Incidental Mutation 'R7849:Robo2'
ID 606845
Institutional Source Beutler Lab
Gene Symbol Robo2
Ensembl Gene ENSMUSG00000052516
Gene Name roundabout guidance receptor 2
Synonyms 2600013A04Rik, 9430089E08Rik, D230004I22Rik
Accession Numbers
Essential gene? Probably essential (E-score: 0.952) question?
Stock # R7849 (G1)
Quality Score 225.009
Status Not validated
Chromosome 16
Chromosomal Location 73688727-74208713 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 73770132 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 531 (T531A)
Ref Sequence ENSEMBL: ENSMUSP00000112776 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000117200] [ENSMUST00000117785] [ENSMUST00000226478] [ENSMUST00000227347]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000102329
Predicted Effect probably benign
Transcript: ENSMUST00000116586
AA Change: T535A

PolyPhen 2 Score 0.052 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000112285
Gene: ENSMUSG00000052516
AA Change: T535A

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 43 117 3.56e-9 SMART
IGc2 145 210 3.33e-9 SMART
IGc2 237 300 6.59e-13 SMART
IGc2 330 402 1.3e-11 SMART
IGc2 434 499 3.73e-12 SMART
FN3 526 608 1.42e-15 SMART
FN3 640 725 3.54e-2 SMART
FN3 740 827 6.15e-11 SMART
transmembrane domain 864 886 N/A INTRINSIC
low complexity region 1044 1069 N/A INTRINSIC
low complexity region 1076 1087 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117200
AA Change: T531A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000113795
Gene: ENSMUSG00000052516
AA Change: T531A

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 43 117 3.56e-9 SMART
IGc2 145 210 3.33e-9 SMART
IGc2 237 300 6.59e-13 SMART
IGc2 326 398 1.3e-11 SMART
IGc2 430 495 3.73e-12 SMART
FN3 522 604 1.42e-15 SMART
FN3 636 721 3.54e-2 SMART
FN3 736 823 6.15e-11 SMART
transmembrane domain 860 882 N/A INTRINSIC
low complexity region 1040 1065 N/A INTRINSIC
low complexity region 1072 1083 N/A INTRINSIC
low complexity region 1191 1199 N/A INTRINSIC
low complexity region 1210 1234 N/A INTRINSIC
low complexity region 1318 1342 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000117785
AA Change: T531A

PolyPhen 2 Score 0.882 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000112776
Gene: ENSMUSG00000052516
AA Change: T531A

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
IGc2 43 117 3.56e-9 SMART
IGc2 145 210 3.33e-9 SMART
IGc2 237 300 6.59e-13 SMART
IGc2 326 398 1.3e-11 SMART
IGc2 430 495 3.73e-12 SMART
FN3 522 604 1.42e-15 SMART
FN3 636 721 3.54e-2 SMART
FN3 736 823 6.15e-11 SMART
transmembrane domain 860 882 N/A INTRINSIC
low complexity region 1072 1107 N/A INTRINSIC
low complexity region 1114 1125 N/A INTRINSIC
low complexity region 1233 1241 N/A INTRINSIC
low complexity region 1252 1276 N/A INTRINSIC
low complexity region 1351 1362 N/A INTRINSIC
low complexity region 1451 1475 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000226478
AA Change: T535A

PolyPhen 2 Score 0.402 (Sensitivity: 0.89; Specificity: 0.89)
