Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,823,595 (GRCm39) |
F374S |
possibly damaging |
Het |
Abca14 |
T |
A |
7: 119,823,644 (GRCm39) |
Y390* |
probably null |
Het |
Abca9 |
T |
C |
11: 110,054,206 (GRCm39) |
|
probably null |
Het |
Anxa1 |
G |
T |
19: 20,352,662 (GRCm39) |
S304* |
probably null |
Het |
Aspm |
G |
A |
1: 139,406,690 (GRCm39) |
R1859Q |
probably damaging |
Het |
Atp13a5 |
A |
T |
16: 29,197,314 (GRCm39) |
N14K |
probably damaging |
Het |
Bmpr1a |
G |
T |
14: 34,163,148 (GRCm39) |
H81N |
possibly damaging |
Het |
Camkv |
C |
T |
9: 107,824,296 (GRCm39) |
T236I |
probably damaging |
Het |
Carm1 |
T |
A |
9: 21,490,789 (GRCm39) |
M219K |
probably damaging |
Het |
Ccdc162 |
T |
C |
10: 41,474,507 (GRCm39) |
R1352G |
probably benign |
Het |
Cd200l1 |
A |
T |
16: 45,263,007 (GRCm39) |
V44D |
possibly damaging |
Het |
Cib1 |
A |
G |
7: 79,878,211 (GRCm39) |
L89P |
probably damaging |
Het |
Col6a5 |
C |
T |
9: 105,822,833 (GRCm39) |
E175K |
unknown |
Het |
Crebbp |
A |
G |
16: 4,031,023 (GRCm39) |
F22S |
probably damaging |
Het |
Csn1s1 |
T |
C |
5: 87,824,482 (GRCm39) |
|
probably null |
Het |
Dchs1 |
A |
T |
7: 105,408,212 (GRCm39) |
H1873Q |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,012,396 (GRCm39) |
D1901G |
probably damaging |
Het |
Dock10 |
G |
T |
1: 80,519,016 (GRCm39) |
T1235N |
probably benign |
Het |
Eddm3b |
T |
A |
14: 51,354,110 (GRCm39) |
S33T |
probably damaging |
Het |
Fam151b |
A |
T |
13: 92,610,567 (GRCm39) |
M74K |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,476,158 (GRCm39) |
F1735I |
probably damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,863,751 (GRCm39) |
R2508G |
probably benign |
Het |
Fip1l1 |
T |
G |
5: 74,756,524 (GRCm39) |
S505R |
probably damaging |
Het |
Gm21886 |
ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG |
ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG |
18: 80,133,040 (GRCm39) |
|
probably benign |
Het |
Gpr180 |
A |
G |
14: 118,395,452 (GRCm39) |
I295V |
probably benign |
Het |
Gtf3c2 |
G |
A |
5: 31,331,151 (GRCm39) |
T175I |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,244,741 (GRCm39) |
Y733H |
probably damaging |
Het |
Irs1 |
T |
A |
1: 82,264,652 (GRCm39) |
Q1188L |
probably benign |
Het |
Kcnk5 |
T |
C |
14: 20,192,046 (GRCm39) |
R372G |
probably benign |
Het |
Kdm5b |
T |
A |
1: 134,541,664 (GRCm39) |
N746K |
possibly damaging |
Het |
Kdm7a |
T |
C |
6: 39,123,903 (GRCm39) |
I754V |
probably benign |
Het |
Mad2l1bp |
G |
A |
17: 46,458,891 (GRCm39) |
T213I |
possibly damaging |
Het |
Map2 |
G |
T |
1: 66,419,684 (GRCm39) |
R5L |
probably damaging |
Het |
Map4 |
G |
A |
9: 109,901,702 (GRCm39) |
V781M |
possibly damaging |
Het |
Mbd2 |
A |
G |
18: 70,713,864 (GRCm39) |
D231G |
probably damaging |
Het |
Negr1 |
C |
A |
3: 156,721,906 (GRCm39) |
P160Q |
probably damaging |
Het |
Nfya |
A |
T |
17: 48,700,489 (GRCm39) |
|
probably benign |
Het |
Nlk |
T |
C |
11: 78,586,758 (GRCm39) |
Q112R |
probably benign |
