Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130213A22Rik |
C |
A |
11: 69,012,301 (GRCm39) |
G26* |
probably null |
Het |
Abca5 |
T |
A |
11: 110,201,059 (GRCm39) |
Y447F |
probably damaging |
Het |
Acox2 |
A |
G |
14: 8,248,061 (GRCm38) |
I407T |
probably benign |
Het |
Adam8 |
T |
C |
7: 139,567,520 (GRCm39) |
N408D |
probably damaging |
Het |
Adgre1 |
A |
T |
17: 57,708,925 (GRCm39) |
T39S |
probably benign |
Het |
Akap12 |
G |
A |
10: 4,307,590 (GRCm39) |
V1467I |
probably benign |
Het |
Arid1b |
T |
A |
17: 5,386,790 (GRCm39) |
|
probably null |
Het |
Atp2c2 |
A |
G |
8: 120,462,035 (GRCm39) |
I303V |
possibly damaging |
Het |
Bpifc |
C |
T |
10: 85,827,118 (GRCm39) |
V144I |
probably benign |
Het |
Camk4 |
A |
G |
18: 33,291,907 (GRCm39) |
E189G |
possibly damaging |
Het |
Casz1 |
A |
G |
4: 149,024,046 (GRCm39) |
|
probably benign |
Het |
Ccdc134 |
T |
C |
15: 82,015,643 (GRCm39) |
V41A |
possibly damaging |
Het |
Chrd |
A |
T |
16: 20,557,660 (GRCm39) |
T753S |
probably damaging |
Het |
Cracd |
A |
G |
5: 76,988,739 (GRCm39) |
D30G |
probably damaging |
Het |
Cyb561a3 |
T |
C |
19: 10,562,735 (GRCm39) |
V125A |
probably benign |
Het |
D630039A03Rik |
T |
A |
4: 57,910,606 (GRCm39) |
T69S |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,410,842 (GRCm39) |
F1687S |
probably damaging |
Het |
Dlgap4 |
T |
C |
2: 156,591,267 (GRCm39) |
S818P |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,320,174 (GRCm39) |
I3965T |
probably damaging |
Het |
Dnai2 |
G |
T |
11: 114,623,781 (GRCm39) |
G15W |
probably damaging |
Het |
Dsg1c |
A |
G |
18: 20,410,109 (GRCm39) |
I526V |
probably benign |
Het |
Gli1 |
A |
T |
10: 127,166,088 (GRCm39) |
V1055E |
probably damaging |
Het |
Hand2 |
G |
T |
8: 57,775,011 (GRCm39) |
A24S |
probably benign |
Het |
Helb |
T |
C |
10: 119,941,942 (GRCm39) |
I249V |
probably benign |
Het |
Hspa4l |
G |
A |
3: 40,727,074 (GRCm39) |
V492M |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,266,660 (GRCm39) |
I1916T |
probably damaging |
Het |
Igfals |
G |
A |
17: 25,100,579 (GRCm39) |
V557I |
possibly damaging |
Het |
Itpa |
T |
G |
2: 130,522,930 (GRCm39) |
S176A |
probably damaging |
Het |
Kcnu1 |
T |
A |
8: 26,375,345 (GRCm39) |
L353H |
probably damaging |
Het |
Klhl1 |
A |
G |
14: 96,755,615 (GRCm39) |
F47L |
probably benign |
Het |
Klhl13 |
T |
C |
X: 23,151,415 (GRCm39) |
D21G |
probably benign |
Het |
Krt26 |
T |
C |
11: 99,225,570 (GRCm39) |
K304E |
probably damaging |
Het |
Krt9 |
C |
T |
11: 100,081,675 (GRCm39) |
V285I |
probably damaging |
Het |
Mansc1 |
T |
C |
6: 134,587,146 (GRCm39) |
R344G |
possibly damaging |
Het |
Mier2 |
G |
T |
10: 79,377,631 (GRCm39) |
P439T |
possibly damaging |
Het |
Mppe1 |
T |
A |
18: 67,358,957 (GRCm39) |
|
probably null |
Het |
Nedd4l |
G |
A |
18: 65,300,606 (GRCm39) |
A243T |