Predicted Effect probably benign
Transcript: ENSMUST00000227347
AA Change: T535A

PolyPhen 2 Score 0.398 (Sensitivity: 0.89; Specificity: 0.89)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the ROBO family, part of the immunoglobulin superfamily of proteins that are highly conserved from fly to human. The encoded protein is a transmembrane receptor for the slit homolog 2 protein and functions in axon guidance and cell migration. Mutations in this gene are associated with vesicoureteral reflux, characterized by the backward flow of urine from the bladder into the ureters or the kidney. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]
PHENOTYPE: Homozygous mutants display postnatal lethality, abnormal ureteric bud development, multiple fused kidneys, multiple ureters, and abnormal commissural axon growth. [provided by MGI curators]
Allele List at MGI

All alleles(6) : Targeted(3) Gene trapped(3)

Other mutations in this stock
Total: 94 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agap1 T C 1: 89,558,141 (GRCm39) V143A probably damaging Het
Agmo A G 12: 37,292,044 (GRCm39) R2G probably benign Het
Alms1 A T 6: 85,598,479 (GRCm39) I1102L possibly damaging Het
Ankrd13a T C 5: 114,929,343 (GRCm39) I140T possibly damaging Het
Arhgef10l T A 4: 140,311,245 (GRCm39) probably null Het
Atxn2l A T 7: 126,092,345 (GRCm39) H967Q possibly damaging Het
B3galnt2 A T 13: 14,169,077 (GRCm39) N370I probably benign Het
Bltp1 T A 3: 37,080,477 (GRCm39) I325N Het
Cacna1e C T 1: 154,509,464 (GRCm39) D264N probably damaging Het
Ccdc112 A T 18: 46,429,390 (GRCm39) Y103N probably benign Het
Ccdc68 A C 18: 70,080,246 (GRCm39) E197A probably damaging Het
Cdr1 AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC X: 60,228,130 (GRCm39) probably benign Het
Cntn3 T C 6: 102,242,392 (GRCm39) M418V probably benign Het
Cpne4 T A 9: 104,563,718 (GRCm39) C32S probably damaging Het
Csf2rb2 A T 15: 78,168,621 (GRCm39) S845T probably benign Het
Ctnnd2 T G 15: 31,027,733 (GRCm39) V1219G probably damaging Het
Cyp4f14 G A 17: 33,128,325 (GRCm39) A230V probably benign Het
Cyth1 TGGGCAA T 11: 118,074,749 (GRCm39) probably null Het
Dmxl1 T A 18: 50,094,214 (GRCm39) C2897S probably benign Het
Elavl2 T A 4: 91,260,280 (GRCm39) probably benign Het
Elp1 A T 4: 56,758,968 (GRCm39) S1191T possibly damaging Het
Fam135a T C 1: 24,083,331 (GRCm39) E298G probably damaging Het
Fbn1 A T 2: 125,151,405 (GRCm39) I2534N probably damaging Het
Fibin A G 2: 110,192,825 (GRCm39) S106P probably damaging Het
Fndc3a C T 14: 72,802,100 (GRCm39) V568M probably benign Het
Frem2 A G 3: 53,479,795 (GRCm39) F1966S probably damaging Het
Gata4 T G 14: 63,442,174 (GRCm39) E216A possibly damaging Het
Gmps T A 3: 63,922,984 (GRCm39) V649E probably benign Het
Golga4 A T 9: 118,388,379 (GRCm39) N1834Y possibly damaging Het
Gpr89 A T 3: 96,778,806 (GRCm39) Y422* probably null Het
Gzmc A T 14: 56,469,829 (GRCm39) F157Y probably benign Het
