Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
T |
11: 109,847,901 (GRCm39) |
T798K |
possibly damaging |
Het |
Abtb1 |
T |
C |
6: 88,813,536 (GRCm39) |
T401A |
probably benign |
Het |
Adsl |
G |
T |
15: 80,846,943 (GRCm39) |
E70* |
probably null |
Het |
Ahcyl2 |
A |
G |
6: 29,768,583 (GRCm39) |
|
probably benign |
Het |
Akr1a1 |
A |
G |
4: 116,493,850 (GRCm39) |
V310A |
probably benign |
Het |
Alpk3 |
T |
A |
7: 80,726,679 (GRCm39) |
C121* |
probably null |
Het |
Amph |
T |
A |
13: 19,132,625 (GRCm39) |
I8N |
probably damaging |
Het |
Ano2 |
G |
A |
6: 125,840,420 (GRCm39) |
A364T |
probably damaging |
Het |
Apbb2 |
T |
C |
5: 66,557,520 (GRCm39) |
T314A |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atf7ip |
A |
G |
6: 136,564,258 (GRCm39) |
T834A |
probably benign |
Het |
Brca2 |
T |
G |
5: 150,463,663 (GRCm39) |
D1142E |
probably benign |
Het |
Brd10 |
T |
C |
19: 29,693,814 (GRCm39) |
N1960S |
probably damaging |
Het |
Cap2 |
A |
G |
13: 46,768,823 (GRCm39) |
S210G |
probably benign |
Het |
Capn2 |
C |
A |
1: 182,300,525 (GRCm39) |
E596D |
possibly damaging |
Het |
Cdc27 |
A |
T |
11: 104,413,648 (GRCm39) |
S358R |
probably benign |
Het |
Cdhr3 |
C |
T |
12: 33,095,204 (GRCm39) |
G622S |
probably null |
Het |
Clip2 |
A |
G |
5: 134,532,081 (GRCm39) |
Y540H |
probably benign |
Het |
Crhr1 |
A |
T |
11: 104,023,898 (GRCm39) |
M1L |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,273,340 (GRCm39) |
T831A |
probably damaging |
Het |
Cwc22 |
T |
C |
2: 77,755,003 (GRCm39) |
|
probably benign |
Het |
Cyp3a25 |
T |
A |
5: 145,921,763 (GRCm39) |
K390N |
probably damaging |
Het |
Cyp4a31 |
T |
C |
4: 115,423,810 (GRCm39) |
|
probably null |
Het |
Cytip |
A |
C |
2: 58,024,158 (GRCm39) |
S221A |
probably benign |
Het |
Dagla |
G |
A |
19: 10,240,550 (GRCm39) |
R227C |
possibly damaging |
Het |
Dhx57 |
A |
G |
17: 80,560,514 (GRCm39) |
|
probably null |
Het |
Dnah2 |
A |
T |
11: 69,405,630 (GRCm39) |
D627E |
probably damaging |
Het |
Dock8 |
A |
G |
19: 25,138,422 (GRCm39) |
E1249G |
probably benign |
Het |
Dpysl3 |
A |
G |
18: 43,475,393 (GRCm39) |
V31A |
probably benign |
Het |
Ecpas |
A |
G |
4: 58,805,539 (GRCm39) |
|
probably null |
Het |
Fan1 |
T |
C |
7: 64,022,554 (GRCm39) |
N233S |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,918,547 (GRCm39) |
I3528F |
probably damaging |
Het |
Glipr1 |
T |
A |
10: 111,832,765 (GRCm39) |
M58L |
possibly damaging |
Het |
Gm10509 |
C |
T |
17: 21,909,765 (GRCm39) |
P31S |
possibly damaging |
Het |
Gm5070 |
T |
C |
3: 95,318,355 (GRCm39) |
|
noncoding transcript |
Het |
Gramd1a |
T |
C |
7: 30,841,998 (GRCm39) |
N138S |
probably damaging |
Het |
Grk5 |
T |
C |
19: 61,078,410 (GRCm39) |
V489A |
probably damaging |
Het |
Hmcn2 |
C |
T |
2: 31,273,704 (GRCm39) |
S1352L |
probably damaging |
Het |
Hoxa5 |
G |
A |
6: 52,179,712 (GRCm39) |
T221I |
probably damaging |
Het |
Hsd17b2 |
C |
A |
8: 118,485,488 (GRCm39) |
P317Q |
possibly damaging |
Het |
Ifi213 |
T |
A |
1: 173,417,408 (GRCm39) |
S335C |
probably damaging |
Het |
Izumo4 |
A |
T |
10: 80,539,729 (GRCm39) |
D156V |
probably damaging |
Het |
Kmt2d |
C |
T |
15: 98,759,661 (GRCm39) |
G1199E |
unknown |
Het |
Lipk |
T |
C |
19: 34,016,491 (GRCm39) |
W240R |
probably benign |
Het |
Lpar5 |
A |
G |
6: 125,058,378 (GRCm39) |
D33G |
possibly damaging |
Het |
Lrp11 |
A |
