Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adhfe1 |
A |
G |
1: 9,631,851 (GRCm39) |
|
probably benign |
Het |
Anln |
T |
C |
9: 22,286,340 (GRCm39) |
T322A |
possibly damaging |
Het |
Best3 |
A |
T |
10: 116,844,907 (GRCm39) |
Y354F |
probably benign |
Het |
Cd44 |
C |
T |
2: 102,661,699 (GRCm39) |
V509I |
possibly damaging |
Het |
Cdk5rap1 |
T |
C |
2: 154,184,315 (GRCm39) |
N529S |
probably damaging |
Het |
Cnst |
A |
G |
1: 179,450,378 (GRCm39) |
D614G |
possibly damaging |
Het |
Cpq |
T |
C |
15: 33,213,008 (GRCm39) |
I9T |
probably benign |
Het |
Cyp2j6 |
T |
C |
4: 96,419,936 (GRCm39) |
H265R |
probably damaging |
Het |
Dctn1 |
T |
A |
6: 83,168,621 (GRCm39) |
M458K |
probably damaging |
Het |
Disc1 |
A |
C |
8: 125,858,899 (GRCm39) |
I454L |
probably benign |
Het |
Dnaja4 |
A |
G |
9: 54,607,023 (GRCm39) |
E4G |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Eipr1 |
C |
A |
12: 28,878,855 (GRCm39) |
N136K |
probably benign |
Het |
Fut11 |
A |
G |
14: 20,746,229 (GRCm39) |
N357S |
probably damaging |
Het |
Gbp2b |
C |
T |
3: 142,304,015 (GRCm39) |
P37S |
probably damaging |
Het |
Ghr |
T |
G |
15: 3,349,622 (GRCm39) |
K519Q |
probably damaging |
Het |
Gipr |
C |
A |
7: 18,893,689 (GRCm39) |
C328F |
probably damaging |
Het |
Gm27013 |
A |
T |
6: 130,654,633 (GRCm39) |
N276K |
probably damaging |
Het |
Got2 |
C |
A |
8: 96,598,951 (GRCm39) |
K150N |
probably benign |
Het |
Gucy2c |
A |
G |
6: 136,744,033 (GRCm39) |
S189P |
possibly damaging |
Het |
H2-T5 |
C |
A |
17: 36,476,308 (GRCm39) |
G347* |
probably null |
Het |
Hells |
T |
C |
19: 38,932,189 (GRCm39) |
V153A |
probably benign |
Het |
Ighd |
G |
A |
12: 113,378,047 (GRCm39) |
|
probably benign |
Het |
Inhca |
C |
T |
9: 103,143,420 (GRCm39) |
V361M |
probably damaging |
Het |
Itga4 |
A |
C |
2: 79,145,973 (GRCm39) |
D725A |
possibly damaging |
Het |
Itgbl1 |
T |
A |
14: 124,204,151 (GRCm39) |
L414Q |
possibly damaging |
Het |
Kat2b-ps |
A |
G |
5: 93,539,585 (GRCm39) |
|
noncoding transcript |
Het |
Lrrc1 |
A |
T |
9: 77,364,740 (GRCm39) |
S192T |
probably benign |
Het |
Mc2r |
A |
T |
18: 68,541,274 (GRCm39) |
N6K |
probably benign |
Het |
Moxd2 |
A |
C |
6: 40,856,270 (GRCm39) |
L534W |
probably damaging |
Het |
Myh4 |
A |
T |
11: 67,146,235 (GRCm39) |
D1431V |
probably damaging |
Het |
Naa15 |
T |
A |
3: 51,364,706 (GRCm39) |
|
probably null |
Het |
Naa16 |
G |
A |
14: 79,614,855 (GRCm39) |
T215I |
possibly damaging |
Het |
Ntng1 |
A |
T |
3: 110,042,645 (GRCm39) |
Y60* |
probably null |
Het |
Or1e29 |
T |
C |
11: 73,668,084 (GRCm39) |
Y23C |
possibly damaging |
Het |
Or2g25 |
A |
T |
17: 37,970,612 (GRCm39) |
V204E |
probably damaging |
Het |
Pccb |
T |
C |
9: 100,867,296 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
C |
A |
12: 82,041,713 (GRCm39) |
P2115Q |
probably damaging |
Het |
Pfkfb3 |
G |
A |
2: 11,488,825 (GRCm39) |
T313I |
probably damaging |
Het |
Pld1 |
A |
G |
3: 28,178,731 (GRCm39) |
N875S |
probably damaging |
Het |
Rabgap1l |
C |
A |
1: 160,549,809 (GRCm39) |
V266L |
probably damaging |
Het |
Reep6 |
A |
G |
10: 80,171,009 (GRCm39) |
D295G |
probably damaging |
Het |
Sass6 |
T |
C |
3: 116,403,947 (GRCm39) |
L195P |
