Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001K19Rik |
A |
G |
12: 110,635,184 (GRCm39) |
V118A |
probably benign |
Het |
Accsl |
C |
T |
2: 93,696,160 (GRCm39) |
G146D |
possibly damaging |
Het |
Acsm1 |
A |
T |
7: 119,237,305 (GRCm39) |
H206L |
probably damaging |
Het |
Acta2 |
A |
G |
19: 34,219,186 (GRCm39) |
Y339H |
probably damaging |
Het |
Adcy2 |
T |
C |
13: 68,779,073 (GRCm39) |
D989G |
probably damaging |
Het |
Ahnak |
G |
A |
19: 8,979,507 (GRCm39) |
A264T |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,987,191 (GRCm39) |
D2825G |
possibly damaging |
Het |
Akt1 |
G |
T |
12: 112,623,587 (GRCm39) |
T291K |
probably damaging |
Het |
Arhgap24 |
A |
G |
5: 103,040,551 (GRCm39) |
D589G |
probably damaging |
Het |
B4galnt3 |
G |
A |
6: 120,192,396 (GRCm39) |
Q447* |
probably null |
Het |
BC024063 |
C |
T |
10: 81,945,993 (GRCm39) |
R538C |
possibly damaging |
Het |
Bod1l |
A |
G |
5: 41,951,676 (GRCm39) |
S2912P |
possibly damaging |
Het |
Bysl |
A |
G |
17: 47,912,710 (GRCm39) |
V360A |
possibly damaging |
Het |
C1qb |
A |
G |
4: 136,607,877 (GRCm39) |
V162A |
possibly damaging |
Het |
Ccdc57 |
G |
A |
11: 120,764,567 (GRCm39) |
P736L |
probably benign |
Het |
Cep290 |
T |
A |
10: 100,373,580 (GRCm39) |
F1287I |
probably damaging |
Het |
Cntn1 |
T |
C |
15: 92,130,156 (GRCm39) |
|
probably null |
Het |
Col6a3 |
C |
T |
1: 90,750,013 (GRCm39) |
G274R |
probably damaging |
Het |
Cplane1 |
G |
T |
15: 8,210,399 (GRCm39) |
V291F |
probably damaging |
Het |
Cyb5r4 |
T |
C |
9: 86,937,835 (GRCm39) |
C285R |
probably damaging |
Het |
Cyp4f39 |
G |
A |
17: 32,708,629 (GRCm39) |
C392Y |
probably damaging |
Het |
Dcun1d3 |
A |
T |
7: 119,458,734 (GRCm39) |
D100E |
probably damaging |
Het |
Dhx58 |
A |
T |
11: 100,588,997 (GRCm39) |
D516E |
probably benign |
Het |
Dock5 |
T |
A |
14: 68,065,951 (GRCm39) |
I351F |
probably benign |
Het |
Elmod2 |
A |
C |
8: 84,046,041 (GRCm39) |
|
probably null |
Het |
Endov |
G |
A |
11: 119,398,077 (GRCm39) |
A281T |
probably benign |
Het |
Epyc |
A |
G |
10: 97,485,562 (GRCm39) |
M1V |
probably null |
Het |
Espnl |
T |
A |
1: 91,251,290 (GRCm39) |
H128Q |
probably damaging |
Het |
Fam20a |
A |
T |
11: 109,565,454 (GRCm39) |
C452* |
probably null |
Het |
Fam241b |
A |
G |
10: 61,944,733 (GRCm39) |
V88A |
probably damaging |
Het |
Fbxl9 |
A |
G |
8: 106,042,299 (GRCm39) |
|
probably benign |
Het |
Fgd3 |
A |
T |
13: 49,450,166 (GRCm39) |
S28T |
possibly damaging |
Het |
Fmn1 |
C |
A |
2: 113,356,025 (GRCm39) |
P920Q |
unknown |
Het |
Gpr139 |
G |
C |
7: 118,744,089 (GRCm39) |
D165E |
probably benign |
Het |
Hoxb1 |
A |
G |
11: 96,257,927 (GRCm39) |
T286A |
possibly damaging |
Het |
Ifi204 |
T |
A |
1: 173,587,134 (GRCm39) |
E174D |
probably benign |
Het |
