Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449I24Rik |
T |
C |
5: 146,439,662 (GRCm39) |
I81T |
probably benign |
Het |
Akr1c19 |
G |
A |
13: 4,286,223 (GRCm39) |
V74M |
probably damaging |
Het |
Alb |
C |
A |
5: 90,620,507 (GRCm39) |
T539K |
probably benign |
Het |
B4galnt2 |
G |
A |
11: 95,760,223 (GRCm39) |
T268I |
possibly damaging |
Het |
Bcl7b |
G |
A |
5: 135,205,986 (GRCm39) |
E58K |
possibly damaging |
Het |
Calr3 |
C |
T |
8: 73,178,487 (GRCm39) |
S372N |
unknown |
Het |
Cdcp3 |
T |
A |
7: 130,844,871 (GRCm39) |
V588E |
probably damaging |
Het |
Cdh20 |
A |
T |
1: 104,875,047 (GRCm39) |
|
probably null |
Het |
Cdh20 |
A |
C |
1: 109,976,677 (GRCm39) |
E114A |
probably benign |
Het |
Cep70 |
A |
G |
9: 99,144,686 (GRCm39) |
R74G |
possibly damaging |
Het |
Chrna6 |
A |
G |
8: 27,897,109 (GRCm39) |
F256S |
probably damaging |
Het |
Cic |
A |
G |
7: 24,984,551 (GRCm39) |
T996A |
probably benign |
Het |
Clstn2 |
A |
G |
9: 97,351,817 (GRCm39) |
V536A |
possibly damaging |
Het |
Csmd1 |
A |
T |
8: 16,441,820 (GRCm39) |
M348K |
probably benign |
Het |
Dnah11 |
A |
C |
12: 118,004,744 (GRCm39) |
D2192E |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,352,646 (GRCm39) |
I2600V |
probably benign |
Het |
Dock3 |
A |
C |
9: 106,785,700 (GRCm39) |
S185A |
probably benign |
Het |
Dock4 |
A |
T |
12: 40,780,083 (GRCm39) |
D628V |
possibly damaging |
Het |
Dzank1 |
A |
T |
2: 144,333,718 (GRCm39) |
S371T |
probably benign |
Het |
Fam83b |
A |
T |
9: 76,399,737 (GRCm39) |
N455K |
possibly damaging |
Het |
Fcrlb |
T |
C |
1: 170,736,365 (GRCm39) |
Y137C |
probably damaging |
Het |
Gtf2i |
G |
A |
5: 134,295,471 (GRCm39) |
T327M |
possibly damaging |
Het |
Hspa5 |
T |
A |
2: 34,665,941 (GRCm39) |
M595K |
probably benign |
Het |
Htt |
C |
T |
5: 34,981,252 (GRCm39) |
A875V |
probably benign |
Het |
Hvcn1 |
G |
A |
5: 122,376,701 (GRCm39) |
|
probably null |
Het |
Igsf10 |
A |
G |
3: 59,238,145 (GRCm39) |
S679P |
probably damaging |
Het |
Itsn2 |
A |
G |
12: 4,751,265 (GRCm39) |
H1285R |
probably benign |
Het |
Kcnq4 |
T |
C |
4: 120,559,632 (GRCm39) |
T523A |
probably benign |
Het |
Kif6 |
T |
A |
17: 50,139,214 (GRCm39) |
I562N |
probably benign |
Het |
Klhl9 |
C |
A |
4: 88,638,575 (GRCm39) |
W555C |
probably damaging |
Het |
Krt78 |
T |
C |
15: 101,856,624 (GRCm39) |
T423A |
probably benign |
Het |
Mapk10 |
C |
T |
5: 103,111,362 (GRCm39) |
V391I |
probably benign |
Het |
Noa1 |
T |
C |
5: 77,445,044 (GRCm39) |
M592V |
probably benign |
Het |
Npy5r |
A |
G |
8: 67,133,968 (GRCm39) |
M275T |
possibly damaging |
Het |
Nuak2 |
T |
A |
1: 132,259,695 (GRCm39) |
V499E |
probably benign |
Het |
Or4x6 |
A |
T |
2: 89,949,185 (GRCm39) |
C252* |
probably null |
Het |
Or6c213 |
T |
C |
10: 129,574,559 (GRCm39) |
I76V |
probably benign |
Het |
Otogl |
T |
C |
10: 107,612,970 (GRCm39) |
E2052G |
probably benign |
Het |
Pard3b |
T |
A |
1: 62,198,670 (GRCm39) |
C253S |
possibly damaging |
Het |
Pclo |
T |
C |
5: 14,727,228 (GRCm39) |
S2029P |
unknown |
Het |
Plekhg3 |
A |
G |
12: 76,612,343 (GRCm39) |
I401M |
probably damaging |
Het |
Polg |
A |
T |
7: 79,100,392 (GRCm39) |
C1140S |
probably benign |
Het |
Prl7c1 |
A |
T |
13: 27,962,817 (GRCm39) |
L62H |
probably damaging |
Het |
Psmf1 |
T |
A |
2: 151,576,163 (GRCm39) |
E115V |
probably benign |
Het |
Ptpn9 |
A |
T |
9: 56,964,010 (GRCm39) |
N381I |
possibly damaging |
Het |
Pzp |
A |
G |
6: 128,465,979 (GRCm39) |
S1234P |
probably benign |
Het |
Qrich1 |
A |
G |
9: 108,436,485 (GRCm39) |
T728A |
possibly damaging |
Het |
Ralgps2 |
C |
A |
1: 156,656,636 (GRCm39) |
