Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
A |
G |
11: 84,122,574 (GRCm39) |
N331S |
probably benign |
Het |
Apc |
T |
A |
18: 34,448,997 (GRCm39) |
N1930K |
probably damaging |
Het |
Arhgap28 |
T |
C |
17: 68,171,601 (GRCm39) |
D391G |
probably damaging |
Het |
Atn1 |
G |
T |
6: 124,720,334 (GRCm39) |
|
probably benign |
Het |
C2cd5 |
T |
C |
6: 142,987,216 (GRCm39) |
E471G |
probably damaging |
Het |
Camta1 |
C |
A |
4: 151,159,597 (GRCm39) |
R1614L |
probably damaging |
Het |
Cap2 |
T |
C |
13: 46,714,023 (GRCm39) |
L34P |
probably damaging |
Het |
Cdc42ep2 |
T |
A |
19: 5,968,553 (GRCm39) |
M51L |
probably benign |
Het |
Cntn5 |
C |
T |
9: 9,972,875 (GRCm39) |
A254T |
probably damaging |
Het |
Dicer1 |
A |
T |
12: 104,670,433 (GRCm39) |
L1044H |
probably damaging |
Het |
Dkk3 |
A |
C |
7: 111,757,430 (GRCm39) |
M58R |
probably damaging |
Het |
Dpy19l3 |
G |
A |
7: 35,452,130 (GRCm39) |
R5W |
probably damaging |
Het |
Dsg1c |
C |
T |
18: 20,416,711 (GRCm39) |
P871S |
probably damaging |
Het |
Dusp1 |
A |
T |
17: 26,726,670 (GRCm39) |
S131T |
probably benign |
Het |
Enpp2 |
C |
T |
15: 54,745,555 (GRCm39) |
G314R |
probably damaging |
Het |
Entr1 |
T |
C |
2: 26,277,671 (GRCm39) |
E41G |
possibly damaging |
Het |
Fam222b |
C |
A |
11: 78,045,756 (GRCm39) |
P439Q |
probably benign |
Het |
Fastkd2 |
A |
T |
1: 63,776,970 (GRCm39) |
I369F |
probably benign |
Het |
Fdps |
G |
A |
3: 89,002,201 (GRCm39) |
S205F |
probably damaging |
Het |
Fmo1 |
A |
T |
1: 162,663,773 (GRCm39) |
V252E |
possibly damaging |
Het |
Frmd5 |
A |
G |
2: 121,386,055 (GRCm39) |
Y230H |
probably damaging |
Het |
Gal |
C |
T |
19: 3,461,171 (GRCm39) |
V88I |
probably benign |
Het |
Gnptab |
T |
C |
10: 88,272,387 (GRCm39) |
I1009T |
probably damaging |
Het |
Idh2 |
C |
T |
7: 79,748,005 (GRCm39) |
A232T |
probably damaging |
Het |
Klhdc7a |
A |
T |
4: 139,694,016 (GRCm39) |
D310E |
probably benign |
Het |
Klk4 |
T |
C |
7: 43,533,432 (GRCm39) |
M97T |
probably benign |
Het |
Krt82 |
C |
T |
15: 101,454,028 (GRCm39) |
V227M |
probably damaging |
Het |
Lpp |
T |
C |
16: 24,580,587 (GRCm39) |
V226A |
probably damaging |
Het |
Mbd1 |
AGCTGACTCGGTAC |
A |
18: 74,406,312 (GRCm39) |
|
probably null |
Het |
Mcm10 |
T |
C |
2: 5,008,965 (GRCm39) |
K335E |
possibly damaging |
Het |
Mpv17l |
A |
T |
16: 13,758,863 (GRCm39) |
I96L |
probably benign |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Myb |
T |
C |
10: 21,030,611 (GRCm39) |
D62G |
possibly damaging |
Het |
Nasp |
A |
T |
4: 116,467,892 (GRCm39) |
N364K |
probably benign |
Het |
Npsr1 |
A |
G |
9: 24,224,573 (GRCm39) |
N317D |
probably damaging |
Het |
Nup210 |
A |
G |
6: 91,005,777 (GRCm39) |
V619A |
possibly damaging |
Het |
Oser1 |
C |
T |
2: 163,253,316 (GRCm39) |
|
probably null |
Het |
Pcdhb4 |
T |
C |
18: 37,442,268 (GRCm39) |
F526S |
probably damaging |
Het |
Plekhh3 |
T |
C |
11: 101,055,967 (GRCm39) |
N444S |
probably damaging |
Het |
Pnpla5 |
G |
T |
15: 84,004,920 (GRCm39) |
L144M |
probably damaging |
Het |
Pou2f2 |
G |
A |
7: 24,815,501 (GRCm39) |
Q89* |
probably null |
Het |
Ptprb |
A |
G |
10: 116,186,083 (GRCm39) |
I1713V |
probably benign |
Het |
Ptprd |
A |
G |
4: 76,046,902 (GRCm39) |
Y442H |
probably damaging |
Het |
Rad21 |
A |
T |
15: 51,837,259 (GRCm39) |
I152N |
possibly damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,723,823 (GRCm39) |
S1568P |
probably damaging |
Het |
Rhag |
T |
A |
17: 41,145,618 (GRCm39) |
V357E |
probably damaging |
