Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
a |
A |
G |
2: 154,889,649 (GRCm39) |
R72G |
probably benign |
Het |
Adgrb1 |
T |
A |
15: 74,412,411 (GRCm39) |
|
probably null |
Het |
Akr1b7 |
G |
A |
6: 34,395,929 (GRCm39) |
A144T |
possibly damaging |
Het |
Anapc5 |
C |
T |
5: 122,926,001 (GRCm39) |
V685I |
probably benign |
Het |
Apba3 |
T |
C |
10: 81,108,946 (GRCm39) |
Y570H |
probably damaging |
Het |
Arf5 |
C |
T |
6: 28,424,783 (GRCm39) |
Q71* |
probably null |
Het |
Arl15 |
C |
T |
13: 114,104,196 (GRCm39) |
S111F |
probably damaging |
Het |
Ash1l |
C |
T |
3: 88,890,571 (GRCm39) |
L817F |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Blvra |
G |
T |
2: 126,927,989 (GRCm39) |
E80* |
probably null |
Het |
Bmp10 |
A |
C |
6: 87,411,441 (GRCm39) |
E411D |
probably benign |
Het |
Ccdc148 |
T |
C |
2: 58,892,128 (GRCm39) |
E188G |
probably damaging |
Het |
Ces1a |
A |
G |
8: 93,766,179 (GRCm39) |
L145P |
possibly damaging |
Het |
Chsy3 |
G |
A |
18: 59,312,561 (GRCm39) |
V345I |
probably damaging |
Het |
Ckmt2 |
T |
A |
13: 92,003,964 (GRCm39) |
I345F |
probably benign |
Het |
Col5a2 |
T |
A |
1: 45,415,964 (GRCm39) |
E1394D |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,121,018 (GRCm39) |
N1492S |
probably damaging |
Het |
Dock3 |
T |
C |
9: 106,870,743 (GRCm39) |
N557S |
probably benign |
Het |
Edem2 |
G |
A |
2: 155,544,479 (GRCm39) |
R424C |
probably damaging |
Het |
Eya1 |
A |
T |
1: 14,340,998 (GRCm39) |
F163I |
probably damaging |
Het |
Ezh1 |
A |
C |
11: 101,099,011 (GRCm39) |
S290A |
probably benign |
Het |
Fam83f |
T |
G |
15: 80,576,468 (GRCm39) |
V373G |
possibly damaging |
Het |
Fam83h |
A |
T |
15: 75,874,146 (GRCm39) |
Y1064N |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,035,633 (GRCm39) |
H3095L |
probably benign |
Het |
Fbxo38 |
A |
C |
18: 62,639,711 (GRCm39) |
I1051S |
possibly damaging |
Het |
Galnt6 |
G |
C |
15: 100,612,122 (GRCm39) |
C173W |
probably damaging |
Het |
Gcc2 |
T |
A |
10: 58,105,362 (GRCm39) |
C99* |
probably null |
Het |
Gcn1 |
A |
T |
5: 115,736,884 (GRCm39) |
M1276L |
probably benign |
Het |
Gm266 |
T |
G |
12: 111,452,116 (GRCm39) |
Q30P |
possibly damaging |
Het |
Gsdma |
A |
T |
11: 98,563,838 (GRCm39) |
E264V |
probably damaging |
Het |
Ift74 |
A |
G |
4: 94,515,496 (GRCm39) |
T138A |
probably benign |
Het |
Ikzf1 |
T |
G |
11: 11,719,473 (GRCm39) |
H480Q |
probably damaging |
Het |
Ints14 |
T |
G |
9: 64,887,077 (GRCm39) |
L336R |
probably damaging |
Het |
Irak1 |
G |
T |
X: 73,066,218 (GRCm39) |
P197Q |
possibly damaging |
Het |
Kcna6 |
A |
G |
6: 126,716,322 (GRCm39) |
V189A |
possibly damaging |
Het |
Kcnh4 |
A |
G |
11: 100,650,421 (GRCm39) |
M4T |
probably damaging |
Het |
Kif4 |
A |
G |
X: 99,709,323 (GRCm39) |
S315G |
probably benign |
Het |
L3mbtl1 |
T |
A |
2: 162,801,990 (GRCm39) |
|
probably null |
Het |
Lrwd1 |
T |
A |
5: 136,159,332 (GRCm39) |
Y431F |
probably damaging |
Het |
Madd |
A |
G |
2: 90,994,367 (GRCm39) |
V884A |
probably damaging |
Het |
Maz |
C |
A |
7: 126,624,677 (GRCm39) |
C281F |
probably damaging |
Het |
Mb |
G |
T |
15: 76,906,759 (GRCm39) |
Q9K |
