Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
A |
G |
14: 29,706,056 (GRCm39) |
M99V |
possibly damaging |
Het |
Adamtsl2 |
T |
A |
2: 26,993,078 (GRCm39) |
C703S |
possibly damaging |
Het |
Aldh3a2 |
G |
A |
11: 61,155,133 (GRCm39) |
S137L |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Aoc1 |
A |
T |
6: 48,882,379 (GRCm39) |
K107M |
possibly damaging |
Het |
Aoc1l1 |
A |
T |
6: 48,952,849 (GRCm39) |
Y258F |
probably damaging |
Het |
Bltp2 |
T |
A |
11: 78,153,624 (GRCm39) |
S56R |
probably damaging |
Het |
Bmp8a |
G |
T |
4: 123,210,758 (GRCm39) |
S252R |
possibly damaging |
Het |
C7 |
T |
C |
15: 5,088,901 (GRCm39) |
I13M |
probably benign |
Het |
Cblb |
T |
A |
16: 51,959,974 (GRCm39) |
D322E |
possibly damaging |
Het |
Cfap54 |
G |
A |
10: 92,768,583 (GRCm39) |
T180I |
probably damaging |
Het |
Clrn2 |
C |
T |
5: 45,617,453 (GRCm39) |
A108V |
probably damaging |
Het |
Cspg4 |
T |
A |
9: 56,793,796 (GRCm39) |
D510E |
probably damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,766,415 (GRCm39) |
N393K |
possibly damaging |
Het |
Dcaf5 |
T |
C |
12: 80,410,843 (GRCm39) |
Y294C |
probably damaging |
Het |
Dclk3 |
T |
A |
9: 111,298,088 (GRCm39) |
M544K |
probably benign |
Het |
Ell3 |
A |
T |
2: 121,269,946 (GRCm39) |
F388I |
probably damaging |
Het |
Fam78b |
A |
G |
1: 166,906,329 (GRCm39) |
I163V |
probably damaging |
Het |
Gnptab |
T |
C |
10: 88,269,943 (GRCm39) |
L882P |
probably damaging |
Het |
Herc2 |
A |
T |
7: 55,854,481 (GRCm39) |
D3802V |
possibly damaging |
Het |
Hs3st5 |
A |
G |
10: 36,709,410 (GRCm39) |
E315G |
probably benign |
Het |
Idh3b |
A |
T |
2: 130,125,974 (GRCm39) |
|
probably null |
Het |
Lama4 |
G |
A |
10: 38,949,639 (GRCm39) |
E911K |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,404,800 (GRCm39) |
I436T |
probably damaging |
Het |
Mgam |
C |
A |
6: 40,736,714 (GRCm39) |
S871* |
probably null |
Het |
Mtmr7 |
A |
G |
8: 41,013,923 (GRCm39) |
S212P |
probably damaging |
Het |
Mylk2 |
A |
G |
2: 152,761,336 (GRCm39) |
T480A |
probably damaging |
Het |
Myo3a |
A |
T |
2: 22,287,437 (GRCm39) |
N191I |
probably damaging |
Het |
Nanog |
C |
T |
6: 122,688,734 (GRCm39) |
S105F |
probably damaging |
Het |
Nanos2 |
A |
G |
7: 18,721,564 (GRCm39) |
Y12C |
probably damaging |
Het |
Nsg1 |
C |
T |
5: 38,312,987 (GRCm39) |
V71I |
probably benign |
Het |
Or10g3 |
A |
T |
14: 52,610,408 (GRCm39) |
I34N |
probably damaging |
Het |
Or13a1 |
T |
C |
6: 116,471,386 (GRCm39) |
L272S |
probably benign |
Het |
Or2ad1 |
C |
T |
13: 21,326,337 (GRCm39) |
V297I |
probably benign |
Het |
Or51a42 |
A |
T |
7: 103,707,930 (GRCm39) |
I293N |
probably damaging |
Het |
Or5b105 |
G |
T |
19: 13,080,568 (GRCm39) |
Y33* |
probably null |
Het |
Pcdhb17 |
A |
G |
18: 37,619,701 (GRCm39) |
Q497R |
probably benign |
Het |
Pcsk7 |
C |
A |
9: 45,837,284 (GRCm39) |
P536Q |
probably damaging |
Het |
Phactr4 |
G |
A |
4: 132,104,559 (GRCm39) |
T256I |
probably benign |
Het |
Phyhip |
A |
G |
14: 70,704,731 (GRCm39) |
K317E |
probably damaging |
Het |
Pkhd1 |
C |
T |
1: 20,604,782 (GRCm39) |
G1178R |
probably damaging |
Het |
Ppp1r9a |
G |
A |
6: 5,057,557 (GRCm39) |
G544D |
probably damaging |
Het |
Ptpn3 |
T |
C |
4: 57,225,775 (GRCm39) |
D480G |
probably benign |
Het |
Ptprn2 |
A |
T |
12: 117,217,235 (GRCm39) |
K918N |
probably damaging |
Het |
Rab42 |
T |
C |
4: 132,029,658 (GRCm39) |
D188G |
probably benign |
Het |
Rasgrf2 |
C |
A |
13: 92,131,795 (GRCm39) |
D20Y |
probably damaging |
Het |
Ryr2 |
G |
A |
13: 11,794,152 (GRCm39) |
T942I |
probably benign |
Het |
Sbpl |
T |
C |
17: 24,172,328 (GRCm39) |
K197R |
