Incidental Mutation 'R1899:Robo4'
ID |
214101 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Robo4
|
Ensembl Gene |
ENSMUSG00000032125 |
Gene Name |
roundabout guidance receptor 4 |
Synonyms |
Magic roundabout, 1200012D01Rik |
MMRRC Submission |
039919-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.224)
|
Stock # |
R1899 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
9 |
Chromosomal Location |
37313198-37325319 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to T
at 37315366 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000150722
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000102895]
[ENSMUST00000115046]
[ENSMUST00000115048]
[ENSMUST00000156972]
[ENSMUST00000214185]
|
AlphaFold |
Q8C310 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000102895
|
SMART Domains |
Protein: ENSMUSP00000099959 Gene: ENSMUSG00000032125
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
37 |
N/A |
INTRINSIC |
IG
|
48 |
144 |
2.51e0 |
SMART |
IGc2
|
160 |
225 |
6.86e-11 |
SMART |
FN3
|
263 |
343 |
2.05e0 |
SMART |
FN3
|
358 |
440 |
1.27e-3 |
SMART |
low complexity region
|
488 |
494 |
N/A |
INTRINSIC |
low complexity region
|
544 |
562 |
N/A |
INTRINSIC |
low complexity region
|
720 |
733 |
N/A |
INTRINSIC |
low complexity region
|
748 |
762 |
N/A |
INTRINSIC |
low complexity region
|
775 |
799 |
N/A |
INTRINSIC |
low complexity region
|
855 |
866 |
N/A |
INTRINSIC |
low complexity region
|
871 |
880 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000115046
|
SMART Domains |
Protein: ENSMUSP00000110698 Gene: ENSMUSG00000032125
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
37 |
N/A |
INTRINSIC |
IG
|
48 |
144 |
2.51e0 |
SMART |
IGc2
|
160 |
225 |
6.86e-11 |
SMART |
FN3
|
263 |
343 |
2.05e0 |
SMART |
FN3
|
358 |
440 |
1.27e-3 |
SMART |
low complexity region
|
484 |
500 |
N/A |
INTRINSIC |
low complexity region
|
540 |
546 |
N/A |
INTRINSIC |
low complexity region
|
596 |
614 |
N/A |
INTRINSIC |
low complexity region
|
747 |
756 |
N/A |
INTRINSIC |
low complexity region
|
779 |
792 |
N/A |
INTRINSIC |
low complexity region
|
807 |
821 |
N/A |
INTRINSIC |
low complexity region
|
834 |
858 |
N/A |
INTRINSIC |
low complexity region
|
914 |
925 |
N/A |
INTRINSIC |
low complexity region
|
930 |
939 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000115048
|
SMART Domains |
Protein: ENSMUSP00000110700 Gene: ENSMUSG00000032125
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
37 |
N/A |
INTRINSIC |
IG
|
48 |
144 |
2.51e0 |
SMART |
IGc2
|
160 |
225 |
6.86e-11 |
SMART |
FN3
|
263 |
343 |
2.05e0 |
SMART |
FN3
|
358 |
440 |
1.27e-3 |
SMART |
low complexity region
|
488 |
494 |
N/A |
INTRINSIC |
low complexity region
|
544 |
562 |
N/A |
INTRINSIC |
low complexity region
|
695 |
704 |
N/A |
INTRINSIC |
low complexity region
|
727 |
740 |
N/A |
INTRINSIC |
low complexity region
|
755 |
769 |
N/A |
INTRINSIC |
low complexity region
|
782 |
806 |
N/A |
INTRINSIC |
low complexity region
|
862 |
873 |
N/A |
INTRINSIC |
low complexity region
|
878 |
887 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000156972
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000214185
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.6%
- 20x: 93.4%
|
Validation Efficiency |
94% (94/100) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a reporter/null allele display enhanced VEGF-induced endothelial migration, tube formation and vascular permeability, and show increased pathologic angiogenesis and vascular leak in models of oxygen-induced retinopathy and choroidal neovascularization. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
T |
A |
5: 109,884,664 (GRCm39) |
Q398L |
probably benign |
Het |
