Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam5 |
A |
T |
8: 25,276,264 (GRCm39) |
C468S |
probably damaging |
Het |
Adamts7 |
G |
A |
9: 90,077,296 (GRCm39) |
R1321H |
probably damaging |
Het |
Adra2c |
T |
C |
5: 35,437,792 (GRCm39) |
V188A |
possibly damaging |
Het |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Ap1g1 |
A |
G |
8: 110,564,423 (GRCm39) |
N323D |
probably damaging |
Het |
Arhgap15 |
A |
T |
2: 43,638,876 (GRCm39) |
|
probably benign |
Het |
Arhgef33 |
T |
C |
17: 80,667,882 (GRCm39) |
|
probably null |
Het |
Armc1 |
C |
T |
3: 19,211,700 (GRCm39) |
C40Y |
probably benign |
Het |
Arsk |
C |
A |
13: 76,214,928 (GRCm39) |
V309F |
probably damaging |
Het |
Atp4b |
A |
T |
8: 13,443,489 (GRCm39) |
M63K |
probably damaging |
Het |
Cacna1s |
T |
C |
1: 136,033,286 (GRCm39) |
L1237P |
probably damaging |
Het |
Ccnt2 |
A |
G |
1: 127,702,020 (GRCm39) |
E19G |
probably damaging |
Het |
Ccr2 |
A |
C |
9: 123,906,131 (GRCm39) |
Y137S |
probably damaging |
Het |
Cdc40 |
C |
T |
10: 40,717,480 (GRCm39) |
D404N |
probably damaging |
Het |
Cfh |
A |
T |
1: 140,046,323 (GRCm39) |
|
probably null |
Het |
Chd5 |
T |
A |
4: 152,450,862 (GRCm39) |
V662E |
probably benign |
Het |
Cnga4 |
A |
G |
7: 105,057,220 (GRCm39) |
D544G |
probably benign |
Het |
Col6a3 |
C |
G |
1: 90,695,328 (GRCm39) |
|
probably benign |
Het |
Coro6 |
T |
A |
11: 77,357,265 (GRCm39) |
I158N |
probably damaging |
Het |
Cpa1 |
A |
G |
6: 30,642,992 (GRCm39) |
S307G |
probably damaging |
Het |
Depdc5 |
T |
A |
5: 33,081,587 (GRCm39) |
M583K |
probably benign |
Het |
Dock2 |
G |
T |
11: 34,223,252 (GRCm39) |
S1170* |
probably null |
Het |
Dusp16 |
A |
T |
6: 134,694,933 (GRCm39) |
S633T |
probably benign |
Het |
Esco1 |
T |
C |
18: 10,572,123 (GRCm39) |
E739G |
probably damaging |
Het |
Fam193a |
T |
A |
5: 34,577,501 (GRCm39) |
|
probably null |
Het |
Fat4 |
G |
A |
3: 38,942,592 (GRCm39) |
S495N |
probably benign |
Het |
Galnt10 |
A |
G |
11: 57,675,409 (GRCm39) |
Y556C |
probably damaging |
Het |
Garin5b |
T |
A |
7: 4,760,814 (GRCm39) |
T633S |
|
Het |
Gc |
A |
T |
5: 89,591,311 (GRCm39) |
D142E |
probably benign |
Het |
Gda |
A |
T |
19: 21,377,952 (GRCm39) |
F369Y |
probably damaging |
Het |
Glce |
A |
T |
9: 61,968,103 (GRCm39) |
S349R |
probably benign |
Het |
Glp2r |
A |
G |
11: 67,612,901 (GRCm39) |
L351P |
probably damaging |
Het |
Gtf2h5 |
C |
CA |
17: 6,134,833 (GRCm39) |
|
probably null |
Het |
Gxylt2 |
A |
T |
6: 100,764,284 (GRCm39) |
Y323F |
probably benign |
Het |
Hmmr |
T |
C |
11: 40,598,858 (GRCm39) |
N589D |
probably damaging |
Het |
Hsd17b3 |
A |
C |
13: 64,210,712 (GRCm39) |
D214E |
probably benign |
Het |
Kat6a |
A |
G |
8: 23,429,022 (GRCm39) |
D1459G |
possibly damaging |
Het |
Lad1 |
G |
A |
1: 135,758,933 (GRCm39) |
R465H |
probably benign |
Het |
Lcmt1 |
T |
A |
7: 122,999,691 (GRCm39) |
D46E |
probably damaging |
Het |
Map4k1 |
G |
A |
7: 28,686,542 (GRCm39) |
D155N |
probably damaging |
Het |
Mylk |
G |
T |
16: 34,741,427 (GRCm39) |
R796L |
probably benign |
Het |
Nat8l |
T |
A |
5: 34,154,510 (GRCm39) |
L108Q |
probably damaging |
Het |
Nlrp5 |
T |
C |
7: 23,118,172 (GRCm39) |
V632A |
probably benign |
Het |
Nr3c2 |
A |
G |
8: 77,636,387 (GRCm39) |
E496G |
probably damaging |
Het |
Or8b12 |
G |
T |
9: 37,658,174 (GRCm39) |
C248F |
probably benign |
Het |
Or8b56 |
A |
T |
9: 38,738,995 (GRCm39) |
I3F |
probably benign |
Het |
Papln |
A |
G |
12: 83,829,764 (GRCm39) |
K962E |
probably damaging |
Het |
Pcdha8 |
T |
A |
18: 37,127,372 (GRCm39) |
M618K |
probably benign |
Het |
Pclo |
A |
G |
5: 14,764,580 (GRCm39) |
D1066G |
|
Het |