G |
10: 7,471,961 (GRCm39) |
D219G |
probably damaging |
Het |
Lrrcc1 |
T |
C |
3: 14,624,285 (GRCm39) |
|
probably benign |
Het |
Man2a1 |
T |
C |
17: 65,047,837 (GRCm39) |
C252R |
probably damaging |
Het |
Map2k5 |
A |
G |
9: 63,142,585 (GRCm39) |
F354L |
possibly damaging |
Het |
Mlh3 |
T |
C |
12: 85,312,919 (GRCm39) |
|
probably benign |
Het |
Mmp28 |
A |
G |
11: 83,335,045 (GRCm39) |
I331T |
probably damaging |
Het |
Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
Myo3a |
A |
T |
2: 22,345,091 (GRCm39) |
Y509F |
probably damaging |
Het |
Nckap1 |
A |
G |
2: 80,348,242 (GRCm39) |
S898P |
possibly damaging |
Het |
Nectin1 |
T |
A |
9: 43,702,374 (GRCm39) |
Y40* |
probably null |
Het |
Neurl1a |
T |
A |
19: 47,245,898 (GRCm39) |
V493E |
probably benign |
Het |
Ntf3 |
A |
C |
6: 126,079,209 (GRCm39) |
I99S |
probably benign |
Het |
Or10ag53 |
T |
C |
2: 87,083,054 (GRCm39) |
S258P |
possibly damaging |
Het |
Or1l4 |
C |
G |
2: 37,091,992 (GRCm39) |
H246Q |
probably damaging |
Het |
Or1p1c |
A |
G |
11: 74,161,066 (GRCm39) |
T284A |
probably benign |
Het |
Or2ak5 |
A |
T |
11: 58,611,133 (GRCm39) |
V247E |
probably damaging |
Het |
Or2i1 |
A |
G |
17: 37,507,722 (GRCm39) |
|
probably benign |
Het |
Or2y1c |
T |
A |
11: 49,361,795 (GRCm39) |
F272L |
probably benign |
Het |
Or6k8-ps1 |
C |
T |
1: 173,979,780 (GRCm39) |
R233C |
probably benign |
Het |
Otof |
G |
A |
5: 30,536,054 (GRCm39) |
T1343I |
probably benign |
Het |
Otop2 |
A |
T |
11: 115,215,454 (GRCm39) |
Y125F |
probably benign |
Het |
Pate3 |
G |
A |
9: 35,557,401 (GRCm39) |
T85I |
probably benign |
Het |
Pdpk1 |
A |
T |
17: 24,317,150 (GRCm39) |
|
probably benign |
Het |
Phf11d |
T |
C |
14: 59,593,778 (GRCm39) |
H132R |
probably benign |
Het |
Pik3c3 |
G |
A |
18: 30,477,130 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
C |
A |
1: 20,417,681 (GRCm39) |
G2490V |
probably damaging |
Het |
Prkdc |
G |
A |
16: 15,577,469 (GRCm39) |
D2372N |
probably damaging |
Het |
Ptprq |
C |
T |
10: 107,554,339 (GRCm39) |
E129K |
probably damaging |
Het |
Pym1 |
G |
A |
10: 128,601,913 (GRCm39) |
|
probably benign |
Het |
Ralgapb |
T |
A |
2: 158,334,372 (GRCm39) |
V1027E |
probably damaging |
Het |
Rita1 |
T |
C |
5: 120,747,645 (GRCm39) |
T218A |
possibly damaging |
Het |
Rrh |
T |
A |
3: 129,606,282 (GRCm39) |
T218S |
probably damaging |
Het |
Scaper |
C |
T |
9: 55,767,184 (GRCm39) |
A416T |
probably damaging |
Het |
Scn3a |
A |
G |
2: 65,314,716 (GRCm39) |
L1115P |
probably damaging |
Het |
Serpinb6e |
A |
T |
13: 34,017,217 (GRCm39) |
S268T |
probably damaging |
Het |
Skic3 |
C |
A |
13: 76,278,407 (GRCm39) |
H574N |
probably benign |
Het |
Slc1a6 |
G |
A |
10: 78,648,765 (GRCm39) |
W495* |
probably null |
Het |
Slc32a1 |
A |
G |
2: 158,453,298 (GRCm39) |
H46R |
probably benign |
Het |
Slc37a1 |
C |
T |
17: 31,519,405 (GRCm39) |
|
probably benign |
Het |
Slc6a5 |
T |
A |
7: 49,606,173 (GRCm39) |
W694R |
probably benign |
Het |
Smarcd2 |
A |
T |
11: 106,158,222 (GRCm39) |
D113E |
probably benign |
Het |
Sod3 |
G |
T |
5: 52,525,504 (GRCm39) |
V68L |
probably benign |
Het |
Srpk3 |
G |
A |
X: 72,821,561 (GRCm39) |
R425Q |
possibly damaging |
Het |
Sspo |
A |
T |
6: 48,469,820 (GRCm39) |
Q4506L |
possibly damaging |
Het |
Stam2 |
T |
A |
2: 52,606,539 (GRCm39) |
E115D |
probably damaging |
Het |
Sult1c2 |
A |
T |
