Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
9530002B09Rik |
T |
A |
4: 122,583,115 (GRCm39) |
|
probably benign |
Het |
Acadl |
C |
T |
1: 66,880,905 (GRCm39) |
|
probably null |
Het |
Afap1l1 |
A |
T |
18: 61,872,193 (GRCm39) |
|
probably null |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ano5 |
T |
G |
7: 51,235,134 (GRCm39) |
L639R |
probably damaging |
Het |
Arhgap26 |
T |
C |
18: 39,439,781 (GRCm39) |
S71P |
probably damaging |
Het |
B3gnt2 |
A |
G |
11: 22,786,735 (GRCm39) |
L151P |
probably damaging |
Het |
Bach1 |
A |
T |
16: 87,526,513 (GRCm39) |
K658N |
probably damaging |
Het |
Bdnf |
C |
A |
2: 109,554,247 (GRCm39) |
T207K |
probably damaging |
Het |
Bod1l |
G |
T |
5: 41,962,499 (GRCm39) |
T2746K |
probably damaging |
Het |
Brwd1 |
A |
G |
16: 95,847,665 (GRCm39) |
S652P |
probably benign |
Het |
Ccnt1 |
A |
T |
15: 98,449,823 (GRCm39) |
H156Q |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,735,225 (GRCm39) |
I1021N |
possibly damaging |
Het |
Cnep1r1 |
G |
T |
8: 88,845,445 (GRCm39) |
|
probably benign |
Het |
Cntn6 |
C |
T |
6: 104,838,783 (GRCm39) |
R946* |
probably null |
Het |
Dnaaf3 |
T |
C |
7: 4,526,798 (GRCm39) |
I426M |
possibly damaging |
Het |
Dnajc13 |
A |
T |
9: 104,098,640 (GRCm39) |
I471N |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Emx2 |
A |
G |
19: 59,450,130 (GRCm39) |
N149S |
probably benign |
Het |
Fbln7 |
G |
T |
2: 128,719,386 (GRCm39) |
R61L |
probably damaging |
Het |
Fgb |
C |
A |
3: 82,956,996 (GRCm39) |
D25Y |
probably benign |
Het |
Filip1 |
A |
G |
9: 79,727,498 (GRCm39) |
S374P |
probably damaging |
Het |
Fry |
T |
A |
5: 150,293,584 (GRCm39) |
|
probably benign |
Het |
Gm12695 |
T |
C |
4: 96,657,963 (GRCm39) |
T69A |
probably benign |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Hdlbp |
A |
G |
1: 93,349,602 (GRCm39) |
|
probably benign |
Het |
Hunk |
G |
A |
16: 90,278,133 (GRCm39) |
|
probably null |
Het |
Ifnb1 |
T |
A |
4: 88,440,996 (GRCm39) |
I6F |
possibly damaging |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,753,251 (GRCm39) |
V720A |
probably benign |
Het |
Invs |
T |
A |
4: 48,396,287 (GRCm39) |
L320Q |
probably damaging |
Het |
Jpt2 |
G |
A |
17: 25,167,713 (GRCm39) |
Q79* |
probably null |
Het |
Lingo2 |
A |
G |
4: 35,709,179 (GRCm39) |
L267P |
probably benign |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Meiob |
G |
T |
17: 25,037,290 (GRCm39) |
R56L |
probably damaging |
Het |
Mindy3 |
A |
T |
2: 12,424,060 (GRCm39) |
S2T |
probably damaging |
Het |
Mrm3 |
A |
T |
11: 76,141,147 (GRCm39) |
D385V |
probably damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Nav1 |
C |
T |
1: 135,376,742 (GRCm39) |
R1694Q |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,875,567 (GRCm39) |
V1701A |
probably damaging |
Het |
Nipal4 |
T |
G |
11: 46,047,622 (GRCm39) |
D104A |
probably damaging |
Het |
Npas4 |
A |
G |
19: 5,037,442 (GRCm39) |
V284A |
probably damaging |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Obscn |
G |
A |
11: 59,026,558 (GRCm39) |
A215V |
possibly damaging |
Het |
Or4c113 |
A |
G |
2: 88,885,243 (GRCm39) |
Y176H |
probably damaging |
Het |
Or8b12i |
G |
T |
9: 20,082,850 (GRCm39) |
Q6K |
probably benign |
Het |
Or8g24 |
T |
C |
9: 38,989,510 (GRCm39) |
Y177C |
probably damaging |
Het |
Pgs1 |
G |
A |
11: 117,905,396 (GRCm39) |
|
probably benign |
Het |
Phc2 |
T |
C |
4: 128,640,929 (GRCm39) |
F672S |
probably damaging |
Het |
Phldb2 |
A |
T |
16: 45,591,121 (GRCm39) |
L970Q |
probably damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Ppip5k1 |
A |
G |
2: 121,173,352 (GRCm39) |
|
probably benign |
Het |
Prune2 |
A |
G |
19: 17,098,042 (GRCm39) |
D1182G |
possibly damaging |
Het |
Psg25 |
G |
A |
7: 18,263,487 (GRCm39) |
T112I |
probably damaging |
Het |
Sec61g |
T |
C |
11: 16,458,124 (GRCm39) |
T24A |
probably benign |
Het |
