Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
C |
A |
2: 25,330,878 (GRCm39) |
R1189S |
possibly damaging |
Het |
Abcf2 |
T |
C |
5: 24,770,970 (GRCm39) |
Q594R |
probably benign |
Het |
Abhd18 |
G |
A |
3: 40,888,215 (GRCm39) |
S353N |
probably benign |
Het |
Adrb1 |
G |
T |
19: 56,712,046 (GRCm39) |
A415S |
probably benign |
Het |
Art2b |
T |
C |
7: 101,229,680 (GRCm39) |
N73S |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
CACTGGTTCTGTGGT |
CACTGGTTCTGTGGTTACTGGTTCTGTGGT |
3: 95,795,480 (GRCm39) |
|
probably benign |
Het |
BC028528 |
ACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC |
ACTGGTTCTGTGGTCTCTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC |
3: 95,795,451 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
A |
G |
8: 85,338,914 (GRCm39) |
M1753V |
possibly damaging |
Het |
Cbx8 |
A |
T |
11: 118,930,287 (GRCm39) |
I102N |
possibly damaging |
Het |
Ccdc178 |
T |
A |
18: 22,238,620 (GRCm39) |
E332D |
probably benign |
Het |
Cdhr17 |
T |
A |
5: 17,031,944 (GRCm39) |
V533D |
possibly damaging |
Het |
Cfap74 |
G |
A |
4: 155,550,809 (GRCm39) |
|
probably benign |
Het |
Cmas |
A |
G |
6: 142,702,526 (GRCm39) |
T10A |
probably damaging |
Het |
Cyb561d1 |
A |
T |
3: 108,107,475 (GRCm39) |
L51H |
probably benign |
Het |
D030056L22Rik |
A |
T |
19: 18,694,629 (GRCm39) |
N128I |
probably damaging |
Het |
D130043K22Rik |
G |
T |
13: 25,048,764 (GRCm39) |
A423S |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,475,795 (GRCm39) |
I1349T |
probably benign |
Het |
Dnajb3 |
T |
G |
1: 88,132,736 (GRCm39) |
D222A |
probably damaging |
Het |
Dtx1 |
T |
C |
5: 120,819,422 (GRCm39) |
E592G |
probably damaging |
Het |
Dzank1 |
C |
T |
2: 144,332,056 (GRCm39) |
G427R |
possibly damaging |
Het |
E130308A19Rik |
A |
C |
4: 59,719,991 (GRCm39) |
K508Q |
probably damaging |
Het |
Eif4e1b |
T |
A |
13: 54,931,916 (GRCm39) |
|
probably null |
Het |
Ell2 |
A |
G |
13: 75,904,495 (GRCm39) |
M159V |
probably null |
Het |
Eml4 |
G |
A |
17: 83,758,446 (GRCm39) |
V377I |
probably benign |
Het |
Fryl |
A |
T |
5: 73,207,773 (GRCm39) |
S2466T |
probably benign |
Het |
Gfpt1 |
C |
A |
6: 87,054,071 (GRCm39) |
T426K |
probably damaging |
Het |
Gm49355 |
T |
C |
14: 12,307,173 (GRCm38) |
|
probably benign |
Het |
Gm5114 |
T |
C |
7: 39,058,624 (GRCm39) |
I332V |
probably benign |
Het |
Gpr15 |
T |
A |
16: 58,539,105 (GRCm39) |
|
probably benign |
Het |
Gpr179 |
T |
C |
11: 97,225,684 (GRCm39) |
E2157G |
probably benign |
Het |
Gramd4 |
A |
G |
15: 86,016,170 (GRCm39) |
N482S |
probably benign |
Het |
Hfm1 |
A |
T |
5: 107,028,343 (GRCm39) |
I829K |
probably benign |
Het |
Hydin |
A |
T |
8: 111,139,916 (GRCm39) |
E728D |
possibly damaging |
Het |
Ifngr2 |
T |
A |
16: 91,356,895 (GRCm39) |
V143E |
probably damaging |
Het |
Ift172 |
T |
C |
5: 31,414,730 (GRCm39) |
D1390G |
probably benign |
Het |
Kdf1 |
A |
T |
4: 133,256,138 (GRCm39) |
D285V |
probably damaging |
Het |
Mast4 |
C |
T |
13: 102,941,155 (GRCm39) |
V301I |
probably damaging |
Het |
Mdn1 |
G |
A |
4: 32,726,942 (GRCm39) |
|
probably null |
Het |
Megf11 |
A |
G |
9: 64,613,132 (GRCm39) |
E1016G |
probably damaging |
Het |
Mixl1 |
G |
A |
1: 180,524,453 (GRCm39) |
A42V |
possibly damaging |
Het |
Mpp2 |
A |
G |
11: 101,950,154 (GRCm39) |
W567R |
probably damaging |
Het |
