Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
G |
T |
5: 64,056,182 (GRCm39) |
|
probably benign |
Het |
2510039O18Rik |
T |
C |
4: 148,026,022 (GRCm39) |
S181P |
probably benign |
Het |
4930522L14Rik |
A |
T |
5: 109,884,440 (GRCm39) |
C473S |
possibly damaging |
Het |
4930523C07Rik |
A |
T |
1: 159,872,149 (GRCm39) |
|
noncoding transcript |
Het |
Aak1 |
A |
G |
6: 86,963,300 (GRCm39) |
K910R |
unknown |
Het |
Abca2 |
A |
G |
2: 25,332,864 (GRCm39) |
D1521G |
probably benign |
Het |
Adamts20 |
C |
A |
15: 94,241,924 (GRCm39) |
D695Y |
probably damaging |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
Bltp3a |
A |
G |
17: 28,104,905 (GRCm39) |
N533S |
probably damaging |
Het |
Bspry |
T |
A |
4: 62,400,904 (GRCm39) |
I132N |
possibly damaging |
Het |
Cfap300 |
A |
G |
9: 8,027,178 (GRCm39) |
V120A |
probably damaging |
Het |
Cfh |
T |
C |
1: 140,064,004 (GRCm39) |
Y424C |
probably damaging |
Het |
Chd2 |
T |
C |
7: 73,085,709 (GRCm39) |
R1642G |
possibly damaging |
Het |
Chrm2 |
A |
G |
6: 36,501,097 (GRCm39) |
D318G |
probably benign |
Het |
Chrna4 |
A |
G |
2: 180,670,413 (GRCm39) |
S448P |
probably damaging |
Het |
Cldn8 |
A |
C |
16: 88,359,619 (GRCm39) |
M102R |
probably damaging |
Het |
Dock8 |
T |
C |
19: 25,042,754 (GRCm39) |
V112A |
probably benign |
Het |
Fbxo42 |
C |
A |
4: 140,927,861 (GRCm39) |
R714S |
probably damaging |
Het |
Fmo1 |
G |
A |
1: 162,661,281 (GRCm39) |
A334V |
possibly damaging |
Het |
Gpr68 |
A |
T |
12: 100,865,650 (GRCm39) |
|
probably benign |
Het |
Gramd4 |
A |
G |
15: 86,014,361 (GRCm39) |
K345R |
probably damaging |
Het |
Gtpbp1 |
T |
G |
15: 79,600,398 (GRCm39) |
S444A |
probably damaging |
Het |
Kat2b-ps |
A |
T |
5: 93,540,443 (GRCm39) |
|
noncoding transcript |
Het |
Klhl25 |
T |
A |
7: 75,515,162 (GRCm39) |
F23I |
probably damaging |
Het |
Lamc1 |
A |
G |
1: 153,097,274 (GRCm39) |
I1590T |
probably damaging |
Het |
Lhfpl4 |
A |
G |
6: 113,170,805 (GRCm39) |
I127T |
possibly damaging |
Het |
Lrrc71 |
A |
G |
3: 87,650,143 (GRCm39) |
S286P |
possibly damaging |
Het |
Man1c1 |
A |
T |
4: 134,430,329 (GRCm39) |
V151D |
probably damaging |
Het |
Mipol1 |
G |
A |
12: 57,350,310 (GRCm39) |
R36Q |
possibly damaging |
Het |
Nuggc |
T |
A |
14: 65,848,659 (GRCm39) |
W187R |
probably benign |
Het |
Or4a71 |
A |
G |
2: 89,357,987 (GRCm39) |
Y256H |
probably damaging |
Het |
Pkhd1 |
G |
A |
1: 20,593,538 (GRCm39) |
T1525I |
probably damaging |
Het |
Pomp |
A |
G |
5: 147,812,289 (GRCm39) |
E125G |
probably damaging |
Het |
Ptar1 |
G |
T |
19: 23,671,695 (GRCm39) |
G33C |
probably damaging |
Het |
Ptpn3 |
A |
G |
4: 57,235,355 (GRCm39) |
S335P |
probably damaging |
Het |
Pus7 |
A |
G |
5: 23,951,487 (GRCm39) |
Y521H |
probably benign |
Het |
Shank1 |
C |
T |
7: 43,969,076 (GRCm39) |
R324* |
probably null |
Het |
Slc12a3 |
A |
T |
8: 95,069,713 (GRCm39) |
I541F |
probably damaging |
