Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
A |
G |
15: 11,215,821 (GRCm39) |
M281V |
probably damaging |
Het |
Ap1g1 |
A |
T |
8: 110,570,986 (GRCm39) |
D423V |
probably damaging |
Het |
Arel1 |
A |
G |
12: 84,968,030 (GRCm39) |
|
probably null |
Het |
Arhgap33 |
T |
C |
7: 30,228,075 (GRCm39) |
|
probably null |
Het |
Arhgef18 |
T |
G |
8: 3,489,575 (GRCm39) |
Y302* |
probably null |
Het |
Blm |
T |
C |
7: 80,131,118 (GRCm39) |
|
probably null |
Het |
Cep295 |
T |
G |
9: 15,264,354 (GRCm39) |
E97D |
probably damaging |
Het |
Cep295nl |
T |
C |
11: 118,223,335 (GRCm39) |
D503G |
possibly damaging |
Het |
Chchd2 |
G |
T |
5: 129,912,989 (GRCm39) |
A29E |
probably damaging |
Het |
Cic |
A |
G |
7: 24,987,559 (GRCm39) |
|
probably null |
Het |
Cmtr1 |
C |
T |
17: 29,921,147 (GRCm39) |
L798F |
probably benign |
Het |
Col11a2 |
C |
A |
17: 34,283,771 (GRCm39) |
|
probably benign |
Het |
Crispld2 |
A |
G |
8: 120,742,078 (GRCm39) |
Y142C |
probably damaging |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Dsp |
G |
A |
13: 38,380,427 (GRCm39) |
D1792N |
probably damaging |
Het |
Esp4 |
C |
A |
17: 40,913,284 (GRCm39) |
N50K |
probably benign |
Het |
Fbxo21 |
T |
C |
5: 118,133,451 (GRCm39) |
S404P |
probably damaging |
Het |
Ggnbp2 |
A |
G |
11: 84,725,259 (GRCm39) |
F639L |
probably benign |
Het |
Golph3l |
G |
A |
3: 95,524,436 (GRCm39) |
G229D |
probably damaging |
Het |
Hlx |
G |
T |
1: 184,459,838 (GRCm39) |
S433R |
probably benign |
Het |
Kdm2b |
T |
A |
5: 123,018,762 (GRCm39) |
S233C |
probably damaging |
Het |
Krt14 |
C |
T |
11: 100,097,939 (GRCm39) |
G115R |
unknown |
Het |
Ldb3 |
A |
G |
14: 34,289,353 (GRCm39) |
|
probably null |
Het |
Lrp1 |
T |
A |
10: 127,391,607 (GRCm39) |
E2937D |
probably damaging |
Het |
Mark2 |
G |
C |
19: 7,260,112 (GRCm39) |
S111C |
probably damaging |
Het |
Naa20 |
T |
A |
2: 145,753,715 (GRCm39) |
|
probably null |
Het |
Ndufa8 |
A |
T |
2: 35,926,527 (GRCm39) |
W170R |
probably damaging |
Het |
Nlrp2 |
A |
T |
7: 5,328,041 (GRCm39) |
L671I |
probably damaging |
Het |
Or52e19b |
T |
A |
7: 103,032,407 (GRCm39) |
R267S |
probably benign |
Het |
Or5b108 |
T |
A |
19: 13,168,673 (GRCm39) |
I214K |
probably damaging |
Het |
Ptgir |
A |
G |
7: 16,640,794 (GRCm39) |
M29V |
possibly damaging |
Het |
Ptpro |
A |
G |
6: 137,426,885 (GRCm39) |
D280G |
probably benign |
Het |
Reps1 |
A |
G |
10: 17,972,031 (GRCm39) |
E361G |
probably damaging |
Het |
Rgs6 |
A |
G |
12: 83,138,578 (GRCm39) |
E304G |
probably damaging |
Het |
Slc5a10 |
C |
T |
11: 61,610,760 (GRCm39) |
G5R |
probably null |
Het |
Sohlh1 |
A |
G |
2: 25,734,648 (GRCm39) |
I215T |
probably benign |
Het |
Stag1 |
T |
A |
9: 100,771,648 (GRCm39) |
V691D |
probably damaging |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Tmed8 |
A |
G |
12: 87,221,031 (GRCm39) |
V185A |
probably damaging |
Het |
Trim71 |
A |
G |
9: 114,341,840 (GRCm39) |
F814S |
probably damaging |
Het |
Trmt9b |
T |
C |
8: 36,972,804 (GRCm39) |
C85R |
probably damaging |
Het |
Tsnax |
A |
T |
8: 125,742,428 (GRCm39) |
K52N |
probably damaging |
Het |
Tubgcp3 |
T |
C |
8: 12,682,292 (GRCm39) |
T676A |
probably benign |
Het |
|
Other mutations in Siglece |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0502:Siglece
|
UTSW |
7 |
43,309,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R1766:Siglece
|
UTSW |
7 |
43,300,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R1772:Siglece
|
UTSW |
7 |
43,308,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Siglece
|
UTSW |
7 |
43,309,360 (GRCm39) |
missense |
probably benign |
0.01 |
R1854:Siglece
|
UTSW |
7 |
43,309,360 (GRCm39) |
missense |
probably benign |
0.01 |
R1914:Siglece
|
UTSW |
7 |
43,307,219 (GRCm39) |
missense |
probably benign |
0.03 |
R2060:Siglece
|
UTSW |
7 |
43,307,210 (GRCm39) |
missense |
probably benign |
0.25 |
R4461:Siglece
|
UTSW |
7 |
43,300,929 (GRCm39) |
missense |
probably benign |
0.00 |
R4924:Siglece
|
UTSW |
7 |
43,309,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Siglece
|
UTSW |
7 |
43,308,396 (GRCm39) |
critical splice donor site |
probably null |
|
R5864:Siglece
|
UTSW |
7 |
43,308,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R5956:Siglece
|
UTSW |
7 |
43,308,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R7111:Siglece
|
UTSW |
7 |
43,309,327 (GRCm39) |
missense |
probably damaging |
0.99 |
R8395:Siglece
|
UTSW |
7 |
43,305,523 (GRCm39) |
missense |
probably benign |
0.03 |
R8490:Siglece
|
UTSW |
7 |
43,309,486 (GRCm39) |
missense |
probably benign |
|
R9218:Siglece
|
UTSW |
7 |
43,307,162 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9535:Siglece
|
UTSW |
7 |
43,307,055 (GRCm39) |
missense |
probably benign |
0.00 |
|