Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
A |
T |
5: 146,121,677 (GRCm39) |
I74N |
probably damaging |
Het |
Abca6 |
A |
T |
11: 110,132,479 (GRCm39) |
V272D |
possibly damaging |
Het |
Acot11 |
A |
T |
4: 106,619,690 (GRCm39) |
S163R |
probably benign |
Het |
Adcy5 |
T |
C |
16: 34,977,205 (GRCm39) |
L246P |
probably damaging |
Het |
Adgra1 |
A |
T |
7: 139,427,573 (GRCm39) |
|
probably null |
Het |
Adgra2 |
A |
G |
8: 27,612,055 (GRCm39) |
T1335A |
probably damaging |
Het |
Aoc1l2 |
A |
T |
6: 48,908,062 (GRCm39) |
Y354F |
probably damaging |
Het |
Armt1 |
T |
C |
10: 4,403,475 (GRCm39) |
S187P |
probably damaging |
Het |
Azin1 |
T |
C |
15: 38,501,749 (GRCm39) |
M1V |
probably null |
Het |
B430305J03Rik |
C |
T |
3: 61,271,256 (GRCm39) |
C163Y |
unknown |
Het |
Cables1 |
T |
C |
18: 11,973,064 (GRCm39) |
S68P |
possibly damaging |
Het |
Cacna1d |
A |
G |
14: 29,900,663 (GRCm39) |
F341L |
probably benign |
Het |
Ccdc90b |
T |
A |
7: 92,221,776 (GRCm39) |
H118Q |
probably damaging |
Het |
Ccn5 |
T |
C |
2: 163,670,772 (GRCm39) |
F93S |
probably benign |
Het |
Celf1 |
T |
A |
2: 90,833,602 (GRCm39) |
C119* |
probably null |
Het |
Cfap57 |
C |
T |
4: 118,450,293 (GRCm39) |
V610M |
possibly damaging |
Het |
Chrm4 |
T |
A |
2: 91,757,595 (GRCm39) |
M1K |
probably null |
Het |
Chrnd |
C |
T |
1: 87,125,201 (GRCm39) |
T418I |
probably damaging |
Het |
Coch |
G |
T |
12: 51,640,344 (GRCm39) |
|
probably benign |
Het |
Cop1 |
A |
G |
1: 159,112,118 (GRCm39) |
T345A |
probably benign |
Het |
Cops6 |
A |
G |
5: 138,161,842 (GRCm39) |
T96A |
probably benign |
Het |
Corin |
T |
C |
5: 72,462,398 (GRCm39) |
I945V |
probably benign |
Het |
Cyp2c67 |
G |
T |
19: 39,605,783 (GRCm39) |
T371N |
probably benign |
Het |
Dap |
T |
A |
15: 31,273,454 (GRCm39) |
*103R |
probably null |
Het |
Defb35 |
T |
A |
8: 22,430,773 (GRCm39) |
V49E |
unknown |
Het |
Dmtf1 |
T |
A |
5: 9,199,016 (GRCm39) |
D39V |
possibly damaging |
Het |
Dmtn |
T |
C |
14: 70,855,460 (GRCm39) |
T10A |
probably damaging |
Het |
Dnajc1 |
C |
T |
2: 18,298,783 (GRCm39) |
E264K |
probably benign |
Het |
Dtx3l |
A |
T |
16: 35,753,771 (GRCm39) |
N278K |
possibly damaging |
Het |
Fam161a |
T |
A |
11: 22,970,037 (GRCm39) |
S72T |
possibly damaging |
Het |
Fnbp4 |
T |
A |
2: 90,576,140 (GRCm39) |
S114T |
unknown |
Het |
Fzd8 |
A |
T |
18: 9,214,171 (GRCm39) |
T418S |
probably damaging |
Het |
Gclc |
A |
G |
9: 77,692,653 (GRCm39) |
Y264C |
probably benign |
Het |
Ggn |
G |
A |
7: 28,872,459 (GRCm39) |
C649Y |
possibly damaging |
Het |
Gys1 |
A |
G |
7: 45,089,092 (GRCm39) |
|
probably null |
Het |
Hsd3b1 |
T |
C |
3: 98,760,526 (GRCm39) |
Y155C |
probably damaging |
