Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
A |
G |
16: 16,939,260 (GRCm39) |
L41P |
probably damaging |
Het |
Aff4 |
C |
T |
11: 53,290,446 (GRCm39) |
L469F |
probably damaging |
Het |
AI182371 |
G |
A |
2: 34,975,366 (GRCm39) |
H288Y |
probably benign |
Het |
AK157302 |
A |
T |
13: 21,679,827 (GRCm39) |
K118* |
probably null |
Het |
Arhgef2 |
G |
A |
3: 88,543,351 (GRCm39) |
R454Q |
probably damaging |
Het |
Asb17 |
C |
T |
3: 153,550,322 (GRCm39) |
T118M |
probably damaging |
Het |
Atp7b |
A |
G |
8: 22,503,600 (GRCm39) |
V718A |
possibly damaging |
Het |
Cdca2 |
A |
G |
14: 67,952,287 (GRCm39) |
L28S |
probably damaging |
Het |
Cdh20 |
G |
T |
1: 109,976,594 (GRCm39) |
L86F |
probably damaging |
Het |
Cela2a |
A |
T |
4: 141,545,350 (GRCm39) |
|
probably null |
Het |
Cers3 |
T |
A |
7: 66,433,162 (GRCm39) |
Y160N |
probably damaging |
Het |
Chmp2b |
A |
G |
16: 65,343,877 (GRCm39) |
V56A |
probably benign |
Het |
Cryl1 |
A |
G |
14: 57,635,880 (GRCm39) |
V9A |
unknown |
Het |
Dmbt1 |
A |
T |
7: 130,699,305 (GRCm39) |
H978L |
possibly damaging |
Het |
Dnm1 |
C |
T |
2: 32,204,949 (GRCm39) |
V673M |
probably damaging |
Het |
Dtx4 |
T |
A |
19: 12,462,646 (GRCm39) |
K378* |
probably null |
Het |
Extl1 |
A |
T |
4: 134,090,491 (GRCm39) |
M328K |
possibly damaging |
Het |
Fcgbp |
T |
C |
7: 27,806,628 (GRCm39) |
S2199P |
probably benign |
Het |
Glis3 |
G |
T |
19: 28,508,702 (GRCm39) |
N427K |
probably benign |
Het |
Hdac7 |
T |
C |
15: 97,691,944 (GRCm39) |
K810E |
probably benign |
Het |
Hesx1 |
A |
G |
14: 26,723,434 (GRCm39) |
E88G |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,350,361 (GRCm39) |
Q5086L |
possibly damaging |
Het |
Ier3 |
A |
G |
17: 36,133,101 (GRCm39) |
T128A |
probably benign |
Het |
Igsf10 |
G |
T |
3: 59,239,101 (GRCm39) |
T360K |
probably damaging |
Het |
Ilkap |
A |
C |
1: 91,312,345 (GRCm39) |
C2G |
possibly damaging |
Het |
Itih1 |
A |
G |
14: 30,660,028 (GRCm39) |
F231S |
probably damaging |
Het |
Jrkl |
A |
T |
9: 13,244,913 (GRCm39) |
Y249* |
probably null |
Het |
Kat6a |
AGAGGAGGAGGAGGAGGAGGAGGAG |
AGAGGAGGAGGAGGAGGAGGAG |
8: 23,425,663 (GRCm39) |
|
probably benign |
Het |
Kcnh5 |
T |
A |
12: 74,945,230 (GRCm39) |
|
probably null |
Het |
Kcnj11 |
G |
T |
7: 45,748,781 (GRCm39) |
L181I |
probably damaging |
Het |
Klhl2 |
T |
C |
8: 65,202,804 (GRCm39) |
T465A |
probably benign |
Het |
Krt90 |
T |
A |
15: 101,471,046 (GRCm39) |
Y72F |
probably benign |
Het |
Lig4 |
G |
A |
8: 10,022,766 (GRCm39) |
T338I |
probably benign |
Het |
Lrrc37 |
T |
C |
11: 103,511,285 (GRCm39) |
T228A |
unknown |
Het |
Magel2 |
T |
C |
7: 62,030,540 (GRCm39) |
V1148A |
unknown |
Het |
Mak |
C |
A |
13: 41,186,020 (GRCm39) |
E549D |
probably benign |
Het |
Marf1 |
G |
T |
16: 13,950,293 (GRCm39) |
S1001Y |
probably damaging |
Het |
Mcoln1 |
G |
A |
8: 3,561,787 (GRCm39) |
V446I |
probably damaging |
Het |
Meig1 |
T |
C |
2: 3,410,290 (GRCm39) |
N70S |
probably benign |
Het |
Mfsd14a |
G |
A |
3: 116,441,479 (GRCm39) |
T108I |
probably damaging |
Het |
Mocs1 |
G |