Igf2bp2 |
A |
G |
16: 21,880,632 (GRCm39) |
I555T |
possibly damaging |
Het |
Ighv1-85 |
A |
G |
12: 115,963,799 (GRCm39) |
I67T |
probably damaging |
Het |
Ihh |
G |
C |
1: 74,990,306 (GRCm39) |
P23R |
unknown |
Het |
Irx2 |
T |
C |
13: 72,779,396 (GRCm39) |
S227P |
probably damaging |
Het |
Itga4 |
A |
G |
2: 79,086,526 (GRCm39) |
I68V |
probably benign |
Het |
Jsrp1 |
T |
A |
10: 80,647,906 (GRCm39) |
T51S |
probably benign |
Het |
Khdc4 |
T |
C |
3: 88,619,002 (GRCm39) |
S569P |
probably damaging |
Het |
Kifc2 |
G |
T |
15: 76,547,010 (GRCm39) |
G306V |
probably damaging |
Het |
L3mbtl2 |
T |
A |
15: 81,551,588 (GRCm39) |
S85T |
possibly damaging |
Het |
Lama1 |
T |
C |
17: 68,074,380 (GRCm39) |
S944P |
|
Het |
Lama4 |
T |
A |
10: 38,902,631 (GRCm39) |
C202S |
probably damaging |
Het |
Morc3 |
G |
A |
16: 93,646,061 (GRCm39) |
D218N |
probably damaging |
Het |
Mrtfb |
T |
A |
16: 13,223,718 (GRCm39) |
Y866* |
probably null |
Het |
Myorg |
A |
G |
4: 41,498,577 (GRCm39) |
I351T |
probably damaging |
Het |
N4bp2l1 |
G |
A |
5: 150,496,389 (GRCm39) |
T179I |
probably damaging |
Het |
Nsd2 |
A |
G |
5: 34,049,380 (GRCm39) |
D1205G |
probably damaging |
Het |
Or10x1 |
T |
C |
1: 174,196,759 (GRCm39) |
V92A |
probably benign |
Het |
Or5an11 |
T |
C |
19: 12,246,068 (GRCm39) |
V158A |
probably benign |
Het |
Parl |
T |
C |
16: 20,106,625 (GRCm39) |
T195A |
probably benign |
Het |
Phrf1 |
A |
G |
7: 140,820,846 (GRCm39) |
I158V |
unknown |
Het |
Phtf1 |
T |
C |
3: 103,904,980 (GRCm39) |
F543L |
possibly damaging |
Het |
Plod2 |
T |
A |
9: 92,466,611 (GRCm39) |
D190E |
probably damaging |
Het |
Polr1a |
G |
T |
6: 71,927,863 (GRCm39) |
K871N |
possibly damaging |
Het |
Ppp2r5a |
A |
T |
1: 191,089,998 (GRCm39) |
I252K |
probably damaging |
Het |
Ptgir |
T |
A |
7: 16,640,973 (GRCm39) |
D88E |
probably damaging |
Het |
Raly |
T |
C |
2: 154,699,340 (GRCm39) |
V48A |
probably damaging |
Het |
Ripor1 |
T |
A |
8: 106,344,447 (GRCm39) |
L527* |
probably null |
Het |
Rnf213 |
T |
C |
11: 119,307,373 (GRCm39) |
S678P |
|
Het |
Rpf1 |
T |
A |
3: 146,212,918 (GRCm39) |
Q306L |
probably benign |
Het |
Rpl14 |
T |
C |
9: 120,403,171 (GRCm39) |
I122T |
probably damaging |
Het |
Scn9a |
C |
A |
2: 66,314,748 (GRCm39) |
A1657S |
possibly damaging |
Het |
Serpinb10 |
A |
G |
1: 107,474,477 (GRCm39) |
Y213C |
probably damaging |
Het |
Slc25a23 |
A |
G |
17: 57,359,827 (GRCm39) |
L308P |
probably damaging |
Het |
Smg9 |
T |
A |
7: 24,120,058 (GRCm39) |
M387K |
probably benign |
Het |
Socs3 |
G |
A |
11: 117,858,614 (GRCm39) |
P148L |
probably benign |
Het |
Susd3 |
A |
G |
13: 49,401,906 (GRCm39) |
L14P |
probably benign |
Het |
Syt14 |
T |
A |
1: 192,662,858 (GRCm39) |
M80L |
probably benign |
Het |
Tmprss2 |
T |
A |