probably benign |
Het |
Mllt10 |
A |
G |
2: 18,167,380 (GRCm39) |
N435S |
probably benign |
Het |
Mrm3 |
T |
C |
11: 76,135,347 (GRCm39) |
M186T |
possibly damaging |
Het |
Naprt |
T |
C |
15: 75,763,637 (GRCm39) |
Y395C |
probably damaging |
Het |
Nccrp1 |
T |
A |
7: 28,246,334 (GRCm39) |
Q76L |
probably benign |
Het |
Nlgn1 |
T |
A |
3: 26,187,414 (GRCm39) |
N157I |
probably damaging |
Het |
Nmi |
T |
C |
2: 51,838,719 (GRCm39) |
T272A |
probably benign |
Het |
Obscn |
C |
T |
11: 59,022,484 (GRCm39) |
V754M |
probably damaging |
Het |
Pcdhb12 |
A |
G |
18: 37,569,265 (GRCm39) |
E137G |
probably damaging |
Het |
Pdk2 |
A |
G |
11: 94,918,088 (GRCm39) |
Y382H |
probably damaging |
Het |
Phka1 |
C |
T |
X: 101,653,807 (GRCm39) |
R290H |
probably damaging |
Het |
Pick1 |
T |
A |
15: 79,139,781 (GRCm39) |
|
probably benign |
Het |
Pik3r2 |
T |
C |
8: 71,222,029 (GRCm39) |
I585V |
probably benign |
Het |
Pitrm1 |
A |
T |
13: 6,607,809 (GRCm39) |
Y268F |
probably damaging |
Het |
Polr2b |
G |
A |
5: 77,468,817 (GRCm39) |
E198K |
probably damaging |
Het |
Prelid3b |
T |
C |
2: 174,311,243 (GRCm39) |
N9D |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,256,937 (GRCm39) |
N1216K |
probably damaging |
Het |
Prkab2 |
A |
T |
3: 97,574,711 (GRCm39) |
M236L |
possibly damaging |
Het |
Prkar2b |
T |
A |
12: 32,017,279 (GRCm39) |
N257I |
probably damaging |
Het |
Prkcd |
A |
G |
14: 30,327,808 (GRCm39) |
C208R |
probably damaging |
Het |
Prkch |
T |
A |
12: 73,749,290 (GRCm39) |
S347T |
probably benign |
Het |
Prr12 |
A |
G |
7: 44,695,506 (GRCm39) |
V1320A |
unknown |
Het |
Ptk2 |
A |
G |
15: 73,114,255 (GRCm39) |
V701A |
possibly damaging |
Het |
Ptpra |
G |
T |
2: 130,381,655 (GRCm39) |
R372L |
probably damaging |
Het |
Ptx3 |
T |
A |
3: 66,132,187 (GRCm39) |
I236N |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,833,134 (GRCm39) |
|
probably null |
Het |
Rgr |
T |
A |
14: 36,760,809 (GRCm39) |
|
probably null |
Het |
Rgs7 |
T |
A |
1: 174,918,639 (GRCm39) |
N235I |
probably damaging |
Het |
Rgsl1 |
T |
A |
1: 153,693,295 (GRCm39) |
M629L |
probably benign |
Het |
Rpgrip1 |
A |
T |
14: 52,387,024 (GRCm39) |
E781V |
probably benign |
Het |
Rrh |
T |
C |
3: 129,604,336 (GRCm39) |
I288M |
probably damaging |
Het |
Rtf1 |
T |
A |
2: 119,535,999 (GRCm39) |
H184Q |
probably benign |
Het |
Rusc1 |
T |
C |
3: 88,999,014 (GRCm39) |
D256G |
probably benign |
Het |
Scap |
T |
C |
9: 110,210,341 (GRCm39) |
Y917H |
probably damaging |
Het |
Scn9a |
T |
C |
2: 66,314,396 (GRCm39) |
E1774G |
probably damaging |
Het |
Sec11c |
A |
T |
18: 65,933,720 (GRCm39) |
T9S |
probably benign |
Het |
Slc24a2 |
C |
T |
4: 86,909,592 (GRCm39) |
V664I |
probably benign |
Het |
Stim2 |
A |
G |
5: 54,261,819 (GRCm39) |
Q237R |
probably damaging |
Het |
Synpo2 |
T |
A |
3: 122,873,537 (GRCm39) |
H1143L |
probably benign |
Het |
Syt4 |
A |
G |
18: 31,573,520 (GRCm39) |
Y332H |
probably damaging |
Het |
Tcf23 |
G |
A |
5: 31,130,919 (GRCm39) |
D186N |
probably benign |
Het |
Tcf3 |
C |
A |
10: 80,246,040 (GRCm39) |
G628W |
probably damaging |
Het |
Tcof1 |
T |
C |
18: 60,965,857 (GRCm39) |
E415G |