4930596D02Rik |
T |
G |
14: 35,532,089 (GRCm39) |
K162T |
probably damaging |
Het |
Abca8b |
G |
T |
11: 109,828,744 (GRCm39) |
T1353K |
possibly damaging |
Het |
Abcg3 |
A |
C |
5: 105,086,065 (GRCm39) |
C565G |
probably damaging |
Het |
Actr3b |
G |
A |
5: 26,034,536 (GRCm39) |
V185I |
possibly damaging |
Het |
Akap6 |
A |
T |
12: 53,188,635 (GRCm39) |
E2016D |
possibly damaging |
Het |
Aldh3b2 |
T |
C |
19: 4,028,662 (GRCm39) |
V148A |
possibly damaging |
Het |
Ankfy1 |
C |
T |
11: 72,645,233 (GRCm39) |
Q771* |
probably null |
Het |
Anks1b |
A |
G |
10: 90,096,618 (GRCm39) |
D425G |
probably damaging |
Het |
Arrb1 |
T |
C |
7: 99,231,504 (GRCm39) |
|
probably benign |
Het |
Atg2a |
C |
A |
19: 6,295,097 (GRCm39) |
T170N |
probably damaging |
Het |
Atp8b5 |
C |
T |
4: 43,361,804 (GRCm39) |
R617C |
possibly damaging |
Het |
Bicra |
T |
C |
7: 15,721,676 (GRCm39) |
T614A |
possibly damaging |
Het |
Cacna1i |
A |
G |
15: 80,275,843 (GRCm39) |
D167G |
possibly damaging |
Het |
Calr4 |
T |
G |
4: 109,103,490 (GRCm39) |
|
probably null |
Het |
Camsap3 |
G |
T |
8: 3,653,922 (GRCm39) |
E515* |
probably null |
Het |
Casp8ap2 |
T |
C |
4: 32,643,647 (GRCm39) |
S907P |
probably damaging |
Het |
Cdk19 |
T |
A |
10: 40,355,776 (GRCm39) |
|
probably benign |
Het |
Chst14 |
A |
G |
2: 118,757,496 (GRCm39) |
M122V |
possibly damaging |
Het |
Cntn4 |
A |
G |
6: 106,652,774 (GRCm39) |
M748V |
probably benign |
Het |
Col7a1 |
A |
G |
9: 108,807,956 (GRCm39) |
D2552G |
unknown |
Het |
Cpeb2 |
C |
A |
5: 43,434,930 (GRCm39) |
P600Q |
probably damaging |
Het |
Cyp2a5 |
C |
T |
7: 26,538,458 (GRCm39) |
R274* |
probably null |
Het |
Dele1 |
T |
C |
18: 38,391,395 (GRCm39) |
W378R |
probably benign |
Het |
Dexi |
A |
G |
16: 10,360,382 (GRCm39) |
F58S |
probably damaging |
Het |
Dlg5 |
C |
A |
14: 24,198,368 (GRCm39) |
G1522W |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,244,286 (GRCm39) |
H1048R |
probably benign |
Het |
Dpp4 |
T |
C |
2: 62,175,394 (GRCm39) |
|
probably benign |
Het |
Dusp10 |
A |
T |
1: 183,801,377 (GRCm39) |
K381N |
possibly damaging |
Het |
Ercc4 |
A |
G |
16: 12,965,651 (GRCm39) |
E761G |
probably damaging |
Het |
Ern2 |
T |
C |
7: 121,783,065 (GRCm39) |
|
probably benign |
Het |
Fam83f |
A |
T |
15: 80,576,281 (GRCm39) |
T311S |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,153,004 (GRCm39) |
D3736G |
probably benign |
Het |
Fgf11 |
G |
T |
11: 69,692,279 (GRCm39) |
T58K |
probably benign |
Het |
Galntl5 |
C |
G |
5: 25,403,530 (GRCm39) |
S167* |
probably null |
Het |
Glg1 |
T |
G |
8: 111,892,306 (GRCm39) |
E846D |
probably benign |
Het |
Grm8 |
C |
A |
6: 28,125,894 (GRCm39) |
E77D |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,533,202 (GRCm39) |
D3028E |
probably damaging |
Het |
Htt |
A |
G |
5: 35,064,429 (GRCm39) |
I2943V |
probably benign |
Het |
Ift80 |
T |
C |
3: 68,825,846 (GRCm39) |
K498R |
probably benign |
Het |
Ipo9 |
A |
T |
1: 135,327,884 (GRCm39) |
M509K |
probably damaging |
Het |
Kcnj3 |
T |
C |
2: 55,327,256 (GRCm39) |
V15A |
probably damaging |
Het |
Kcnn3 |
A |
T |
3: 89,427,762 (GRCm39) |
|
probably benign |
Het |
Larp1b |
T |
A |
3: 40,918,519 (GRCm39) |
D53E |
probably benign |
Het |
Ltf |
T |
C |
9: 110,851,913 (GRCm39) |
F117L |
possibly damaging |
Het |
Maml1 |
A |
G |
11: 50,156,957 (GRCm39) |
L406P |
probably damaging |
Het |
Mnx1 |
G |
A |
5: 29,678,955 (GRCm39) |
A376V |
unknown |
Het |
Mroh2a |
G |
A |
1: 88,163,098 (GRCm39) |
R376H |
probably benign |
Het |
Mrpl4 |
A |
G |
9: 20,918,127 (GRCm39) |
Y111C |
probably damaging |
Het |
Mto1 |
T |
C |
9: 78,368,799 (GRCm39) |
|
probably benign |
Het |
Nalcn |
A |
T |
14: 123,553,538 (GRCm39) |
M972K |
possibly damaging |
