Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
T |
9: 46,215,593 (GRCm39) |
F318I |
probably damaging |
Het |
Bfsp2 |
T |
C |
9: 103,327,074 (GRCm39) |
K221R |
probably benign |
Het |
Cacna1b |
A |
C |
2: 24,569,485 (GRCm39) |
M813R |
probably benign |
Het |
Chaf1a |
T |
C |
17: 56,372,226 (GRCm39) |
L798P |
probably damaging |
Het |
Chd8 |
G |
A |
14: 52,474,428 (GRCm39) |
T201I |
probably benign |
Het |
Col23a1 |
T |
C |
11: 51,464,861 (GRCm39) |
S436P |
probably benign |
Het |
Cubn |
T |
C |
2: 13,340,978 (GRCm39) |
I2248V |
probably benign |
Het |
Cyp4f39 |
A |
G |
17: 32,710,163 (GRCm39) |
I440M |
probably benign |
Het |
Dhcr24 |
G |
T |
4: 106,429,499 (GRCm39) |
E191* |
probably null |
Het |
Dlg5 |
T |
C |
14: 24,220,612 (GRCm39) |
D522G |
probably damaging |
Het |
Dnaja4 |
A |
T |
9: 54,616,506 (GRCm39) |
M170L |
probably benign |
Het |
Dop1b |
T |
C |
16: 93,567,895 (GRCm39) |
S1441P |
possibly damaging |
Het |
Efcab3 |
C |
T |
11: 104,642,737 (GRCm39) |
T1120I |
possibly damaging |
Het |
Egr2 |
T |
A |
10: 67,376,702 (GRCm39) |
S383T |
probably damaging |
Het |
Elovl1 |
A |
G |
4: 118,288,303 (GRCm39) |
D94G |
probably damaging |
Het |
Erbb4 |
A |
G |
1: 68,385,788 (GRCm39) |
V267A |
probably damaging |
Het |
Esp38 |
T |
A |
17: 40,264,275 (GRCm39) |
I11N |
probably damaging |
Het |
Esrrb |
T |
C |
12: 86,468,740 (GRCm39) |
|
probably null |
Het |
Fbxo24 |
A |
T |
5: 137,611,327 (GRCm39) |
S488T |
probably damaging |
Het |
Fgfr1 |
T |
G |
8: 26,060,882 (GRCm39) |
V618G |
probably damaging |
Het |
Gak |
C |
T |
5: 108,754,743 (GRCm39) |
|
probably null |
Het |
Gpr61 |
A |
T |
3: 108,058,077 (GRCm39) |
C195S |
probably damaging |
Het |
Greb1l |
A |
C |
18: 10,555,011 (GRCm39) |
N1686H |
probably damaging |
Het |
Hapln4 |
T |
C |
8: 70,540,788 (GRCm39) |
F274L |
probably benign |
Het |
Hoxc10 |
A |
T |
15: 102,875,912 (GRCm39) |
Q207L |
probably benign |
Het |
Hspa12a |
A |
G |
19: 58,787,914 (GRCm39) |
V636A |
probably benign |
Het |
Il22ra2 |
T |
A |
10: 19,508,618 (GRCm39) |
F215L |
probably benign |
Het |
Il36b |
A |
G |
2: 24,044,672 (GRCm39) |
N24S |
probably benign |
Het |
Kank1 |
G |
A |
19: 25,389,117 (GRCm39) |
G930D |
probably benign |
Het |
Kif13a |
T |
C |
13: 46,905,945 (GRCm39) |
D666G |
possibly damaging |
Het |
Krt86 |
A |
T |
15: 101,371,639 (GRCm39) |
I70F |
probably benign |
Het |
Lgi4 |
A |
T |
7: 30,762,548 (GRCm39) |
I112F |
probably damaging |
Het |
Lrrc8c |
T |
G |
5: 105,754,558 (GRCm39) |
I111S |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,862,753 (GRCm39) |
N600S |
probably damaging |
Het |
Mbd3l2 |
A |
T |
9: 18,356,254 (GRCm39) |
D193V |
probably damaging |
Het |
Mroh5 |
T |
A |
15: 73,661,940 (GRCm39) |
D417V |
probably damaging |
Het |
Ms4a18 |
A |
T |
19: 10,974,695 (GRCm39) |
V332D |
possibly damaging |
Het |
Mtarc1 |
G |
A |
1: 184,527,632 (GRCm39) |
T276I |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,581,599 (GRCm39) |
I2488N |
unknown |
Het |
Myrf |
C |
G |
19: 10,193,831 (GRCm39) |
A532P |
probably damaging |
Het |
Nav3 |
T |
C |
10: 109,688,996 (GRCm39) |
N427S |
probably benign |
Het |
Neb |
T |
C |
2: 52,102,600 (GRCm39) |
S4315G |
probably damaging |
Het |
Nyap2 |
A |
G |
1: 81,218,983 (GRCm39) |
D335G |
probably damaging |
Het |
Olfm4 |
T |
C |
14: 80,251,755 (GRCm39) |
L225P |
probably benign |
Het |
Or10z1 |
A |
T |
1: 174,078,302 (GRCm39) |
|
probably null |
Het |
Or4c104 |
T |
A |
2: 88,586,437 (GRCm39) |
N194I |
probably damaging |
Het |
Or51ac3 |
A |
T |
7: 103,213,961 (GRCm39) |
I175K |
possibly damaging |
Het |
Or8s2 |
T |
C |
15: 98,276,145 (GRCm39) |
N282S |
probably damaging |
Het |
Pcdhac2 |
T |
G |
18: 37,279,139 (GRCm39) |
Y706* |
probably null |
Het |
Pgbd1 |
A |
G |
13: 21,607,190 (GRCm39) |
S335P |
probably damaging |
Het |
Pkhd1l1 |
A |
C |
15: 44,393,214 (GRCm39) |
I1850L |
possibly damaging |
Het |
Pogz |
T |
C |
3: 94,778,318 (GRCm39) |
