Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
C |
T |
3: 121,919,962 (GRCm39) |
|
probably null |
Het |
Acyp1 |
C |
T |
12: 85,325,679 (GRCm39) |
V107I |
probably null |
Het |
Aftph |
T |
C |
11: 20,676,144 (GRCm39) |
|
probably null |
Het |
Agtpbp1 |
A |
T |
13: 59,692,167 (GRCm39) |
|
probably null |
Het |
Arhgap30 |
T |
C |
1: 171,235,297 (GRCm39) |
V557A |
probably damaging |
Het |
Asb3 |
T |
A |
11: 31,031,493 (GRCm39) |
M410K |
probably benign |
Het |
B4galnt2 |
T |
C |
11: 95,759,460 (GRCm39) |
|
probably null |
Het |
Birc2 |
A |
G |
9: 7,860,262 (GRCm39) |
|
probably null |
Het |
Cav2 |
A |
T |
6: 17,286,950 (GRCm39) |
N69Y |
probably damaging |
Het |
Cc2d2b |
G |
A |
19: 40,784,111 (GRCm39) |
C826Y |
probably benign |
Het |
Cenpf |
T |
A |
1: 189,385,051 (GRCm39) |
T2410S |
probably benign |
Het |
Chchd1 |
A |
G |
14: 20,753,448 (GRCm39) |
D24G |
probably benign |
Het |
Cmip |
G |
A |
8: 118,163,618 (GRCm39) |
G450S |
probably benign |
Het |
Col11a1 |
C |
T |
3: 114,006,099 (GRCm39) |
Q534* |
probably null |
Het |
Col3a1 |
G |
T |
1: 45,377,782 (GRCm39) |
|
probably benign |
Het |
Cox4i1 |
T |
C |
8: 121,399,969 (GRCm39) |
I31T |
possibly damaging |
Het |
Cstf3 |
G |
T |
2: 104,477,112 (GRCm39) |
V168F |
probably damaging |
Het |
Dapk1 |
T |
C |
13: 60,873,154 (GRCm39) |
I352T |
probably benign |
Het |
Ddx52 |
T |
C |
11: 83,846,128 (GRCm39) |
V456A |
probably damaging |
Het |
Dmxl2 |
A |
T |
9: 54,323,372 (GRCm39) |
H1337Q |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,675,221 (GRCm39) |
T369A |
probably benign |
Het |
Dppa1 |
T |
A |
11: 46,516,422 (GRCm39) |
I8F |
unknown |
Het |
Ebf1 |
G |
T |
11: 44,774,641 (GRCm39) |
V213F |
probably damaging |
Het |
Foxb2 |
C |
A |
19: 16,850,197 (GRCm39) |
E270* |
probably null |
Het |
Gclc |
A |
T |
9: 77,695,527 (GRCm39) |
R450W |
probably damaging |
Het |
Grin2d |
T |
C |
7: 45,511,692 (GRCm39) |
E251G |
probably damaging |
Het |
Hal |
A |
T |
10: 93,336,539 (GRCm39) |
N423Y |
probably damaging |
Het |
Krtap4-8 |
T |
A |
11: 99,670,917 (GRCm39) |
I185F |
unknown |
Het |
Lrp3 |
T |
A |
7: 34,910,862 (GRCm39) |
Q61L |
probably benign |
Het |
Met |
A |
C |
6: 17,571,466 (GRCm39) |
Q1296H |
probably damaging |
Het |
Mphosph9 |
T |
A |
5: 124,435,762 (GRCm39) |
N557I |
possibly damaging |
Het |
Mrpl46 |
C |
A |
7: 78,432,729 (GRCm39) |
W16C |
probably benign |
Het |
Myh13 |
G |
A |
11: 67,241,245 (GRCm39) |
R874Q |
probably damaging |
Het |
Nelfb |
G |
A |
2: 25,093,393 (GRCm39) |
T453I |
probably benign |
Het |
Nos2 |
A |
G |
11: 78,843,780 (GRCm39) |
D909G |
probably damaging |
Het |
Nr5a2 |
T |
C |
1: 136,810,082 (GRCm39) |
E431G |
possibly damaging |
Het |
Nsmce2 |
A |
G |
15: 59,463,573 (GRCm39) |
D149G |
probably benign |
Het |
Or52b1 |
C |
T |
7: 104,979,234 (GRCm39) |
R55H |
probably benign |
Het |
Or5ac21 |
T |
C |
16: 59,124,004 (GRCm39) |
F164L |
probably benign |
Het |
Pcbp4 |
C |
A |
9: 106,337,847 (GRCm39) |
|
probably null |
Het |
Peg10 |
A |
G |
6: 4,757,137 (GRCm39) |
|
probably benign |
Het |
Pms2 |
C |
T |
5: 143,862,237 (GRCm39) |
P154L |
probably benign |
Het |
Pou6f2 |
A |
C |
13: 18,303,772 (GRCm39) |
L112R |
probably benign |
Het |
Pramel30 |
T |
C |
4: 144,059,548 (GRCm39) |
W420R |
probably benign |
Het |
Prdm6 |
A |
T |
18: 53,598,118 (GRCm39) |
|
probably benign |
Het |
Prob1 |
G |
A |
18: 35,788,207 (GRCm39) |
R12W |
probably damaging |
Het |
Rif1 |
T |
A |
2: 51,968,275 (GRCm39) |
|
probably null |
Het |
Rpl9-ps6 |
A |
G |
19: 32,443,543 (GRCm39) |
S137P |
probably benign |
Het |
Rsf1 |
GGCG |
GGCGACGGCAGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Homo |
Sec23ip |
A |
G |
7: 128,354,573 (GRCm39) |
|
silent |
Het |
Slc38a9 |
T |
C |
13: 112,826,714 (GRCm39) |
C151R |
probably benign |
Het |
Slc39a8 |
T |
C |
3: 135,554,941 (GRCm39) |
|
probably null |
Het |
Slc6a18 |
C |
A |
13: 73,826,110 (GRCm39) |
|
probably benign |
Het |
Snw1 |
T |
C |
12: 87,511,480 (GRCm39) |
D57G |
probably damaging |
Het |
Sox6 |
C |
G |
7: 115,140,966 (GRCm39) |
R505P |
probably damaging |
Het |
Speg |
T |
C |
1: 75,387,039 (GRCm39) |