Het |
Nemf |
T |
C |
12: 69,393,152 (GRCm39) |
I225V |
probably null |
Het |
Nipal4 |
T |
G |
11: 46,041,058 (GRCm39) |
D379A |
probably damaging |
Het |
Nktr |
A |
G |
9: 121,577,932 (GRCm39) |
|
probably benign |
Het |
Nlrp5 |
A |
G |
7: 23,104,222 (GRCm39) |
T28A |
probably benign |
Het |
Nxph1 |
T |
A |
6: 9,247,622 (GRCm39) |
Y198N |
probably damaging |
Het |
Or4c123 |
T |
C |
2: 89,127,014 (GRCm39) |
N200S |
probably damaging |
Het |
Or5an10 |
T |
C |
19: 12,275,707 (GRCm39) |
Y263C |
probably damaging |
Het |
Or8u10 |
A |
T |
2: 85,916,064 (GRCm39) |
V19D |
probably benign |
Het |
P2rx7 |
A |
G |
5: 122,811,799 (GRCm39) |
Y370C |
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,209,384 (GRCm39) |
|
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,216,305 (GRCm39) |
D1401G |
probably damaging |
Het |
Plxnd1 |
A |
G |
6: 115,946,324 (GRCm39) |
L879P |
probably benign |
Het |
Polr2a |
A |
T |
11: 69,634,772 (GRCm39) |
I636N |
probably damaging |
Het |
Prex2 |
G |
T |
1: 11,232,590 (GRCm39) |
E886* |
probably null |
Het |
Proca1 |
A |
T |
11: 78,095,847 (GRCm39) |
I73F |
probably damaging |
Het |
Prss55 |
A |
T |
14: 64,316,839 (GRCm39) |
V101E |
probably benign |
Het |
Psg26 |
T |
A |
7: 18,212,350 (GRCm39) |
H335L |
probably benign |
Het |
Rai1 |
A |
G |
11: 60,076,746 (GRCm39) |
E270G |
probably benign |
Het |
Reep1 |
A |
G |
6: 71,757,781 (GRCm39) |
N127D |
probably benign |
Het |
Rims1 |
G |
T |
1: 22,498,725 (GRCm39) |
P769Q |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,606,222 (GRCm39) |
D888E |
probably benign |
Het |
Scamp3 |
A |
G |
3: 89,087,567 (GRCm39) |
N135D |
probably damaging |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Sema4f |
A |
G |
6: 82,895,010 (GRCm39) |
M395T |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,825,534 (GRCm39) |
|
probably null |
Het |
Sik2 |
A |
T |
9: 50,906,974 (GRCm39) |
|
probably benign |
Het |
Smtn |
G |
T |
11: 3,481,326 (GRCm39) |
A223D |
possibly damaging |
Het |
Spen |
T |
C |
4: 141,197,654 (GRCm39) |
T3405A |
probably benign |
Het |
Srebf1 |
A |
G |
11: 60,094,312 (GRCm39) |
L601P |
probably damaging |
Het |
Srsf11 |
A |
T |
3: 157,737,217 (GRCm39) |
|
probably benign |
Het |
Tacc2 |
T |
G |
7: 130,225,932 (GRCm39) |
S891R |
possibly damaging |
Het |
Tbc1d17 |
T |
A |
7: 44,491,057 (GRCm39) |
|
probably benign |
Het |
Tgfbr3l |
C |
A |
8: 4,299,600 (GRCm39) |
R128S |
probably damaging |
Het |
Thsd1 |
G |
A |
8: 22,742,334 (GRCm39) |
|
probably benign |
Het |
Tlx3 |
T |
C |
11: 33,153,072 (GRCm39) |
S130G |
probably benign |
Het |
Tmem25 |
A |
T |
9: 44,709,513 (GRCm39) |
|
probably null |
Het |
Trak2 |
A |
T |
1: 58,985,495 (GRCm39) |
M1K |
probably null |
Het |
Trappc12 |
C |
T |
12: 28,796,984 (GRCm39) |
E183K |
probably damaging |
Het |
Ubl3 |
A |
G |
5: 148,446,090 (GRCm39) |
V71A |
possibly damaging |
Het |
Unc50 |
A |
G |
1: 37,477,880 (GRCm39) |
Y254C |
probably damaging |
Het |
Unkl |
T |
C |
17: 25,448,434 (GRCm39) |
|
probably null |
Het |
Uso1 |
T |
A |
5: 92,349,051 (GRCm39) |
S819T |
probably benign |
Het |
Yes1 |
A |
T |
5: 32,802,395 (GRCm39) |
R103S |
probably damaging |
Het |
Zfp131 |
A |
G |
13: 120,228,561 (GRCm39) |
V396A |
probably damaging |
Het |
Zfp553 |
T |
C |
7: 126,834,826 (GRCm39) |
I127T |
possibly damaging |
Het |
Zfp599 |
A |
T |
9: 22,162,845 (GRCm39) |
N102K |
probably benign |
Het |
Zmynd10 |
A |
T |
9: 107,427,236 (GRCm39) |
Q288L |
probably benign |
Het |
|
Other mutations in Robo4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Robo4
|
APN |
9 |
37,322,400 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00392:Robo4
|
APN |
9 |
37,319,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00491:Robo4