V304A |
possibly damaging |
Het |
Rap1a |
T |
C |
3: 105,646,856 (GRCm39) |
I100V |
probably damaging |
Het |
Slc4a4 |
A |
T |
5: 89,194,123 (GRCm39) |
K201M |
probably damaging |
Het |
Slc6a1 |
T |
C |
6: 114,281,022 (GRCm39) |
F8S |
possibly damaging |
Het |
St18 |
T |
G |
1: 6,880,839 (GRCm39) |
M444R |
possibly damaging |
Het |
Tgm1 |
A |
G |
14: 55,947,000 (GRCm39) |
V336A |
probably damaging |
Het |
Tle6 |
G |
T |
10: 81,429,868 (GRCm39) |
T400K |
probably damaging |
Het |
Tmem181a |
T |
C |
17: 6,348,481 (GRCm39) |
W328R |
probably damaging |
Het |
Trim7 |
T |
C |
11: 48,729,721 (GRCm39) |
F193L |
probably benign |
Het |
Txndc16 |
A |
T |
14: 45,410,046 (GRCm39) |
M178K |
probably damaging |
Het |
Unc80 |
C |
T |
1: 66,560,740 (GRCm39) |
H823Y |
possibly damaging |
Het |
Vmn1r74 |
A |
G |
7: 11,581,243 (GRCm39) |
Y181C |
probably damaging |
Het |
Vmn2r56 |
T |
A |
7: 12,446,890 (GRCm39) |
K421* |
probably null |
Het |
Vwa7 |
T |
G |
17: 35,242,406 (GRCm39) |
S503R |
probably benign |
Het |
Washc5 |
G |
A |
15: 59,221,991 (GRCm39) |
T135M |
probably damaging |
Het |
Wdr6 |
T |
C |
9: 108,451,322 (GRCm39) |
I854V |
probably benign |
Het |
Zfp507 |
A |
G |
7: 35,493,148 (GRCm39) |
C632R |
probably damaging |
Het |
|
Other mutations in Syna |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Syna
|
APN |
5 |
134,588,571 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01128:Syna
|
APN |
5 |
134,588,334 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03183:Syna
|
APN |
5 |
134,587,144 (GRCm39) |
missense |
probably benign |
0.03 |
R0051:Syna
|
UTSW |
5 |
134,588,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Syna
|
UTSW |
5 |
134,588,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R0137:Syna
|
UTSW |
5 |
134,588,314 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0920:Syna
|
UTSW |
5 |
134,587,956 (GRCm39) |
missense |
probably benign |
0.12 |
R1525:Syna
|
UTSW |
5 |
134,588,112 (GRCm39) |
missense |
probably benign |
|
R1801:Syna
|
UTSW |
5 |
134,588,943 (GRCm39) |
missense |
probably benign |
0.02 |
R1813:Syna
|
UTSW |
5 |
134,588,006 (GRCm39) |
missense |
probably benign |
0.06 |
R1866:Syna
|
UTSW |
5 |
134,588,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Syna
|
UTSW |
5 |
134,588,106 (GRCm39) |
missense |
probably benign |
|
R1896:Syna
|
UTSW |
5 |
134,588,006 (GRCm39) |
missense |
probably benign |
0.06 |
R3896:Syna
|
UTSW |
5 |
134,587,165 (GRCm39) |
nonsense |
probably null |
|
R4674:Syna
|
UTSW |
5 |
134,587,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R4730:Syna
|
UTSW |
5 |
134,587,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R5124:Syna
|
UTSW |
5 |
134,588,424 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5482:Syna
|
UTSW |
5 |
134,588,028 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6130:Syna
|
UTSW |
5 |
134,587,122 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6196:Syna
|
UTSW |
5 |
134,588,466 (GRCm39) |
missense |
probably benign |
0.14 |
R6243:Syna
|
UTSW |
5 |
134,588,968 (GRCm39) |
start gained |
probably benign |
|
R6945:Syna
|
UTSW |
5 |
134,587,815 (GRCm39) |
missense |
probably damaging |
0.97 |
R7999:Syna
|
UTSW |
5 |
134,588,046 (GRCm39) |
missense |
probably benign |
|
R8320:Syna
|
UTSW |
5 |
134,588,574 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8783:Syna
|
UTSW |
5 |
134,588,723 (GRCm39) |
missense |
probably benign |
0.01 |
R8784:Syna
|
UTSW |
5 |
134,588,723 (GRCm39) |
missense |
probably benign |
0.01 |
R8785:Syna
|
UTSW |
5 |
134,588,723 (GRCm39) |
missense |
probably benign |
0.01 |
R8786:Syna
|
UTSW |
5 |
134,588,723 (GRCm39) |
missense |
probably benign |
0.01 |
R8787:Syna
|
UTSW |
5 |
134,588,723 (GRCm39) |
missense |
probably benign |
0.01 |
X0022:Syna
|
UTSW |
5 |
134,588,427 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Syna
|
UTSW |
5 |
134,587,383 (GRCm39) |
missense |
probably benign |
0.01 |
|