Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
A |
G |
3: 124,373,527 (GRCm39) |
S23P |
possibly damaging |
Het |
Adam1a |
T |
C |
5: 121,657,439 (GRCm39) |
Y618C |
probably benign |
Het |
Amigo2 |
A |
C |
15: 97,143,107 (GRCm39) |
S438R |
probably benign |
Het |
Atp5me |
T |
C |
5: 108,581,922 (GRCm39) |
I21V |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,365,017 (GRCm39) |
|
probably benign |
Het |
Dock2 |
A |
G |
11: 34,260,390 (GRCm39) |
Y984H |
probably damaging |
Het |
Dpysl2 |
T |
A |
14: 67,045,367 (GRCm39) |
I469F |
possibly damaging |
Het |
Edem3 |
C |
T |
1: 151,694,379 (GRCm39) |
T886I |
probably benign |
Het |
Gart |
T |
C |
16: 91,422,400 (GRCm39) |
T706A |
probably benign |
Het |
Gfpt2 |
A |
T |
11: 49,698,517 (GRCm39) |
|
probably benign |
Het |
Gm11541 |
T |
G |
11: 94,586,495 (GRCm39) |
D84A |
unknown |
Het |
Gne |
T |
C |
4: 44,041,860 (GRCm39) |
|
probably null |
Het |
Gria4 |
A |
T |
9: 4,503,652 (GRCm39) |
D321E |
probably benign |
Het |
Ift122 |
T |
G |
6: 115,889,565 (GRCm39) |
|
probably null |
Het |
Lcp2 |
A |
T |
11: 33,997,345 (GRCm39) |
|
probably benign |
Het |
Mcm2 |
C |
T |
6: 88,868,948 (GRCm39) |
|
probably benign |
Het |
Or8b54 |
A |
G |
9: 38,687,225 (GRCm39) |
I225V |
probably benign |
Het |
Ptpru |
C |
A |
4: 131,496,803 (GRCm39) |
|
probably benign |
Het |
Rpap2 |
T |
C |
5: 107,751,492 (GRCm39) |
|
probably null |
Het |
Slc25a39 |
T |
C |
11: 102,295,726 (GRCm39) |
T138A |
probably damaging |
Het |
St6galnac1 |
A |
C |
11: 116,660,165 (GRCm39) |
S49R |
probably benign |
Het |
Stat1 |
T |
C |
1: 52,178,502 (GRCm39) |
L312P |
probably damaging |
Het |
Tmem198 |
T |
C |
1: 75,461,014 (GRCm39) |
|
probably benign |
Het |
Top2a |
A |
T |
11: 98,901,856 (GRCm39) |
L458Q |
probably damaging |
Het |
Treml4 |
T |
C |
17: 48,572,023 (GRCm39) |
|
probably benign |
Het |
Trpm6 |
A |
G |
19: 18,786,933 (GRCm39) |
D503G |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,775,617 (GRCm39) |
E1854D |
unknown |
Het |
Ubqln3 |
A |
T |
7: 103,791,403 (GRCm39) |
M229K |
possibly damaging |
Het |
|
Other mutations in Zfyve9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00162:Zfyve9
|
APN |
4 |
108,499,304 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01161:Zfyve9
|
APN |
4 |
108,538,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01404:Zfyve9
|
APN |
4 |
108,539,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01655:Zfyve9
|
APN |
4 |
108,499,289 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Zfyve9
|
APN |
4 |
108,531,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02593:Zfyve9
|
APN |
4 |
108,539,420 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03169:Zfyve9
|
APN |
4 |
108,553,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:Zfyve9
|
APN |
4 |
108,546,406 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03288:Zfyve9
|
APN |
4 |
108,580,996 (GRCm39) |
splice site |
probably benign |
|
R0008:Zfyve9
|
UTSW |
4 |
108,575,902 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0008:Zfyve9
|
UTSW |
4 |
108,575,902 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0104:Zfyve9
|
UTSW |
4 |
108,575,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R0104:Zfyve9
|
UTSW |
4 |
108,575,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R0362:Zfyve9
|
UTSW |
4 |
108,538,166 (GRCm39) |
missense |
probably damaging |
0.96 |
R0502:Zfyve9
|
UTSW |
4 |
108,576,961 (GRCm39) |
nonsense |
probably null |
|
R0503:Zfyve9
|
UTSW |
4 |
108,576,961 (GRCm39) |
nonsense |
probably null |
|
R0557:Zfyve9
|
UTSW |
4 |
108,531,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R0835:Zfyve9
|
UTSW |
4 |
108,575,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R1215:Zfyve9
|
UTSW |
4 |
108,507,426 (GRCm39) |
missense |
probably benign |
0.32 |
R1245:Zfyve9
|
UTSW |
4 |
108,550,508 (GRCm39) |
intron |
probably benign |
|
R1527:Zfyve9
|
UTSW |
4 |
108,552,964 (GRCm39) |
critical splice donor site |
probably null |
|
R1638:Zfyve9
|
UTSW |
4 |
108,542,104 (GRCm39) |
critical splice donor site |
probably null |
|
R1653:Zfyve9
|
UTSW |
4 |
108,517,774 (GRCm39) |
nonsense |
probably null |
|
R1728:Zfyve9
|
UTSW |
4 |
108,575,698 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1729:Zfyve9
|
UTSW |
4 |
108,575,698 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1861:Zfyve9
