Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AC133488.1 |
A |
T |
16: 18,440,075 (GRCm39) |
V363E |
probably benign |
Het |
Adamts16 |
A |
G |
13: 70,901,408 (GRCm39) |
S890P |
probably benign |
Het |
Amd1 |
A |
G |
10: 40,169,158 (GRCm39) |
|
probably null |
Het |
Apcs |
A |
G |
1: 172,722,061 (GRCm39) |
I95T |
probably damaging |
Het |
Arhgap18 |
A |
G |
10: 26,730,886 (GRCm39) |
D188G |
probably benign |
Het |
Arhgap42 |
C |
T |
9: 9,011,419 (GRCm39) |
V456M |
probably damaging |
Het |
Atp2a2 |
T |
C |
5: 122,599,633 (GRCm39) |
Y586C |
probably damaging |
Het |
Cbr1 |
G |
C |
16: 93,406,794 (GRCm39) |
G170A |
probably benign |
Het |
Cdh23 |
T |
A |
10: 60,270,283 (GRCm39) |
|
probably benign |
Het |
Clcn3 |
A |
G |
8: 61,382,136 (GRCm39) |
I511T |
probably damaging |
Het |
Col28a1 |
T |
A |
6: 8,014,993 (GRCm39) |
D804V |
probably damaging |
Het |
Csmd2 |
A |
G |
4: 128,443,007 (GRCm39) |
T3253A |
|
Het |
Csta3 |
G |
A |
16: 36,038,069 (GRCm39) |
V69I |
probably benign |
Het |
Cyp2c40 |
A |
T |
19: 39,762,317 (GRCm39) |
D443E |
probably damaging |
Het |
Cyp7b1 |
A |
G |
3: 18,151,476 (GRCm39) |
C246R |
probably benign |
Het |
Dmxl1 |
C |
G |
18: 50,072,639 (GRCm39) |
N2744K |
probably damaging |
Het |
Dnai4 |
A |
G |
4: 102,916,930 (GRCm39) |
M592T |
probably damaging |
Het |
Dpyd |
T |
A |
3: 118,710,897 (GRCm39) |
I435N |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,189,436 (GRCm39) |
L1194Q |
possibly damaging |
Het |
Firrm |
A |
G |
1: 163,814,514 (GRCm39) |
I143T |
probably damaging |
Het |
Gabrg1 |
A |
T |
5: 70,939,622 (GRCm39) |
I170N |
possibly damaging |
Het |
Gon4l |
C |
T |
3: 88,815,484 (GRCm39) |
P2016S |
probably benign |
Het |
Hax1 |
T |
C |
3: 89,903,127 (GRCm39) |
R251G |
probably damaging |
Het |
Hbq1b |
A |
T |
11: 32,237,228 (GRCm39) |
K41* |
probably null |
Het |
Ido2 |
G |
A |
8: 25,023,933 (GRCm39) |
P302S |
probably damaging |
Het |
Igf2bp2 |
G |
A |
16: 21,900,502 (GRCm39) |
T213I |
probably damaging |
Het |
Itga2 |
A |
T |
13: 115,014,298 (GRCm39) |
L210* |
probably null |
Het |
Kdm1b |
G |
A |
13: 47,225,458 (GRCm39) |
S547N |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Lyz2 |
A |
T |
10: 117,116,562 (GRCm39) |
C95* |
probably null |
Het |
Mafa |
A |
T |
15: 75,619,048 (GRCm39) |
S242T |
possibly damaging |
Het |
Mapk1 |
T |
C |
16: 16,856,300 (GRCm39) |
|
probably null |
Het |
Mta1 |
T |
A |
12: 113,100,025 (GRCm39) |
V645E |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,363,529 (GRCm39) |
I2280T |
unknown |
Het |
Naa35 |
T |
C |
13: 59,772,341 (GRCm39) |
I438T |
possibly damaging |
Het |
Necab2 |
T |
C |
8: 120,189,303 (GRCm39) |
Y158H |
probably damaging |
Het |
Nphp3 |
T |
A |
9: 103,897,980 (GRCm39) |
L523Q |
probably damaging |
Het |
Ogdh |
A |
T |
11: 6,290,488 (GRCm39) |
I369F |
probably benign |
Het |
Pglyrp4 |
C |
T |
3: 90,635,238 (GRCm39) |
Q28* |
probably null |
Het |
Pla2g4a |
C |
T |
1: 149,747,230 (GRCm39) |
V319I |
probably benign |
Het |
Plk3 |
ACACTCAC |
ACAC |
4: 116,989,090 (GRCm39) |
|
probably benign |
Het |
Prdm6 |
C |
A |
18: 53,598,019 (GRCm39) |
A127D |
unknown |
Het |
Prop1 |
T |
G |
11: 50,843,037 (GRCm39) |
E50A |
|
Het |
Ripk1 |
A |
G |
13: 34,212,184 (GRCm39) |
N498S |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,374,742 (GRCm39) |
N5069S |
|
Het |
Saa3 |
T |
C |
7: 46,362,121 (GRCm39) |
D41G |
probably damaging |
Het |
Setd2 |
T |
C |
9: 110,374,385 (GRCm39) |
|
probably null |
Het |
Shbg |
G |
A |
11: 69,506,430 (GRCm39) |
L327F |
probably benign |
Het |
Slc12a5 |
G |
A |
2: 164,835,876 (GRCm39) |
|
probably benign |
Het |
Slc1a4 |
C |
T |
11: 20,258,527 (GRCm39) |
G304D |
probably damaging |
Het |
Slf1 |
T |
C |
13: 77,249,073 (GRCm39) |
K372E |
probably benign |
Het |
Smad2 |
T |
A |
18: 76,395,573 (GRCm39) |
I4N |
possibly damaging |
Het |
Smad6 |
A |
C |
9: 63,914,870 (GRCm39) |