Hdhd2 A G 18: 77,052,962 (GRCm39) D204G probably damaging Het
Hspa4 T G 11: 53,171,530 (GRCm39) T225P possibly damaging Het
Klhl30 T A 1: 91,287,059 (GRCm39) D448E probably benign Het
Kptn A G 7: 15,853,966 (GRCm39) Y28C probably damaging Het
Krt10 A T 11: 99,278,432 (GRCm39) N242K probably damaging Het
Krt6b A T 15: 101,587,009 (GRCm39) N254K probably damaging Het
Lama5 G T 2: 179,843,605 (GRCm39) D447E probably damaging Het
Lgr6 T C 1: 134,915,419 (GRCm39) Y720C probably damaging Het
Macf1 G C 4: 123,301,392 (GRCm39) P1037A probably benign Het
Map3k19 C T 1: 127,751,383 (GRCm39) G656D probably benign Het
Mroh7 A C 4: 106,578,287 (GRCm39) N130K probably benign Het
Muc16 T C 9: 18,551,801 (GRCm39) T4831A probably benign Het
Nfkb1 A T 3: 135,291,173 (GRCm39) L533H Het
Oaf G A 9: 43,134,077 (GRCm39) R215C probably damaging Het
Or4x11 A G 2: 89,867,626 (GRCm39) Y121C probably damaging Het
Or51k1 C A 7: 103,661,510 (GRCm39) R133L possibly damaging Het
Or5m3b G A 2: 85,871,949 (GRCm39) V97I probably benign Het
Or8a1 A G 9: 37,642,003 (GRCm39) I92T probably damaging Het
Or8g2b A G 9: 39,751,618 (GRCm39) D296G possibly damaging Het
Otub1 T C 19: 7,177,425 (GRCm39) D74G probably damaging Het
Oxct2b A G 4: 123,010,680 (GRCm39) E200G probably damaging Het
Pcdh1 T C 18: 38,322,662 (GRCm39) D1057G probably benign Het
Pkd1 T A 17: 24,805,174 (GRCm39) V3242E probably damaging Het
Pkd1l3 CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA 8: 110,350,420 (GRCm39) probably benign Het
Pla2g4e T A 2: 120,015,803 (GRCm39) D247V probably benign Het
Pole T A 5: 110,480,414 (GRCm39) M1995K probably benign Het
Ppargc1a T C 5: 51,705,855 (GRCm39) E76G probably benign Het
Pten G T 19: 32,777,396 (GRCm39) R130L probably damaging Het
Ptprj A T 2: 90,274,804 (GRCm39) V1186D probably damaging Het
Rab4a T A 8: 124,532,876 (GRCm39) M1K probably null Het
Rapgef3 C A 15: 97,656,271 (GRCm39) probably null Het
Rarb C A 14: 16,548,473 (GRCm38) V83F probably damaging Het
Rgs22 A T 15: 36,099,858 (GRCm39) F410I probably damaging Het
Rhpn2 A C 7: 35,080,912 (GRCm39) E459A probably benign Het
Rims4 A T 2: 163,705,974 (GRCm39) L220Q probably damaging Het
Sbf2 T C 7: 109,971,717 (GRCm39) H839R probably damaging Het
Setbp1 T C 18: 78,900,068 (GRCm39) R1200G probably benign Het
Slc12a8 C A 16: 33,444,930 (GRCm39) P275T probably damaging Het
Slc23a1 G T 18: 35,757,554 (GRCm39) T239N probably benign Het
Slc37a3 T A 6: 39,341,517 (GRCm39) T40S possibly damaging Het
Speer4c1 T C 5: 15,915,925 (GRCm39) probably null Het
Tet1 A T 10: 62,655,252 (GRCm39) H1556Q possibly damaging Het
Tfcp2l1 T A 1: 118,603,325 (GRCm39) D454E probably damaging Het
Timd6 T A 11: 46,468,058 (GRCm39) I44K not run Het
Tmem123 A T 9: 7,790,890 (GRCm39) M64L probably benign Het
Tmem62 A T 2: 120,814,853 (GRCm39) H172L probably benign Het
Trim15 T G 17: 37,177,764 (GRCm39) Y77S probably benign Het
Trim37 T A 11: 87,092,270 (GRCm39) V693E possibly damaging Het
Trim65 A G 11: 116,017,082 (GRCm39) L460S probably damaging Het
