Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130401M01Rik |
A |
T |
15: 57,892,132 (GRCm39) |
N158K |
probably benign |
Het |
Acnat1 |
G |
C |
4: 49,447,457 (GRCm39) |
P357A |
probably damaging |
Het |
Akap6 |
T |
A |
12: 53,119,240 (GRCm39) |
C1102* |
probably null |
Het |
Calb2 |
C |
T |
8: 110,883,635 (GRCm39) |
|
probably benign |
Het |
Cdh15 |
G |
A |
8: 123,583,374 (GRCm39) |
R59H |
probably benign |
Het |
Csgalnact1 |
TGG |
TG |
8: 68,913,737 (GRCm39) |
|
probably null |
Het |
Dmtf1 |
A |
G |
5: 9,182,454 (GRCm39) |
|
probably benign |
Het |
Frem1 |
A |
G |
4: 82,932,351 (GRCm39) |
F117L |
probably damaging |
Het |
Gab2 |
A |
G |
7: 96,921,236 (GRCm39) |
T204A |
probably benign |
Het |
Gapdh |
T |
C |
6: 125,139,583 (GRCm39) |
N229S |
possibly damaging |
Het |
Gm3604 |
A |
T |
13: 62,517,868 (GRCm39) |
C163* |
probably null |
Het |
Iqub |
G |
C |
6: 24,462,036 (GRCm39) |
|
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
L1td1 |
A |
G |
4: 98,625,755 (GRCm39) |
E650G |
possibly damaging |
Het |
Lilra5 |
G |
A |
7: 4,241,756 (GRCm39) |
G185D |
probably damaging |
Het |
Lpin1 |
A |
G |
12: 16,615,584 (GRCm39) |
S323P |
possibly damaging |
Het |
Mmp7 |
C |
A |
9: 7,692,219 (GRCm39) |
S31R |
probably benign |
Het |
Myo1h |
G |
A |
5: 114,466,801 (GRCm39) |
C283Y |
probably benign |
Het |
Nfkbiz |
A |
G |
16: 55,639,991 (GRCm39) |
L122P |
probably damaging |
Het |
Or10c1 |
A |
G |
17: 37,522,427 (GRCm39) |
F106L |
possibly damaging |
Het |
Or1e35 |
T |
C |
11: 73,797,484 (GRCm39) |
Y278C |
possibly damaging |
Het |
Paqr8 |
A |
G |
1: 21,005,257 (GRCm39) |
E137G |
probably damaging |
Het |
Pde4b |
G |
A |
4: 102,456,840 (GRCm39) |
A429T |
probably damaging |
Het |
Pes1 |
T |
C |
11: 3,925,736 (GRCm39) |
|
probably benign |
Het |
Reln |
A |
T |
5: 22,245,418 (GRCm39) |
I730N |
possibly damaging |
Het |
Sh3rf1 |
C |
T |
8: 61,679,321 (GRCm39) |
P121L |
probably benign |
Het |
Skint9 |
T |
G |
4: 112,248,148 (GRCm39) |
I199L |
probably benign |
Het |
Slc13a4 |
C |
T |
6: 35,245,861 (GRCm39) |
V595M |
probably damaging |
Het |
Smarca2 |
A |
G |
19: 26,661,222 (GRCm39) |
E939G |
possibly damaging |
Het |
Spg11 |
A |
G |
2: 121,913,879 (GRCm39) |
|
probably null |
Het |
Trpm1 |
T |
A |
7: 63,849,061 (GRCm39) |
Y102* |
probably null |
Het |
Usp42 |
A |
G |
5: 143,702,954 (GRCm39) |
S556P |
probably benign |
Het |
Zfp957 |
A |
G |
14: 79,450,332 (GRCm39) |
V489A |
probably damaging |
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 |
|
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 |
|