Mrgpra6 |
A |
G |
7: 46,838,697 (GRCm39) |
L136P |
probably damaging |
Het |
Mroh7 |
T |
A |
4: 106,557,434 (GRCm39) |
I759L |
probably benign |
Het |
Nrxn2 |
A |
G |
19: 6,500,609 (GRCm39) |
D277G |
probably benign |
Het |
Nup210l |
A |
T |
3: 90,027,234 (GRCm39) |
K205N |
probably benign |
Het |
Or4g17 |
A |
G |
2: 111,209,620 (GRCm39) |
I92V |
possibly damaging |
Het |
Or4p4b-ps1 |
A |
G |
2: 88,453,939 (GRCm39) |
*97W |
probably null |
Het |
Or52e19b |
T |
C |
7: 103,032,303 (GRCm39) |
E302G |
probably benign |
Het |
Or5al6 |
A |
T |
2: 85,976,681 (GRCm39) |
Y132* |
probably null |
Het |
Oxnad1 |
C |
T |
14: 31,807,576 (GRCm39) |
|
probably benign |
Het |
Pamr1 |
C |
T |
2: 102,472,549 (GRCm39) |
T616I |
probably benign |
Het |
Pcdhgb5 |
C |
T |
18: 37,866,592 (GRCm39) |
H796Y |
possibly damaging |
Het |
Pdlim7 |
G |
T |
13: 55,656,041 (GRCm39) |
D126E |
probably benign |
Het |
Pfdn2 |
C |
T |
1: 171,185,465 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
T |
A |
18: 63,216,032 (GRCm39) |
|
probably null |
Het |
Pms2 |
A |
T |
5: 143,848,842 (GRCm39) |
I43L |
probably benign |
Het |
Prex2 |
T |
A |
1: 11,232,487 (GRCm39) |
S851R |
probably benign |
Het |
Ptpn4 |
T |
A |
1: 119,671,151 (GRCm39) |
E202D |
possibly damaging |
Het |
Rnf40 |
T |
A |
7: 127,193,849 (GRCm39) |
V455E |
probably damaging |
Het |
Rp1l1 |
A |
G |
14: 64,266,169 (GRCm39) |
N585S |
probably benign |
Het |
Rrp12 |
A |
G |
19: 41,878,582 (GRCm39) |
S188P |
probably damaging |
Het |
Rsbn1l |
T |
A |
5: 21,101,482 (GRCm39) |
H686L |
probably benign |
Het |
Runx2 |
C |
T |
17: 45,046,203 (GRCm39) |
V107I |
possibly damaging |
Het |
Rusc2 |
A |
G |
4: 43,422,846 (GRCm39) |
I994M |
probably benign |
Het |
Ryr1 |
T |
A |
7: 28,808,812 (GRCm39) |
D420V |
probably benign |
Het |
Sash1 |
T |
C |
10: 8,605,612 (GRCm39) |
Q926R |
probably benign |
Het |
Scgb3a2 |
T |
A |
18: 43,897,499 (GRCm39) |
I6N |
probably damaging |
Het |
Sdc3 |
T |
A |
4: 130,544,233 (GRCm39) |
|
probably benign |
Het |
Sik2 |
A |
G |
9: 50,808,755 (GRCm39) |
V658A |
probably benign |
Het |
Slc25a39 |
A |
G |
11: 102,296,601 (GRCm39) |
V81A |
probably damaging |
Het |
Snai2 |
T |
A |
16: 14,526,113 (GRCm39) |
S255T |
possibly damaging |
Het |
Sorbs1 |
A |
T |
19: 40,316,060 (GRCm39) |
Y371* |
probably null |
Het |
Spata31d1b |
A |
T |
13: 59,863,236 (GRCm39) |
H128L |
probably benign |
Het |
Spdl1 |
A |
T |
11: 34,721,706 (GRCm39) |
M1K |
probably null |
Het |
Tgm3 |
T |
A |
2: 129,868,697 (GRCm39) |
N211K |
probably benign |
Het |
Tmem116 |
T |
C |
5: 121,606,050 (GRCm39) |
|
probably null |
Het |
Tmem132e |
T |
A |
11: 82,329,212 (GRCm39) |
|
probably null |
Het |
Tmem53 |
T |
C |
4: 117,125,705 (GRCm39) |
C251R |
probably damaging |
Het |
Trcg1 |
A |
C |
9: 57,152,856 (GRCm39) |
D551A |
probably damaging |
Het |
Trp63 |
T |
A |
16: 25,620,843 (GRCm39) |
F12I |
probably benign |
Het |
Ttn |
C |
T |
2: 76,709,401 (GRCm39) |
|
probably null |
Het |
Tubgcp4 |
T |
C |
2: 121,025,946 (GRCm39) |
V596A |
probably benign |
Het |
Ugt2a3 |
A |
C |
5: 87,473,491 (GRCm39) |
H475Q |
probably damaging |
Het |
Unc79 |
G |
A |
12: 103,025,759 (GRCm39) |
R382K |
probably damaging |
Het |
Vmn2r58 |
T |
C |
7: 41,513,662 (GRCm39) |
H327R |
possibly damaging |
Het |
Vmn2r7 |
G |
A |
3: 64,623,987 (GRCm39) |
T111I |
