Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp8a1 |
G |
T |
5: 67,824,943 (GRCm39) |
T796K |
probably benign |
Het |
Atr |
T |
C |
9: 95,744,916 (GRCm39) |
S78P |
probably damaging |
Het |
Calb2 |
C |
T |
8: 110,875,141 (GRCm39) |
|
probably null |
Het |
Ccdc88c |
G |
T |
12: 100,879,591 (GRCm39) |
S1843R |
possibly damaging |
Het |
Cdca7 |
A |
G |
2: 72,310,042 (GRCm39) |
S77G |
probably damaging |
Het |
Cnot2 |
C |
T |
10: 116,417,379 (GRCm39) |
|
probably benign |
Het |
Cstf2t |
T |
A |
19: 31,060,482 (GRCm39) |
V6D |
possibly damaging |
Het |
Cybc1 |
A |
G |
11: 121,114,934 (GRCm39) |
|
probably benign |
Het |
Dido1 |
T |
C |
2: 180,314,085 (GRCm39) |
I852V |
probably damaging |
Het |
Dmgdh |
C |
T |
13: 93,825,138 (GRCm39) |
Q154* |
probably null |
Het |
Dnah12 |
T |
C |
14: 26,491,979 (GRCm39) |
F1138S |
probably damaging |
Het |
Dnah12 |
G |
A |
14: 26,598,915 (GRCm39) |
A998T |
possibly damaging |
Het |
Dusp5 |
T |
G |
19: 53,526,032 (GRCm39) |
Y225D |
probably damaging |
Het |
Fam193a |
G |
A |
5: 34,600,715 (GRCm39) |
D601N |
probably benign |
Het |
Fbxo41 |
A |
G |
6: 85,461,024 (GRCm39) |
I228T |
probably damaging |
Het |
Fmo2 |
T |
C |
1: 162,715,277 (GRCm39) |
K115R |
probably benign |
Het |
Gak |
G |
T |
5: 108,724,432 (GRCm39) |
Q1093K |
probably benign |
Het |
Gm5277 |
G |
T |
3: 78,799,493 (GRCm39) |
|
noncoding transcript |
Het |
Hgsnat |
A |
G |
8: 26,458,389 (GRCm39) |
|
probably null |
Het |
Hycc1 |
T |
C |
5: 24,170,120 (GRCm39) |
T410A |
probably benign |
Het |
Irag1 |
T |
C |
7: 110,523,048 (GRCm39) |
M338V |
probably benign |
Het |
Map3k3 |
G |
A |
11: 106,039,694 (GRCm39) |
R278H |
probably damaging |
Het |
Muc4 |
T |
C |
16: 32,555,154 (GRCm39) |
|
probably benign |
Het |
Nectin3 |
C |
A |
16: 46,268,953 (GRCm39) |
R483L |
probably benign |
Het |
Nop2 |
G |
T |
6: 125,110,515 (GRCm39) |
R47L |
probably damaging |
Het |
Ntng1 |
A |
G |
3: 109,842,312 (GRCm39) |
S154P |
probably damaging |
Het |
Olfml2b |
T |
C |
1: 170,496,791 (GRCm39) |
I474T |
probably benign |
Het |
Optc |
G |
T |
1: 133,831,492 (GRCm39) |
T138K |
possibly damaging |
Het |
Or7g25 |
T |
C |
9: 19,160,525 (GRCm39) |
T57A |
probably damaging |
Het |
Or8k22 |
C |
G |
2: 86,163,644 (GRCm39) |
D19H |
probably benign |
Het |
Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
Pabir3 |
G |
A |
X: 52,382,376 (GRCm39) |
R94H |
possibly damaging |
Het |
Pard3 |
C |
T |
8: 128,125,108 (GRCm39) |
P421S |
probably benign |
Het |
Pcdhb22 |
G |
T |
18: 37,653,474 (GRCm39) |
E647D |
probably benign |
Het |
Pclo |
A |
G |
5: 14,730,006 (GRCm39) |
|
probably benign |
Het |
Prkce |
G |
T |
17: 86,798,178 (GRCm39) |
|
probably null |
Het |
Prr12 |
T |
C |
7: 44,697,947 (GRCm39) |
D656G |
unknown |
Het |
Ptprk |
A |
T |
10: 28,342,048 (GRCm39) |
D485V |
probably damaging |
Het |
Ptprn2 |
T |
C |
12: 116,839,620 (GRCm39) |
L381P |
probably damaging |
Het |
Rnf144b |
T |
C |
13: 47,361,013 (GRCm39) |
I51T |
probably benign |
Het |
Rpl10l |
T |
C |
12: 66,330,512 (GRCm39) |
D207G |
probably benign |
Het |
Sh3glb2 |
A |
T |
2: 30,240,711 (GRCm39) |
V118E |
probably damaging |
Het |
Sipa1l2 |
C |
T |
8: 126,219,163 (GRCm39) |
G58D |
probably damaging |
Het |
Slc5a4a |
C |
T |
10: 75,984,196 (GRCm39) |
A46V |
probably damaging |
Het |
Spmip8 |
T |
A |
8: 96,039,638 (GRCm39) |
Y18* |
probably null |
Het |
Tgm7 |
C |
A |
2: 120,929,069 (GRCm39) |
|
probably null |
Het |
Tjap1 |
A |
G |
17: 46,569,718 (GRCm39) |
V424A |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,773,864 (GRCm39) |
I414F |
probably damaging |
Het |
Tsr3 |
C |
G |
17: 25,460,723 (GRCm39) |
D196E |
probably benign |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,134 (GRCm39) |
H95L |
probably benign |
Het |
Vmn2r97 |
T |
A |
17: 19,149,333 (GRCm39) |
N240K |
probably benign |
Het |
Xdh |
C |
A |
17: 74,205,339 (GRCm39) |
G1042V |
probably damaging |
Het |
Zcchc4 |
A |
G |
5: 52,941,409 (GRCm39) |
D68G |
probably damaging |
Het |
|
Other mutations in Cfap47 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01285:Cfap47
|
APN |
X |
78,532,764 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01679:Cfap47
|
APN |
X |
78,376,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02025:Cfap47
|
APN |
X |
78,554,036 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02632:Cfap47
|
APN |
X |
78,540,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Cfap47
|
UTSW |
X |
78,553,507 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1551:Cfap47
|
UTSW |
X |
78,532,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2121:Cfap47
|
UTSW |
X |
78,553,927 (GRCm39) |
missense |
probably benign |
0.04 |
R2124:Cfap47
|
UTSW |
X |
78,553,927 (GRCm39) |
missense |
probably benign |
0.04 |
R2192:Cfap47
|
UTSW |
X |
78,454,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R3725:Cfap47
|
UTSW |
X |
78,553,621 (GRCm39) |
missense |
probably damaging |
0.97 |
R4304:Cfap47
|
UTSW |
X |
78,541,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4305:Cfap47
|
UTSW |
X |
78,541,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4522:Cfap47
|
UTSW |
X |
78,553,601 (GRCm39) |
missense |
possibly damaging |
0.63 |
Z1088:Cfap47
|
UTSW |
X |
78,374,420 (GRCm39) |
nonsense |
probably null |
|
Z1088:Cfap47
|
UTSW |
X |
78,374,419 (GRCm39) |
missense |
probably damaging |
1.00 |
|