Ttc39a T C 4: 109,279,687 (GRCm39) V109A probably benign Het
Ttc7 A G 17: 87,600,374 (GRCm39) M163V probably null Het
Vps13b T C 15: 35,423,378 (GRCm39) S233P probably damaging Het
Vwf T C 6: 125,633,766 (GRCm39) L2084P Het
Wasl A G 6: 24,633,922 (GRCm39) V114A possibly damaging Het
Wdr5 A G 2: 27,409,463 (GRCm39) S62G probably damaging Het
Wfdc11 G T 2: 164,507,445 (GRCm39) S4* probably null Het
Wfikkn2 C A 11: 94,129,810 (GRCm39) M110I probably benign Het
Wiz T G 17: 32,576,760 (GRCm39) E588A probably benign Het
Xylt1 A G 7: 117,255,891 (GRCm39) H821R probably benign Het
Zbtb7c A T 18: 76,278,772 (GRCm39) H410L probably benign Het
Zc3h18 T A 8: 123,110,710 (GRCm39) D186E probably damaging Het
Zfp687 G T 3: 94,917,673 (GRCm39) L700I possibly damaging Het
Zmym2 T A 14: 57,184,020 (GRCm39) M994K probably benign Het
Other mutations in Robo2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00666:Robo2 APN 16 73,758,588 (GRCm39) missense probably benign
IGL00849:Robo2 APN 16 73,770,665 (GRCm39) missense possibly damaging 0.80
IGL00908:Robo2 APN 16 73,782,579 (GRCm39) missense probably damaging 0.98
IGL00944:Robo2 APN 16 73,730,585 (GRCm39) missense possibly damaging 0.92
IGL00955:Robo2 APN 16 73,812,860 (GRCm39) missense probably damaging 1.00
IGL00970:Robo2 APN 16 73,693,934 (GRCm39) missense probably benign 0.00
IGL01020:Robo2 APN 16 73,725,039 (GRCm39) missense probably benign 0.06
IGL01347:Robo2 APN 16 74,149,744 (GRCm39) missense probably damaging 1.00
IGL02280:Robo2 APN 16 73,843,704 (GRCm39) missense probably damaging 1.00
IGL02424:Robo2 APN 16 73,770,189 (GRCm39) missense possibly damaging 0.89
IGL03376:Robo2 APN 16 73,753,380 (GRCm39) missense probably damaging 1.00
LCD18:Robo2 UTSW 16 74,055,954 (GRCm38) intron probably benign
P0018:Robo2 UTSW 16 73,843,694 (GRCm39) missense possibly damaging 0.82
R0314:Robo2 UTSW 16 73,753,525 (GRCm39) missense probably damaging 1.00
R0324:Robo2 UTSW 16 73,764,739 (GRCm39) missense probably damaging 1.00
R0539:Robo2 UTSW 16 73,782,462 (GRCm39) splice site probably benign
R0620:Robo2 UTSW 16 73,764,690 (GRCm39) missense possibly damaging 0.92
R0630:Robo2 UTSW 16 73,713,093 (GRCm39) missense probably benign 0.05
R0701:Robo2 UTSW 16 73,843,762 (GRCm39) missense probably damaging 1.00
R1155:Robo2 UTSW 16 73,831,996 (GRCm39) missense probably damaging 1.00
R1168:Robo2 UTSW 16 73,745,184 (GRCm39) missense probably damaging 1.00
R1195:Robo2 UTSW 16 73,713,016 (GRCm39) splice site probably null
R1195:Robo2 UTSW 16 73,713,016 (GRCm39) splice site probably null
R1195:Robo2 UTSW 16 73,713,016 (GRCm39) splice site probably null
R1317:Robo2 UTSW 16 73,831,912 (GRCm39) missense probably damaging 1.00
R1422:Robo2 UTSW 16 73,775,336 (GRCm39) missense probably damaging 0.99
R1452:Robo2 UTSW 16 73,758,798 (GRCm39) missense probably damaging 1.00
R1649:Robo2 UTSW 16 73,695,889 (GRCm39) missense probably benign 0.36
R1709:Robo2 UTSW 16 73,753,411 (GRCm39) missense possibly damaging 0.83
