Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano1 |
T |
C |
7: 144,190,882 (GRCm39) |
I401V |
possibly damaging |
Het |
Ap2a2 |
A |
T |
7: 141,184,932 (GRCm39) |
|
probably benign |
Het |
Apol7c |
T |
A |
15: 77,410,637 (GRCm39) |
D103V |
probably damaging |
Het |
Arid4a |
T |
C |
12: 71,119,507 (GRCm39) |
|
probably null |
Het |
Atp2a1 |
A |
G |
7: 126,049,479 (GRCm39) |
V521A |
probably benign |
Het |
Ccdc88c |
G |
T |
12: 100,883,062 (GRCm39) |
D1603E |
probably benign |
Het |
Clec4f |
T |
C |
6: 83,630,182 (GRCm39) |
I125M |
probably benign |
Het |
Dsc1 |
T |
C |
18: 20,227,679 (GRCm39) |
I520V |
probably benign |
Het |
Eomes |
G |
A |
9: 118,311,334 (GRCm39) |
A386T |
probably damaging |
Het |
Hectd4 |
G |
T |
5: 121,445,013 (GRCm39) |
M1420I |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,508,303 (GRCm39) |
|
probably benign |
Het |
Ighv6-3 |
G |
A |
12: 114,355,335 (GRCm39) |
T118I |
possibly damaging |
Het |
Krt82 |
A |
G |
15: 101,453,958 (GRCm39) |
F250S |
probably damaging |
Het |
Ltb |
A |
G |
17: 35,413,576 (GRCm39) |
T27A |
probably benign |
Het |
Mex3b |
T |
A |
7: 82,518,911 (GRCm39) |
S409T |
probably benign |
Het |
Mki67 |
A |
T |
7: 135,315,745 (GRCm39) |
I39N |
probably damaging |
Het |
Or51a7 |
A |
G |
7: 102,615,235 (GRCm39) |
|
probably benign |
Het |
Palmd |
A |
G |
3: 116,717,922 (GRCm39) |
S192P |
probably damaging |
Het |
Pcdh20 |
A |
T |
14: 88,704,636 (GRCm39) |
M888K |
probably benign |
Het |
Pclo |
A |
T |
5: 14,731,083 (GRCm39) |
H3195L |
unknown |
Het |
Pgm2 |
A |
T |
5: 64,260,225 (GRCm39) |
I137F |
possibly damaging |
Het |
Polq |
T |
A |
16: 36,837,671 (GRCm39) |
N194K |
probably damaging |
Het |
Rmnd1 |
T |
C |
10: 4,360,793 (GRCm39) |
|
probably null |
Het |
Rnf114 |
T |
C |
2: 167,354,459 (GRCm39) |
M180T |
probably damaging |
Het |
Sap30 |
A |
G |
8: 57,938,123 (GRCm39) |
F165L |
possibly damaging |
Het |
Scgb3a2 |
T |
A |
18: 43,900,059 (GRCm39) |
|
probably benign |
Het |
Sftpa1 |
A |
T |
14: 40,854,527 (GRCm39) |
N38I |
probably benign |
Het |
Sumf1 |
A |
G |
6: 108,152,977 (GRCm39) |
F137S |
probably damaging |
Het |
Tln2 |
C |
A |
9: 67,219,093 (GRCm39) |
R284L |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,570,703 (GRCm39) |
R26730Q |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,540,808 (GRCm39) |
R25732S |
probably damaging |
Het |
Tubgcp4 |
T |
C |
2: 121,004,082 (GRCm39) |
V41A |
probably benign |
Het |
Usp53 |
T |
A |
3: 122,751,367 (GRCm39) |
Q230L |
probably damaging |
Het |
Vmn2r57 |
T |
C |
7: 41,074,467 (GRCm39) |
E532G |
probably damaging |
Het |
Vps9d1 |
G |
T |
8: 123,972,769 (GRCm39) |
N454K |
probably damaging |
Het |
Wdr55 |
T |
C |
18: 36,895,132 (GRCm39) |
|
probably null |
Het |
Zfp263 |
T |
A |
16: 3,566,776 (GRCm39) |
C76S |
probably benign |
Het |
|
Other mutations in Gldc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Gldc
|
APN |
19 |
30,092,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01016:Gldc
|
APN |
19 |
30,110,893 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01510:Gldc
|
APN |
19 |
30,091,121 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01516:Gldc
|
APN |
19 |
30,076,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01598:Gldc
|
APN |
19 |
30,111,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01646:Gldc
|
APN |
19 |
30,078,165 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02024:Gldc
|
APN |
19 |
30,078,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02125:Gldc
|
APN |
19 |
30,124,641 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02548:Gldc
|
APN |
19 |
30,077,299 (GRCm39) |
missense |
probably benign |
|
IGL02711:Gldc
|
APN |
19 |
30,122,546 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02818:Gldc
|
APN |
19 |
30,113,909 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02982:Gldc
|
APN |
19 |
30,122,545 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03165:Gldc
|
APN |
19 |
30,076,393 (GRCm39) |
missense |
possibly damaging |
0.61 |
jojoba
|
UTSW |
19 |
30,110,912 (GRCm39) |
missense |
probably damaging |
1.00 |
miserable
|
UTSW |
19 |
30,128,936 (GRCm39) |
missense |
probably damaging |
1.00 |
Urchin
|
UTSW |
19 |
30,096,002 (GRCm39) |
missense |
probably damaging |
0.98 |
I2289:Gldc
|
UTSW |
19 |
30,124,576 (GRCm39) |
nonsense |
probably null |
|
R0180:Gldc
|
UTSW |
19 |
30,078,217 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0269:Gldc
|
UTSW |
19 |
30,096,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R0277:Gldc
|
UTSW |
19 |
30,093,851 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1085:Gldc
|
UTSW |
