Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 8,988,021 (GRCm39) |
K3102E |
possibly damaging |
Het |
Akap13 |
T |
C |
7: 75,351,902 (GRCm39) |
|
probably null |
Het |
Akp3 |
A |
T |
1: 87,055,485 (GRCm39) |
T511S |
unknown |
Het |
Alkal2 |
T |
A |
12: 30,934,889 (GRCm39) |
L36Q |
probably damaging |
Het |
Arhgef17 |
A |
T |
7: 100,529,218 (GRCm39) |
V523E |
probably damaging |
Het |
Asah1 |
G |
T |
8: 41,813,332 (GRCm39) |
T27K |
possibly damaging |
Het |
Bag2 |
A |
G |
1: 33,786,034 (GRCm39) |
V96A |
probably damaging |
Het |
Bicd1 |
C |
T |
6: 149,421,901 (GRCm39) |
A874V |
probably damaging |
Het |
C4b |
T |
C |
17: 34,961,391 (GRCm39) |
I189M |
probably benign |
Het |
Calcr |
A |
G |
6: 3,708,538 (GRCm39) |
I216T |
probably damaging |
Het |
Cdk5rap2 |
T |
A |
4: 70,184,970 (GRCm39) |
D1160V |
probably damaging |
Het |
Cep128 |
A |
T |
12: 91,315,625 (GRCm39) |
I87K |
probably damaging |
Het |
Cep170b |
C |
G |
12: 112,707,275 (GRCm39) |
H1256Q |
probably benign |
Het |
Chd2 |
A |
T |
7: 73,134,232 (GRCm39) |
V705E |
probably damaging |
Het |
Clec12b |
T |
A |
6: 129,356,923 (GRCm39) |
I172L |
probably benign |
Het |
Cobl |
A |
T |
11: 12,256,948 (GRCm39) |
|
probably benign |
Het |
Col5a2 |
T |
A |
1: 45,429,202 (GRCm39) |
D972V |
probably damaging |
Het |
Csrp1 |
A |
T |
1: 135,678,797 (GRCm39) |
N174I |
probably damaging |
Het |
Dnah7a |
T |
A |
1: 53,444,866 (GRCm39) |
H3946L |
probably benign |
Het |
Dnajc21 |
A |
T |
15: 10,462,001 (GRCm39) |
D133E |
probably benign |
Het |
Dvl3 |
T |
A |
16: 20,345,026 (GRCm39) |
I353N |
probably damaging |
Het |
Elavl3 |
A |
T |
9: 21,930,029 (GRCm39) |
S292T |
probably benign |
Het |
Ephb2 |
T |
C |
4: 136,498,923 (GRCm39) |
N52S |
probably damaging |
Het |
Gaa |
T |
A |
11: 119,171,361 (GRCm39) |
M671K |
possibly damaging |
Het |
Gabrg3 |
T |
C |
7: 56,423,032 (GRCm39) |
D222G |
possibly damaging |
Het |
Gk5 |
C |
T |
9: 96,022,709 (GRCm39) |
Q182* |
probably null |
Het |
Gm14403 |
A |
T |
2: 177,199,054 (GRCm39) |
H50L |
possibly damaging |
Het |
Gzma |
T |
C |
13: 113,234,794 (GRCm39) |
T66A |
probably damaging |
Het |
Hint2 |
T |
C |
4: 43,656,445 (GRCm39) |
|
probably benign |
Het |
Hnmt |
A |
T |
2: 23,904,251 (GRCm39) |
W137R |
probably damaging |
Het |
Hoga1 |
T |
C |
19: 42,048,402 (GRCm39) |
V90A |
probably benign |
Het |
Idua |
A |
T |
5: 108,828,090 (GRCm39) |
|
probably benign |
Het |
Kif1a |
A |
C |
1: 92,983,489 (GRCm39) |
S669R |
probably damaging |
Het |
Klhdc7b |
A |
T |
15: 89,271,862 (GRCm39) |
M915L |
possibly damaging |
Het |
Klhl41 |
A |
G |
2: 69,500,815 (GRCm39) |
Y92C |
probably damaging |
Het |
Klrc2 |
A |
T |
6: 129,633,420 (GRCm39) |
C186S |
probably damaging |
Het |
Lmo7 |
A |
G |
14: 102,166,772 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
T |
C |
10: 103,051,301 (GRCm39) |
M484V |
probably benign |
Het |
