Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930516K23Rik |
A |
G |
7: 103,708,212 (GRCm39) |
I199T |
probably benign |
Het |
Adam23 |
T |
G |
1: 63,602,495 (GRCm39) |
|
probably null |
Het |
Adamts8 |
C |
T |
9: 30,865,787 (GRCm39) |
T445I |
probably benign |
Het |
Ahi1 |
T |
C |
10: 20,864,524 (GRCm39) |
V752A |
probably damaging |
Het |
Arfgef1 |
T |
C |
1: 10,223,903 (GRCm39) |
Q1465R |
probably damaging |
Het |
Arfgef1 |
G |
T |
1: 10,223,904 (GRCm39) |
Q1465K |
probably damaging |
Het |
Bicra |
T |
C |
7: 15,706,130 (GRCm39) |
E1437G |
probably damaging |
Het |
Cdc42ep4 |
C |
T |
11: 113,619,998 (GRCm39) |
S131N |
possibly damaging |
Het |
Ces1f |
G |
A |
8: 93,994,625 (GRCm39) |
P262L |
probably benign |
Het |
Chrna2 |
A |
T |
14: 66,388,398 (GRCm39) |
|
probably null |
Het |
Cspg4 |
G |
A |
9: 56,797,420 (GRCm39) |
V1295M |
possibly damaging |
Het |
D5Ertd579e |
T |
C |
5: 36,773,100 (GRCm39) |
T432A |
probably benign |
Het |
Dach1 |
A |
T |
14: 98,140,633 (GRCm39) |
S456R |
probably damaging |
Het |
Dhx37 |
T |
C |
5: 125,499,231 (GRCm39) |
D659G |
probably benign |
Het |
Dscaml1 |
T |
C |
9: 45,585,821 (GRCm39) |
V586A |
probably damaging |
Het |
Efhb |
G |
T |
17: 53,770,196 (GRCm39) |
L38I |
probably benign |
Het |
Fbxw10 |
T |
C |
11: 62,738,429 (GRCm39) |
S108P |
possibly damaging |
Het |
Fmnl2 |
A |
G |
2: 52,987,344 (GRCm39) |
N313S |
possibly damaging |
Het |
Gga3 |
T |
C |
11: 115,482,102 (GRCm39) |
E172G |
probably damaging |
Het |
Ggta1 |
A |
G |
2: 35,292,734 (GRCm39) |
V191A |
possibly damaging |
Het |
Golm1 |
ACTTCTTCT |
ACTTCT |
13: 59,797,390 (GRCm39) |
|
probably benign |
Het |
Hcn4 |
C |
T |
9: 58,731,228 (GRCm39) |
T145M |
unknown |
Het |
Kirrel3 |
T |
C |
9: 34,946,202 (GRCm39) |
S654P |
probably damaging |
Het |
Klrb1 |
A |
T |
6: 128,687,486 (GRCm39) |
|
probably null |
Het |
Lipk |
T |
A |
19: 34,017,794 (GRCm39) |
Y277* |
probably null |
Het |
Ly6g |
A |
C |
15: 75,030,398 (GRCm39) |
N49T |
possibly damaging |
Het |
Ms4a4c |
A |
T |
19: 11,392,191 (GRCm39) |
Q4L |
probably benign |
Het |
Nfya |
A |
C |
17: 48,699,932 (GRCm39) |
|
probably benign |
Het |
Nub1 |
T |
C |
5: 24,913,709 (GRCm39) |
V530A |
probably benign |
Het |
Ocln |
A |
T |
13: 100,675,796 (GRCm39) |
Y232* |
probably null |
Het |
Or10ag59 |
A |
G |
2: 87,405,857 (GRCm39) |
N143S |
possibly damaging |
Het |
Or2r2 |
A |
G |
6: 42,463,947 (GRCm39) |
F60S |
probably damaging |
Het |
Or4d2b |
C |
T |
11: 87,780,324 (GRCm39) |
V133I |
probably benign |
Het |
Or5b114-ps1 |
A |
G |
19: 13,352,815 (GRCm39) |
H163R |
unknown |
Het |
Otogl |
G |
A |
10: 107,649,911 (GRCm39) |
A1148V |
probably benign |
Het |
Paqr5 |
C |
T |
9: 61,880,113 (GRCm39) |
W46* |
probably null |
Het |
Psd2 |
C |
A |
18: 36,113,385 (GRCm39) |
L286M |
probably damaging |
Het |
Ptpn4 |
A |
T |
1: 119,612,311 (GRCm39) |
Y27* |
probably null |
Het |
Ripk2 |
A |
G |
