Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
T |
C |
7: 78,761,065 (GRCm39) |
W1926R |
probably damaging |
Het |
Arhgef25 |
T |
C |
10: 127,023,063 (GRCm39) |
T106A |
probably benign |
Het |
Baz1b |
G |
A |
5: 135,239,629 (GRCm39) |
R243Q |
probably damaging |
Het |
Cdhr3 |
A |
G |
12: 33,099,068 (GRCm39) |
Y508H |
probably benign |
Het |
Cyp2d9 |
T |
A |
15: 82,336,680 (GRCm39) |
W10R |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 50,013,858 (GRCm39) |
T1549A |
possibly damaging |
Het |
Dnah8 |
A |
T |
17: 31,070,705 (GRCm39) |
R4464W |
probably damaging |
Het |
Dpp4 |
G |
A |
2: 62,217,477 (GRCm39) |
T40M |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,607,654 (GRCm39) |
H2723R |
possibly damaging |
Het |
E2f3 |
C |
T |
13: 30,095,289 (GRCm39) |
S333N |
probably damaging |
Het |
Fam120a |
G |
T |
13: 49,121,069 (GRCm39) |
A79E |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,877,399 (GRCm39) |
S3405P |
probably benign |
Het |
Gaa |
T |
C |
11: 119,174,531 (GRCm39) |
S793P |
possibly damaging |
Het |
Galc |
A |
C |
12: 98,193,540 (GRCm39) |
F350V |
probably damaging |
Het |
Garre1 |
A |
G |
7: 33,955,916 (GRCm39) |
V391A |
possibly damaging |
Het |
Gm136 |
A |
G |
4: 34,746,541 (GRCm39) |
C157R |
probably damaging |
Het |
Gm3327 |
A |
C |
14: 44,363,720 (GRCm39) |
N108T |
unknown |
Het |
H2-M10.2 |
A |
G |
17: 36,596,771 (GRCm39) |
Y102H |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,490,972 (GRCm39) |
D4192E |
probably benign |
Het |
Hpse2 |
A |
C |
19: 43,001,482 (GRCm39) |
|
probably null |
Het |
Idh3a |
T |
C |
9: 54,510,633 (GRCm39) |
V362A |
probably benign |
Het |
Kdm7a |
A |
T |
6: 39,147,697 (GRCm39) |
|
probably null |
Het |
Lrba |
G |
A |
3: 86,439,394 (GRCm39) |
R1977H |
probably damaging |
Het |
Magi2 |
A |
T |
5: 19,883,750 (GRCm39) |
Y134F |
probably benign |
Het |
Mamdc4 |
T |
C |
2: 25,455,914 (GRCm39) |
Y801C |
probably damaging |
Het |
Maml1 |
T |
C |
11: 50,149,371 (GRCm39) |
T790A |
probably benign |
Het |
Map3k19 |
A |
G |
1: 127,750,823 (GRCm39) |
Y843H |
probably damaging |
Het |
Mdfic |
A |
T |
6: 15,741,041 (GRCm39) |
H45L |
possibly damaging |
Het |
Mlx |
C |
T |
11: 100,979,080 (GRCm39) |
T87I |
probably benign |
Het |
Mms22l |
T |
A |
4: 24,521,269 (GRCm39) |
I382K |
probably benign |
Het |
Mtf1 |
A |
G |
4: 124,732,697 (GRCm39) |
N585S |
probably benign |
Het |
Mylk2 |
C |
T |
2: 152,755,588 (GRCm39) |
P251S |
probably damaging |
Het |
Myorg |
A |
G |
4: 41,499,165 (GRCm39) |
V155A |
probably benign |
Het |
Nox4 |
A |
T |
7: 86,955,958 (GRCm39) |
T157S |
probably benign |
Het |
Oas2 |
A |
T |
5: 120,886,682 (GRCm39) |
H161Q |
probably benign |
Het |
Obscn |
A |
T |
11: 58,994,268 (GRCm39) |
V1563E |
probably damaging |
Het |
Or2n1b |
T |
C |
17: 38,460,322 (GRCm39) |
V281A |
possibly damaging |
Het |
Or55b3 |
T |
C |
7: 102,126,354 (GRCm39) |
K241R |
probably damaging |
Het |
Or6c203 |
A |
C |
10: 129,009,966 (GRCm39) |
F308C |
probably benign |
Het |
Pcdhb11 |
T |
A |
18: 37,555,375 (GRCm39) |
I235N |
probably benign |
Het |
Pcsk5 |
A |
T |
19: 17,443,522 (GRCm39) |
C1212* |
probably null |
Het |
Ptges |
C |
T |
2: 30,782,722 (GRCm39) |
G110D |
possibly damaging |
Het |
Rsph4a |
A |
T |
10: 33,784,094 (GRCm39) |
I239L |
possibly damaging |
Het |
Setx |
A |
G |
2: 29,034,813 (GRCm39) |
I433V |
probably benign |
Het |
Smyd4 |
T |
C |
