Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
A |
T |
19: 31,910,062 (GRCm39) |
S285C |
possibly damaging |
Het |
Abcc9 |
A |
T |
6: 142,610,351 (GRCm39) |
N604K |
probably benign |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Adgrl3 |
A |
G |
5: 81,919,491 (GRCm39) |
T1192A |
probably damaging |
Het |
Aldh1l2 |
A |
T |
10: 83,326,478 (GRCm39) |
Y800N |
probably damaging |
Het |
Ano3 |
A |
T |
2: 110,491,832 (GRCm39) |
V865D |
probably damaging |
Het |
App |
A |
T |
16: 84,810,568 (GRCm39) |
L545Q |
probably damaging |
Het |
Atp10a |
A |
G |
7: 58,453,215 (GRCm39) |
D798G |
probably damaging |
Het |
B3galnt2 |
T |
C |
13: 14,166,059 (GRCm39) |
V318A |
probably benign |
Het |
Clcn3 |
T |
A |
8: 61,394,382 (GRCm39) |
D49V |
possibly damaging |
Het |
Clcn6 |
T |
A |
4: 148,108,651 (GRCm39) |
K126M |
possibly damaging |
Het |
Cntln |
T |
A |
4: 84,914,722 (GRCm39) |
S510T |
probably damaging |
Het |
Csk |
A |
C |
9: 57,535,477 (GRCm39) |
C290W |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,012,349 (GRCm39) |
M1502K |
probably damaging |
Het |
Dpy19l2 |
T |
A |
9: 24,607,218 (GRCm39) |
N81I |
possibly damaging |
Het |
Dpyd |
T |
A |
3: 118,710,748 (GRCm39) |
C385* |
probably null |
Het |
Dst |
G |
A |
1: 34,238,634 (GRCm39) |
V1765I |
probably benign |
Het |
Eif5b |
A |
G |
1: 38,071,447 (GRCm39) |
S459G |
probably benign |
Het |
Fam83d |
A |
G |
2: 158,621,768 (GRCm39) |
I160V |
possibly damaging |
Het |
Fat3 |
A |
G |
9: 15,942,476 (GRCm39) |
F1299L |
probably damaging |
Het |
Fmn1 |
A |
G |
2: 113,196,141 (GRCm39) |
I614V |
unknown |
Het |
Fsd1l |
T |
A |
4: 53,679,854 (GRCm39) |
V184E |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,626,727 (GRCm39) |
V1328A |
probably damaging |
Het |
Ganab |
T |
A |
19: 8,889,016 (GRCm39) |
N572K |
probably null |
Het |
Gbp10 |
T |
A |
5: 105,368,942 (GRCm39) |
D299V |
possibly damaging |
Het |
Gpr83 |
T |
G |
9: 14,779,563 (GRCm39) |
L205R |
probably damaging |
Het |
Hapln2 |
G |
A |
3: 87,930,936 (GRCm39) |
P152S |
probably damaging |
Het |
Htatip2 |
T |
C |
7: 49,423,140 (GRCm39) |
Y232H |
probably benign |
Het |
Itga2b |
C |
T |
11: 102,358,252 (GRCm39) |
V158I |
probably damaging |
Het |
Kansl3 |
T |
C |
1: 36,390,864 (GRCm39) |
D390G |
probably damaging |
Het |
Kcnh2 |
T |
C |
5: 24,556,235 (GRCm39) |
D16G |
probably benign |
Het |
Kctd8 |
A |
T |
5: 69,498,353 (GRCm39) |
F98I |
probably damaging |
Het |
Kif21b |
A |
T |
1: 136,077,049 (GRCm39) |
E357V |
probably damaging |
Het |
Kmt5c |
C |
T |
7: 4,749,594 (GRCm39) |
R371C |
probably damaging |
Het |
Kndc1 |
T |
C |
7: 139,490,220 (GRCm39) |
F241L |
probably benign |
Het |
Lrba |
A |
G |
3: 86,447,312 (GRCm39) |
D2052G |
probably damaging |
Het |
Lsr |
T |
A |
7: 30,658,698 (GRCm39) |
I54F |
probably damaging |
Het |
Matk |
G |
T |
10: 81,094,328 (GRCm39) |
L28F |
probably benign |
Het |
Mdn1 |
T |
C |
4: 32,750,318 (GRCm39) |
L4429P |
