Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
C |
T |
11: 109,688,225 (GRCm39) |
S90N |
probably benign |
Het |
Apc2 |
C |
T |
10: 80,137,676 (GRCm39) |
T39I |
possibly damaging |
Het |
Arfgef3 |
C |
T |
10: 18,500,896 (GRCm39) |
R1118K |
probably null |
Het |
Arhgef12 |
T |
C |
9: 42,908,956 (GRCm39) |
D658G |
possibly damaging |
Het |
Asph |
G |
T |
4: 9,453,315 (GRCm39) |
R736S |
probably benign |
Het |
Brd8 |
A |
T |
18: 34,744,279 (GRCm39) |
V183E |
probably damaging |
Het |
C1rl |
G |
A |
6: 124,470,869 (GRCm39) |
G59E |
probably damaging |
Het |
Cacna1i |
C |
A |
15: 80,273,411 (GRCm39) |
A1699D |
probably damaging |
Het |
Card6 |
G |
T |
15: 5,128,214 (GRCm39) |
Q1061K |
probably benign |
Het |
Cd163 |
G |
T |
6: 124,294,540 (GRCm39) |
C566F |
probably damaging |
Het |
Cd84 |
C |
T |
1: 171,712,173 (GRCm39) |
T263I |
possibly damaging |
Het |
Cep63 |
T |
C |
9: 102,464,112 (GRCm39) |
I740V |
possibly damaging |
Het |
Chaf1b |
C |
A |
16: 93,691,791 (GRCm39) |
A279D |
probably damaging |
Het |
Chsy3 |
A |
T |
18: 59,309,488 (GRCm39) |
Y247F |
probably damaging |
Het |
Cpxm1 |
G |
A |
2: 130,235,466 (GRCm39) |
L509F |
possibly damaging |
Het |
Disc1 |
A |
T |
8: 125,875,204 (GRCm39) |
Q558L |
possibly damaging |
Het |
Dnah3 |
A |
T |
7: 119,525,672 (GRCm39) |
L3894Q |
probably damaging |
Het |
Dnmt1 |
G |
T |
9: 20,847,870 (GRCm39) |
T105N |
possibly damaging |
Het |
Dock6 |
A |
T |
9: 21,716,139 (GRCm39) |
L1732Q |
probably damaging |
Het |
Dsc2 |
T |
C |
18: 20,179,303 (GRCm39) |
N255S |
probably benign |
Het |
Dsel |
A |
T |
1: 111,790,242 (GRCm39) |
Y98N |
probably damaging |
Het |
Enox1 |
T |
A |
14: 77,848,814 (GRCm39) |
I375N |
possibly damaging |
Het |
Epha4 |
T |
A |
1: 77,351,405 (GRCm39) |
|
probably null |
Het |
Fktn |
A |
G |
4: 53,761,220 (GRCm39) |
I446V |
probably benign |
Het |
Garin4 |
T |
C |
1: 190,895,678 (GRCm39) |
R322G |
probably benign |
Het |
Gm7361 |
G |
T |
5: 26,466,097 (GRCm39) |
R153L |
probably damaging |
Het |
Grin2c |
C |
T |
11: 115,151,679 (GRCm39) |
V94I |
probably benign |
Het |
Kalrn |
T |
G |
16: 33,796,108 (GRCm39) |
L1222F |
probably damaging |
Het |
Krt80 |
T |
C |
15: 101,249,590 (GRCm39) |
K255E |
probably damaging |
Het |
Lcn6 |
T |
A |
2: 25,570,787 (GRCm39) |
|
probably null |
Het |
Lonp2 |
T |
G |
8: 87,358,078 (GRCm39) |
L100V |
probably damaging |
Het |
Lyn |
G |
A |
4: 3,789,912 (GRCm39) |
A482T |
probably damaging |
Het |
Mapk4 |
A |
G |
18: 74,064,010 (GRCm39) |
F404S |
probably damaging |
Het |
Mast2 |
T |
C |
4: 116,173,747 (GRCm39) |
|
probably null |
Het |
Medag |
T |
C |
5: 149,345,600 (GRCm39) |
Y94H |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,037,911 (GRCm39) |
L809P |
possibly damaging |
Het |
Mgam |
T |
C |
6: 40,734,421 (GRCm39) |
S743P |
probably damaging |
Het |
Mia2 |
C |
A |
12: 59,155,619 (GRCm39) |
T445K |
possibly damaging |
Het |
Mtcl3 |
A |
T |
10: 29,022,931 (GRCm39) |
|
probably null |
Het |
Nars1 |
C |
G |
18: 64,645,120 (GRCm39) |
A43P |
probably damaging |
Het |
Nav3 |
