Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,831,615 (GRCm39) |
|
probably benign |
Het |
Adam20 |
A |
G |
8: 41,248,907 (GRCm39) |
D339G |
probably benign |
Het |
Adam3 |
T |
A |
8: 25,193,821 (GRCm39) |
Y397F |
probably benign |
Het |
Ago3 |
C |
T |
4: 126,248,829 (GRCm39) |
G574E |
probably damaging |
Het |
Angptl4 |
T |
A |
17: 33,999,800 (GRCm39) |
Y133F |
probably benign |
Het |
Ankrd61 |
T |
C |
5: 143,831,759 (GRCm39) |
D15G |
possibly damaging |
Het |
Arfgap1 |
T |
A |
2: 180,615,330 (GRCm39) |
S174T |
possibly damaging |
Het |
Arhgap12 |
T |
C |
18: 6,034,539 (GRCm39) |
D549G |
possibly damaging |
Het |
Arhgap25 |
T |
C |
6: 87,453,254 (GRCm39) |
E182G |
probably benign |
Het |
Astn1 |
T |
G |
1: 158,496,327 (GRCm39) |
I1127S |
probably benign |
Het |
Bivm |
T |
C |
1: 44,168,526 (GRCm39) |
|
probably null |
Het |
Cdc42bpa |
T |
A |
1: 179,945,258 (GRCm39) |
S952T |
possibly damaging |
Het |
Cfap44 |
T |
A |
16: 44,255,923 (GRCm39) |
L1005Q |
probably damaging |
Het |
Cmklr1 |
G |
C |
5: 113,752,043 (GRCm39) |
H319Q |
probably benign |
Het |
Cog1 |
T |
C |
11: 113,544,807 (GRCm39) |
F330L |
possibly damaging |
Het |
Dnah2 |
T |
G |
11: 69,435,208 (GRCm39) |
D54A |
probably benign |
Het |
Dntt |
A |
T |
19: 41,044,197 (GRCm39) |
|
probably null |
Het |
Eml2 |
A |
G |
7: 18,925,620 (GRCm39) |
S240G |
probably benign |
Het |
Fam174b |
G |
A |
7: 73,416,371 (GRCm39) |
|
probably benign |
Het |
Fancd2 |
T |
C |
6: 113,512,762 (GRCm39) |
S33P |
possibly damaging |
Het |
Fars2 |
A |
T |
13: 36,430,402 (GRCm39) |
M277L |
probably benign |
Het |
Ifnar1 |
G |
A |
16: 91,302,150 (GRCm39) |
G542S |
probably benign |
Het |
Itih5 |
T |
C |
2: 10,191,831 (GRCm39) |
V122A |
probably benign |
Het |
Jph3 |
A |
G |
8: 122,516,201 (GRCm39) |
I740V |
probably benign |
Het |
Mettl25b |
G |
A |
3: 87,834,978 (GRCm39) |
H57Y |
probably benign |
Het |
Mpeg1 |
A |
T |
19: 12,440,014 (GRCm39) |
T491S |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,055,605 (GRCm39) |
I998L |
possibly damaging |
Het |
Nrxn1 |
G |
A |
17: 90,869,233 (GRCm39) |
Q124* |
probably null |
Het |
Nup188 |
T |
A |
2: 30,222,461 (GRCm39) |
S1028T |
possibly damaging |
Het |
Nxf1 |
A |
T |
19: 8,745,118 (GRCm39) |
H456L |
probably damaging |
Het |
Or2aj6 |
T |
A |
16: 19,443,743 (GRCm39) |
I36F |
possibly damaging |
Het |
Or2n1d |
C |
A |
17: 38,646,434 (GRCm39) |
P129T |
probably damaging |
Het |
Or5af2 |
T |
A |
11: 58,707,959 (GRCm39) |
S42T |
possibly damaging |
Het |
Or5w19 |
T |
A |
2: 87,698,543 (GRCm39) |
D69E |
probably damaging |
Het |
Or6c66 |
T |
A |
10: 129,461,820 (GRCm39) |
I37F |
possibly damaging |
Het |
Otx2 |
T |
C |
14: 48,896,227 (GRCm39) |
N277S |
probably damaging |
Het |
Pax4 |
T |
C |
6: 28,445,201 (GRCm39) |
N158S |
probably benign |
Het |
Pgm2 |
T |
G |
5: 64,261,159 (GRCm39) |
S218A |
probably benign |
Het |
Plb1 |
T |
C |
5: 32,521,402 (GRCm39) |
S1418P |
probably benign |
Het |
Prkd3 |
T |
A |
17: 79,292,751 (GRCm39) |
D107V |
probably damaging |
Het |
Prl2a1 |
A |
G |
13: 27,992,398 (GRCm39) |
E174G |
probably benign |
Het |
Prr7 |
C |
T |
13: 55,620,574 (GRCm39) |
P194L |
probably damaging |
Het |
Psmd2 |
T |
C |
16: 20,470,994 (GRCm39) |
S46P |
probably damaging |
Het |
Ptbp2 |
C |
T |
3: 119,541,258 (GRCm39) |
A231T |
possibly damaging |
Het |
Rae1 |
A |
G |
2: 172,854,016 (GRCm39) |
T265A |
probably benign |
Het |
Sct |
T |
C |