Lzts1 |
A |
G |
8: 69,591,729 (GRCm39) |
S140P |
possibly damaging |
Het |
Mgat5b |
T |
A |
11: 116,864,226 (GRCm39) |
V464E |
probably damaging |
Het |
Mms19 |
A |
T |
19: 41,944,305 (GRCm39) |
D298E |
possibly damaging |
Het |
Muc5ac |
T |
C |
7: 141,347,452 (GRCm39) |
|
probably null |
Het |
Mycbp2 |
T |
A |
14: 103,524,770 (GRCm39) |
K597I |
probably damaging |
Het |
Myo18a |
C |
A |
11: 77,745,513 (GRCm39) |
D1619E |
probably benign |
Het |
Nipbl |
C |
T |
15: 8,388,391 (GRCm39) |
V410I |
probably benign |
Het |
Or14j10 |
T |
A |
17: 37,935,323 (GRCm39) |
I68F |
probably benign |
Het |
Or4c101 |
T |
A |
2: 88,389,849 (GRCm39) |
M1K |
probably null |
Het |
Or4f60 |
A |
T |
2: 111,902,013 (GRCm39) |
M305K |
probably benign |
Het |
Or52h1 |
T |
C |
7: 103,829,091 (GRCm39) |
I175V |
probably benign |
Het |
Or5b95 |
A |
T |
19: 12,658,336 (GRCm39) |
Y288F |
probably damaging |
Het |
Or7g32 |
A |
T |
9: 19,388,853 (GRCm39) |
M231K |
probably benign |
Het |
Or8u10 |
T |
C |
2: 85,915,503 (GRCm39) |
N206S |
probably damaging |
Het |
Otog |
A |
T |
7: 45,936,871 (GRCm39) |
T1527S |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,125,516 (GRCm39) |
M53K |
possibly damaging |
Het |
Pask |
A |
G |
1: 93,265,065 (GRCm39) |
|
probably null |
Het |
Pcca |
G |
A |
14: 123,124,481 (GRCm39) |
C684Y |
probably damaging |
Het |
Pcdhb10 |
A |
G |
18: 37,546,219 (GRCm39) |
T432A |
possibly damaging |
Het |
Peak1 |
T |
C |
9: 56,166,039 (GRCm39) |
N630D |
probably damaging |
Het |
Plbd2 |
A |
T |
5: 120,631,231 (GRCm39) |
|
probably null |
Het |
Plekhg5 |
T |
C |
4: 152,188,797 (GRCm39) |
V200A |
probably benign |
Het |
Pola2 |
A |
G |
19: 6,011,198 (GRCm39) |
V42A |
probably benign |
Het |
Ppfibp2 |
T |
A |
7: 107,337,097 (GRCm39) |
W572R |
probably damaging |
Het |
Ppp6r1 |
C |
T |
7: 4,636,771 (GRCm39) |
E679K |
probably benign |
Het |
Pramel11 |
A |
T |
4: 143,622,337 (GRCm39) |
H339Q |
probably damaging |
Het |
Prdx3 |
G |
A |
19: 60,859,963 (GRCm39) |
A70V |
probably damaging |
Het |
Prkd2 |
T |
C |
7: 16,577,717 (GRCm39) |
F57L |
probably benign |
Het |
Prodh2 |
A |
G |
7: 30,206,171 (GRCm39) |
T324A |
possibly damaging |
Het |
Ptdss1 |
T |
C |
13: 67,120,604 (GRCm39) |
F267L |
probably damaging |
Het |
Rai14 |
T |
A |
15: 10,593,137 (GRCm39) |
H169L |
probably benign |
Het |
Rere |
A |
G |
4: 150,701,700 (GRCm39) |
H1360R |
probably damaging |
Het |
Rfc3 |
C |
T |
5: 151,573,444 (GRCm39) |
V40I |
probably benign |
Het |
Rims1 |
T |
A |
1: 22,577,590 (GRCm39) |
T219S |
probably damaging |
Het |
Rnf169 |
T |
C |
7: 99,576,338 (GRCm39) |
R289G |
possibly damaging |
Het |
Senp7 |
T |
C |
16: 56,004,512 (GRCm39) |
|
silent |
Het |
Sfmbt2 |
A |
T |
2: 10,573,184 (GRCm39) |
I571F |
probably damaging |
Het |
Slc11a2 |
C |
A |
15: 100,301,068 (GRCm39) |
K328N |
probably benign |
Het |
Slc25a10 |
A |
G |
