Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam22 |
A |
T |
5: 8,167,634 (GRCm39) |
S675R |
probably damaging |
Het |
Akap5 |
A |
T |
12: 76,376,122 (GRCm39) |
H518L |
possibly damaging |
Het |
Ankfn1 |
T |
C |
11: 89,296,423 (GRCm39) |
D102G |
probably damaging |
Het |
Aox3 |
A |
T |
1: 58,177,391 (GRCm39) |
Y202F |
probably benign |
Het |
Arhgef37 |
G |
A |
18: 61,637,427 (GRCm39) |
L412F |
possibly damaging |
Het |
B4galt3 |
C |
T |
1: 171,100,118 (GRCm39) |
P121L |
probably damaging |
Het |
BC034090 |
C |
T |
1: 155,097,178 (GRCm39) |
R640Q |
probably damaging |
Het |
Bhmt |
A |
T |
13: 93,761,900 (GRCm39) |
Y128N |
probably damaging |
Het |
Bin3 |
A |
G |
14: 70,372,222 (GRCm39) |
E173G |
probably damaging |
Het |
C1qtnf1 |
T |
A |
11: 118,339,110 (GRCm39) |
F260Y |
probably benign |
Het |
Ccdc14 |
G |
T |
16: 34,511,092 (GRCm39) |
G22V |
possibly damaging |
Het |
Ccnc |
A |
T |
4: 21,741,955 (GRCm39) |
I135L |
possibly damaging |
Het |
Chd3 |
T |
C |
11: 69,239,878 (GRCm39) |
D1650G |
probably benign |
Het |
Cherp |
A |
C |
8: 73,228,613 (GRCm39) |
N14K |
probably damaging |
Het |
Clint1 |
C |
T |
11: 45,784,919 (GRCm39) |
T306I |
possibly damaging |
Het |
Cyb5r1 |
T |
A |
1: 134,335,315 (GRCm39) |
Y85N |
probably damaging |
Het |
D830013O20Rik |
A |
G |
12: 73,418,162 (GRCm39) |
|
noncoding transcript |
Het |
Dapk1 |
A |
T |
13: 60,869,671 (GRCm39) |
K304N |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,044,449 (GRCm39) |
N3169Y |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 7,169,589 (GRCm39) |
I296K |
probably benign |
Het |
Elp2 |
A |
T |
18: 24,764,515 (GRCm39) |
T621S |
probably benign |
Het |
Eml6 |
G |
T |
11: 29,781,128 (GRCm39) |
Q635K |
possibly damaging |
Het |
Exph5 |
G |
A |
9: 53,278,466 (GRCm39) |
M192I |
possibly damaging |
Het |
Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
Gas6 |
C |
T |
8: 13,518,266 (GRCm39) |
V523M |
probably damaging |
Het |
Ggn |
A |
T |
7: 28,873,188 (GRCm39) |
|
probably null |
Het |
Gimap8 |
A |
G |
6: 48,633,287 (GRCm39) |
T369A |
probably damaging |
Het |
Gtpbp6 |
G |
A |
5: 110,252,790 (GRCm39) |
A354V |
probably damaging |
Het |
Habp4 |
G |
A |
13: 64,317,995 (GRCm39) |
|
probably null |
Het |
Has2 |
A |
G |
15: 56,531,264 (GRCm39) |
W484R |
probably damaging |
Het |
Herc4 |
G |
T |
10: 63,079,817 (GRCm39) |
|
probably benign |
Het |
Igf2 |
C |
A |
7: 142,208,136 (GRCm39) |
E106D |
probably damaging |
Het |
Il17rb |
A |
T |
14: 29,718,797 (GRCm39) |
C428* |
probably null |
Het |
Ipo11 |
A |
T |
13: 107,056,130 (GRCm39) |
N47K |
probably benign |
Het |
Itga4 |
T |
G |
2: 79,108,138 (GRCm39) |
S197A |
probably damaging |
Het |
Itpr1 |
T |
A |
6: 108,417,497 (GRCm39) |
M1788K |
probably benign |
Het |
Kbtbd3 |
C |
T |
9: 4,330,919 (GRCm39) |
T431I |
probably benign |
Het |
Kif5a |
A |
T |
10: 127,075,044 (GRCm39) |
V523E |
probably benign |
Het |
Klhl41 |
A |
T |
2: 69,513,840 (GRCm39) |
D573V |
possibly damaging |
Het |
Kndc1 |
C |
A |
7: 139,501,196 (GRCm39) |
H828Q |
possibly damaging |
Het |
Leng8 |
T |
A |
7: 4,146,609 (GRCm39) |
V407D |
probably damaging |
Het |
Mamdc2 |
C |
T |
19: 23,288,215 (GRCm39) |
E608K |
probably benign |
Het |
Mcf2 |
T |
A |
X: 59,122,574 (GRCm39) |
R850S |
probably damaging |
Het |
Mmp2 |
A |
G |
8: 93,576,831 (GRCm39) |
N618S |
probably benign |
Het |
Morn5 |
A |
T |
2: 35,942,950 (GRCm39) |
M17L |
probably benign |
Het |
Nme8 |
T |
C |
13: 19,881,053 (GRCm39) |
N26S |
probably damaging |
Het |
Nostrin |
C |
A |
2: 68,975,111 (GRCm39) |
|
probably null |
Het |
Npy4r |
T |
A |
14: 33,869,154 (GRCm39) |
I45F |
possibly damaging |
Het |
Or13a21 |
T |
A |
7: 139,999,024 (GRCm39) |
I221F |
probably damaging |
Het |
Or1j11 |
A |
G |
2: 36,311,931 (GRCm39) |
