Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
G |
A |
10: 29,100,896 (GRCm39) |
R423K |
probably benign |
Het |
Acot7 |
T |
C |
4: 152,307,575 (GRCm39) |
S170P |
probably damaging |
Het |
Arhgap40 |
A |
G |
2: 158,380,620 (GRCm39) |
Q341R |
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,082,189 (GRCm39) |
E1206G |
possibly damaging |
Het |
Arpp21 |
T |
A |
9: 112,008,133 (GRCm39) |
K122N |
probably damaging |
Het |
Arsi |
T |
C |
18: 61,049,726 (GRCm39) |
L203P |
possibly damaging |
Het |
C1rb |
A |
T |
6: 124,557,488 (GRCm39) |
I542F |
probably benign |
Het |
Cadm3 |
C |
A |
1: 173,171,956 (GRCm39) |
V206L |
probably benign |
Het |
Card11 |
T |
C |
5: 140,885,419 (GRCm39) |
D380G |
probably damaging |
Het |
Ccdc42 |
A |
T |
11: 68,488,534 (GRCm39) |
Q164L |
probably benign |
Het |
Ccnd1 |
A |
G |
7: 144,491,622 (GRCm39) |
|
probably null |
Het |
Cep120 |
T |
C |
18: 53,871,578 (GRCm39) |
D98G |
probably damaging |
Het |
Chrd |
A |
G |
16: 20,554,155 (GRCm39) |
T336A |
probably benign |
Het |
Clca3a2 |
C |
A |
3: 144,790,726 (GRCm39) |
A449S |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,657,245 (GRCm39) |
F844L |
probably benign |
Het |
Fbxo11 |
T |
A |
17: 88,308,245 (GRCm39) |
I480F |
|
Het |
Fcrl5 |
A |
G |
3: 87,350,930 (GRCm39) |
T147A |
probably benign |
Het |
Gm15130 |
T |
A |
2: 110,969,320 (GRCm39) |
I133F |
|
Het |
Gpr155 |
C |
T |
2: 73,212,329 (GRCm39) |
W98* |
probably null |
Het |
Hspa4 |
A |
G |
11: 53,162,863 (GRCm39) |
S408P |
probably damaging |
Het |
Il12rb2 |
G |
A |
6: 67,333,635 (GRCm39) |
R215C |
possibly damaging |
Het |
Itga5 |
T |
A |
15: 103,265,741 (GRCm39) |
|
probably null |
Het |
Kcnip3 |
T |
A |
2: 127,323,703 (GRCm39) |
|
probably null |
Het |
Krt12 |
A |
G |
11: 99,309,309 (GRCm39) |
|
probably null |
Het |
Marchf3 |
A |
T |
18: 56,916,163 (GRCm39) |
S177R |
probably benign |
Het |
Minpp1 |
T |
G |
19: 32,468,803 (GRCm39) |
F229V |
probably damaging |
Het |
Muc2 |
G |
A |
7: 141,282,543 (GRCm39) |
|
probably null |
Het |
Myh10 |
A |
G |
11: 68,676,735 (GRCm39) |
T906A |
probably benign |
Het |
Myh13 |
A |
G |
11: 67,218,056 (GRCm39) |
D43G |
probably benign |
Het |
Nacad |
C |
T |
11: 6,549,071 (GRCm39) |
D1327N |
probably benign |
Het |
Nbeal1 |
A |
T |
1: 60,331,048 (GRCm39) |
Y2219F |
probably damaging |
Het |
Nckap5 |
A |
G |
1: 125,953,163 (GRCm39) |
S1130P |
probably benign |
Het |
Pfkfb3 |
T |
C |
2: 11,486,719 (GRCm39) |
N415S |
probably benign |
Het |
Plxdc2 |
A |
G |
2: 16,665,678 (GRCm39) |
I293V |
possibly damaging |
Het |
Prpf38a |
A |
T |
4: 108,436,277 (GRCm39) |
I12N |
probably damaging |
Het |
Ptprt |
C |
T |
2: 161,372,413 (GRCm39) |
V1420M |
probably damaging |
Het |
Qars1 |
A |
G |
9: 108,386,670 (GRCm39) |
D161G |
probably damaging |
Het |
Scaf8 |
T |
A |
17: 3,247,549 (GRCm39) |
D957E |
probably damaging |
Het |
Scn7a |
T |
C |
2: 66,506,689 (GRCm39) |
Y1400C |
probably damaging |
Het |
Sis |
T |
C |
3: 72,832,801 (GRCm39) |
I999V |
probably benign |
Het |
Sorcs2 |
A |
T |
5: 36,181,958 (GRCm39) |
L1054H |
probably damaging |
Het |
Sptbn1 |
C |
T |
11: 30,088,455 (GRCm39) |
A906T |
probably damaging |
Het |
Srd5a2 |
A |
G |
17: 74,331,541 (GRCm39) |
