Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933412E24Rik |
T |
C |
15: 59,887,321 (GRCm39) |
Y373C |
probably benign |
Het |
Abca12 |
T |
G |
1: 71,341,822 (GRCm39) |
Q1046H |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,714,415 (GRCm39) |
F956S |
probably benign |
Het |
Alk |
A |
G |
17: 72,212,152 (GRCm39) |
V797A |
possibly damaging |
Het |
Ascl2 |
A |
G |
7: 142,522,217 (GRCm39) |
L77P |
probably benign |
Het |
Aspm |
A |
T |
1: 139,405,639 (GRCm39) |
I1509F |
probably damaging |
Het |
AY358078 |
A |
T |
14: 52,043,089 (GRCm39) |
Y259F |
unknown |
Het |
Cbs |
G |
A |
17: 31,835,126 (GRCm39) |
A450V |
probably benign |
Het |
Cdh26 |
C |
T |
2: 178,123,425 (GRCm39) |
R675C |
possibly damaging |
Het |
Cfap126 |
T |
C |
1: 170,953,769 (GRCm39) |
I113T |
probably damaging |
Het |
Clk4 |
A |
G |
11: 51,158,155 (GRCm39) |
D53G |
possibly damaging |
Het |
Dab1 |
T |
C |
4: 104,577,747 (GRCm39) |
L272P |
probably benign |
Het |
Dmtf1 |
A |
T |
5: 9,182,454 (GRCm39) |
|
probably null |
Het |
Dph5 |
A |
C |
3: 115,722,359 (GRCm39) |
D279A |
probably benign |
Het |
Fbxw19 |
T |
A |
9: 109,307,717 (GRCm39) |
T461S |
probably benign |
Het |
G3bp1 |
T |
C |
11: 55,389,452 (GRCm39) |
F383L |
probably damaging |
Het |
Gcg |
T |
C |
2: 62,307,282 (GRCm39) |
D93G |
probably damaging |
Het |
Gmps |
A |
G |
3: 63,901,365 (GRCm39) |
T395A |
probably damaging |
Het |
H2-Ob |
A |
G |
17: 34,461,633 (GRCm39) |
D124G |
probably damaging |
Het |
Itga8 |
G |
T |
2: 12,237,697 (GRCm39) |
A341E |
probably damaging |
Het |
Itih3 |
A |
G |
14: 30,634,831 (GRCm39) |
|
probably null |
Het |
Kcnh4 |
C |
T |
11: 100,637,758 (GRCm39) |
G633E |
probably benign |
Het |
Kif2c |
C |
T |
4: 117,029,489 (GRCm39) |
R215Q |
possibly damaging |
Het |
Letm1 |
A |
C |
5: 33,919,074 (GRCm39) |
|
probably benign |
Het |
Lypd8l |
T |
C |
11: 58,503,331 (GRCm39) |
|
probably benign |
Het |
Mmp3 |
A |
G |
9: 7,450,165 (GRCm39) |
D299G |
probably damaging |
Het |
Myh8 |
G |
T |
11: 67,189,405 (GRCm39) |
A1194S |
probably benign |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Nfib |
A |
C |
4: 82,416,775 (GRCm39) |
Y87D |
probably damaging |
Het |
Nlrp4a |
T |
C |
7: 26,162,045 (GRCm39) |
|
probably benign |
Het |
Nsmce1 |
A |
T |
7: 125,071,408 (GRCm39) |
|
probably benign |
Het |
Odad2 |
T |
A |
18: 7,286,758 (GRCm39) |
I158F |
probably benign |
Het |
Or7g12 |
T |
G |
9: 18,899,551 (GRCm39) |
V89G |
probably benign |
Het |
Or7g27 |
A |
T |
9: 19,250,475 (GRCm39) |
T240S |
probably damaging |
Het |
Patj |
C |
A |
4: 98,576,393 (GRCm39) |
Q1193K |
probably damaging |
Het |
Pcdhb5 |
G |
A |
18: 37,455,596 (GRCm39) |
V659M |
probably damaging |
Het |
Pkd1l3 |
C |
G |
8: 110,350,281 (GRCm39) |
D375E |
possibly damaging |
Het |
Pmis2 |
T |
C |
7: 30,370,817 (GRCm39) |
I46V |
probably benign |
Het |
Ppp2r5e |
A |
G |
12: 75,509,216 (GRCm39) |
|
probably benign |
Het |
Prom2 |
A |
G |
2: 127,370,709 (GRCm39) |
F825S |
probably damaging |
Het |
Rab11fip2 |
G |
A |
19: 59,894,675 (GRCm39) |
A524V |
possibly damaging |
Het |
Rb1cc1 |
A |
C |
1: 6,333,491 (GRCm39) |
|
probably null |
Het |
Rwdd3 |
G |
C |
3: 120,952,668 (GRCm39) |
Q180E |
possibly damaging |
Het |
Sema6a |
G |
A |
18: 47,423,112 (GRCm39) |
|
probably null |
Het |
Sgcg |
A |
T |
14: 61,459,135 (GRCm39) |
C265S |
probably damaging |
Het |
Slc16a3 |
T |
C |
11: 120,848,878 (GRCm39) |
S445P |
possibly damaging |
Het |
Slc22a3 |
G |
A |
17: 12,677,380 (GRCm39) |
Q263* |
probably null |
Het |
Sorcs3 |
A |
G |
19: 48,736,758 (GRCm39) |
T694A |
probably benign |
Het |
Tbc1d15 |
T |
C |
10: 115,055,077 (GRCm39) |
K322E |
probably damaging |
Het |
Tecta |
G |
T |
9: 42,284,369 (GRCm39) |
F905L |
probably benign |
Het |
Tmeff1 |
A |
G |
4: 48,636,853 (GRCm39) |
I184V |
possibly damaging |
Het |
Ttf1 |
A |
G |
2: 28,955,419 (GRCm39) |
H261R |
possibly damaging |
Het |
Ttll6 |
T |
A |
11: 96,036,417 (GRCm39) |
L349M |
probably damaging |
Het |
Ubac2 |
G |
A |
14: 122,211,031 (GRCm39) |
V134M |
