Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
A |
G |
16: 14,261,319 (GRCm39) |
E699G |
probably damaging |
Het |
Ap4e1 |
T |
A |
2: 126,906,899 (GRCm39) |
V1053D |
possibly damaging |
Het |
Apobec1 |
T |
A |
6: 122,558,456 (GRCm39) |
I100F |
probably damaging |
Het |
Atp6v1g3 |
G |
T |
1: 138,211,480 (GRCm39) |
K53N |
probably damaging |
Het |
Bag3 |
C |
T |
7: 128,147,830 (GRCm39) |
R482W |
probably damaging |
Het |
Brme1 |
C |
T |
8: 84,894,114 (GRCm39) |
T427I |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,279,279 (GRCm39) |
T2007A |
possibly damaging |
Het |
Cd44 |
T |
C |
2: 102,731,687 (GRCm39) |
D2G |
probably damaging |
Het |
Cdadc1 |
T |
A |
14: 59,827,372 (GRCm39) |
I100F |
possibly damaging |
Het |
Cdh16 |
A |
G |
8: 105,344,677 (GRCm39) |
F485L |
probably damaging |
Het |
Cdhr5 |
T |
A |
7: 140,849,110 (GRCm39) |
K817* |
probably null |
Het |
Cfap46 |
G |
T |
7: 139,258,493 (GRCm39) |
P260Q |
probably damaging |
Het |
Clec11a |
C |
T |
7: 43,955,832 (GRCm39) |
E72K |
possibly damaging |
Het |
Cnr2 |
C |
A |
4: 135,644,076 (GRCm39) |
N51K |
probably damaging |
Het |
Col3a1 |
T |
A |
1: 45,370,872 (GRCm39) |
|
probably benign |
Het |
Cxcr1 |
G |
A |
1: 74,230,987 (GRCm39) |
T345M |
probably damaging |
Het |
Cyp2s1 |
T |
C |
7: 25,515,744 (GRCm39) |
|
probably null |
Het |
Dalrd3 |
C |
T |
9: 108,449,489 (GRCm39) |
T474M |
probably damaging |
Het |
Ddit4 |
C |
T |
10: 59,787,327 (GRCm39) |
S3N |
probably benign |
Het |
Ddx41 |
T |
C |
13: 55,683,708 (GRCm39) |
K108E |
possibly damaging |
Het |
Ece2 |
A |
T |
16: 20,462,477 (GRCm39) |
H732L |
probably benign |
Het |
Etv3 |
T |
G |
3: 87,443,322 (GRCm39) |
L302R |
possibly damaging |
Het |
Fam135b |
A |
G |
15: 71,333,985 (GRCm39) |
S1070P |
probably damaging |
Het |
Fhip1b |
A |
T |
7: 105,039,089 (GRCm39) |
I50N |
probably damaging |
Het |
Gm11567 |
T |
A |
11: 99,770,437 (GRCm39) |
I125N |
unknown |
Het |
Grm3 |
A |
G |
5: 9,620,536 (GRCm39) |
L236P |
probably benign |
Het |
Hip1 |
T |
A |
5: 135,461,939 (GRCm39) |
R97* |
probably null |
Het |
Hoxa5 |
T |
C |
6: 52,181,197 (GRCm39) |
Y45C |
probably damaging |
Het |
Ighg1 |
T |
A |
12: 113,292,654 (GRCm39) |
H305L |
probably damaging |
Het |
Inpp5b |
T |
A |
4: 124,676,229 (GRCm39) |
C362S |
probably benign |
Het |
Kif1c |
A |
G |
11: 70,599,273 (GRCm39) |
K391E |
probably benign |
Het |
Klf9 |
T |
C |
19: 23,119,246 (GRCm39) |
V43A |
probably benign |
Het |
Krt28 |
T |
A |
11: 99,265,320 (GRCm39) |
I116F |
probably damaging |
Het |
Lct |
A |
T |
1: 128,222,969 (GRCm39) |
D1439E |
probably damaging |
Het |
Liph |
G |
A |
16: 21,784,745 (GRCm39) |
T284M |
possibly damaging |
Het |
Lrrc75b |
T |
C |
10: 75,393,055 (GRCm39) |
K98R |
possibly damaging |
Het |
Lypd4 |
T |
C |
7: 24,564,604 (GRCm39) |
Q178R |
probably benign |
Het |
Map1a |
T |
A |
2: 121,136,524 (GRCm39) |
S2209T |
probably damaging |
Het |
Map3k21 |
C |
T |
8: 126,665,563 (GRCm39) |
T584I |
probably benign |
Het |
Map3k6 |
T |
C |
4: 132,972,855 (GRCm39) |
V338A |
probably damaging |
Het |
Mapk8ip3 |
A |
T |
