Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432M17Rik |
T |
C |
3: 121,473,172 (GRCm39) |
F109S |
unknown |
Het |
Ankhd1 |
A |
T |
18: 36,694,111 (GRCm39) |
|
probably null |
Het |
Atp8a1 |
C |
T |
5: 67,863,248 (GRCm39) |
|
probably null |
Het |
Ccdc136 |
G |
T |
6: 29,417,497 (GRCm39) |
V707F |
probably benign |
Het |
Ccdc157 |
A |
T |
11: 4,100,078 (GRCm39) |
C91* |
probably null |
Het |
Ceacam3 |
T |
A |
7: 16,892,296 (GRCm39) |
N346K |
possibly damaging |
Het |
Cfap251 |
A |
G |
5: 123,460,626 (GRCm39) |
D1196G |
probably benign |
Het |
Chd4 |
A |
G |
6: 125,077,551 (GRCm39) |
E74G |
probably damaging |
Het |
Cntn1 |
A |
G |
15: 92,192,892 (GRCm39) |
M665V |
probably benign |
Het |
Crtc2 |
C |
T |
3: 90,168,348 (GRCm39) |
Q364* |
probably null |
Het |
Csf1r |
T |
A |
18: 61,262,796 (GRCm39) |
I857N |
probably damaging |
Het |
Dner |
C |
T |
1: 84,558,460 (GRCm39) |
G168D |
probably damaging |
Het |
Edar |
T |
C |
10: 58,443,182 (GRCm39) |
T315A |
probably benign |
Het |
Egflam |
A |
G |
15: 7,333,493 (GRCm39) |
V153A |
probably damaging |
Het |
Enoph1 |
T |
C |
5: 100,211,682 (GRCm39) |
I193T |
possibly damaging |
Het |
Epc1 |
A |
G |
18: 6,462,969 (GRCm39) |
I9T |
probably damaging |
Het |
Fbxw18 |
T |
A |
9: 109,522,246 (GRCm39) |
I208F |
possibly damaging |
Het |
Gm4841 |
A |
G |
18: 60,403,364 (GRCm39) |
V243A |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,869,534 (GRCm39) |
V4297A |
probably damaging |
Het |
Itsn2 |
C |
T |
12: 4,677,960 (GRCm39) |
P106S |
probably benign |
Het |
Kcnu1 |
A |
G |
8: 26,352,486 (GRCm39) |
T218A |
probably damaging |
Het |
Kif1a |
A |
G |
1: 92,946,220 (GRCm39) |
S1677P |
probably damaging |
Het |
Meis3 |
T |
A |
7: 15,917,989 (GRCm39) |
V307E |
probably damaging |
Het |
Nadk2 |
A |
C |
15: 9,108,401 (GRCm39) |
I417L |
probably benign |
Het |
Nav2 |
AAGCAGCAGCAGCAGCAGCAGCAGCA |
AAGCAGCAGCAGCAGCAGCAGCA |
7: 49,058,440 (GRCm39) |
|
probably benign |
Het |
Neb |
A |
T |
2: 52,171,515 (GRCm39) |
N1659K |
probably benign |
Het |
Nhsl3 |
T |
C |
4: 129,118,005 (GRCm39) |
T208A |
possibly damaging |
Het |
Or10w1 |
T |
C |
19: 13,632,630 (GRCm39) |
V274A |
probably benign |
Het |
Or8g32 |
T |
C |
9: 39,305,785 (GRCm39) |
S233P |
probably damaging |
Het |
Or8s5 |
G |
A |
15: 98,238,246 (GRCm39) |
A208V |
probably benign |
Het |
Pde3b |
A |
T |
7: 114,093,772 (GRCm39) |
N339Y |
probably damaging |
Het |
Pde8b |
A |
G |
13: 95,223,361 (GRCm39) |
F298L |
possibly damaging |
Het |
Phtf1 |
G |
A |
3: 103,906,603 (GRCm39) |
R606H |
probably damaging |
Het |
Psd4 |
A |
G |
2: 24,290,528 (GRCm39) |
D535G |
possibly damaging |
Het |
Rad51ap1 |
A |
G |
6: 126,905,121 (GRCm39) |
V130A |
probably damaging |
Het |
Rbm11 |
T |
C |
16: 75,393,474 (GRCm39) |
F57L |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,671,401 (GRCm39) |
V1334A |
possibly damaging |
Het |
Satb2 |
T |
C |
1: 56,870,686 (GRCm39) |
E433G |
probably damaging |
Het |
Sema6b |
G |
A |
17: 56,435,413 (GRCm39) |
R277* |
probably null |
Het |
Sepsecs |
A |
T |
5: 52,805,015 (GRCm39) |
S349T |
probably benign |
Het |
Slc35b2 |
T |
C |
17: 45,877,424 (GRCm39) |
Y184H |
probably damaging |