4: 16,158,275 (GRCm39) |
|
probably null |
Het |
Rsf1 |
G |
GACGGCGGCA |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Sbk2 |
C |
T |
7: 4,967,146 (GRCm39) |
|
probably null |
Het |
Sec16a |
G |
A |
2: 26,320,498 (GRCm39) |
R1361C |
probably damaging |
Het |
Sspo |
A |
C |
6: 48,466,728 (GRCm39) |
D4072A |
probably benign |
Het |
St6galnac3 |
T |
C |
3: 152,912,345 (GRCm39) |
Y214C |
probably damaging |
Het |
Sugp1 |
T |
A |
8: 70,513,202 (GRCm39) |
D256E |
possibly damaging |
Het |
Sugt1 |
A |
G |
14: 79,834,847 (GRCm39) |
Y90C |
probably benign |
Het |
Taok2 |
A |
G |
7: 126,469,564 (GRCm39) |
I1088T |
probably damaging |
Het |
Tasor2 |
A |
T |
13: 3,624,819 (GRCm39) |
D1710E |
probably benign |
Het |
Tmc7 |
T |
A |
7: 118,146,901 (GRCm39) |
T459S |
probably benign |
Het |
Tmed11 |
T |
C |
5: 108,926,780 (GRCm39) |
Y164C |
probably damaging |
Het |
Tmem275 |
A |
G |
4: 115,755,491 (GRCm39) |
T97A |
unknown |
Het |
Tmem63b |
T |
C |
17: 45,977,558 (GRCm39) |
E356G |
probably benign |
Het |
Ttc13 |
T |
C |
8: 125,415,357 (GRCm39) |
I261V |
probably benign |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Vmn1r73 |
A |
T |
7: 11,490,544 (GRCm39) |
K121* |
probably null |
Het |
Zc3h12d |
A |
T |
10: 7,715,644 (GRCm39) |
S16C |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,807,812 (GRCm39) |
M1744K |
probably damaging |
Het |
|
Other mutations in Krt15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02194:Krt15
|
APN |
11 |
100,022,839 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02304:Krt15
|
APN |
11 |
100,024,503 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0361:Krt15
|
UTSW |
11 |
100,024,007 (GRCm39) |
missense |
probably benign |
0.13 |
R1562:Krt15
|
UTSW |
11 |
100,024,007 (GRCm39) |
missense |
probably benign |
0.13 |
R2113:Krt15
|
UTSW |
11 |
100,026,484 (GRCm39) |
missense |
unknown |
|
R4858:Krt15
|
UTSW |
11 |
100,022,897 (GRCm39) |
missense |
probably benign |
0.00 |
R5185:Krt15
|
UTSW |
11 |
100,024,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R7294:Krt15
|
UTSW |
11 |
100,022,848 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7371:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7372:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7389:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7390:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7391:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7392:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7420:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7421:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7423:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7424:Krt15
|
UTSW |
11 |
100,026,386 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9405:Krt15
|
UTSW |
11 |
100,022,961 (GRCm39) |
missense |
probably benign |
0.37 |
X0025:Krt15
|
UTSW |
11 |
100,026,343 (GRCm39) |
missense |
probably benign |
0.01 |
|