Het |
Rnf121 |
A |
T |
7: 101,678,324 (GRCm39) |
D174E |
possibly damaging |
Het |
Sf3b4 |
T |
C |
3: 96,080,298 (GRCm39) |
Y16H |
probably damaging |
Het |
Slc1a3 |
C |
T |
15: 8,668,619 (GRCm39) |
V449I |
probably damaging |
Het |
Slc20a2 |
A |
G |
8: 23,058,409 (GRCm39) |
I648M |
probably benign |
Het |
Slc25a25 |
T |
A |
2: 32,307,834 (GRCm39) |
I254F |
probably damaging |
Het |
Slit3 |
A |
G |
11: 35,591,109 (GRCm39) |
H1307R |
probably damaging |
Het |
Sorl1 |
C |
A |
9: 41,943,205 (GRCm39) |
M890I |
probably damaging |
Het |
Supt16 |
A |
C |
14: 52,414,175 (GRCm39) |
M468R |
probably benign |
Het |
Taf4b |
T |
C |
18: 14,916,817 (GRCm39) |
S56P |
probably benign |
Het |
Tapt1 |
T |
C |
5: 44,375,443 (GRCm39) |
|
probably null |
Het |
Tmco3 |
T |
G |
8: 13,346,027 (GRCm39) |
C288W |
probably damaging |
Het |
Tpcn2 |
A |
G |
7: 144,830,911 (GRCm39) |
Y145H |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,712,061 (GRCm39) |
|
probably benign |
Het |
Usb1 |
G |
T |
8: 96,071,946 (GRCm39) |
W215C |
probably damaging |
Het |
Usp2 |
C |
G |
9: 44,004,047 (GRCm39) |
T305R |
probably damaging |
Het |
Vmn1r13 |
G |
A |
6: 57,187,690 (GRCm39) |
S283N |
probably benign |
Het |
Vps54 |
A |
G |
11: 21,256,381 (GRCm39) |
K467E |
possibly damaging |
Het |
Wnk2 |
G |
T |
13: 49,221,604 (GRCm39) |
S1121Y |
probably damaging |
Het |
Zbed6 |
A |
T |
1: 133,584,522 (GRCm39) |
D938E |
probably damaging |
Het |
|
Other mutations in Adk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01113:Adk
|
APN |
14 |
21,142,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01403:Adk
|
APN |
14 |
21,284,983 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01701:Adk
|
APN |
14 |
21,153,922 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02405:Adk
|
APN |
14 |
21,153,899 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02808:Adk
|
APN |
14 |
21,153,901 (GRCm39) |
missense |
probably benign |
0.08 |
jeopardy
|
UTSW |
14 |
21,284,982 (GRCm39) |
missense |
probably damaging |
0.99 |
presumption
|
UTSW |
14 |
21,290,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Adk
|
UTSW |
14 |
21,473,604 (GRCm39) |
missense |
probably benign |
0.35 |
R0904:Adk
|
UTSW |
14 |
21,142,496 (GRCm39) |
missense |
probably damaging |
0.96 |
R1448:Adk
|
UTSW |
14 |
21,102,708 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R1695:Adk
|
UTSW |
14 |
21,431,668 (GRCm39) |
missense |
probably benign |
0.01 |
R2048:Adk
|
UTSW |
14 |
21,368,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Adk
|
UTSW |
14 |
21,419,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Adk
|
UTSW |
14 |
21,290,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Adk
|
UTSW |
14 |
21,473,616 (GRCm39) |
missense |
probably benign |
0.03 |
R6770:Adk
|
UTSW |
14 |
21,284,982 (GRCm39) |
missense |
probably damaging |
0.99 |
R6932:Adk
|
UTSW |
14 |
21,126,376 (GRCm39) |
start codon destroyed |
probably null |
0.23 |
R7146:Adk
|
UTSW |
14 |
21,376,682 (GRCm39) |
missense |
|
|
R7257:Adk
|
UTSW |
14 |
21,102,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R7491:Adk
|
UTSW |
14 |
21,284,997 (GRCm39) |
missense |
probably damaging |
0.96 |
R7806:Adk
|
UTSW |
14 |
21,376,679 (GRCm39) |
missense |
|
|
R7922:Adk
|
UTSW |
14 |
21,368,111 (GRCm39) |
missense |
probably benign |
|
R8465:Adk
|
UTSW |
14 |
21,153,892 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9709:Adk
|
UTSW |
14 |
21,126,386 (GRCm39) |
missense |
probably benign |
0.04 |
|