Het |
Obscn |
C |
A |
11: 58,947,009 (GRCm39) |
A4339S |
probably damaging |
Het |
Or3a10 |
A |
G |
11: 73,935,782 (GRCm39) |
F106S |
possibly damaging |
Het |
Or5b99 |
A |
T |
19: 12,976,445 (GRCm39) |
I32F |
probably damaging |
Het |
Pcdhb12 |
A |
G |
18: 37,570,590 (GRCm39) |
T579A |
probably benign |
Het |
Pcdhb2 |
G |
A |
18: 37,429,715 (GRCm39) |
V563M |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,208,729 (GRCm39) |
R2545G |
probably benign |
Het |
Plcb1 |
A |
G |
2: 135,179,439 (GRCm39) |
N616D |
probably damaging |
Het |
Pogk |
A |
T |
1: 166,226,394 (GRCm39) |
F586I |
probably damaging |
Het |
Polr1f |
T |
A |
12: 33,483,526 (GRCm39) |
Y93N |
probably damaging |
Het |
Prkg2 |
T |
A |
5: 99,119,815 (GRCm39) |
I435F |
possibly damaging |
Het |
Prrt4 |
T |
C |
6: 29,177,665 (GRCm39) |
T35A |
probably damaging |
Het |
Rad17 |
A |
G |
13: 100,767,576 (GRCm39) |
S342P |
probably damaging |
Het |
Rpl36-ps4 |
A |
G |
17: 88,228,574 (GRCm39) |
T40A |
probably damaging |
Het |
Skint5 |
T |
C |
4: 113,374,349 (GRCm39) |
T1247A |
unknown |
Het |
Slc22a14 |
A |
G |
9: 118,998,778 (GRCm39) |
L182P |
possibly damaging |
Het |
Slc35b3 |
T |
C |
13: 39,138,097 (GRCm39) |
D104G |
probably damaging |
Het |
Sult2a1 |
A |
G |
7: 13,530,342 (GRCm39) |
F266L |
probably damaging |
Het |
Sult2a2 |
A |
T |
7: 13,467,484 (GRCm39) |
M1L |
probably damaging |
Het |
Tat |
T |
A |
8: 110,718,337 (GRCm39) |
I74N |
probably damaging |
Het |
Trappc6a |
G |
T |
7: 19,249,923 (GRCm39) |
|
probably benign |
Het |
Usp44 |
A |
G |
10: 93,682,129 (GRCm39) |
E193G |
possibly damaging |
Het |
Virma |
C |
T |
4: 11,519,047 (GRCm39) |
Q765* |
probably null |
Het |
Vmn1r46 |
T |
C |
6: 89,954,053 (GRCm39) |
S301P |
probably damaging |
Het |
Vmn2r116 |
A |
T |
17: 23,620,467 (GRCm39) |
I734F |
probably damaging |
Het |
Vmn2r5 |
A |
T |
3: 64,398,522 (GRCm39) |
V819D |
probably damaging |
Het |
Vmn2r74 |
A |
G |
7: 85,606,569 (GRCm39) |
I259T |
probably damaging |
Het |
Vps13a |
A |
G |
19: 16,723,340 (GRCm39) |
I286T |
probably damaging |
Het |
Wdr73 |
T |
C |
7: 80,550,131 (GRCm39) |
I55V |
probably benign |
Het |
Znhit2 |
A |
T |
19: 6,111,803 (GRCm39) |
R183* |
probably null |
Het |
|
Other mutations in Csf2rb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00565:Csf2rb
|
APN |
15 |
78,232,714 (GRCm39) |
nonsense |
probably null |
|
IGL00979:Csf2rb
|
APN |
15 |
78,232,304 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01613:Csf2rb
|
APN |
15 |
78,219,502 (GRCm39) |
intron |
probably benign |
|
IGL01724:Csf2rb
|
APN |
15 |
78,220,614 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01942:Csf2rb
|
APN |
15 |
78,224,692 (GRCm39) |
missense |
probably benign |
|
IGL02479:Csf2rb
|
APN |
15 |
78,225,924 (GRCm39) |
nonsense |
probably null |
|
3-1:Csf2rb
|
UTSW |
15 |
78,228,803 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02802:Csf2rb
|
UTSW |
15 |
78,223,103 (GRCm39) |
missense |
probably benign |
0.00 |
R0133:Csf2rb
|
UTSW |
15 |