Het |
Slc7a2 |
T |
C |
8: 41,368,067 (GRCm39) |
|
probably null |
Het |
Smc1b |
T |
A |
15: 84,955,066 (GRCm39) |
Y1062F |
probably benign |
Het |
Snrnp70 |
G |
A |
7: 45,026,476 (GRCm39) |
R298* |
probably null |
Het |
Sntb1 |
C |
G |
15: 55,506,191 (GRCm39) |
G461R |
probably damaging |
Het |
Taar8c |
A |
T |
10: 23,977,246 (GRCm39) |
C189S |
probably damaging |
Het |
Tas1r2 |
T |
A |
4: 139,382,672 (GRCm39) |
D103E |
probably damaging |
Het |
Timd2 |
T |
C |
11: 46,568,087 (GRCm39) |
I236V |
probably benign |
Het |
Tmem87a |
A |
G |
2: 120,208,407 (GRCm39) |
V316A |
probably damaging |
Het |
Treml2 |
T |
A |
17: 48,607,601 (GRCm39) |
L16Q |
probably damaging |
Het |
Zcchc14 |
G |
A |
8: 122,335,337 (GRCm39) |
|
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,013,178 (GRCm39) |
Y567H |
probably damaging |
Het |
Zfp551 |
G |
A |
7: 12,150,087 (GRCm39) |
R441* |
probably null |
Het |
Zfp930 |
A |
G |
8: 69,679,373 (GRCm39) |
I59M |
probably benign |
Het |
|
Other mutations in Krt14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01759:Krt14
|
APN |
11 |
100,095,242 (GRCm39) |
splice site |
probably benign |
|
R0449:Krt14
|
UTSW |
11 |
100,098,221 (GRCm39) |
missense |
unknown |
|
R0848:Krt14
|
UTSW |
11 |
100,095,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R1302:Krt14
|
UTSW |
11 |
100,094,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R2024:Krt14
|
UTSW |
11 |
100,098,044 (GRCm39) |
missense |
unknown |
|
R2088:Krt14
|
UTSW |
11 |
100,094,949 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2161:Krt14
|
UTSW |
11 |
100,097,939 (GRCm39) |
missense |
unknown |
|
R3878:Krt14
|
UTSW |
11 |
100,097,915 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5015:Krt14
|
UTSW |
11 |
100,098,032 (GRCm39) |
nonsense |
probably null |
|
R5474:Krt14
|
UTSW |
11 |
100,095,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Krt14
|
UTSW |
11 |
100,096,451 (GRCm39) |
missense |
probably benign |
0.44 |
R5707:Krt14
|
UTSW |
11 |
100,095,584 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6072:Krt14
|
UTSW |
11 |
100,097,992 (GRCm39) |
missense |
unknown |
|
R6523:Krt14
|
UTSW |
11 |
100,095,923 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6622:Krt14
|
UTSW |
11 |
100,094,786 (GRCm39) |
missense |
probably benign |
0.00 |
R7082:Krt14
|
UTSW |
11 |
100,094,167 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7239:Krt14
|
UTSW |
11 |
100,095,081 (GRCm39) |
missense |
probably benign |
0.03 |
R7350:Krt14
|
UTSW |
11 |
100,095,926 (GRCm39) |
nonsense |
probably null |
|
R8055:Krt14
|
UTSW |
11 |
100,095,584 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8233:Krt14
|
UTSW |
11 |
100,094,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R9043:Krt14
|
UTSW |
11 |
100,095,464 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9116:Krt14
|
UTSW |
11 |
100,095,904 (GRCm39) |
missense |
probably benign |
0.31 |
R9725:Krt14
|
UTSW |
11 |
100,097,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R9784:Krt14
|
UTSW |
11 |
100,097,966 (GRCm39) |
missense |
unknown |
|
X0020:Krt14
|
UTSW |
11 |
100,095,932 (GRCm39) |
critical splice acceptor site |
probably null |
|
|