Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
T |
13: 81,640,656 (GRCm39) |
C3357S |
probably benign |
Het |
Ago1 |
T |
A |
4: 126,357,650 (GRCm39) |
|
probably null |
Het |
Akap10 |
A |
T |
11: 61,781,129 (GRCm39) |
D562E |
possibly damaging |
Het |
Akr1b7 |
G |
A |
6: 34,395,929 (GRCm39) |
A144T |
possibly damaging |
Het |
Ankle1 |
A |
G |
8: 71,860,562 (GRCm39) |
T340A |
probably benign |
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 |
Asph |
G |
A |
4: 9,517,671 (GRCm39) |
Q468* |
probably null |
Het |
Bcam |
G |
T |
7: 19,492,352 (GRCm39) |
A581E |
possibly damaging |
Het |
Blvra |
G |
T |
2: 126,927,989 (GRCm39) |
E80* |
probably null |
Het |
Ccr6 |
T |
C |
17: 8,474,914 (GRCm39) |
F40L |
possibly damaging |
Het |
Cfap161 |
A |
T |
7: 83,425,184 (GRCm39) |
N302K |
possibly damaging |
Het |
Ckmt2 |
T |
A |
13: 92,003,964 (GRCm39) |
I345F |
probably benign |
Het |
Cpsf6 |
A |
G |
10: 117,202,025 (GRCm39) |
|
probably benign |
Het |
Ctnna1 |
A |
G |
18: 35,285,678 (GRCm39) |
N8S |
possibly damaging |
Het |
Cyp2d11 |
A |
G |
15: 82,275,954 (GRCm39) |
L209P |
probably damaging |
Het |
Dab2 |
T |
C |
15: 6,465,096 (GRCm39) |
V628A |
probably damaging |
Het |
Dcstamp |
C |
T |
15: 39,618,571 (GRCm39) |
Q327* |
probably null |
Het |
Defb38 |
A |
T |
8: 19,073,483 (GRCm39) |
Y63* |
probably null |
Het |
Dlg5 |
A |
T |
14: 24,227,826 (GRCm39) |
L365* |
probably null |
Het |
Dnai7 |
C |
T |
6: 145,150,967 (GRCm39) |
|
probably null |
Het |
Dnmt3l |
C |
A |
10: 77,899,130 (GRCm39) |
L110I |
probably damaging |
Het |
Exoc3l2 |
G |
T |
7: 19,228,907 (GRCm39) |
L108F |
possibly damaging |
Het |
Exoc4 |
T |
A |
6: 33,324,760 (GRCm39) |
N351K |
possibly damaging |
Het |
Fam83h |
C |
A |
15: 75,876,582 (GRCm39) |
E252* |
probably null |
Het |
Fancm |
A |
G |
12: 65,123,948 (GRCm39) |
D202G |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,490,500 (GRCm39) |
V3804E |
probably benign |
Het |
Fbxw28 |
T |
C |
9: 109,159,985 (GRCm39) |
T190A |
probably benign |
Het |
Fer1l4 |
T |
C |
2: 155,881,038 (GRCm39) |
T843A |
probably benign |
Het |
Fnip1 |
A |
T |
11: 54,391,450 (GRCm39) |
H461L |
probably damaging |
Het |
Gcn1 |
A |
T |
5: 115,736,884 (GRCm39) |
M1276L |
probably benign |
Het |
Gemin4 |
A |
G |
11: 76,101,827 (GRCm39) |
V978A |
possibly damaging |
Het |
Gm7247 |
A |
T |
14: 51,602,792 (GRCm39) |
I43F |
probably damaging |
Het |
Gm9978 |
C |
T |
10: 78,322,731 (GRCm39) |
|
noncoding transcript |
Het |
Gpr4 |
T |
C |
7: 18,957,070 (GRCm39) |
S331P |
probably damaging |
Het |
Hspa1a |
T |
A |
17: 35,189,455 (GRCm39) |
N483Y |
probably damaging |
Het |
Ift74 |
A |
G |
4: 94,515,496 (GRCm39) |
T138A |
probably benign |
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 |
Kif4 |
A |
G |
X: 99,709,323 (GRCm39) |
S315G |
probably benign |
Het |
L3mbtl1 |
T |
A |
2: 162,801,990 (GRCm39) |
|
probably null |
Het |
Lamb3 |
A |
G |
1: 193,016,489 (GRCm39) |
R657G |
probably benign |
Het |
Ldc1 |
C |
A |
4: 130,109,156 (GRCm39) |
V295L |
possibly damaging |
Het |
Lrp2 |
A |
C |
