Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
T |
C |
14: 59,379,623 (GRCm39) |
N137S |
probably benign |
Het |
4930505A04Rik |
T |
A |
11: 30,404,880 (GRCm39) |
|
probably null |
Het |
Abcc8 |
A |
G |
7: 45,803,977 (GRCm39) |
I399T |
probably benign |
Het |
Aldh3b2 |
A |
C |
19: 4,029,461 (GRCm39) |
Q278P |
probably benign |
Het |
Baiap3 |
T |
C |
17: 25,469,096 (GRCm39) |
N229S |
probably benign |
Het |
Chrdl2 |
T |
C |
7: 99,666,292 (GRCm39) |
S71P |
possibly damaging |
Het |
Cmbl |
A |
G |
15: 31,585,541 (GRCm39) |
M142V |
possibly damaging |
Het |
Cpt1b |
A |
G |
15: 89,306,490 (GRCm39) |
|
probably null |
Het |
Crybg3 |
T |
C |
16: 59,378,651 (GRCm39) |
K868E |
probably benign |
Het |
Efl1 |
A |
G |
7: 82,411,986 (GRCm39) |
I792V |
probably benign |
Het |
Evx2 |
A |
G |
2: 74,486,321 (GRCm39) |
L356S |
probably benign |
Het |
Hspa14 |
C |
T |
2: 3,513,670 (GRCm39) |
|
probably null |
Het |
Ighv5-8 |
C |
T |
12: 113,618,813 (GRCm39) |
A76V |
unknown |
Het |
Il7r |
A |
G |
15: 9,516,504 (GRCm39) |
F99S |
probably damaging |
Het |
Klra2 |
A |
T |
6: 131,222,273 (GRCm39) |
V6D |
possibly damaging |
Het |
Lce3c |
T |
C |
3: 92,852,760 (GRCm39) |
S74P |
unknown |
Het |
Nectin2 |
C |
T |
7: 19,467,137 (GRCm39) |
|
probably null |
Het |
Nfil3 |
A |
G |
13: 53,121,849 (GRCm39) |
S352P |
probably benign |
Het |
Nme6 |
T |
A |
9: 109,664,394 (GRCm39) |
M1K |
probably null |
Het |
Or52z13 |
A |
T |
7: 103,247,404 (GRCm39) |
I294F |
probably damaging |
Het |
Otogl |
A |
G |
10: 107,722,326 (GRCm39) |
|
probably null |
Het |
Plcb1 |
T |
C |
2: 135,159,710 (GRCm39) |
V391A |
probably damaging |
Het |
Ptf1a |
T |
A |
2: 19,450,746 (GRCm39) |
D25E |
probably damaging |
Het |
Ralbp1 |
C |
T |
17: 66,159,748 (GRCm39) |
R505H |
probably benign |
Het |
Scube1 |
T |
C |
15: 83,492,492 (GRCm39) |
Y944C |
probably damaging |
Het |
Sdk2 |
A |
G |
11: 113,729,542 (GRCm39) |
I1039T |
probably benign |
Het |
Senp7 |
G |
T |
16: 55,990,190 (GRCm39) |
W646L |
possibly damaging |
Het |
Sphkap |
A |
T |
1: 83,253,797 (GRCm39) |
N1317K |
probably benign |
Het |
Strc |
G |
T |
2: 121,209,490 (GRCm39) |
Q278K |
probably benign |
Het |
Tbc1d30 |
T |
A |
10: 121,183,013 (GRCm39) |
R142* |
probably null |
Het |
Tmtc3 |
T |
C |
10: 100,282,808 (GRCm39) |
I916V |
probably damaging |
Het |
Tomm40l |
A |
T |
1: 171,048,776 (GRCm39) |
H79Q |
probably damaging |
Het |
Txndc12 |
T |
A |
4: 108,713,420 (GRCm39) |
|
probably null |
Het |
Vmn2r2 |
T |
C |
3: 64,044,858 (GRCm39) |
N96S |
probably damaging |
Het |
Vmn2r27 |
T |
C |
6: 124,168,776 (GRCm39) |
T785A |
possibly damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zfp462 |
A |
G |
4: 55,011,862 (GRCm39) |
D1276G |
probably damaging |
Het |
|
Other mutations in Arl8b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01919:Arl8b
|
APN |
6 |
108,798,518 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03135:Arl8b
|
APN |
6 |
108,795,506 (GRCm39) |
missense |
probably benign |
0.10 |
R0486:Arl8b
|
UTSW |
6 |
108,792,287 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0544:Arl8b
|
UTSW |
6 |
108,760,189 (GRCm39) |
start gained |
probably benign |
|
R1018:Arl8b
|
UTSW |
6 |
108,795,572 (GRCm39) |
missense |
probably damaging |
0.98 |
R2248:Arl8b
|
UTSW |
6 |
108,760,304 (GRCm39) |
missense |
probably benign |
0.00 |
R2351:Arl8b
|
UTSW |
6 |
108,798,484 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3815:Arl8b
|
UTSW |
6 |
108,790,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R3816:Arl8b
|
UTSW |
6 |
108,790,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Arl8b
|
UTSW |
6 |
108,760,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6480:Arl8b
|
UTSW |
6 |
108,792,010 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7147:Arl8b
|
UTSW |
6 |
108,791,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R8478:Arl8b
|
UTSW |
6 |
108,760,285 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8828:Arl8b
|
UTSW |
6 |
108,792,250 (GRCm39) |
missense |
probably benign |
0.00 |
|