F152S |
probably benign |
Het |
Stkld1 |
T |
A |
2: 26,835,888 (GRCm39) |
L241* |
probably null |
Het |
Strip2 |
A |
T |
6: 29,923,912 (GRCm39) |
|
probably null |
Het |
Tcaf1 |
A |
C |
6: 42,650,363 (GRCm39) |
Y905* |
probably null |
Het |
Tet2 |
T |
C |
3: 133,179,404 (GRCm39) |
I1254V |
probably benign |
Het |
Tiam2 |
A |
T |
17: 3,487,522 (GRCm39) |
N681I |
probably damaging |
Het |
Trappc6a |
A |
G |
7: 19,248,124 (GRCm39) |
|
probably null |
Het |
Trav12-2 |
A |
T |
14: 53,854,223 (GRCm39) |
K66* |
probably null |
Het |
Ttn |
T |
A |
2: 76,597,841 (GRCm39) |
I19691F |
probably damaging |
Het |
Tubgcp5 |
A |
T |
7: 55,450,444 (GRCm39) |
Q185L |
possibly damaging |
Het |
Vmn1r44 |
A |
T |
6: 89,869,192 (GRCm39) |
|
probably benign |
Het |
Vps13a |
T |
C |
19: 16,628,820 (GRCm39) |
D2717G |
possibly damaging |
Het |
Vps13d |
A |
T |
4: 144,904,633 (GRCm39) |
Y133* |
probably null |
Het |
Zer1 |
T |
C |
2: 30,000,385 (GRCm39) |
D265G |
probably damaging |
Het |
Zfp710 |
A |
G |
7: 79,730,859 (GRCm39) |
D12G |
possibly damaging |
Het |
|
Other mutations in Zfp819 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Zfp819
|
APN |
7 |
43,261,403 (GRCm39) |
splice site |
probably benign |
|
IGL01732:Zfp819
|
APN |
7 |
43,265,846 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02139:Zfp819
|
APN |
7 |
43,261,534 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02276:Zfp819
|
APN |
7 |
43,261,428 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0306:Zfp819
|
UTSW |
7 |
43,266,621 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0620:Zfp819
|
UTSW |
7 |
43,265,868 (GRCm39) |
missense |
probably benign |
0.07 |
R1301:Zfp819
|
UTSW |
7 |
43,266,524 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1314:Zfp819
|
UTSW |
7 |
43,266,480 (GRCm39) |
missense |
probably benign |
0.27 |
R1980:Zfp819
|
UTSW |
7 |
43,265,885 (GRCm39) |
missense |
probably benign |
|
R4545:Zfp819
|
UTSW |
7 |
43,267,209 (GRCm39) |
missense |
probably damaging |
0.98 |
R4993:Zfp819
|
UTSW |
7 |
43,266,720 (GRCm39) |
missense |
probably benign |
0.37 |
R5053:Zfp819
|
UTSW |
7 |
43,266,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R6080:Zfp819
|
UTSW |
7 |
43,266,120 (GRCm39) |
missense |
probably benign |
0.00 |
R7289:Zfp819
|
UTSW |
7 |
43,266,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7387:Zfp819
|
UTSW |
7 |
43,262,065 (GRCm39) |
critical splice donor site |
probably null |
|
R7608:Zfp819
|
UTSW |
7 |
43,266,357 (GRCm39) |
missense |
probably benign |
|
R7863:Zfp819
|
UTSW |
7 |
43,267,316 (GRCm39) |
missense |
probably benign |
0.17 |
R8026:Zfp819
|
UTSW |
7 |
43,267,319 (GRCm39) |
missense |
probably benign |
0.44 |
R8080:Zfp819
|
UTSW |
7 |
43,267,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Zfp819
|
UTSW |
7 |
43,266,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R9073:Zfp819
|
UTSW |
7 |
43,266,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R9199:Zfp819
|
UTSW |
7 |
43,267,203 (GRCm39) |
missense |
probably benign |
0.04 |
R9792:Zfp819
|
UTSW |
7 |
43,261,519 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Zfp819
|
UTSW |
7 |
43,267,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|