T |
C |
10: 109,688,984 (GRCm39) |
N431S |
possibly damaging |
Het |
Ndufaf5 |
A |
G |
2: 140,019,220 (GRCm39) |
|
probably null |
Het |
Nlrp1b |
T |
G |
11: 71,072,124 (GRCm39) |
E573A |
probably damaging |
Het |
Nlrp3 |
T |
C |
11: 59,433,949 (GRCm39) |
V4A |
probably benign |
Het |
Or2y1d |
G |
A |
11: 49,321,329 (GRCm39) |
G9R |
probably benign |
Het |
Or56b2 |
A |
T |
7: 104,337,420 (GRCm39) |
Y66F |
probably benign |
Het |
Or5ac15 |
T |
C |
16: 58,940,052 (GRCm39) |
N127S |
possibly damaging |
Het |
Pcdhb12 |
A |
T |
18: 37,569,754 (GRCm39) |
D300V |
probably damaging |
Het |
Pik3c2a |
A |
T |
7: 115,968,083 (GRCm39) |
C804S |
probably benign |
Het |
Pkp4 |
A |
T |
2: 59,167,963 (GRCm39) |
Q725L |
probably damaging |
Het |
Ptpre |
T |
A |
7: 135,255,657 (GRCm39) |
S119T |
probably benign |
Het |
Ptprk |
G |
A |
10: 28,259,643 (GRCm39) |
R361H |
probably damaging |
Het |
Ptprr |
T |
C |
10: 116,024,268 (GRCm39) |
V193A |
probably benign |
Het |
Rfx2 |
C |
T |
17: 57,115,263 (GRCm39) |
A19T |
probably benign |
Het |
Rgs4 |
T |
A |
1: 169,572,880 (GRCm39) |
M19L |
probably benign |
Het |
Rnf157 |
T |
C |
11: 116,249,541 (GRCm39) |
H225R |
probably damaging |
Het |
Rnf44 |
A |
T |
13: 54,829,592 (GRCm39) |
D341E |
possibly damaging |
Het |
Sct |
T |
A |
7: 140,858,767 (GRCm39) |
Q55L |
probably damaging |
Het |
Sh3rf1 |
A |
T |
8: 61,814,779 (GRCm39) |
H446L |
possibly damaging |
Het |
Shisa3 |
A |
T |
5: 67,768,402 (GRCm39) |
I101F |
probably damaging |
Het |
Slc6a13 |
A |
G |
6: 121,313,885 (GRCm39) |
I543V |
probably benign |
Het |
Spef2 |
G |
A |
15: 9,634,738 (GRCm39) |
A1024V |
probably damaging |
Het |
St6galnac6 |
T |
C |
2: 32,509,521 (GRCm39) |
S330P |
probably damaging |
Het |
Stard9 |
G |
T |
2: 120,534,203 (GRCm39) |
A3487S |
probably benign |
Het |
Suclg2 |
T |
C |
6: 95,632,532 (GRCm39) |
S46G |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,147,868 (GRCm39) |
V6469A |
possibly damaging |
Het |
Tada2b |
C |
T |
5: 36,641,139 (GRCm39) |
G88D |
probably damaging |
Het |
Tll1 |
A |
T |
8: 64,570,937 (GRCm39) |
|
probably null |
Het |
Tph2 |
T |
A |
10: 115,020,712 (GRCm39) |
H28L |
probably benign |
Het |
Trmt6 |
C |
A |
2: 132,657,755 (GRCm39) |
V34L |
possibly damaging |
Het |
Ttc22 |
A |
G |
4: 106,491,408 (GRCm39) |
T204A |
probably damaging |
Het |
Umodl1 |
A |
T |
17: 31,206,942 (GRCm39) |
M778L |
probably benign |
Het |
Vcan |
T |
C |
13: 89,810,065 (GRCm39) |
H2282R |
probably damaging |
Het |
Vmn2r77 |
T |
A |
7: 86,461,123 (GRCm39) |
S816R |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,858,969 (GRCm39) |
F2806L |
probably damaging |
Het |
Zbtb4 |
C |
A |
11: 69,669,995 (GRCm39) |
A906D |
probably damaging |
Het |
Zscan29 |
A |
G |
2: 120,995,260 (GRCm39) |
V421A |
probably benign |
Het |
|
Other mutations in Bcas1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01647:Bcas1
|
APN |
2 |
170,191,172 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01714:Bcas1
|
APN |
2 |
170,226,102 (GRCm39) |
splice site |
probably benign |
|
