Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310002L09Rik |
A |
G |
4: 73,861,424 (GRCm39) |
S59P |
probably damaging |
Het |
Abcc8 |
G |
T |
7: 45,816,418 (GRCm39) |
H241N |
|
Het |
Acsm1 |
T |
C |
7: 119,258,385 (GRCm39) |
S493P |
probably damaging |
Het |
Agtr1a |
T |
C |
13: 30,565,049 (GRCm39) |
I38T |
probably damaging |
Het |
Ahnak |
T |
C |
19: 8,989,099 (GRCm39) |
I3461T |
probably benign |
Het |
Brip1 |
T |
C |
11: 86,039,227 (GRCm39) |
K436E |
possibly damaging |
Het |
Cdhr1 |
T |
A |
14: 36,809,405 (GRCm39) |
T299S |
probably benign |
Het |
Cr2 |
T |
C |
1: 194,853,424 (GRCm39) |
D18G |
probably damaging |
Het |
Cyp51 |
T |
C |
5: 4,150,202 (GRCm39) |
I174V |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,328,754 (GRCm39) |
Y3290N |
probably damaging |
Het |
Fcho1 |
T |
G |
8: 72,169,790 (GRCm39) |
K111T |
possibly damaging |
Het |
Firrm |
C |
T |
1: 163,789,541 (GRCm39) |
V665I |
probably benign |
Het |
Gli2 |
A |
T |
1: 118,763,935 (GRCm39) |
D1405E |
probably damaging |
Het |
Gsg1l2 |
A |
G |
11: 67,680,399 (GRCm39) |
H278R |
possibly damaging |
Het |
H2-K2 |
T |
C |
17: 34,216,294 (GRCm39) |
H284R |
probably damaging |
Het |
Ighv1-62-1 |
C |
T |
12: 115,350,735 (GRCm39) |
W5* |
probably null |
Het |
Ighv1-81 |
T |
A |
12: 115,883,988 (GRCm39) |
T88S |
probably benign |
Het |
Igkv4-57 |
T |
A |
6: 69,553,256 (GRCm39) |
M19L |
probably benign |
Het |
Klk1b3 |
G |
T |
7: 43,849,729 (GRCm39) |
W38L |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,689,762 (GRCm39) |
S2835P |
probably damaging |
Het |
Lhx8 |
T |
C |
3: 154,028,024 (GRCm39) |
N145S |
possibly damaging |
Het |
Mfsd6 |
A |
T |
1: 52,748,454 (GRCm39) |
L137H |
probably damaging |
Het |
Mmp12 |
GTAATAATAATAATAATAAT |
GTAATAATAATAATAAT |
9: 7,348,446 (GRCm39) |
|
probably benign |
Het |
Mpst |
A |
T |
15: 78,294,270 (GRCm39) |
M1L |
possibly damaging |
Het |
Mrpl2 |
T |
A |
17: 46,957,238 (GRCm39) |
|
probably benign |
Het |
Mybpc3 |
T |
C |
2: 90,954,294 (GRCm39) |
V224A |
probably damaging |
Het |
Nol4l |
T |
C |
2: 153,262,651 (GRCm39) |
D63G |
probably damaging |
Het |
Or8g36 |
A |
T |
9: 39,422,910 (GRCm39) |
Y35* |
probably null |
Het |
Patz1 |
C |
T |
11: 3,240,660 (GRCm39) |
T16I |
probably damaging |
Het |
Pcdha3 |
A |
G |
18: 37,080,154 (GRCm39) |
I299V |
probably benign |
Het |
Pcdhb18 |
G |
T |
18: 37,623,537 (GRCm39) |
R289L |
probably benign |
Het |
Pcdhga6 |
A |
T |
18: 37,841,562 (GRCm39) |
R427S |
probably benign |
Het |
Pcdhga8 |
T |
A |
18: 37,859,955 (GRCm39) |
V337E |
probably damaging |
Het |
Pik3c2b |
T |
A |
1: 133,016,068 (GRCm39) |
W877R |
probably benign |
Het |
Plcg2 |
T |
C |
8: 118,231,114 (GRCm39) |
|
probably null |
Het |
Prp2 |
C |
A |
6: 132,577,581 (GRCm39) |
H289Q |
unknown |
Het |
Rac2 |
A |
G |
15: 78,446,112 (GRCm39) |
L192P |
probably damaging |
Het |
Rfx4 |
T |
A |
10: 84,675,936 (GRCm39) |
Y51N |
probably damaging |
Het |
Rptn |
A |
T |
3: 93,302,332 (GRCm39) |
Q16L |
possibly damaging |
Het |
Ryr1 |
C |
T |
7: 28,801,358 (GRCm39) |
G802D |
probably damaging |
Het |
Shroom3 |