17: 25,122,285 (GRCm39) |
V699E |
possibly damaging |
Het |
Mtarc1 |
A |
C |
1: 184,543,116 (GRCm39) |
S71A |
probably damaging |
Het |
Nckap1l |
T |
C |
15: 103,363,452 (GRCm39) |
S53P |
probably benign |
Het |
Nt5e |
T |
C |
9: 88,209,740 (GRCm39) |
M1T |
probably null |
Het |
Nudt22 |
T |
C |
19: 6,972,896 (GRCm39) |
H64R |
probably damaging |
Het |
Or1o11 |
A |
T |
17: 37,756,663 (GRCm39) |
T84S |
probably damaging |
Het |
Or2t44 |
A |
T |
11: 58,677,654 (GRCm39) |
Y198F |
probably damaging |
Het |
Or2w3 |
T |
C |
11: 58,557,225 (GRCm39) |
I280T |
possibly damaging |
Het |
Or52b1 |
A |
T |
7: 104,978,772 (GRCm39) |
V209D |
probably damaging |
Het |
Or5ac16 |
A |
G |
16: 59,022,369 (GRCm39) |
L140P |
probably damaging |
Het |
Or8k17 |
T |
C |
2: 86,066,276 (GRCm39) |
N294S |
probably damaging |
Het |
Otogl |
T |
C |
10: 107,722,413 (GRCm39) |
I314V |
probably benign |
Het |
Pan2 |
G |
T |
10: 128,143,969 (GRCm39) |
E106D |
probably benign |
Het |
Papss1 |
T |
A |
3: 131,337,565 (GRCm39) |
Y554* |
probably null |
Het |
Pcnx1 |
T |
C |
12: 81,941,803 (GRCm39) |
V67A |
possibly damaging |
Het |
Pdpk1 |
A |
C |
17: 24,325,829 (GRCm39) |
Y122* |
probably null |
Het |
Pkd1l1 |
A |
T |
11: 8,829,202 (GRCm39) |
N1463K |
probably damaging |
Het |
Ptgfrn |
C |
A |
3: 100,950,678 (GRCm39) |
M878I |
probably damaging |
Het |
Ranbp3 |
G |
A |
17: 57,017,703 (GRCm39) |
G453E |
probably benign |
Het |
Rapgef2 |
T |
C |
3: 79,002,157 (GRCm39) |
D261G |
probably damaging |
Het |
Reep2 |
A |
G |
18: 34,979,271 (GRCm39) |
S199G |
probably benign |
Het |
Rnpep |
G |
A |
1: 135,205,259 (GRCm39) |
T202I |
probably damaging |
Het |
Sass6 |
T |
A |
3: 116,401,145 (GRCm39) |
|
probably null |
Het |
Sema3e |
A |
G |
5: 14,212,257 (GRCm39) |
D111G |
probably damaging |
Het |
Slc29a4 |
A |
G |
5: 142,697,727 (GRCm39) |
E60G |
probably damaging |
Het |
Spata31g1 |
T |
C |
4: 42,971,831 (GRCm39) |
L388P |
possibly damaging |
Het |
Spata31h1 |
T |
A |
10: 82,120,317 (GRCm39) |
Q4231L |
probably damaging |
Het |
Sptlc3 |
T |
C |
2: 139,388,328 (GRCm39) |
Y107H |
probably damaging |
Het |
Stx6 |
T |
C |
1: 155,073,925 (GRCm39) |
I245T |
probably benign |
Het |
Syne2 |
T |
C |
12: 75,965,306 (GRCm39) |
S774P |
probably damaging |
Het |
Tbc1d16 |
T |
A |
11: 119,049,617 (GRCm39) |
Q293L |
probably damaging |
Het |
Tbc1d30 |
T |
C |
10: 121,132,692 (GRCm39) |
D224G |
probably damaging |
Het |
Tbc1d32 |
T |
A |
10: 56,026,973 (GRCm39) |
N759Y |
possibly damaging |
Het |
Tdrd12 |
G |
T |
7: 35,210,725 (GRCm39) |
A166E |
probably damaging |
Het |
Tex14 |
A |
G |
11: 87,405,046 (GRCm39) |
R653G |
probably benign |
Het |
Them6 |
A |
T |
15: 74,593,654 (GRCm39) |
R171W |
probably null |
Het |
Tln2 |
T |
C |
9: 67,203,640 (GRCm39) |
T489A |
probably benign |
Het |
Tmem87a |
A |
G |
2: 120,234,427 (GRCm39) |
F39L |
probably benign |
Het |
Toporsl |
T |
A |
4: 52,611,515 (GRCm39) |
C469* |
probably null |
Het |
Tpr |
T |
C |
1: 150,299,569 (GRCm39) |
S1147P |
probably damaging |
Het |
Trp53bp1 |
T |
C |
2: 121,067,143 (GRCm39) |
M528V |