probably damaging |
Het |
Med29 |
CCTGCTGCTGCTGCTGC |
CCTGCTGCTGCTGC |
7: 28,091,935 (GRCm39) |
|
probably benign |
Het |
Msln |
G |
T |
17: 25,969,250 (GRCm39) |
Q407K |
possibly damaging |
Het |
Msr1 |
C |
T |
8: 40,034,868 (GRCm39) |
G428R |
probably damaging |
Het |
Myof |
A |
G |
19: 37,899,417 (GRCm39) |
I1040T |
probably damaging |
Het |
Nckap5 |
A |
G |
1: 125,954,171 (GRCm39) |
S794P |
probably benign |
Het |
Nfkbiz |
C |
T |
16: 55,639,354 (GRCm39) |
|
probably null |
Het |
Nr2c1 |
C |
T |
10: 94,031,044 (GRCm39) |
S535L |
probably damaging |
Het |
Opn3 |
A |
C |
1: 175,519,870 (GRCm39) |
L78R |
probably damaging |
Het |
Or11h4b |
G |
A |
14: 50,918,711 (GRCm39) |
R127C |
probably benign |
Het |
Or52n3 |
A |
T |
7: 104,530,199 (GRCm39) |
D95V |
possibly damaging |
Het |
Or5b12 |
A |
T |
19: 12,897,299 (GRCm39) |
C125S |
probably damaging |
Het |
Otulinl |
T |
A |
15: 27,664,876 (GRCm39) |
I27L |
probably benign |
Het |
Pcdhb9 |
A |
G |
18: 37,535,632 (GRCm39) |
N542S |
probably damaging |
Het |
Pdc |
T |
A |
1: 150,209,178 (GRCm39) |
N220K |
probably benign |
Het |
Pde6c |
A |
T |
19: 38,150,797 (GRCm39) |
N569Y |
probably damaging |
Het |
Pgm1 |
A |
T |
4: 99,820,814 (GRCm39) |
K219M |
probably damaging |
Het |
Pitpnb |
C |
T |
5: 111,494,992 (GRCm39) |
T99M |
possibly damaging |
Het |
Pou6f2 |
T |
A |
13: 18,326,589 (GRCm39) |
Q71L |
probably damaging |
Het |
Pramel24 |
T |
G |
4: 143,453,629 (GRCm39) |
W246G |
probably benign |
Het |
Prkd1 |
C |
A |
12: 50,413,139 (GRCm39) |
L677F |
probably damaging |
Het |
Rnft2 |
T |
A |
5: 118,339,450 (GRCm39) |
K362M |
possibly damaging |
Het |
Rprd1a |
T |
A |
18: 24,639,904 (GRCm39) |
E259V |
possibly damaging |
Het |
Scara3 |
A |
T |
14: 66,169,230 (GRCm39) |
I129N |
probably damaging |
Het |
Scgb1a1 |
A |
T |
19: 9,062,753 (GRCm39) |
|
probably null |
Het |
Sec16b |
A |
T |
1: 157,359,746 (GRCm39) |
|
probably null |
Het |
Slc18a1 |
A |
T |
8: 69,524,753 (GRCm39) |
M167K |
probably damaging |
Het |
Slc6a15 |
C |
T |
10: 103,254,086 (GRCm39) |
A674V |
probably benign |
Het |
Slc6a3 |
T |
C |
13: 73,715,676 (GRCm39) |
F437S |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Stag1 |
T |
A |
9: 100,658,837 (GRCm39) |
N141K |
probably damaging |
Het |
Sun2 |
T |
C |
15: 79,614,433 (GRCm39) |
E321G |
probably damaging |
Het |
Taar2 |
C |
A |
10: 23,817,327 (GRCm39) |
T289K |
possibly damaging |
Het |
Taar2 |
T |
C |
10: 23,817,407 (GRCm39) |
Y316H |
probably benign |
Het |
Tbcd |
T |
A |
11: 121,493,809 (GRCm39) |
|
probably null |
Het |
Tecr |
G |
A |
8: 84,298,904 (GRCm39) |
T106I |
probably damaging |
Het |
Thoc2l |
T |
C |
5: 104,667,842 (GRCm39) |
L788P |
possibly damaging |
Het |
Tmem60 |
T |
G |
5: 21,091,628 (GRCm39) |
V131G |
probably benign |
Het |
Uimc1 |
A |
G |
13: 55,223,804 (GRCm39) |
V156A |
probably benign |
Het |
Usp28 |
G |
A |
9: 48,921,581 (GRCm39) |
W266* |
probably null |
Het |
Vmn2r17 |
T |
