Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
C |
T |
6: 128,547,442 (GRCm39) |
E343K |
possibly damaging |
Het |
Abcc9 |
T |
C |
6: 142,571,763 (GRCm39) |
I1087V |
probably benign |
Het |
Bcam |
A |
C |
7: 19,494,042 (GRCm39) |
Y416* |
probably null |
Het |
Bhlhe22 |
T |
A |
3: 18,109,960 (GRCm39) |
C337S |
probably damaging |
Het |
Cerkl |
T |
C |
2: 79,223,364 (GRCm39) |
D119G |
probably benign |
Het |
Cog6 |
T |
C |
3: 52,909,825 (GRCm39) |
|
probably benign |
Het |
Dchs1 |
T |
C |
7: 105,408,312 (GRCm39) |
D1840G |
probably damaging |
Het |
Dhx16 |
G |
T |
17: 36,196,396 (GRCm39) |
M521I |
probably benign |
Het |
Dnaja2 |
A |
G |
8: 86,273,329 (GRCm39) |
I196T |
probably damaging |
Het |
Fbxw7 |
T |
C |
3: 84,811,369 (GRCm39) |
Y165H |
possibly damaging |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm3371 |
A |
G |
14: 44,646,178 (GRCm39) |
Y96H |
probably damaging |
Het |
H2-T10 |
G |
A |
17: 36,431,608 (GRCm39) |
A82V |
possibly damaging |
Het |
Hydin |
A |
G |
8: 111,217,350 (GRCm39) |
T1413A |
possibly damaging |
Het |
Krt23 |
T |
A |
11: 99,383,665 (GRCm39) |
M76L |
possibly damaging |
Het |
Lipe |
A |
T |
7: 25,082,701 (GRCm39) |
M504K |
possibly damaging |
Het |
Lrrc37 |
T |
A |
11: 103,503,759 (GRCm39) |
R560S |
probably benign |
Het |
Lta4h |
T |
A |
10: 93,307,232 (GRCm39) |
|
probably benign |
Het |
Ltbp2 |
T |
C |
12: 84,877,522 (GRCm39) |
T348A |
probably damaging |
Het |
Mybpc2 |
C |
A |
7: 44,159,322 (GRCm39) |
|
probably benign |
Het |
Or51r1 |
T |
C |
7: 102,227,734 (GRCm39) |
|
probably null |
Het |
Or52r1b |
T |
A |
7: 102,691,357 (GRCm39) |
S219T |
probably damaging |
Het |
Pdp2 |
G |
A |
8: 105,320,824 (GRCm39) |
M224I |
probably benign |
Het |
Pimreg |
C |
T |
11: 71,935,804 (GRCm39) |
|
probably benign |
Het |
Pld1 |
A |
T |
3: 28,178,766 (GRCm39) |
S887C |
probably damaging |
Het |
Ppp1r3g |
G |
A |
13: 36,152,978 (GRCm39) |
A133T |
possibly damaging |
Het |
Prpf8 |
G |
A |
11: 75,390,818 (GRCm39) |
G1323D |
probably damaging |
Het |
Rab3ip |
A |
G |
10: 116,773,300 (GRCm39) |
|
probably null |
Het |
Rpain |
A |
G |
11: 70,861,358 (GRCm39) |
H9R |
possibly damaging |
Het |
Scin |
T |
C |
12: 40,110,490 (GRCm39) |
|
probably benign |
Het |
Serpinb6d |
A |
G |
13: 33,855,369 (GRCm39) |
T348A |
probably benign |
Het |
Smad3 |
A |
G |
9: 63,664,835 (GRCm39) |
L42P |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r13 |
G |
A |
5: 109,322,085 (GRCm39) |
T204I |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,660,561 (GRCm39) |
N1272D |
probably damaging |
Het |
|
Other mutations in Smr3a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Smr3a
|
APN |
5 |
88,155,919 (GRCm39) |
utr 3 prime |
probably benign |
|
R0410:Smr3a
|
UTSW |
5 |
88,156,070 (GRCm39) |
intron |
probably benign |
|
R1817:Smr3a
|
UTSW |
5 |
88,155,917 (GRCm39) |
utr 3 prime |
probably benign |
|
R4166:Smr3a
|
UTSW |
5 |
88,156,013 (GRCm39) |
intron |
probably benign |
|
R4977:Smr3a
|
UTSW |
5 |
88,155,962 (GRCm39) |
critical splice donor site |
probably null |
|
R5367:Smr3a
|
UTSW |
5 |
88,155,897 (GRCm39) |
utr 3 prime |
probably benign |
|
R5933:Smr3a
|
UTSW |
5 |
88,155,873 (GRCm39) |
splice site |
probably null |
|
R6944:Smr3a
|
UTSW |
5 |
88,155,949 (GRCm39) |
utr 3 prime |
probably benign |
|
R7899:Smr3a
|
UTSW |
5 |
88,156,086 (GRCm39) |
missense |
unknown |
|
R8444:Smr3a
|
UTSW |
5 |
88,152,611 (GRCm39) |
missense |
unknown |
|
|