2: 69,313,729 (GRCm39) |
V2334G |
probably benign |
Het |
Lrwd1 |
T |
A |
5: 136,159,332 (GRCm39) |
Y431F |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 126,650,781 (GRCm39) |
H261L |
probably benign |
Het |
Meis1 |
G |
T |
11: 18,831,679 (GRCm39) |
P453Q |
probably damaging |
Het |
Mettl16 |
G |
T |
11: 74,693,755 (GRCm39) |
M255I |
probably benign |
Het |
Mllt10 |
A |
G |
2: 18,167,380 (GRCm39) |
N435S |
probably benign |
Het |
Mta2 |
T |
C |
19: 8,920,880 (GRCm39) |
I27T |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,114,328 (GRCm39) |
I771V |
probably benign |
Het |
Nisch |
A |
T |
14: 30,899,242 (GRCm39) |
|
probably benign |
Het |
Npc1 |
G |
A |
18: 12,329,613 (GRCm39) |
P990L |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 91,011,705 (GRCm39) |
I308K |
probably damaging |
Het |
Or13l2 |
C |
A |
3: 97,317,765 (GRCm39) |
C244F |
probably damaging |
Het |
Or1ad6 |
A |
T |
11: 50,860,147 (GRCm39) |
I101F |
probably damaging |
Het |
Or5h17 |
T |
C |
16: 58,820,783 (GRCm39) |
L245P |
possibly damaging |
Het |
Otogl |
T |
C |
10: 107,694,779 (GRCm39) |
D823G |
probably benign |
Het |
P2rx7 |
A |
G |
5: 122,819,329 (GRCm39) |
T584A |
probably benign |
Het |
Pals1 |
T |
C |
12: 78,856,696 (GRCm39) |
F180L |
possibly damaging |
Het |
Pank1 |
T |
A |
19: 34,818,486 (GRCm39) |
I18F |
probably damaging |
Het |
Pgap3 |
A |
G |
11: 98,281,933 (GRCm39) |
L126P |
probably damaging |
Het |
Pgap6 |
C |
T |
17: 26,336,858 (GRCm39) |
L259F |
possibly damaging |
Het |
Phka1 |
C |
T |
X: 101,653,807 (GRCm39) |
R290H |
probably damaging |
Het |
Pkd2 |
G |
A |
5: 104,631,042 (GRCm39) |
E489K |
probably damaging |
Het |
Prdm16 |
T |
A |
4: 154,432,382 (GRCm39) |
S296C |
probably null |
Het |
Prex2 |
T |
A |
1: 11,256,937 (GRCm39) |
N1216K |
probably damaging |
Het |
Prmt7 |
A |
G |
8: 106,953,930 (GRCm39) |
T124A |
probably damaging |
Het |
Ptpra |
G |
T |
2: 130,381,655 (GRCm39) |
R372L |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rap2b |
G |
T |
3: 61,272,512 (GRCm39) |
G12V |
probably damaging |
Het |
Rassf4 |
A |
G |
6: 116,622,088 (GRCm39) |
F168S |
possibly damaging |
Het |
Rtf1 |
T |
A |
2: 119,535,999 (GRCm39) |
H184Q |
probably benign |
Het |
Sacs |
A |
G |
14: 61,451,220 (GRCm39) |
K4422R |
probably benign |
Het |
Sec11c |
A |
T |
18: 65,933,720 (GRCm39) |
T9S |
probably benign |
Het |
Sema3d |
C |
T |
5: 12,613,240 (GRCm39) |
T439I |
probably benign |
Het |
Sephs1 |
A |
G |
2: 4,904,351 (GRCm39) |
N243S |
probably benign |
Het |
Setd2 |
TTGGGA |
T |
9: 110,433,212 (GRCm39) |
|
probably null |
Het |
Setx |
A |
G |
2: 29,020,313 (GRCm39) |
D100G |
probably benign |
Het |
Slc22a7 |
C |
A |
17: 46,744,898 (GRCm39) |
V383L |
possibly damaging |
Het |
Slc25a40 |
T |
C |
5: 8,480,417 (GRCm39) |
C56R |
probably damaging |
Het |
Stk38l |
T |
A |
6: 146,670,344 (GRCm39) |
L229I |
probably damaging |
Het |
Sult2a5 |
T |
C |
7: 13,359,359 (GRCm39) |
S112P |
probably damaging |
Het |
Syt4 |
A |
G |
18: 31,573,520 (GRCm39) |
Y332H |
probably damaging |
Het |
Tcof1 |
T |
C |
18: 60,965,857 (GRCm39) |
