Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp6 |
A |
T |
3: 97,073,266 (GRCm39) |
E102D |
probably benign |
Het |
Acss1 |
T |
A |
2: 150,461,688 (GRCm39) |
R632* |
probably null |
Het |
Adamtsl1 |
G |
T |
4: 86,259,450 (GRCm39) |
C832F |
probably damaging |
Het |
Adgrg6 |
T |
G |
10: 14,344,573 (GRCm39) |
M127L |
probably damaging |
Het |
Alkbh1 |
A |
T |
12: 87,487,095 (GRCm39) |
Y91* |
probably null |
Het |
Arhgap35 |
A |
T |
7: 16,298,786 (GRCm39) |
I93N |
probably damaging |
Het |
Asic2 |
A |
T |
11: 81,858,657 (GRCm39) |
D118E |
probably benign |
Het |
Asprv1 |
G |
T |
6: 86,605,762 (GRCm39) |
V203L |
probably damaging |
Het |
Atad2b |
G |
A |
12: 5,081,726 (GRCm39) |
D1212N |
probably benign |
Het |
Atp4a |
A |
G |
7: 30,424,105 (GRCm39) |
I960V |
probably benign |
Het |
Bin1 |
G |
T |
18: 32,552,932 (GRCm39) |
E186* |
probably null |
Het |
Bmp10 |
A |
G |
6: 87,410,651 (GRCm39) |
Y148C |
probably damaging |
Het |
Ccdc152 |
T |
A |
15: 3,310,137 (GRCm39) |
D246V |
probably damaging |
Het |
Cdc16 |
A |
G |
8: 13,827,605 (GRCm39) |
T504A |
probably benign |
Het |
Cdh9 |
A |
T |
15: 16,823,261 (GRCm39) |
D81V |
probably damaging |
Het |
Cep162 |
A |
T |
9: 87,086,250 (GRCm39) |
S1025T |
probably benign |
Het |
Cidea |
A |
G |
18: 67,493,283 (GRCm39) |
I101V |
probably benign |
Het |
Clock |
G |
A |
5: 76,384,145 (GRCm39) |
S478L |
possibly damaging |
Het |
Cp |
T |
A |
3: 20,020,494 (GRCm39) |
N162K |
probably benign |
Het |
Crb1 |
C |
T |
1: 139,164,978 (GRCm39) |
E1110K |
probably damaging |
Het |
Cyp2b13 |
A |
T |
7: 25,780,416 (GRCm39) |
I146L |
possibly damaging |
Het |
D630045J12Rik |
A |
G |
6: 38,172,429 (GRCm39) |
S580P |
possibly damaging |
Het |
Dars2 |
T |
C |
1: 160,885,113 (GRCm39) |
E224G |
probably damaging |
Het |
Dcbld2 |
A |
G |
16: 58,244,941 (GRCm39) |
T72A |
possibly damaging |
Het |
Ddx11 |
A |
T |
17: 66,433,193 (GRCm39) |
I8F |
possibly damaging |
Het |
Dennd2d |
T |
C |
3: 106,407,244 (GRCm39) |
F432L |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,823,608 (GRCm39) |
V543A |
probably benign |
Het |
Eef2k |
G |
A |
7: 120,488,491 (GRCm39) |
|
probably null |
Het |
Elmo1 |
A |
G |
13: 20,474,610 (GRCm39) |
M345V |
probably benign |
Het |
Ephb4 |
A |
G |
5: 137,359,560 (GRCm39) |
M377V |
probably benign |
Het |
Erbb4 |
C |
A |
1: 68,293,758 (GRCm39) |
R711L |
probably damaging |
Het |
Fads1 |
A |
G |
19: 10,162,361 (GRCm39) |
E95G |
probably damaging |
Het |
Farsa |
G |
A |
8: 85,594,278 (GRCm39) |
|
probably null |
Het |
Galntl6 |
A |
G |
8: 58,230,293 (GRCm39) |
S42P |
probably damaging |
Het |
Gga2 |
G |
A |
7: 121,589,672 (GRCm39) |
T559M |
probably benign |
Het |
Glipr1l2 |
G |
A |
10: 111,928,465 (GRCm39) |
G120D |
probably damaging |
Het |
Gm14226 |
A |
T |
2: 154,866,114 (GRCm39) |
I24L |
unknown |
Het |
Gprc5b |
G |
T |
7: 118,583,492 (GRCm39) |
R126S |
probably damaging |
Het |
Gys1 |
A |
G |
7: 45,092,360 (GRCm39) |
D321G |
probably damaging |
Het |
Hdlbp |
C |
T |
1: 93,358,005 (GRCm39) |
A299T |
probably benign |
Het |
Hic2 |
A |
G |
16: 17,076,979 (GRCm39) |
T603A |
probably damaging |
Het |
Hoxa11 |
A |
T |
6: 52,220,524 (GRCm39) |
I253N |
probably damaging |
Het |
Iglon5 |
A |
T |
7: 43,126,064 (GRCm39) |
D222E |
probably benign |
Het |
Inpp5d |
T |
A |
1: 87,645,500 (GRCm39) |
S1023T |
possibly damaging |
Het |
Kif21a |
C |
T |
15: 90,828,064 (GRCm39) |
A1233T |
probably benign |
Het |
Kif9 |
A |
T |
9: 110,350,421 (GRCm39) |
T771S |
possibly damaging |