probably damaging |
Het |
Slc25a27 |
A |
G |
17: 43,977,821 (GRCm39) |
S25P |
probably damaging |
Het |
Smok2b |
T |
A |
17: 13,454,011 (GRCm39) |
M57K |
probably benign |
Het |
Sp110 |
C |
G |
1: 85,516,839 (GRCm39) |
E219D |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,465,405 (GRCm39) |
V71A |
possibly damaging |
Het |
Stab1 |
G |
A |
14: 30,881,261 (GRCm39) |
L590F |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,527,500 (GRCm39) |
Y1252* |
probably null |
Het |
Syde2 |
T |
A |
3: 145,712,881 (GRCm39) |
D1006E |
probably damaging |
Het |
Syde2 |
CAGTT |
CAGTTAGTT |
3: 145,707,163 (GRCm39) |
|
probably null |
Het |
Tmc5 |
G |
A |
7: 118,244,609 (GRCm39) |
A496T |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,566,704 (GRCm39) |
V28063A |
probably damaging |
Het |
Usp25 |
A |
C |
16: 76,874,007 (GRCm39) |
I528L |
probably benign |
Het |
Vmn1r58 |
C |
T |
7: 5,413,666 (GRCm39) |
S188N |
probably benign |
Het |
Wfikkn2 |
A |
T |
11: 94,129,173 (GRCm39) |
C323S |
probably damaging |
Het |
Zfy1 |
A |
C |
Y: 732,964 (GRCm39) |
S290A |
unknown |
Het |
|
Other mutations in Ptpn20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Ptpn20
|
APN |
14 |
33,344,576 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01510:Ptpn20
|
APN |
14 |
33,360,343 (GRCm39) |
splice site |
probably null |
|
R2057:Ptpn20
|
UTSW |
14 |
33,352,942 (GRCm39) |
missense |
probably damaging |
0.98 |
R2262:Ptpn20
|
UTSW |
14 |
33,334,268 (GRCm39) |
missense |
probably benign |
|
R3106:Ptpn20
|
UTSW |
14 |
33,334,253 (GRCm39) |
missense |
probably benign |
|
R3430:Ptpn20
|
UTSW |
14 |
33,336,485 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4645:Ptpn20
|
UTSW |
14 |
33,353,169 (GRCm39) |
missense |
probably benign |
|
R4928:Ptpn20
|
UTSW |
14 |
33,336,446 (GRCm39) |
missense |
probably benign |
0.00 |
R4962:Ptpn20
|
UTSW |
14 |
33,336,416 (GRCm39) |
missense |
probably benign |
0.02 |
R5163:Ptpn20
|
UTSW |
14 |
33,353,068 (GRCm39) |
missense |
probably benign |
0.07 |
R5275:Ptpn20
|
UTSW |
14 |
33,353,149 (GRCm39) |
missense |
probably benign |
0.00 |
R6325:Ptpn20
|
UTSW |
14 |
33,352,962 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6651:Ptpn20
|
UTSW |
14 |
33,354,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R6831:Ptpn20
|
UTSW |
14 |
33,354,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R6903:Ptpn20
|
UTSW |
14 |
33,336,461 (GRCm39) |
missense |
probably damaging |
0.98 |
R7034:Ptpn20
|
UTSW |
14 |
33,336,392 (GRCm39) |
makesense |
probably null |
|
R7036:Ptpn20
|
UTSW |
14 |
33,336,392 (GRCm39) |
makesense |
probably null |
|
R7265:Ptpn20
|
UTSW |
14 |
33,336,481 (GRCm39) |
missense |
probably benign |
0.05 |
R7654:Ptpn20
|
UTSW |
14 |
33,360,281 (GRCm39) |
missense |
probably benign |
0.18 |
R7735:Ptpn20
|
UTSW |
14 |
33,352,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R7761:Ptpn20
|
UTSW |
14 |
33,344,509 (GRCm39) |
missense |
probably benign |
0.18 |
R8314:Ptpn20
|
UTSW |
14 |
33,344,504 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9356:Ptpn20
|
UTSW |
14 |
33,352,865 (GRCm39) |
nonsense |
probably null |
|
R9690:Ptpn20
|
UTSW |
14 |
33,353,176 (GRCm39) |
missense |
probably benign |
0.31 |
|