Incidental Mutation 'R0595:Apob'
ID 55080
Institutional Source Beutler Lab
Gene Symbol Apob
Ensembl Gene ENSMUSG00000020609
Gene Name apolipoprotein B
Synonyms apob-100, apob-48
MMRRC Submission 038785-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.859) question?
Stock # R0595 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 8027648-8066835 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 8058369 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 2251 (V2251I)
Ref Sequence ENSEMBL: ENSMUSP00000035761 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037520] [ENSMUST00000037811] [ENSMUST00000171239]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000037520
AA Change: V2251I

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000035761
Gene: ENSMUSG00000020609
AA Change: V2251I

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
LPD_N 33 585 6.03e-94 SMART
DUF1943 619 932 7.88e-97 SMART
Pfam:DUF1081 945 1059 9.4e-32 PFAM
low complexity region 1100 1109 N/A INTRINSIC
Blast:LPD_N 1249 1311 9e-22 BLAST
low complexity region 1632 1644 N/A INTRINSIC
internal_repeat_1 1882 2038 6.61e-9 PROSPERO
SCOP:d1gw5a_ 2105 2577 9e-5 SMART
internal_repeat_1 2973 3150 6.61e-9 PROSPERO
low complexity region 3561 3580 N/A INTRINSIC
low complexity region 3928 3936 N/A INTRINSIC
Pfam:ApoB100_C 4401 4456 5.6e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000037811
AA Change: V2284I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000036044
Gene: ENSMUSG00000020609
AA Change: V2284I

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
LPD_N 46 598 6.03e-94 SMART
DUF1943 632 945 7.88e-97 SMART
Pfam:DUF1081 960 1070 6.3e-39 PFAM
low complexity region 1113 1122 N/A INTRINSIC
Blast:LPD_N 1282 1344 1e-21 BLAST
low complexity region 1665 1677 N/A INTRINSIC
internal_repeat_1 1915 2071 6.6e-9 PROSPERO
SCOP:d1gw5a_ 2138 2610 9e-5 SMART
internal_repeat_1 3006 3183 6.6e-9 PROSPERO
low complexity region 3594 3613 N/A INTRINSIC
low complexity region 3961 3969 N/A INTRINSIC
Pfam:ApoB100_C 4434 4490 1.6e-32 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000171239
SMART Domains Protein: ENSMUSP00000129496
Gene: ENSMUSG00000020609

DomainStartEndE-ValueType
low complexity region 348 356 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.3%
  • 20x: 94.5%
Validation Efficiency 100% (50/50)
MGI Phenotype FUNCTION: This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. It occurs in plasma as two main isoforms, apoB-48 and apoB-100. Unlike the apoB-48 and apoB-100 structural equivalents in human, which are synthesized exclusively in the gut and liver, respectively, the mouse apoB-48 isoform is also found in mouse liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2179 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mutants usually die by midgestation and longer survivors exhibit exencephaly. Heterozygotes show reduced plasma cholesterol and apolipoprotein levels. Single isoform B100 and B48 null mutants are viable. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb1a T A 5: 8,790,417 (GRCm39) D1093E probably damaging Het
