Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
G |
7: 120,000,972 (GRCm39) |
M1503V |
possibly damaging |
Het |
Abraxas1 |
A |
T |
5: 100,966,403 (GRCm39) |
V53D |
probably damaging |
Het |
Bub1b |
T |
C |
2: 118,461,463 (GRCm39) |
S672P |
probably damaging |
Het |
Cacng7 |
A |
T |
7: 3,415,420 (GRCm39) |
I262F |
probably benign |
Het |
Capzb |
T |
G |
4: 139,006,738 (GRCm39) |
|
probably benign |
Het |
Ccdc149 |
A |
G |
5: 52,561,493 (GRCm39) |
V229A |
probably damaging |
Het |
Cfap69 |
A |
G |
5: 5,676,020 (GRCm39) |
L225P |
probably damaging |
Het |
Cftr |
A |
G |
6: 18,268,095 (GRCm39) |
T685A |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,611,041 (GRCm39) |
T177M |
probably damaging |
Het |
Creb3l3 |
T |
G |
10: 80,920,881 (GRCm39) |
D383A |
probably benign |
Het |
Cyp2j8 |
T |
A |
4: 96,395,578 (GRCm39) |
I16F |
probably benign |
Het |
Dnah5 |
G |
T |
15: 28,343,754 (GRCm39) |
A2385S |
probably damaging |
Het |
Enox1 |
A |
G |
14: 77,816,493 (GRCm39) |
I158V |
probably benign |
Het |
Erich3 |
A |
T |
3: 154,433,033 (GRCm39) |
T139S |
probably damaging |
Het |
Fam186b |
A |
T |
15: 99,169,170 (GRCm39) |
S926T |
possibly damaging |
Het |
Gjd2 |
C |
A |
2: 113,841,965 (GRCm39) |
V171F |
possibly damaging |
Het |
Helz2 |
A |
T |
2: 180,879,082 (GRCm39) |
|
probably benign |
Het |
Herc1 |
T |
TTN |
9: 66,341,345 (GRCm39) |
|
probably benign |
Het |
Impg1 |
A |
T |
9: 80,252,500 (GRCm39) |
V483E |
probably benign |
Het |
Irx4 |
A |
G |
13: 73,415,799 (GRCm39) |
N196S |
probably damaging |
Het |
Kcnip1 |
T |
C |
11: 33,580,597 (GRCm39) |
D213G |
probably damaging |
Het |
Lmntd1 |
T |
A |
6: 145,359,140 (GRCm39) |
T191S |
probably benign |
Het |
Med12l |
T |
A |
3: 59,159,771 (GRCm39) |
N1273K |
probably benign |
Het |
Musk |
T |
C |
4: 58,373,036 (GRCm39) |
C654R |
probably damaging |
Het |
Nlrp4d |
A |
T |
7: 10,115,951 (GRCm39) |
S274T |
noncoding transcript |
Het |
Omd |
A |
G |
13: 49,745,814 (GRCm39) |
H408R |
probably benign |
Het |
Pbld2 |
C |
T |
10: 62,907,791 (GRCm39) |
A219V |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,381,025 (GRCm39) |
T333S |
probably damaging |
Het |
Pramel32 |
C |
T |
4: 88,548,292 (GRCm39) |
E38K |
probably damaging |
Het |
Ptpn1 |
T |
C |
2: 167,816,683 (GRCm39) |
I246T |
probably damaging |
Het |
Sap18b |
G |
T |
8: 96,551,998 (GRCm39) |
A3S |
unknown |
Het |
Sptbn5 |
G |
A |
2: 119,876,965 (GRCm39) |
|
probably benign |
Het |
Sstr4 |
G |
T |
2: 148,237,652 (GRCm39) |
V88F |
possibly damaging |
Het |
Tdpoz4 |
A |
T |
3: 93,704,806 (GRCm39) |
T368S |
probably benign |
Het |
Tmcc2 |
T |
C |
1: 132,288,221 (GRCm39) |
N489D |
probably damaging |
Het |
Tnfrsf9 |
T |
C |
4: 151,014,331 (GRCm39) |
V10A |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,907,778 (GRCm39) |
V1274E |
probably damaging |
Het |
Ube3b |
T |
A |
5: 114,544,221 (GRCm39) |
|
probably null |
Het |
Vwa5a |
A |
T |
9: 38,633,874 (GRCm39) |
I26F |
probably damaging |
Het |
|
Other mutations in C1qtnf7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01323:C1qtnf7
|
APN |
5 |
43,766,602 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01411:C1qtnf7
|
APN |
5 |
43,766,403 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R1464:C1qtnf7
|
UTSW |
5 |
43,766,481 (GRCm39) |
missense |
probably benign |
0.18 |
R1464:C1qtnf7
|
UTSW |
5 |
43,766,481 (GRCm39) |
missense |
probably benign |
0.18 |
R1630:C1qtnf7
|
UTSW |
5 |
43,766,503 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2883:C1qtnf7
|
UTSW |
5 |
43,773,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R4441:C1qtnf7
|
UTSW |
5 |
43,766,612 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4569:C1qtnf7
|
UTSW |
5 |
43,766,549 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5101:C1qtnf7
|
UTSW |
5 |
43,773,314 (GRCm39) |
nonsense |
probably null |
|
R5180:C1qtnf7
|
UTSW |
5 |
43,773,156 (GRCm39) |
missense |
probably benign |
0.19 |
R5886:C1qtnf7
|
UTSW |
5 |
43,772,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5997:C1qtnf7
|
UTSW |
5 |
43,773,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:C1qtnf7
|
UTSW |
5 |
43,766,436 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6971:C1qtnf7
|
UTSW |
5 |
43,766,392 (GRCm39) |
splice site |
probably null |
|
R7615:C1qtnf7
|
UTSW |
5 |
43,773,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:C1qtnf7
|
UTSW |
5 |
43,773,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R8942:C1qtnf7
|
UTSW |
5 |
43,773,583 (GRCm39) |
missense |
probably benign |
0.01 |
R9300:C1qtnf7
|
UTSW |
5 |
43,766,441 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9777:C1qtnf7
|
UTSW |
5 |
43,673,313 (GRCm39) |
start gained |
probably benign |
|
|