Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
T |
C |
3: 36,123,920 (GRCm39) |
V75A |
probably benign |
Het |
Ace |
G |
C |
11: 105,865,652 (GRCm39) |
W628C |
probably damaging |
Het |
Adh4 |
T |
C |
3: 138,127,996 (GRCm39) |
S141P |
probably benign |
Het |
Apob |
T |
C |
12: 8,061,384 (GRCm39) |
Y3256H |
possibly damaging |
Het |
B3galnt1 |
G |
T |
3: 69,482,282 (GRCm39) |
N326K |
probably benign |
Het |
Bltp3a |
T |
G |
17: 28,095,964 (GRCm39) |
|
probably null |
Het |
Catsperb |
T |
C |
12: 101,516,070 (GRCm39) |
F569L |
probably damaging |
Het |
Cecr2 |
A |
G |
6: 120,732,478 (GRCm39) |
I225V |
probably benign |
Het |
Cox5b |
A |
G |
1: 36,731,510 (GRCm39) |
|
probably null |
Het |
Crybg1 |
T |
C |
10: 43,834,332 (GRCm39) |
D1953G |
probably damaging |
Het |
Dnaaf5 |
C |
T |
5: 139,167,215 (GRCm39) |
T707M |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Ebf1 |
G |
A |
11: 44,882,295 (GRCm39) |
R409Q |
probably damaging |
Het |
Eef2k |
G |
A |
7: 120,484,645 (GRCm39) |
A256T |
probably damaging |
Het |
Eef2k |
C |
A |
7: 120,484,646 (GRCm39) |
A256D |
probably damaging |
Het |
Evl |
C |
G |
12: 108,647,781 (GRCm39) |
T294S |
probably benign |
Het |
Eya2 |
T |
C |
2: 165,573,548 (GRCm39) |
Y288H |
probably damaging |
Het |
Ezh2 |
A |
T |
6: 47,509,014 (GRCm39) |
|
probably null |
Het |
Fam171a1 |
T |
C |
2: 3,226,426 (GRCm39) |
Y395H |
probably benign |
Het |
Gas2l3 |
C |
A |
10: 89,249,837 (GRCm39) |
R427L |
probably damaging |
Het |
Gli2 |
T |
A |
1: 118,783,233 (GRCm39) |
I91F |
probably damaging |
Het |
Gm4884 |
T |
C |
7: 40,692,318 (GRCm39) |
S96P |
probably damaging |
Het |
Gprc5d |
T |
A |
6: 135,093,031 (GRCm39) |
D292V |
probably benign |
Het |
Herc1 |
A |
G |
9: 66,355,505 (GRCm39) |
K2252R |
probably benign |
Het |
Il1rl1 |
A |
T |
1: 40,489,285 (GRCm39) |
M346L |
probably benign |
Het |
Kcng4 |
A |
T |
8: 120,352,617 (GRCm39) |
M431K |
possibly damaging |
Het |
Kifbp |
A |
T |
10: 62,414,020 (GRCm39) |
V46E |
probably damaging |
Het |
Large1 |
A |
G |
8: 73,774,937 (GRCm39) |
F258L |
possibly damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,852,662 (GRCm39) |
C1001S |
probably damaging |
Het |
Micu1 |
A |
G |
10: 59,663,054 (GRCm39) |
Q328R |
probably benign |
Het |
Mmp11 |
G |
A |
10: 75,761,290 (GRCm39) |
P437S |
probably damaging |
Het |
Msh6 |
T |
A |
17: 88,287,716 (GRCm39) |
F119I |
possibly damaging |
Het |
Myo6 |
A |
G |
9: 80,149,531 (GRCm39) |
E159G |
probably damaging |
Het |
Negr1 |
T |
A |
3: 156,721,833 (GRCm39) |
Y136N |
probably damaging |
Het |
Nol9 |
T |
A |
4: 152,130,428 (GRCm39) |
C321S |
probably damaging |
Het |
Nos1 |
T |
C |
5: 118,043,378 (GRCm39) |
F551S |
probably benign |
Het |
Nup153 |
C |
A |
13: 46,837,629 (GRCm39) |
G1198C |
probably damaging |
Het |
Omd |
T |
C |
13: 49,743,552 (GRCm39) |
S201P |
