Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd5 |
A |
G |
2: 22,989,579 (GRCm39) |
N401D |
probably benign |
Het |
Agtpbp1 |
T |
A |
13: 59,644,829 (GRCm39) |
D679V |
possibly damaging |
Het |
Akap8 |
A |
G |
17: 32,524,622 (GRCm39) |
V558A |
probably benign |
Het |
Arrdc2 |
C |
T |
8: 71,290,171 (GRCm39) |
R170Q |
probably benign |
Het |
Atg10 |
A |
T |
13: 91,189,027 (GRCm39) |
H94Q |
probably damaging |
Het |
Atg4a-ps |
G |
A |
3: 103,552,837 (GRCm39) |
A168V |
probably damaging |
Het |
Crb2 |
G |
T |
2: 37,673,395 (GRCm39) |
R97L |
probably benign |
Het |
Dnaja1 |
C |
T |
4: 40,724,052 (GRCm39) |
A71V |
possibly damaging |
Het |
Dysf |
G |
A |
6: 84,163,491 (GRCm39) |
|
probably null |
Het |
G6pd2 |
A |
G |
5: 61,966,869 (GRCm39) |
R215G |
probably damaging |
Het |
Hcn3 |
A |
G |
3: 89,054,920 (GRCm39) |
S776P |
probably benign |
Het |
Mafa |
A |
G |
15: 75,619,147 (GRCm39) |
S209P |
probably benign |
Het |
Mug2 |
A |
G |
6: 122,051,683 (GRCm39) |
|
probably null |
Het |
Myh14 |
T |
C |
7: 44,265,687 (GRCm39) |
D1564G |
possibly damaging |
Het |
Ncor2 |
T |
A |
5: 125,102,824 (GRCm39) |
I1792F |
probably damaging |
Het |
Nod2 |
T |
C |
8: 89,379,519 (GRCm39) |
F7L |
probably benign |
Het |
Odad2 |
G |
A |
18: 7,222,625 (GRCm39) |
S548L |
probably benign |
Het |
Or10d5 |
A |
G |
9: 39,861,660 (GRCm39) |
S136P |
probably benign |
Het |
Or1m1 |
T |
A |
9: 18,666,775 (GRCm39) |
D52V |
probably damaging |
Het |
Or2aa1 |
T |
C |
11: 59,480,265 (GRCm39) |
T217A |
probably benign |
Het |
Pak3 |
T |
C |
X: 142,547,972 (GRCm39) |
V318A |
probably damaging |
Het |
Pik3ap1 |
T |
C |
19: 41,290,970 (GRCm39) |
T521A |
probably benign |
Het |
Pkdcc |
G |
C |
17: 83,523,378 (GRCm39) |
A162P |
probably benign |
Het |
Rassf4 |
A |
G |
6: 116,618,701 (GRCm39) |
V194A |
probably damaging |
Het |
Scp2d1 |
T |
A |
2: 144,665,868 (GRCm39) |
I69N |
probably damaging |
Het |
Spg11 |
A |
G |
2: 121,905,782 (GRCm39) |
S1288P |
probably damaging |
Het |
Sptb |
A |
G |
12: 76,645,532 (GRCm39) |
S2019P |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,021,004 (GRCm39) |
L630* |
probably null |
Het |
Trim41 |
TTCCTCCTCCTCCTCCTCCTCCTCCTCC |
TTCCTCCTCCTCCTCCTCCTCCTCC |
11: 48,707,084 (GRCm39) |
|
probably benign |
Het |
Trpc1 |
C |
T |
9: 95,605,182 (GRCm39) |
R159H |
probably damaging |
Het |
Zbtb14 |
C |
T |
17: 69,695,214 (GRCm39) |
P304L |
probably damaging |
Het |
|
Other mutations in Ift140 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00753:Ift140
|
APN |
17 |
25,274,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00966:Ift140
|
APN |
17 |
25,237,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01082:Ift140
|
APN |
17 |
25,267,429 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01394:Ift140
|
APN |
17 |
25,313,676 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01816:Ift140
|
APN |
17 |
25,305,999 (GRCm39) |
splice site |
probably null |
|
IGL01994:Ift140
|
APN |
17 |
25,267,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02102:Ift140
|
APN |
17 |
25,252,104 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02207:Ift140
|
APN |
17 |
25,274,572 (GRCm39) |
missense |
probably benign |
|
IGL02493:Ift140
|
APN |
17 |
25,306,898 (GRCm39) |
nonsense |
probably null |