11: 75,281,927 (GRCm39) |
S467P |
probably benign |
Het |
Snai2 |
A |
T |
16: 14,523,866 (GRCm39) |
H10L |
possibly damaging |
Het |
Snw1 |
T |
C |
12: 87,497,589 (GRCm39) |
I467V |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,883,420 (GRCm39) |
C301S |
probably damaging |
Het |
Tax1bp1 |
T |
A |
6: 52,735,342 (GRCm39) |
|
probably null |
Het |
Tmem70 |
C |
A |
1: 16,735,575 (GRCm39) |
P15Q |
probably benign |
Het |
Tmem87a |
T |
C |
2: 120,224,859 (GRCm39) |
E134G |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,200,516 (GRCm39) |
|
probably benign |
Het |
Ugt2b37 |
C |
T |
5: 87,402,569 (GRCm39) |
V21M |
probably damaging |
Het |
Ugt2b38 |
T |
A |
5: 87,569,551 (GRCm39) |
I259F |
probably damaging |
Het |
Zfp804a |
T |
A |
2: 82,066,188 (GRCm39) |
L53Q |
probably damaging |
Het |
|
Other mutations in Krt6b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Krt6b
|
APN |
15 |
101,588,267 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01653:Krt6b
|
APN |
15 |
101,587,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01900:Krt6b
|
APN |
15 |
101,585,981 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL03187:Krt6b
|
APN |
15 |
101,588,392 (GRCm39) |
missense |
probably benign |
|
R0511:Krt6b
|
UTSW |
15 |
101,586,042 (GRCm39) |
splice site |
probably benign |
|
R0788:Krt6b
|
UTSW |
15 |
101,585,954 (GRCm39) |
missense |
probably damaging |
0.96 |
R1370:Krt6b
|
UTSW |
15 |
101,585,987 (GRCm39) |
missense |
probably damaging |
0.96 |
R1481:Krt6b
|
UTSW |
15 |
101,586,809 (GRCm39) |
missense |
probably benign |
0.05 |
R2007:Krt6b
|
UTSW |
15 |
101,586,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Krt6b
|
UTSW |
15 |
101,586,999 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2166:Krt6b
|
UTSW |
15 |
101,587,050 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2227:Krt6b
|
UTSW |
15 |
101,587,557 (GRCm39) |
missense |
probably damaging |
0.96 |
R2495:Krt6b
|
UTSW |
15 |
101,586,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Krt6b
|
UTSW |
15 |
101,586,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R4969:Krt6b
|
UTSW |
15 |
101,588,460 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6301:Krt6b
|
UTSW |
15 |
101,587,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R6646:Krt6b
|
UTSW |
15 |
101,585,649 (GRCm39) |
missense |
probably damaging |
0.98 |
R7232:Krt6b
|
UTSW |
15 |
101,586,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7406:Krt6b
|
UTSW |
15 |
101,587,513 (GRCm39) |
missense |
probably benign |
0.04 |
R7414:Krt6b
|
UTSW |
15 |
101,587,449 (GRCm39) |
missense |
probably benign |
0.05 |
R7849:Krt6b
|
UTSW |
15 |
101,587,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Krt6b
|
UTSW |
15 |
101,588,577 (GRCm39) |
missense |
probably damaging |
0.96 |
R8348:Krt6b
|
UTSW |
15 |
101,586,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Krt6b
|
UTSW |
15 |
101,586,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R8736:Krt6b
|
UTSW |
15 |
101,587,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R9466:Krt6b
|
UTSW |
15 |
101,586,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9633:Krt6b
|
UTSW |
15 |
101,586,996 (GRCm39) |
missense |
probably benign |
0.00 |
R9720:Krt6b
|
UTSW |
15 |
101,588,226 (GRCm39) |
missense |
probably benign |
0.40 |
Z1177:Krt6b
|
UTSW |
15 |
101,586,767 (GRCm39) |
missense |
probably damaging |
1.00 |
|