possibly damaging |
Het |
Tlr5 |
T |
C |
1: 182,803,194 (GRCm39) |
W833R |
probably damaging |
Het |
Tmem132b |
A |
G |
5: 125,699,615 (GRCm39) |
E92G |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,577,352 (GRCm39) |
S24514T |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,382,484 (GRCm39) |
E587G |
probably benign |
Het |
Ubr4 |
A |
T |
4: 139,156,922 (GRCm39) |
K2316* |
probably null |
Het |
Usp20 |
T |
A |
2: 30,906,317 (GRCm39) |
C562S |
probably damaging |
Het |
Vat1 |
A |
T |
11: 101,356,568 (GRCm39) |
V131E |
probably damaging |
Het |
Vgll1 |
A |
C |
X: 56,137,790 (GRCm39) |
K53T |
probably damaging |
Het |
Zfp1005 |
T |
A |
2: 150,109,819 (GRCm39) |
C170S |
unknown |
Het |
Zfp592 |
G |
A |
7: 80,674,544 (GRCm39) |
V503M |
probably damaging |
Het |
Zfp786 |
A |
G |
6: 47,803,931 (GRCm39) |
V37A |
probably damaging |
Het |
Zscan30 |
A |
G |
18: 24,104,173 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Exoc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Exoc4
|
APN |
6 |
33,895,334 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00433:Exoc4
|
APN |
6 |
33,273,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00833:Exoc4
|
APN |
6 |
33,948,859 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Exoc4
|
APN |
6 |
33,282,335 (GRCm39) |
splice site |
probably benign |
|
IGL01559:Exoc4
|
APN |
6 |
33,243,011 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01812:Exoc4
|
APN |
6 |
33,734,894 (GRCm39) |
splice site |
probably benign |
|
IGL01926:Exoc4
|
APN |
6 |
33,839,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02270:Exoc4
|
APN |
6 |
33,556,961 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02316:Exoc4
|
APN |
6 |
33,887,519 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02332:Exoc4
|
APN |
6 |
33,226,175 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02668:Exoc4
|
APN |
6 |
33,898,467 (GRCm39) |
missense |
probably benign |
0.00 |
slacker
|
UTSW |
6 |
33,735,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Exoc4
|
UTSW |
6 |
33,273,857 (GRCm39) |
splice site |
probably null |
|
R0134:Exoc4
|
UTSW |
6 |
33,948,881 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0234:Exoc4
|
UTSW |
6 |
33,839,022 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0234:Exoc4
|
UTSW |
6 |
33,839,022 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0538:Exoc4
|
UTSW |
6 |
33,948,998 (GRCm39) |
missense |
probably benign |
0.09 |
R1033:Exoc4
|
UTSW |
6 |
33,242,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Exoc4
|
UTSW |
6 |
33,895,359 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1109:Exoc4
|
UTSW |
6 |
33,418,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Exoc4
|
UTSW |
6 |
33,734,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Exoc4
|
UTSW |
6 |
33,243,026 (GRCm39) |
missense |
probably damaging |
0.96 |
R2078:Exoc4
|
UTSW |
6 |
33,887,522 (GRCm39) |
missense |
probably benign |
0.06 |
R2115:Exoc4
|
UTSW |
6 |
33,324,760 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2117:Exoc4
|
UTSW |
6 |
33,324,760 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2133:Exoc4
|
UTSW |