R1751:Robo2 UTSW 16 73,831,912 (GRCm39) missense probably damaging 1.00
R1761:Robo2 UTSW 16 73,831,912 (GRCm39) missense probably damaging 1.00
R1885:Robo2 UTSW 16 73,713,033 (GRCm39) missense probably benign 0.00
R1911:Robo2 UTSW 16 73,755,213 (GRCm39) missense probably damaging 1.00
R1919:Robo2 UTSW 16 73,696,042 (GRCm39) missense probably benign
R2005:Robo2 UTSW 16 73,730,003 (GRCm39) missense possibly damaging 0.82
R2851:Robo2 UTSW 16 73,758,776 (GRCm39) missense probably damaging 1.00
R3732:Robo2 UTSW 16 73,717,635 (GRCm39) missense possibly damaging 0.64
R3732:Robo2 UTSW 16 73,717,635 (GRCm39) missense possibly damaging 0.64
R3733:Robo2 UTSW 16 73,717,635 (GRCm39) missense possibly damaging 0.64
R3734:Robo2 UTSW 16 73,717,635 (GRCm39) missense possibly damaging 0.64
R3913:Robo2 UTSW 16 73,831,893 (GRCm39) missense probably damaging 1.00
R3956:Robo2 UTSW 16 73,758,755 (GRCm39) missense probably damaging 1.00
R4394:Robo2 UTSW 16 73,745,267 (GRCm39) missense probably benign 0.13
R4426:Robo2 UTSW 16 73,745,154 (GRCm39) missense probably damaging 1.00
R4437:Robo2 UTSW 16 73,770,132 (GRCm39) missense possibly damaging 0.88
R4454:Robo2 UTSW 16 74,149,407 (GRCm39) intron probably benign
R4478:Robo2 UTSW 16 73,812,761 (GRCm39) missense probably damaging 1.00
R4586:Robo2 UTSW 16 73,758,761 (GRCm39) missense probably damaging 0.96
R4621:Robo2 UTSW 16 73,782,821 (GRCm39) missense probably benign 0.00
R4673:Robo2 UTSW 16 73,701,266 (GRCm39) splice site probably null
R4798:Robo2 UTSW 16 74,149,633 (GRCm39) missense probably damaging 1.00
R4812:Robo2 UTSW 16 73,713,176 (GRCm39) missense probably benign 0.00
R4855:Robo2 UTSW 16 73,768,079 (GRCm39) missense probably damaging 1.00
R4910:Robo2 UTSW 16 73,730,666 (GRCm39) missense probably damaging 0.99
R4916:Robo2 UTSW 16 73,695,803 (GRCm39) missense possibly damaging 0.53
R4948:Robo2 UTSW 16 74,149,726 (GRCm39) missense possibly damaging 0.88
R5325:Robo2 UTSW 16 73,770,673 (GRCm39) missense possibly damaging 0.72
R5326:Robo2 UTSW 16 73,695,853 (GRCm39) missense probably benign 0.20
R5447:Robo2 UTSW 16 73,770,654 (GRCm39) nonsense probably null
R5542:Robo2 UTSW 16 73,695,853 (GRCm39) missense probably benign 0.20
R5545:Robo2 UTSW 16 73,758,635 (GRCm39) missense probably damaging 1.00
R5646:Robo2 UTSW 16 73,758,707 (GRCm39) missense probably damaging 0.99
R5734:Robo2 UTSW 16 74,149,672 (GRCm39) missense probably damaging 1.00
R5892:Robo2 UTSW 16 73,692,668 (GRCm39) utr 3 prime probably benign
R5960:Robo2 UTSW 16 73,730,603 (GRCm39) missense probably damaging 1.00
R6126:Robo2 UTSW 16 73,717,570 (GRCm39) missense probably benign 0.00
R6130:Robo2 UTSW 16 73,717,570 (GRCm39) missense probably benign 0.00
R6153:Robo2 UTSW 16 73,717,617 (GRCm39) missense probably damaging 1.00
R6240:Robo2 UTSW 16 73,779,027 (GRCm39) missense probably damaging 1.00
R6247:Robo2 UTSW 16 73,764,672 (GRCm39) missense probably damaging 1.00
R6304:Robo2 UTSW 16 73,755,196 (GRCm39) missense probably damaging 1.00