possibly damaging |
Het |
Zfp318 |
T |
A |
17: 46,708,138 (GRCm39) |
Y399N |
probably damaging |
Het |
|
Other mutations in Chat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00861:Chat
|
APN |
14 |
32,170,980 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01618:Chat
|
APN |
14 |
32,168,849 (GRCm39) |
splice site |
probably null |
|
IGL02192:Chat
|
APN |
14 |
32,145,279 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02418:Chat
|
APN |
14 |
32,168,906 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02851:Chat
|
APN |
14 |
32,180,570 (GRCm39) |
missense |
probably benign |
|
IGL02966:Chat
|
APN |
14 |
32,170,903 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Chat
|
APN |
14 |
32,174,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Chat
|
UTSW |
14 |
32,130,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Chat
|
UTSW |
14 |
32,142,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Chat
|
UTSW |
14 |
32,142,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Chat
|
UTSW |
14 |
32,168,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Chat
|
UTSW |
14 |
32,130,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Chat
|
UTSW |
14 |
32,146,148 (GRCm39) |
missense |
probably benign |
0.03 |
R1973:Chat
|
UTSW |
14 |
32,146,148 (GRCm39) |
missense |
probably benign |
0.03 |
R2061:Chat
|
UTSW |
14 |
32,168,830 (GRCm39) |
missense |
probably benign |
0.00 |
R2270:Chat
|
UTSW |
14 |
32,176,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R4012:Chat
|
UTSW |
14 |
32,145,269 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4601:Chat
|
UTSW |
14 |
32,146,112 (GRCm39) |
missense |
probably benign |
0.00 |
R4620:Chat
|
UTSW |
14 |
32,175,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Chat
|
UTSW |
14 |
32,175,694 (GRCm39) |
missense |
probably benign |
|
R4885:Chat
|
UTSW |
14 |
32,176,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Chat
|
UTSW |
14 |
32,170,934 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4940:Chat
|
UTSW |
14 |
32,141,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:Chat
|
UTSW |
14 |
32,142,771 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5094:Chat
|
UTSW |
14 |
32,130,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Chat
|
UTSW |
14 |
32,170,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Chat
|
UTSW |
14 |
32,170,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6621:Chat
|
UTSW |
14 |
32,140,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R6648:Chat
|
UTSW |
14 |
32,176,651 (GRCm39) |
missense |
probably benign |
0.17 |
R7203:Chat
|
UTSW |
14 |
32,141,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7336:Chat
|
UTSW |
14 |
32,145,213 (GRCm39) |
splice site |
probably null |
|
R7530:Chat
|
UTSW |
14 |
32,130,915 (GRCm39) |
nonsense |
probably null |
|
R8782:Chat
|
UTSW |
14 |
32,146,155 (GRCm39) |
missense |
probably benign |
0.00 |
R8941:Chat
|
UTSW |
14 |
32,130,963 (GRCm39) |
missense |
probably benign |
0.43 |
R9496:Chat
|
UTSW |
14 |
32,148,119 (GRCm39) |
missense |
probably benign |
0.00 |
R9560:Chat
|
UTSW |
14 |
32,170,942 (GRCm39) |
nonsense |
probably null |
|
X0014:Chat
|
UTSW |
14 |
32,168,890 (GRCm39) |
missense |
probably benign |
0.01 |
X0066:Chat
|
UTSW |
14 |
32,175,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|