Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Bcam |
T |
G |
7: 19,490,738 (GRCm39) |
E586D |
probably benign |
Het |
Bmp7 |
A |
C |
2: 172,721,283 (GRCm39) |
I264S |
probably benign |
Het |
Casz1 |
G |
A |
4: 149,028,943 (GRCm39) |
M1129I |
probably benign |
Het |
Ccdc59 |
T |
A |
10: 105,677,455 (GRCm39) |
N31K |
probably benign |
Het |
Cfap61 |
A |
G |
2: 145,887,376 (GRCm39) |
Y607C |
probably benign |
Het |
Cnga1 |
T |
C |
5: 72,761,597 (GRCm39) |
E639G |
probably benign |
Het |
Coch |
T |
A |
12: 51,643,366 (GRCm39) |
|
probably null |
Het |
Col6a6 |
A |
C |
9: 105,657,883 (GRCm39) |
Y776* |
probably null |
Het |
Cyp1a1 |
T |
G |
9: 57,609,073 (GRCm39) |
L318R |
probably damaging |
Het |
Cyp3a16 |
T |
A |
5: 145,389,666 (GRCm39) |
Y233F |
probably benign |
Het |
Dgkz |
G |
T |
2: 91,795,817 (GRCm39) |
R42S |
probably damaging |
Het |
Dner |
A |
G |
1: 84,673,218 (GRCm39) |
Y78H |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,163,922 (GRCm39) |
N3111S |
probably damaging |
Het |
Frmpd2 |
T |
C |
14: 33,260,246 (GRCm39) |
S768P |
probably benign |
Het |
Gpr12 |
T |
A |
5: 146,520,094 (GRCm39) |
Y276F |
possibly damaging |
Het |
Hace1 |
C |
T |
10: 45,562,792 (GRCm39) |
P769L |
probably benign |
Het |
Hapln1 |
G |
A |
13: 89,753,347 (GRCm39) |
R171H |
probably damaging |
Het |
Hlx |
T |
G |
1: 184,464,125 (GRCm39) |
T72P |
probably benign |
Het |
Iqcm |
G |
T |
8: 76,304,596 (GRCm39) |
C119F |
probably benign |
Het |
Katna1 |
G |
T |
10: 7,637,075 (GRCm39) |
A409S |
probably benign |
Het |
Kcnip2 |
A |
T |
19: 45,782,729 (GRCm39) |
I204N |
probably damaging |
Het |
Kel |
G |
T |
6: 41,675,310 (GRCm39) |
Q314K |
probably benign |
Het |
Klf5 |
T |
C |
14: 99,536,444 (GRCm39) |
V5A |
probably damaging |
Het |
Lax1 |
A |
T |
1: 133,607,896 (GRCm39) |
C282S |
probably benign |
Het |
Lyar |
A |
G |
5: 38,388,295 (GRCm39) |
T274A |
probably benign |
Het |
Mboat1 |
A |
G |
13: 30,415,959 (GRCm39) |
H306R |
possibly damaging |
Het |
Morn5 |
A |
T |
2: 35,947,082 (GRCm39) |
Y120F |
probably benign |
Het |
Mrgprx2 |
T |
C |
7: 48,132,240 (GRCm39) |
T193A |
probably benign |
Het |
Myh10 |
T |
A |
11: 68,583,327 (GRCm39) |
W8R |
unknown |
Het |
Nfasc |
A |
G |
1: 132,533,269 (GRCm39) |
V644A |
probably damaging |
Het |
Nup153 |
G |
T |
13: 46,842,855 (GRCm39) |
|
probably null |
Het |
Nup50l |
T |
C |
6: 96,141,866 (GRCm39) |
K393E |
possibly damaging |
Het |
Or1o4 |
T |
A |
17: 37,590,991 (GRCm39) |
M107L |
probably benign |
Het |
Or4x6 |
A |
T |
2: 89,949,173 (GRCm39) |
Y256* |
probably null |
Het |
Or5h19 |
A |
T |
16: 58,856,325 (GRCm39) |
Y258* |
probably null |
Het |
Orc4 |
A |
T |
2: 48,800,203 (GRCm39) |
V315E |
possibly damaging |
Het |
Pcsk5 |
T |
A |
19: 17,443,549 (GRCm39) |
|
probably null |
Het |
Pif1 |
A |
G |
9: 65,502,073 (GRCm39) |
D635G |
probably benign |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Ppfia2 |
A |
G |
10: 106,310,648 (GRCm39) |
T52A |
probably damaging |
Het |
Ppp1r36 |
A |
T |
12: 76,485,180 (GRCm39) |
D301V |
probably damaging |
Het |
Prss46 |
A |
G |
9: 110,680,500 (GRCm39) |
N215S |
probably benign |
Het |
Qser1 |
A |
C |
2: 104,619,312 (GRCm39) |
V410G |
probably damaging |
Het |
Reln |
A |
C |
5: 22,155,870 (GRCm39) |
N2207K |
probably damaging |
Het |
Rimkla |
A |
G |
4: 119,327,810 (GRCm39) |
V180A |
probably benign |
Het |
Rpa1 |
CA |
C |
11: 75,198,050 (GRCm39) |
|
probably null |
Het |
Rsph3a |
G |
T |
17: 8,165,050 (GRCm39) |
E137* |
probably null |
Het |
Spata31f1a |
A |
G |
4: 42,850,765 (GRCm39) |
S464P |
possibly damaging |
Het |
Sqle |
C |
A |
15: 59,196,315 (GRCm39) |
H369Q |
probably damaging |
