Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap8 |
A |
G |
17: 32,535,429 (GRCm39) |
F195S |
possibly damaging |
Het |
Aldh3a1 |
G |
A |
11: 61,106,362 (GRCm39) |
A246T |
probably damaging |
Het |
Caskin1 |
T |
A |
17: 24,718,539 (GRCm39) |
N331K |
probably damaging |
Het |
Ceacam5 |
G |
A |
7: 17,491,562 (GRCm39) |
S644N |
possibly damaging |
Het |
Csmd3 |
A |
T |
15: 47,710,648 (GRCm39) |
D1646E |
probably damaging |
Het |
Cyp4a12a |
A |
C |
4: 115,184,471 (GRCm39) |
K282T |
probably benign |
Het |
Dtnb |
C |
T |
12: 3,641,962 (GRCm39) |
R42* |
probably null |
Het |
Dyrk3 |
A |
G |
1: 131,057,219 (GRCm39) |
I318T |
probably damaging |
Het |
Fhip2b |
G |
A |
14: 70,824,025 (GRCm39) |
T535M |
probably damaging |
Het |
Gm11110 |
T |
C |
17: 57,410,435 (GRCm39) |
|
probably benign |
Het |
Gm8674 |
T |
A |
13: 50,055,792 (GRCm39) |
|
noncoding transcript |
Het |
Igfn1 |
A |
G |
1: 135,926,379 (GRCm39) |
S24P |
probably benign |
Het |
Inpp4b |
A |
G |
8: 82,678,890 (GRCm39) |
M307V |
possibly damaging |
Het |
Ism2 |
T |
C |
12: 87,333,871 (GRCm39) |
N58S |
probably benign |
Het |
Kmt2a |
A |
C |
9: 44,731,394 (GRCm39) |
|
probably benign |
Het |
Limk1 |
A |
G |
5: 134,701,523 (GRCm39) |
|
probably null |
Het |
Lrrc14 |
T |
A |
15: 76,597,318 (GRCm39) |
|
probably null |
Het |
Mapt |
C |
T |
11: 104,189,548 (GRCm39) |
R189* |
probably null |
Het |
Meltf |
C |
T |
16: 31,715,343 (GRCm39) |
R679* |
probably null |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Mug2 |
T |
C |
6: 122,024,465 (GRCm39) |
|
probably benign |
Het |
Myo15a |
G |
A |
11: 60,401,126 (GRCm39) |
|
probably null |
Het |
Nup98 |
T |
C |
7: 101,834,084 (GRCm39) |
T293A |
probably benign |
Het |
Nwd2 |
A |
T |
5: 63,957,504 (GRCm39) |
Y278F |
probably damaging |
Het |
Or12d12 |
T |
A |
17: 37,610,761 (GRCm39) |
D184V |
probably benign |
Het |
Phactr4 |
A |
C |
4: 132,097,058 (GRCm39) |
D496E |
probably benign |
Het |
Pramel6 |
T |
A |
2: 87,341,140 (GRCm39) |
|
probably null |
Het |
Ptprq |
C |
T |
10: 107,418,337 (GRCm39) |
A1680T |
probably damaging |
Het |
Retnlb |
T |
A |
16: 48,639,008 (GRCm39) |
C70S |
probably damaging |
Het |
Ros1 |
C |
A |
10: 52,004,512 (GRCm39) |
|
probably null |
Het |
Sez6l |
T |
C |
5: 112,574,615 (GRCm39) |
D875G |
probably damaging |
Het |
Slc18b1 |
T |
G |
10: 23,698,874 (GRCm39) |
M348R |
probably damaging |
Het |
Slc36a3 |
G |
T |
11: 55,033,607 (GRCm39) |
T137K |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,650,327 (GRCm39) |
N865D |
probably damaging |
Het |
Spg11 |
C |
T |
2: 121,901,534 (GRCm39) |
V1469I |
probably benign |
Het |
Unc13c |
G |
T |
9: 73,837,935 (GRCm39) |
A972D |
possibly damaging |
Het |
Vwa3a |
T |
C |
7: 120,398,334 (GRCm39) |
L945P |
probably damaging |
Het |
|
Other mutations in Sp9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03129:Sp9
|
APN |
2 |
73,103,865 (GRCm39) |
missense |
probably benign |
0.00 |
R0604:Sp9
|
UTSW |
2 |
73,103,982 (GRCm39) |
missense |
probably benign |
0.00 |
R0718:Sp9
|
UTSW |
2 |
73,104,171 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3747:Sp9
|
UTSW |
2 |
73,104,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R4335:Sp9
|
UTSW |
2 |
73,104,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Sp9
|
UTSW |
2 |
73,103,962 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4875:Sp9
|
UTSW |
2 |
73,103,962 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5341:Sp9
|
UTSW |
2 |
73,104,858 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5389:Sp9
|
UTSW |
2 |
73,104,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R5891:Sp9
|
UTSW |
2 |
73,104,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R6938:Sp9
|
UTSW |
2 |
73,103,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R7092:Sp9
|
UTSW |
2 |
73,104,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R7699:Sp9
|
UTSW |
2 |
73,103,724 (GRCm39) |
missense |
probably damaging |
0.98 |
R8336:Sp9
|
UTSW |
2 |
73,104,796 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8809:Sp9
|
UTSW |
2 |
73,104,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R8900:Sp9
|
UTSW |
2 |
73,103,863 (GRCm39) |
missense |
probably benign |
0.03 |
R9057:Sp9
|
UTSW |
2 |
73,103,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R9225:Sp9
|
UTSW |
2 |
73,103,839 (GRCm39) |
nonsense |
probably null |
|
R9335:Sp9
|
UTSW |
2 |
73,104,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R9462:Sp9
|
UTSW |
2 |
73,104,243 (GRCm39) |
missense |
probably benign |
0.23 |
Z1088:Sp9
|
UTSW |
2 |
73,103,574 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Sp9
|
UTSW |
2 |
73,103,800 (GRCm39) |
missense |
probably damaging |
0.98 |
|