A |
17: 49,761,386 (GRCm39) |
M493I |
probably damaging |
Het |
Mrpl11 |
C |
A |
19: 5,012,497 (GRCm39) |
A26E |
probably damaging |
Het |
Myh6 |
A |
T |
14: 55,191,251 (GRCm39) |
D863E |
probably benign |
Het |
Myom2 |
T |
A |
8: 15,134,555 (GRCm39) |
Y453N |
probably damaging |
Het |
Nhlh1 |
A |
G |
1: 171,881,524 (GRCm39) |
I114T |
probably damaging |
Het |
Odr4 |
A |
G |
1: 150,258,086 (GRCm39) |
V183A |
possibly damaging |
Het |
Or12j4 |
A |
C |
7: 140,046,504 (GRCm39) |
H130P |
probably benign |
Het |
Or2y3 |
G |
T |
17: 38,393,071 (GRCm39) |
P266Q |
probably damaging |
Het |
Or4k5 |
A |
T |
14: 50,386,154 (GRCm39) |
M59K |
probably damaging |
Het |
Or5k17 |
G |
T |
16: 58,746,486 (GRCm39) |
F149L |
probably benign |
Het |
Or5p80 |
C |
G |
7: 108,229,984 (GRCm39) |
P262A |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,764,309 (GRCm39) |
S976P |
probably benign |
Het |
Pde3a |
G |
A |
6: 141,429,640 (GRCm39) |
E734K |
possibly damaging |
Het |
Pdzd2 |
A |
T |
15: 12,375,879 (GRCm39) |
S1419T |
probably benign |
Het |
Pdzd8 |
T |
A |
19: 59,288,853 (GRCm39) |
Y849F |
probably damaging |
Het |
Phldb3 |
A |
G |
7: 24,312,070 (GRCm39) |
E128G |
probably damaging |
Het |
Polg |
A |
G |
7: 79,111,468 (GRCm39) |
I261T |
possibly damaging |
Het |
Ppp1r35 |
T |
C |
5: 137,778,267 (GRCm39) |
M254T |
probably benign |
Het |
Ppp3ca |
G |
T |
3: 136,596,211 (GRCm39) |
R292M |
possibly damaging |
Het |
Ptk7 |
T |
A |
17: 46,890,543 (GRCm39) |
T430S |
probably benign |
Het |
Ptrh1 |
T |
A |
2: 32,667,040 (GRCm39) |
N144K |
possibly damaging |
Het |
Rbfox1 |
A |
G |
16: 7,111,946 (GRCm39) |
T211A |
possibly damaging |
Het |
Rbpjl |
A |
G |
2: 164,256,343 (GRCm39) |
D443G |
possibly damaging |
Het |
Rcc1 |
A |
G |
4: 132,065,360 (GRCm39) |
|
probably null |
Het |
Rimbp2 |
G |
T |
5: 128,865,229 (GRCm39) |
S706R |
probably damaging |
Het |
Rsph10b |
G |
C |
5: 143,898,074 (GRCm39) |
E96D |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,438,514 (GRCm39) |
I1784K |
probably benign |
Het |
Sfxn2 |
A |
G |
19: 46,579,985 (GRCm39) |
|
probably null |
Het |
Slamf6 |
T |
A |
1: 171,765,575 (GRCm39) |
L233Q |
probably damaging |
Het |
Slc17a5 |
A |
T |
9: 78,484,455 (GRCm39) |
Y102N |
probably damaging |
Het |
Slc25a53 |
T |
C |
X: 135,884,216 (GRCm39) |
T42A |
probably damaging |
Het |
Slco1a8 |
T |
C |
6: 141,926,670 (GRCm39) |
D552G |
probably damaging |
Het |
Smg7 |
G |
A |
1: 152,716,064 (GRCm39) |
T1057I |
possibly damaging |
Het |
Speer2 |
T |
A |
16: 69,657,485 (GRCm39) |
T53S |
possibly damaging |
Het |
Srm |
A |
C |
4: 148,676,948 (GRCm39) |
I100L |
probably benign |
Het |
Stoml3 |
A |
C |
3: 53,415,008 (GRCm39) |
N267H |
probably damaging |
Het |
Thsd7a |
A |
C |
6: 12,379,632 (GRCm39) |
C931G |
probably damaging |
Het |
Tlr11 |
A |
G |
14: 50,598,139 (GRCm39) |
I42V |
probably benign |
Het |
Tmigd1 |
T |
C |
11: 76,800,999 (GRCm39) |
V162A |
probably benign |
Het |
Tmx3 |
A |
G |
18: 90,528,505 (GRCm39) |
|
probably null |
Het |
Topors |
T |
A |
4: 40,262,790 (GRCm39) |
R165W |