|
APN |
9 |
37,317,231 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL00792:Robo4
|
APN |
9 |
37,319,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01062:Robo4
|
APN |
9 |
37,317,296 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01287:Robo4
|
APN |
9 |
37,324,336 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02289:Robo4
|
APN |
9 |
37,319,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02486:Robo4
|
APN |
9 |
37,319,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Robo4
|
APN |
9 |
37,324,678 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02898:Robo4
|
APN |
9 |
37,319,472 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02965:Robo4
|
APN |
9 |
37,321,765 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03071:Robo4
|
APN |
9 |
37,315,580 (GRCm39) |
splice site |
probably benign |
|
IGL03102:Robo4
|
APN |
9 |
37,315,481 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Robo4
|
UTSW |
9 |
37,317,106 (GRCm39) |
intron |
probably benign |
|
PIT4305001:Robo4
|
UTSW |
9 |
37,322,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Robo4
|
UTSW |
9 |
37,315,773 (GRCm39) |
missense |
probably benign |
0.03 |
R0068:Robo4
|
UTSW |
9 |
37,315,773 (GRCm39) |
missense |
probably benign |
0.03 |
R0233:Robo4
|
UTSW |
9 |
37,313,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Robo4
|
UTSW |
9 |
37,313,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R0416:Robo4
|
UTSW |
9 |
37,316,062 (GRCm39) |
splice site |
probably benign |
|
R1005:Robo4
|
UTSW |
9 |
37,319,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1174:Robo4
|
UTSW |
9 |
37,324,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1183:Robo4
|
UTSW |
9 |
37,319,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1254:Robo4
|
UTSW |
9 |
37,322,136 (GRCm39) |
critical splice donor site |
probably null |
|
R1398:Robo4
|
UTSW |
9 |
37,319,372 (GRCm39) |
critical splice donor site |
probably null |
|
R1505:Robo4
|
UTSW |
9 |
37,314,523 (GRCm39) |
missense |
probably damaging |
0.98 |
R1701:Robo4
|
UTSW |
9 |
37,314,739 (GRCm39) |
missense |
probably benign |
0.44 |
R1834:Robo4
|
UTSW |
9 |
37,324,355 (GRCm39) |
missense |
probably benign |
0.09 |
R2203:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R2204:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R2351:Robo4
|
UTSW |
9 |
37,322,956 (GRCm39) |
missense |
probably benign |
0.01 |
R2448:Robo4
|
UTSW |
9 |
37,313,958 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2847:Robo4
|
UTSW |
9 |
37,315,772 (GRCm39) |
nonsense |
probably null |
|
R2851:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R2852:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R2877:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R3123:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R3124:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R3125:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R3805:Robo4
|
UTSW |
9 |
37,315,734 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3806:Robo4
|
UTSW |
9 |
37,315,734 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3892:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R3905:Robo4
|
UTSW |
9 |
37,314,801 (GRCm39) |
nonsense |
probably null |
|
R3938:Robo4
|
UTSW |
9 |
37,313,313 (GRCm39) |
start gained |
probably benign |
|
R4261:Robo4
|
UTSW |
9 |
37,316,877 (GRCm39) |
missense |
probably benign |
0.04 |
R4434:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R4435:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R4561:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R4562:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R4568:Robo4
|
UTSW |
9 |
37,316,118 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4695:Robo4