19 |
30,128,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Gldc
|
UTSW |
19 |
30,138,162 (GRCm39) |
intron |
probably benign |
|
R1500:Gldc
|
UTSW |
19 |
30,091,225 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1507:Gldc
|
UTSW |
19 |
30,096,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1592:Gldc
|
UTSW |
19 |
30,138,077 (GRCm39) |
intron |
probably benign |
|
R1593:Gldc
|
UTSW |
19 |
30,091,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R1675:Gldc
|
UTSW |
19 |
30,120,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1869:Gldc
|
UTSW |
19 |
30,116,732 (GRCm39) |
missense |
probably benign |
|
R1965:Gldc
|
UTSW |
19 |
30,114,513 (GRCm39) |
nonsense |
probably null |
|
R2312:Gldc
|
UTSW |
19 |
30,078,226 (GRCm39) |
missense |
probably damaging |
0.98 |
R2425:Gldc
|
UTSW |
19 |
30,109,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R3836:Gldc
|
UTSW |
19 |
30,096,075 (GRCm39) |
splice site |
probably benign |
|
R3837:Gldc
|
UTSW |
19 |
30,096,075 (GRCm39) |
splice site |
probably benign |
|
R3839:Gldc
|
UTSW |
19 |
30,096,075 (GRCm39) |
splice site |
probably benign |
|
R4191:Gldc
|
UTSW |
19 |
30,123,058 (GRCm39) |
missense |
probably damaging |
0.96 |
R4380:Gldc
|
UTSW |
19 |
30,138,168 (GRCm39) |
intron |
probably benign |
|
R4508:Gldc
|
UTSW |
19 |
30,120,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Gldc
|
UTSW |
19 |
30,151,839 (GRCm39) |
missense |
probably benign |
|
R4655:Gldc
|
UTSW |
19 |
30,138,102 (GRCm39) |
intron |
probably benign |
|
R4842:Gldc
|
UTSW |
19 |
30,111,132 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5070:Gldc
|
UTSW |
19 |
30,095,998 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5085:Gldc
|
UTSW |
19 |
30,128,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Gldc
|
UTSW |
19 |
30,123,125 (GRCm39) |
missense |
probably damaging |
0.96 |
R5368:Gldc
|
UTSW |
19 |
30,135,921 (GRCm39) |
missense |
probably benign |
|
R5718:Gldc
|
UTSW |
19 |
30,088,172 (GRCm39) |
nonsense |
probably null |
|
R5878:Gldc
|
UTSW |
19 |
30,120,867 (GRCm39) |
splice site |
probably null |
|
R6192:Gldc
|
UTSW |
19 |
30,111,172 (GRCm39) |
missense |
probably damaging |
0.98 |
R6453:Gldc
|
UTSW |
19 |
30,093,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R6777:Gldc
|
UTSW |
19 |
30,110,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6865:Gldc
|
UTSW |
19 |
30,111,162 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7332:Gldc
|
UTSW |
19 |
30,093,926 (GRCm39) |
missense |
probably damaging |
0.99 |
R7390:Gldc
|
UTSW |
19 |
30,077,314 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7647:Gldc
|
UTSW |
19 |
30,096,067 (GRCm39) |
missense |
probably damaging |
0.96 |
R8081:Gldc
|
UTSW |
19 |
30,135,987 (GRCm39) |
frame shift |
probably null |
|
R8171:Gldc
|
UTSW |
19 |
30,111,161 (GRCm39) |
missense |
probably benign |
0.24 |
R8321:Gldc
|
UTSW |
19 |
30,120,807 (GRCm39) |
nonsense |
probably null |
|
R8374:Gldc
|
UTSW |
19 |
30,114,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R8503:Gldc
|
UTSW |
19 |
30,077,254 (GRCm39) |
missense |
probably benign |
0.26 |
R8510:Gldc
|
UTSW |
19 |
30,093,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R8785:Gldc
|
UTSW |
19 |
30,092,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R8818:Gldc
|
UTSW |
19 |
30,078,212 (GRCm39) |
missense |
probably benign |
0.05 |
R8820:Gldc
|
UTSW |
19 |
30,078,212 (GRCm39) |
missense |
probably benign |
0.05 |
R8829:Gldc
|
UTSW |
19 |
30,078,212 (GRCm39) |
missense |
probably benign |
0.05 |
R8830:Gldc
|
UTSW |
19 |
30,078,212 (GRCm39) |
missense |
probably benign |
0.05 |
R8859:Gldc
|
UTSW |
19 |
30,116,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Gldc
|
UTSW |
19 |
30,111,156 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8935:Gldc
|
UTSW |
19 |
30,109,093 (GRCm39) |
missense |
probably benign |
0.00 |
R8940:Gldc
|
UTSW |
19 |
30,128,884 (GRCm39) |
missense |
probably benign |
|
R9070:Gldc
|
UTSW |
19 |
30,080,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Gldc
|
UTSW |
19 |
30,077,314 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9144:Gldc
|
UTSW |
19 |
30,114,593 (GRCm39) |
missense |
|
|
R9163:Gldc
|
UTSW |
19 |
30,111,686 (GRCm39) |
missense |
probably benign |
0.13 |
R9429:Gldc
|
UTSW |
19 |
30,091,172 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1177:Gldc
|
UTSW |
19 |
30,123,148 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1177:Gldc
|
UTSW |
19 |
30,088,179 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Gldc
|
UTSW |
19 |
30,088,178 (GRCm39) |
missense |
probably damaging |
1.00 |
|