Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510009E07Rik |
T |
C |
16: 21,472,310 (GRCm39) |
D60G |
probably damaging |
Het |
Abca2 |
T |
A |
2: 25,335,975 (GRCm39) |
|
probably null |
Het |
Adamts14 |
C |
T |
10: 61,065,455 (GRCm39) |
R348H |
probably damaging |
Het |
Aimp2 |
A |
T |
5: 143,843,524 (GRCm39) |
I22N |
probably damaging |
Het |
Cacna1c |
A |
G |
6: 118,653,405 (GRCm39) |
|
probably benign |
Het |
Cfap221 |
A |
T |
1: 119,860,575 (GRCm39) |
Y684N |
possibly damaging |
Het |
Cldn6 |
T |
A |
17: 23,900,698 (GRCm39) |
|
probably benign |
Het |
Copb2 |
A |
G |
9: 98,450,130 (GRCm39) |
M30V |
probably benign |
Het |
Dcaf17 |
G |
A |
2: 70,908,503 (GRCm39) |
E243K |
probably benign |
Het |
Dhx35 |
T |
C |
2: 158,669,836 (GRCm39) |
Y257H |
probably damaging |
Het |
Dnai3 |
C |
T |
3: 145,788,759 (GRCm39) |
G274E |
probably benign |
Het |
Dzank1 |
A |
T |
2: 144,323,645 (GRCm39) |
Y600* |
probably null |
Het |
Flvcr1 |
T |
A |
1: 190,747,686 (GRCm39) |
R201* |
probably null |
Het |
Fstl4 |
G |
A |
11: 53,077,102 (GRCm39) |
V620I |
probably benign |
Het |
Gm21976 |
G |
A |
13: 98,439,069 (GRCm39) |
V20M |
probably benign |
Het |
Ifi208 |
T |
C |
1: 173,506,604 (GRCm39) |
|
probably null |
Het |
Kdm4c |
T |
C |
4: 74,263,738 (GRCm39) |
V674A |
probably benign |
Het |
Lig1 |
T |
A |
7: 13,035,378 (GRCm39) |
Y612* |
probably null |
Het |
Marco |
A |
G |
1: 120,413,432 (GRCm39) |
V295A |
probably benign |
Het |
Myo5c |
T |
C |
9: 75,150,162 (GRCm39) |
|
probably benign |
Het |
Or1e34 |
A |
G |
11: 73,779,075 (GRCm39) |
L41P |
probably damaging |
Het |
Or51a42 |
T |
C |
7: 103,708,623 (GRCm39) |
Y62C |
probably damaging |
Het |
Or6c217 |
T |
A |
10: 129,738,528 (GRCm39) |
D17V |
possibly damaging |
Het |
Pkd1l1 |
A |
G |
11: 8,911,971 (GRCm39) |
M245T |
unknown |
Het |
Pomt1 |
A |
G |
2: 32,131,784 (GRCm39) |
I158V |
probably benign |
Het |
Ptpn21 |
A |
G |
12: 98,646,727 (GRCm39) |
W967R |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,875,533 (GRCm39) |
M270K |
possibly damaging |
Het |
Spats2 |
A |
G |
15: 99,078,474 (GRCm39) |
E179G |
possibly damaging |
Het |
Tapbp |
T |
C |
17: 34,138,866 (GRCm39) |
V11A |
probably benign |
Het |
Tasor |
T |
G |
14: 27,170,163 (GRCm39) |
L364R |
probably damaging |
Het |
Tonsl |
A |
G |
15: 76,522,696 (GRCm39) |
F185S |
possibly damaging |
Het |
Trpm1 |
A |
G |
7: 63,893,198 (GRCm39) |
I901V |
probably damaging |
Het |
Tulp2 |
A |
G |
7: 45,171,332 (GRCm39) |
N371S |
probably damaging |
Het |
Unc5d |
A |
T |
8: 29,209,854 (GRCm39) |
V433D |
probably damaging |
Het |
Wasf3 |
G |
A |
5: 146,392,461 (GRCm39) |
R177Q |
probably damaging |
Het |
Zfp715 |
A |
T |
7: 42,949,173 (GRCm39) |
H262Q |
possibly damaging |
Het |
Zftraf1 |
A |
G |
15: 76,530,738 (GRCm39) |
I194T |
probably damaging |
Het |
|
Other mutations in Cfap300 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Cfap300
|
APN |
9 |
8,042,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Cfap300
|
UTSW |
9 |
8,027,184 (GRCm39) |
missense |
probably benign |
0.40 |
R0725:Cfap300
|
UTSW |
9 |
8,027,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Cfap300
|
UTSW |
9 |
8,022,457 (GRCm39) |
missense |
probably benign |
0.03 |
R1735:Cfap300
|
UTSW |
9 |
8,027,266 (GRCm39) |
missense |
probably benign |
0.01 |
R2140:Cfap300
|
UTSW |
9 |
8,022,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R2966:Cfap300
|
UTSW |
9 |
8,027,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4165:Cfap300
|
UTSW |
9 |
8,026,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Cfap300
|
UTSW |
9 |
8,026,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:Cfap300
|
UTSW |
9 |
8,027,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Cfap300
|
UTSW |
9 |
8,022,494 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7797:Cfap300
|
UTSW |
9 |
8,027,130 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7979:Cfap300
|
UTSW |
9 |
8,027,111 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8061:Cfap300
|
UTSW |
9 |
8,042,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|