I174V |
probably benign |
Het |
Or2aj5 |
C |
T |
16: 19,424,881 (GRCm39) |
C179Y |
probably benign |
Het |
Or2w1 |
T |
A |
13: 21,317,659 (GRCm39) |
M238K |
probably benign |
Het |
Or2w3b |
T |
C |
11: 58,623,214 (GRCm39) |
Y259C |
possibly damaging |
Het |
Or4a70 |
A |
G |
2: 89,324,342 (GRCm39) |
F105L |
probably benign |
Het |
Or5d36 |
A |
G |
2: 87,901,063 (GRCm39) |
V221A |
probably benign |
Het |
Oxt |
A |
G |
2: 130,418,572 (GRCm39) |
D61G |
probably damaging |
Het |
Patl1 |
T |
C |
19: 11,917,181 (GRCm39) |
L676P |
probably damaging |
Het |
Pcdhb20 |
G |
A |
18: 37,638,127 (GRCm39) |
G218R |
probably damaging |
Het |
Pdgfrb |
T |
A |
18: 61,194,566 (GRCm39) |
S114R |
probably benign |
Het |
Pfdn5 |
A |
G |
15: 102,234,956 (GRCm39) |
N54S |
possibly damaging |
Het |
Phldb1 |
G |
T |
9: 44,639,333 (GRCm39) |
T15N |
possibly damaging |
Het |
Pink1 |
A |
C |
4: 138,045,316 (GRCm39) |
S253A |
probably null |
Het |
Plag1 |
A |
T |
4: 3,904,870 (GRCm39) |
L107Q |
probably damaging |
Het |
Pld5 |
C |
A |
1: 175,791,579 (GRCm39) |
V476L |
probably benign |
Het |
Pramel28 |
A |
T |
4: 143,692,637 (GRCm39) |
D121E |
probably benign |
Het |
Prrt2 |
C |
T |
7: 126,618,581 (GRCm39) |
A295T |
probably damaging |
Het |
Ptgs1 |
A |
G |
2: 36,127,668 (GRCm39) |
I76V |
probably benign |
Het |
Ptprz1 |
A |
G |
6: 23,001,026 (GRCm39) |
T1039A |
probably benign |
Het |
Rbm20 |
G |
A |
19: 53,847,859 (GRCm39) |
C1135Y |
probably damaging |
Het |
Recql5 |
A |
T |
11: 115,787,923 (GRCm39) |
N465K |
probably benign |
Het |
Rgs12 |
A |
G |
5: 35,187,872 (GRCm39) |
S510G |
probably benign |
Het |
Satb1 |
G |
A |
17: 52,089,816 (GRCm39) |
Q344* |
probably null |
Het |
Sdr16c5 |
A |
G |
4: 3,996,244 (GRCm39) |
I283T |
probably benign |
Het |
Serpinb3c |
T |
C |
1: 107,199,574 (GRCm39) |
S316G |
possibly damaging |
Het |
Siglec1 |
A |
T |
2: 130,925,277 (GRCm39) |
Y395N |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,651,701 (GRCm39) |
I5V |
probably benign |
Het |
Slc27a2 |
T |
C |
2: 126,395,535 (GRCm39) |
V154A |
probably damaging |
Het |
Slc27a5 |
A |
G |
7: 12,731,634 (GRCm39) |
L119S |
probably damaging |
Het |
Slc35g2 |
T |
A |
9: 100,435,120 (GRCm39) |
T184S |
possibly damaging |
Het |
Slc4a7 |
C |
T |
14: 14,733,727 (GRCm38) |
R46* |
probably null |
Het |
Smcr8 |
T |
C |
11: 60,669,010 (GRCm39) |
F53L |
probably damaging |
Het |
Spag9 |
T |
A |
11: 93,983,201 (GRCm39) |
L504* |
probably null |
Het |
Spata31d1a |
A |
G |
13: 59,850,370 (GRCm39) |
I586T |
possibly damaging |
Het |
Spata31d1c |
A |
T |
13: 65,183,041 (GRCm39) |
E194D |
possibly damaging |
Het |
Spats2 |
A |
G |
15: 99,076,375 (GRCm39) |
E151G |
probably damaging |
Het |
Sugp2 |
T |
A |
8: 70,695,861 (GRCm39) |
L278Q |
possibly damaging |
Het |
Sult2a7 |
T |
A |
7: 14,207,322 (GRCm39) |
|
probably benign |
Het |
Syde2 |
G |
T |
3: 145,694,163 (GRCm39) |
G137V |
possibly damaging |
Het |
Synj1 |
A |
T |
16: 90,735,584 (GRCm39) |
F1456L |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,220,862 (GRCm39) |
|
probably benign |
Het |
Timd4 |
C |
A |
11: 46,710,857 (GRCm39) |
T253K |
possibly damaging |
Het |
Tlr3 |
G |
T |
8: 45,855,823 (GRCm39) |
T119N |
possibly damaging |
Het |
Tmc6 |
A |
G |
11: 117,660,232 (GRCm39) |
Y669H |
probably damaging |
Het |
Tmem221 |
T |
C |
8: 72,008,458 (GRCm39) |
E194G |
probably benign |
Het |
Tmem232 |
C |
A |
17: 65,807,167 (GRCm39) |
V9F |
probably benign |
Het |
Tpm1 |
G |
A |
9: 66,941,247 (GRCm39) |
Q135* |
probably null |
Het |
Trank1 |
A |
G |
9: 111,194,096 (GRCm39) |
T707A |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,665,917 (GRCm39) |
Y896* |
probably null |
Het |
Tuba4a |
A |
T |
1: 75,192,983 (GRCm39) |
Y210* |
probably null |
Het |
Tut7 |