Skint1 |
T |
A |
4: 111,882,730 (GRCm39) |
V258D |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,353,472 (GRCm39) |
|
probably null |
Het |
Sox2 |
C |
A |
3: 34,705,456 (GRCm39) |
Q298K |
possibly damaging |
Het |
Spatc1 |
T |
A |
15: 76,167,737 (GRCm39) |
|
probably null |
Het |
Szt2 |
T |
C |
4: 118,231,177 (GRCm39) |
M2529V |
unknown |
Het |
Thrap3 |
T |
C |
4: 126,069,189 (GRCm39) |
Y654C |
possibly damaging |
Het |
Tpp2 |
T |
G |
1: 44,017,598 (GRCm39) |
I734S |
possibly damaging |
Het |
Troap |
T |
C |
15: 98,980,344 (GRCm39) |
L508P |
probably benign |
Het |
Ttc28 |
C |
A |
5: 111,373,799 (GRCm39) |
F1078L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,544,717 (GRCm39) |
N32795S |
probably damaging |
Het |
Ubap2 |
C |
T |
4: 41,199,872 (GRCm39) |
A752T |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,240,100 (GRCm39) |
E95G |
probably benign |
Het |
Vmn1r55 |
A |
G |
7: 5,150,048 (GRCm39) |
V125A |
possibly damaging |
Het |
Vstm2a |
A |
T |
11: 16,211,483 (GRCm39) |
I98F |
probably benign |
Het |
Zdhhc13 |
T |
A |
7: 48,466,175 (GRCm39) |
V284D |
probably benign |
Het |
Zfp668 |
C |
A |
7: 127,466,203 (GRCm39) |
R327L |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
Het |
|
Other mutations in Acss1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Acss1
|
APN |
2 |
150,461,606 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01594:Acss1
|
APN |
2 |
150,463,450 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01781:Acss1
|
APN |
2 |
150,479,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02189:Acss1
|
APN |
2 |
150,471,788 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02735:Acss1
|
APN |
2 |
150,480,387 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Acss1
|
APN |
2 |
150,466,792 (GRCm39) |
splice site |
probably benign |
|
IGL03399:Acss1
|
APN |
2 |
150,479,798 (GRCm39) |
missense |
probably damaging |
1.00 |
Cutlass
|
UTSW |
2 |
150,510,051 (GRCm39) |
nonsense |
probably null |
|
oathkeeper
|
UTSW |
2 |
150,501,823 (GRCm39) |
missense |
possibly damaging |
0.58 |
oilseller
|
UTSW |
2 |
150,509,801 (GRCm39) |
splice site |
probably null |
|
scimitar
|
UTSW |
2 |
150,470,412 (GRCm39) |
critical splice donor site |
probably null |
|
R0058:Acss1
|
UTSW |
2 |
150,470,459 (GRCm39) |
missense |
probably damaging |
0.97 |
R0063:Acss1
|
UTSW |
2 |
150,469,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Acss1
|
UTSW |
2 |
150,469,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Acss1
|
UTSW |
2 |
150,484,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R1651:Acss1
|
UTSW |
2 |
150,480,357 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4414:Acss1
|
UTSW |
2 |
150,501,823 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4559:Acss1
|
UTSW |
2 |
150,480,405 (GRCm39) |
missense |
probably benign |
0.19 |
R4893:Acss1
|
UTSW |
2 |
150,471,786 (GRCm39) |
missense |
probably damaging |
0.97 |
R6408:Acss1
|
UTSW |
2 |
150,470,412 (GRCm39) |
critical splice donor site |
probably null |
|
R6459:Acss1
|
UTSW |
2 |
150,509,840 (GRCm39) |
missense |
probably damaging |
0.97 |
R7593:Acss1
|
UTSW |
2 |
150,461,688 (GRCm39) |
nonsense |
probably null |
|
R7598:Acss1
|
UTSW |
2 |
150,480,370 (GRCm39) |
missense |
probably benign |
0.12 |
R8084:Acss1
|
UTSW |
2 |
150,484,701 (GRCm39) |
missense |
probably damaging |
0.99 |
R8087:Acss1
|
UTSW |
2 |
150,484,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Acss1
|
UTSW |
2 |
150,509,801 (GRCm39) |
splice site |
probably null |
|
R8213:Acss1
|
UTSW |
2 |
150,461,630 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8972:Acss1
|
UTSW |
2 |
150,484,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R9064:Acss1
|
UTSW |
2 |
150,463,510 (GRCm39) |
missense |
probably benign |
0.00 |
R9708:Acss1
|
UTSW |
2 |
150,471,752 (GRCm39) |
missense |
probably damaging |
1.00 |
|