Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
T |
A |
11: 7,089,095 (GRCm39) |
V503E |
possibly damaging |
Het |
Alk |
C |
A |
17: 72,181,938 (GRCm39) |
V1362L |
probably damaging |
Het |
Ankrd55 |
T |
A |
13: 112,492,453 (GRCm39) |
I208N |
possibly damaging |
Het |
Asap2 |
T |
A |
12: 21,268,191 (GRCm39) |
I319N |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,891,696 (GRCm39) |
I1036T |
probably benign |
Het |
B4gat1 |
T |
C |
19: 5,089,560 (GRCm39) |
F186L |
probably benign |
Het |
C3 |
T |
A |
17: 57,521,831 (GRCm39) |
T1079S |
probably damaging |
Het |
Cacul1 |
G |
T |
19: 60,525,902 (GRCm39) |
T287K |
possibly damaging |
Het |
Cbr3 |
G |
C |
16: 93,487,614 (GRCm39) |
G266R |
probably damaging |
Het |
Cd63 |
T |
A |
10: 128,748,160 (GRCm39) |
|
probably null |
Het |
Chd7 |
G |
A |
4: 8,866,382 (GRCm39) |
M851I |
probably damaging |
Het |
Chst13 |
T |
A |
6: 90,286,554 (GRCm39) |
H136L |
probably benign |
Het |
Cyp2d22 |
T |
C |
15: 82,258,014 (GRCm39) |
T179A |
probably benign |
Het |
Dclre1b |
A |
T |
3: 103,711,053 (GRCm39) |
V286E |
probably damaging |
Het |
Defb45 |
G |
A |
2: 152,435,154 (GRCm39) |
|
probably benign |
Het |
Dlg1 |
T |
C |
16: 31,610,704 (GRCm39) |
|
probably null |
Het |
Dock3 |
A |
G |
9: 106,901,002 (GRCm39) |
V321A |
probably benign |
Het |
Dytn |
A |
T |
1: 63,716,396 (GRCm39) |
V59E |
possibly damaging |
Het |
Efcab3 |
T |
C |
11: 104,612,227 (GRCm39) |
|
probably benign |
Het |
Eif2ak1 |
A |
G |
5: 143,823,733 (GRCm39) |
I393M |
probably damaging |
Het |
Fbxo34 |
T |
A |
14: 47,767,176 (GRCm39) |
F179I |
probably damaging |
Het |
Fmo5 |
T |
A |
3: 97,549,041 (GRCm39) |
Y230N |
probably benign |
Het |
Fzd9 |
T |
G |
5: 135,278,317 (GRCm39) |
|
probably null |
Het |
Gata2 |
T |
C |
6: 88,177,722 (GRCm39) |
S251P |
probably benign |
Het |
Gigyf1 |
A |
G |
5: 137,523,959 (GRCm39) |
D1043G |
probably damaging |
Het |
Gm10322 |
T |
A |
10: 59,452,125 (GRCm39) |
S81T |
probably benign |
Het |
Gm15517 |
A |
T |
7: 43,910,066 (GRCm39) |
|
probably benign |
Het |
Haus4 |
T |
C |
14: 54,781,676 (GRCm39) |
T232A |
probably benign |
Het |
Hgfac |
A |
T |
5: 35,202,751 (GRCm39) |
H417L |
probably damaging |
Het |
Iqgap2 |
T |
C |
13: 95,772,118 (GRCm39) |
K1354E |
possibly damaging |
Het |
Kcnk12 |
C |
A |
17: 88,054,077 (GRCm39) |
R195L |
probably benign |
Het |
Kcnn2 |
A |
T |
18: 45,725,412 (GRCm39) |
I303F |
probably damaging |
Het |
Kcnt1 |
T |
C |
2: 25,798,122 (GRCm39) |
F879S |
probably damaging |
Het |
Kndc1 |
T |
C |
7: 139,475,133 (GRCm39) |
F11L |
probably benign |
Het |
Kpna7 |
A |
G |
5: 144,926,605 (GRCm39) |
F449S |
probably damaging |
Het |
Krt77 |
G |
T |
15: 101,773,888 (GRCm39) |
N255K |
probably benign |
Het |
Lair1 |
A |
T |
7: 4,013,844 (GRCm39) |
D134E |
probably damaging |
Het |
Loxhd1 |
T |
C |
18: 77,490,211 (GRCm39) |
V1318A |
probably damaging |
Het |
Marchf10 |
A |
T |
11: 105,292,972 (GRCm39) |
V145D |
possibly damaging |
Het |
Mcpt1 |
T |
A |
14: 56,256,969 (GRCm39) |
M169K |
probably benign |
Het |
Mdc1 |
T |
A |
17: 36,158,712 (GRCm39) |
V364E |
probably benign |
Het |
Mfsd11 |
T |
C |
11: 116,762,210 (GRCm39) |
F270S |
probably damaging |
Het |