probably benign |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or1e35 |
T |
C |
11: 73,797,452 (GRCm39) |
I289V |
probably damaging |
Het |
Or4c120 |
C |
A |
2: 89,000,744 (GRCm39) |
V271F |
probably benign |
Het |
Or51l14 |
A |
G |
7: 103,100,919 (GRCm39) |
Y125C |
probably damaging |
Het |
Or51l14 |
C |
A |
7: 103,100,920 (GRCm39) |
Y125* |
probably null |
Het |
Oxct1 |
G |
T |
15: 4,064,832 (GRCm39) |
A57S |
probably benign |
Het |
Pcdhga7 |
T |
G |
18: 37,850,433 (GRCm39) |
S813R |
probably damaging |
Het |
Pcmtd2 |
A |
T |
2: 181,496,787 (GRCm39) |
I255F |
possibly damaging |
Het |
Pdk1 |
T |
G |
2: 71,713,913 (GRCm39) |
M186R |
possibly damaging |
Het |
Pelp1 |
T |
C |
11: 70,285,925 (GRCm39) |
T648A |
probably damaging |
Het |
Phldb2 |
A |
T |
16: 45,628,621 (GRCm39) |
S570R |
possibly damaging |
Het |
Pramel16 |
T |
A |
4: 143,675,690 (GRCm39) |
T379S |
probably benign |
Het |
Ptprj |
T |
C |
2: 90,299,992 (GRCm39) |
T270A |
possibly damaging |
Het |
Reln |
C |
T |
5: 22,160,179 (GRCm39) |
G2130D |
probably damaging |
Het |
Rims1 |
A |
T |
1: 22,358,844 (GRCm39) |
Y663* |
probably null |
Het |
Rit2 |
T |
C |
18: 31,286,817 (GRCm39) |
T123A |
probably benign |
Het |
Rmdn2 |
A |
T |
17: 79,975,418 (GRCm39) |
E302D |
probably benign |
Het |
Ryr1 |
T |
C |
7: 28,801,283 (GRCm39) |
E827G |
possibly damaging |
Het |
Siglec1 |
C |
T |
2: 130,923,264 (GRCm39) |
G494R |
probably damaging |
Het |
Slc16a14 |
T |
A |
1: 84,890,318 (GRCm39) |
Y329F |
probably damaging |
Het |
Slc35d1 |
A |
T |
4: 103,071,978 (GRCm39) |
L8Q |
possibly damaging |
Het |
Smpdl3a |
C |
T |
10: 57,677,163 (GRCm39) |
S57L |
possibly damaging |
Het |
Snx9 |
T |
C |
17: 5,978,528 (GRCm39) |
V566A |
probably damaging |
Het |
Spaca1 |
A |
T |
4: 34,029,095 (GRCm39) |
I126N |
probably damaging |
Het |
Spred1 |
T |
G |
2: 116,994,052 (GRCm39) |
I94S |
probably damaging |
Het |
Tardbp |
T |
C |
4: 148,706,494 (GRCm39) |
D105G |
possibly damaging |
Het |
Tet2 |
T |
C |
3: 133,182,326 (GRCm39) |
S1213G |
probably benign |
Het |
Trak1 |
A |
T |
9: 121,196,121 (GRCm39) |
|
probably benign |
Het |
Trem3 |
G |
A |
17: 48,556,756 (GRCm39) |
V76M |
possibly damaging |
Het |
Ttc13 |
G |
T |
8: 125,421,674 (GRCm39) |
Y250* |
probably null |
Het |
Ttll5 |
T |
G |
12: 85,969,819 (GRCm39) |
S714R |
possibly damaging |
Het |
Ube2l6 |
T |
G |
2: 84,633,220 (GRCm39) |
|
probably null |
Het |
Ubr3 |
T |
C |
2: 69,803,679 (GRCm39) |
S1090P |
probably damaging |
Het |
Vezt |
T |
C |
10: 93,806,372 (GRCm39) |
T680A |
probably benign |
Het |
Virma |
A |
G |
4: 11,546,297 (GRCm39) |
K1762E |
probably damaging |
Het |
Vps53 |
A |
G |
11: 76,057,074 (GRCm39) |
S57P |
probably damaging |
Het |
Vwa7 |
G |
T |
17: 35,236,822 (GRCm39) |
D130Y |
probably damaging |
Het |
Vwa8 |
T |
G |
14: 79,302,342 (GRCm39) |
F1004V |
probably damaging |
Het |