17: 54,280,953 (GRCm39) |
L50H |
probably damaging |
Het |
Tbc1d22a |
T |
C |
15: 86,119,770 (GRCm39) |
V22A |
possibly damaging |
Het |
Togaram1 |
T |
G |
12: 65,042,409 (GRCm39) |
V1156G |
probably damaging |
Het |
Tpp1 |
T |
C |
7: 105,398,854 (GRCm39) |
T192A |
probably benign |
Het |
Ush1c |
A |
G |
7: 45,859,325 (GRCm39) |
L498P |
probably damaging |
Het |
Vit |
A |
C |
17: 78,930,265 (GRCm39) |
Q410P |
probably benign |
Het |
Vmn2r27 |
C |
T |
6: 124,208,593 (GRCm39) |
G51S |
probably benign |
Het |
Zfp341 |
A |
G |
2: 154,488,054 (GRCm39) |
E839G |
possibly damaging |
Het |
Zhx3 |
G |
A |
2: 160,622,275 (GRCm39) |
L631F |
probably benign |
Het |
Zmpste24 |
T |
C |
4: 120,944,513 (GRCm39) |
E95G |
possibly damaging |
Het |
|
Other mutations in Khnyn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01746:Khnyn
|
APN |
14 |
56,124,439 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01924:Khnyn
|
APN |
14 |
56,132,426 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01990:Khnyn
|
APN |
14 |
56,125,045 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0310:Khnyn
|
UTSW |
14 |
56,125,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Khnyn
|
UTSW |
14 |
56,124,195 (GRCm39) |
missense |
probably benign |
0.30 |
R4333:Khnyn
|
UTSW |
14 |
56,131,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R4334:Khnyn
|
UTSW |
14 |
56,131,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Khnyn
|
UTSW |
14 |
56,124,438 (GRCm39) |
missense |
probably benign |
0.02 |
R4731:Khnyn
|
UTSW |
14 |
56,123,946 (GRCm39) |
splice site |
probably null |
|
R4732:Khnyn
|
UTSW |
14 |
56,123,946 (GRCm39) |
splice site |
probably null |
|
R4733:Khnyn
|
UTSW |
14 |
56,123,946 (GRCm39) |
splice site |
probably null |
|
R5063:Khnyn
|
UTSW |
14 |
56,124,660 (GRCm39) |
nonsense |
probably null |
|
R5434:Khnyn
|
UTSW |
14 |
56,124,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Khnyn
|
UTSW |
14 |
56,124,523 (GRCm39) |
missense |
probably benign |
|
R5928:Khnyn
|
UTSW |
14 |
56,123,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R6144:Khnyn
|
UTSW |
14 |
56,125,296 (GRCm39) |
missense |
probably damaging |
0.98 |
R6147:Khnyn
|
UTSW |
14 |
56,125,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R6353:Khnyn
|
UTSW |
14 |
56,131,760 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7179:Khnyn
|
UTSW |
14 |
56,131,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7658:Khnyn
|
UTSW |
14 |
56,124,596 (GRCm39) |
nonsense |
probably null |
|
R7755:Khnyn
|
UTSW |
14 |
56,125,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Khnyn
|
UTSW |
14 |
56,125,303 (GRCm39) |
critical splice donor site |
probably null |
|
R7947:Khnyn
|
UTSW |
14 |
56,125,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R8006:Khnyn
|
UTSW |
14 |
56,125,047 (GRCm39) |
missense |
probably benign |
0.11 |
R8546:Khnyn
|
UTSW |
14 |
56,123,275 (GRCm39) |
missense |
probably benign |
0.00 |
R8753:Khnyn
|
UTSW |
14 |
56,125,223 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8877:Khnyn
|
UTSW |
14 |
56,131,782 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8901:Khnyn
|
UTSW |
14 |
56,124,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Khnyn
|
UTSW |
14 |
56,124,735 (GRCm39) |
missense |
probably benign |
0.00 |
R9541:Khnyn
|
UTSW |
14 |
56,124,109 (GRCm39) |
missense |
possibly damaging |
0.63 |
|