Het |
Htatip2 |
A |
G |
7: 49,422,354 (GRCm39) |
K191E |
probably benign |
Het |
Ik |
A |
T |
18: 36,881,275 (GRCm39) |
S79C |
probably null |
Het |
Kin |
G |
A |
2: 10,096,604 (GRCm39) |
R151Q |
probably benign |
Het |
Kpna2rt |
G |
A |
17: 90,217,563 (GRCm39) |
T61I |
probably benign |
Het |
Mast4 |
A |
G |
13: 102,874,986 (GRCm39) |
S1461P |
probably damaging |
Het |
Melk |
T |
A |
4: 44,360,885 (GRCm39) |
V555E |
probably damaging |
Het |
Met |
G |
A |
6: 17,491,316 (GRCm39) |
C26Y |
probably damaging |
Het |
Mfsd6 |
A |
T |
1: 52,748,633 (GRCm39) |
F77L |
probably damaging |
Het |
Mib1 |
T |
A |
18: 10,741,011 (GRCm39) |
D86E |
probably damaging |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Or12e8 |
G |
A |
2: 87,188,426 (GRCm39) |
V213I |
probably benign |
Het |
Or56b1b |
T |
G |
7: 108,164,919 (GRCm39) |
S28R |
probably benign |
Het |
Or7a36 |
A |
T |
10: 78,820,331 (GRCm39) |
K236* |
probably null |
Het |
Or8g21 |
A |
G |
9: 38,906,437 (GRCm39) |
I98T |
probably benign |
Het |
Patj |
A |
T |
4: 98,480,170 (GRCm39) |
I1296L |
probably benign |
Het |
Pcdh1 |
C |
T |
18: 38,336,270 (GRCm39) |
V122M |
probably benign |
Het |
Pcdhac2 |
A |
T |
18: 37,277,946 (GRCm39) |
I309F |
possibly damaging |
Het |
Phf8-ps |
A |
G |
17: 33,286,101 (GRCm39) |
Y234H |
probably damaging |
Het |
Phtf1 |
A |
G |
3: 103,906,012 (GRCm39) |
S565G |
probably damaging |
Het |
Plekha2 |
A |
C |
8: 25,578,411 (GRCm39) |
F30V |
probably damaging |
Het |
Ptbp1 |
A |
G |
10: 79,692,222 (GRCm39) |
M20V |
unknown |
Het |
Pth2r |
A |
G |
1: 65,427,779 (GRCm39) |
D484G |
probably benign |
Het |
Rapgef2 |
G |
A |
3: 78,995,210 (GRCm39) |
Q665* |
probably null |
Het |
Scamp1 |
G |
A |
13: 94,369,648 (GRCm39) |
T59I |
probably benign |
Het |
Sema4a |
T |
A |
3: 88,357,416 (GRCm39) |
D230V |
probably damaging |
Het |
Snw1 |
C |
T |
12: 87,515,415 (GRCm39) |
G45R |
possibly damaging |
Het |
Sox30 |
T |
A |
11: 45,875,347 (GRCm39) |
|
probably null |
Het |
Sspo |
T |
A |
6: 48,450,886 (GRCm39) |
I2665K |
probably benign |
Het |
Stx5a |
T |
A |
19: 8,732,641 (GRCm39) |
W437R |
unknown |
Het |
Tln1 |
A |
G |
4: 43,542,602 (GRCm39) |
V1402A |
probably benign |
Het |
Tpm1 |
A |
G |
9: 66,935,383 (GRCm39) |
L244P |
probably benign |
Het |
Try5 |
T |
A |
6: 41,290,388 (GRCm39) |
E32V |
probably benign |
Het |
Ttn |
T |
C |
2: 76,552,073 (GRCm39) |
N31188S |
probably benign |
Het |
Tulp1 |
T |
C |
17: 28,582,379 (GRCm39) |
|
probably null |
Het |
Usp13 |
T |
G |
3: 32,919,892 (GRCm39) |
|
probably null |
Het |
Vax2 |
A |
G |
6: 83,688,298 (GRCm39) |
E7G |
possibly damaging |
Het |
Vmn2r45 |
A |
T |
7: 8,488,612 (GRCm39) |
Y139* |
probably null |
Het |