E415G |
possibly damaging |
Het |
Tenm2 |
A |
G |
11: 35,915,681 (GRCm39) |
L1951P |
probably damaging |
Het |
Tlr9 |
A |
G |
9: 106,102,536 (GRCm39) |
N609S |
probably damaging |
Het |
Tmem120a |
A |
T |
5: 135,764,977 (GRCm39) |
S266T |
possibly damaging |
Het |
Tmem132b |
A |
G |
5: 125,699,615 (GRCm39) |
E92G |
probably damaging |
Het |
Tnfrsf18 |
T |
A |
4: 156,112,973 (GRCm39) |
V196E |
probably damaging |
Het |
Trpc1 |
A |
T |
9: 95,599,637 (GRCm39) |
L474H |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,807,316 (GRCm39) |
V1020A |
probably damaging |
Het |
Usp20 |
T |
A |
2: 30,906,317 (GRCm39) |
C562S |
probably damaging |
Het |
Usp47 |
T |
A |
7: 111,666,443 (GRCm39) |
|
probably null |
Het |
Vgll1 |
A |
C |
X: 56,137,790 (GRCm39) |
K53T |
probably damaging |
Het |
Vmn1r26 |
T |
C |
6: 57,985,335 (GRCm39) |
N285D |
possibly damaging |
Het |
Zfp445 |
T |
A |
9: 122,682,502 (GRCm39) |
K480* |
probably null |
Het |
Zfp786 |
A |
G |
6: 47,803,931 (GRCm39) |
V37A |
probably damaging |
Het |
Zfp821 |
A |
G |
8: 110,447,851 (GRCm39) |
E64G |
probably damaging |
Het |
Zfp994 |
T |
A |
17: 22,419,962 (GRCm39) |
D329V |
probably damaging |
Het |
Zkscan8 |
T |
C |
13: 21,704,488 (GRCm39) |
S484G |
probably damaging |
Het |
|
Other mutations in Rapgef5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Rapgef5
|
APN |
12 |
117,677,917 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01405:Rapgef5
|
APN |
12 |
117,685,115 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01611:Rapgef5
|
APN |
12 |
117,717,154 (GRCm39) |
splice site |
probably benign |
|
IGL01720:Rapgef5
|
APN |
12 |
117,577,055 (GRCm39) |
splice site |
probably benign |
|
IGL01958:Rapgef5
|
APN |
12 |
117,694,386 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02093:Rapgef5
|
APN |
12 |
117,682,867 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03210:Rapgef5
|
APN |
12 |
117,706,607 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03370:Rapgef5
|
APN |
12 |
117,694,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03397:Rapgef5
|
APN |
12 |
117,712,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:Rapgef5
|
UTSW |
12 |
117,652,896 (GRCm39) |
missense |
probably benign |
0.11 |
R0026:Rapgef5
|
UTSW |
12 |
117,652,896 (GRCm39) |
missense |
probably benign |
0.11 |
R0100:Rapgef5
|
UTSW |
12 |
117,685,034 (GRCm39) |
missense |
probably benign |
0.05 |
R0173:Rapgef5
|
UTSW |
12 |
117,652,411 (GRCm39) |
missense |
probably benign |
0.00 |
R0834:Rapgef5
|
UTSW |
12 |
117,610,741 (GRCm39) |
splice site |
probably benign |
|
R1331:Rapgef5
|
UTSW |
12 |
117,685,084 (GRCm39) |
missense |
probably benign |
0.04 |
R1505:Rapgef5
|
UTSW |
12 |
117,652,354 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1546:Rapgef5
|
UTSW |
12 |
117,610,721 (GRCm39) |
missense |
probably benign |
0.00 |
R1577:Rapgef5
|
UTSW |
12 |
117,558,911 (GRCm39) |
missense |
probably benign |
0.28 |
R1597:Rapgef5
|
UTSW |
12 |
117,621,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Rapgef5
|
UTSW |
12 |
