Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
T |
A |
11: 101,301,971 (GRCm39) |
I332F |
probably damaging |
Het |
Acp3 |
G |
T |
9: 104,201,916 (GRCm39) |
Q76K |
probably damaging |
Het |
Anp32e |
A |
T |
3: 95,842,181 (GRCm39) |
I100L |
probably benign |
Het |
Ccdc13 |
C |
A |
9: 121,660,085 (GRCm39) |
L76F |
probably damaging |
Het |
Cd44 |
T |
C |
2: 102,731,738 (GRCm39) |
|
probably null |
Het |
Chka |
A |
G |
19: 3,932,038 (GRCm39) |
|
probably benign |
Het |
Cnot6 |
A |
T |
11: 49,579,999 (GRCm39) |
S98T |
probably benign |
Het |
Cth |
A |
G |
3: 157,624,136 (GRCm39) |
F127S |
probably benign |
Het |
Dnah9 |
C |
A |
11: 65,741,829 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
C |
6: 84,184,070 (GRCm39) |
|
probably benign |
Het |
Flad1 |
T |
A |
3: 89,318,494 (GRCm39) |
I20F |
probably damaging |
Het |
Gm20730 |
C |
T |
6: 43,058,656 (GRCm39) |
S52N |
probably benign |
Het |
Gpr89 |
A |
G |
3: 96,800,260 (GRCm39) |
S113P |
probably benign |
Het |
Hivep1 |
A |
T |
13: 42,337,787 (GRCm39) |
H2622L |
possibly damaging |
Het |
Hlcs |
T |
C |
16: 94,068,840 (GRCm39) |
N274D |
probably benign |
Het |
Ido2 |
T |
C |
8: 25,023,771 (GRCm39) |
I356V |
probably benign |
Het |
Insyn2b |
T |
C |
11: 34,353,007 (GRCm39) |
S350P |
probably benign |
Het |
Itgam |
A |
G |
7: 127,711,458 (GRCm39) |
|
probably null |
Het |
Lama1 |
C |
A |
17: 68,086,041 (GRCm39) |
|
probably null |
Het |
Lrrc4b |
T |
A |
7: 44,111,982 (GRCm39) |
V618E |
probably damaging |
Het |
Man1a2 |
A |
G |
3: 100,539,913 (GRCm39) |
I176T |
possibly damaging |
Het |
Mns1 |
A |
G |
9: 72,346,730 (GRCm39) |
E71G |
probably damaging |
Het |
Ncoa6 |
T |
A |
2: 155,248,858 (GRCm39) |
N1482I |
probably damaging |
Het |
Neto2 |
C |
A |
8: 86,389,924 (GRCm39) |
E180* |
probably null |
Het |
Psmb7 |
A |
T |
2: 38,503,440 (GRCm39) |
|
probably benign |
Het |
Rin2 |
C |
T |
2: 145,664,550 (GRCm39) |
T60M |
probably benign |
Het |
Slc28a3 |
A |
G |
13: 58,706,092 (GRCm39) |
V639A |
probably benign |
Het |
Tenm2 |
A |
T |
11: 35,915,147 (GRCm39) |
I2129N |
probably damaging |
Het |
Topaz1 |
A |
G |
9: 122,626,848 (GRCm39) |
D1492G |
possibly damaging |
Het |
Trank1 |
G |
A |
9: 111,207,887 (GRCm39) |
G1711R |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 63,867,451 (GRCm39) |
|
probably benign |
Het |
Ugt1a6a |
T |
A |
1: 88,066,251 (GRCm39) |
V19E |
probably benign |
Het |
Vmn2r60 |
A |
T |
7: 41,785,125 (GRCm39) |
E112D |
probably damaging |
Het |
Wdr4 |
T |
G |
17: 31,731,195 (GRCm39) |
Q55P |
probably damaging |
Het |
Xpnpep1 |
G |
A |
19: 52,992,250 (GRCm39) |
|
probably benign |
Het |
Zfyve16 |
A |
T |
13: 92,657,769 (GRCm39) |
L714Q |
probably damaging |
Het |
|
Other mutations in Herpud2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01310:Herpud2
|
APN |
9 |
25,062,247 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01325:Herpud2
|
APN |
9 |
25,025,207 (GRCm39) |
missense |
probably benign |
|
R1793:Herpud2
|
UTSW |
9 |
25,021,953 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3976:Herpud2
|
UTSW |
9 |
25,021,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Herpud2
|
UTSW |
9 |
25,036,285 (GRCm39) |
missense |
probably benign |
0.05 |
R5291:Herpud2
|
UTSW |
9 |
25,036,256 (GRCm39) |
missense |
probably benign |
|
R5922:Herpud2
|
UTSW |
9 |
25,020,280 (GRCm39) |
missense |
probably benign |
0.00 |
R6062:Herpud2
|
UTSW |
9 |
25,020,284 (GRCm39) |
missense |
probably damaging |
0.96 |
R6200:Herpud2
|
UTSW |
9 |
25,062,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Herpud2
|
UTSW |
9 |
25,020,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R7649:Herpud2
|
UTSW |
9 |
25,021,902 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9330:Herpud2
|
UTSW |
9 |
25,036,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R9539:Herpud2
|
UTSW |
9 |
25,041,936 (GRCm39) |
missense |
probably damaging |
0.96 |
X0063:Herpud2
|
UTSW |
9 |
25,062,165 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Herpud2
|
UTSW |
9 |
25,041,918 (GRCm39) |
missense |
not run |
|
Z1177:Herpud2
|
UTSW |
9 |
25,041,918 (GRCm39) |
missense |
not run |
|
|