Aldh2 G T 5: 121,711,563 (GRCm39) A276D probably damaging Het
Aldh2 C T 5: 121,711,564 (GRCm39) A276T probably damaging Het
Aldh7a1 C T 18: 56,679,965 (GRCm39) probably benign Het
Ano1 C T 7: 144,143,890 (GRCm39) R964H possibly damaging Het
Atp6v1e1 A G 6: 120,778,091 (GRCm39) V148A probably benign Het
Bbs9 T A 9: 22,408,111 (GRCm39) H73Q probably benign Het
Brca1 A G 11: 101,415,713 (GRCm39) V807A probably benign Het
Cacna1b C T 2: 24,540,001 (GRCm39) probably benign Het
Cadps2 A T 6: 23,321,703 (GRCm39) probably null Het
Cep152 T C 2: 125,436,983 (GRCm39) Q519R probably damaging Het
Cep295 A C 9: 15,243,487 (GRCm39) Y1608* probably null Het
Cfap54 T C 10: 92,720,598 (GRCm39) I2619V unknown Het
Dnajb9 A G 12: 44,255,067 (GRCm39) V7A probably benign Het
Ep400 T C 5: 110,851,408 (GRCm39) K1358R unknown Het
Fbxw7 C A 3: 84,884,674 (GRCm39) probably null Het
Fsip2 T C 2: 82,777,296 (GRCm39) Y108H probably damaging Het
Ggt6 T A 11: 72,328,493 (GRCm39) L331Q probably damaging Het
Ifitm1 T A 7: 140,548,242 (GRCm39) I25N possibly damaging Het
Krt75 C T 15: 101,476,789 (GRCm39) E367K probably damaging Het
Lifr A G 15: 7,206,950 (GRCm39) Y487C probably damaging Het
Map3k6 G T 4: 132,968,574 (GRCm39) G59W probably damaging Het
Mme A G 3: 63,235,602 (GRCm39) T129A probably benign Het
Mmp10 G A 9: 7,508,199 (GRCm39) E442K probably benign Het
Myh13 T C 11: 67,235,672 (GRCm39) S646P probably benign Het
Nbea A T 3: 55,535,917 (GRCm39) I2889N probably benign Het
Nlrp4d T A 7: 10,114,972 (GRCm39) K581N probably benign Het
Nr3c2 C T 8: 77,636,233 (GRCm39) P445S possibly damaging Het
Or5p63 A T 7: 107,810,868 (GRCm39) N289K probably damaging Het
Pck1 T A 2: 172,998,822 (GRCm39) V360E probably damaging Het
Plekha7 T C 7: 115,744,203 (GRCm39) D766G probably damaging Het
Prag1 A G 8: 36,614,156 (GRCm39) N1236S probably damaging Het
Prkdc A C 16: 15,625,952 (GRCm39) Q3326P probably damaging Het
Prrc2b T C 2: 32,073,189 (GRCm39) M57T probably damaging Het
Rb1 A T 14: 73,511,120 (GRCm39) F330I probably damaging Het
Rufy4 A G 1: 74,180,089 (GRCm39) E448G possibly damaging Het
Scn10a T A 9: 119,495,129 (GRCm39) M371L probably benign Het
Sgta T C 10: 80,884,742 (GRCm39) D189G probably damaging Het
Spata31d1b A G 13: 59,864,091 (GRCm39) H413R probably benign Het
Stau2 T C 1: 16,510,674 (GRCm39) T95A probably damaging Het
Supt4a C T 11: 87,633,982 (GRCm39) probably null Het
Tanc2 A G 11: 105,605,003 (GRCm39) probably null Het
Tap2 T A 17: 34,431,328 (GRCm39) V422D probably damaging Het
Tas2r138 A G 6: 40,589,799 (GRCm39) L149P probably damaging Het
Tex15 T C 8: 34,062,645 (GRCm39) S692P probably damaging Het
Tgm2 C T 2: 157,984,962 (GRCm39) R48H probably damaging Het
Ticrr T A 7: 79,345,311 (GRCm39) F1725L possibly damaging Het
