Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810459M11Rik |
G |
T |
1: 85,974,087 (GRCm39) |
V135F |
possibly damaging |
Het |
Aatk |
T |
C |
11: 119,902,603 (GRCm39) |
T541A |
probably benign |
Het |
Abcc1 |
T |
C |
16: 14,240,991 (GRCm39) |
L516P |
probably damaging |
Het |
Actl6a |
T |
A |
3: 32,776,791 (GRCm39) |
V350E |
possibly damaging |
Het |
Afm |
A |
G |
5: 90,674,222 (GRCm39) |
K245E |
possibly damaging |
Het |
Agr3 |
T |
C |
12: 35,996,915 (GRCm39) |
V63A |
probably damaging |
Het |
Arhgef28 |
A |
T |
13: 98,083,383 (GRCm39) |
M1162K |
probably damaging |
Het |
Casq2 |
T |
A |
3: 101,994,113 (GRCm39) |
C53* |
probably null |
Het |
Ccdc181 |
T |
C |
1: 164,107,470 (GRCm39) |
V51A |
probably benign |
Het |
Cd101 |
A |
G |
3: 100,926,310 (GRCm39) |
|
probably benign |
Het |
Csdc2 |
T |
C |
15: 81,832,801 (GRCm39) |
V69A |
probably benign |
Het |
Cyp2c23 |
A |
T |
19: 44,009,997 (GRCm39) |
|
probably benign |
Het |
Dnph1 |
A |
G |
17: 46,809,427 (GRCm39) |
|
probably benign |
Het |
Egf |
T |
C |
3: 129,474,796 (GRCm39) |
T1124A |
probably benign |
Het |
Gpr45 |
A |
G |
1: 43,072,371 (GRCm39) |
E338G |
possibly damaging |
Het |
Grb14 |
A |
C |
2: 64,768,762 (GRCm39) |
L98R |
probably damaging |
Het |
Gucy1a1 |
T |
C |
3: 82,026,224 (GRCm39) |
S77G |
possibly damaging |
Het |
Helb |
A |
G |
10: 119,925,390 (GRCm39) |
S996P |
probably benign |
Het |
Huwe1 |
A |
G |
X: 150,669,762 (GRCm39) |
E1405G |
probably damaging |
Het |
Ifi47 |
T |
C |
11: 48,986,617 (GRCm39) |
I128T |
probably benign |
Het |
Ift140 |
T |
A |
17: 25,309,736 (GRCm39) |
Y1089N |
probably damaging |
Het |
Ift56 |
A |
C |
6: 38,402,097 (GRCm39) |
S530R |
probably benign |
Het |
Il1r1 |
A |
T |
1: 40,341,569 (GRCm39) |
H324L |
probably benign |
Het |
Irx1 |
C |
T |
13: 72,107,974 (GRCm39) |
R236H |
probably benign |
Het |
Itpr3 |
T |
C |
17: 27,323,530 (GRCm39) |
V1185A |
probably benign |
Het |
Kif19a |
T |
C |
11: 114,676,396 (GRCm39) |
V450A |
possibly damaging |
Het |
Krtap21-1 |
G |
T |
16: 89,200,446 (GRCm39) |
Y65* |
probably null |
Het |
Ltn1 |
A |
T |
16: 87,176,693 (GRCm39) |
N1704K |
possibly damaging |
Het |
Med1 |
T |
C |
11: 98,047,335 (GRCm39) |
|
probably benign |
Het |
Meis2 |
T |
A |
2: 115,893,804 (GRCm39) |
H36L |
probably damaging |
Het |
Mier2 |
T |
C |
10: 79,385,456 (GRCm39) |
N124S |
probably damaging |
Het |
Mmp20 |
A |
G |
9: 7,654,171 (GRCm39) |
|
probably null |
Het |
Muc4 |
A |
G |
16: 32,569,212 (GRCm39) |
T91A |
possibly damaging |
Het |
Myo3b |
T |
A |
2: 70,119,745 (GRCm39) |
V935E |
probably benign |
Het |
Ndufa7 |
T |
C |
17: 34,048,632 (GRCm39) |
|
probably benign |
Het |
Nobox |
A |
T |
6: 43,282,617 (GRCm39) |
N263K |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,018,890 (GRCm39) |
D684G |
probably damaging |
Het |
Odr4 |
C |
A |
1: 150,260,179 (GRCm39) |
|
probably null |
Het |
Or2t1 |
A |
G |
14: 14,328,789 (GRCm38) |
H226R |
probably benign |
Het |
Or4c12b |
T |
A |
2: 89,647,508 (GRCm39) |
Y273* |
probably null |
Het |
Or5p69 |
C |
A |
7: 107,967,336 (GRCm39) |
T213K |
probably damaging |
Het |
Or5w13 |
T |
C |
2: 87,523,344 (GRCm39) |
N294S |
probably damaging |
Het |
Or6aa1 |
T |
C |
7: 86,043,743 (GRCm39) |
|
probably benign |
Het |