6 |
33,887,473 (GRCm39) |
missense |
probably benign |
|
R2133:Exoc4
|
UTSW |
6 |
33,735,093 (GRCm39) |
missense |
probably benign |
0.00 |
R2308:Exoc4
|
UTSW |
6 |
33,895,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R3412:Exoc4
|
UTSW |
6 |
33,242,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R3794:Exoc4
|
UTSW |
6 |
33,452,932 (GRCm39) |
missense |
probably benign |
|
R3885:Exoc4
|
UTSW |
6 |
33,243,066 (GRCm39) |
critical splice donor site |
probably null |
|
R4378:Exoc4
|
UTSW |
6 |
33,792,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R4534:Exoc4
|
UTSW |
6 |
33,254,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R4535:Exoc4
|
UTSW |
6 |
33,254,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R4536:Exoc4
|
UTSW |
6 |
33,254,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Exoc4
|
UTSW |
6 |
33,415,340 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4617:Exoc4
|
UTSW |
6 |
33,839,139 (GRCm39) |
missense |
probably benign |
0.00 |
R4771:Exoc4
|
UTSW |
6 |
33,418,884 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4851:Exoc4
|
UTSW |
6 |
33,895,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R4921:Exoc4
|
UTSW |
6 |
33,887,452 (GRCm39) |
missense |
probably benign |
|
R5358:Exoc4
|
UTSW |
6 |
33,242,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R5767:Exoc4
|
UTSW |
6 |
33,895,367 (GRCm39) |
missense |
probably benign |
|
R6014:Exoc4
|
UTSW |
6 |
33,452,932 (GRCm39) |
missense |
probably benign |
|
R6132:Exoc4
|
UTSW |
6 |
33,735,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Exoc4
|
UTSW |
6 |
33,309,218 (GRCm39) |
missense |
probably damaging |
0.99 |
R6583:Exoc4
|
UTSW |
6 |
33,792,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Exoc4
|
UTSW |
6 |
33,898,388 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6973:Exoc4
|
UTSW |
6 |
33,556,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7112:Exoc4
|
UTSW |
6 |
33,898,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7129:Exoc4
|
UTSW |
6 |
33,948,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Exoc4
|
UTSW |
6 |
33,415,408 (GRCm39) |
missense |
probably benign |
0.07 |
R7547:Exoc4
|
UTSW |
6 |
33,816,056 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7885:Exoc4
|
UTSW |
6 |
33,735,001 (GRCm39) |
missense |
probably benign |
0.00 |
R8024:Exoc4
|
UTSW |
6 |
33,324,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Exoc4
|
UTSW |
6 |
33,309,191 (GRCm39) |
missense |
probably benign |
0.45 |
R8118:Exoc4
|
UTSW |
6 |
33,948,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Exoc4
|
UTSW |
6 |
33,887,473 (GRCm39) |
missense |
probably benign |
|
R8485:Exoc4
|
UTSW |
6 |
33,898,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R9226:Exoc4
|
UTSW |
6 |
33,895,359 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9402:Exoc4
|
UTSW |
6 |
33,453,078 (GRCm39) |
makesense |
probably null |
|
R9612:Exoc4
|
UTSW |
6 |
33,226,161 (GRCm39) |
missense |
probably benign |
0.19 |
R9711:Exoc4
|
UTSW |
6 |
33,452,991 (GRCm39) |
missense |
unknown |
|
X0066:Exoc4
|
UTSW |
6 |
33,792,625 (GRCm39) |
missense |
probably damaging |
0.99 |
|