Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,234,200 (GRCm39) |
C1067S |
possibly damaging |
Het |
Agbl3 |
T |
A |
6: 34,834,688 (GRCm39) |
S952R |
possibly damaging |
Het |
Ano9 |
A |
G |
7: 140,686,698 (GRCm39) |
Y429H |
probably damaging |
Het |
Bbs7 |
C |
A |
3: 36,667,415 (GRCm39) |
R7L |
probably damaging |
Het |
Birc2 |
T |
A |
9: 7,849,684 (GRCm39) |
D535V |
possibly damaging |
Het |
Catsper4 |
A |
G |
4: 133,945,240 (GRCm39) |
V206A |
probably damaging |
Het |
Ccdc73 |
T |
G |
2: 104,822,482 (GRCm39) |
S810R |
possibly damaging |
Het |
Cd177 |
A |
T |
7: 24,443,698 (GRCm39) |
L800* |
probably null |
Het |
Cd34 |
T |
C |
1: 194,630,316 (GRCm39) |
|
probably null |
Het |
Cep78 |
G |
A |
19: 15,959,150 (GRCm39) |
R95* |
probably null |
Het |
Cfap69 |
T |
C |
5: 5,713,996 (GRCm39) |
D12G |
probably benign |
Het |
Cpne7 |
A |
G |
8: 123,854,171 (GRCm39) |
D286G |
probably benign |
Het |
Cwc22 |
ATCTCTCTCTCTCTCTCT |
ATCTCTCTCTCTCTCT |
2: 77,759,803 (GRCm39) |
|
probably null |
Het |
Cxcl5 |
A |
T |
5: 90,907,565 (GRCm39) |
I46L |
probably benign |
Het |
Cyp19a1 |
C |
T |
9: 54,087,540 (GRCm39) |
G59D |
probably damaging |
Het |
Dclre1c |
A |
G |
2: 3,438,742 (GRCm39) |
D35G |
probably damaging |
Het |
Defa41 |
A |
G |
8: 21,692,428 (GRCm39) |
N83S |
probably benign |
Het |
Dvl1 |
A |
G |
4: 155,939,409 (GRCm39) |
Y279C |
probably damaging |
Het |
Fes |
A |
G |
7: 80,030,044 (GRCm39) |
L578P |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Fmn2 |
T |
C |
1: 174,494,229 (GRCm39) |
S1248P |
probably damaging |
Het |
Fmo1 |
T |
G |
1: 162,679,088 (GRCm39) |
S53R |
probably damaging |
Het |
Gabrg1 |
A |
T |
5: 70,931,804 (GRCm39) |
M313K |
probably damaging |
Het |
Galnt10 |
T |
C |
11: 57,675,474 (GRCm39) |
C578R |
probably damaging |
Het |
Gpr39 |
T |
C |
1: 125,800,323 (GRCm39) |
V358A |
probably damaging |
Het |
Gsap |
A |
G |
5: 21,431,323 (GRCm39) |
R216G |
probably damaging |
Het |
Gsap |
A |
T |
5: 21,475,575 (GRCm39) |
T570S |
probably benign |
Het |
Gucy2d |
A |
T |
7: 98,093,030 (GRCm39) |
I136L |
probably benign |
Het |
Hap1 |
A |
T |
11: 100,240,218 (GRCm39) |
V294E |
probably damaging |
Het |
Ipo8 |
A |
G |
6: 148,701,278 (GRCm39) |
V514A |
probably damaging |
Het |
Irf5 |
T |
C |
6: 29,535,958 (GRCm39) |
L324P |
probably damaging |
Het |
Itsn1 |
C |
T |
16: 91,613,740 (GRCm39) |
R251C |
probably damaging |
Het |
Klf11 |
T |
C |
12: 24,701,567 (GRCm39) |
|
probably null |
Het |
Kpna6 |
G |
A |
4: 129,543,099 (GRCm39) |
Q439* |
probably null |
Het |
Mark4 |
A |
T |
7: 19,163,441 (GRCm39) |
S563T |
probably benign |
Het |
Mrpl21 |
A |
T |
19: 3,333,084 (GRCm39) |
I5L |
probably benign |
Het |
Muc4 |
T |
C |
16: 32,753,802 (GRCm38) |
I1226T |
probably benign |
Het |
Myrf |
G |
A |
19: 10,189,839 (GRCm39) |
T815I |
probably damaging |
Het |
Olfr515-ps1 |
A |
T |
7: 108,444,178 (GRCm39) |
|
probably null |
Het |
Or10d4c |
G |
T |
9: 39,558,555 (GRCm39) |
D178Y |
probably damaging |
Het |
Or11g27 |
A |
G |
14: 50,771,778 (GRCm39) |
N303S |
probably benign |
Het |
Or4c15 |
C |
T |
2: 88,760,597 (GRCm39) |
V21I |
probably benign |
Het |
Or52n3 |
A |
G |
7: 104,530,289 (GRCm39) |
Y125C |
possibly damaging |
Het |
Os9 |
T |
C |
10: 126,935,812 (GRCm39) |
D280G |
probably benign |
Het |
Pcdhb14 |
A |
G |
18: 37,582,283 (GRCm39) |
N463S |
probably damaging |
Het |
Pex19 |
G |
A |
1: 171,961,606 (GRCm39) |
E271K |
probably damaging |
Het |
Ppdpf |
G |
A |
2: 180,829,641 (GRCm39) |
S32N |