R6337:Robo2 UTSW 16 73,725,039 (GRCm39) missense probably benign 0.06
R6431:Robo2 UTSW 16 73,843,697 (GRCm39) nonsense probably null
R6440:Robo2 UTSW 16 73,713,010 (GRCm39) missense probably benign 0.31
R6596:Robo2 UTSW 16 73,767,996 (GRCm39) missense probably damaging 1.00
R6919:Robo2 UTSW 16 73,758,755 (GRCm39) missense probably damaging 1.00
R6927:Robo2 UTSW 16 73,778,946 (GRCm39) missense probably damaging 1.00
R7029:Robo2 UTSW 16 73,745,225 (GRCm39) missense probably damaging 1.00
R7078:Robo2 UTSW 16 74,149,504 (GRCm39) missense probably damaging 1.00
R7092:Robo2 UTSW 16 73,753,531 (GRCm39) missense probably damaging 0.99
R7136:Robo2 UTSW 16 73,753,438 (GRCm39) missense probably damaging 0.99
R7192:Robo2 UTSW 16 73,717,638 (GRCm39) missense probably benign 0.19
R7569:Robo2 UTSW 16 73,832,003 (GRCm39) missense possibly damaging 0.82
R7686:Robo2 UTSW 16 73,755,293 (GRCm39) missense probably damaging 1.00
R7720:Robo2 UTSW 16 73,693,903 (GRCm39) missense probably benign 0.00
R7772:Robo2 UTSW 16 73,758,777 (GRCm39) missense probably benign 0.24
R7822:Robo2 UTSW 16 73,770,059 (GRCm39) missense probably damaging 1.00
R7881:Robo2 UTSW 16 73,717,585 (GRCm39) missense probably benign 0.00
R7897:Robo2 UTSW 16 73,695,838 (GRCm39) missense probably benign
R8135:Robo2 UTSW 16 73,730,048 (GRCm39) missense probably benign 0.04
R8297:Robo2 UTSW 16 73,812,814 (GRCm39) nonsense probably null
R8307:Robo2 UTSW 16 73,753,498 (GRCm39) missense probably damaging 1.00
R8379:Robo2 UTSW 16 73,730,588 (GRCm39) missense probably damaging 0.99
R8393:Robo2 UTSW 16 73,775,382 (GRCm39) missense probably damaging 1.00
R8474:Robo2 UTSW 16 73,745,150 (GRCm39) missense probably damaging 1.00
R8500:Robo2 UTSW 16 73,745,228 (GRCm39) missense probably damaging 1.00
R8721:Robo2 UTSW 16 73,703,798 (GRCm39) missense
R8734:Robo2 UTSW 16 73,764,651 (GRCm39) splice site probably benign
R8735:Robo2 UTSW 16 73,755,247 (GRCm39) missense probably damaging 1.00
R8840:Robo2 UTSW 16 73,782,570 (GRCm39) missense probably damaging 1.00
R8937:Robo2 UTSW 16 73,770,150 (GRCm39) missense probably damaging 1.00
R8937:Robo2 UTSW 16 73,770,149 (GRCm39) missense probably damaging 1.00
R8968:Robo2 UTSW 16 73,767,941 (GRCm39) critical splice donor site probably null
R9134:Robo2 UTSW 16 73,703,738 (GRCm39) missense
R9622:Robo2 UTSW 16 73,729,952 (GRCm39) missense probably benign 0.02
R9662:Robo2 UTSW 16 73,758,566 (GRCm39) critical splice donor site probably null
R9708:Robo2 UTSW 16 73,770,197 (GRCm39) missense possibly damaging 0.70
R9779:Robo2 UTSW 16 73,767,965 (GRCm39) missense probably damaging 0.97
X0063:Robo2 UTSW 16 73,842,716 (GRCm39) missense probably damaging 1.00
Z1176:Robo2 UTSW 16 73,730,479 (GRCm39) missense probably benign 0.35
Z1177:Robo2 UTSW 16 73,737,187 (GRCm39) critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- AACTTGTCCTGGACATAAACCATC -3'
(R):5'- AGCTTACCACCGTCTGATTTATG -3'

Sequencing Primer
(F):5'- GTCCTGGACATAAACCATCAGGTTG -3'
(R):5'- CCACCGTCTGATTTATGAAGATG -3'
Posted On 2019-12-20