|
probably null |
Het |
Spire2 |
C |
T |
8: 124,083,585 (GRCm39) |
R190C |
probably damaging |
Het |
Stard9 |
A |
C |
2: 120,528,864 (GRCm39) |
H1707P |
possibly damaging |
Het |
Tenm3 |
G |
T |
8: 48,796,278 (GRCm39) |
T237K |
probably damaging |
Het |
Themis2 |
T |
A |
4: 132,523,573 (GRCm39) |
E31V |
possibly damaging |
Het |
Trim56 |
T |
G |
5: 137,143,375 (GRCm39) |
Q47P |
probably damaging |
Het |
Trim58 |
T |
C |
11: 58,542,090 (GRCm39) |
I350T |
probably benign |
Het |
Ttll7 |
C |
T |
3: 146,649,811 (GRCm39) |
P639S |
probably benign |
Het |
Ubxn6 |
A |
G |
17: 56,377,650 (GRCm39) |
|
probably null |
Het |
Vmn2r114 |
A |
T |
17: 23,528,850 (GRCm39) |
F417L |
probably benign |
Het |
Vmn2r29 |
T |
A |
7: 7,234,421 (GRCm39) |
M822L |
probably benign |
Het |
Vps9d1 |
T |
C |
8: 123,980,746 (GRCm39) |
D27G |
probably damaging |
Het |
Wdr3 |
C |
T |
3: 100,046,040 (GRCm39) |
R931Q |
probably damaging |
Het |
Whamm |
G |
A |
7: 81,228,050 (GRCm39) |
|
probably null |
Het |
Zcchc24 |
T |
C |
14: 25,757,457 (GRCm39) |
H142R |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,806,894 (GRCm39) |
K2050R |
probably damaging |
Het |
|
Other mutations in Arhgap15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01533:Arhgap15
|
APN |
2 |
44,133,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01779:Arhgap15
|
APN |
2 |
43,955,057 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02011:Arhgap15
|
APN |
2 |
43,670,767 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02506:Arhgap15
|
APN |
2 |
43,953,820 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02659:Arhgap15
|
APN |
2 |
43,953,849 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02711:Arhgap15
|
APN |
2 |
44,006,674 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02944:Arhgap15
|
APN |
2 |
44,032,362 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02989:Arhgap15
|
APN |
2 |
43,670,748 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4468001:Arhgap15
|
UTSW |
2 |
44,133,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0140:Arhgap15
|
UTSW |
2 |
44,212,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R0403:Arhgap15
|
UTSW |
2 |
43,953,778 (GRCm39) |
missense |
probably damaging |
0.98 |
R0557:Arhgap15
|
UTSW |
2 |
44,006,629 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0616:Arhgap15
|
UTSW |
2 |
44,006,729 (GRCm39) |
critical splice donor site |
probably null |
|
R1122:Arhgap15
|
UTSW |
2 |
44,032,307 (GRCm39) |
missense |
probably benign |
0.43 |
R1958:Arhgap15
|
UTSW |
2 |
44,133,136 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2258:Arhgap15
|
UTSW |
2 |
44,276,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2905:Arhgap15
|
UTSW |
2 |
43,953,798 (GRCm39) |
missense |
probably damaging |
0.97 |
R4788:Arhgap15
|
UTSW |
2 |
43,638,902 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R4793:Arhgap15
|
UTSW |
2 |
44,032,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5040:Arhgap15
|
UTSW |
2 |
43,734,825 (GRCm39) |
critical splice donor site |
probably null |
|
R5093:Arhgap15
|
UTSW |
2 |
44,212,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R5114:Arhgap15
|
UTSW |
2 |
43,670,630 (GRCm39) |
missense |
probably benign |
0.03 |
R5202:Arhgap15
|
UTSW |
2 |
43,953,869 (GRCm39) |
missense |
probably benign |
0.22 |
R5446:Arhgap15
|
UTSW |
2 |
43,718,772 (GRCm39) |
missense |
probably benign |
0.00 |
R5661:Arhgap15
|
UTSW |
2 |
44,212,739 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7392:Arhgap15
|
UTSW |
2 |
43,953,786 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7502:Arhgap15
|
UTSW |
2 |
43,670,630 (GRCm39) |
missense |
probably benign |
0.03 |
R7630:Arhgap15
|
UTSW |
2 |
43,670,648 (GRCm39) |
missense |
probably benign |
0.01 |
R7658:Arhgap15
|
UTSW |
2 |
44,032,280 (GRCm39) |
missense |
probably benign |
0.18 |
R7735:Arhgap15
|
UTSW |
2 |
44,006,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R8734:Arhgap15
|
UTSW |
2 |
44,133,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Arhgap15
|
UTSW |
2 |
43,638,876 (GRCm39) |
start gained |
probably benign |
|
|