A323S |
probably benign |
Het |
Rimbp3 |
T |
C |
16: 17,028,910 (GRCm39) |
V778A |
possibly damaging |
Het |
Scn1a |
A |
T |
2: 66,116,349 (GRCm39) |
L430* |
probably null |
Het |
Sema7a |
A |
T |
9: 57,862,363 (GRCm39) |
I189F |
probably damaging |
Het |
Slc22a8 |
T |
C |
19: 8,571,386 (GRCm39) |
I39T |
probably benign |
Het |
Stap2 |
T |
C |
17: 56,309,023 (GRCm39) |
T115A |
probably benign |
Het |
Stmn4 |
A |
G |
14: 66,595,388 (GRCm39) |
I138V |
probably benign |
Het |
Suds3 |
C |
T |
5: 117,236,335 (GRCm39) |
|
probably null |
Het |
Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
Tet1 |
A |
C |
10: 62,714,825 (GRCm39) |
D323E |
probably benign |
Het |
Tia1 |
A |
G |
6: 86,401,347 (GRCm39) |
D140G |
probably damaging |
Het |
Trio |
C |
T |
15: 27,852,010 (GRCm39) |
R827H |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,625,397 (GRCm39) |
|
probably null |
Het |
Unc80 |
T |
C |
1: 66,549,866 (GRCm39) |
V708A |
probably benign |
Het |
Vmn1r194 |
A |
T |
13: 22,428,772 (GRCm39) |
T130S |
probably benign |
Het |
Wfikkn2 |
A |
G |
11: 94,129,755 (GRCm39) |
C129R |
probably damaging |
Het |
Zkscan5 |
A |
C |
5: 145,157,676 (GRCm39) |
H726P |
probably damaging |
Het |
|
Other mutations in Acnat2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00655:Acnat2
|
APN |
4 |
49,383,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01321:Acnat2
|
APN |
4 |
49,380,269 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01891:Acnat2
|
APN |
4 |
49,383,395 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01993:Acnat2
|
APN |
4 |
49,380,131 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02517:Acnat2
|
APN |
4 |
49,380,647 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02517:Acnat2
|
APN |
4 |
49,380,639 (GRCm39) |
nonsense |
probably null |
|
IGL03249:Acnat2
|
APN |
4 |
49,381,787 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4494001:Acnat2
|
UTSW |
4 |
49,383,133 (GRCm39) |
missense |
probably benign |
0.16 |
R0050:Acnat2
|
UTSW |
4 |
49,380,586 (GRCm39) |
missense |
probably benign |
0.03 |
R0462:Acnat2
|
UTSW |
4 |
49,383,084 (GRCm39) |
critical splice donor site |
probably null |
|
R0482:Acnat2
|
UTSW |
4 |
49,383,534 (GRCm39) |
missense |
probably benign |
0.09 |
R0590:Acnat2
|
UTSW |
4 |
49,383,273 (GRCm39) |
missense |
probably benign |
0.00 |
R0616:Acnat2
|
UTSW |
4 |
49,380,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R1099:Acnat2
|
UTSW |
4 |
49,380,484 (GRCm39) |
missense |
probably benign |
0.01 |
R1678:Acnat2
|
UTSW |
4 |
49,380,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R1710:Acnat2
|
UTSW |
4 |
49,380,587 (GRCm39) |
missense |
probably benign |
0.16 |
R2190:Acnat2
|
UTSW |
4 |
49,383,551 (GRCm39) |
start codon destroyed |
probably benign |
|
R4863:Acnat2
|
UTSW |
4 |
49,380,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R5031:Acnat2
|
UTSW |
4 |
49,380,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R5194:Acnat2
|
UTSW |
4 |
49,380,452 (GRCm39) |
missense |
probably benign |
|
R5936:Acnat2
|
UTSW |
4 |
49,383,362 (GRCm39) |
missense |
probably benign |
0.00 |
R6451:Acnat2
|
UTSW |
4 |
49,380,262 (GRCm39) |
missense |
probably benign |
0.00 |
R6526:Acnat2
|
UTSW |
4 |
49,383,497 (GRCm39) |
missense |
probably benign |
0.00 |
R6759:Acnat2
|
UTSW |
4 |
49,380,254 (GRCm39) |
missense |
probably benign |
0.01 |
R7180:Acnat2
|
UTSW |
4 |
49,381,803 (GRCm39) |
nonsense |
probably null |
|
R7356:Acnat2
|
UTSW |
4 |
49,383,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R9626:Acnat2
|
UTSW |
4 |
49,380,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|