Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf3 |
T |
C |
5: 30,410,607 (GRCm39) |
|
probably benign |
Het |
Ahrr |
G |
A |
13: 74,431,143 (GRCm39) |
|
probably benign |
Het |
Aoc1l3 |
A |
T |
6: 48,965,840 (GRCm39) |
H616L |
probably damaging |
Het |
Bbs7 |
T |
C |
3: 36,661,866 (GRCm39) |
|
probably null |
Het |
Cacna1h |
T |
C |
17: 25,599,818 (GRCm39) |
K1566E |
probably damaging |
Het |
Ccdc73 |
C |
T |
2: 104,811,332 (GRCm39) |
|
probably benign |
Het |
Cd74 |
A |
T |
18: 60,942,143 (GRCm39) |
H124L |
probably benign |
Het |
Cd74 |
A |
T |
18: 60,936,968 (GRCm39) |
|
probably benign |
Het |
Cdk5rap2 |
T |
C |
4: 70,161,696 (GRCm39) |
E270G |
probably benign |
Het |
Ces2a |
G |
A |
8: 105,468,028 (GRCm39) |
D520N |
probably benign |
Het |
Cldnd1 |
T |
A |
16: 58,551,622 (GRCm39) |
|
probably benign |
Het |
Cox17 |
T |
A |
16: 38,167,532 (GRCm39) |
C24S |
possibly damaging |
Het |
Cyp2b9 |
T |
A |
7: 25,886,178 (GRCm39) |
|
probably benign |
Het |
Dennd4a |
T |
C |
9: 64,803,997 (GRCm39) |
L1112P |
probably benign |
Het |
Dennd4c |
T |
C |
4: 86,699,814 (GRCm39) |
S222P |
probably damaging |
Het |
Dhx37 |
T |
A |
5: 125,508,680 (GRCm39) |
Q85L |
probably benign |
Het |
Egfem1 |
G |
T |
3: 29,637,068 (GRCm39) |
C192F |
probably damaging |
Het |
Eif3f |
A |
T |
7: 108,540,212 (GRCm39) |
N336Y |
possibly damaging |
Het |
Evc2 |
T |
A |
5: 37,574,793 (GRCm39) |
L1016Q |
probably damaging |
Het |
Fam135b |
T |
C |
15: 71,493,881 (GRCm39) |
K16R |
probably damaging |
Het |
Fcho1 |
A |
G |
8: 72,162,643 (GRCm39) |
Y725H |
probably damaging |
Het |
Frem1 |
T |
C |
4: 82,918,335 (GRCm39) |
I536V |
probably benign |
Het |
Galnt2l |
G |
A |
8: 122,997,337 (GRCm39) |
|
probably benign |
Het |
Ginm1 |
T |
C |
10: 7,651,138 (GRCm39) |
|
probably benign |
Het |
Glrb |
A |
T |
3: 80,767,622 (GRCm39) |
|
probably benign |
Het |
Glt6d1 |
C |
A |
2: 25,684,739 (GRCm39) |
|
probably null |
Het |
Gm10320 |
T |
C |
13: 98,626,054 (GRCm39) |
Y110C |
probably damaging |
Het |
Gm3985 |
A |
T |
8: 33,432,484 (GRCm39) |
|
noncoding transcript |
Het |
Gm5422 |
A |
G |
10: 31,125,750 (GRCm39) |
|
noncoding transcript |
Het |
Igkv6-29 |
A |
T |
6: 70,115,754 (GRCm39) |
|
probably benign |
Het |
Inpp5d |
G |
A |
1: 87,625,268 (GRCm39) |
|
probably null |
Het |
Itpr3 |
T |
G |
17: 27,339,951 (GRCm39) |
V2610G |
probably damaging |
Het |
Kmt5c |
T |
A |
7: 4,749,207 (GRCm39) |
M88K |
probably benign |
Het |
Lrp12 |
C |
T |
15: 39,741,672 (GRCm39) |
A367T |
probably damaging |
Het |
Ltbp1 |
A |
G |
17: 75,670,386 (GRCm39) |
T1476A |
probably damaging |
Het |
Mcoln2 |
C |
T |
3: 145,889,316 (GRCm39) |
T374M |
probably damaging |
Het |
Milr1 |
T |
G |
11: 106,657,829 (GRCm39) |
*209G |
probably null |
Het |
Mitf |
A |
G |
6: 97,784,242 (GRCm39) |
K33R |
probably benign |
