Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630095N17Rik |
T |
C |
1: 75,197,181 (GRCm39) |
|
probably benign |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adgrv1 |
A |
G |
13: 81,624,683 (GRCm39) |
L3762P |
probably damaging |
Het |
Amn1 |
G |
A |
6: 149,086,522 (GRCm39) |
R4W |
probably damaging |
Het |
Atxn1 |
G |
T |
13: 45,720,347 (GRCm39) |
T516N |
possibly damaging |
Het |
Atxn7 |
A |
T |
14: 14,089,260 (GRCm38) |
T259S |
probably benign |
Het |
Bsn |
C |
G |
9: 107,982,710 (GRCm39) |
R3681P |
unknown |
Het |
Ccdc110 |
T |
G |
8: 46,393,646 (GRCm39) |
S119R |
probably benign |
Het |
Ccdc202 |
C |
A |
14: 96,119,807 (GRCm39) |
A188E |
probably benign |
Het |
Ceacam20 |
A |
T |
7: 19,704,318 (GRCm39) |
Q123L |
possibly damaging |
Het |
Clip3 |
A |
G |
7: 29,998,274 (GRCm39) |
D240G |
possibly damaging |
Het |
Col24a1 |
T |
C |
3: 145,004,588 (GRCm39) |
F22S |
probably benign |
Het |
Dlg5 |
T |
A |
14: 24,227,860 (GRCm39) |
M354L |
probably benign |
Het |
Dnajb12 |
GC |
G |
10: 59,728,574 (GRCm39) |
|
probably null |
Het |
Dnase1l3 |
A |
G |
14: 7,967,847 (GRCm38) |
V282A |
probably damaging |
Het |
Dnhd1 |
G |
A |
7: 105,364,028 (GRCm39) |
G4127S |
probably damaging |
Het |
Eed |
G |
A |
7: 89,617,001 (GRCm39) |
R165W |
probably damaging |
Het |
Ephb2 |
C |
T |
4: 136,388,717 (GRCm39) |
V627M |
probably damaging |
Het |
Fancc |
T |
C |
13: 63,465,201 (GRCm39) |
E502G |
possibly damaging |
Het |
Fbf1 |
T |
C |
11: 116,048,646 (GRCm39) |
D105G |
probably damaging |
Het |
Fer |
T |
A |
17: 64,344,580 (GRCm39) |
Y246* |
probably null |
Het |
Fer1l6 |
A |
G |
15: 58,532,674 (GRCm39) |
K1792E |
probably damaging |
Het |
Foxi2 |
A |
G |
7: 135,013,376 (GRCm39) |
D202G |
probably damaging |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
H2-DMb2 |
G |
T |
17: 34,364,445 (GRCm39) |
|
probably null |
Het |
Helq |
G |
T |
5: 100,934,916 (GRCm39) |
D491E |
probably benign |
Het |
Hgsnat |
A |
G |
8: 26,436,362 (GRCm39) |
V564A |
possibly damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hs3st5 |
T |
A |
10: 36,709,425 (GRCm39) |
V320D |
probably damaging |
Het |
Ifit1bl1 |
A |
T |
19: 34,571,197 (GRCm39) |
L420* |
probably null |
Het |
Ift80 |
T |
G |
3: 68,875,196 (GRCm39) |
N178T |
probably benign |
Het |
Ing4 |
C |
T |
6: 125,024,023 (GRCm39) |
T89I |
possibly damaging |
Het |
Lcp1 |
G |
A |
14: 75,449,948 (GRCm39) |
D386N |
probably benign |
Het |
Mdc1 |
T |
A |
17: 36,159,438 (GRCm39) |
I606K |
probably benign |
Het |
Mllt10 |
T |
A |
2: 18,114,656 (GRCm39) |
M120K |
probably damaging |
Het |
Morc1 |
G |
T |
16: 48,269,711 (GRCm39) |
L89F |
probably benign |
Het |
Mroh2a |
GCCC |
GC |
1: 88,159,979 (GRCm39) |
|
probably null |
Het |
Nav3 |
C |
A |
10: 109,552,413 (GRCm39) |
D1810Y |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,926,919 (GRCm39) |
T5532M |
probably damaging |
Het |
Opn3 |
C |
T |
1: 175,493,153 (GRCm39) |
R137H |
probably damaging |
Het |
Or12j2 |
C |
T |
7: 139,916,065 (GRCm39) |
Q97* |
probably null |
Het |
Or2d36 |
A |
G |
7: 106,747,297 (GRCm39) |
N258S |
probably benign |
Het |
Palld |
G |
A |
8: 61,969,619 (GRCm39) |
A993V |
probably damaging |
Het |
Ppp1r12c |
A |
T |
7: 4,489,355 (GRCm39) |
|
probably null |
Het |
Prdm4 |
TCTCCTCCT |
TCTCCT |
10: 85,728,987 (GRCm39) |
|
probably null |
Het |
Rapgef2 |
A |
T |
3: 78,995,950 (GRCm39) |
|
probably null |
Het |
Ring1 |
T |
C |
17: 34,240,432 (GRCm39) |
E382G |
possibly damaging |
Het |
Rpl22l1 |
T |
A |
3: 28,860,969 (GRCm39) |
N61K |
probably benign |
Het |
Rpp14 |
A |
G |
14: 8,090,558 (GRCm38) |
|
probably null |
Het |
Rusc2 |
C |
T |
4: 43,415,932 (GRCm39) |
Q413* |
probably null |
Het |
Slco3a1 |
A |
G |
7: 73,968,247 (GRCm39) |
I491T |
possibly damaging |
Het |
Smtnl1 |
C |
T |
2: 84,648,739 (GRCm39) |
V172I |