Mfsd4b2 |
T |
G |
10: 39,798,031 (GRCm39) |
D108A |
probably benign |
Het |
Mink1 |
A |
T |
11: 70,500,885 (GRCm39) |
|
probably benign |
Het |
Mmp25 |
T |
C |
17: 23,850,048 (GRCm39) |
Y504C |
probably damaging |
Het |
Ms4a13 |
C |
T |
19: 11,168,870 (GRCm39) |
V52I |
probably benign |
Het |
Msh4 |
C |
T |
3: 153,573,360 (GRCm39) |
|
probably null |
Het |
Muc5b |
T |
G |
7: 141,412,158 (GRCm39) |
S1701R |
unknown |
Het |
Naalad2 |
A |
T |
9: 18,241,937 (GRCm39) |
S656T |
probably benign |
Het |
Ncapd2 |
T |
C |
6: 125,164,052 (GRCm39) |
Y64C |
probably damaging |
Het |
Ncapg2 |
T |
A |
12: 116,389,420 (GRCm39) |
S347T |
possibly damaging |
Het |
Ndufb11b |
T |
C |
15: 81,864,872 (GRCm39) |
S38P |
probably benign |
Het |
Nipal4 |
T |
C |
11: 46,042,166 (GRCm39) |
T172A |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,961,905 (GRCm39) |
K652R |
probably benign |
Het |
Nrxn3 |
G |
T |
12: 89,478,855 (GRCm39) |
A983S |
possibly damaging |
Het |
Or4a76 |
T |
A |
2: 89,461,143 (GRCm39) |
Y33F |
probably damaging |
Het |
Or4ac1-ps1 |
T |
C |
2: 88,370,588 (GRCm39) |
|
noncoding transcript |
Het |
Or4c115 |
T |
A |
2: 88,928,269 (GRCm39) |
M1L |
probably damaging |
Het |
Or4k77 |
T |
C |
2: 111,199,088 (GRCm39) |
M37T |
probably benign |
Het |
Or51m1 |
A |
G |
7: 103,578,239 (GRCm39) |
T70A |
possibly damaging |
Het |
Or8g24 |
A |
T |
9: 38,989,263 (GRCm39) |
Y259* |
probably null |
Het |
Or8k37 |
A |
C |
2: 86,469,488 (GRCm39) |
L188R |
probably damaging |
Het |
P2rx4 |
T |
A |
5: 122,857,228 (GRCm39) |
S155T |
probably benign |
Het |
P2rx4 |
T |
G |
5: 122,865,271 (GRCm39) |
Y299D |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,693,372 (GRCm39) |
L7F |
probably null |
Het |
Pdss2 |
T |
C |
10: 43,097,793 (GRCm39) |
|
silent |
Het |
Pfkl |
A |
G |
10: 77,827,204 (GRCm39) |
V494A |
possibly damaging |
Het |
Prep |
G |
T |
10: 44,943,460 (GRCm39) |
D12Y |
possibly damaging |
Het |
Prg4 |
A |
G |
1: 150,328,101 (GRCm39) |
F188S |
probably damaging |
Het |
Ripor3 |
T |
C |
2: 167,839,207 (GRCm39) |
Y98C |
probably damaging |
Het |
Rnf216 |
T |
A |
5: 143,054,069 (GRCm39) |
|
probably null |
Het |
Rnf24 |
A |
G |
2: 131,164,165 (GRCm39) |
|
probably benign |
Het |
Rps18-ps6 |
G |
A |
13: 97,896,901 (GRCm39) |
R66* |
probably null |
Het |
Scn3a |
A |
G |
2: 65,327,742 (GRCm39) |
M916T |
probably benign |
Het |
Scnm1 |
T |
C |
3: 95,037,596 (GRCm39) |
I157V |
probably benign |
Het |
Sh2b3 |
C |
G |
5: 121,967,084 (GRCm39) |
R10P |
possibly damaging |
Het |
Slc25a27 |
T |
C |
17: 43,960,585 (GRCm39) |
D211G |
probably damaging |
Het |
Slc36a4 |
A |
T |
9: 15,638,324 (GRCm39) |
Y250F |
probably damaging |
Het |
Slc4a1 |
T |
A |
11: 102,247,351 (GRCm39) |
E448V |
probably damaging |
Het |
Slit1 |
C |
A |
19: 41,731,735 (GRCm39) |
C38F |
probably damaging |
Het |
Spock3 |
T |
A |
8: 63,808,334 (GRCm39) |
N410K |
unknown |
Het |
Supt20 |
G |
T |
3: 54,619,628 (GRCm39) |
W370L |
probably benign |
Het |
Tas2r139 |
T |
A |
6: 42,118,430 (GRCm39) |
N187K |
probably damaging |
Het |
Tbc1d9b |
G |
A |
11: 50,031,311 (GRCm39) |
V111I |
probably benign |
Het |
Thsd7b |
T |
A |
1: 130,138,057 (GRCm39) |
Y1578* |
probably null |