Het |
Slc12a9 |
G |
A |
5: 137,319,775 (GRCm39) |
P580L |
probably benign |
Het |
Spz1 |
A |
G |
13: 92,711,837 (GRCm39) |
L213P |
probably damaging |
Het |
Strn |
A |
G |
17: 79,043,891 (GRCm39) |
V9A |
probably damaging |
Het |
Sytl5 |
A |
T |
X: 9,826,262 (GRCm39) |
N412Y |
probably damaging |
Het |
Tert |
T |
A |
13: 73,775,594 (GRCm39) |
F115Y |
probably damaging |
Het |
Tmem67 |
T |
A |
4: 12,051,473 (GRCm39) |
N785I |
possibly damaging |
Het |
Trf |
T |
C |
9: 103,089,075 (GRCm39) |
N243S |
possibly damaging |
Het |
Ttc3 |
T |
C |
16: 94,211,817 (GRCm39) |
|
probably null |
Het |
Vmn2r22 |
T |
C |
6: 123,614,817 (GRCm39) |
T258A |
possibly damaging |
Het |
Vps13b |
A |
C |
15: 35,770,899 (GRCm39) |
Q2114P |
probably damaging |
Het |
Wdfy1 |
T |
A |
1: 79,691,583 (GRCm39) |
R275* |
probably null |
Het |
Wnt2b |
A |
G |
3: 104,860,256 (GRCm39) |
L217S |
probably damaging |
Het |
|
Other mutations in Ints12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00585:Ints12
|
APN |
3 |
132,806,570 (GRCm39) |
critical splice donor site |
probably null |
|
R0243:Ints12
|
UTSW |
3 |
132,814,806 (GRCm39) |
missense |
probably benign |
0.37 |
R0847:Ints12
|
UTSW |
3 |
132,814,603 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2118:Ints12
|
UTSW |
3 |
132,814,921 (GRCm39) |
missense |
probably damaging |
0.98 |
R2323:Ints12
|
UTSW |
3 |
132,815,126 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2324:Ints12
|
UTSW |
3 |
132,815,126 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2384:Ints12
|
UTSW |
3 |
132,814,864 (GRCm39) |
splice site |
probably null |
|
R3055:Ints12
|
UTSW |
3 |
132,815,126 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3056:Ints12
|
UTSW |
3 |
132,815,126 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3919:Ints12
|
UTSW |
3 |
132,806,444 (GRCm39) |
missense |
probably benign |
|
R4594:Ints12
|
UTSW |
3 |
132,814,629 (GRCm39) |
missense |
probably benign |
0.00 |
R4598:Ints12
|
UTSW |
3 |
132,804,214 (GRCm39) |
missense |
probably benign |
|
R4599:Ints12
|
UTSW |
3 |
132,804,214 (GRCm39) |
missense |
probably benign |
|
R4702:Ints12
|
UTSW |
3 |
132,802,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R5083:Ints12
|
UTSW |
3 |
132,806,538 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5507:Ints12
|
UTSW |
3 |
132,814,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Ints12
|
UTSW |
3 |
132,804,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R6647:Ints12
|
UTSW |
3 |
132,802,639 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8245:Ints12
|
UTSW |
3 |
132,814,633 (GRCm39) |
missense |
probably benign |
|
R8887:Ints12
|
UTSW |
3 |
132,815,003 (GRCm39) |
missense |
probably damaging |
0.99 |
R9779:Ints12
|
UTSW |
3 |
132,812,752 (GRCm39) |
missense |
probably benign |
0.30 |
Z1176:Ints12
|
UTSW |
3 |
132,808,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|