probably benign |
Het |
Spats2l |
T |
A |
1: 57,939,780 (GRCm39) |
|
probably null |
Het |
Spire1 |
T |
A |
18: 67,639,716 (GRCm39) |
N266Y |
probably damaging |
Het |
Stox2 |
T |
C |
8: 47,646,041 (GRCm39) |
H473R |
probably damaging |
Het |
Syne2 |
C |
T |
12: 76,141,232 (GRCm39) |
R121* |
probably null |
Het |
Synrg |
G |
A |
11: 83,893,066 (GRCm39) |
|
probably null |
Het |
Tm9sf1 |
C |
T |
14: 55,875,554 (GRCm39) |
V397M |
probably damaging |
Het |
Trabd |
T |
C |
15: 88,966,187 (GRCm39) |
M48T |
probably benign |
Het |
Ttn |
T |
A |
2: 76,537,577 (GRCm39) |
I26457F |
possibly damaging |
Het |
Uggt2 |
C |
T |
14: 119,278,939 (GRCm39) |
R856Q |
probably benign |
Het |
Ugt1a5 |
T |
A |
1: 88,094,039 (GRCm39) |
M89K |
probably benign |
Het |
Vmn2r53 |
A |
T |
7: 12,335,347 (GRCm39) |
S104R |
probably damaging |
Het |
Zdhhc12 |
A |
T |
2: 29,982,496 (GRCm39) |
L53Q |
probably null |
Het |
|
Other mutations in C8b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:C8b
|
APN |
4 |
104,658,531 (GRCm39) |
splice site |
probably benign |
|
IGL01145:C8b
|
APN |
4 |
104,637,777 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01768:C8b
|
APN |
4 |
104,644,151 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02347:C8b
|
APN |
4 |
104,644,151 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02488:C8b
|
APN |
4 |
104,661,278 (GRCm39) |
missense |
probably benign |
|
IGL02957:C8b
|
APN |
4 |
104,623,652 (GRCm39) |
missense |
probably benign |
|
IGL02979:C8b
|
APN |
4 |
104,631,585 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02995:C8b
|
APN |
4 |
104,658,525 (GRCm39) |
splice site |
probably benign |
|
IGL03294:C8b
|
APN |
4 |
104,637,888 (GRCm39) |
missense |
probably benign |
0.06 |
R0568:C8b
|
UTSW |
4 |
104,650,577 (GRCm39) |
missense |
probably benign |
0.39 |
R1015:C8b
|
UTSW |
4 |
104,644,157 (GRCm39) |
missense |
probably benign |
0.19 |
R1191:C8b
|
UTSW |
4 |
104,650,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:C8b
|
UTSW |
4 |
104,641,679 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3824:C8b
|
UTSW |
4 |
104,640,206 (GRCm39) |
missense |
probably benign |
0.42 |
R4611:C8b
|
UTSW |
4 |
104,647,841 (GRCm39) |
missense |
probably damaging |
0.98 |
R4756:C8b
|
UTSW |
4 |
104,644,083 (GRCm39) |
missense |
probably benign |
|
R4845:C8b
|
UTSW |
4 |
104,649,009 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5355:C8b
|
UTSW |
4 |
104,637,860 (GRCm39) |
missense |
probably benign |
0.01 |
R5436:C8b
|
UTSW |
4 |
104,657,546 (GRCm39) |
nonsense |
probably null |
|
R5967:C8b
|
UTSW |
4 |
104,650,530 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6744:C8b
|
UTSW |
4 |
104,631,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R6899:C8b
|
UTSW |
4 |
104,644,071 (GRCm39) |
missense |
probably benign |
0.02 |
R6977:C8b
|
UTSW |
4 |
104,644,193 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7088:C8b
|
UTSW |
4 |
104,650,540 (GRCm39) |
missense |
probably benign |
0.12 |
R7224:C8b
|
UTSW |
4 |
104,637,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:C8b
|
UTSW |
4 |
104,637,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8058:C8b
|
UTSW |
4 |
104,647,811 (GRCm39) |
missense |
probably damaging |
0.96 |
R8437:C8b
|
UTSW |
4 |
104,644,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R8821:C8b
|
UTSW |
4 |
104,647,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8831:C8b
|
UTSW |
4 |
104,647,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:C8b
|
UTSW |
4 |
104,641,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R9237:C8b
|
UTSW |
4 |
104,650,481 (GRCm39) |
missense |
probably benign |
0.00 |
R9294:C8b
|
UTSW |
4 |
104,644,192 (GRCm39) |
missense |
probably benign |
0.04 |
R9789:C8b
|
UTSW |
4 |
104,640,191 (GRCm39) |
missense |
probably benign |
0.00 |
|