Het |
Klre1 |
T |
A |
6: 129,560,150 (GRCm39) |
C141S |
probably damaging |
Het |
Lats1 |
A |
G |
10: 7,577,476 (GRCm39) |
Y200C |
probably damaging |
Het |
Lgr4 |
T |
A |
2: 109,829,801 (GRCm39) |
L247H |
probably damaging |
Het |
Lrrc37a |
T |
C |
11: 103,391,778 (GRCm39) |
K1216E |
probably benign |
Het |
Lrrc41 |
G |
A |
4: 115,950,141 (GRCm39) |
R518H |
possibly damaging |
Het |
Lrrk1 |
A |
G |
7: 65,958,439 (GRCm39) |
V320A |
probably benign |
Het |
Mcm9 |
C |
T |
10: 53,506,088 (GRCm39) |
R62H |
probably benign |
Het |
Mmp10 |
T |
G |
9: 7,503,154 (GRCm39) |
L38R |
probably damaging |
Het |
Mroh8 |
A |
G |
2: 157,071,867 (GRCm39) |
L546P |
probably damaging |
Het |
Mtcl2 |
A |
T |
2: 156,882,776 (GRCm39) |
D425E |
probably benign |
Het |
Myt1 |
T |
A |
2: 181,439,532 (GRCm39) |
D393E |
possibly damaging |
Het |
Mzb1 |
A |
T |
18: 35,780,901 (GRCm39) |
I129N |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,826,955 (GRCm38) |
D51G |
probably benign |
Het |
Nme5 |
A |
G |
18: 34,700,201 (GRCm39) |
I148T |
probably benign |
Het |
Nr2e1 |
G |
A |
10: 42,439,475 (GRCm39) |
P348L |
probably damaging |
Het |
Nrp2 |
A |
G |
1: 62,758,203 (GRCm39) |
E63G |
probably damaging |
Het |
Or2d2 |
A |
T |
7: 106,727,782 (GRCm39) |
S273T |
probably damaging |
Het |
Or51ab3 |
A |
T |
7: 103,200,956 (GRCm39) |
|
probably benign |
Het |
Or52e3 |
A |
G |
7: 102,869,471 (GRCm39) |
E182G |
probably damaging |
Het |
Or52e5 |
A |
G |
7: 104,718,704 (GRCm39) |
H10R |
probably benign |
Het |
Or56a3 |
A |
G |
7: 104,735,372 (GRCm39) |
T150A |
probably benign |
Het |
Pak5 |
A |
G |
2: 135,942,884 (GRCm39) |
S419P |
probably benign |
Het |
Pfas |
C |
A |
11: 68,881,921 (GRCm39) |
M25I |
|
Het |
Prdm9 |
A |
G |
17: 15,764,867 (GRCm39) |
S638P |
possibly damaging |
Het |
Psd |
G |
A |
19: 46,301,352 (GRCm39) |
T954I |
possibly damaging |
Het |
Psph |
T |
C |
5: 129,864,337 (GRCm39) |
|
probably benign |
Het |
Ptprf |
A |
G |
4: 118,069,593 (GRCm39) |
I1517T |
probably benign |
Het |
Rassf8 |
A |
G |
6: 145,761,129 (GRCm39) |
R152G |
probably benign |
Het |
Rfx3 |
G |
A |
19: 27,827,139 (GRCm39) |
T149I |
probably benign |
Het |
Rfx8 |
A |
T |
1: 39,722,838 (GRCm39) |
F260I |
probably damaging |
Het |
Rnft1 |
C |
T |
11: 86,384,023 (GRCm39) |
Q308* |
probably null |
Het |
Rock2 |
A |
G |
12: 17,008,241 (GRCm39) |
N528S |
probably benign |
Het |
Rpp25l |
T |
C |
4: 41,712,305 (GRCm39) |
R157G |
unknown |
Het |
Ryr1 |
A |
T |
7: 28,735,528 (GRCm39) |
N4083K |
probably damaging |
Het |
Scd1 |
G |
T |
19: 44,388,739 (GRCm39) |
T237N |
probably benign |
Het |
Sema3d |
T |
C |
5: 12,558,112 (GRCm39) |
F215L |
probably benign |
Het |
Sema7a |
C |
T |
9: 57,867,858 (GRCm39) |
T478I |
probably benign |
Het |
Sftpc |
T |
C |
14: 70,759,623 (GRCm39) |
T99A |
possibly damaging |
Het |
Slc25a4 |
G |
A |
8: 46,662,241 (GRCm39) |
T139I |
probably damaging |
Het |
Snx27 |
T |
C |
3: 94,410,272 (GRCm39) |
E468G |
possibly damaging |
Het |
Snx33 |
T |
C |
9: 56,834,058 (GRCm39) |
K4E |
possibly damaging |
Het |
Soat1 |
A |
T |
1: 156,268,148 (GRCm39) |
L253* |
probably null |
Het |
Sycp2l |
A |
T |
13: 41,326,192 (GRCm39) |
N749I |
probably damaging |
Het |
Synj2bp |
A |
T |
12: 81,557,664 (GRCm39) |
I47N |
probably damaging |
Het |
Tmem82 |
T |
A |
4: 141,343,605 (GRCm39) |
I222F |
probably damaging |
Het |
Ube2o |
A |
T |
11: 116,471,905 (GRCm39) |
L112Q |
possibly damaging |
Het |
Vmn1r204 |
G |
A |
13: 22,740,754 (GRCm39) |
W128* |