Tnpo2 T A 8: 85,778,670 (GRCm39) C672* probably null Het
Xkr9 A G 1: 13,771,008 (GRCm39) I175V probably benign Het
Zfp428 T A 7: 24,214,803 (GRCm39) S140T probably benign Het
Other mutations in Apob
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00402:Apob APN 12 8,043,065 (GRCm39) splice site probably benign
IGL00421:Apob APN 12 8,060,197 (GRCm39) missense probably damaging 0.99
IGL00658:Apob APN 12 8,059,471 (GRCm39) missense probably benign 0.08
IGL00768:Apob APN 12 8,052,107 (GRCm39) missense probably damaging 1.00
IGL00833:Apob APN 12 8,060,101 (GRCm39) missense probably benign 0.14
IGL00926:Apob APN 12 8,065,421 (GRCm39) missense probably benign 0.01
IGL01065:Apob APN 12 8,053,299 (GRCm39) missense probably damaging 0.99
IGL01313:Apob APN 12 8,050,898 (GRCm39) missense probably damaging 1.00
IGL01419:Apob APN 12 8,052,251 (GRCm39) missense probably damaging 0.99
IGL01461:Apob APN 12 8,051,884 (GRCm39) missense probably benign 0.13
IGL02002:Apob APN 12 8,044,822 (GRCm39) missense probably benign 0.03
IGL02031:Apob APN 12 8,065,222 (GRCm39) missense probably benign
IGL02102:Apob APN 12 8,039,407 (GRCm39) missense possibly damaging 0.94
IGL02115:Apob APN 12 8,042,923 (GRCm39) missense probably benign 0.06
IGL02513:Apob APN 12 8,042,979 (GRCm39) missense probably benign 0.01
IGL02967:Apob APN 12 8,065,366 (GRCm39) nonsense probably null
IGL03005:Apob APN 12 8,043,059 (GRCm39) splice site probably benign
IGL03011:Apob APN 12 8,047,883 (GRCm39) missense probably damaging 1.00
IGL03116:Apob APN 12 8,066,350 (GRCm39) missense probably damaging 0.98
IGL03215:Apob APN 12 8,063,818 (GRCm39) missense possibly damaging 0.92
IGL03227:Apob APN 12 8,066,089 (GRCm39) missense probably benign 0.04
Aesthete UTSW 12 8,060,080 (GRCm39) nonsense probably null
Essence UTSW 12 8,057,769 (GRCm39) nonsense probably null
Ethos UTSW 12 8,040,394 (GRCm39) missense probably null 1.00
IGL02835:Apob UTSW 12 8,065,097 (GRCm39) missense possibly damaging 0.86
IGL02837:Apob UTSW 12 8,055,102 (GRCm39) missense probably damaging 1.00
R0071:Apob UTSW 12 8,052,111 (GRCm39) missense probably damaging 0.98
R0071:Apob UTSW 12 8,052,111 (GRCm39) missense probably damaging 0.98
R0116:Apob UTSW 12 8,039,113 (GRCm39) unclassified probably benign
R0180:Apob UTSW 12 8,058,285 (GRCm39) nonsense probably null
R0288:Apob UTSW 12 8,040,779 (GRCm39) nonsense probably null
R0295:Apob UTSW 12 8,052,181 (GRCm39) nonsense probably null
R0305:Apob UTSW 12 8,062,210 (GRCm39) missense probably damaging 1.00
R0312:Apob UTSW 12 8,059,034 (GRCm39) missense probably benign
R0324:Apob UTSW 12 8,060,521 (GRCm39) missense probably benign 0.41
R0326:Apob UTSW 12 8,040,307 (GRCm39) missense probably damaging 1.00
R0363:Apob UTSW 12 8,060,136 (GRCm39) missense probably damaging 1.00
R0390:Apob UTSW 12 8,038,678 (GRCm39) missense probably damaging 0.99
R0462:Apob UTSW 12 8,050,896 (GRCm39) missense probably damaging 1.00
R0471:Apob UTSW 12 8,040,406 (GRCm39) missense probably damaging 1.00
