Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,832,214 (GRCm39) |
|
probably null |
Het |
Abca3 |
T |
A |
17: 24,605,250 (GRCm39) |
V716D |
possibly damaging |
Het |
Adprhl1 |
C |
T |
8: 13,298,682 (GRCm39) |
V83I |
probably damaging |
Het |
Alkbh1 |
A |
G |
12: 87,478,215 (GRCm39) |
V232A |
probably damaging |
Het |
Arhgef10l |
T |
A |
4: 140,302,642 (GRCm39) |
I271F |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,407,584 (GRCm39) |
M2157K |
possibly damaging |
Het |
Capn13 |
G |
A |
17: 73,629,049 (GRCm39) |
S586L |
probably benign |
Het |
Cd3g |
A |
T |
9: 44,885,459 (GRCm39) |
|
probably null |
Het |
Cfap54 |
A |
T |
10: 92,704,603 (GRCm39) |
Y2826N |
unknown |
Het |
Cmas |
T |
C |
6: 142,710,283 (GRCm39) |
V134A |
probably damaging |
Het |
Cnp |
A |
G |
11: 100,469,814 (GRCm39) |
H250R |
probably damaging |
Het |
Dact1 |
G |
A |
12: 71,364,688 (GRCm39) |
A453T |
probably benign |
Het |
Dcaf6 |
T |
A |
1: 165,179,623 (GRCm39) |
R506* |
probably null |
Het |
Dph1 |
A |
G |
11: 75,081,272 (GRCm39) |
V5A |
probably benign |
Het |
Entpd3 |
A |
G |
9: 120,387,568 (GRCm39) |
Y255C |
probably damaging |
Het |
Etl4 |
A |
T |
2: 20,811,957 (GRCm39) |
T1715S |
probably damaging |
Het |
Exd2 |
T |
A |
12: 80,539,334 (GRCm39) |
H466Q |
probably damaging |
Het |
Fbln2 |
A |
G |
6: 91,246,181 (GRCm39) |
N1056S |
probably damaging |
Het |
Fcrl5 |
A |
T |
3: 87,351,502 (GRCm39) |
Q250L |
possibly damaging |
Het |
Fignl2 |
A |
G |
15: 100,951,301 (GRCm39) |
V327A |
unknown |
Het |
Gm10226 |
T |
A |
17: 21,910,866 (GRCm39) |
C34S |
possibly damaging |
Het |
H2bc6 |
A |
T |
13: 23,769,938 (GRCm39) |
M1K |
probably null |
Het |
Kdm6b |
A |
G |
11: 69,296,960 (GRCm39) |
S436P |
possibly damaging |
Het |
Lmnb2 |
G |
T |
10: 80,753,991 (GRCm39) |
A21E |
possibly damaging |
Het |
Mcf2l |
A |
T |
8: 12,930,127 (GRCm39) |
E49V |
probably benign |
Het |
Muc2 |
A |
G |
7: 141,290,942 (GRCm39) |
E76G |
|
Het |
Naa60 |
T |
C |
16: 3,718,573 (GRCm39) |
I135T |
probably benign |
Het |
Neb |
T |
C |
2: 52,097,713 (GRCm39) |
Y4924C |
possibly damaging |
Het |
Nlrp10 |
T |
A |
7: 108,524,656 (GRCm39) |
I275F |
probably damaging |
Het |
Nr3c2 |
T |
C |
8: 77,636,174 (GRCm39) |
V425A |
possibly damaging |
Het |
Nynrin |
G |
A |
14: 56,103,420 (GRCm39) |
G755S |
probably damaging |
Het |
Or5d41 |
T |
C |
2: 88,054,429 (GRCm39) |
T316A |
probably damaging |
Het |
Padi2 |
T |
A |
4: 140,651,656 (GRCm39) |
D135E |
probably benign |
Het |
Pcdha6 |
T |
A |
18: 37,103,034 (GRCm39) |
S742R |
probably benign |
Het |
Pcdhgb5 |
T |
A |
18: 37,866,007 (GRCm39) |
S601T |
probably damaging |
Het |
Pira13 |
T |
C |
7: 3,826,246 (GRCm39) |
N249S |
unknown |
Het |
Polr1b |
C |
A |
2: 128,967,464 (GRCm39) |
F952L |
probably damaging |
Het |
Prr15l |
T |
C |
11: 96,825,390 (GRCm39) |
W7R |
possibly damaging |
Het |
Ptpn23 |
G |
A |
9: 110,215,368 (GRCm39) |
H1431Y |
possibly damaging |
Het |
Rnf20 |
C |
T |
4: 49,644,592 (GRCm39) |
Q286* |
probably null |
Het |
Rptor |
T |
C |
11: 119,783,453 (GRCm39) |
I1149T |
probably benign |
Het |
Sfrp2 |
A |
G |
3: 83,674,086 (GRCm39) |
I80V |
probably benign |
Het |
Slc38a2 |
T |
C |
15: 96,588,033 (GRCm39) |
D497G |
probably benign |
Het |
Slc43a1 |
T |
A |
2: 84,671,197 (GRCm39) |
M44K |
probably damaging |
Het |
Stil |
T |
A |
4: 114,890,035 (GRCm39) |
V841E |
possibly damaging |
Het |
Stip1 |
T |
A |
19: 6,999,141 (GRCm39) |
H479L |
probably benign |
Het |
Supt6 |
A |
G |
11: 78,100,355 (GRCm39) |
Y1486H |
probably damaging |
Het |
Taf6 |
T |
C |
5: 138,180,282 (GRCm39) |
D324G |
probably damaging |
Het |
Tgif1 |
T |
A |
17: 71,158,452 (GRCm39) |
|
probably benign |
Het |
Tmprss11f |
T |
C |
5: 86,681,605 (GRCm39) |
E216G |
probably benign |
Het |
Tmprss7 |
C |
A |
16: 45,488,014 (GRCm39) |
A472S |
probably benign |
Het |
Trpm1 |
T |
A |
7: 63,897,939 (GRCm39) |
F1191I |
probably benign |
Het |
Tspan12 |
T |
A |
6: 21,836,442 (GRCm39) |
N40I |
probably damaging |
Het |
Ttll3 |
AAGTA |
AAGTACAGTA |
6: 113,376,120 (GRCm39) |
|
probably null |
Het |
Unc13c |
A |
T |
9: 73,602,232 (GRCm39) |
I1338N |
probably damaging |
Het |
Vegfc |
T |
A |
8: 54,530,835 (GRCm39) |
S8T |
unknown |
Het |
Vmn1r59 |
T |
A |
7: 5,457,634 (GRCm39) |
Q42L |
probably damaging |
Het |
Vmn2r-ps117 |
A |
T |
17: 19,043,934 (GRCm39) |
I337F |
probably damaging |
Het |
Xylb |
G |
A |
9: 119,209,766 (GRCm39) |
|
probably null |
Het |
Zfp551 |
T |
A |
7: 12,152,569 (GRCm39) |
I55F |
probably damaging |
Het |
Zfp972 |
T |
C |
2: 177,563,532 (GRCm39) |
N27S |
probably benign |
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 |
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 |
|
R8743:Nucb2
|
UTSW |
7 |
116,128,065 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|