Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
T |
C |
10: 10,325,780 (GRCm39) |
I56M |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,545,542 (GRCm39) |
L5581* |
probably null |
Het |
Arpc2 |
C |
A |
1: 74,301,645 (GRCm39) |
H193N |
probably benign |
Het |
B3galt5 |
A |
G |
16: 96,116,384 (GRCm39) |
T6A |
probably benign |
Het |
Bod1l |
A |
T |
5: 41,976,103 (GRCm39) |
V1737E |
probably benign |
Het |
Cacfd1 |
T |
G |
2: 26,903,440 (GRCm39) |
|
probably benign |
Het |
Cdc42ep4 |
A |
T |
11: 113,620,192 (GRCm39) |
D66E |
probably benign |
Het |
Cldn1 |
G |
T |
16: 26,181,969 (GRCm39) |
T80N |
probably damaging |
Het |
Cmtm1 |
C |
A |
8: 105,037,583 (GRCm39) |
|
probably benign |
Het |
Cntnap5c |
A |
T |
17: 58,411,693 (GRCm39) |
I526F |
probably benign |
Het |
Copb1 |
T |
C |
7: 113,836,032 (GRCm39) |
K450E |
probably benign |
Het |
Crebrf |
A |
C |
17: 26,976,823 (GRCm39) |
I416L |
probably benign |
Het |
Csmd3 |
C |
A |
15: 48,177,408 (GRCm39) |
V377F |
possibly damaging |
Het |
Cyp1a2 |
T |
C |
9: 57,588,313 (GRCm39) |
K304E |
probably damaging |
Het |
Cyp2d26 |
A |
G |
15: 82,674,774 (GRCm39) |
S403P |
possibly damaging |
Het |
Cyp4a12a |
T |
A |
4: 115,183,476 (GRCm39) |
C198* |
probably null |
Het |
Ddx11 |
A |
G |
17: 66,437,012 (GRCm39) |
D102G |
|
Het |
Dpys |
T |
A |
15: 39,710,114 (GRCm39) |
Q105L |
probably null |
Het |
Dsn1 |
C |
A |
2: 156,838,162 (GRCm39) |
R334L |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Epha8 |
G |
T |
4: 136,659,054 (GRCm39) |
H867N |
probably damaging |
Het |
Ephb3 |
T |
C |
16: 21,040,781 (GRCm39) |
L643P |
probably damaging |
Het |
Fbxo44 |
G |
T |
4: 148,243,010 (GRCm39) |
H83Q |
probably benign |
Het |
Gm13102 |
T |
C |
4: 143,835,807 (GRCm39) |
Y477H |
possibly damaging |
Het |
Gm7347 |
T |
C |
5: 26,262,276 (GRCm39) |
T82A |
probably benign |
Het |
Gss |
C |
A |
2: 155,429,385 (GRCm39) |
A36S |
probably benign |
Het |
Hepacam |
A |
G |
9: 37,292,056 (GRCm39) |
D128G |
probably benign |
Het |
Hepacam2 |
C |
A |
6: 3,483,332 (GRCm39) |
V226F |
probably damaging |
Het |
Hgfac |
T |
C |
5: 35,201,739 (GRCm39) |
Y291H |
probably damaging |
Het |
Ip6k2 |
G |
A |
9: 108,674,466 (GRCm39) |
R88H |
probably benign |
Het |
Kcnf1 |
T |
C |
12: 17,225,082 (GRCm39) |
M380V |
probably damaging |
Het |
Kcnj1 |
A |
T |
9: 32,305,400 (GRCm39) |
|
probably benign |
Het |
Kcnk12 |
T |
C |
17: 88,054,164 (GRCm39) |
E166G |
probably damaging |
Het |
Kctd16 |
T |
C |
18: 40,391,996 (GRCm39) |
C195R |
probably damaging |
Het |
Kif28 |
T |
A |
1: 179,527,018 (GRCm39) |
I718F |
probably benign |
Het |
Lce1e |
T |
A |
3: 92,615,240 (GRCm39) |
K36* |
probably null |
Het |
Map4 |
T |
C |
9: 109,863,687 (GRCm39) |
L304P |
probably benign |
Het |
Mettl17 |
C |
T |
14: 52,129,074 (GRCm39) |
|
probably benign |
Het |
Mpp4 |
T |
C |
1: 59,160,518 (GRCm39) |
D595G |
probably damaging |
Het |
Myo18a |
A |
G |
11: 77,732,349 (GRCm39) |
K1282E |
probably damaging |
Het |
Nf2 |
A |
T |
11: 4,766,137 (GRCm39) |
V131D |
possibly damaging |
Het |
Or7g35 |
T |
C |
9: 19,496,730 (GRCm39) |
V299A |
probably benign |
Het |
Or8b3 |
A |
T |
9: 38,314,916 (GRCm39) |
M249L |
probably benign |
Het |
Oxsr1 |
A |
G |
9: 119,093,843 (GRCm39) |
L270S |
probably benign |
Het |
Plekhg2 |
G |
A |
7: 28,062,309 (GRCm39) |
T536I |
probably damaging |
Het |
Ppp1r9a |
T |
A |
6: 4,906,363 (GRCm39) |
V306D |
probably benign |
Het |
Ptk6 |
C |
T |
2: 180,837,605 (GRCm39) |
C438Y |
probably benign |
Het |
Scfd1 |
T |
C |
12: 51,492,461 (GRCm39) |
V590A |
probably damaging |
Het |
Serpina1b |
A |
G |
12: 103,695,531 (GRCm39) |
S337P |
probably damaging |
Het |
Skor2 |
T |
A |
18: 76,946,622 (GRCm39) |
C115S |
unknown |
Het |
Slc2a7 |
T |
C |
4: 150,249,629 (GRCm39) |
S407P |
probably damaging |
Het |
Slc8a1 |
A |
G |
17: 81,955,683 (GRCm39) |
