Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4gnt |
T |
A |
9: 99,502,536 (GRCm39) |
M232K |
possibly damaging |
Het |
Abcc1 |
T |
C |
16: 14,222,927 (GRCm39) |
S243P |
probably damaging |
Het |
Acsl1 |
T |
C |
8: 46,974,486 (GRCm39) |
Y320H |
probably damaging |
Het |
Adam11 |
A |
G |
11: 102,653,090 (GRCm39) |
S61G |
probably benign |
Het |
Adamts1 |
G |
A |
16: 85,592,302 (GRCm39) |
T965I |
probably benign |
Het |
Adcyap1r1 |
T |
A |
6: 55,456,182 (GRCm39) |
M190K |
probably damaging |
Het |
Ankrd2 |
T |
A |
19: 42,033,358 (GRCm39) |
L300Q |
|
Het |
Ankrd27 |
A |
T |
7: 35,291,294 (GRCm39) |
Q30L |
possibly damaging |
Het |
Atp8b5 |
T |
A |
4: 43,305,798 (GRCm39) |
I114K |
probably damaging |
Het |
Atrn |
A |
T |
2: 130,786,809 (GRCm39) |
I205F |
probably damaging |
Het |
BC035947 |
A |
G |
1: 78,488,561 (GRCm39) |
|
probably benign |
Het |
Boc |
C |
T |
16: 44,311,692 (GRCm39) |
R677H |
|
Het |
Calhm6 |
A |
G |
10: 34,003,643 (GRCm39) |
F88S |
probably benign |
Het |
Ccdc121rt3 |
T |
A |
5: 112,502,939 (GRCm39) |
E255V |
probably benign |
Het |
Dpysl3 |
G |
T |
18: 43,462,922 (GRCm39) |
T485K |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,194,038 (GRCm39) |
D867G |
possibly damaging |
Het |
Fam178b |
G |
A |
1: 36,603,517 (GRCm39) |
T478I |
probably damaging |
Het |
Foxd2 |
G |
T |
4: 114,764,850 (GRCm39) |
T390K |
possibly damaging |
Het |
Furin |
A |
G |
7: 80,040,645 (GRCm39) |
V731A |
probably benign |
Het |
Grin2a |
T |
A |
16: 9,471,466 (GRCm39) |
I601F |
possibly damaging |
Het |
Hat1 |
G |
A |
2: 71,250,959 (GRCm39) |
R169Q |
possibly damaging |
Het |
Ighe |
G |
C |
12: 113,236,851 (GRCm39) |
Q6E |
|
Het |
Ighv8-2 |
T |
C |
12: 114,426,179 (GRCm39) |
I31V |
probably benign |
Het |
Klk1 |
A |
G |
7: 43,878,104 (GRCm39) |
D120G |
probably damaging |
Het |
Kmt2e |
A |
G |
5: 23,702,982 (GRCm39) |
D1054G |
probably benign |
Het |
Maco1 |
A |
T |
4: 134,557,993 (GRCm39) |
Y173* |
probably null |
Het |
Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
Mfsd4b1 |
T |
C |
10: 39,878,865 (GRCm39) |
E344G |
probably damaging |
Het |
Mns1 |
A |
G |
9: 72,346,556 (GRCm39) |
K13R |
probably benign |
Het |
Mrpl43 |
C |
T |
19: 44,994,346 (GRCm39) |
S91N |
probably benign |
Het |
Mtbp |
T |
C |
15: 55,481,032 (GRCm39) |
S706P |
probably benign |
Het |
Nelfb |
A |
T |
2: 25,095,145 (GRCm39) |
V348D |
probably damaging |
Het |
Or1l8 |
T |
A |
2: 36,817,416 (GRCm39) |
K237* |
probably null |
Het |
Or5p72 |
A |
T |
7: 108,021,924 (GRCm39) |
I49F |
probably benign |
Het |
Or7g20 |
C |
T |
9: 18,947,241 (GRCm39) |
A274V |
possibly damaging |
Het |
Or8k18 |
G |
A |
2: 86,085,428 (GRCm39) |
S203L |
probably benign |
Het |
Or8s8 |
T |
C |
15: 98,354,713 (GRCm39) |
I174T |
possibly damaging |
Het |
Pde6c |
T |
C |
19: 38,140,009 (GRCm39) |
I324T |
possibly damaging |
Het |
Phlpp2 |
T |
A |
8: 110,660,655 (GRCm39) |
L770* |
probably null |
Het |
Pik3c2b |
T |
A |
1: 133,019,338 (GRCm39) |
F1029I |
possibly damaging |
Het |
Rfx2 |
A |
T |
17: 57,087,890 (GRCm39) |
S500R |
probably benign |
Het |
Sarm1 |
T |
C |
11: 78,365,743 (GRCm39) |
M761V |
probably benign |
Het |
Serpina1a |
A |
G |
12: 103,822,140 (GRCm39) |
L264P |
possibly damaging |
Het |
Slc37a1 |
G |
T |
17: 31,556,965 (GRCm39) |
G377V |
probably damaging |
Het |
Slc38a4 |
T |
A |
15: 96,906,378 (GRCm39) |
M364L |
probably damaging |
Het |
Slc7a15 |
A |
G |
12: 8,580,280 (GRCm39) |
F384S |
probably benign |
Het |