Zfp423 |
T |
C |
8: 88,631,155 (GRCm39) |
D21G |
probably benign |
Het |
|
Other mutations in Focad |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00326:Focad
|
APN |
4 |
88,275,711 (GRCm39) |
missense |
unknown |
|
IGL00562:Focad
|
APN |
4 |
88,267,046 (GRCm39) |
missense |
unknown |
|
IGL00563:Focad
|
APN |
4 |
88,267,046 (GRCm39) |
missense |
unknown |
|
IGL00900:Focad
|
APN |
4 |
88,047,260 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00984:Focad
|
APN |
4 |
88,263,022 (GRCm39) |
missense |
unknown |
|
IGL01016:Focad
|
APN |
4 |
88,310,252 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01069:Focad
|
APN |
4 |
88,244,383 (GRCm39) |
missense |
unknown |
|
IGL01305:Focad
|
APN |
4 |
88,311,784 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01409:Focad
|
APN |
4 |
88,260,542 (GRCm39) |
missense |
unknown |
|
IGL01447:Focad
|
APN |
4 |
88,244,465 (GRCm39) |
missense |
unknown |
|
IGL01521:Focad
|
APN |
4 |
88,328,927 (GRCm39) |
makesense |
probably null |
|
IGL01672:Focad
|
APN |
4 |
88,278,827 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01739:Focad
|
APN |
4 |
88,289,043 (GRCm39) |
missense |
unknown |
|
IGL02082:Focad
|
APN |
4 |
88,148,815 (GRCm39) |
nonsense |
probably null |
|
IGL02139:Focad
|
APN |
4 |
88,047,291 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02381:Focad
|
APN |
4 |
88,192,327 (GRCm39) |
splice site |
probably benign |
|
IGL02898:Focad
|
APN |
4 |
88,310,234 (GRCm39) |
missense |
probably benign |
0.02 |
certitude
|
UTSW |
4 |
88,096,370 (GRCm39) |
missense |
probably damaging |
1.00 |
impression
|
UTSW |
4 |
88,196,479 (GRCm39) |
missense |
unknown |
|
Microscope
|
UTSW |
4 |
88,260,441 (GRCm39) |
missense |
unknown |
|
Nuance
|
UTSW |
4 |
88,115,083 (GRCm39) |
intron |
probably benign |
|
Objective
|
UTSW |
4 |
88,319,305 (GRCm39) |
nonsense |
probably null |
|
ANU22:Focad
|
UTSW |
4 |
88,311,784 (GRCm39) |
missense |
probably benign |
0.32 |
R0025:Focad
|
UTSW |
4 |
88,327,196 (GRCm39) |
missense |
probably benign |
0.02 |
R0554:Focad
|
UTSW |
4 |
88,267,126 (GRCm39) |
missense |
unknown |
|
R0617:Focad
|
UTSW |
4 |
88,039,525 (GRCm39) |
unclassified |
probably benign |
|
R0688:Focad
|
UTSW |
4 |
88,192,450 (GRCm39) |
missense |
unknown |
|
R0746:Focad
|
UTSW |
4 |
88,315,451 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0907:Focad
|
UTSW |
4 |
88,196,498 (GRCm39) |
critical splice donor site |
probably null |
|
R1109:Focad
|
UTSW |
4 |
88,114,984 (GRCm39) |
intron |
probably benign |
|
R1136:Focad
|
UTSW |
4 |
88,244,417 (GRCm39) |
missense |
unknown |
|
R1185:Focad
|
UTSW |
4 |
88,096,424 (GRCm39) |
missense |
probably benign |
0.40 |
R1185:Focad