|
IGL02735:Ift140
|
APN |
17 |
25,253,009 (GRCm39) |
splice site |
probably benign |
|
IGL02902:Ift140
|
APN |
17 |
25,309,736 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03037:Ift140
|
APN |
17 |
25,311,368 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03122:Ift140
|
APN |
17 |
25,305,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:Ift140
|
APN |
17 |
25,311,800 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03271:Ift140
|
APN |
17 |
25,306,880 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03358:Ift140
|
APN |
17 |
25,306,958 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4515001:Ift140
|
UTSW |
17 |
25,305,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R0100:Ift140
|
UTSW |
17 |
25,309,928 (GRCm39) |
nonsense |
probably null |
|
R0100:Ift140
|
UTSW |
17 |
25,309,928 (GRCm39) |
nonsense |
probably null |
|
R0197:Ift140
|
UTSW |
17 |
25,309,907 (GRCm39) |
missense |
probably benign |
0.09 |
R0238:Ift140
|
UTSW |
17 |
25,264,497 (GRCm39) |
nonsense |
probably null |
|
R0238:Ift140
|
UTSW |
17 |
25,264,497 (GRCm39) |
nonsense |
probably null |
|
R0239:Ift140
|
UTSW |
17 |
25,264,497 (GRCm39) |
nonsense |
probably null |
|
R0239:Ift140
|
UTSW |
17 |
25,264,497 (GRCm39) |
nonsense |
probably null |
|
R0355:Ift140
|
UTSW |
17 |
25,267,409 (GRCm39) |
nonsense |
probably null |
|
R0399:Ift140
|
UTSW |
17 |
25,269,314 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0574:Ift140
|
UTSW |
17 |
25,270,734 (GRCm39) |
splice site |
probably null |
|
R0610:Ift140
|
UTSW |
17 |
25,254,777 (GRCm39) |
missense |
probably benign |
0.06 |
R0701:Ift140
|
UTSW |
17 |
25,309,907 (GRCm39) |
missense |
probably benign |
0.09 |
R0883:Ift140
|
UTSW |
17 |
25,309,907 (GRCm39) |
missense |
probably benign |
0.09 |
R0900:Ift140
|
UTSW |
17 |
25,254,786 (GRCm39) |
missense |
probably benign |
0.22 |
R1167:Ift140
|
UTSW |
17 |
25,254,719 (GRCm39) |
missense |
probably benign |
0.01 |
R1295:Ift140
|
UTSW |
17 |
25,307,907 (GRCm39) |
critical splice donor site |
probably null |
|
R1588:Ift140
|
UTSW |
17 |
25,306,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Ift140
|
UTSW |
17 |
25,307,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1637:Ift140
|
UTSW |
17 |
25,244,608 (GRCm39) |
missense |
probably benign |
0.40 |
R1854:Ift140
|
UTSW |
17 |
25,254,813 (GRCm39) |
missense |
probably benign |
0.05 |
R2397:Ift140
|
UTSW |
17 |
25,239,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Ift140
|
UTSW |
17 |
25,255,282 (GRCm39) |
missense |
probably benign |
0.02 |
R3433:Ift140
|
UTSW |
17 |
25,255,282 (GRCm39) |
missense |
probably benign |
0.02 |
R3878:Ift140
|
UTSW |
17 |
25,247,918 (GRCm39) |
missense |
probably benign |
0.25 |
R4559:Ift140
|
UTSW |
17 |
25,309,741 (GRCm39) |
missense |
probably damaging |
0.97 |
R4670:Ift140
|
UTSW |
17 |
25,317,935 (GRCm39) |
unclassified |
probably benign |
|
R4711:Ift140
|
UTSW |
17 |
25,313,691 (GRCm39) |
splice site |
probably null |
|
R4934:Ift140
|
UTSW |
17 |
25,267,462 (GRCm39) |
missense |
probably benign |
|
R4949:Ift140
|
UTSW |
17 |
25,313,639 (GRCm39) |
missense |
probably benign |
0.06 |
R4982:Ift140
|
UTSW |
17 |
25,255,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R5099:Ift140
|
UTSW |
17 |
