Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330161L09Rik |
T |
C |
12: 103,373,848 (GRCm39) |
|
probably benign |
Het |
Ablim1 |
T |
C |
19: 57,032,245 (GRCm39) |
D638G |
possibly damaging |
Het |
Adam1b |
A |
G |
5: 121,638,777 (GRCm39) |
|
probably benign |
Het |
Aim2 |
T |
C |
1: 173,287,279 (GRCm39) |
M93T |
probably benign |
Het |
Alpk2 |
T |
C |
18: 65,440,151 (GRCm39) |
E414G |
possibly damaging |
Het |
Ap1b1 |
T |
C |
11: 4,965,613 (GRCm39) |
F51L |
probably damaging |
Het |
Bard1 |
T |
A |
1: 71,114,550 (GRCm39) |
K144* |
probably null |
Het |
Begain |
G |
T |
12: 108,999,843 (GRCm39) |
Y514* |
probably null |
Het |
Cfap251 |
G |
A |
5: 123,392,438 (GRCm39) |
|
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,824,197 (GRCm39) |
Y58C |
probably damaging |
Het |
Cfap54 |
A |
T |
10: 92,722,229 (GRCm39) |
D2437E |
unknown |
Het |
Chd2 |
A |
G |
7: 73,079,735 (GRCm39) |
S1722P |
probably benign |
Het |
Clec5a |
C |
T |
6: 40,562,137 (GRCm39) |
G9E |
probably damaging |
Het |
Cog4 |
A |
G |
8: 111,585,214 (GRCm39) |
Y292C |
possibly damaging |
Het |
Col3a1 |
C |
T |
1: 45,369,305 (GRCm39) |
P331S |
unknown |
Het |
Ctsk |
T |
C |
3: 95,413,988 (GRCm39) |
I245T |
probably benign |
Het |
Dthd1 |
T |
C |
5: 62,979,251 (GRCm39) |
Y304H |
probably damaging |
Het |
Dthd1 |
T |
C |
5: 63,000,222 (GRCm39) |
S515P |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Eci2 |
A |
G |
13: 35,174,699 (GRCm39) |
|
probably null |
Het |
Ecm1 |
C |
T |
3: 95,643,254 (GRCm39) |
A349T |
probably benign |
Het |
Efemp2 |
A |
G |
19: 5,525,190 (GRCm39) |
E32G |
probably damaging |
Het |
Flt4 |
C |
A |
11: 49,516,131 (GRCm39) |
T78K |
probably benign |
Het |
Foxg1 |
A |
G |
12: 49,431,708 (GRCm39) |
|
probably benign |
Het |
Fv1 |
T |
C |
4: 147,954,619 (GRCm39) |
V395A |
possibly damaging |
Het |
Gcfc2 |
C |
A |
6: 81,900,759 (GRCm39) |
D24E |
probably benign |
Het |
Gpha2 |
T |
G |
19: 6,277,532 (GRCm39) |
V96G |
probably damaging |
Het |
Gse1 |
A |
G |
8: 121,293,719 (GRCm39) |
Y228C |
probably damaging |
Het |
Hmgxb3 |
T |
C |
18: 61,288,458 (GRCm39) |
R470G |
possibly damaging |
Het |
Ildr1 |
A |
G |
16: 36,542,341 (GRCm39) |
E247G |
probably damaging |
Het |
Ktn1 |
T |
A |
14: 47,931,345 (GRCm39) |
M646K |
possibly damaging |
Het |
Lrrc37a |
T |
A |
11: 103,388,648 (GRCm39) |
H2259L |
unknown |
Het |
Map1b |
A |
T |
13: 99,567,629 (GRCm39) |
H1697Q |
unknown |
Het |
Mdn1 |
A |
G |
4: 32,700,409 (GRCm39) |
E1456G |
probably damaging |
Het |
Mta1 |
C |
T |
12: 113,095,248 (GRCm39) |
T467I |
probably damaging |
Het |
Nav1 |
C |
T |
1: 135,376,742 (GRCm39) |
R1694Q |
probably damaging |
Het |
Ncoa5 |
C |
A |
2: 164,854,838 (GRCm39) |
D95Y |
possibly damaging |
Het |
Nfatc1 |
A |
T |
18: 80,678,879 (GRCm39) |
C836* |
probably null |
Het |
Nr3c2 |
T |
C |
8: 77,635,156 (GRCm39) |
S86P |
possibly damaging |
Het |
Nup153 |
A |
G |
13: 46,837,404 (GRCm39) |