11: 120,387,202 (GRCm39) |
|
probably benign |
Het |
Slc38a8 |
T |
C |
8: 120,207,488 (GRCm39) |
*433W |
probably null |
Het |
Slco1a5 |
A |
C |
6: 142,183,320 (GRCm39) |
|
probably null |
Het |
Smc6 |
T |
A |
12: 11,339,995 (GRCm39) |
N434K |
probably benign |
Het |
Syndig1 |
A |
T |
2: 149,741,428 (GRCm39) |
I5F |
possibly damaging |
Het |
Syt5 |
T |
C |
7: 4,546,018 (GRCm39) |
Q124R |
probably benign |
Het |
Taok3 |
A |
C |
5: 117,344,785 (GRCm39) |
M171L |
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,560,709 (GRCm39) |
D389G |
probably benign |
Het |
Tcaf2 |
G |
A |
6: 42,619,707 (GRCm39) |
R107C |
possibly damaging |
Het |
Tex14 |
C |
A |
11: 87,426,452 (GRCm39) |
H1159Q |
probably damaging |
Het |
Tmprss11d |
T |
A |
5: 86,474,388 (GRCm39) |
M190L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,768,867 (GRCm39) |
T2856S |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,171,998 (GRCm39) |
M2997K |
probably damaging |
Het |
Unc5c |
C |
T |
3: 141,383,886 (GRCm39) |
A88V |
probably damaging |
Het |
Use1 |
T |
C |
8: 71,820,398 (GRCm39) |
|
probably benign |
Het |
Vmn1r43 |
T |
C |
6: 89,847,354 (GRCm39) |
N44S |
probably damaging |
Het |
Vmn1r89 |
T |
A |
7: 12,954,146 (GRCm39) |
V294D |
possibly damaging |
Het |
Vmn2r11 |
A |
T |
5: 109,194,869 (GRCm39) |
V819E |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,977 (GRCm39) |
M271L |
probably benign |
Het |
Vmn2r52 |
T |
C |
7: 9,905,059 (GRCm39) |
Y260C |
probably damaging |
Het |
Vmn2r67 |
T |
A |
7: 84,799,151 (GRCm39) |
R519* |
probably null |
Het |
Vmn2r69 |
T |
A |
7: 85,056,404 (GRCm39) |
D578V |
probably damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,262,343 (GRCm39) |
Y132C |
probably damaging |
Het |
Wdr74 |
T |
A |
19: 8,715,240 (GRCm39) |
V133E |
probably damaging |
Het |
Zfp318 |
T |
A |
17: 46,720,170 (GRCm39) |
|
probably benign |
Het |
Zfp810 |
A |
T |
9: 22,194,467 (GRCm39) |
S74T |
probably benign |
Het |
|
Other mutations in Nfx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01377:Nfx1
|
APN |
4 |
40,977,241 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01998:Nfx1
|
APN |
4 |
41,004,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02072:Nfx1
|
APN |
4 |
41,016,119 (GRCm39) |
missense |
probably benign |
|
IGL02170:Nfx1
|
APN |
4 |
41,018,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02188:Nfx1
|
APN |
4 |
40,993,827 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02502:Nfx1
|
APN |
4 |
40,976,345 (GRCm39) |
splice site |
probably benign |
|
IGL02674:Nfx1
|
APN |
4 |
40,999,717 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03007:Nfx1
|
APN |
4 |
40,984,962 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03092:Nfx1
|
APN |
4 |
41,024,851 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03303:Nfx1
|
APN |
4 |
41,004,323 (GRCm39) |
splice site |
probably benign |