Plau |
A |
C |
14: 20,889,965 (GRCm39) |
D270A |
possibly damaging |
Het |
Pof1b |
T |
C |
X: 111,558,809 (GRCm39) |
|
probably null |
Het |
Pramel23 |
A |
G |
4: 143,424,913 (GRCm39) |
C177R |
probably damaging |
Het |
Prtn3 |
A |
T |
10: 79,717,767 (GRCm39) |
|
probably null |
Het |
Ptges3 |
T |
A |
10: 127,904,616 (GRCm39) |
D26E |
probably benign |
Het |
Pxmp2 |
T |
C |
5: 110,429,160 (GRCm39) |
E99G |
probably benign |
Het |
Rasgef1a |
A |
G |
6: 118,060,068 (GRCm39) |
R106G |
probably benign |
Het |
Rnf208 |
T |
C |
2: 25,133,774 (GRCm39) |
V156A |
probably benign |
Het |
Rps6ka1 |
A |
T |
4: 133,599,292 (GRCm39) |
I45N |
possibly damaging |
Het |
Rps6ka4 |
C |
T |
19: 6,809,623 (GRCm39) |
|
probably null |
Het |
Rsbn1 |
G |
T |
3: 103,860,972 (GRCm39) |
C466F |
possibly damaging |
Het |
Shkbp1 |
A |
T |
7: 27,042,141 (GRCm39) |
C605S |
probably damaging |
Het |
Slc2a10 |
G |
A |
2: 165,360,142 (GRCm39) |
D531N |
probably benign |
Het |
Sox13 |
A |
G |
1: 133,317,204 (GRCm39) |
L143P |
probably damaging |
Het |
Stx2 |
C |
T |
5: 129,069,285 (GRCm39) |
R142Q |
probably damaging |
Het |
Tanc1 |
T |
A |
2: 59,623,431 (GRCm39) |
|
probably benign |
Het |
Tubgcp5 |
C |
T |
7: 55,456,355 (GRCm39) |
Q316* |
probably null |
Het |
Ubc |
A |
G |
5: 125,463,293 (GRCm39) |
V678A |
probably benign |
Het |
Unc5d |
G |
A |
8: 29,365,634 (GRCm39) |
T117I |
probably damaging |
Het |
Vmn2r4 |
T |
C |
3: 64,314,337 (GRCm39) |
I126V |
probably benign |
Het |
Zfp410 |
T |
A |
12: 84,378,594 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Nipal1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Nipal1
|
APN |
5 |
72,816,067 (GRCm39) |
missense |
probably benign |
|
IGL01894:Nipal1
|
APN |
5 |
72,820,882 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01962:Nipal1
|
APN |
5 |
72,825,401 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02145:Nipal1
|
APN |
5 |
72,824,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02934:Nipal1
|
APN |
5 |
72,805,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03024:Nipal1
|
APN |
5 |
72,820,968 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03237:Nipal1
|
APN |
5 |
72,824,150 (GRCm39) |
missense |
probably damaging |
0.99 |
R0848:Nipal1
|
UTSW |
5 |
72,825,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R1024:Nipal1
|
UTSW |
5 |
72,825,334 (GRCm39) |
frame shift |
probably null |
|
R2106:Nipal1
|
UTSW |
5 |
72,820,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R2883:Nipal1
|
UTSW |
5 |
72,825,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R2932:Nipal1
|
UTSW |
5 |
72,824,978 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5364:Nipal1
|
UTSW |
5 |
72,825,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Nipal1
|
UTSW |
5 |
72,820,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6523:Nipal1
|
UTSW |
5 |
72,824,951 (GRCm39) |
missense |
probably damaging |
0.97 |
R7185:Nipal1
|
UTSW |
5 |
72,824,198 (GRCm39) |
missense |
probably damaging |
0.98 |
R7436:Nipal1
|
UTSW |
5 |
72,824,984 (GRCm39) |
missense |
probably benign |
0.00 |
R9388:Nipal1
|
UTSW |
5 |
72,825,557 (GRCm39) |
makesense |
probably null |
|
RF011:Nipal1
|
UTSW |
5 |
72,824,156 (GRCm39) |
missense |
probably damaging |
1.00 |
|