A |
G |
13: 59,959,352 (GRCm39) |
V372A |
probably damaging |
Het |
Vegfa |
T |
G |
17: 46,336,284 (GRCm39) |
I279L |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,349,804 (GRCm39) |
T593S |
probably damaging |
Het |
Vmn2r93 |
A |
G |
17: 18,536,840 (GRCm39) |
I508V |
probably benign |
Het |
Vps33a |
G |
T |
5: 123,669,244 (GRCm39) |
|
probably null |
Het |
Wasl |
T |
A |
6: 24,624,360 (GRCm39) |
N231I |
probably damaging |
Het |
Zbtb39 |
A |
G |
10: 127,578,703 (GRCm39) |
N426D |
probably benign |
Het |
Zeb2 |
T |
G |
2: 44,887,962 (GRCm39) |
H350P |
probably damaging |
Het |
Zfp112 |
T |
C |
7: 23,824,725 (GRCm39) |
F231S |
possibly damaging |
Het |
Zfp180 |
T |
C |
7: 23,803,943 (GRCm39) |
S121P |
probably benign |
Het |
|
Other mutations in Grm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Grm5
|
APN |
7 |
87,779,989 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00970:Grm5
|
APN |
7 |
87,453,104 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01286:Grm5
|
APN |
7 |
87,251,773 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01307:Grm5
|
APN |
7 |
87,724,220 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01603:Grm5
|
APN |
7 |
87,252,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01646:Grm5
|
APN |
7 |
87,689,267 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01705:Grm5
|
APN |
7 |
87,779,254 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02184:Grm5
|
APN |
7 |
87,675,650 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02504:Grm5
|
APN |
7 |
87,779,980 (GRCm39) |
missense |
probably benign |
|
IGL02689:Grm5
|
APN |
7 |
87,251,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02725:Grm5
|
APN |
7 |
87,723,873 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Grm5
|
APN |
7 |
87,723,918 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03106:Grm5
|
APN |
7 |
87,685,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03257:Grm5
|
APN |
7 |
87,252,106 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03291:Grm5
|
APN |
7 |
87,780,004 (GRCm39) |
missense |
probably damaging |
1.00 |
BB004:Grm5
|
UTSW |
7 |
87,685,382 (GRCm39) |
missense |
probably benign |
0.16 |
BB014:Grm5
|
UTSW |
7 |
87,685,382 (GRCm39) |
missense |
probably benign |
0.16 |
R0078:Grm5
|
UTSW |
7 |
87,724,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Grm5
|
UTSW |
7 |
87,252,163 (GRCm39) |
missense |
probably damaging |
0.97 |
R0318:Grm5
|
UTSW |
7 |
87,252,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R0364:Grm5
|
UTSW |
7 |
87,723,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Grm5
|
UTSW |
7 |
87,723,584 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0454:Grm5
|
UTSW |
7 |
87,779,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Grm5
|
UTSW |
7 |
87,779,989 (GRCm39) |
missense |
probably benign |
0.00 |
R0562:Grm5
|
UTSW |
7 |
87,252,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Grm5
|
UTSW |
7 |
87,685,311 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2384:Grm5
|
UTSW |
7 |
87,251,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Grm5
|
UTSW |
7 |
87,685,299 (GRCm39) |
missense |
probably benign |
0.21 |
R2870:Grm5
|
UTSW |
7 |
87,251,930 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2870:Grm5
|
UTSW |
7 |
87,251,930 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3861:Grm5
|
UTSW |
7 |
87,779,202 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4451:Grm5
|
UTSW |
7 |
87,724,340 (GRCm39) |
critical splice donor site |
probably null |
|
R4626:Grm5
|
UTSW |
7 |
87,779,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Grm5
|
UTSW |
7 |
87,624,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4914:Grm5
|
UTSW |
7 |
87,779,337 (GRCm39) |
missense |
