Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
G |
A |
11: 58,771,054 (GRCm39) |
A179T |
probably benign |
Het |
Abca6 |
A |
G |
11: 110,138,090 (GRCm39) |
|
probably null |
Het |
Agps |
A |
C |
2: 75,662,585 (GRCm39) |
D10A |
probably damaging |
Het |
Atad2b |
T |
A |
12: 5,081,578 (GRCm39) |
D1162E |
probably benign |
Het |
Atp13a4 |
T |
C |
16: 29,239,659 (GRCm39) |
K851R |
unknown |
Het |
Cdh15 |
A |
G |
8: 123,586,029 (GRCm39) |
D136G |
probably damaging |
Het |
Cdk5rap1 |
A |
T |
2: 154,190,585 (GRCm39) |
Y459N |
probably damaging |
Het |
Cep192 |
A |
T |
18: 67,989,354 (GRCm39) |
K1834* |
probably null |
Het |
Cfap221 |
C |
T |
1: 119,853,361 (GRCm39) |
V778I |
probably benign |
Het |
Chpf |
G |
A |
1: 75,452,854 (GRCm39) |
T362I |
probably benign |
Het |
Cyp4x1 |
T |
C |
4: 114,991,069 (GRCm39) |
R36G |
probably damaging |
Het |
D16Ertd472e |
T |
A |
16: 78,342,052 (GRCm39) |
Q276L |
probably damaging |
Het |
Dapk3 |
T |
C |
10: 81,025,825 (GRCm39) |
Y39H |
probably damaging |
Het |
Eefsec |
T |
C |
6: 88,353,337 (GRCm39) |
T111A |
probably damaging |
Het |
Ehbp1l1 |
G |
A |
19: 5,758,371 (GRCm39) |
R1714C |
unknown |
Het |
Flcn |
A |
G |
11: 59,694,609 (GRCm39) |
V121A |
probably damaging |
Het |
Gaa |
G |
T |
11: 119,165,958 (GRCm39) |
D423Y |
probably damaging |
Het |
Gaa |
A |
C |
11: 119,165,959 (GRCm39) |
D423A |
probably benign |
Het |
Garnl3 |
A |
G |
2: 32,893,881 (GRCm39) |
I694T |
probably damaging |
Het |
Gm5114 |
T |
A |
7: 39,058,242 (GRCm39) |
Q459L |
probably damaging |
Het |
H1f0 |
C |
T |
15: 78,912,947 (GRCm39) |
P9L |
probably damaging |
Het |
Hmmr |
A |
G |
11: 40,612,655 (GRCm39) |
|
probably null |
Het |
Klra5 |
C |
A |
6: 129,883,686 (GRCm39) |
W147L |
possibly damaging |
Het |
Lmnb1 |
G |
A |
18: 56,873,114 (GRCm39) |
|
probably null |
Het |
Lrp2 |
T |
C |
2: 69,288,832 (GRCm39) |
Y3678C |
probably damaging |
Het |
Map7 |
T |
C |
10: 20,153,981 (GRCm39) |
V699A |
unknown |
Het |
Mme |
G |
T |
3: 63,272,306 (GRCm39) |
G635V |
possibly damaging |
Het |
Mroh8 |
A |
T |
2: 157,071,948 (GRCm39) |
I519N |
possibly damaging |
Het |
Mrps11 |
T |
C |
7: 78,442,390 (GRCm39) |
S157P |
probably damaging |
Het |
Muc16 |
T |
C |
9: 18,572,061 (GRCm39) |
T153A |
unknown |
Het |
Nlrp1b |
A |
G |
11: 71,072,913 (GRCm39) |
V310A |
probably damaging |
Het |
Oas1f |
T |
C |
5: 120,993,592 (GRCm39) |
V268A |
probably damaging |
Het |
Or56a3b |
T |
A |
7: 104,770,817 (GRCm39) |
I51N |
|
Het |
Or6y1 |
A |
T |
1: 174,276,233 (GRCm39) |
T15S |
probably benign |
Het |
Padi4 |
A |
G |
4: 140,479,950 (GRCm39) |
L401P |
probably benign |
Het |
Pdzd7 |
A |
G |
19: 45,016,056 (GRCm39) |
*1022Q |
probably null |
Het |
Plcl2 |
C |
A |
17: 50,915,391 (GRCm39) |
T800K |
probably damaging |
Het |
Polr1has |
TCACCACCACCACCACCACCACCAC |
TCACCACCACCACCACCACCAC |
17: 37,275,939 (GRCm39) |
|
probably benign |
Het |
Ppp1r37 |
A |
T |
7: 19,295,796 (GRCm39) |
F54I |
probably damaging |
Het |
Prl7c1 |
T |
A |
13: 27,957,870 (GRCm39) |
Y190F |
probably benign |
Het |
Prpf8 |
A |
G |
11: 75,397,212 (GRCm39) |
E2015G |
possibly damaging |
Het |
Rpap3 |
A |
G |
15: 97,579,641 (GRCm39) |
V457A |
|
Het |
Samd13 |
A |
T |
3: 146,368,510 (GRCm39) |
D27E |
|
Het |
Sephs1 |
A |
T |
2: 4,889,174 (GRCm39) |
|
probably benign |
Het |
Slc22a20 |
T |
G |
19: 6,023,024 (GRCm39) |
Q373P |
probably damaging |
Het |
Sp100 |
A |
G |
1: 85,629,179 (GRCm39) |
*483W |
probably null |
Het |
Src |
A |
T |
2: 157,307,852 (GRCm39) |
T254S |
probably damaging |
Het |
St6galnac2 |
A |
T |
11: 116,569,344 (GRCm39) |
M301K |