|
K7371:Nfx1
|
UTSW |
4 |
40,976,803 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4498001:Nfx1
|
UTSW |
4 |
40,977,244 (GRCm39) |
missense |
probably benign |
|
R0032:Nfx1
|
UTSW |
4 |
41,015,321 (GRCm39) |
missense |
probably benign |
0.00 |
R0032:Nfx1
|
UTSW |
4 |
41,015,321 (GRCm39) |
missense |
probably benign |
0.00 |
R0069:Nfx1
|
UTSW |
4 |
40,986,688 (GRCm39) |
splice site |
probably benign |
|
R1056:Nfx1
|
UTSW |
4 |
41,003,057 (GRCm39) |
missense |
probably damaging |
0.97 |
R1449:Nfx1
|
UTSW |
4 |
40,976,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Nfx1
|
UTSW |
4 |
40,977,004 (GRCm39) |
missense |
probably benign |
|
R1636:Nfx1
|
UTSW |
4 |
41,016,072 (GRCm39) |
splice site |
probably null |
|
R1882:Nfx1
|
UTSW |
4 |
41,009,240 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2089:Nfx1
|
UTSW |
4 |
40,977,004 (GRCm39) |
missense |
probably benign |
|
R2091:Nfx1
|
UTSW |
4 |
40,977,004 (GRCm39) |
missense |
probably benign |
|
R2091:Nfx1
|
UTSW |
4 |
40,977,004 (GRCm39) |
missense |
probably benign |
|
R3792:Nfx1
|
UTSW |
4 |
41,004,357 (GRCm39) |
nonsense |
probably null |
|
R3793:Nfx1
|
UTSW |
4 |
41,004,357 (GRCm39) |
nonsense |
probably null |
|
R4668:Nfx1
|
UTSW |
4 |
40,976,367 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4678:Nfx1
|
UTSW |
4 |
41,012,070 (GRCm39) |
missense |
probably benign |
0.01 |
R4894:Nfx1
|
UTSW |
4 |
40,996,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R4972:Nfx1
|
UTSW |
4 |
40,976,375 (GRCm39) |
missense |
probably benign |
0.36 |
R5066:Nfx1
|
UTSW |
4 |
40,991,868 (GRCm39) |
missense |
probably benign |
|
R5389:Nfx1
|
UTSW |
4 |
40,985,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R5429:Nfx1
|
UTSW |
4 |
41,004,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Nfx1
|
UTSW |
4 |
40,984,973 (GRCm39) |
missense |
probably null |
1.00 |
R5915:Nfx1
|
UTSW |
4 |
40,977,285 (GRCm39) |
missense |
probably benign |
0.02 |
R6286:Nfx1
|
UTSW |
4 |
40,986,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Nfx1
|
UTSW |
4 |
40,976,851 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7409:Nfx1
|
UTSW |
4 |
41,021,830 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7523:Nfx1
|
UTSW |
4 |
41,016,119 (GRCm39) |
missense |
probably benign |
|
R7916:Nfx1
|
UTSW |
4 |
40,977,142 (GRCm39) |
missense |
probably benign |
0.11 |
R8497:Nfx1
|
UTSW |
4 |
40,976,968 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8799:Nfx1
|
UTSW |
4 |
41,023,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R9154:Nfx1
|
UTSW |
4 |
40,990,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R9364:Nfx1
|
UTSW |
4 |
41,023,756 (GRCm39) |
missense |
probably benign |
0.31 |
R9497:Nfx1
|
UTSW |
4 |
40,994,104 (GRCm39) |
missense |
probably benign |
0.00 |
X0025:Nfx1
|
UTSW |
4 |
40,976,422 (GRCm39) |
missense |
possibly damaging |
0.83 |
|