|
UTSW |
4 |
108,539,492 (GRCm39) |
splice site |
probably benign |
|
R1983:Zfyve9
|
UTSW |
4 |
108,546,386 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2050:Zfyve9
|
UTSW |
4 |
108,576,500 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2050:Zfyve9
|
UTSW |
4 |
108,575,800 (GRCm39) |
missense |
probably benign |
0.05 |
R2246:Zfyve9
|
UTSW |
4 |
108,546,461 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2338:Zfyve9
|
UTSW |
4 |
108,517,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R2697:Zfyve9
|
UTSW |
4 |
108,553,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R3522:Zfyve9
|
UTSW |
4 |
108,576,940 (GRCm39) |
missense |
probably benign |
0.45 |
R4030:Zfyve9
|
UTSW |
4 |
108,576,898 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4247:Zfyve9
|
UTSW |
4 |
108,576,389 (GRCm39) |
missense |
probably benign |
0.28 |
R4273:Zfyve9
|
UTSW |
4 |
108,538,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Zfyve9
|
UTSW |
4 |
108,501,565 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4835:Zfyve9
|
UTSW |
4 |
108,575,195 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4871:Zfyve9
|
UTSW |
4 |
108,538,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R4881:Zfyve9
|
UTSW |
4 |
108,584,688 (GRCm39) |
splice site |
probably null |
|
R4974:Zfyve9
|
UTSW |
4 |
108,538,097 (GRCm39) |
critical splice donor site |
probably null |
|
R5024:Zfyve9
|
UTSW |
4 |
108,548,866 (GRCm39) |
missense |
probably benign |
0.18 |
R5481:Zfyve9
|
UTSW |
4 |
108,501,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R5660:Zfyve9
|
UTSW |
4 |
108,576,365 (GRCm39) |
missense |
probably benign |
|
R5965:Zfyve9
|
UTSW |
4 |
108,548,878 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5996:Zfyve9
|
UTSW |
4 |
108,576,557 (GRCm39) |
missense |
probably benign |
0.07 |
R6315:Zfyve9
|
UTSW |
4 |
108,531,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R6772:Zfyve9
|
UTSW |
4 |
108,496,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6865:Zfyve9
|
UTSW |
4 |
108,501,558 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7112:Zfyve9
|
UTSW |
4 |
108,507,519 (GRCm39) |
missense |
probably benign |
0.00 |
R7258:Zfyve9
|
UTSW |
4 |
108,514,151 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7266:Zfyve9
|
UTSW |
4 |
108,575,744 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7287:Zfyve9
|
UTSW |
4 |
108,575,453 (GRCm39) |
missense |
probably benign |
0.00 |
R7356:Zfyve9
|
UTSW |
4 |
108,576,212 (GRCm39) |
missense |
probably benign |
0.01 |
R7389:Zfyve9
|
UTSW |
4 |
108,550,515 (GRCm39) |
critical splice donor site |
probably null |
|
R7729:Zfyve9
|
UTSW |
4 |
108,548,973 (GRCm39) |
missense |
probably benign |
0.01 |
R7780:Zfyve9
|
UTSW |
4 |
108,576,298 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7801:Zfyve9
|
UTSW |
4 |
108,542,192 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8069:Zfyve9
|
UTSW |
4 |
108,542,215 (GRCm39) |
missense |
probably benign |
0.32 |
R8201:Zfyve9
|
UTSW |
4 |
108,507,474 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8221:Zfyve9
|
UTSW |
4 |
108,576,877 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8682:Zfyve9
|
UTSW |
4 |
108,576,539 (GRCm39) |
missense |
probably benign |
0.30 |
R8948:Zfyve9
|
UTSW |
4 |
108,499,288 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8960:Zfyve9
|
UTSW |
4 |
108,501,558 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9123:Zfyve9
|
UTSW |
4 |
108,575,760 (GRCm39) |
missense |
probably benign |
0.30 |
R9135:Zfyve9
|
UTSW |
4 |
108,539,386 (GRCm39) |
nonsense |
probably null |
|
R9439:Zfyve9
|
UTSW |
4 |
108,501,538 (GRCm39) |
missense |
probably benign |
0.33 |
R9449:Zfyve9
|
UTSW |
4 |
108,576,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R9560:Zfyve9
|
UTSW |
4 |
108,575,334 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9603:Zfyve9
|
UTSW |
4 |
108,499,288 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9657:Zfyve9
|
UTSW |
4 |
108,575,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R9691:Zfyve9
|
UTSW |
4 |
108,576,305 (GRCm39) |
missense |
probably benign |
|
R9717:Zfyve9
|
UTSW |
4 |
108,539,334 (GRCm39) |
missense |
probably benign |
0.11 |
Z1176:Zfyve9
|
UTSW |
4 |
108,499,404 (GRCm39) |
missense |
possibly damaging |
0.85 |
|