Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
C |
A |
11: 9,265,416 (GRCm39) |
F3030L |
probably benign |
Het |
Abca13 |
A |
T |
11: 9,347,841 (GRCm39) |
I3565F |
probably damaging |
Het |
Ak7 |
A |
T |
12: 105,708,600 (GRCm39) |
I352F |
probably damaging |
Het |
Alkal2 |
G |
T |
12: 30,934,850 (GRCm39) |
G23V |
probably damaging |
Het |
Anapc7 |
C |
T |
5: 122,566,342 (GRCm39) |
P84S |
probably benign |
Het |
Apol7a |
A |
T |
15: 77,273,547 (GRCm39) |
I305N |
probably damaging |
Het |
Asf1b |
C |
T |
8: 84,694,559 (GRCm39) |
R108C |
probably damaging |
Het |
Bicd1 |
A |
T |
6: 149,421,989 (GRCm39) |
E903D |
probably benign |
Het |
Bpifb3 |
A |
T |
2: 153,767,715 (GRCm39) |
I263F |
probably benign |
Het |
Cavin3 |
T |
A |
7: 105,130,228 (GRCm39) |
S195C |
probably damaging |
Het |
Chsy3 |
C |
A |
18: 59,312,585 (GRCm39) |
R353S |
probably damaging |
Het |
Col5a2 |
A |
G |
1: 45,481,890 (GRCm39) |
V78A |
unknown |
Het |
Cpxm1 |
C |
T |
2: 130,236,146 (GRCm39) |
E339K |
probably damaging |
Het |
Cyp26c1 |
G |
T |
19: 37,675,660 (GRCm39) |
A175S |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,327,489 (GRCm39) |
T2069S |
probably benign |
Het |
Ednrb |
A |
G |
14: 104,057,383 (GRCm39) |
F393S |
probably damaging |
Het |
Fstl4 |
T |
C |
11: 53,053,502 (GRCm39) |
S385P |
possibly damaging |
Het |
Gabpb2 |
G |
A |
3: 95,112,109 (GRCm39) |
S40L |
probably damaging |
Het |
Gabrb1 |
T |
C |
5: 72,187,172 (GRCm39) |
I155T |
probably damaging |
Het |
Hc |
T |
A |
2: 34,873,731 (GRCm39) |
N1668Y |
probably benign |
Het |
Kcnh1 |
A |
G |
1: 192,117,124 (GRCm39) |
H670R |
probably damaging |
Het |
Lrfn2 |
T |
A |
17: 49,403,851 (GRCm39) |
M658K |
possibly damaging |
Het |
Lrrc1 |
T |
A |
9: 77,365,129 (GRCm39) |
N184I |
probably damaging |
Het |
Lrrc69 |
T |
C |
4: 14,795,994 (GRCm39) |
I18V |
probably benign |
Het |
Lvrn |
G |
A |
18: 46,983,289 (GRCm39) |
V11M |
probably damaging |
Het |
Map4k4 |
T |
C |
1: 40,063,801 (GRCm39) |
S1199P |
possibly damaging |
Het |
Mib1 |
T |
C |
18: 10,768,233 (GRCm39) |
|
probably null |
Het |
Mpv17l |
A |
T |
16: 13,758,863 (GRCm39) |
I96L |
probably benign |
Het |
Myo18b |
C |
T |
5: 112,908,259 (GRCm39) |
V2005I |
possibly damaging |
Het |
Myo6 |
T |
A |
9: 80,162,206 (GRCm39) |
H314Q |
unknown |
Het |
Nat8f6 |
A |
C |
6: 85,785,888 (GRCm39) |
M87R |
probably benign |
Het |
Net1 |
A |
G |
13: 3,943,458 (GRCm39) |
|
probably benign |
Het |
Notch4 |
C |
T |
17: 34,787,228 (GRCm39) |
T294I |
possibly damaging |
Het |
Nrros |
A |
G |
16: 31,966,456 (GRCm39) |
L36P |
probably damaging |
Het |
Or8b12i |
T |
C |
9: 20,082,037 (GRCm39) |
M277V |
probably benign |
Het |
Or8c9 |
G |
C |
9: 38,241,231 (GRCm39) |
W113S |
probably benign |
Het |
Padi3 |
T |
C |
4: 140,525,407 (GRCm39) |
H202R |
probably damaging |
Het |
Pik3ap1 |
A |
T |
19: 41,316,538 (GRCm39) |
M284K |
probably damaging |
Het |
Prr27 |
C |
A |
5: 87,990,710 (GRCm39) |
Y107* |
probably null |
Het |
Rab5c |
G |
T |
11: 100,607,609 (GRCm39) |
N188K |
probably damaging |
Het |
Rlf |
A |
T |
4: 121,005,532 (GRCm39) |
S1259R |
probably damaging |