Het |
Srebf2 |
T |
A |
15: 82,057,016 (GRCm39) |
D250E |
probably damaging |
Het |
Svs3b |
A |
T |
2: 164,097,567 (GRCm39) |
C251* |
probably null |
Het |
Tdrd9 |
A |
T |
12: 111,997,649 (GRCm39) |
N713Y |
possibly damaging |
Het |
Terf2ip |
T |
C |
8: 112,738,717 (GRCm39) |
S202P |
possibly damaging |
Het |
Trank1 |
A |
G |
9: 111,194,096 (GRCm39) |
T707A |
probably benign |
Het |
Trav8-1 |
T |
G |
14: 53,707,688 (GRCm39) |
D109E |
possibly damaging |
Het |
Trem2 |
T |
A |
17: 48,658,777 (GRCm39) |
S181T |
probably benign |
Het |
Trim37 |
A |
G |
11: 87,037,863 (GRCm39) |
N199S |
probably benign |
Het |
Tshz3 |
T |
C |
7: 36,468,583 (GRCm39) |
F191L |
probably damaging |
Het |
Ubxn8 |
A |
G |
8: 34,111,712 (GRCm39) |
M227T |
probably damaging |
Het |
Uggt2 |
T |
A |
14: 119,296,519 (GRCm39) |
I448F |
possibly damaging |
Het |
Usp47 |
T |
A |
7: 111,687,132 (GRCm39) |
L697M |
probably damaging |
Het |
Vmn2r52 |
T |
C |
7: 9,893,300 (GRCm39) |
D613G |
probably benign |
Het |
Wdr81 |
T |
C |
11: 75,338,828 (GRCm39) |
T1444A |
probably benign |
Het |
Zfp423 |
T |
C |
8: 88,622,304 (GRCm39) |
Y11C |
unknown |
Het |
Zw10 |
T |
A |
9: 48,982,933 (GRCm39) |
D521E |
probably benign |
Het |
|
Other mutations in Gm45861 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6286:Gm45861
|
UTSW |
8 |
28,019,619 (GRCm39) |
missense |
unknown |
|
R6580:Gm45861
|
UTSW |
8 |
28,034,979 (GRCm39) |
missense |
unknown |
|
R6650:Gm45861
|
UTSW |
8 |
27,995,043 (GRCm39) |
missense |
unknown |
|
R6784:Gm45861
|
UTSW |
8 |
27,990,086 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6881:Gm45861
|
UTSW |
8 |
28,025,279 (GRCm39) |
splice site |
probably null |
|
R6909:Gm45861
|
UTSW |
8 |
28,017,109 (GRCm39) |
missense |
unknown |
|
R6929:Gm45861
|
UTSW |
8 |
28,014,462 (GRCm39) |
missense |
unknown |
|
R6959:Gm45861
|
UTSW |
8 |
28,038,213 (GRCm39) |
critical splice donor site |
probably null |
|
R7023:Gm45861
|
UTSW |
8 |
28,071,034 (GRCm39) |
missense |
unknown |
|
R7157:Gm45861
|
UTSW |
8 |
28,032,537 (GRCm39) |
missense |
unknown |
|
R7157:Gm45861
|
UTSW |
8 |
28,032,536 (GRCm39) |
nonsense |
probably null |
|
R7453:Gm45861
|
UTSW |
8 |
28,031,686 (GRCm39) |
missense |
unknown |
|
R7462:Gm45861
|
UTSW |
8 |
28,024,517 (GRCm39) |
critical splice donor site |
probably null |
|
R7545:Gm45861
|
UTSW |
8 |
28,071,032 (GRCm39) |
missense |
unknown |
|
R7674:Gm45861
|
UTSW |
8 |
28,030,147 (GRCm39) |
missense |
unknown |
|
R7840:Gm45861
|
UTSW |
8 |
28,072,751 (GRCm39) |
missense |
unknown |
|
R8092:Gm45861
|
UTSW |
8 |
28,057,823 (GRCm39) |
missense |
unknown |
|
R8242:Gm45861
|
UTSW |
8 |
28,038,821 (GRCm39) |
missense |
unknown |
|
R8856:Gm45861
|
UTSW |
8 |
28,010,788 (GRCm39) |
missense |
unknown |
|
R8900:Gm45861
|
UTSW |
8 |
28,019,632 (GRCm39) |
missense |
unknown |
|
R8988:Gm45861
|
UTSW |
8 |
28,032,531 (GRCm39) |
missense |
unknown |
|
R9067:Gm45861
|
UTSW |
8 |
27,995,043 (GRCm39) |
missense |
unknown |
|
R9251:Gm45861
|
UTSW |
8 |
28,032,589 (GRCm39) |
critical splice donor site |
probably null |
|
R9266:Gm45861
|
UTSW |
8 |
28,074,674 (GRCm39) |
missense |
unknown |
|
R9455:Gm45861
|
UTSW |
8 |
28,041,394 (GRCm39) |
nonsense |
probably null |
|
R9643:Gm45861
|
UTSW |
8 |
27,994,083 (GRCm39) |
missense |
unknown |
|
R9684:Gm45861
|
UTSW |
8 |
28,014,601 (GRCm39) |
missense |
unknown |
|
R9729:Gm45861
|
UTSW |
8 |
28,045,436 (GRCm39) |
missense |
unknown |
|
Z1176:Gm45861
|
UTSW |
8 |
28,074,897 (GRCm39) |
missense |
unknown |
|
Z1177:Gm45861
|
UTSW |
8 |
28,059,979 (GRCm39) |
missense |
unknown |
|
Z1177:Gm45861
|
UTSW |
8 |
28,025,397 (GRCm39) |
missense |
unknown |
|
|