78,223,204 (GRCm39) |
unclassified |
probably benign |
|
R0179:Csf2rb
|
UTSW |
15 |
78,220,572 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0487:Csf2rb
|
UTSW |
15 |
78,232,531 (GRCm39) |
missense |
probably benign |
0.00 |
R1544:Csf2rb
|
UTSW |
15 |
78,224,955 (GRCm39) |
missense |
probably benign |
0.02 |
R1619:Csf2rb
|
UTSW |
15 |
78,219,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R1690:Csf2rb
|
UTSW |
15 |
78,232,844 (GRCm39) |
missense |
probably benign |
0.11 |
R1831:Csf2rb
|
UTSW |
15 |
78,232,453 (GRCm39) |
missense |
probably benign |
0.03 |
R3970:Csf2rb
|
UTSW |
15 |
78,225,667 (GRCm39) |
missense |
probably benign |
|
R4922:Csf2rb
|
UTSW |
15 |
78,230,667 (GRCm39) |
missense |
probably benign |
0.02 |
R5151:Csf2rb
|
UTSW |
15 |
78,224,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5202:Csf2rb
|
UTSW |
15 |
78,233,257 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5398:Csf2rb
|
UTSW |
15 |
78,232,820 (GRCm39) |
missense |
probably benign |
|
R5496:Csf2rb
|
UTSW |
15 |
78,224,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:Csf2rb
|
UTSW |
15 |
78,233,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6166:Csf2rb
|
UTSW |
15 |
78,228,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R6347:Csf2rb
|
UTSW |
15 |
78,229,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R6350:Csf2rb
|
UTSW |
15 |
78,229,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R6899:Csf2rb
|
UTSW |
15 |
78,224,902 (GRCm39) |
missense |
probably benign |
0.01 |
R6984:Csf2rb
|
UTSW |
15 |
78,229,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R7484:Csf2rb
|
UTSW |
15 |
78,223,099 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7671:Csf2rb
|
UTSW |
15 |
78,223,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Csf2rb
|
UTSW |
15 |
78,225,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Csf2rb
|
UTSW |
15 |
78,228,771 (GRCm39) |
missense |
probably benign |
0.00 |
R7861:Csf2rb
|
UTSW |
15 |
78,233,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R8135:Csf2rb
|
UTSW |
15 |
78,232,319 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8154:Csf2rb
|
UTSW |
15 |
78,224,642 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8299:Csf2rb
|
UTSW |
15 |
78,230,669 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8315:Csf2rb
|
UTSW |
15 |
78,231,581 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8926:Csf2rb
|
UTSW |
15 |
78,224,749 (GRCm39) |
missense |
probably benign |
|
R8948:Csf2rb
|
UTSW |
15 |
78,232,520 (GRCm39) |
missense |
probably benign |
0.05 |
R9265:Csf2rb
|
UTSW |
15 |
78,232,746 (GRCm39) |
missense |
probably benign |
0.08 |
R9510:Csf2rb
|
UTSW |
15 |
78,229,760 (GRCm39) |
critical splice donor site |
probably null |
|
R9755:Csf2rb
|
UTSW |
15 |
78,232,824 (GRCm39) |
nonsense |
probably null |
|
X0024:Csf2rb
|
UTSW |
15 |
78,220,560 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Csf2rb
|
UTSW |
15 |
78,233,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|