probably benign |
Het |
Prdm2 |
A |
G |
4: 142,859,477 (GRCm39) |
I1271T |
probably benign |
Het |
Rbbp4 |
T |
C |
4: 129,215,751 (GRCm39) |
T262A |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Spaca9 |
G |
A |
2: 28,583,793 (GRCm39) |
R64W |
probably damaging |
Het |
Sult1e1 |
A |
T |
5: 87,727,770 (GRCm39) |
S171T |
probably damaging |
Het |
Tns1 |
T |
C |
1: 73,992,612 (GRCm39) |
T689A |
probably damaging |
Het |
Unc13c |
G |
C |
9: 73,600,648 (GRCm39) |
N1365K |
probably benign |
Het |
Vmn2r52 |
T |
C |
7: 9,905,090 (GRCm39) |
I250V |
probably benign |
Het |
Vmn2r55 |
C |
A |
7: 12,402,069 (GRCm39) |
L406F |
probably benign |
Het |
Wdcp |
T |
C |
12: 4,900,621 (GRCm39) |
V159A |
possibly damaging |
Het |
Zbtb3 |
C |
T |
19: 8,781,560 (GRCm39) |
A391V |
probably benign |
Het |
Znhit1 |
A |
T |
5: 137,011,487 (GRCm39) |
S109T |
probably benign |
Het |
|
Other mutations in AAdacl4fm3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00661:AAdacl4fm3
|
APN |
4 |
144,430,263 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01985:AAdacl4fm3
|
APN |
4 |
144,442,024 (GRCm39) |
nonsense |
probably null |
|
IGL02587:AAdacl4fm3
|
APN |
4 |
144,429,969 (GRCm39) |
missense |
possibly damaging |
0.94 |
P0018:AAdacl4fm3
|
UTSW |
4 |
144,429,767 (GRCm39) |
missense |
probably benign |
0.00 |
R0395:AAdacl4fm3
|
UTSW |
4 |
144,429,765 (GRCm39) |
missense |
probably benign |
0.14 |
R1617:AAdacl4fm3
|
UTSW |
4 |
144,441,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R3802:AAdacl4fm3
|
UTSW |
4 |
144,430,074 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4409:AAdacl4fm3
|
UTSW |
4 |
144,447,872 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4577:AAdacl4fm3
|
UTSW |
4 |
144,430,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R4603:AAdacl4fm3
|
UTSW |
4 |
144,429,798 (GRCm39) |
missense |
probably benign |
0.00 |
R5069:AAdacl4fm3
|
UTSW |
4 |
144,430,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:AAdacl4fm3
|
UTSW |
4 |
144,430,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R5802:AAdacl4fm3
|
UTSW |
4 |
144,430,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:AAdacl4fm3
|
UTSW |
4 |
144,429,766 (GRCm39) |
missense |
probably benign |
|
R6466:AAdacl4fm3
|
UTSW |
4 |
144,430,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R6655:AAdacl4fm3
|
UTSW |
4 |
144,431,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7006:AAdacl4fm3
|
UTSW |
4 |
144,447,853 (GRCm39) |
missense |
probably benign |
0.00 |
R7021:AAdacl4fm3
|
UTSW |
4 |
144,442,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R7030:AAdacl4fm3
|
UTSW |
4 |
144,430,173 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7514:AAdacl4fm3
|
UTSW |
4 |
144,429,798 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7773:AAdacl4fm3
|
UTSW |
4 |
144,430,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R7791:AAdacl4fm3
|
UTSW |
4 |
144,430,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:AAdacl4fm3
|
UTSW |
4 |
144,429,972 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8082:AAdacl4fm3
|
UTSW |
4 |
144,441,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:AAdacl4fm3
|
UTSW |
4 |
144,442,011 (GRCm39) |
missense |
probably benign |
0.04 |
R9721:AAdacl4fm3
|
UTSW |
4 |
144,429,942 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:AAdacl4fm3
|
UTSW |
4 |
144,429,895 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:AAdacl4fm3
|
UTSW |
4 |
144,430,216 (GRCm39) |
missense |
possibly damaging |
0.87 |
|