probably null |
Het |
Vmn2r114 |
A |
T |
17: 23,510,817 (GRCm39) |
Y554* |
probably null |
Het |
Vmn2r62 |
A |
T |
7: 42,437,213 (GRCm39) |
Y424N |
possibly damaging |
Het |
Vmn2r70 |
A |
T |
7: 85,215,312 (GRCm39) |
L74* |
probably null |
Het |
Vmp1 |
T |
A |
11: 86,477,377 (GRCm39) |
Y341F |
probably benign |
Het |
Vps13a |
A |
T |
19: 16,703,027 (GRCm39) |
V642D |
probably damaging |
Het |
Vps33a |
T |
C |
5: 123,674,619 (GRCm39) |
M383V |
probably benign |
Het |
Vwf |
G |
A |
6: 125,624,731 (GRCm39) |
V1827I |
|
Het |
Zc3hav1 |
A |
G |
6: 38,306,121 (GRCm39) |
Y644H |
probably benign |
Het |
Zfp429 |
A |
C |
13: 67,538,410 (GRCm39) |
C345G |
probably damaging |
Het |
Zfp595 |
T |
C |
13: 67,464,823 (GRCm39) |
H483R |
probably benign |
Het |
Zfp748 |
G |
T |
13: 67,690,638 (GRCm39) |
H207Q |
probably benign |
Het |
Zfp758 |
T |
C |
17: 22,593,939 (GRCm39) |
S142P |
probably damaging |
Het |
Znfx1 |
A |
C |
2: 166,898,145 (GRCm39) |
S260A |
probably benign |
Het |
|
Other mutations in 0610040J01Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:0610040J01Rik
|
APN |
5 |
64,055,726 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02229:0610040J01Rik
|
APN |
5 |
64,055,696 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02389:0610040J01Rik
|
APN |
5 |
64,053,826 (GRCm39) |
missense |
probably null |
1.00 |
IGL02411:0610040J01Rik
|
APN |
5 |
64,055,459 (GRCm39) |
missense |
probably benign |
0.31 |
R0243:0610040J01Rik
|
UTSW |
5 |
64,055,806 (GRCm39) |
missense |
probably benign |
0.10 |
R0411:0610040J01Rik
|
UTSW |
5 |
64,053,834 (GRCm39) |
splice site |
probably benign |
|
R1978:0610040J01Rik
|
UTSW |
5 |
64,055,880 (GRCm39) |
nonsense |
probably null |
|
R2072:0610040J01Rik
|
UTSW |
5 |
64,056,080 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2202:0610040J01Rik
|
UTSW |
5 |
64,056,011 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3161:0610040J01Rik
|
UTSW |
5 |
64,053,833 (GRCm39) |
splice site |
probably benign |
|
R3162:0610040J01Rik
|
UTSW |
5 |
64,053,833 (GRCm39) |
splice site |
probably benign |
|
R4428:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4429:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4430:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4431:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4464:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4465:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4467:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4491:0610040J01Rik
|
UTSW |
5 |
64,055,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5161:0610040J01Rik
|
UTSW |
5 |
64,055,344 (GRCm39) |
nonsense |
probably null |
|
R6115:0610040J01Rik
|
UTSW |
5 |
64,055,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6273:0610040J01Rik
|
UTSW |
5 |
64,055,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7445:0610040J01Rik
|
UTSW |
5 |
64,055,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R8070:0610040J01Rik
|
UTSW |
5 |
64,055,510 (GRCm39) |
missense |
probably benign |
0.01 |
R8140:0610040J01Rik
|
UTSW |
5 |
64,055,954 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8165:0610040J01Rik
|
UTSW |
5 |
64,055,289 (GRCm39) |
splice site |
probably null |
|
R8557:0610040J01Rik
|
UTSW |
5 |
64,055,954 (GRCm39) |
missense |
probably benign |
0.04 |
R9671:0610040J01Rik
|
UTSW |
5 |
64,055,948 (GRCm39) |
nonsense |
probably null |
|
R9782:0610040J01Rik
|
UTSW |
5 |
64,053,796 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|