Het |
Mon2 |
A |
C |
10: 122,868,599 (GRCm39) |
S485A |
probably damaging |
Het |
Mpdu1 |
C |
T |
11: 69,549,667 (GRCm39) |
G47R |
probably damaging |
Het |
Ms4a4d |
A |
G |
19: 11,532,190 (GRCm39) |
N112S |
probably damaging |
Het |
Mybpc3 |
G |
A |
2: 90,965,178 (GRCm39) |
W1082* |
probably null |
Het |
Myl3 |
A |
C |
9: 110,596,997 (GRCm39) |
D119A |
probably damaging |
Het |
Naa15 |
A |
T |
3: 51,343,634 (GRCm39) |
|
probably null |
Het |
Nav3 |
A |
G |
10: 109,659,087 (GRCm39) |
|
probably benign |
Het |
Nek7 |
T |
A |
1: 138,471,942 (GRCm39) |
Q66L |
possibly damaging |
Het |
Nktr |
G |
A |
9: 121,570,232 (GRCm39) |
|
probably benign |
Het |
Nlgn1 |
G |
T |
3: 25,490,006 (GRCm39) |
|
probably benign |
Het |
Npr1 |
T |
C |
3: 90,362,139 (GRCm39) |
E1002G |
probably damaging |
Het |
Nup133 |
A |
T |
8: 124,631,318 (GRCm39) |
I1072N |
probably damaging |
Het |
Oc90 |
C |
T |
15: 65,748,397 (GRCm39) |
C371Y |
probably damaging |
Het |
Or5ak24 |
A |
T |
2: 85,260,239 (GRCm39) |
D311E |
probably benign |
Het |
Or7g20 |
A |
T |
9: 18,946,618 (GRCm39) |
L66F |
probably damaging |
Het |
Or8b42 |
A |
T |
9: 38,342,216 (GRCm39) |
I213F |
possibly damaging |
Het |
Pradc1 |
A |
T |
6: 85,424,213 (GRCm39) |
N44K |
probably damaging |
Het |
Pradc1 |
T |
C |
6: 85,424,602 (GRCm39) |
D116G |
probably damaging |
Het |
Ptprk |
G |
A |
10: 28,461,965 (GRCm39) |
C91Y |
probably damaging |
Het |
Pus7 |
T |
C |
5: 23,952,843 (GRCm39) |
I491V |
probably benign |
Het |
Rock1 |
T |
A |
18: 10,084,380 (GRCm39) |
D951V |
probably damaging |
Het |
Scgb2b26 |
T |
A |
7: 33,643,774 (GRCm39) |
E55D |
probably damaging |
Het |
Scn8a |
T |
C |
15: 100,911,454 (GRCm39) |
V958A |
probably damaging |
Het |
Sec14l1 |
T |
C |
11: 117,034,596 (GRCm39) |
|
probably benign |
Het |
Sec24c |
A |
G |
14: 20,739,329 (GRCm39) |
|
probably benign |
Het |
Sema6b |
C |
T |
17: 56,431,105 (GRCm39) |
E853K |
probably benign |
Het |
Sgk1 |
G |
A |
10: 21,873,337 (GRCm39) |
|
probably null |
Het |
Shprh |
C |
T |
10: 11,027,675 (GRCm39) |
T94I |
probably benign |
Het |
Slc16a3 |
T |
C |
11: 120,847,531 (GRCm39) |
S240P |
probably benign |
Het |
Slc5a8 |
T |
C |
10: 88,722,452 (GRCm39) |
V95A |
probably benign |
Het |
Smg1 |
A |
T |
7: 117,771,082 (GRCm39) |
|
probably benign |
Het |
Spta1 |
G |
A |
1: 174,045,509 (GRCm39) |
V1556I |
probably benign |
Het |
Trappc14 |
T |
C |
5: 138,258,555 (GRCm39) |
|
probably null |
Het |
Trappc4 |
G |
A |
9: 44,316,528 (GRCm39) |
|
probably benign |
Het |
Tubgcp6 |
A |
G |
15: 88,987,386 (GRCm39) |
S1188P |
probably benign |
Het |
Txlna |
T |
G |
4: 129,522,879 (GRCm39) |
D487A |
probably benign |
Het |
Ube2d2b |
T |
C |
5: 107,978,502 (GRCm39) |
F51S |
possibly damaging |
Het |
Vmn2r6 |
G |
A |
3: 64,466,966 (GRCm39) |
Q178* |
probably null |
Het |
Wdfy3 |
T |
