Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
C |
11: 110,039,615 (GRCm39) |
D466G |
probably benign |
Het |
Asb4 |
A |
T |
6: 5,390,771 (GRCm39) |
M55L |
probably benign |
Het |
Atxn7l1 |
T |
C |
12: 33,375,954 (GRCm39) |
S10P |
probably damaging |
Het |
Bola3 |
T |
C |
6: 83,328,249 (GRCm39) |
L45P |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,255,134 (GRCm39) |
|
probably null |
Het |
Cfap54 |
A |
G |
10: 92,675,333 (GRCm39) |
S2863P |
possibly damaging |
Het |
Cyb5r3 |
A |
G |
15: 83,044,330 (GRCm39) |
V180A |
possibly damaging |
Het |
Dglucy |
A |
T |
12: 100,807,648 (GRCm39) |
T186S |
probably benign |
Het |
Eml5 |
A |
T |
12: 98,768,724 (GRCm39) |
|
probably benign |
Het |
Fam90a1a |
G |
A |
8: 22,451,432 (GRCm39) |
D98N |
probably damaging |
Het |
Fbxo16 |
T |
A |
14: 65,524,606 (GRCm39) |
L42Q |
probably damaging |
Het |
Fbxw16 |
A |
G |
9: 109,268,697 (GRCm39) |
V231A |
probably benign |
Het |
Fermt3 |
G |
A |
19: 6,979,792 (GRCm39) |
A447V |
possibly damaging |
Het |
Fignl2 |
A |
G |
15: 100,950,467 (GRCm39) |
L605P |
unknown |
Het |
Gcsam |
T |
G |
16: 45,440,192 (GRCm39) |
N78K |
probably damaging |
Het |
Gdf2 |
T |
A |
14: 33,666,791 (GRCm39) |
V171D |
probably damaging |
Het |
Gm28042 |
C |
T |
2: 119,867,237 (GRCm39) |
H218Y |
probably benign |
Het |
Herpud2 |
A |
G |
9: 25,021,734 (GRCm39) |
V304A |
probably damaging |
Het |
Kcnma1 |
C |
T |
14: 24,053,815 (GRCm39) |
|
probably null |
Het |
Lrp3 |
T |
C |
7: 34,903,530 (GRCm39) |
D251G |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,852,339 (GRCm39) |
V957A |
possibly damaging |
Het |
Mepe |
C |
T |
5: 104,484,944 (GRCm39) |
P28L |
probably benign |
Het |
Muc2 |
T |
A |
7: 141,300,541 (GRCm39) |
|
probably benign |
Het |
Nt5dc2 |
T |
C |
14: 30,860,832 (GRCm39) |
S439P |
probably damaging |
Het |
Opn4 |
C |
T |
14: 34,319,066 (GRCm39) |
R173H |
probably benign |
Het |
Or2k2 |
A |
G |
4: 58,785,164 (GRCm39) |
L186P |
probably damaging |
Het |
Or4f14 |
C |
T |
2: 111,742,951 (GRCm39) |
G108D |
possibly damaging |
Het |
Phf8-ps |
A |
T |
17: 33,285,405 (GRCm39) |
S466T |
probably benign |
Het |
Ppp1r12a |
T |
C |
10: 108,089,341 (GRCm39) |
V660A |
probably benign |
Het |
Rab18 |
T |
A |
18: 6,778,529 (GRCm39) |
D53E |
probably benign |
Het |
Rel |
A |
G |
11: 23,692,939 (GRCm39) |
S365P |
probably benign |
Het |
Rhbg |
C |
A |
3: 88,151,843 (GRCm39) |
G383V |
probably damaging |
Het |
Rnps1-ps |
A |
T |
6: 7,983,149 (GRCm39) |
|
noncoding transcript |
Het |
Rp1l1 |
T |
A |
14: 64,267,758 (GRCm39) |
Y1115N |
probably damaging |
Het |
Runx2 |
T |
C |
17: 44,920,966 (GRCm39) |
T339A |
possibly damaging |
Het |
Ryr3 |
T |
C |
2: 112,506,182 (GRCm39) |
E3455G |
possibly damaging |
Het |
Serpina1d |
A |
T |
12: 103,734,107 (GRCm39) |
S66T |
probably benign |
Het |
Setd3 |
T |
C |
12: 108,131,417 (GRCm39) |