probably benign |
Het |
Trpm6 |
T |
A |
19: 18,807,571 (GRCm39) |
C1039S |
probably damaging |
Het |
Ttc16 |
T |
A |
2: 32,665,348 (GRCm39) |
S5C |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,617,412 (GRCm39) |
Y14607C |
probably damaging |
Het |
Usp6nl |
T |
C |
2: 6,435,275 (GRCm39) |
F345L |
probably damaging |
Het |
Vmn1r205 |
C |
T |
13: 22,776,206 (GRCm39) |
G299R |
probably benign |
Het |
Vmn2r74 |
G |
A |
7: 85,606,588 (GRCm39) |
H253Y |
probably benign |
Het |
Vps13d |
A |
T |
4: 144,896,872 (GRCm39) |
D343E |
possibly damaging |
Het |
Vwf |
A |
G |
6: 125,580,381 (GRCm39) |
E543G |
|
Het |
Zfat |
A |
T |
15: 68,052,765 (GRCm39) |
V343E |
probably damaging |
Het |
Zfp316 |
T |
C |
5: 143,249,846 (GRCm39) |
E139G |
unknown |
Het |
Zfp943 |
T |
A |
17: 22,211,813 (GRCm39) |
C300S |
probably damaging |
Het |
Zkscan16 |
A |
G |
4: 58,957,748 (GRCm39) |
K677E |
probably benign |
Het |
|
Other mutations in Dnaaf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01678:Dnaaf10
|
APN |
11 |
17,182,790 (GRCm39) |
missense |
probably benign |
|
IGL01801:Dnaaf10
|
APN |
11 |
17,169,015 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02573:Dnaaf10
|
APN |
11 |
17,162,136 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02985:Dnaaf10
|
APN |
11 |
17,179,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03148:Dnaaf10
|
APN |
11 |
17,179,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03147:Dnaaf10
|
UTSW |
11 |
17,179,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R0244:Dnaaf10
|
UTSW |
11 |
17,179,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Dnaaf10
|
UTSW |
11 |
17,179,821 (GRCm39) |
missense |
probably benign |
0.33 |
R1013:Dnaaf10
|
UTSW |
11 |
17,178,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R1660:Dnaaf10
|
UTSW |
11 |
17,177,183 (GRCm39) |
missense |
probably benign |
0.00 |
R2030:Dnaaf10
|
UTSW |
11 |
17,179,832 (GRCm39) |
missense |
probably benign |
|
R4663:Dnaaf10
|
UTSW |
11 |
17,182,853 (GRCm39) |
missense |
probably benign |
0.01 |
R4676:Dnaaf10
|
UTSW |
11 |
17,179,794 (GRCm39) |
missense |
probably benign |
0.00 |
R4822:Dnaaf10
|
UTSW |
11 |
17,177,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Dnaaf10
|
UTSW |
11 |
17,172,220 (GRCm39) |
missense |
probably damaging |
0.97 |
R5439:Dnaaf10
|
UTSW |
11 |
17,162,031 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5473:Dnaaf10
|
UTSW |
11 |
17,174,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R5771:Dnaaf10
|
UTSW |
11 |
17,174,638 (GRCm39) |
missense |
probably benign |
0.00 |
R6680:Dnaaf10
|
UTSW |
11 |
17,179,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Dnaaf10
|
UTSW |
11 |
17,172,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7367:Dnaaf10
|
UTSW |
11 |
17,182,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7693:Dnaaf10
|
UTSW |
11 |
17,162,064 (GRCm39) |
missense |
probably benign |
0.25 |
R7785:Dnaaf10
|
UTSW |
11 |
17,179,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnaaf10
|
UTSW |
11 |
17,178,184 (GRCm39) |
missense |
probably damaging |
1.00 |
|