16: 97,369,616 (GRCm39) |
Y386F |
possibly damaging |
Het |
Tmx3 |
T |
A |
18: 90,558,195 (GRCm39) |
S416T |
probably benign |
Het |
Treh |
A |
G |
9: 44,597,245 (GRCm39) |
T555A |
probably benign |
Het |
Ttc5 |
T |
G |
14: 51,003,400 (GRCm39) |
Q428P |
probably damaging |
Het |
Vmn2r73 |
A |
G |
7: 85,521,192 (GRCm39) |
S259P |
possibly damaging |
Het |
Vps4b |
A |
T |
1: 106,719,434 (GRCm39) |
V38E |
probably damaging |
Het |
Wdr83 |
C |
A |
8: 85,802,890 (GRCm39) |
R177L |
probably benign |
Het |
Zfp780b |
A |
G |
7: 27,662,588 (GRCm39) |
F656L |
possibly damaging |
Het |
Zfp995 |
A |
T |
17: 22,099,641 (GRCm39) |
F198I |
probably benign |
Het |
Zswim8 |
A |
T |
14: 20,771,552 (GRCm39) |
Y1495F |
probably damaging |
Het |
|
Other mutations in Narf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Narf
|
APN |
11 |
121,129,344 (GRCm39) |
critical splice donor site |
probably null |
|
R0128:Narf
|
UTSW |
11 |
121,141,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Narf
|
UTSW |
11 |
121,143,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R1326:Narf
|
UTSW |
11 |
121,133,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Narf
|
UTSW |
11 |
121,129,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2049:Narf
|
UTSW |
11 |
121,141,195 (GRCm39) |
nonsense |
probably null |
|
R2078:Narf
|
UTSW |
11 |
121,136,220 (GRCm39) |
missense |
probably benign |
0.03 |
R3711:Narf
|
UTSW |
11 |
121,137,764 (GRCm39) |
nonsense |
probably null |
|
R3967:Narf
|
UTSW |
11 |
121,129,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3968:Narf
|
UTSW |
11 |
121,129,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3970:Narf
|
UTSW |
11 |
121,129,247 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4128:Narf
|
UTSW |
11 |
121,141,261 (GRCm39) |
splice site |
probably null |
|
R4913:Narf
|
UTSW |
11 |
121,135,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Narf
|
UTSW |
11 |
121,135,765 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4946:Narf
|
UTSW |
11 |
121,141,179 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5404:Narf
|
UTSW |
11 |
121,133,452 (GRCm39) |
missense |
probably benign |
0.00 |
R5799:Narf
|
UTSW |
11 |
121,135,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6753:Narf
|
UTSW |
11 |
121,133,452 (GRCm39) |
missense |
probably benign |
0.00 |
R6912:Narf
|
UTSW |
11 |
121,129,287 (GRCm39) |
missense |
probably benign |
0.00 |
R8056:Narf
|
UTSW |
11 |
121,136,170 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8559:Narf
|
UTSW |
11 |
121,141,258 (GRCm39) |
critical splice donor site |
probably null |
|
R9021:Narf
|
UTSW |
11 |
121,136,209 (GRCm39) |
missense |
probably damaging |
0.98 |
X0011:Narf
|
UTSW |
11 |
121,141,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|