7: 140,859,007 (GRCm39) |
E2G |
unknown |
Het |
Sec14l3 |
T |
G |
11: 4,015,007 (GRCm39) |
|
probably null |
Het |
Sfxn3 |
T |
A |
19: 45,038,727 (GRCm39) |
N131K |
probably damaging |
Het |
Slc18a2 |
A |
T |
19: 59,282,326 (GRCm39) |
D511V |
probably benign |
Het |
Slc20a2 |
T |
C |
8: 23,025,457 (GRCm39) |
I53T |
probably damaging |
Het |
Smad4 |
T |
C |
18: 73,782,941 (GRCm39) |
D331G |
probably damaging |
Het |
Srms |
C |
T |
2: 180,848,050 (GRCm39) |
R485H |
|
Het |
Szt2 |
C |
A |
4: 118,242,630 (GRCm39) |
A1486S |
possibly damaging |
Het |
Tmem87b |
C |
T |
2: 128,684,615 (GRCm39) |
Q459* |
probably null |
Het |
Vdr |
A |
T |
15: 97,782,753 (GRCm39) |
I23N |
probably damaging |
Het |
Vmn1r204 |
T |
C |
13: 22,740,564 (GRCm39) |
V65A |
possibly damaging |
Het |
Vps33b |
A |
G |
7: 79,939,743 (GRCm39) |
D498G |
probably benign |
Het |
Zfp442 |
T |
A |
2: 150,250,093 (GRCm39) |
Y603F |
probably benign |
Het |
Zfp853 |
T |
A |
5: 143,275,320 (GRCm39) |
Q115L |
unknown |
Het |
Zmiz2 |
C |
A |
11: 6,348,271 (GRCm39) |
Q303K |
probably benign |
Het |
|
Other mutations in Krtap16-1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Krtap16-1
|
APN |
11 |
99,876,557 (GRCm39) |
nonsense |
probably null |
|
IGL00578:Krtap16-1
|
APN |
11 |
99,876,121 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02324:Krtap16-1
|
APN |
11 |
99,877,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R0200:Krtap16-1
|
UTSW |
11 |
99,876,123 (GRCm39) |
missense |
probably damaging |
0.96 |
R0617:Krtap16-1
|
UTSW |
11 |
99,877,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Krtap16-1
|
UTSW |
11 |
99,876,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Krtap16-1
|
UTSW |
11 |
99,876,602 (GRCm39) |
nonsense |
probably null |
|
R2130:Krtap16-1
|
UTSW |
11 |
99,876,602 (GRCm39) |
nonsense |
probably null |
|
R2177:Krtap16-1
|
UTSW |
11 |
99,877,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R4455:Krtap16-1
|
UTSW |
11 |
99,876,559 (GRCm39) |
missense |
probably benign |
0.44 |
R4716:Krtap16-1
|
UTSW |
11 |
99,876,000 (GRCm39) |
missense |
probably damaging |
0.99 |
R5111:Krtap16-1
|
UTSW |
11 |
99,877,378 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5122:Krtap16-1
|
UTSW |
11 |
99,876,523 (GRCm39) |
missense |
probably damaging |
0.96 |
R5254:Krtap16-1
|
UTSW |
11 |
99,876,424 (GRCm39) |
nonsense |
probably null |
|
R5481:Krtap16-1
|
UTSW |
11 |
99,876,153 (GRCm39) |
missense |
probably damaging |
0.98 |
R6557:Krtap16-1
|
UTSW |
11 |
99,875,956 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6884:Krtap16-1
|
UTSW |
11 |
99,877,284 (GRCm39) |
nonsense |
probably null |
|
R7085:Krtap16-1
|
UTSW |
11 |
99,877,111 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7675:Krtap16-1
|
UTSW |
11 |
99,876,259 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8517:Krtap16-1
|
UTSW |
11 |
99,876,524 (GRCm39) |
nonsense |
probably null |
|
R8903:Krtap16-1
|
UTSW |
11 |
99,877,170 (GRCm39) |
missense |
probably damaging |
0.96 |
R9047:Krtap16-1
|
UTSW |
11 |
99,877,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Krtap16-1
|
UTSW |
11 |
99,876,071 (GRCm39) |
missense |
probably benign |
0.02 |
R9243:Krtap16-1
|
UTSW |
11 |
99,876,644 (GRCm39) |
nonsense |
probably null |
|
R9262:Krtap16-1
|
UTSW |
11 |
99,876,994 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Krtap16-1
|
UTSW |
11 |
99,876,423 (GRCm39) |
missense |
possibly damaging |
0.95 |
|