A |
5: 109,576,202 (GRCm39) |
S358T |
probably damaging |
Het |
Wwc2 |
T |
A |
8: 48,321,701 (GRCm39) |
Y471F |
unknown |
Het |
Ythdc1 |
C |
T |
5: 86,983,579 (GRCm39) |
R675C |
probably damaging |
Het |
Zfp30 |
T |
C |
7: 29,493,029 (GRCm39) |
S428P |
probably damaging |
Het |
Zfp462 |
T |
A |
4: 55,008,768 (GRCm39) |
C245S |
probably benign |
Het |
Zscan30 |
T |
C |
18: 24,104,455 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Ranbp17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Ranbp17
|
APN |
11 |
33,443,402 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00582:Ranbp17
|
APN |
11 |
33,454,683 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00698:Ranbp17
|
APN |
11 |
33,391,910 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00789:Ranbp17
|
APN |
11 |
33,193,249 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01304:Ranbp17
|
APN |
11 |
33,216,147 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01936:Ranbp17
|
APN |
11 |
33,437,689 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01937:Ranbp17
|
APN |
11 |
33,278,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01945:Ranbp17
|
APN |
11 |
33,278,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01993:Ranbp17
|
APN |
11 |
33,450,770 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02588:Ranbp17
|
APN |
11 |
33,167,361 (GRCm39) |
missense |
probably benign |
|
IGL02870:Ranbp17
|
APN |
11 |
33,193,262 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03149:Ranbp17
|
APN |
11 |
33,193,183 (GRCm39) |
missense |
possibly damaging |
0.76 |
PIT4445001:Ranbp17
|
UTSW |
11 |
33,431,020 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4480001:Ranbp17
|
UTSW |
11 |
33,247,340 (GRCm39) |
critical splice donor site |
probably null |
|
R0079:Ranbp17
|
UTSW |
11 |
33,450,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R0395:Ranbp17
|
UTSW |
11 |
33,424,896 (GRCm39) |
missense |
probably benign |
|
R1456:Ranbp17
|
UTSW |
11 |
33,216,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Ranbp17
|
UTSW |
11 |
33,247,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R1542:Ranbp17
|
UTSW |
11 |
33,214,672 (GRCm39) |
missense |
probably benign |
|
R1770:Ranbp17
|
UTSW |
11 |
33,167,301 (GRCm39) |
missense |
probably benign |
0.31 |
R2216:Ranbp17
|
UTSW |
11 |
33,431,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Ranbp17
|
UTSW |
11 |
33,193,122 (GRCm39) |
missense |
probably benign |
|
R2883:Ranbp17
|
UTSW |
11 |
33,454,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R3498:Ranbp17
|
UTSW |
11 |
33,169,203 (GRCm39) |
small deletion |
probably benign |
|
R3499:Ranbp17
|
UTSW |
11 |
33,169,203 (GRCm39) |
small deletion |
probably benign |
|
R3721:Ranbp17
|
UTSW |
11 |
33,169,203 (GRCm39) |
small deletion |
probably benign |
|
R3788:Ranbp17
|
UTSW |
11 |
33,169,203 (GRCm39) |
small deletion |
probably benign |
|
R3790:Ranbp17
|
UTSW |
11 |
33,169,203 (GRCm39) |