possibly damaging |
Het |
Tnfsf13 |
A |
T |
11: 69,576,010 (GRCm39) |
W26R |
probably damaging |
Het |
Trbv28 |
T |
A |
6: 41,248,687 (GRCm39) |
D72E |
probably benign |
Het |
Trim75 |
T |
A |
8: 65,436,561 (GRCm39) |
|
probably benign |
Het |
Ttc39d |
T |
C |
17: 80,524,754 (GRCm39) |
F471S |
probably damaging |
Het |
Vav1 |
C |
T |
17: 57,613,191 (GRCm39) |
P621L |
probably benign |
Het |
Vezt |
A |
T |
10: 93,832,856 (GRCm39) |
L185* |
probably null |
Het |
Vmn2r42 |
T |
C |
7: 8,187,295 (GRCm39) |
I826V |
probably benign |
Het |
Vmn2r67 |
G |
A |
7: 84,800,697 (GRCm39) |
T413M |
probably benign |
Het |
Vnn1 |
G |
A |
10: 23,776,723 (GRCm39) |
C358Y |
probably damaging |
Het |
Wdr83os |
G |
C |
8: 85,808,638 (GRCm39) |
W106C |
probably damaging |
Het |
Wdr95 |
T |
C |
5: 149,475,917 (GRCm39) |
S72P |
probably damaging |
Het |
Zfp423 |
T |
A |
8: 88,508,251 (GRCm39) |
T698S |
probably damaging |
Het |
Zfp521 |
G |
A |
18: 13,977,293 (GRCm39) |
T1040I |
probably damaging |
Het |
Zmym2 |
T |
A |
14: 57,180,770 (GRCm39) |
V894E |
probably damaging |
Het |
|
Other mutations in Zfp563 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01629:Zfp563
|
APN |
17 |
33,323,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01981:Zfp563
|
APN |
17 |
33,324,383 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02407:Zfp563
|
APN |
17 |
33,323,795 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02662:Zfp563
|
APN |
17 |
33,321,253 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03220:Zfp563
|
APN |
17 |
33,323,661 (GRCm39) |
missense |
probably benign |
0.44 |
R0241:Zfp563
|
UTSW |
17 |
33,323,659 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0241:Zfp563
|
UTSW |
17 |
33,323,659 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0537:Zfp563
|
UTSW |
17 |
33,323,659 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0552:Zfp563
|
UTSW |
17 |
33,323,659 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1544:Zfp563
|
UTSW |
17 |
33,324,187 (GRCm39) |
missense |
probably benign |
0.01 |
R3763:Zfp563
|
UTSW |
17 |
33,323,902 (GRCm39) |
nonsense |
probably null |
|
R3979:Zfp563
|
UTSW |
17 |
33,324,701 (GRCm39) |
missense |
probably benign |
0.03 |
R4938:Zfp563
|
UTSW |
17 |
33,324,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5280:Zfp563
|
UTSW |
17 |
33,323,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R5383:Zfp563
|
UTSW |
17 |
33,323,681 (GRCm39) |
missense |
probably benign |
|
R5485:Zfp563
|
UTSW |
17 |
33,308,540 (GRCm39) |
unclassified |
probably benign |
|
R5524:Zfp563
|
UTSW |
17 |
33,321,515 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5567:Zfp563
|
UTSW |
17 |
33,308,431 (GRCm39) |
unclassified |
probably benign |
|
R5736:Zfp563
|
UTSW |
17 |
33,323,960 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5758:Zfp563
|
UTSW |
17 |
33,323,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Zfp563
|
UTSW |
17 |
33,323,935 (GRCm39) |
missense |
probably damaging |
0.96 |
R6034:Zfp563
|
UTSW |
17 |
33,323,935 (GRCm39) |
missense |
probably damaging |
0.96 |
R6532:Zfp563
|
UTSW |
17 |
33,324,672 (GRCm39) |
missense |
probably benign |
0.21 |
R9241:Zfp563
|
UTSW |
17 |
33,321,520 (GRCm39) |
missense |
probably benign |
0.10 |
R9360:Zfp563
|
UTSW |
17 |
33,324,428 (GRCm39) |
missense |
probably benign |
0.38 |
R9410:Zfp563
|
UTSW |
17 |
33,321,320 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Zfp563
|
UTSW |
17 |
33,323,999 (GRCm39) |
missense |
probably benign |
|
X0023:Zfp563
|
UTSW |
17 |
33,324,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|