Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
G |
A |
15: 76,834,475 (GRCm39) |
V124I |
probably damaging |
Het |
1700123K08Rik |
C |
T |
5: 138,560,751 (GRCm39) |
A215T |
probably benign |
Het |
Aen |
G |
A |
7: 78,557,050 (GRCm39) |
M299I |
probably damaging |
Het |
Apc2 |
G |
A |
10: 80,147,820 (GRCm39) |
C929Y |
probably damaging |
Het |
Arap2 |
T |
C |
5: 62,807,199 (GRCm39) |
H1156R |
probably benign |
Het |
Arhgap9 |
A |
G |
10: 127,164,821 (GRCm39) |
T582A |
probably damaging |
Het |
Ccdc57 |
T |
A |
11: 120,752,085 (GRCm39) |
H832L |
probably benign |
Het |
Ces3b |
T |
C |
8: 105,818,206 (GRCm39) |
S92P |
probably benign |
Het |
Ces5a |
A |
G |
8: 94,252,172 (GRCm39) |
|
probably null |
Het |
Cfap206 |
C |
T |
4: 34,721,562 (GRCm39) |
S162N |
probably damaging |
Het |
Cpb2 |
T |
A |
14: 75,508,215 (GRCm39) |
D225E |
probably damaging |
Het |
Cpne8 |
C |
T |
15: 90,499,313 (GRCm39) |
|
probably null |
Het |
Cux2 |
G |
A |
5: 122,005,414 (GRCm39) |
T924M |
possibly damaging |
Het |
Dtl |
T |
A |
1: 191,293,651 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
A |
6: 84,176,767 (GRCm39) |
I1912N |
possibly damaging |
Het |
Edc4 |
T |
A |
8: 106,613,766 (GRCm39) |
F369I |
probably benign |
Het |
Fibcd1 |
T |
C |
2: 31,711,531 (GRCm39) |
E298G |
probably benign |
Het |
Frem1 |
C |
T |
4: 82,932,104 (GRCm39) |
R199H |
probably benign |
Het |
Gadl1 |
T |
C |
9: 115,783,907 (GRCm39) |
|
probably null |
Het |
Hipk1 |
G |
A |
3: 103,685,015 (GRCm39) |
T200I |
possibly damaging |
Het |
Ighv14-2 |
C |
T |
12: 113,958,379 (GRCm39) |
V21I |
possibly damaging |
Het |
Kank4 |
A |
T |
4: 98,666,632 (GRCm39) |
I605N |
probably damaging |
Het |
Krt88 |
T |
G |
15: 101,351,508 (GRCm39) |
*172G |
probably null |
Het |
Lmf2 |
C |
A |
15: 89,237,091 (GRCm39) |
A408S |
probably benign |
Het |
Lsm12 |
T |
C |
11: 102,054,896 (GRCm39) |
|
probably benign |
Het |
Myo3b |
A |
G |
2: 70,075,735 (GRCm39) |
I580V |
probably benign |
Het |
Myt1 |
T |
C |
2: 181,467,749 (GRCm39) |
M1061T |
probably damaging |
Het |
Nup133 |
G |
A |
8: 124,657,721 (GRCm39) |
R405* |
probably null |
Het |
Or1ad1 |
A |
T |
11: 50,875,830 (GRCm39) |
I101F |
possibly damaging |
Het |
Or5m3 |
A |
G |
2: 85,838,891 (GRCm39) |
Y257C |
probably damaging |
Het |
Or8g2 |
A |
T |
9: 39,821,902 (GRCm39) |
M268L |
possibly damaging |
Het |
Pcnx1 |
A |
G |
12: 81,964,918 (GRCm39) |
R362G |
probably benign |
Het |
Pomt2 |
G |
T |
12: 87,157,078 (GRCm39) |
T747K |
probably damaging |
Het |
Rgma |
G |
A |
7: 73,067,239 (GRCm39) |
A165T |
probably damaging |
Het |
Rhbdf2 |
T |
C |
11: 116,492,577 (GRCm39) |
D437G |
possibly damaging |
Het |
Rpl5 |
T |
C |
5: 108,055,145 (GRCm39) |
|
probably null |
Het |
Rtkn2 |
A |
G |
10: 67,877,494 (GRCm39) |
D518G |
probably benign |
Het |
Sclt1 |
T |
C |
3: 41,696,426 (GRCm39) |
|
probably benign |
Het |
Sidt2 |
C |
T |
9: 45,854,375 (GRCm39) |
V616I |
possibly damaging |
Het |
Ska2 |
A |
G |
11: 87,000,091 (GRCm39) |
|
probably benign |
Het |
Slc13a4 |
C |
A |
6: 35,245,817 (GRCm39) |
L609F |
probably damaging |
Het |
Sorbs3 |
T |
C |
14: 70,428,604 (GRCm39) |
E390G |
probably damaging |
Het |
Syt15 |
T |
C |
14: 33,946,881 (GRCm39) |
V220A |
possibly damaging |
Het |
Tob1 |
T |
C |
11: 94,104,881 (GRCm39) |
F139S |
probably damaging |
Het |
Yars2 |
C |
T |
16: 16,124,406 (GRCm39) |
R338* |
probably null |
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 |
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 |
|
R7242:Focad
|
UTSW |
4 |
88,228,143 (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 |
|