R0532:Apob UTSW 12 8,066,188 (GRCm39) missense possibly damaging 0.48
R0548:Apob UTSW 12 8,056,282 (GRCm39) missense probably damaging 1.00
R0560:Apob UTSW 12 8,055,101 (GRCm39) missense probably damaging 1.00
R0600:Apob UTSW 12 8,056,440 (GRCm39) missense probably damaging 1.00
R0626:Apob UTSW 12 8,066,193 (GRCm39) missense probably benign 0.45
R0685:Apob UTSW 12 8,060,742 (GRCm39) missense probably benign
R0765:Apob UTSW 12 8,066,518 (GRCm39) missense probably benign
R0790:Apob UTSW 12 8,060,245 (GRCm39) missense probably damaging 1.00
R0918:Apob UTSW 12 8,033,941 (GRCm39) missense probably benign 0.10
R0962:Apob UTSW 12 8,039,191 (GRCm39) missense probably damaging 0.98
R1055:Apob UTSW 12 8,044,963 (GRCm39) missense probably damaging 1.00
R1077:Apob UTSW 12 8,056,017 (GRCm39) missense probably benign
R1143:Apob UTSW 12 8,062,354 (GRCm39) missense probably benign 0.26
R1163:Apob UTSW 12 8,061,654 (GRCm39) missense probably damaging 1.00
R1266:Apob UTSW 12 8,056,093 (GRCm39) missense probably benign 0.37
R1434:Apob UTSW 12 8,059,715 (GRCm39) missense probably damaging 1.00
R1442:Apob UTSW 12 8,036,165 (GRCm39) missense probably benign 0.31
R1445:Apob UTSW 12 8,066,084 (GRCm39) missense possibly damaging 0.48
R1459:Apob UTSW 12 8,061,937 (GRCm39) missense possibly damaging 0.92
R1459:Apob UTSW 12 8,056,047 (GRCm39) missense probably benign
R1465:Apob UTSW 12 8,061,421 (GRCm39) missense possibly damaging 0.91
R1465:Apob UTSW 12 8,061,421 (GRCm39) missense possibly damaging 0.91
R1508:Apob UTSW 12 8,061,481 (GRCm39) missense possibly damaging 0.92
R1518:Apob UTSW 12 8,039,207 (GRCm39) missense probably benign 0.01
R1531:Apob UTSW 12 8,047,880 (GRCm39) missense possibly damaging 0.65
R1547:Apob UTSW 12 8,053,368 (GRCm39) missense probably benign 0.08
R1574:Apob UTSW 12 8,040,839 (GRCm39) missense possibly damaging 0.51
R1574:Apob UTSW 12 8,040,839 (GRCm39) missense possibly damaging 0.51
R1682:Apob UTSW 12 8,062,365 (GRCm39) missense probably benign 0.00
R1709:Apob UTSW 12 8,059,306 (GRCm39) missense probably damaging 0.98
R1718:Apob UTSW 12 8,066,087 (GRCm39) missense probably benign 0.02
R1752:Apob UTSW 12 8,038,766 (GRCm39) missense probably benign 0.01
R1781:Apob UTSW 12 8,059,603 (GRCm39) missense possibly damaging 0.96
R1818:Apob UTSW 12 8,063,064 (GRCm39) missense possibly damaging 0.93
R1818:Apob UTSW 12 8,056,834 (GRCm39) missense probably damaging 0.98
R1842:Apob UTSW 12 8,061,559 (GRCm39) missense probably damaging 1.00
R1843:Apob UTSW 12 8,057,602 (GRCm39) missense possibly damaging 0.65
R1853:Apob UTSW 12 8,060,928 (GRCm39) nonsense probably null
R1990:Apob UTSW 12 8,051,039 (GRCm39) missense probably damaging 1.00
R2016:Apob UTSW 12 8,057,751 (GRCm39) missense possibly damaging 0.48
R2017:Apob UTSW 12 8,057,751 (GRCm39) missense possibly damaging 0.48
R2023:Apob UTSW 12 8,061,090 (GRCm39) missense probably benign 0.01