Phip |
A |
T |
9: 82,809,140 (GRCm39) |
M446K |
probably benign |
Het |
Pkn3 |
A |
G |
2: 29,973,318 (GRCm39) |
K380R |
probably benign |
Het |
Potefam1 |
T |
C |
2: 111,000,017 (GRCm39) |
T198A |
unknown |
Het |
Ppa1 |
C |
A |
10: 61,496,758 (GRCm39) |
A82E |
possibly damaging |
Het |
Prune2 |
A |
C |
19: 17,096,920 (GRCm39) |
D808A |
probably benign |
Het |
Psme4 |
T |
G |
11: 30,828,467 (GRCm39) |
L1829R |
probably damaging |
Het |
Rtp4 |
A |
C |
16: 23,431,866 (GRCm39) |
K133Q |
possibly damaging |
Het |
Scaf11 |
C |
T |
15: 96,313,669 (GRCm39) |
A1371T |
probably benign |
Het |
Serpinb9g |
A |
T |
13: 33,678,931 (GRCm39) |
H267L |
probably benign |
Het |
Slc47a2 |
T |
G |
11: 61,233,588 (GRCm39) |
D6A |
probably benign |
Het |
Slco1a4 |
A |
T |
6: 141,765,255 (GRCm39) |
V329D |
possibly damaging |
Het |
Smg6 |
T |
C |
11: 74,820,859 (GRCm39) |
S377P |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,971,030 (GRCm39) |
H121R |
probably benign |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Taar2 |
A |
T |
10: 23,817,369 (GRCm39) |
Y303F |
probably damaging |
Het |
Tgm6 |
A |
G |
2: 129,985,418 (GRCm39) |
D407G |
probably damaging |
Het |
Twf2 |
A |
G |
9: 106,090,010 (GRCm39) |
E153G |
possibly damaging |
Het |
Upb1 |
A |
G |
10: 75,275,710 (GRCm39) |
Y365C |
probably damaging |
Het |
Vmn2r4 |
A |
T |
3: 64,317,247 (GRCm39) |
S164T |
possibly damaging |
Het |
Wtip |
C |
T |
7: 33,824,979 (GRCm39) |
G202R |
possibly damaging |
Het |
Zfhx4 |
G |
A |
3: 5,309,084 (GRCm39) |
C770Y |
probably damaging |
Het |
|
Other mutations in Nucb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00423:Nucb2
|
APN |
7 |
116,121,066 (GRCm39) |
splice site |
probably benign |
|
IGL02347:Nucb2
|
APN |
7 |
116,135,113 (GRCm39) |
missense |
probably benign |
0.00 |
R0017:Nucb2
|
UTSW |
7 |
116,132,386 (GRCm39) |
missense |
probably benign |
0.01 |
R0017:Nucb2
|
UTSW |
7 |
116,132,386 (GRCm39) |
missense |
probably benign |
0.01 |
R0207:Nucb2
|
UTSW |
7 |
116,135,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Nucb2
|
UTSW |
7 |
116,135,086 (GRCm39) |
splice site |
probably benign |
|
R1526:Nucb2
|
UTSW |
7 |
116,123,642 (GRCm39) |
critical splice donor site |
probably null |
|
R3964:Nucb2
|
UTSW |
7 |
116,128,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R3966:Nucb2
|
UTSW |
7 |
116,128,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R4154:Nucb2
|
UTSW |
7 |
116,126,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4619:Nucb2
|
UTSW |
7 |
116,127,059 (GRCm39) |
critical splice donor site |
probably null |
|
R4705:Nucb2
|
UTSW |
7 |
116,139,262 (GRCm39) |
critical splice donor site |
probably null |
|
R4913:Nucb2
|
UTSW |
7 |
116,123,540 (GRCm39) |
nonsense |
probably null |
|
R4934:Nucb2
|
UTSW |
7 |
116,139,199 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5210:Nucb2
|
UTSW |
7 |
116,128,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R7227:Nucb2
|
UTSW |
7 |
116,125,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Nucb2
|
UTSW |
7 |
116,128,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7899:Nucb2
|
UTSW |
7 |
116,121,205 (GRCm39) |
missense |
probably benign |
0.01 |
R8200:Nucb2
|
UTSW |
7 |
116,132,398 (GRCm39) |
critical splice donor site |
probably null |
|
R8818:Nucb2
|
UTSW |
7 |
116,121,136 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8977:Nucb2
|
UTSW |
7 |
116,128,063 (GRCm39) |
missense |
probably benign |
0.05 |
R9072:Nucb2
|
UTSW |
7 |
116,125,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R9182:Nucb2
|
UTSW |
7 |
116,121,070 (GRCm39) |
critical splice acceptor site |
probably null |
|
|