S452P |
probably damaging |
Het |
Spata31d1c |
A |
G |
13: 65,182,893 (GRCm39) |
D145G |
possibly damaging |
Het |
Spata6 |
C |
A |
4: 111,632,024 (GRCm39) |
T145K |
probably damaging |
Het |
Stab1 |
C |
T |
14: 30,863,501 (GRCm39) |
R2087H |
probably benign |
Het |
Stk24 |
C |
T |
14: 121,539,657 (GRCm39) |
V180M |
probably benign |
Het |
Trrap |
A |
G |
5: 144,781,051 (GRCm39) |
T3271A |
probably damaging |
Het |
Tyro3 |
T |
A |
2: 119,647,147 (GRCm39) |
W755R |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,689,711 (GRCm39) |
|
probably null |
Het |
Uts2b |
T |
C |
16: 27,179,793 (GRCm39) |
|
probably null |
Het |
Vmn2r105 |
T |
A |
17: 20,428,889 (GRCm39) |
H729L |
probably damaging |
Het |
Vps35l |
T |
A |
7: 118,409,144 (GRCm39) |
V635D |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 101,999,225 (GRCm39) |
I3068V |
probably benign |
Het |
Zfp457 |
G |
A |
13: 67,441,763 (GRCm39) |
H175Y |
probably damaging |
Het |
Zfp758 |
A |
G |
17: 22,592,712 (GRCm39) |
D40G |
probably damaging |
Het |
|
Other mutations in Irx5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01735:Irx5
|
APN |
8 |
93,087,331 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01870:Irx5
|
APN |
8 |
93,086,405 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Irx5
|
APN |
8 |
93,086,155 (GRCm39) |
splice site |
probably benign |
|
IGL02481:Irx5
|
APN |
8 |
93,087,307 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02597:Irx5
|
APN |
8 |
93,087,400 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03257:Irx5
|
APN |
8 |
93,087,258 (GRCm39) |
missense |
probably benign |
0.00 |
R0784:Irx5
|
UTSW |
8 |
93,087,118 (GRCm39) |
missense |
probably benign |
|
R1498:Irx5
|
UTSW |
8 |
93,086,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Irx5
|
UTSW |
8 |
93,086,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Irx5
|
UTSW |
8 |
93,086,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Irx5
|
UTSW |
8 |
93,086,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Irx5
|
UTSW |
8 |
93,086,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Irx5
|
UTSW |
8 |
93,084,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R3875:Irx5
|
UTSW |
8 |
93,086,793 (GRCm39) |
missense |
probably benign |
0.00 |
R3942:Irx5
|
UTSW |
8 |
93,086,314 (GRCm39) |
missense |
probably damaging |
0.98 |
R4361:Irx5
|
UTSW |
8 |
93,085,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R4574:Irx5
|
UTSW |
8 |
93,084,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R4994:Irx5
|
UTSW |
8 |
93,087,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Irx5
|
UTSW |
8 |
93,086,541 (GRCm39) |
missense |
probably benign |
0.01 |
R5884:Irx5
|
UTSW |
8 |
93,087,258 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5988:Irx5
|
UTSW |
8 |
93,087,299 (GRCm39) |
nonsense |
probably null |
|
R6339:Irx5
|
UTSW |
8 |
93,086,481 (GRCm39) |
missense |
probably damaging |
0.99 |
R6466:Irx5
|
UTSW |
8 |
93,086,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R6595:Irx5
|
UTSW |
8 |
93,086,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7344:Irx5
|
UTSW |
8 |
93,086,183 (GRCm39) |
missense |
probably benign |
0.24 |
R8166:Irx5
|
UTSW |
8 |
93,086,712 (GRCm39) |
splice site |
probably null |
|
R8215:Irx5
|
UTSW |
8 |
93,086,241 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8396:Irx5
|
UTSW |
8 |
93,086,962 (GRCm39) |
missense |
probably benign |
0.12 |
R8695:Irx5
|
UTSW |
8 |
93,087,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R8991:Irx5
|
UTSW |
8 |
93,087,135 (GRCm39) |
nonsense |
probably null |
|
R9412:Irx5
|
UTSW |
8 |
93,086,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R9522:Irx5
|
UTSW |
8 |
93,087,259 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9708:Irx5
|
UTSW |
8 |
93,087,118 (GRCm39) |
missense |
probably benign |
0.25 |
|