probably benign |
Het |
Notch4 |
T |
A |
17: 34,797,043 (GRCm39) |
C934* |
probably null |
Het |
Nsmce3 |
C |
T |
7: 64,521,916 (GRCm39) |
D251N |
probably damaging |
Het |
Or10a49 |
C |
T |
7: 108,468,335 (GRCm39) |
V9M |
probably damaging |
Het |
Or12d12 |
T |
A |
17: 37,610,870 (GRCm39) |
T148S |
probably benign |
Het |
Or3a10 |
A |
G |
11: 73,935,525 (GRCm39) |
C192R |
probably damaging |
Het |
Or4f6 |
T |
C |
2: 111,838,668 (GRCm39) |
T288A |
possibly damaging |
Het |
Or5l13 |
T |
A |
2: 87,779,874 (GRCm39) |
R234S |
probably damaging |
Het |
Or8g23 |
A |
G |
9: 38,971,470 (GRCm39) |
I164T |
probably benign |
Het |
Pdzd7 |
T |
C |
19: 45,034,067 (GRCm39) |
T6A |
probably benign |
Het |
Picalm |
T |
A |
7: 89,838,427 (GRCm39) |
F493Y |
probably damaging |
Het |
Prl7d1 |
A |
G |
13: 27,900,651 (GRCm39) |
M1T |
probably null |
Het |
Prl8a1 |
T |
C |
13: 27,759,441 (GRCm39) |
K199E |
possibly damaging |
Het |
Rims1 |
C |
T |
1: 22,498,740 (GRCm39) |
R764H |
probably damaging |
Het |
Rnf17 |
G |
T |
14: 56,712,870 (GRCm39) |
R779L |
possibly damaging |
Het |
Rufy2 |
T |
C |
10: 62,833,916 (GRCm39) |
L294P |
probably damaging |
Het |
Sgsh |
A |
G |
11: 119,241,773 (GRCm39) |
L111P |
probably damaging |
Het |
Slc22a30 |
G |
T |
19: 8,314,213 (GRCm39) |
T491K |
probably benign |
Het |
Slc35b3 |
T |
C |
13: 39,127,044 (GRCm39) |
N20D |
possibly damaging |
Het |
Slc5a4a |
T |
C |
10: 76,017,489 (GRCm39) |
F429L |
probably benign |
Het |
Sulf1 |
T |
C |
1: 12,887,636 (GRCm39) |
I270T |
probably damaging |
Het |
Tmem51 |
T |
C |
4: 141,759,059 (GRCm39) |
T230A |
probably damaging |
Het |
Tnc |
T |
A |
4: 63,926,947 (GRCm39) |
I860F |
probably damaging |
Het |
Trh |
A |
T |
6: 92,220,679 (GRCm39) |
V61E |
possibly damaging |
Het |
Ttn |
T |
G |
2: 76,584,443 (GRCm39) |
T22222P |
probably damaging |
Het |
Uroc1 |
A |
T |
6: 90,338,494 (GRCm39) |
K652* |
probably null |
Het |
Usp34 |
C |
T |
11: 23,439,033 (GRCm39) |
P3532S |
possibly damaging |
Het |
Vmn2r120 |
A |
T |
17: 57,831,954 (GRCm39) |
F278L |
probably benign |
Het |
Vmn2r7 |
A |
G |
3: 64,627,032 (GRCm39) |
F86L |
possibly damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,315,856 (GRCm39) |
I70K |
possibly damaging |
Het |
Vps13a |
C |
T |
19: 16,722,317 (GRCm39) |
A332T |
probably benign |
Het |
Zfp568 |
T |
A |
7: 29,722,821 (GRCm39) |
C589S |
probably damaging |
Het |
|
Other mutations in Far2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01131:Far2
|
APN |
6 |
148,052,096 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01650:Far2
|
APN |
6 |
148,074,985 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01899:Far2
|
APN |
6 |
148,047,527 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02524:Far2
|
APN |
6 |
148,052,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02756:Far2
|
APN |
6 |