R2037:Apob UTSW 12 8,057,488 (GRCm39) missense probably benign 0.37
R2054:Apob UTSW 12 8,063,134 (GRCm39) missense probably damaging 1.00
R2057:Apob UTSW 12 8,052,164 (GRCm39) nonsense probably null
R2085:Apob UTSW 12 8,062,240 (GRCm39) missense probably damaging 1.00
R2159:Apob UTSW 12 8,060,081 (GRCm39) missense probably benign 0.12
R2209:Apob UTSW 12 8,057,752 (GRCm39) missense probably benign 0.28
R2249:Apob UTSW 12 8,057,499 (GRCm39) missense probably damaging 1.00
R2254:Apob UTSW 12 8,061,256 (GRCm39) missense possibly damaging 0.92
R2265:Apob UTSW 12 8,065,475 (GRCm39) missense possibly damaging 0.74
R2266:Apob UTSW 12 8,065,475 (GRCm39) missense possibly damaging 0.74
R2267:Apob UTSW 12 8,065,475 (GRCm39) missense possibly damaging 0.74
R2268:Apob UTSW 12 8,065,475 (GRCm39) missense possibly damaging 0.74
R2296:Apob UTSW 12 8,044,879 (GRCm39) missense probably damaging 0.97
R2897:Apob UTSW 12 8,060,356 (GRCm39) missense probably damaging 1.00
R3431:Apob UTSW 12 8,060,778 (GRCm39) missense probably damaging 1.00
R3723:Apob UTSW 12 8,061,763 (GRCm39) missense possibly damaging 0.46
R3723:Apob UTSW 12 8,056,327 (GRCm39) missense probably damaging 1.00
R3899:Apob UTSW 12 8,065,849 (GRCm39) missense possibly damaging 0.87
R4020:Apob UTSW 12 8,044,914 (GRCm39) nonsense probably null
R4050:Apob UTSW 12 8,065,390 (GRCm39) missense probably benign 0.02
R4351:Apob UTSW 12 8,043,054 (GRCm39) missense probably benign 0.03
R4365:Apob UTSW 12 8,066,083 (GRCm39) missense possibly damaging 0.95
R4366:Apob UTSW 12 8,066,083 (GRCm39) missense possibly damaging 0.95
R4456:Apob UTSW 12 8,065,445 (GRCm39) missense probably damaging 1.00
R4458:Apob UTSW 12 8,065,445 (GRCm39) missense probably damaging 1.00
R4600:Apob UTSW 12 8,058,568 (GRCm39) missense probably damaging 1.00
R4611:Apob UTSW 12 8,061,331 (GRCm39) missense probably damaging 1.00
R4646:Apob UTSW 12 8,062,759 (GRCm39) missense probably benign 0.21
R4678:Apob UTSW 12 8,045,585 (GRCm39) missense probably damaging 1.00
R4685:Apob UTSW 12 8,056,456 (GRCm39) missense probably benign 0.00
R4707:Apob UTSW 12 8,056,205 (GRCm39) missense probably damaging 0.96
R4726:Apob UTSW 12 8,040,267 (GRCm39) missense probably damaging 0.98
R4792:Apob UTSW 12 8,058,051 (GRCm39) missense probably benign 0.26
R4822:Apob UTSW 12 8,065,741 (GRCm39) missense probably benign 0.04
R4834:Apob UTSW 12 8,064,101 (GRCm39) missense possibly damaging 0.49
R4835:Apob UTSW 12 8,065,391 (GRCm39) missense possibly damaging 0.56
R4887:Apob UTSW 12 8,063,099 (GRCm39) missense probably damaging 1.00
R4910:Apob UTSW 12 8,057,848 (GRCm39) missense probably damaging 1.00
R5072:Apob UTSW 12 8,058,714 (GRCm39) missense probably benign 0.00
R5073:Apob UTSW 12 8,055,219 (GRCm39) critical splice donor site probably null
R5074:Apob UTSW 12 8,055,219 (GRCm39) critical splice donor site probably null
R5101:Apob UTSW 12 8,061,934 (GRCm39) missense probably benign 0.09
R5123:Apob UTSW 12 8,057,630 (GRCm39) splice site probably null
