Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy7 |
G |
C |
8: 89,035,362 (GRCm39) |
V89L |
probably benign |
Het |
Aebp2 |
T |
A |
6: 140,588,021 (GRCm39) |
S364T |
probably damaging |
Het |
Akr1b10 |
C |
T |
6: 34,369,388 (GRCm39) |
T206I |
probably benign |
Het |
Ap4e1 |
C |
T |
2: 126,903,846 (GRCm39) |
S916F |
probably benign |
Het |
Apob |
C |
T |
12: 8,044,914 (GRCm39) |
Q845* |
probably null |
Het |
Asb4 |
A |
G |
6: 5,390,803 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,066,724 (GRCm39) |
|
probably benign |
Het |
C1ra |
A |
T |
6: 124,496,736 (GRCm39) |
T391S |
probably benign |
Het |
Catsperg2 |
C |
A |
7: 29,416,429 (GRCm39) |
D328Y |
probably damaging |
Het |
Ciapin1 |
G |
T |
8: 95,555,814 (GRCm39) |
L119M |
probably damaging |
Het |
Crhr2 |
A |
G |
6: 55,077,765 (GRCm39) |
|
probably benign |
Het |
Cyp2j6 |
A |
G |
4: 96,406,407 (GRCm39) |
S455P |
probably benign |
Het |
Dctn4 |
G |
A |
18: 60,671,329 (GRCm39) |
|
probably benign |
Het |
Defa25 |
C |
T |
8: 21,575,245 (GRCm39) |
R75C |
probably benign |
Het |
Dnajc10 |
T |
C |
2: 80,175,296 (GRCm39) |
L561P |
probably damaging |
Het |
Dnajc7 |
A |
T |
11: 100,482,292 (GRCm39) |
F185L |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,844,267 (GRCm39) |
I1175V |
probably benign |
Het |
Drosha |
T |
G |
15: 12,837,422 (GRCm39) |
L302R |
possibly damaging |
Het |
Efcab5 |
C |
T |
11: 76,994,930 (GRCm39) |
V1214I |
probably benign |
Het |
Erich3 |
G |
A |
3: 154,419,686 (GRCm39) |
R260H |
probably damaging |
Het |
Fam168b |
T |
C |
1: 34,867,860 (GRCm39) |
T47A |
possibly damaging |
Het |
Gorasp1 |
G |
A |
9: 119,757,936 (GRCm39) |
R290C |
probably benign |
Het |
Gtf2a1 |
A |
G |
12: 91,539,351 (GRCm39) |
S94P |
possibly damaging |
Het |
Ighv1-53 |
C |
T |
12: 115,122,442 (GRCm39) |
C5Y |
probably benign |
Het |
Impdh1 |
T |
C |
6: 29,202,693 (GRCm39) |
I446V |
probably benign |
Het |
Krtap5-1 |
T |
C |
7: 141,850,094 (GRCm39) |
|
probably null |
Het |
Lipo3 |
T |
A |
19: 33,764,804 (GRCm39) |
I17L |
probably benign |
Het |
Lrrc37 |
A |
G |
11: 103,506,119 (GRCm39) |
S1950P |
probably benign |
Het |
Med12l |
A |
C |
3: 59,155,363 (GRCm39) |
Q1181P |
probably damaging |
Het |
Mtrf1l |
T |
C |
10: 5,767,454 (GRCm39) |
T221A |
probably benign |
Het |
Muc21 |
T |
C |
17: 35,930,953 (GRCm39) |
|
probably benign |
Het |
Mxi1 |
C |
A |
19: 53,360,160 (GRCm39) |
A294E |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,359,883 (GRCm39) |
E451G |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,359,902 (GRCm39) |
I445V |
probably benign |
Het |
Nfrkb |
T |
A |
9: 31,325,407 (GRCm39) |
L950Q |
possibly damaging |
Het |
Nherf4 |
A |
T |
9: 44,162,117 (GRCm39) |
|
probably null |
Het |
Oplah |
A |
G |
15: 76,181,476 (GRCm39) |
Y1155H |
probably damaging |
Het |
Or5b105 |
T |
G |
19: 13,079,790 (GRCm39) |
K287Q |
probably damaging |
Het |
Pcnx1 |
C |
T |
12: 81,965,018 (GRCm39) |
T395I |
probably damaging |
Het |
Pitrm1 |
A |
G |
13: 6,606,723 (GRCm39) |
H259R |
probably damaging |
Het |
Pllp |
C |
A |
8: 95,406,072 (GRCm39) |
M70I |
