29,704,673 (GRCm39) |
Q58* |
probably null |
Het |
Adamts20 |
A |
C |
15: 94,180,985 (GRCm39) |
|
probably null |
Het |
Alpk3 |
T |
A |
7: 80,728,327 (GRCm39) |
S486T |
possibly damaging |
Het |
Cep162 |
T |
A |
9: 87,104,227 (GRCm39) |
E553V |
probably damaging |
Het |
Epha5 |
T |
C |
5: 84,304,360 (GRCm39) |
I370V |
possibly damaging |
Het |
Ets1 |
A |
T |
9: 32,664,093 (GRCm39) |
|
probably null |
Het |
Fbxo38 |
C |
T |
18: 62,666,634 (GRCm39) |
E180K |
probably damaging |
Het |
Fscn1 |
A |
G |
5: 142,957,741 (GRCm39) |
D296G |
probably damaging |
Het |
Glul |
A |
G |
1: 153,783,779 (GRCm39) |
I325V |
probably benign |
Het |
Keg1 |
A |
G |
19: 12,693,274 (GRCm39) |
D99G |
probably benign |
Het |
Krt1 |
A |
T |
15: 101,758,702 (GRCm39) |
V154D |
possibly damaging |
Het |
Mdfic |
T |
A |
6: 15,770,324 (GRCm39) |
I110N |
probably damaging |
Het |
Myo1g |
T |
C |
11: 6,462,509 (GRCm39) |
N541D |
probably damaging |
Het |
Nos3 |
T |
A |
5: 24,588,622 (GRCm39) |
V1116D |
probably damaging |
Het |
Or8h8 |
A |
G |
2: 86,753,441 (GRCm39) |
I145T |
probably benign |
Het |
Piwil2 |
G |
T |
14: 70,611,785 (GRCm39) |
Q954K |
probably benign |
Het |
Ppm1l |
T |
C |
3: 69,224,916 (GRCm39) |
M6T |
probably damaging |
Het |
Scn3a |
T |
A |
2: 65,327,907 (GRCm39) |
E861V |
possibly damaging |
Het |
Senp2 |
C |
T |
16: 21,845,474 (GRCm39) |
T236M |
possibly damaging |
Het |
Sgo2b |
A |
T |
8: 64,384,528 (GRCm39) |
V156D |
probably damaging |
Het |
Sis |
T |
C |
3: 72,814,475 (GRCm39) |
Y1585C |
probably damaging |
Het |
Slc22a22 |
A |
G |
15: 57,114,365 (GRCm39) |
S321P |
probably benign |
Het |
Slu7 |
T |
A |
11: 43,328,975 (GRCm39) |
Y66N |
probably damaging |
Het |
Stra6l |
A |
G |
4: 45,879,473 (GRCm39) |
H365R |
probably benign |
Het |
Stt3b |
T |
C |
9: 115,096,410 (GRCm39) |
T246A |
probably benign |
Het |
Taf1c |
T |
G |
8: 120,330,986 (GRCm39) |
N44T |
possibly damaging |
Het |
Tcirg1 |
C |
T |
19: 3,951,933 (GRCm39) |
V376M |
probably damaging |
Het |
Tkt |
A |
G |
14: 30,271,280 (GRCm39) |
D17G |
probably damaging |
Het |
Tle6 |
G |
A |
10: 81,427,810 (GRCm39) |
H482Y |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 84,889,689 (GRCm39) |
V672A |
probably benign |
Het |
Zdbf2 |
T |
G |
1: 63,344,679 (GRCm39) |
D1019E |
possibly damaging |
Het |
Zfp608 |
A |
T |
18: 55,032,150 (GRCm39) |
C597S |
possibly damaging |
Het |
|
Other mutations in Zfp986 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4548:Zfp986
|
UTSW |
4 |
145,625,928 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4142001:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R0126:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R1835:Zfp986
|
UTSW |
4 |
145,625,805 (GRCm39) |
missense |
probably benign |
0.00 |
R3926:Zfp986
|
UTSW |
4 |
145,619,090 (GRCm39) |
splice site |
probably benign |
|
R4287:Zfp986
|
UTSW |
4 |
145,619,088 (GRCm39) |
critical splice donor site |
probably null |
|
R4401:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R7836:Zfp986
|
UTSW |
4 |
145,625,691 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8108:Zfp986
|
UTSW |
4 |
145,625,875 (GRCm39) |
missense |
probably benign |
0.02 |
R8738:Zfp986
|
UTSW |
4 |
145,625,550 (GRCm39) |
missense |
probably benign |
0.04 |
R9153:Zfp986
|
UTSW |
4 |
145,626,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Zfp986
|
UTSW |
4 |
145,625,798 (GRCm39) |
missense |
probably benign |
0.01 |
R9212:Zfp986
|
UTSW |
4 |
145,625,798 (GRCm39) |
missense |
probably benign |
0.01 |
R9235:Zfp986
|
UTSW |
4 |
145,625,759 (GRCm39) |
missense |
probably benign |
0.09 |
R9326:Zfp986
|
UTSW |
4 |
145,626,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R9691:Zfp986
|
UTSW |
4 |
145,626,070 (GRCm39) |
missense |
probably benign |
0.25 |
|