R5133:Apob UTSW 12 8,058,898 (GRCm39) missense probably damaging 0.99
R5135:Apob UTSW 12 8,060,086 (GRCm39) missense probably damaging 1.00
R5137:Apob UTSW 12 8,061,384 (GRCm39) missense possibly damaging 0.63
R5160:Apob UTSW 12 8,062,126 (GRCm39) missense possibly damaging 0.90
R5173:Apob UTSW 12 8,058,238 (GRCm39) missense probably benign 0.00
R5202:Apob UTSW 12 8,063,737 (GRCm39) missense probably damaging 0.98
R5229:Apob UTSW 12 8,027,806 (GRCm39) missense probably benign
R5292:Apob UTSW 12 8,055,912 (GRCm39) missense probably benign 0.01
R5378:Apob UTSW 12 8,061,865 (GRCm39) missense probably damaging 0.99
R5494:Apob UTSW 12 8,061,762 (GRCm39) missense probably damaging 0.99
R5517:Apob UTSW 12 8,040,906 (GRCm39) missense probably damaging 1.00
R5576:Apob UTSW 12 8,048,662 (GRCm39) missense probably damaging 1.00
R5582:Apob UTSW 12 8,060,788 (GRCm39) missense probably damaging 1.00
R5629:Apob UTSW 12 8,057,847 (GRCm39) missense probably damaging 1.00
R5678:Apob UTSW 12 8,041,494 (GRCm39) missense possibly damaging 0.92
R5732:Apob UTSW 12 8,060,353 (GRCm39) missense probably benign 0.15
R5734:Apob UTSW 12 8,038,781 (GRCm39) missense probably damaging 1.00
R5742:Apob UTSW 12 8,057,191 (GRCm39) missense probably damaging 1.00
R5751:Apob UTSW 12 8,062,619 (GRCm39) nonsense probably null
R5776:Apob UTSW 12 8,056,149 (GRCm39) missense possibly damaging 0.57
R5778:Apob UTSW 12 8,065,074 (GRCm39) missense probably benign 0.45
R5783:Apob UTSW 12 8,051,022 (GRCm39) missense probably damaging 1.00
R5786:Apob UTSW 12 8,065,304 (GRCm39) missense possibly damaging 0.48
R5837:Apob UTSW 12 8,053,277 (GRCm39) missense probably benign 0.04
R5857:Apob UTSW 12 8,065,397 (GRCm39) missense probably benign 0.00
R6029:Apob UTSW 12 8,066,243 (GRCm39) missense probably damaging 0.99
R6032:Apob UTSW 12 8,045,513 (GRCm39) missense probably benign 0.02
R6032:Apob UTSW 12 8,045,513 (GRCm39) missense probably benign 0.02
R6086:Apob UTSW 12 8,065,164 (GRCm39) missense probably benign
R6110:Apob UTSW 12 8,061,883 (GRCm39) missense probably damaging 1.00
R6131:Apob UTSW 12 8,065,874 (GRCm39) missense probably benign 0.17
R6157:Apob UTSW 12 8,056,077 (GRCm39) missense probably benign
R6179:Apob UTSW 12 8,055,060 (GRCm39) nonsense probably null
R6247:Apob UTSW 12 8,051,801 (GRCm39) missense probably damaging 1.00
R6279:Apob UTSW 12 8,057,769 (GRCm39) nonsense probably null
R6300:Apob UTSW 12 8,057,769 (GRCm39) nonsense probably null
R6320:Apob UTSW 12 8,039,194 (GRCm39) missense probably benign 0.27
R6339:Apob UTSW 12 8,066,188 (GRCm39) missense probably damaging 0.99
R6353:Apob UTSW 12 8,059,421 (GRCm39) missense probably damaging 1.00
R6395:Apob UTSW 12 8,058,507 (GRCm39) missense probably benign 0.45
R6441:Apob UTSW 12 8,037,796 (GRCm39) missense probably damaging 1.00
R6492:Apob UTSW 12 8,058,261 (GRCm39) missense probably damaging 0.99
R6495:Apob UTSW 12 8,040,394 (GRCm39) missense probably null 1.00