Het |
Rrm2 |
T |
C |
12: 24,762,751 (GRCm39) |
V298A |
probably damaging |
Het |
Rtn4rl2 |
A |
T |
2: 84,711,033 (GRCm39) |
L77H |
possibly damaging |
Het |
Skint4 |
A |
G |
4: 111,975,173 (GRCm39) |
I44M |
probably damaging |
Het |
Spaca7 |
T |
C |
8: 12,648,998 (GRCm39) |
I164T |
probably benign |
Het |
Spg7 |
A |
G |
8: 123,800,568 (GRCm39) |
S153G |
probably damaging |
Het |
Spink5 |
T |
C |
18: 44,123,786 (GRCm39) |
S358P |
probably benign |
Het |
Stx5a |
T |
C |
19: 8,732,462 (GRCm39) |
M377T |
unknown |
Het |
Tchh |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
3: 93,354,015 (GRCm39) |
|
probably benign |
Het |
Ttc41 |
A |
G |
10: 86,599,844 (GRCm39) |
D1048G |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,557,509 (GRCm39) |
W29862R |
probably damaging |
Het |
Vmn1r203 |
T |
G |
13: 22,709,154 (GRCm39) |
*312G |
probably null |
Het |
Vmn2r74 |
T |
G |
7: 85,601,914 (GRCm39) |
T575P |
possibly damaging |
Het |
Zfp14 |
A |
T |
7: 29,738,579 (GRCm39) |
N135K |
possibly damaging |
Het |
|
Other mutations in Krt31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02313:Krt31
|
APN |
11 |
99,939,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02433:Krt31
|
APN |
11 |
99,939,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R0393:Krt31
|
UTSW |
11 |
99,941,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R0667:Krt31
|
UTSW |
11 |
99,938,951 (GRCm39) |
missense |
probably benign |
0.02 |
R1224:Krt31
|
UTSW |
11 |
99,940,690 (GRCm39) |
critical splice donor site |
probably null |
|
R1544:Krt31
|
UTSW |
11 |
99,938,699 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1891:Krt31
|
UTSW |
11 |
99,938,634 (GRCm39) |
missense |
probably damaging |
0.98 |
R1940:Krt31
|
UTSW |
11 |
99,939,069 (GRCm39) |
missense |
probably benign |
0.03 |
R1987:Krt31
|
UTSW |
11 |
99,940,406 (GRCm39) |
missense |
probably benign |
0.00 |
R2761:Krt31
|
UTSW |
11 |
99,938,691 (GRCm39) |
missense |
probably benign |
0.01 |
R2870:Krt31
|
UTSW |
11 |
99,938,699 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2870:Krt31
|
UTSW |
11 |
99,938,699 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3980:Krt31
|
UTSW |
11 |
99,939,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R4809:Krt31
|
UTSW |
11 |
99,940,748 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4822:Krt31
|
UTSW |
11 |
99,938,610 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4931:Krt31
|
UTSW |
11 |
99,940,983 (GRCm39) |
missense |
probably benign |
0.05 |
R6146:Krt31
|
UTSW |
11 |
99,939,056 (GRCm39) |
missense |
probably benign |
0.21 |
R6722:Krt31
|
UTSW |
11 |
99,939,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R6811:Krt31
|
UTSW |
11 |
99,939,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6996:Krt31
|
UTSW |
11 |
99,938,558 (GRCm39) |
missense |
probably benign |
0.19 |
R7300:Krt31
|
UTSW |
11 |
99,938,612 (GRCm39) |
missense |
probably damaging |
0.96 |
R7548:Krt31
|
UTSW |
11 |
99,940,346 (GRCm39) |
missense |
probably damaging |
0.98 |
X0028:Krt31
|
UTSW |
11 |
99,938,534 (GRCm39) |
missense |
probably damaging |
1.00 |
|