C |
5: 101,996,215 (GRCm39) |
T3234A |
probably damaging |
Het |
Ylpm1 |
C |
A |
12: 85,075,800 (GRCm39) |
Q384K |
probably damaging |
Het |
Zbtb41 |
T |
G |
1: 139,351,268 (GRCm39) |
V127G |
probably damaging |
Het |
Zfp605 |
T |
A |
5: 110,275,400 (GRCm39) |
C173S |
probably benign |
Het |
Zfp608 |
A |
T |
18: 55,028,286 (GRCm39) |
|
probably benign |
Het |
Zhx2 |
T |
C |
15: 57,684,670 (GRCm39) |
V13A |
possibly damaging |
Het |
|
Other mutations in Fam114a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00655:Fam114a2
|
APN |
11 |
57,378,413 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00943:Fam114a2
|
APN |
11 |
57,405,099 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
IGL01809:Fam114a2
|
APN |
11 |
57,404,461 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01972:Fam114a2
|
APN |
11 |
57,400,220 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02541:Fam114a2
|
APN |
11 |
57,390,627 (GRCm39) |
missense |
probably benign |
0.41 |
R1594:Fam114a2
|
UTSW |
11 |
57,404,066 (GRCm39) |
critical splice donor site |
probably null |
|
R1645:Fam114a2
|
UTSW |
11 |
57,390,621 (GRCm39) |
missense |
probably benign |
0.00 |
R2426:Fam114a2
|
UTSW |
11 |
57,383,906 (GRCm39) |
missense |
probably benign |
0.00 |
R3021:Fam114a2
|
UTSW |
11 |
57,390,625 (GRCm39) |
missense |
probably benign |
0.01 |
R3107:Fam114a2
|
UTSW |
11 |
57,390,561 (GRCm39) |
missense |
probably benign |
0.39 |
R6149:Fam114a2
|
UTSW |
11 |
57,378,415 (GRCm39) |
missense |
probably benign |
0.05 |
R6248:Fam114a2
|
UTSW |
11 |
57,383,942 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6306:Fam114a2
|
UTSW |
11 |
57,404,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R6933:Fam114a2
|
UTSW |
11 |
57,374,897 (GRCm39) |
missense |
probably benign |
0.04 |
R7485:Fam114a2
|
UTSW |
11 |
57,404,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Fam114a2
|
UTSW |
11 |
57,404,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7487:Fam114a2
|
UTSW |
11 |
57,404,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7531:Fam114a2
|
UTSW |
11 |
57,404,542 (GRCm39) |
missense |
probably benign |
|
R7601:Fam114a2
|
UTSW |
11 |
57,405,042 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7662:Fam114a2
|
UTSW |
11 |
57,398,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R8033:Fam114a2
|
UTSW |
11 |
57,398,333 (GRCm39) |
missense |
probably damaging |
0.99 |
R9335:Fam114a2
|
UTSW |
11 |
57,397,748 (GRCm39) |
missense |
possibly damaging |
0.94 |
RF024:Fam114a2
|
UTSW |
11 |
57,383,859 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Fam114a2
|
UTSW |
11 |
57,404,084 (GRCm39) |
missense |
probably benign |
0.05 |
Z1186:Fam114a2
|
UTSW |
11 |
57,390,581 (GRCm39) |
missense |
probably benign |
0.04 |
Z1186:Fam114a2
|
UTSW |
11 |
57,390,623 (GRCm39) |
missense |