K3R |
possibly damaging |
Het |
Spg7 |
A |
G |
8: 123,806,187 (GRCm39) |
D299G |
probably damaging |
Het |
Sptbn5 |
C |
T |
2: 119,878,742 (GRCm39) |
|
noncoding transcript |
Het |
Srcap |
A |
G |
7: 127,148,411 (GRCm39) |
T1859A |
probably benign |
Het |
Suox |
A |
G |
10: 128,506,906 (GRCm39) |
V374A |
probably damaging |
Het |
Tesk1 |
C |
T |
4: 43,445,786 (GRCm39) |
P280S |
possibly damaging |
Het |
Tsc22d1 |
T |
C |
14: 76,656,049 (GRCm39) |
S761P |
probably damaging |
Het |
Tubal3 |
C |
T |
13: 3,982,946 (GRCm39) |
S242L |
probably benign |
Het |
Ugt2b1 |
C |
A |
5: 87,065,534 (GRCm39) |
V502L |
probably benign |
Het |
|
Other mutations in Prdm6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00473:Prdm6
|
APN |
18 |
53,673,357 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00743:Prdm6
|
APN |
18 |
53,673,300 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02183:Prdm6
|
APN |
18 |
53,597,749 (GRCm39) |
unclassified |
probably benign |
|
R1720:Prdm6
|
UTSW |
18 |
53,673,272 (GRCm39) |
missense |
probably benign |
0.29 |
R1879:Prdm6
|
UTSW |
18 |
53,701,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Prdm6
|
UTSW |
18 |
53,669,796 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1962:Prdm6
|
UTSW |
18 |
53,701,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Prdm6
|
UTSW |
18 |
53,598,031 (GRCm39) |
unclassified |
probably benign |
|
R3973:Prdm6
|
UTSW |
18 |
53,673,278 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3974:Prdm6
|
UTSW |
18 |
53,673,278 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3975:Prdm6
|
UTSW |
18 |
53,673,278 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4012:Prdm6
|
UTSW |
18 |
53,673,390 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5144:Prdm6
|
UTSW |
18 |
53,598,110 (GRCm39) |
unclassified |
probably benign |
|
R5640:Prdm6
|
UTSW |
18 |
53,669,813 (GRCm39) |
critical splice donor site |
probably null |
|
R6113:Prdm6
|
UTSW |
18 |
53,606,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Prdm6
|
UTSW |
18 |
53,669,751 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6747:Prdm6
|
UTSW |
18 |
53,598,118 (GRCm39) |
unclassified |
probably benign |
|
R6784:Prdm6
|
UTSW |
18 |
53,669,698 (GRCm39) |
missense |
probably benign |
0.04 |
R7363:Prdm6
|
UTSW |
18 |
53,598,199 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8365:Prdm6
|
UTSW |
18 |
53,685,137 (GRCm39) |
missense |
probably benign |
0.22 |
R8469:Prdm6
|
UTSW |
18 |
53,597,758 (GRCm39) |
unclassified |
probably benign |
|
R8827:Prdm6
|
UTSW |
18 |
53,701,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R8977:Prdm6
|
UTSW |
18 |
53,701,373 (GRCm39) |
missense |
probably damaging |
0.99 |
R9132:Prdm6
|
UTSW |
18 |
53,598,019 (GRCm39) |
missense |
unknown |
|
R9159:Prdm6
|
UTSW |
18 |
53,598,019 (GRCm39) |
missense |
unknown |
|
|