probably benign |
0.00 |
R5122:Grm5
|
UTSW |
7 |
87,724,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Grm5
|
UTSW |
7 |
87,724,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Grm5
|
UTSW |
7 |
87,723,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R5684:Grm5
|
UTSW |
7 |
87,779,853 (GRCm39) |
missense |
probably benign |
|
R5715:Grm5
|
UTSW |
7 |
87,779,464 (GRCm39) |
missense |
probably benign |
0.05 |
R5759:Grm5
|
UTSW |
7 |
87,675,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R5844:Grm5
|
UTSW |
7 |
87,453,232 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5889:Grm5
|
UTSW |
7 |
87,252,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Grm5
|
UTSW |
7 |
87,675,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Grm5
|
UTSW |
7 |
87,675,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Grm5
|
UTSW |
7 |
87,251,638 (GRCm39) |
unclassified |
probably benign |
|
R6972:Grm5
|
UTSW |
7 |
87,252,131 (GRCm39) |
missense |
probably benign |
0.02 |
R7072:Grm5
|
UTSW |
7 |
87,723,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R7258:Grm5
|
UTSW |
7 |
87,723,914 (GRCm39) |
missense |
probably damaging |
0.96 |
R7316:Grm5
|
UTSW |
7 |
87,624,473 (GRCm39) |
missense |
probably benign |
|
R7434:Grm5
|
UTSW |
7 |
87,779,682 (GRCm39) |
missense |
probably benign |
0.10 |
R7521:Grm5
|
UTSW |
7 |
87,723,480 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7616:Grm5
|
UTSW |
7 |
87,765,409 (GRCm39) |
missense |
probably benign |
|
R7631:Grm5
|
UTSW |
7 |
87,624,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R7655:Grm5
|
UTSW |
7 |
87,779,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7656:Grm5
|
UTSW |
7 |
87,779,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7739:Grm5
|
UTSW |
7 |
87,779,266 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7897:Grm5
|
UTSW |
7 |
87,780,069 (GRCm39) |
missense |
probably benign |
0.14 |
R7927:Grm5
|
UTSW |
7 |
87,685,382 (GRCm39) |
missense |
probably benign |
0.16 |
R7967:Grm5
|
UTSW |
7 |
87,624,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R8260:Grm5
|
UTSW |
7 |
87,724,340 (GRCm39) |
critical splice donor site |
probably null |
|
R8345:Grm5
|
UTSW |
7 |
87,723,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R8460:Grm5
|
UTSW |
7 |
87,252,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R8473:Grm5
|
UTSW |
7 |
87,252,278 (GRCm39) |
missense |
probably damaging |
0.97 |
R8531:Grm5
|
UTSW |
7 |
87,779,724 (GRCm39) |
missense |
probably benign |
0.05 |
R8671:Grm5
|
UTSW |
7 |
87,765,498 (GRCm39) |
critical splice donor site |
probably null |
|
R8805:Grm5
|
UTSW |
7 |
87,453,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R9036:Grm5
|
UTSW |
7 |
87,685,397 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9106:Grm5
|
UTSW |
7 |
87,723,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Grm5
|
UTSW |
7 |
87,689,254 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9189:Grm5
|
UTSW |
7 |
87,724,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R9196:Grm5
|
UTSW |
7 |
87,723,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Grm5
|
UTSW |
7 |
87,723,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R9234:Grm5
|
UTSW |
7 |
87,723,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Grm5
|
UTSW |
7 |
87,723,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Grm5
|
UTSW |
7 |
87,765,484 (GRCm39) |
missense |
probably benign |
0.00 |
R9531:Grm5
|
UTSW |
7 |
87,780,075 (GRCm39) |
makesense |
probably null |
|
R9631:Grm5
|
UTSW |
7 |
87,624,560 (GRCm39) |
missense |
probably damaging |
0.98 |
R9691:Grm5
|
UTSW |
7 |
87,723,903 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Grm5
|
UTSW |
7 |
87,251,923 (GRCm39) |
missense |
probably damaging |
1.00 |
|