148,058,889 (GRCm39) |
missense |
probably damaging |
1.00 |
Galway
|
UTSW |
6 |
148,058,980 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4531001:Far2
|
UTSW |
6 |
148,076,629 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0319:Far2
|
UTSW |
6 |
148,058,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R0654:Far2
|
UTSW |
6 |
148,076,639 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1321:Far2
|
UTSW |
6 |
148,075,034 (GRCm39) |
splice site |
probably benign |
|
R1610:Far2
|
UTSW |
6 |
148,058,956 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2039:Far2
|
UTSW |
6 |
148,067,075 (GRCm39) |
missense |
probably benign |
|
R2471:Far2
|
UTSW |
6 |
148,040,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R3875:Far2
|
UTSW |
6 |
148,052,089 (GRCm39) |
missense |
probably benign |
0.00 |
R3974:Far2
|
UTSW |
6 |
148,052,252 (GRCm39) |
missense |
probably damaging |
0.96 |
R4490:Far2
|
UTSW |
6 |
148,074,907 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4491:Far2
|
UTSW |
6 |
148,074,907 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5034:Far2
|
UTSW |
6 |
148,074,939 (GRCm39) |
missense |
probably benign |
0.43 |
R5421:Far2
|
UTSW |
6 |
148,047,690 (GRCm39) |
splice site |
probably null |
|
R5673:Far2
|
UTSW |
6 |
148,047,602 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6092:Far2
|
UTSW |
6 |
148,076,581 (GRCm39) |
missense |
probably benign |
0.00 |
R6294:Far2
|
UTSW |
6 |
148,058,980 (GRCm39) |
missense |
probably damaging |
0.99 |
R6325:Far2
|
UTSW |
6 |
148,058,995 (GRCm39) |
missense |
probably benign |
0.30 |
R6783:Far2
|
UTSW |
6 |
148,052,273 (GRCm39) |
splice site |
probably null |
|
R7380:Far2
|
UTSW |
6 |
148,082,493 (GRCm39) |
missense |
unknown |
|
R7403:Far2
|
UTSW |
6 |
148,060,475 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7484:Far2
|
UTSW |
6 |
148,075,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Far2
|
UTSW |
6 |
148,075,399 (GRCm39) |
missense |
probably benign |
0.00 |
R8709:Far2
|
UTSW |
6 |
148,067,133 (GRCm39) |
missense |
probably benign |
0.00 |
R8774:Far2
|
UTSW |
6 |
148,047,629 (GRCm39) |
missense |
probably benign |
0.01 |
R8774-TAIL:Far2
|
UTSW |
6 |
148,047,629 (GRCm39) |
missense |
probably benign |
0.01 |
R9177:Far2
|
UTSW |
6 |
148,060,418 (GRCm39) |
missense |
probably benign |
0.00 |
R9268:Far2
|
UTSW |
6 |
148,060,418 (GRCm39) |
missense |
probably benign |
0.00 |
R9504:Far2
|
UTSW |
6 |
148,059,453 (GRCm39) |
missense |
probably damaging |
0.99 |
R9583:Far2
|
UTSW |
6 |
148,059,434 (GRCm39) |
missense |
probably damaging |
0.99 |
R9760:Far2
|
UTSW |
6 |
148,060,448 (GRCm39) |
missense |
probably damaging |
1.00 |
X0053:Far2
|
UTSW |
6 |
148,067,138 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Far2
|
UTSW |
6 |
148,040,156 (GRCm39) |
missense |
probably damaging |
1.00 |
|