25,309,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R5223:Ift140
|
UTSW |
17 |
25,254,786 (GRCm39) |
missense |
probably benign |
0.22 |
R5268:Ift140
|
UTSW |
17 |
25,239,601 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5423:Ift140
|
UTSW |
17 |
25,252,059 (GRCm39) |
missense |
probably damaging |
0.96 |
R5480:Ift140
|
UTSW |
17 |
25,239,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Ift140
|
UTSW |
17 |
25,264,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R5756:Ift140
|
UTSW |
17 |
25,247,787 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5837:Ift140
|
UTSW |
17 |
25,308,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Ift140
|
UTSW |
17 |
25,252,893 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5907:Ift140
|
UTSW |
17 |
25,311,345 (GRCm39) |
missense |
probably benign |
0.02 |
R5966:Ift140
|
UTSW |
17 |
25,313,735 (GRCm39) |
nonsense |
probably null |
|
R6000:Ift140
|
UTSW |
17 |
25,255,934 (GRCm39) |
missense |
probably benign |
0.00 |
R6046:Ift140
|
UTSW |
17 |
25,274,563 (GRCm39) |
missense |
probably benign |
0.00 |
R6050:Ift140
|
UTSW |
17 |
25,309,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R6103:Ift140
|
UTSW |
17 |
25,312,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6239:Ift140
|
UTSW |
17 |
25,247,946 (GRCm39) |
missense |
probably benign |
0.26 |
R6287:Ift140
|
UTSW |
17 |
25,269,408 (GRCm39) |
missense |
probably benign |
|
R6539:Ift140
|
UTSW |
17 |
25,313,643 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6656:Ift140
|
UTSW |
17 |
25,251,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R6723:Ift140
|
UTSW |
17 |
25,252,090 (GRCm39) |
missense |
probably benign |
0.08 |
R6749:Ift140
|
UTSW |
17 |
25,317,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R6892:Ift140
|
UTSW |
17 |
25,239,520 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7151:Ift140
|
UTSW |
17 |
25,274,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R7235:Ift140
|
UTSW |
17 |
25,239,619 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7424:Ift140
|
UTSW |
17 |
25,256,010 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7552:Ift140
|
UTSW |
17 |
25,252,089 (GRCm39) |
missense |
probably benign |
0.02 |
R7560:Ift140
|
UTSW |
17 |
25,311,315 (GRCm39) |
missense |
probably benign |
0.28 |
R7660:Ift140
|
UTSW |
17 |
25,270,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R8105:Ift140
|
UTSW |
17 |
25,255,949 (GRCm39) |
missense |
probably benign |
0.01 |
R8415:Ift140
|
UTSW |
17 |
25,311,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R8437:Ift140
|
UTSW |
17 |
25,313,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R8747:Ift140
|
UTSW |
17 |
25,254,809 (GRCm39) |
missense |
probably benign |
|
R8932:Ift140
|
UTSW |
17 |
25,305,862 (GRCm39) |
missense |
probably benign |
0.03 |
R9226:Ift140
|
UTSW |
17 |
25,317,839 (GRCm39) |
missense |
probably benign |
0.00 |
R9347:Ift140
|
UTSW |
17 |
25,313,753 (GRCm39) |
missense |
probably benign |
0.00 |
R9451:Ift140
|
UTSW |
17 |
25,252,925 (GRCm39) |
missense |
probably benign |
0.33 |
R9456:Ift140
|
UTSW |
17 |
25,254,758 (GRCm39) |
missense |
probably benign |
0.03 |
R9782:Ift140
|
UTSW |
17 |
25,264,151 (GRCm39) |
critical splice donor site |
probably null |
|
|