Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
A2ml1 |
T |
A |
6: 128,526,799 (GRCm39) |
K1071* |
probably null |
Het |
Abca13 |
G |
T |
11: 9,247,752 (GRCm39) |
V2500F |
possibly damaging |
Het |
Adamdec1 |
T |
C |
14: 68,816,633 (GRCm39) |
E85G |
probably damaging |
Het |
Aldh8a1 |
T |
C |
10: 21,264,970 (GRCm39) |
V199A |
probably benign |
Het |
Aoc2 |
G |
A |
11: 101,216,627 (GRCm39) |
V237M |
probably damaging |
Het |
Aplp2 |
C |
T |
9: 31,062,240 (GRCm39) |
R672H |
probably damaging |
Het |
Apob |
A |
G |
12: 8,045,513 (GRCm39) |
N886S |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,718,279 (GRCm39) |
R1991* |
probably null |
Het |
Atp6v1a |
T |
C |
16: 43,927,303 (GRCm39) |
Y328C |
probably damaging |
Het |
Bag4 |
T |
C |
8: 26,267,521 (GRCm39) |
Y103C |
probably damaging |
Het |
Crem |
C |
T |
18: 3,267,673 (GRCm39) |
R190Q |
probably damaging |
Het |
Crybg1 |
A |
G |
10: 43,832,756 (GRCm39) |
S2000P |
probably damaging |
Het |
Cubn |
T |
A |
2: 13,329,995 (GRCm39) |
T2629S |
probably benign |
Het |
Cyp3a44 |
G |
T |
5: 145,714,756 (GRCm39) |
S465Y |
probably damaging |
Het |
Daam2 |
A |
C |
17: 49,793,525 (GRCm39) |
F331V |
probably damaging |
Het |
Dscam |
A |
G |
16: 96,451,191 (GRCm39) |
|
probably null |
Het |
Fam184b |
G |
A |
5: 45,740,238 (GRCm39) |
S316L |
probably benign |
Het |
Fat2 |
G |
C |
11: 55,144,760 (GRCm39) |
T4038S |
probably damaging |
Het |
Fbxl19 |
C |
T |
7: 127,360,437 (GRCm39) |
R439C |
probably damaging |
Het |
Gm3454 |
T |
A |
15: 75,183,448 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch3 |
A |
G |
4: 133,305,617 (GRCm39) |
E284G |
probably benign |
Het |
Grm1 |
A |
T |
10: 10,595,549 (GRCm39) |
I693N |
probably damaging |
Het |
Gsdme |
T |
A |
6: 50,222,934 (GRCm39) |
Q127L |
probably damaging |
Het |
Ifnlr1 |
A |
G |
4: 135,432,937 (GRCm39) |
K458E |
probably benign |
Het |
Kcns2 |
T |
C |
15: 34,839,080 (GRCm39) |
F148L |
probably benign |
Het |
Lama1 |
A |
G |
17: 68,057,638 (GRCm39) |
T571A |
probably benign |
Het |
Loxhd1 |
G |
A |
18: 77,469,254 (GRCm39) |
V108M |
probably damaging |
Het |
Mef2c |
A |
T |
13: 83,810,478 (GRCm39) |
T375S |
probably benign |
Het |
Ncor1 |
A |
T |
11: 62,264,147 (GRCm39) |
D144E |
possibly damaging |
Het |
Nos3 |
A |
T |
5: 24,584,809 (GRCm39) |
T738S |
probably benign |
Het |
Nrxn2 |
A |
T |
19: 6,567,162 (GRCm39) |
T1353S |
probably damaging |
Het |
Or2b7 |
G |
T |
13: 21,740,077 (GRCm39) |
S38R |
probably benign |
Het |
Or4f4b |
T |
C |
2: 111,314,195 (GRCm39) |
L140P |
probably damaging |
Het |
Or8g17 |
A |
G |
9: 38,930,261 (GRCm39) |
I192T |
probably benign |
Het |
Pfpl |
A |
G |
19: 12,406,747 (GRCm39) |
T333A |
probably damaging |
Het |
Postn |
A |
T |
3: 54,284,137 (GRCm39) |
I565F |
possibly damaging |
Het |
Ppef2 |
A |
G |
5: 92,378,383 (GRCm39) |
V604A |
probably benign |
Het |
Pramel13 |
A |
C |
4: 144,119,598 (GRCm39) |
I323S |
possibly damaging |
Het |
Prmt1 |
A |
G |