possibly damaging |
Het |
Ttc17 |
A |
T |
2: 94,196,987 (GRCm39) |
S453R |
possibly damaging |
Het |
Vmn1r49 |
G |
T |
6: 90,049,441 (GRCm39) |
T187N |
probably damaging |
Het |
Zbtb49 |
A |
T |
5: 38,371,464 (GRCm39) |
V139E |
possibly damaging |
Het |
Zfp11 |
T |
C |
5: 129,734,216 (GRCm39) |
H415R |
probably damaging |
Het |
Zfp677 |
A |
T |
17: 21,617,970 (GRCm39) |
K342N |
probably benign |
Het |
Zfp979 |
A |
C |
4: 147,697,915 (GRCm39) |
C265G |
possibly damaging |
Het |
Zfpl1 |
T |
C |
19: 6,134,459 (GRCm39) |
R9G |
probably damaging |
Het |
Zkscan8 |
A |
T |
13: 21,704,759 (GRCm39) |
C321* |
probably null |
Het |
|
Other mutations in Katnal2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00886:Katnal2
|
APN |
18 |
77,090,450 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00976:Katnal2
|
APN |
18 |
77,105,189 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01012:Katnal2
|
APN |
18 |
77,105,250 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01302:Katnal2
|
APN |
18 |
77,134,863 (GRCm39) |
splice site |
probably benign |
|
IGL01377:Katnal2
|
APN |
18 |
77,090,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01532:Katnal2
|
APN |
18 |
77,099,696 (GRCm39) |
missense |
probably benign |
|
IGL03203:Katnal2
|
APN |
18 |
77,095,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R0592:Katnal2
|
UTSW |
18 |
77,090,256 (GRCm39) |
splice site |
probably null |
|
R1348:Katnal2
|
UTSW |
18 |
77,066,238 (GRCm39) |
splice site |
probably null |
|
R1419:Katnal2
|
UTSW |
18 |
77,065,128 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1755:Katnal2
|
UTSW |
18 |
77,099,763 (GRCm39) |
missense |
probably benign |
0.01 |
R1772:Katnal2
|
UTSW |
18 |
77,090,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Katnal2
|
UTSW |
18 |
77,103,719 (GRCm39) |
missense |
probably benign |
0.08 |
R1952:Katnal2
|
UTSW |
18 |
77,067,707 (GRCm39) |
missense |
probably benign |
0.00 |
R2115:Katnal2
|
UTSW |
18 |
77,067,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Katnal2
|
UTSW |
18 |
77,065,239 (GRCm39) |
splice site |
probably null |
|
R5126:Katnal2
|
UTSW |
18 |
77,105,294 (GRCm39) |
missense |
probably benign |
0.13 |
R5141:Katnal2
|
UTSW |
18 |
77,085,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R5315:Katnal2
|
UTSW |
18 |
77,099,705 (GRCm39) |
missense |
probably benign |
0.02 |
R5358:Katnal2
|
UTSW |
18 |
77,105,190 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5412:Katnal2
|
UTSW |
18 |
77,090,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R6289:Katnal2
|
UTSW |
18 |
77,105,151 (GRCm39) |
splice site |
probably null |
|
R6647:Katnal2
|
UTSW |
18 |
77,067,733 (GRCm39) |
missense |
probably benign |
0.01 |
R6919:Katnal2
|
UTSW |
18 |
77,098,734 (GRCm39) |
missense |
probably benign |
0.05 |
R7039:Katnal2
|
UTSW |
18 |
77,134,868 (GRCm39) |
critical splice donor site |
probably null |
|
R7285:Katnal2
|
UTSW |
18 |
77,081,271 (GRCm39) |
missense |
probably benign |
0.20 |
Z1176:Katnal2
|
UTSW |
18 |
77,099,753 (GRCm39) |
missense |
probably benign |
|
|