small deletion |
probably benign |
|
R3914:Ranbp17
|
UTSW |
11 |
33,429,189 (GRCm39) |
missense |
probably benign |
0.02 |
R3915:Ranbp17
|
UTSW |
11 |
33,429,189 (GRCm39) |
missense |
probably benign |
0.02 |
R3949:Ranbp17
|
UTSW |
11 |
33,429,189 (GRCm39) |
missense |
probably benign |
0.02 |
R4021:Ranbp17
|
UTSW |
11 |
33,429,189 (GRCm39) |
missense |
probably benign |
0.02 |
R4022:Ranbp17
|
UTSW |
11 |
33,429,189 (GRCm39) |
missense |
probably benign |
0.02 |
R4027:Ranbp17
|
UTSW |
11 |
33,450,718 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4421:Ranbp17
|
UTSW |
11 |
33,425,056 (GRCm39) |
missense |
probably benign |
0.01 |
R4462:Ranbp17
|
UTSW |
11 |
33,167,421 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4659:Ranbp17
|
UTSW |
11 |
33,216,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4791:Ranbp17
|
UTSW |
11 |
33,437,746 (GRCm39) |
missense |
probably benign |
0.11 |
R4837:Ranbp17
|
UTSW |
11 |
33,278,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4914:Ranbp17
|
UTSW |
11 |
33,163,425 (GRCm39) |
missense |
probably benign |
|
R4939:Ranbp17
|
UTSW |
11 |
33,169,223 (GRCm39) |
missense |
probably benign |
0.31 |
R5119:Ranbp17
|
UTSW |
11 |
33,354,181 (GRCm39) |
makesense |
probably null |
|
R5171:Ranbp17
|
UTSW |
11 |
33,167,419 (GRCm39) |
missense |
probably benign |
|
R5182:Ranbp17
|
UTSW |
11 |
33,169,287 (GRCm39) |
intron |
probably benign |
|
R5288:Ranbp17
|
UTSW |
11 |
33,169,241 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5384:Ranbp17
|
UTSW |
11 |
33,169,241 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5385:Ranbp17
|
UTSW |
11 |
33,169,241 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5398:Ranbp17
|
UTSW |
11 |
33,424,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R6658:Ranbp17
|
UTSW |
11 |
33,169,214 (GRCm39) |
nonsense |
probably null |
|
R6701:Ranbp17
|
UTSW |
11 |
33,425,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Ranbp17
|
UTSW |
11 |
33,167,398 (GRCm39) |
missense |
probably benign |
|
R6869:Ranbp17
|
UTSW |
11 |
33,463,074 (GRCm39) |
start gained |
probably benign |
|
R7096:Ranbp17
|
UTSW |
11 |
33,424,896 (GRCm39) |
missense |
probably benign |
|
R7156:Ranbp17
|
UTSW |
11 |
33,247,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Ranbp17
|
UTSW |
11 |
33,234,114 (GRCm39) |
splice site |
probably null |
|
R7958:Ranbp17
|
UTSW |
11 |
33,437,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:Ranbp17
|
UTSW |
11 |
33,429,232 (GRCm39) |
missense |
probably benign |
0.01 |
R9529:Ranbp17
|
UTSW |
11 |
33,424,826 (GRCm39) |
missense |
unknown |
|
RF016:Ranbp17
|
UTSW |
11 |
33,279,511 (GRCm39) |
missense |
probably damaging |
0.99 |
X0013:Ranbp17
|
UTSW |
11 |
33,239,562 (GRCm39) |
splice site |
probably null |
|
X0024:Ranbp17
|
UTSW |
11 |
33,163,404 (GRCm39) |
makesense |
probably null |
|
Z1176:Ranbp17
|
UTSW |
11 |
33,431,108 (GRCm39) |
missense |
probably damaging |
1.00 |
|