S1273P |
probably benign |
Het |
Or8g52 |
G |
A |
9: 39,631,018 (GRCm39) |
R165Q |
probably benign |
Het |
Pcsk5 |
C |
A |
19: 17,450,423 (GRCm39) |
G1142C |
probably damaging |
Het |
Pgghg |
A |
G |
7: 140,523,453 (GRCm39) |
D244G |
possibly damaging |
Het |
Polr1has |
T |
C |
17: 37,276,336 (GRCm39) |
V306A |
possibly damaging |
Het |
Ppargc1b |
G |
A |
18: 61,444,321 (GRCm39) |
P297S |
probably benign |
Het |
Rad52 |
A |
T |
6: 119,897,855 (GRCm39) |
Q356L |
possibly damaging |
Het |
Rhpn1 |
T |
A |
15: 75,585,083 (GRCm39) |
F507I |
probably damaging |
Het |
Rhpn2 |
T |
C |
7: 35,076,433 (GRCm39) |
M328T |
probably benign |
Het |
Rnf19a |
T |
C |
15: 36,254,665 (GRCm39) |
I298V |
possibly damaging |
Het |
Rwdd2a |
T |
C |
9: 86,456,184 (GRCm39) |
V120A |
probably benign |
Het |
Scml2 |
G |
T |
X: 160,014,442 (GRCm39) |
E566D |
possibly damaging |
Het |
Serpina3a |
G |
A |
12: 104,082,481 (GRCm39) |
A85T |
probably damaging |
Het |
Slc16a11 |
G |
A |
11: 70,106,146 (GRCm39) |
G80D |
probably damaging |
Het |
Slc5a5 |
A |
T |
8: 71,342,395 (GRCm39) |
|
probably null |
Het |
Sparcl1 |
T |
A |
5: 104,236,289 (GRCm39) |
Q488L |
probably damaging |
Het |
Spg21 |
T |
A |
9: 65,391,711 (GRCm39) |
|
probably null |
Het |
Spopfm2 |
A |
G |
3: 94,082,834 (GRCm39) |
S326P |
probably damaging |
Het |
Sry |
T |
C |
Y: 2,662,901 (GRCm39) |
H253R |
unknown |
Het |
Swt1 |
A |
G |
1: 151,279,636 (GRCm39) |
S391P |
probably damaging |
Het |
Uhrf2 |
A |
G |
19: 30,033,888 (GRCm39) |
Y200C |
probably damaging |
Het |
Utp15 |
T |
C |
13: 98,391,493 (GRCm39) |
H248R |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,603,313 (GRCm39) |
|
probably null |
Het |
Vcan |
T |
A |
13: 89,841,422 (GRCm39) |
D414V |
probably damaging |
Het |
Vmn1r56 |
A |
T |
7: 5,199,179 (GRCm39) |
M146K |
probably damaging |
Het |
Zfp143 |
A |
T |
7: 109,685,453 (GRCm39) |
K399N |
probably damaging |
Het |
Zfp516 |
A |
G |
18: 82,975,536 (GRCm39) |
D578G |
probably damaging |
Het |
Zfp90 |
G |
A |
8: 107,152,120 (GRCm39) |
C611Y |
probably damaging |
Het |
|
Other mutations in Ccdc186 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00708:Ccdc186
|
APN |
19 |
56,801,879 (GRCm39) |
missense |
probably benign |
0.18 |
IGL00976:Ccdc186
|
APN |
19 |
56,785,932 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01146:Ccdc186
|
APN |
19 |
56,797,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01316:Ccdc186
|
APN |
19 |
56,801,845 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01627:Ccdc186
|
APN |
19 |
56,780,452 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02325:Ccdc186
|
APN |
19 |
56,801,788 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02755:Ccdc186
|
APN |
19 |
56,801,828 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02899:Ccdc186
|
APN |
19 |
56,781,920 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03408:Ccdc186
|
APN |
19 |
56,787,163 (GRCm39) |