possibly damaging |
Het |
Pop1 |
A |
G |
15: 34,508,926 (GRCm39) |
T334A |
probably benign |
Het |
Prep |
T |
C |
10: 44,968,894 (GRCm39) |
|
probably benign |
Het |
Ptprz1 |
C |
A |
6: 22,959,623 (GRCm39) |
|
probably benign |
Het |
Sbsn |
A |
G |
7: 30,455,390 (GRCm39) |
S170G |
probably damaging |
Het |
Sco1 |
T |
G |
11: 66,954,846 (GRCm39) |
S284A |
probably benign |
Het |
Slc25a10 |
T |
A |
11: 120,388,265 (GRCm39) |
M227K |
probably damaging |
Het |
Trav7-6 |
A |
G |
14: 53,954,638 (GRCm39) |
K56R |
probably benign |
Het |
Ubr4 |
T |
G |
4: 139,179,116 (GRCm39) |
C3322G |
probably damaging |
Het |
Unc5a |
T |
C |
13: 55,151,182 (GRCm39) |
Y608H |
probably damaging |
Het |
Zfand1 |
A |
C |
3: 10,405,816 (GRCm39) |
N262K |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,743,380 (GRCm39) |
R536H |
probably damaging |
Het |
|
Other mutations in Lss |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02164:Lss
|
APN |
10 |
76,372,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02561:Lss
|
APN |
10 |
76,376,264 (GRCm39) |
unclassified |
probably benign |
|
IGL02991:Lss
|
APN |
10 |
76,379,745 (GRCm39) |
unclassified |
probably benign |
|
IGL03059:Lss
|
APN |
10 |
76,367,860 (GRCm39) |
splice site |
probably benign |
|
IGL03328:Lss
|
APN |
10 |
76,376,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03389:Lss
|
APN |
10 |
76,372,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Lss
|
UTSW |
10 |
76,372,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R1529:Lss
|
UTSW |
10 |
76,372,123 (GRCm39) |
nonsense |
probably null |
|
R1727:Lss
|
UTSW |
10 |
76,375,678 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1815:Lss
|
UTSW |
10 |
76,388,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Lss
|
UTSW |
10 |
76,381,296 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2051:Lss
|
UTSW |
10 |
76,367,712 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2061:Lss
|
UTSW |
10 |
76,381,932 (GRCm39) |
splice site |
probably null |
|
R3700:Lss
|
UTSW |
10 |
76,382,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R4619:Lss
|
UTSW |
10 |
76,372,089 (GRCm39) |
missense |
probably benign |
0.11 |
R4995:Lss
|
UTSW |
10 |
76,383,371 (GRCm39) |
missense |
probably benign |
0.10 |
R5056:Lss
|
UTSW |
10 |
76,388,760 (GRCm39) |
splice site |
probably null |
|
R5134:Lss
|
UTSW |
10 |
76,382,070 (GRCm39) |
unclassified |
probably benign |
|
R6074:Lss
|
UTSW |
10 |
76,379,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R6140:Lss
|
UTSW |
10 |
76,386,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R7214:Lss
|
UTSW |
10 |
76,383,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R7717:Lss
|
UTSW |
10 |
76,381,286 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8263:Lss
|
UTSW |
10 |
76,367,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R8350:Lss
|
UTSW |
10 |
76,371,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R8450:Lss
|
UTSW |
10 |
76,371,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R9735:Lss
|
UTSW |
10 |
76,382,615 (GRCm39) |
missense |
probably benign |
|
|