7: 44,626,526 (GRCm39) |
|
probably null |
Het |
Rel |
A |
G |
11: 23,692,684 (GRCm39) |
S450P |
probably benign |
Het |
Rpap2 |
A |
C |
5: 107,745,661 (GRCm39) |
D3A |
probably damaging |
Het |
Shisa9 |
T |
C |
16: 11,802,772 (GRCm39) |
F110L |
possibly damaging |
Het |
Slc25a10 |
A |
T |
11: 120,385,784 (GRCm39) |
|
probably null |
Het |
Slx4 |
A |
T |
16: 3,798,021 (GRCm39) |
F1454L |
probably damaging |
Het |
Smc1b |
A |
T |
15: 84,950,430 (GRCm39) |
V1198D |
possibly damaging |
Het |
Supt5 |
T |
C |
7: 28,015,600 (GRCm39) |
Y879C |
probably damaging |
Het |
Tbx15 |
T |
C |
3: 99,259,833 (GRCm39) |
M568T |
probably benign |
Het |
Tle4 |
T |
C |
19: 14,429,472 (GRCm39) |
H698R |
possibly damaging |
Het |
Trappc9 |
T |
C |
15: 72,797,379 (GRCm39) |
N803D |
probably benign |
Het |
Trim10 |
A |
T |
17: 37,182,606 (GRCm39) |
R157S |
possibly damaging |
Het |
Wsb1 |
T |
C |
11: 79,131,025 (GRCm39) |
|
probably benign |
Het |
Zfp106 |
T |
C |
2: 120,365,874 (GRCm39) |
S178G |
probably benign |
Het |
Zftraf1 |
C |
T |
15: 76,543,058 (GRCm39) |
R34Q |
probably damaging |
Het |
|
Other mutations in Dnajc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01543:Dnajc3
|
APN |
14 |
119,198,274 (GRCm39) |
critical splice donor site |
probably null |
|
ghostly
|
UTSW |
14 |
119,208,192 (GRCm39) |
nonsense |
probably null |
|
vanishing
|
UTSW |
14 |
119,209,799 (GRCm39) |
nonsense |
probably null |
|
R1438:Dnajc3
|
UTSW |
14 |
119,205,518 (GRCm39) |
missense |
probably benign |
|
R1712:Dnajc3
|
UTSW |
14 |
119,195,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Dnajc3
|
UTSW |
14 |
119,210,114 (GRCm39) |
missense |
probably benign |
|
R2261:Dnajc3
|
UTSW |
14 |
119,198,232 (GRCm39) |
missense |
probably damaging |
0.98 |
R2262:Dnajc3
|
UTSW |
14 |
119,198,232 (GRCm39) |
missense |
probably damaging |
0.98 |
R2307:Dnajc3
|
UTSW |
14 |
119,190,633 (GRCm39) |
critical splice donor site |
probably null |
|
R4963:Dnajc3
|
UTSW |
14 |
119,215,585 (GRCm39) |
missense |
probably benign |
0.06 |
R4996:Dnajc3
|
UTSW |
14 |
119,209,839 (GRCm39) |
missense |
probably benign |
|
R5398:Dnajc3
|
UTSW |
14 |
119,209,799 (GRCm39) |
nonsense |
probably null |
|
R5539:Dnajc3
|
UTSW |
14 |
119,208,159 (GRCm39) |
missense |
probably damaging |
0.98 |
R5988:Dnajc3
|
UTSW |
14 |
119,195,376 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6032:Dnajc3
|
UTSW |
14 |
119,205,443 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7361:Dnajc3
|
UTSW |
14 |
119,175,576 (GRCm39) |
missense |
probably benign |
0.01 |
R7486:Dnajc3
|
UTSW |
14 |
119,209,816 (GRCm39) |
missense |
probably benign |
0.01 |
R8086:Dnajc3
|
UTSW |
14 |
119,208,192 (GRCm39) |
nonsense |
probably null |
|
R8092:Dnajc3
|
UTSW |
14 |
119,207,994 (GRCm39) |
splice site |
probably null |
|
R8517:Dnajc3
|
UTSW |
14 |
119,190,589 (GRCm39) |
nonsense |
probably null |
|
R9685:Dnajc3
|
UTSW |
14 |
119,209,775 (GRCm39) |
missense |
probably benign |
0.41 |
|