|
UTSW |
9 |
37,314,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Robo4
|
UTSW |
9 |
37,313,856 (GRCm39) |
missense |
probably benign |
|
R5000:Robo4
|
UTSW |
9 |
37,319,664 (GRCm39) |
missense |
probably benign |
0.02 |
R5056:Robo4
|
UTSW |
9 |
37,316,102 (GRCm39) |
missense |
probably benign |
0.00 |
R5125:Robo4
|
UTSW |
9 |
37,319,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5178:Robo4
|
UTSW |
9 |
37,319,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5278:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5279:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5285:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5347:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5348:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5361:Robo4
|
UTSW |
9 |
37,324,674 (GRCm39) |
missense |
probably benign |
0.01 |
R5403:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5404:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5488:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5489:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5490:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5494:Robo4
|
UTSW |
9 |
37,322,786 (GRCm39) |
frame shift |
probably null |
|
R5629:Robo4
|
UTSW |
9 |
37,319,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R5736:Robo4
|
UTSW |
9 |
37,316,093 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5796:Robo4
|
UTSW |
9 |
37,322,970 (GRCm39) |
missense |
probably benign |
0.00 |
R5987:Robo4
|
UTSW |
9 |
37,322,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Robo4
|
UTSW |
9 |
37,316,926 (GRCm39) |
nonsense |
probably null |
|
R6189:Robo4
|
UTSW |
9 |
37,314,829 (GRCm39) |
missense |
probably benign |
0.35 |
R6365:Robo4
|
UTSW |
9 |
37,322,008 (GRCm39) |
missense |
probably benign |
0.34 |
R6528:Robo4
|
UTSW |
9 |
37,315,664 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6887:Robo4
|
UTSW |
9 |
37,313,363 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7196:Robo4
|
UTSW |
9 |
37,314,001 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7408:Robo4
|
UTSW |
9 |
37,322,277 (GRCm39) |
missense |
probably benign |
0.09 |
R7419:Robo4
|
UTSW |
9 |
37,314,105 (GRCm39) |
missense |
probably benign |
0.18 |
R7486:Robo4
|
UTSW |
9 |
37,316,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R7707:Robo4
|
UTSW |
9 |
37,324,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7839:Robo4
|
UTSW |
9 |
37,322,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Robo4
|
UTSW |
9 |
37,313,931 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8081:Robo4
|
UTSW |
9 |
37,316,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R8280:Robo4
|
UTSW |
9 |
37,315,372 (GRCm39) |
missense |
probably benign |
0.00 |
R8526:Robo4
|
UTSW |
9 |
37,314,801 (GRCm39) |
nonsense |
probably null |
|
R8547:Robo4
|
UTSW |
9 |
37,315,674 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8735:Robo4
|
UTSW |
9 |
37,319,577 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8836:Robo4
|
UTSW |
9 |
37,317,130 (GRCm39) |
missense |
unknown |
|
R8889:Robo4
|
UTSW |
9 |
37,314,601 (GRCm39) |
missense |
probably benign |
0.00 |
R9018:Robo4
|
UTSW |
9 |
37,315,520 (GRCm39) |
missense |
probably benign |
0.00 |
R9182:Robo4
|
UTSW |
9 |
37,313,206 (GRCm39) |
start gained |
probably benign |
|
R9375:Robo4
|
UTSW |
9 |
37,316,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R9621:Robo4
|
UTSW |
9 |
37,317,509 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GTTCAAGGTAAGGTAGGAGACTCC -3'
(R):5'- TCACCTGGGAAGAAGTCAGAGC -3'
Sequencing Primer
(F):5'- AGACTCCAGTTAGTGTGGTCACC -3'
(R):5'- TCATGGCAGCCCTAATCTGAG -3'
|
Posted On |
2014-07-14 |