T |
C |
5: 93,090,930 (GRCm39) |
S1146P |
probably damaging |
Het |
Stam |
T |
C |
2: 14,133,984 (GRCm39) |
|
probably null |
Het |
Vmn2r100 |
A |
G |
17: 19,751,825 (GRCm39) |
M623V |
probably benign |
Het |
Wdr90 |
G |
A |
17: 26,076,146 (GRCm39) |
R104C |
|
Het |
Xkr7 |
T |
C |
2: 152,874,133 (GRCm39) |
F67L |
probably damaging |
Het |
Zfp451 |
A |
T |
1: 33,842,063 (GRCm39) |
|
probably benign |
Het |
Zfp609 |
C |
T |
9: 65,610,561 (GRCm39) |
A801T |
possibly damaging |
Het |
Zfp974 |
A |
T |
7: 27,610,311 (GRCm39) |
H471Q |
possibly damaging |
Het |
|
Other mutations in Bbox1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01686:Bbox1
|
APN |
2 |
110,095,831 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02273:Bbox1
|
APN |
2 |
110,105,961 (GRCm39) |
nonsense |
probably null |
|
IGL02648:Bbox1
|
APN |
2 |
110,135,871 (GRCm39) |
missense |
probably damaging |
1.00 |
E0374:Bbox1
|
UTSW |
2 |
110,098,656 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4434001:Bbox1
|
UTSW |
2 |
110,105,979 (GRCm39) |
missense |
probably benign |
0.01 |
R0047:Bbox1
|
UTSW |
2 |
110,098,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Bbox1
|
UTSW |
2 |
110,098,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R1173:Bbox1
|
UTSW |
2 |
110,095,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R1682:Bbox1
|
UTSW |
2 |
110,122,893 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2510:Bbox1
|
UTSW |
2 |
110,135,976 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R3740:Bbox1
|
UTSW |
2 |
110,135,922 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3741:Bbox1
|
UTSW |
2 |
110,135,922 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4125:Bbox1
|
UTSW |
2 |
110,100,525 (GRCm39) |
missense |
probably benign |
|
R4126:Bbox1
|
UTSW |
2 |
110,100,525 (GRCm39) |
missense |
probably benign |
|
R4128:Bbox1
|
UTSW |
2 |
110,100,525 (GRCm39) |
missense |
probably benign |
|
R4750:Bbox1
|
UTSW |
2 |
110,095,866 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4841:Bbox1
|
UTSW |
2 |
110,134,084 (GRCm39) |
splice site |
probably null |
|
R5621:Bbox1
|
UTSW |
2 |
110,122,868 (GRCm39) |
nonsense |
probably null |
|
R6210:Bbox1
|
UTSW |
2 |
110,100,422 (GRCm39) |
missense |
probably benign |
0.38 |
R6649:Bbox1
|
UTSW |
2 |
110,135,914 (GRCm39) |
missense |
probably benign |
|
R6677:Bbox1
|
UTSW |
2 |
110,135,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Bbox1
|
UTSW |
2 |
110,122,884 (GRCm39) |
missense |
probably benign |
|
R7473:Bbox1
|
UTSW |
2 |
110,095,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7590:Bbox1
|
UTSW |
2 |
110,098,577 (GRCm39) |
missense |
probably benign |
|
R7672:Bbox1
|
UTSW |
2 |
110,135,794 (GRCm39) |
missense |
probably damaging |
0.96 |
R7881:Bbox1
|
UTSW |
2 |
110,122,871 (GRCm39) |
missense |
probably benign |
0.00 |
R9711:Bbox1
|
UTSW |
2 |
110,098,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Bbox1
|
UTSW |
2 |
110,100,418 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Bbox1
|
UTSW |
2 |
110,100,533 (GRCm39) |
missense |
probably benign |
0.22 |
|