R6502:Apob UTSW 12 8,051,814 (GRCm39) missense probably damaging 0.99
R6520:Apob UTSW 12 8,033,124 (GRCm39) missense probably damaging 1.00
R6644:Apob UTSW 12 8,059,077 (GRCm39) missense probably damaging 0.97
R6704:Apob UTSW 12 8,060,379 (GRCm39) missense probably damaging 0.98
R6750:Apob UTSW 12 8,047,853 (GRCm39) missense probably damaging 1.00
R6759:Apob UTSW 12 8,061,049 (GRCm39) missense probably benign 0.06
R6812:Apob UTSW 12 8,033,062 (GRCm39) missense probably damaging 0.98
R6865:Apob UTSW 12 8,058,847 (GRCm39) missense probably benign 0.05
R6873:Apob UTSW 12 8,065,995 (GRCm39) missense probably benign 0.00
R7013:Apob UTSW 12 8,060,080 (GRCm39) nonsense probably null
R7067:Apob UTSW 12 8,059,423 (GRCm39) missense probably damaging 1.00
R7084:Apob UTSW 12 8,059,591 (GRCm39) missense probably benign
R7113:Apob UTSW 12 8,045,539 (GRCm39) missense probably damaging 1.00
R7175:Apob UTSW 12 8,057,034 (GRCm39) missense probably benign 0.33
R7196:Apob UTSW 12 8,033,893 (GRCm39) missense possibly damaging 0.90
R7199:Apob UTSW 12 8,055,072 (GRCm39) missense probably damaging 1.00
R7205:Apob UTSW 12 8,055,087 (GRCm39) missense probably damaging 0.98
R7251:Apob UTSW 12 8,057,037 (GRCm39) missense probably damaging 0.98
R7474:Apob UTSW 12 8,059,185 (GRCm39) missense probably benign 0.29
R7484:Apob UTSW 12 8,056,884 (GRCm39) nonsense probably null
R7538:Apob UTSW 12 8,052,219 (GRCm39) missense probably damaging 0.98
R7636:Apob UTSW 12 8,059,516 (GRCm39) missense possibly damaging 0.86
R7646:Apob UTSW 12 8,059,189 (GRCm39) missense probably damaging 0.99
R7787:Apob UTSW 12 8,040,780 (GRCm39) missense probably damaging 0.97
R7793:Apob UTSW 12 8,058,124 (GRCm39) missense probably damaging 0.99
R7836:Apob UTSW 12 8,051,885 (GRCm39) missense possibly damaging 0.72
R7895:Apob UTSW 12 8,061,933 (GRCm39) missense probably benign 0.00
R8005:Apob UTSW 12 8,059,744 (GRCm39) missense probably benign 0.01
R8013:Apob UTSW 12 8,060,798 (GRCm39) missense possibly damaging 0.94
R8014:Apob UTSW 12 8,060,798 (GRCm39) missense possibly damaging 0.94
R8111:Apob UTSW 12 8,058,801 (GRCm39) missense probably benign 0.16
R8117:Apob UTSW 12 8,056,435 (GRCm39) missense probably damaging 0.99
R8226:Apob UTSW 12 8,059,056 (GRCm39) missense probably benign 0.00
R8244:Apob UTSW 12 8,060,548 (GRCm39) missense probably damaging 0.96
R8280:Apob UTSW 12 8,060,851 (GRCm39) missense possibly damaging 0.46
R8310:Apob UTSW 12 8,059,033 (GRCm39) missense probably benign 0.00
R8327:Apob UTSW 12 8,051,015 (GRCm39) missense possibly damaging 0.72
R8329:Apob UTSW 12 8,061,135 (GRCm39) missense probably damaging 0.98
R8331:Apob UTSW 12 8,051,882 (GRCm39) missense probably benign 0.28
R8351:Apob UTSW 12 8,056,356 (GRCm39) missense probably benign 0.29
R8412:Apob UTSW 12 8,058,069 (GRCm39) missense probably benign 0.33
R8425:Apob UTSW 12 8,038,842 (GRCm39) missense possibly damaging 0.70