missense |
probably benign |
0.00 |
receding
|
UTSW |
19 |
56,788,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R1256:Ccdc186
|
UTSW |
19 |
56,786,053 (GRCm39) |
missense |
probably benign |
0.20 |
R1728:Ccdc186
|
UTSW |
19 |
56,797,652 (GRCm39) |
missense |
probably benign |
0.04 |
R1729:Ccdc186
|
UTSW |
19 |
56,797,652 (GRCm39) |
missense |
probably benign |
0.04 |
R1784:Ccdc186
|
UTSW |
19 |
56,797,652 (GRCm39) |
missense |
probably benign |
0.04 |
R1813:Ccdc186
|
UTSW |
19 |
56,788,601 (GRCm39) |
missense |
probably benign |
0.03 |
R1909:Ccdc186
|
UTSW |
19 |
56,781,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R2319:Ccdc186
|
UTSW |
19 |
56,785,999 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2351:Ccdc186
|
UTSW |
19 |
56,787,129 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2970:Ccdc186
|
UTSW |
19 |
56,795,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R4159:Ccdc186
|
UTSW |
19 |
56,781,924 (GRCm39) |
nonsense |
probably null |
|
R4898:Ccdc186
|
UTSW |
19 |
56,790,432 (GRCm39) |
splice site |
probably null |
|
R4910:Ccdc186
|
UTSW |
19 |
56,787,123 (GRCm39) |
missense |
probably damaging |
0.98 |
R5325:Ccdc186
|
UTSW |
19 |
56,801,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R5338:Ccdc186
|
UTSW |
19 |
56,801,689 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5662:Ccdc186
|
UTSW |
19 |
56,781,920 (GRCm39) |
missense |
probably benign |
|
R5773:Ccdc186
|
UTSW |
19 |
56,801,919 (GRCm39) |
missense |
probably benign |
0.06 |
R6621:Ccdc186
|
UTSW |
19 |
56,801,919 (GRCm39) |
missense |
probably benign |
0.06 |
R6806:Ccdc186
|
UTSW |
19 |
56,788,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Ccdc186
|
UTSW |
19 |
56,780,371 (GRCm39) |
critical splice donor site |
probably null |
|
R6977:Ccdc186
|
UTSW |
19 |
56,787,219 (GRCm39) |
missense |
probably benign |
0.05 |
R7108:Ccdc186
|
UTSW |
19 |
56,787,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Ccdc186
|
UTSW |
19 |
56,780,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7407:Ccdc186
|
UTSW |
19 |
56,801,817 (GRCm39) |
missense |
probably benign |
0.00 |
R7408:Ccdc186
|
UTSW |
19 |
56,796,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R7437:Ccdc186
|
UTSW |
19 |
56,795,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R8219:Ccdc186
|
UTSW |
19 |
56,781,777 (GRCm39) |
missense |
probably benign |
0.42 |
R8422:Ccdc186
|
UTSW |
19 |
56,801,617 (GRCm39) |
missense |
probably benign |
0.26 |
R8537:Ccdc186
|
UTSW |
19 |
56,798,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Ccdc186
|
UTSW |
19 |
56,801,793 (GRCm39) |
missense |
probably damaging |
0.98 |
R8777-TAIL:Ccdc186
|
UTSW |
19 |
56,801,793 (GRCm39) |
missense |
probably damaging |
0.98 |
R9510:Ccdc186
|
UTSW |
19 |
56,802,016 (GRCm39) |
missense |
probably benign |
0.00 |
RF014:Ccdc186
|
UTSW |
19 |
56,801,904 (GRCm39) |
missense |
probably benign |
0.00 |
|