IGL02267:Bcas1
|
APN |
2 |
170,220,708 (GRCm39) |
nonsense |
probably null |
|
IGL02486:Bcas1
|
APN |
2 |
170,248,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Bcas1
|
APN |
2 |
170,208,316 (GRCm39) |
nonsense |
probably null |
|
R0335:Bcas1
|
UTSW |
2 |
170,260,601 (GRCm39) |
missense |
probably damaging |
0.97 |
R1458:Bcas1
|
UTSW |
2 |
170,229,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Bcas1
|
UTSW |
2 |
170,260,584 (GRCm39) |
missense |
probably benign |
0.07 |
R1467:Bcas1
|
UTSW |
2 |
170,229,852 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1467:Bcas1
|
UTSW |
2 |
170,229,852 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1507:Bcas1
|
UTSW |
2 |
170,208,348 (GRCm39) |
missense |
probably damaging |
0.99 |
R1645:Bcas1
|
UTSW |
2 |
170,229,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Bcas1
|
UTSW |
2 |
170,229,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R1990:Bcas1
|
UTSW |
2 |
170,212,397 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2017:Bcas1
|
UTSW |
2 |
170,190,081 (GRCm39) |
splice site |
probably null |
|
R4119:Bcas1
|
UTSW |
2 |
170,220,735 (GRCm39) |
missense |
probably benign |
0.02 |
R4181:Bcas1
|
UTSW |
2 |
170,260,547 (GRCm39) |
missense |
probably benign |
0.26 |
R4302:Bcas1
|
UTSW |
2 |
170,260,547 (GRCm39) |
missense |
probably benign |
0.26 |
R4497:Bcas1
|
UTSW |
2 |
170,248,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R4670:Bcas1
|
UTSW |
2 |
170,226,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R4671:Bcas1
|
UTSW |
2 |
170,226,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Bcas1
|
UTSW |
2 |
170,220,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Bcas1
|
UTSW |
2 |
170,220,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Bcas1
|
UTSW |
2 |
170,220,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Bcas1
|
UTSW |
2 |
170,220,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Bcas1
|
UTSW |
2 |
170,260,538 (GRCm39) |
missense |
probably damaging |
0.98 |
R5354:Bcas1
|
UTSW |
2 |
170,191,316 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5686:Bcas1
|
UTSW |
2 |
170,248,730 (GRCm39) |
missense |
probably benign |
0.03 |
R7566:Bcas1
|
UTSW |
2 |
170,212,369 (GRCm39) |
critical splice donor site |
probably null |
|
R7736:Bcas1
|
UTSW |
2 |
170,229,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7816:Bcas1
|
UTSW |
2 |
170,248,347 (GRCm39) |
missense |
probably benign |
0.11 |
R7850:Bcas1
|
UTSW |
2 |
170,190,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R8078:Bcas1
|
UTSW |
2 |
170,260,532 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8350:Bcas1
|
UTSW |
2 |
170,248,220 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8530:Bcas1
|
UTSW |
2 |
170,229,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Bcas1
|
UTSW |
2 |
170,190,081 (GRCm39) |
splice site |
probably benign |
|
R9272:Bcas1
|
UTSW |
2 |
170,190,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R9469:Bcas1
|
UTSW |
2 |
170,191,292 (GRCm39) |
missense |
possibly damaging |
0.90 |
|