Smyd4 |
T |
C |
11: 75,281,625 (GRCm39) |
V366A |
probably benign |
Het |
Spata31d1b |
T |
A |
13: 59,866,155 (GRCm39) |
V1101D |
possibly damaging |
Het |
Spata31d1e |
C |
T |
13: 59,890,498 (GRCm39) |
D441N |
possibly damaging |
Het |
Stab2 |
C |
A |
10: 86,757,997 (GRCm39) |
M1090I |
probably benign |
Het |
Tex15 |
C |
T |
8: 34,062,457 (GRCm39) |
T903I |
probably damaging |
Het |
Tgds |
A |
T |
14: 118,368,049 (GRCm39) |
Y41* |
probably null |
Het |
Tle4 |
G |
T |
19: 14,495,304 (GRCm39) |
H142N |
probably benign |
Het |
Tlx2 |
T |
C |
6: 83,046,274 (GRCm39) |
|
probably null |
Het |
Tmem151a |
C |
G |
19: 5,131,869 (GRCm39) |
A446P |
probably damaging |
Het |
Tmem205 |
A |
T |
9: 21,832,496 (GRCm39) |
D138E |
probably damaging |
Het |
Tmprss9 |
A |
G |
10: 80,734,042 (GRCm39) |
K1009E |
unknown |
Het |
Tnk2 |
T |
A |
16: 32,498,875 (GRCm39) |
C729* |
probably null |
Het |
Trim46 |
T |
A |
3: 89,142,399 (GRCm39) |
D696V |
probably damaging |
Het |
Tuba3b |
G |
A |
6: 145,564,482 (GRCm39) |
R84Q |
probably benign |
Het |
Unc119b |
C |
T |
5: 115,263,521 (GRCm39) |
D228N |
probably damaging |
Het |
Usp17la |
A |
G |
7: 104,510,864 (GRCm39) |
T490A |
probably benign |
Het |
Zfp267 |
T |
A |
3: 36,219,853 (GRCm39) |
C625* |
probably null |
Het |
Zfp687 |
C |
T |
3: 94,919,768 (GRCm39) |
M1I |
probably null |
Het |
Zfp729a |
T |
C |
13: 67,768,628 (GRCm39) |
T534A |
possibly damaging |
Het |
Zfp985 |
A |
T |
4: 147,668,047 (GRCm39) |
H305L |
probably benign |
Het |
Zscan10 |
C |
T |
17: 23,828,330 (GRCm39) |
Q291* |
probably null |
Het |
|
Other mutations in Lamp5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01544:Lamp5
|
APN |
2 |
135,910,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02145:Lamp5
|
APN |
2 |
135,901,509 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL03058:Lamp5
|
APN |
2 |
135,911,047 (GRCm39) |
missense |
probably benign |
0.03 |
R0392:Lamp5
|
UTSW |
2 |
135,902,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:Lamp5
|
UTSW |
2 |
135,900,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Lamp5
|
UTSW |
2 |
135,911,011 (GRCm39) |
missense |
probably benign |
0.03 |
R2862:Lamp5
|
UTSW |
2 |
135,900,866 (GRCm39) |
missense |
probably benign |
0.37 |
R3954:Lamp5
|
UTSW |
2 |
135,902,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4467:Lamp5
|
UTSW |
2 |
135,900,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R4686:Lamp5
|
UTSW |
2 |
135,900,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4745:Lamp5
|
UTSW |
2 |
135,902,786 (GRCm39) |
missense |
probably benign |
0.09 |
R6394:Lamp5
|
UTSW |
2 |
135,902,929 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6701:Lamp5
|
UTSW |
2 |
135,901,483 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6702:Lamp5
|
UTSW |
2 |
135,901,483 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6703:Lamp5
|
UTSW |
2 |
135,901,483 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6736:Lamp5
|
UTSW |
2 |
135,901,483 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7237:Lamp5
|
UTSW |
2 |
135,901,755 (GRCm39) |
missense |
probably benign |
0.29 |
R7347:Lamp5
|
UTSW |
2 |
135,902,878 (GRCm39) |
missense |
probably benign |
0.10 |
R8895:Lamp5
|
UTSW |
2 |
135,902,874 (GRCm39) |
missense |
probably benign |
0.00 |
R9051:Lamp5
|
UTSW |
2 |
135,911,054 (GRCm39) |
missense |
probably benign |
0.15 |
R9205:Lamp5
|
UTSW |
2 |
135,901,521 (GRCm39) |
missense |
probably damaging |
1.00 |
|