probably damaging |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Vmn2r25 |
T |
G |
6: 123,829,008 (GRCm39) |
I89L |
probably benign |
Het |
Vmn2r6 |
A |
C |
3: 64,463,723 (GRCm39) |
F370L |
probably damaging |
Het |
Vps13b |
T |
A |
15: 35,445,748 (GRCm39) |
Y412* |
probably null |
Het |
Zfp142 |
A |
G |
1: 74,624,570 (GRCm39) |
S85P |
possibly damaging |
Het |
Zfp516 |
G |
A |
18: 82,975,579 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cdh11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00598:Cdh11
|
APN |
8 |
103,377,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01019:Cdh11
|
APN |
8 |
103,406,377 (GRCm39) |
missense |
probably benign |
|
IGL01286:Cdh11
|
APN |
8 |
103,391,261 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01556:Cdh11
|
APN |
8 |
103,406,276 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01964:Cdh11
|
APN |
8 |
103,391,375 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02322:Cdh11
|
APN |
8 |
103,374,151 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03094:Cdh11
|
APN |
8 |
103,385,035 (GRCm39) |
missense |
probably benign |
|
IGL03110:Cdh11
|
APN |
8 |
103,400,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Cdh11
|
APN |
8 |
103,400,655 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0401:Cdh11
|
UTSW |
8 |
103,400,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Cdh11
|
UTSW |
8 |
103,394,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0925:Cdh11
|
UTSW |
8 |
103,361,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Cdh11
|
UTSW |
8 |
103,377,343 (GRCm39) |
missense |
probably benign |
0.06 |
R1624:Cdh11
|
UTSW |
8 |
103,391,233 (GRCm39) |
splice site |
probably benign |
|
R1829:Cdh11
|
UTSW |
8 |
103,361,273 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2029:Cdh11
|
UTSW |
8 |
103,406,404 (GRCm39) |
missense |
probably benign |
0.00 |
R4191:Cdh11
|
UTSW |
8 |
103,377,380 (GRCm39) |
missense |
probably damaging |
0.98 |
R4270:Cdh11
|
UTSW |
8 |
103,391,258 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4271:Cdh11
|
UTSW |
8 |
103,391,258 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4455:Cdh11
|
UTSW |
8 |
103,374,455 (GRCm39) |
missense |
probably benign |
|
R4516:Cdh11
|
UTSW |
8 |
103,400,594 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4900:Cdh11
|
UTSW |
8 |
103,374,090 (GRCm39) |
splice site |
probably null |
|
R5441:Cdh11
|
UTSW |
8 |
103,374,178 (GRCm39) |
missense |
probably benign |
0.11 |
R5699:Cdh11
|
UTSW |
8 |
103,361,175 (GRCm39) |
missense |
probably damaging |
0.96 |
R6170:Cdh11
|
UTSW |
8 |
103,361,442 (GRCm39) |
missense |
probably benign |
0.00 |
R6846:Cdh11
|
UTSW |
8 |
103,391,276 (GRCm39) |
missense |
probably damaging |
0.97 |
R7018:Cdh11
|
UTSW |
8 |
103,360,953 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7095:Cdh11
|
UTSW |
8 |
103,384,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7497:Cdh11
|
UTSW |
8 |
103,400,456 (GRCm39) |
missense |
probably benign |
0.00 |
R7632:Cdh11
|
UTSW |
8 |
103,400,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R7715:Cdh11
|
UTSW |
8 |
103,391,346 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8321:Cdh11
|
UTSW |
8 |
103,361,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R8529:Cdh11
|
UTSW |
8 |
103,391,387 (GRCm39) |
missense |
probably benign |
0.01 |
R8530:Cdh11
|
UTSW |
8 |
103,391,387 (GRCm39) |
missense |
probably benign |
0.01 |
R8682:Cdh11
|
UTSW |
8 |
103,377,348 (GRCm39) |
missense |
probably benign |
0.24 |
R9105:Cdh11
|
UTSW |
8 |
103,360,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R9404:Cdh11
|
UTSW |
8 |
103,406,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Cdh11
|
UTSW |
8 |
103,384,879 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9684:Cdh11
|
UTSW |
8 |
103,391,327 (GRCm39) |
missense |
probably benign |
0.04 |
R9721:Cdh11
|
UTSW |
8 |
103,406,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R9802:Cdh11
|
UTSW |
8 |
103,391,276 (GRCm39) |
missense |
probably damaging |
0.97 |
|