|
UTSW |
4 |
88,096,424 (GRCm39) |
missense |
probably benign |
0.40 |
R1185:Focad
|
UTSW |
4 |
88,096,424 (GRCm39) |
missense |
probably benign |
0.40 |
R1412:Focad
|
UTSW |
4 |
88,196,498 (GRCm39) |
critical splice donor site |
probably null |
|
R1453:Focad
|
UTSW |
4 |
88,275,679 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1697:Focad
|
UTSW |
4 |
88,327,225 (GRCm39) |
missense |
probably damaging |
0.98 |
R1739:Focad
|
UTSW |
4 |
88,316,128 (GRCm39) |
missense |
probably benign |
0.05 |
R1767:Focad
|
UTSW |
4 |
88,275,705 (GRCm39) |
missense |
unknown |
|
R1827:Focad
|
UTSW |
4 |
88,147,620 (GRCm39) |
missense |
probably benign |
0.03 |
R1866:Focad
|
UTSW |
4 |
88,325,402 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1867:Focad
|
UTSW |
4 |
88,096,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R1929:Focad
|
UTSW |
4 |
88,260,449 (GRCm39) |
missense |
unknown |
|
R1929:Focad
|
UTSW |
4 |
88,315,416 (GRCm39) |
missense |
probably benign |
0.32 |
R1937:Focad
|
UTSW |
4 |
88,319,318 (GRCm39) |
start codon destroyed |
probably null |
|
R1989:Focad
|
UTSW |
4 |
88,151,021 (GRCm39) |
critical splice donor site |
probably null |
|
R2176:Focad
|
UTSW |
4 |
88,197,481 (GRCm39) |
missense |
unknown |
|
R2393:Focad
|
UTSW |
4 |
88,039,567 (GRCm39) |
missense |
probably damaging |
0.96 |
R2431:Focad
|
UTSW |
4 |
88,249,264 (GRCm39) |
missense |
unknown |
|
R3195:Focad
|
UTSW |
4 |
88,325,588 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3196:Focad
|
UTSW |
4 |
88,325,588 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3730:Focad
|
UTSW |
4 |
88,327,162 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3772:Focad
|
UTSW |
4 |
88,254,398 (GRCm39) |
splice site |
probably benign |
|
R4391:Focad
|
UTSW |
4 |
88,104,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R4491:Focad
|
UTSW |
4 |
88,278,142 (GRCm39) |
critical splice donor site |
probably null |
|
R4492:Focad
|
UTSW |
4 |
88,278,142 (GRCm39) |
critical splice donor site |
probably null |
|
R4703:Focad
|
UTSW |
4 |
88,260,558 (GRCm39) |
critical splice donor site |
probably null |
|
R4788:Focad
|
UTSW |
4 |
88,275,706 (GRCm39) |
missense |
unknown |
|
R4923:Focad
|
UTSW |
4 |
88,115,083 (GRCm39) |
intron |
probably benign |
|
R5026:Focad
|
UTSW |
4 |
88,262,819 (GRCm39) |
missense |
unknown |
|
R5122:Focad
|
UTSW |
4 |
88,325,602 (GRCm39) |
critical splice donor site |
probably null |
|
R5153:Focad
|
UTSW |
4 |
88,278,121 (GRCm39) |
missense |
unknown |
|
R5369:Focad
|
UTSW |
4 |
88,039,610 (GRCm39) |
splice site |
probably benign |
|
R5414:Focad
|
UTSW |
4 |
88,328,939 (GRCm39) |
utr 3 prime |
probably benign |
|
R5839:Focad
|
UTSW |