R8481:Apob UTSW 12 8,044,807 (GRCm39) splice site probably null
R8493:Apob UTSW 12 8,059,009 (GRCm39) missense possibly damaging 0.87
R8529:Apob UTSW 12 8,057,353 (GRCm39) missense probably damaging 1.00
R8554:Apob UTSW 12 8,037,830 (GRCm39) missense probably damaging 0.98
R8692:Apob UTSW 12 8,058,270 (GRCm39) missense probably damaging 0.98
R8695:Apob UTSW 12 8,057,830 (GRCm39) missense probably damaging 1.00
R8977:Apob UTSW 12 8,065,990 (GRCm39) missense probably damaging 0.99
R9016:Apob UTSW 12 8,035,408 (GRCm39) splice site silent
R9020:Apob UTSW 12 8,063,999 (GRCm39) missense probably damaging 1.00
R9037:Apob UTSW 12 8,066,501 (GRCm39) missense probably benign 0.15
R9053:Apob UTSW 12 8,058,954 (GRCm39) missense possibly damaging 0.72
R9062:Apob UTSW 12 8,058,046 (GRCm39) missense possibly damaging 0.91
R9142:Apob UTSW 12 8,062,705 (GRCm39) missense possibly damaging 0.95
R9180:Apob UTSW 12 8,047,925 (GRCm39) missense probably damaging 1.00
R9205:Apob UTSW 12 8,030,635 (GRCm39) missense probably damaging 0.99
R9248:Apob UTSW 12 8,065,231 (GRCm39) nonsense probably null
R9277:Apob UTSW 12 8,061,183 (GRCm39) missense probably benign 0.01
R9305:Apob UTSW 12 8,058,053 (GRCm39) missense probably benign 0.04
R9358:Apob UTSW 12 8,060,833 (GRCm39) missense probably benign 0.14
R9375:Apob UTSW 12 8,029,261 (GRCm39) missense possibly damaging 0.91
R9385:Apob UTSW 12 8,056,399 (GRCm39) missense possibly damaging 0.91
R9386:Apob UTSW 12 8,056,629 (GRCm39) missense probably damaging 0.99
R9392:Apob UTSW 12 8,057,098 (GRCm39) missense probably benign 0.45
R9470:Apob UTSW 12 8,039,219 (GRCm39) missense possibly damaging 0.94
R9523:Apob UTSW 12 8,052,069 (GRCm39) missense probably damaging 1.00
R9545:Apob UTSW 12 8,033,890 (GRCm39) missense possibly damaging 0.81
R9629:Apob UTSW 12 8,059,054 (GRCm39) missense probably damaging 1.00
R9702:Apob UTSW 12 8,057,559 (GRCm39) missense probably damaging 0.96
R9703:Apob UTSW 12 8,030,507 (GRCm39) missense probably damaging 0.99
R9719:Apob UTSW 12 8,065,464 (GRCm39) missense probably benign 0.15
R9726:Apob UTSW 12 8,056,926 (GRCm39) missense probably damaging 0.99
R9729:Apob UTSW 12 8,066,125 (GRCm39) missense probably damaging 0.99
X0027:Apob UTSW 12 8,057,975 (GRCm39) missense probably benign
Z1088:Apob UTSW 12 8,062,936 (GRCm39) missense possibly damaging 0.95
Z1088:Apob UTSW 12 8,055,945 (GRCm39) nonsense probably null
Z1088:Apob UTSW 12 8,055,074 (GRCm39) missense possibly damaging 0.91
Z1176:Apob UTSW 12 8,054,978 (GRCm39) missense probably benign 0.00
Z1176:Apob UTSW 12 8,048,011 (GRCm39) missense probably damaging 1.00
Z1177:Apob UTSW 12 8,065,249 (GRCm39) frame shift probably null
Z1177:Apob UTSW 12 8,038,765 (GRCm39) missense probably benign 0.43
Predicted Primers PCR Primer
(F):5'- CTGAGCAGACTTCCTCAGCAGATTC -3'
(R):5'- TCAGGCTATATCTGTGGGCCAACTC -3'

Sequencing Primer
(F):5'- CATTATCTGAATGCATCTGACTGGG -3'
(R):5'- CCATTAAAACCTGGATGTGTTGGTC -3'
Posted On 2013-07-11