probably benign |
|
Z1186:Fam114a2
|
UTSW |
11 |
57,405,060 (GRCm39) |
missense |
probably benign |
|
Z1186:Fam114a2
|
UTSW |
11 |
57,380,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1186:Fam114a2
|
UTSW |
11 |
57,374,858 (GRCm39) |
missense |
probably benign |
|
Z1187:Fam114a2
|
UTSW |
11 |
57,390,623 (GRCm39) |
missense |
probably benign |
|
Z1187:Fam114a2
|
UTSW |
11 |
57,405,060 (GRCm39) |
missense |
probably benign |
|
Z1187:Fam114a2
|
UTSW |
11 |
57,374,858 (GRCm39) |
missense |
probably benign |
|
Z1187:Fam114a2
|
UTSW |
11 |
57,380,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1187:Fam114a2
|
UTSW |
11 |
57,390,581 (GRCm39) |
missense |
probably benign |
0.04 |
Z1188:Fam114a2
|
UTSW |
11 |
57,390,581 (GRCm39) |
missense |
probably benign |
0.04 |
Z1188:Fam114a2
|
UTSW |
11 |
57,380,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1188:Fam114a2
|
UTSW |
11 |
57,374,858 (GRCm39) |
missense |
probably benign |
|
Z1188:Fam114a2
|
UTSW |
11 |
57,405,060 (GRCm39) |
missense |
probably benign |
|
Z1188:Fam114a2
|
UTSW |
11 |
57,390,623 (GRCm39) |
missense |
probably benign |
|
Z1189:Fam114a2
|
UTSW |
11 |
57,390,581 (GRCm39) |
missense |
probably benign |
0.04 |
Z1189:Fam114a2
|
UTSW |
11 |
57,380,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1189:Fam114a2
|
UTSW |
11 |
57,374,858 (GRCm39) |
missense |
probably benign |
|
Z1189:Fam114a2
|
UTSW |
11 |
57,405,060 (GRCm39) |
missense |
probably benign |
|
Z1189:Fam114a2
|
UTSW |
11 |
57,390,623 (GRCm39) |
missense |
probably benign |
|
Z1190:Fam114a2
|
UTSW |
11 |
57,390,581 (GRCm39) |
missense |
probably benign |
0.04 |
Z1190:Fam114a2
|
UTSW |
11 |
57,380,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1190:Fam114a2
|
UTSW |
11 |
57,374,858 (GRCm39) |
missense |
probably benign |
|
Z1190:Fam114a2
|
UTSW |
11 |
57,405,060 (GRCm39) |
missense |
probably benign |
|
Z1190:Fam114a2
|
UTSW |
11 |
57,390,623 (GRCm39) |
missense |
probably benign |
|
Z1191:Fam114a2
|
UTSW |
11 |
57,390,581 (GRCm39) |
missense |
probably benign |
0.04 |
Z1191:Fam114a2
|
UTSW |
11 |
57,380,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1191:Fam114a2
|
UTSW |
11 |
57,374,858 (GRCm39) |
missense |
probably benign |
|
Z1191:Fam114a2
|
UTSW |
11 |
57,405,060 (GRCm39) |
missense |
probably benign |
|
Z1191:Fam114a2
|
UTSW |
11 |
57,390,623 (GRCm39) |
missense |
probably benign |
|
Z1192:Fam114a2
|
UTSW |
11 |
57,390,581 (GRCm39) |
missense |
probably benign |
0.04 |
Z1192:Fam114a2
|
UTSW |
11 |
57,380,940 (GRCm39) |
missense |
probably benign |
0.03 |
Z1192:Fam114a2
|
UTSW |
11 |
57,374,858 (GRCm39) |
missense |
probably benign |
|
Z1192:Fam114a2
|
UTSW |
11 |
57,405,060 (GRCm39) |
missense |
probably benign |
|
Z1192:Fam114a2
|
UTSW |
11 |
57,390,623 (GRCm39) |
missense |
probably benign |
|
|