Zfp35 |
A |
T |
18: 24,137,194 (GRCm39) |
K513* |
probably null |
Het |
Zfp384 |
ACAGCAGCAGCAGCAGCAGCAGC |
ACAGCAGCAGCAGCAGCAGC |
6: 125,013,472 (GRCm39) |
|
probably benign |
Het |
Zfp521 |
C |
A |
18: 13,978,505 (GRCm39) |
C636F |
probably damaging |
Het |
|
Other mutations in Kcna5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02379:Kcna5
|
APN |
6 |
126,511,472 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Kcna5
|
UTSW |
6 |
126,510,386 (GRCm39) |
missense |
probably damaging |
0.98 |
R0137:Kcna5
|
UTSW |
6 |
126,510,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R0881:Kcna5
|
UTSW |
6 |
126,511,957 (GRCm39) |
missense |
probably benign |
|
R1436:Kcna5
|
UTSW |
6 |
126,511,724 (GRCm39) |
missense |
probably damaging |
0.99 |
R1561:Kcna5
|
UTSW |
6 |
126,511,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Kcna5
|
UTSW |
6 |
126,510,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Kcna5
|
UTSW |
6 |
126,510,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R3940:Kcna5
|
UTSW |
6 |
126,510,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R4276:Kcna5
|
UTSW |
6 |
126,510,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4372:Kcna5
|
UTSW |
6 |
126,510,320 (GRCm39) |
makesense |
probably null |
|
R4562:Kcna5
|
UTSW |
6 |
126,511,303 (GRCm39) |
missense |
probably benign |
0.00 |
R5130:Kcna5
|
UTSW |
6 |
126,511,496 (GRCm39) |
missense |
probably benign |
0.01 |
R5388:Kcna5
|
UTSW |
6 |
126,511,859 (GRCm39) |
missense |
probably benign |
0.04 |
R5890:Kcna5
|
UTSW |
6 |
126,511,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R7159:Kcna5
|
UTSW |
6 |
126,510,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Kcna5
|
UTSW |
6 |
126,510,806 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7322:Kcna5
|
UTSW |
6 |
126,510,754 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7353:Kcna5
|
UTSW |
6 |
126,511,808 (GRCm39) |
missense |
probably benign |
0.00 |
R7695:Kcna5
|
UTSW |
6 |
126,511,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7775:Kcna5
|
UTSW |
6 |
126,511,768 (GRCm39) |
nonsense |
probably null |
|
R7778:Kcna5
|
UTSW |
6 |
126,511,768 (GRCm39) |
nonsense |
probably null |
|
R7894:Kcna5
|
UTSW |
6 |
126,512,011 (GRCm39) |
missense |
probably damaging |
0.96 |
R7905:Kcna5
|
UTSW |
6 |
126,511,831 (GRCm39) |
missense |
probably benign |
|
R7961:Kcna5
|
UTSW |
6 |
126,510,517 (GRCm39) |
missense |
probably benign |
|
R8009:Kcna5
|
UTSW |
6 |
126,510,517 (GRCm39) |
missense |
probably benign |
|
R8388:Kcna5
|
UTSW |
6 |
126,511,588 (GRCm39) |
missense |
probably benign |
0.08 |
R9725:Kcna5
|
UTSW |
6 |
126,511,844 (GRCm39) |
missense |
probably benign |
|
Z1176:Kcna5
|
UTSW |
6 |
126,510,679 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Kcna5
|
UTSW |
6 |
126,510,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|