Het |
Tln2 |
T |
A |
9: 67,136,685 (GRCm39) |
I1267F |
probably damaging |
Het |
Tnk2 |
G |
A |
16: 32,490,185 (GRCm39) |
V363I |
probably damaging |
Het |
Ttc32 |
A |
G |
12: 9,085,870 (GRCm39) |
K139R |
possibly damaging |
Het |
Vmn1r30 |
G |
C |
6: 58,412,550 (GRCm39) |
T94S |
possibly damaging |
Het |
Vmn1r90 |
G |
A |
7: 14,295,780 (GRCm39) |
T106I |
probably damaging |
Het |
Zfp677 |
T |
A |
17: 21,618,520 (GRCm39) |
C526S |
probably damaging |
Het |
Zfp831 |
T |
G |
2: 174,485,420 (GRCm39) |
S32A |
probably benign |
Het |
|
Other mutations in Fam83g |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02121:Fam83g
|
APN |
11 |
61,575,609 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02958:Fam83g
|
APN |
11 |
61,598,548 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Fam83g
|
UTSW |
11 |
61,594,422 (GRCm39) |
missense |
probably damaging |
0.99 |
R0365:Fam83g
|
UTSW |
11 |
61,593,935 (GRCm39) |
nonsense |
probably null |
|
R0410:Fam83g
|
UTSW |
11 |
61,594,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Fam83g
|
UTSW |
11 |
61,598,489 (GRCm39) |
missense |
probably benign |
0.37 |
R1163:Fam83g
|
UTSW |
11 |
61,594,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1413:Fam83g
|
UTSW |
11 |
61,593,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Fam83g
|
UTSW |
11 |
61,593,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R1916:Fam83g
|
UTSW |
11 |
61,585,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Fam83g
|
UTSW |
11 |
61,593,801 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2105:Fam83g
|
UTSW |
11 |
61,594,284 (GRCm39) |
missense |
probably benign |
0.01 |
R2134:Fam83g
|
UTSW |
11 |
61,594,510 (GRCm39) |
missense |
probably benign |
0.00 |
R2968:Fam83g
|
UTSW |
11 |
61,594,304 (GRCm39) |
missense |
probably damaging |
0.97 |
R4274:Fam83g
|
UTSW |
11 |
61,592,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4753:Fam83g
|
UTSW |
11 |
61,586,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R6280:Fam83g
|
UTSW |
11 |
61,594,008 (GRCm39) |
missense |
probably benign |
0.00 |
R7234:Fam83g
|
UTSW |
11 |
61,593,342 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7257:Fam83g
|
UTSW |
11 |
61,575,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7588:Fam83g
|
UTSW |
11 |
61,575,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R7761:Fam83g
|
UTSW |
11 |
61,575,584 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9624:Fam83g
|
UTSW |
11 |
61,575,328 (GRCm39) |
intron |
probably benign |
|
Z1176:Fam83g
|
UTSW |
11 |
61,598,296 (GRCm39) |
missense |
probably benign |
0.08 |
Z1186:Fam83g
|
UTSW |
11 |
61,594,020 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Fam83g
|
UTSW |
11 |
61,594,020 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Fam83g
|
UTSW |
11 |
61,594,020 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Fam83g
|
UTSW |
11 |
61,594,020 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Fam83g
|
UTSW |
11 |
61,594,020 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Fam83g
|
UTSW |
11 |
61,594,020 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Fam83g
|
UTSW |
11 |
61,594,020 (GRCm39) |
missense |
probably benign |
0.00 |
|