117,652,419 (GRCm39) |
critical splice donor site |
probably null |
|
R2065:Rapgef5
|
UTSW |
12 |
117,547,739 (GRCm39) |
nonsense |
probably null |
|
R2169:Rapgef5
|
UTSW |
12 |
117,679,130 (GRCm39) |
missense |
probably benign |
0.25 |
R2903:Rapgef5
|
UTSW |
12 |
117,677,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Rapgef5
|
UTSW |
12 |
117,692,405 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4004:Rapgef5
|
UTSW |
12 |
117,712,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R4652:Rapgef5
|
UTSW |
12 |
117,677,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R4830:Rapgef5
|
UTSW |
12 |
117,719,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5282:Rapgef5
|
UTSW |
12 |
117,703,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Rapgef5
|
UTSW |
12 |
117,652,346 (GRCm39) |
missense |
probably benign |
0.24 |
R5456:Rapgef5
|
UTSW |
12 |
117,692,381 (GRCm39) |
splice site |
probably null |
|
R5502:Rapgef5
|
UTSW |
12 |
117,685,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R5741:Rapgef5
|
UTSW |
12 |
117,719,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R5771:Rapgef5
|
UTSW |
12 |
117,685,061 (GRCm39) |
missense |
probably benign |
0.45 |
R5905:Rapgef5
|
UTSW |
12 |
117,712,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R5941:Rapgef5
|
UTSW |
12 |
117,692,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R6228:Rapgef5
|
UTSW |
12 |
117,685,398 (GRCm39) |
splice site |
probably null |
|
R6233:Rapgef5
|
UTSW |
12 |
117,703,453 (GRCm39) |
critical splice donor site |
probably null |
|
R6376:Rapgef5
|
UTSW |
12 |
117,684,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R6475:Rapgef5
|
UTSW |
12 |
117,681,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R7063:Rapgef5
|
UTSW |
12 |
117,652,864 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7410:Rapgef5
|
UTSW |
12 |
117,685,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R7445:Rapgef5
|
UTSW |
12 |
117,719,704 (GRCm39) |
missense |
probably benign |
0.00 |
R7690:Rapgef5
|
UTSW |
12 |
117,685,105 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7707:Rapgef5
|
UTSW |
12 |
117,679,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R7815:Rapgef5
|
UTSW |
12 |
117,719,702 (GRCm39) |
missense |
probably benign |
0.10 |
R8461:Rapgef5
|
UTSW |
12 |
117,677,844 (GRCm39) |
missense |
probably benign |
0.00 |
R8475:Rapgef5
|
UTSW |
12 |
117,681,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R8675:Rapgef5
|
UTSW |
12 |
117,547,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Rapgef5
|
UTSW |
12 |
117,545,432 (GRCm39) |
missense |
probably benign |
0.06 |
R9018:Rapgef5
|
UTSW |
12 |
117,712,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R9617:Rapgef5
|
UTSW |
12 |
117,621,930 (GRCm39) |
missense |
probably benign |
0.00 |
X0018:Rapgef5
|
UTSW |
12 |
117,681,950 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Rapgef5
|
UTSW |
12 |
117,558,908 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Rapgef5
|
UTSW |
12 |
117,652,732 (GRCm39) |
missense |
probably damaging |
0.97 |
|