unknown |
Het |
Slc44a1 |
T |
A |
4: 53,561,069 (GRCm39) |
V595E |
probably damaging |
Het |
Slc6a19 |
A |
G |
13: 73,832,463 (GRCm39) |
M410T |
probably damaging |
Het |
Sntb1 |
A |
T |
15: 55,511,351 (GRCm39) |
L411H |
probably damaging |
Het |
Synj2 |
A |
G |
17: 6,073,940 (GRCm39) |
K245E |
probably damaging |
Het |
Tasor2 |
T |
C |
13: 3,625,543 (GRCm39) |
K1469R |
probably benign |
Het |
Tmem131 |
G |
A |
1: 36,864,559 (GRCm39) |
T558I |
probably damaging |
Het |
Tnrc18 |
A |
T |
5: 142,757,288 (GRCm39) |
S1078T |
unknown |
Het |
Trmu |
T |
A |
15: 85,781,302 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,721,430 (GRCm39) |
|
probably benign |
Het |
Tyw3 |
T |
C |
3: 154,293,160 (GRCm39) |
T172A |
probably benign |
Het |
Vldlr |
T |
C |
19: 27,217,121 (GRCm39) |
I348T |
possibly damaging |
Het |
Zfp114 |
A |
G |
7: 23,877,194 (GRCm39) |
D12G |
probably damaging |
Het |
|
Other mutations in Afap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01397:Afap1
|
APN |
5 |
36,126,052 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01730:Afap1
|
APN |
5 |
36,119,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01798:Afap1
|
APN |
5 |
36,093,026 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02188:Afap1
|
APN |
5 |
36,093,421 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03027:Afap1
|
APN |
5 |
36,119,094 (GRCm39) |
missense |
probably benign |
0.00 |
R0124:Afap1
|
UTSW |
5 |
36,102,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Afap1
|
UTSW |
5 |
36,108,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R0532:Afap1
|
UTSW |
5 |
36,125,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0891:Afap1
|
UTSW |
5 |
36,119,196 (GRCm39) |
splice site |
probably null |
|
R1370:Afap1
|
UTSW |
5 |
36,092,944 (GRCm39) |
missense |
unknown |
|
R1378:Afap1
|
UTSW |
5 |
36,126,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Afap1
|
UTSW |
5 |
36,119,081 (GRCm39) |
splice site |
probably benign |
|
R1536:Afap1
|
UTSW |
5 |
36,131,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R2357:Afap1
|
UTSW |
5 |
36,141,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R4737:Afap1
|
UTSW |
5 |
36,119,126 (GRCm39) |
missense |
probably benign |
0.03 |
R5251:Afap1
|
UTSW |
5 |
36,108,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5918:Afap1
|
UTSW |
5 |
36,131,869 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5936:Afap1
|
UTSW |
5 |
36,131,740 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6008:Afap1
|
UTSW |
5 |
36,154,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R6009:Afap1
|
UTSW |
5 |
36,154,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Afap1
|
UTSW |
5 |
36,092,953 (GRCm39) |
missense |
unknown |
|
R7058:Afap1
|
UTSW |
5 |
36,119,604 (GRCm39) |
missense |
probably benign |
0.00 |
R7320:Afap1
|
UTSW |
5 |
36,105,567 (GRCm39) |
missense |
probably damaging |
0.98 |
R7799:Afap1
|
UTSW |
5 |
36,131,742 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7946:Afap1
|
UTSW |
5 |
36,141,396 (GRCm39) |
splice site |
probably null |
|
R7946:Afap1
|
UTSW |
5 |
36,092,995 (GRCm39) |
missense |
probably benign |
0.30 |
R8358:Afap1
|
UTSW |
5 |
36,131,830 (GRCm39) |
missense |
probably benign |
0.30 |
R8446:Afap1
|
UTSW |
5 |
36,144,645 (GRCm39) |
missense |
|
|
R8785:Afap1
|
UTSW |
5 |
36,108,304 (GRCm39) |
nonsense |
probably null |
|
R9013:Afap1
|
UTSW |
5 |
36,133,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9225:Afap1
|
UTSW |
5 |
36,133,968 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9711:Afap1
|
UTSW |
5 |
36,141,540 (GRCm39) |
missense |
probably damaging |
1.00 |
|