S300A |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,127,896 (GRCm39) |
T1705A |
possibly damaging |
Het |
Spem2 |
T |
A |
11: 69,707,414 (GRCm39) |
|
probably benign |
Het |
Syde1 |
T |
C |
10: 78,425,340 (GRCm39) |
S224G |
probably benign |
Het |
Tacc1 |
A |
T |
8: 25,672,151 (GRCm39) |
V359E |
possibly damaging |
Het |
Tex15 |
T |
G |
8: 34,067,554 (GRCm39) |
V2328G |
possibly damaging |
Het |
Tmem43 |
A |
C |
6: 91,459,291 (GRCm39) |
D254A |
probably benign |
Het |
Trav6d-3 |
T |
A |
14: 52,964,210 (GRCm39) |
Y58N |
possibly damaging |
Het |
Trrap |
A |
G |
5: 144,726,362 (GRCm39) |
E437G |
probably benign |
Het |
Wars1 |
A |
G |
12: 108,827,199 (GRCm39) |
F474L |
probably benign |
Het |
Zfp169 |
T |
C |
13: 48,644,557 (GRCm39) |
E190G |
unknown |
Het |
Zfp541 |
T |
A |
7: 15,816,966 (GRCm39) |
V918D |
probably benign |
Het |
Zfp747 |
T |
C |
7: 126,974,922 (GRCm39) |
D26G |
probably damaging |
Het |
|
Other mutations in Cfap53 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00579:Cfap53
|
APN |
18 |
74,438,611 (GRCm39) |
nonsense |
probably null |
|
IGL00667:Cfap53
|
APN |
18 |
74,433,263 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00917:Cfap53
|
APN |
18 |
74,432,367 (GRCm39) |
missense |
probably benign |
0.08 |
R0009:Cfap53
|
UTSW |
18 |
74,432,247 (GRCm39) |
missense |
probably benign |
0.00 |
R0009:Cfap53
|
UTSW |
18 |
74,432,247 (GRCm39) |
missense |
probably benign |
0.00 |
R0035:Cfap53
|
UTSW |
18 |
74,433,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Cfap53
|
UTSW |
18 |
74,433,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Cfap53
|
UTSW |
18 |
74,432,244 (GRCm39) |
missense |
probably benign |
0.09 |
R0601:Cfap53
|
UTSW |
18 |
74,433,221 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0939:Cfap53
|
UTSW |
18 |
74,438,801 (GRCm39) |
missense |
probably null |
0.72 |
R1166:Cfap53
|
UTSW |
18 |
74,433,251 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1588:Cfap53
|
UTSW |
18 |
74,440,444 (GRCm39) |
missense |
probably benign |
|
R2105:Cfap53
|
UTSW |
18 |
74,416,294 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2186:Cfap53
|
UTSW |
18 |
74,462,576 (GRCm39) |
splice site |
probably null |
|
R3723:Cfap53
|
UTSW |
18 |
74,492,640 (GRCm39) |
missense |
probably benign |
0.13 |
R3724:Cfap53
|
UTSW |
18 |
74,492,640 (GRCm39) |
missense |
probably benign |
0.13 |
R3904:Cfap53
|
UTSW |
18 |
74,440,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R5156:Cfap53
|
UTSW |
18 |
74,492,838 (GRCm39) |
utr 3 prime |
probably benign |
|
R5262:Cfap53
|
UTSW |
18 |
74,462,530 (GRCm39) |
missense |
probably benign |
0.39 |
R5928:Cfap53
|
UTSW |
18 |
74,492,811 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6405:Cfap53
|
UTSW |
18 |
74,492,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6653:Cfap53
|
UTSW |
18 |
74,433,280 (GRCm39) |
missense |
probably damaging |
0.97 |
R6675:Cfap53
|
UTSW |
18 |
74,440,447 (GRCm39) |
critical splice donor site |
probably null |
|
R7011:Cfap53
|
UTSW |
18 |
74,462,564 (GRCm39) |
missense |
probably benign |
0.13 |
R7397:Cfap53
|
UTSW |
18 |
74,416,294 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8943:Cfap53
|
UTSW |
18 |
74,432,253 (GRCm39) |
missense |
probably damaging |
0.97 |
R9159:Cfap53
|
UTSW |
18 |
74,416,272 (GRCm39) |
missense |
probably damaging |
0.98 |
R9389:Cfap53
|
UTSW |
18 |
74,432,414 (GRCm39) |
critical splice donor site |
probably null |
|
R9548:Cfap53
|
UTSW |
18 |
74,438,040 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9679:Cfap53
|
UTSW |
18 |
74,492,656 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9792:Cfap53
|
UTSW |
18 |
74,438,741 (GRCm39) |
missense |
probably benign |
0.44 |
R9793:Cfap53
|
UTSW |
18 |
74,438,741 (GRCm39) |
missense |
probably benign |
0.44 |
R9795:Cfap53
|
UTSW |
18 |
74,438,741 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Cfap53
|
UTSW |
18 |
74,438,623 (GRCm39) |
nonsense |
probably null |
|
|