4 |
88,115,083 (GRCm39) |
intron |
probably benign |
|
R5916:Focad
|
UTSW |
4 |
88,275,778 (GRCm39) |
missense |
unknown |
|
R5953:Focad
|
UTSW |
4 |
88,147,572 (GRCm39) |
missense |
probably benign |
0.01 |
R5991:Focad
|
UTSW |
4 |
88,319,256 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6230:Focad
|
UTSW |
4 |
88,260,441 (GRCm39) |
missense |
unknown |
|
R6247:Focad
|
UTSW |
4 |
88,325,377 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6324:Focad
|
UTSW |
4 |
88,319,305 (GRCm39) |
nonsense |
probably null |
|
R6543:Focad
|
UTSW |
4 |
88,197,493 (GRCm39) |
missense |
unknown |
|
R6639:Focad
|
UTSW |
4 |
88,196,479 (GRCm39) |
missense |
unknown |
|
R6802:Focad
|
UTSW |
4 |
88,262,921 (GRCm39) |
missense |
unknown |
|
R6802:Focad
|
UTSW |
4 |
88,192,440 (GRCm39) |
missense |
unknown |
|
R6866:Focad
|
UTSW |
4 |
88,321,623 (GRCm39) |
missense |
probably benign |
0.34 |
R6902:Focad
|
UTSW |
4 |
88,148,713 (GRCm39) |
missense |
unknown |
|
R6928:Focad
|
UTSW |
4 |
88,267,112 (GRCm39) |
missense |
unknown |
|
R7036:Focad
|
UTSW |
4 |
88,042,874 (GRCm39) |
missense |
probably benign |
0.05 |
R7057:Focad
|
UTSW |
4 |
88,192,342 (GRCm39) |
missense |
unknown |
|
R7077:Focad
|
UTSW |
4 |
88,328,914 (GRCm39) |
missense |
unknown |
|
R7357:Focad
|
UTSW |
4 |
88,147,572 (GRCm39) |
missense |
probably benign |
0.19 |
R7380:Focad
|
UTSW |
4 |
88,192,435 (GRCm39) |
missense |
unknown |
|
R7427:Focad
|
UTSW |
4 |
88,286,988 (GRCm39) |
missense |
unknown |
|
R7582:Focad
|
UTSW |
4 |
88,147,615 (GRCm39) |
missense |
probably benign |
0.00 |
R7661:Focad
|
UTSW |
4 |
88,221,772 (GRCm39) |
missense |
unknown |
|
R7688:Focad
|
UTSW |
4 |
88,096,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R7789:Focad
|
UTSW |
4 |
88,147,643 (GRCm39) |
missense |
unknown |
|
R7880:Focad
|
UTSW |
4 |
88,319,407 (GRCm39) |
missense |
unknown |
|
R7887:Focad
|
UTSW |
4 |
88,100,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Focad
|
UTSW |
4 |
88,315,237 (GRCm39) |
missense |
unknown |
|
R8129:Focad
|
UTSW |
4 |
88,151,000 (GRCm39) |
missense |
unknown |
|
R8369:Focad
|
UTSW |
4 |
88,150,905 (GRCm39) |
missense |
unknown |
|
R8837:Focad
|
UTSW |
4 |
88,072,905 (GRCm39) |
missense |
probably damaging |
0.96 |
R9014:Focad
|
UTSW |
4 |
88,275,763 (GRCm39) |
missense |
unknown |
|
R9282:Focad
|
UTSW |
4 |
88,115,059 (GRCm39) |
missense |
unknown |
|
R9431:Focad
|
UTSW |
4 |
88,321,583 (GRCm39) |
missense |
unknown |
|
R9435:Focad
|
UTSW |
4 |
88,267,076 (GRCm39) |
missense |
unknown |
|
R9676:Focad
|
UTSW |
4 |
88,273,682 (GRCm39) |
missense |
unknown |
|
X0035:Focad
|
UTSW |
4 |
88,316,159 (GRCm39) |
missense |
possibly damaging |
0.86 |
|