Incidental Mutation 'R1990:Apob'
ID 224965
Institutional Source Beutler Lab
Gene Symbol Apob
Ensembl Gene ENSMUSG00000020609
Gene Name apolipoprotein B
Synonyms apob-100, apob-48
Accession Numbers
Essential gene? Probably essential (E-score: 0.859) question?
Stock # R1990 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 8027648-8066835 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 8051039 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 1088 (I1088F)
Ref Sequence ENSEMBL: ENSMUSP00000035761 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037520] [ENSMUST00000037811]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000037520
AA Change: I1088F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000035761
Gene: ENSMUSG00000020609
AA Change: I1088F

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 possibly damaging
Transcript: ENSMUST00000037811
AA Change: I1101F

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000036044
Gene: ENSMUSG00000020609
AA Change: I1101F

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
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.5%
Validation Efficiency
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: 97 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik C T 3: 137,771,419 (GRCm39) R203* probably null Het
Acp6 T C 3: 97,083,054 (GRCm39) L355P probably damaging Het
Aebp2 T C 6: 140,579,464 (GRCm39) S234P probably damaging Het
Anapc7 A G 5: 122,577,567 (GRCm39) D374G probably benign Het
Arid4b T C 13: 14,307,021 (GRCm39) V92A probably damaging Het
Armc3 T C 2: 19,297,953 (GRCm39) Y575H probably damaging Het
Asxl2 G T 12: 3,534,558 (GRCm39) G252* probably null Het
Atl1 A T 12: 70,010,102 (GRCm39) K556M probably damaging Het
AU018091 A G 7: 3,212,104 (GRCm39) V206A probably benign Het
Bcas1 A T 2: 170,212,397 (GRCm39) D383E possibly damaging Het
Bmx A G X: 163,015,192 (GRCm39) W257R probably benign Het
Bpifb6 T C 2: 153,747,270 (GRCm39) probably null Het
Cacna1b G A 2: 24,622,318 (GRCm39) P222L probably damaging Het
Cand1 A G 10: 119,045,972 (GRCm39) S978P probably damaging Het
Cap2 T A 13: 46,791,357 (GRCm39) Y175N possibly damaging Het
Caps2 G A 10: 112,036,591 (GRCm39) A384T probably benign Het
Catsperg2 A T 7: 29,420,470 (GRCm39) Y223* probably null Het
Cd81 G T 7: 142,620,938 (GRCm39) G206* probably null Het
Cd84 A G 1: 171,700,317 (GRCm39) T145A possibly damaging Het
Cdkn2aip G T 8: 48,165,211 (GRCm39) N167K probably benign Het
Ceacam14 T A 7: 17,549,290 (GRCm39) L227* probably null Het
Ceacam5 A T 7: 17,491,805 (GRCm39) D725V probably damaging Het
Cldn34a A T X: 151,346,841 (GRCm39) H171L probably benign Het
Col18a1 T C 10: 76,916,988 (GRCm39) I114V unknown Het
Cp A G 3: 20,033,177 (GRCm39) D667G probably damaging Het
Cr2 G A 1: 194,836,458 (GRCm39) P1278S possibly damaging Het
Crat A G 2: 30,295,060 (GRCm39) Y452H possibly damaging Het
Cyp4f13 T A 17: 33,144,542 (GRCm39) H318L probably damaging Het
Dab1 C T 4: 104,588,948 (GRCm39) A524V probably benign Het
Dmbt1 A G 7: 130,660,018 (GRCm39) N527S probably damaging Het
Fcgbpl1 A T 7: 27,853,785 (GRCm39) D1583V probably damaging Het
Fgb G T 3: 82,951,560 (GRCm39) Y256* probably null Het
Frmd3 T A 4: 74,105,676 (GRCm39) S441T probably damaging Het
Glp1r T A 17: 31,149,722 (GRCm39) C329S possibly damaging Het
Gm14190 G T 11: 99,581,431 (GRCm39) Q46K unknown Het
Golt1b T A 6: 142,338,080 (GRCm39) F17Y probably damaging Het
Gsdmc A G 15: 63,673,748 (GRCm39) I179T probably benign Het
Gsdmc2 T A 15: 63,700,086 (GRCm39) M229L probably benign Het
Gulp1 A C 1: 44,805,274 (GRCm39) N121T possibly damaging Het
Ift122 T A 6: 115,901,328 (GRCm39) F1037I probably damaging Het
Ildr1 A T 16: 36,536,568 (GRCm39) Y199F probably damaging Het
Ints2 T A 11: 86,139,760 (GRCm39) H278L possibly damaging Het
Invs T C 4: 48,392,599 (GRCm39) V271A possibly damaging Het
Kcnj2 T C 11: 110,963,709 (GRCm39) I367T probably benign Het
Kif21b T C 1: 136,089,508 (GRCm39) S1115P probably damaging Het
Lce1k A T 3: 92,714,125 (GRCm39) C20S unknown Het
Lcmt2 C A 2: 120,970,762 (GRCm39) R107L probably benign Het
Letm1 A AG 5: 33,926,859 (GRCm39) probably null Het
Lrrc9 A C 12: 72,544,635 (GRCm39) R71S probably damaging Het
Mcc C A 18: 44,624,382 (GRCm39) E213* probably null Het
Mis18bp1 T C 12: 65,205,468 (GRCm39) T235A probably benign Het
Mta2 C T 19: 8,919,696 (GRCm39) probably benign Het
Nebl T A 2: 17,457,321 (GRCm39) I80F probably damaging Het
Nek10 A G 14: 14,860,764 (GRCm38) T467A probably benign Het
Nexn A T 3: 151,958,576 (GRCm39) F106I probably damaging Het
Nrdc T A 4: 108,896,972 (GRCm39) Y282* probably null Het
Nxf3 G A X: 134,976,583 (GRCm39) P380S possibly damaging Het
Oma1 C T 4: 103,178,971 (GRCm39) T208I probably damaging Het
Or1a1 T C 11: 74,086,989 (GRCm39) V220A probably damaging Het
Or4c31 A G 2: 88,291,686 (GRCm39) M1V probably null Het
Or4d10c C A 19: 12,065,620 (GRCm39) V179F probably damaging Het
Or4p21 A G 2: 88,277,033 (GRCm39) L83P probably damaging Het
Or51a42 A T 7: 103,708,335 (GRCm39) I158N possibly damaging Het
Or52l1 A T 7: 104,830,221 (GRCm39) C115S probably damaging Het
Or5p66 C A 7: 107,885,566 (GRCm39) G256* probably null Het
Or5p70 A G 7: 107,995,041 (GRCm39) Y238C probably benign Het
Panx2 A T 15: 88,953,941 (GRCm39) Y632F possibly damaging Het
Pdia4 T C 6: 47,773,589 (GRCm39) T587A probably benign Het
Piezo2 A T 18: 63,207,733 (GRCm39) L1426Q probably null Het
Pigk T A 3: 152,450,131 (GRCm39) Y212N probably damaging Het
Pramel22 T A 4: 143,380,838 (GRCm39) Y395F probably damaging Het
Prl3b1 C T 13: 27,429,775 (GRCm39) T71I possibly damaging Het
Rab3gap1 A G 1: 127,870,166 (GRCm39) E929G possibly damaging Het
Rabl3 T C 16: 37,384,079 (GRCm39) I162T probably benign Het
Rasgrf2 T A 13: 92,172,473 (GRCm39) T188S probably damaging Het
Slc12a2 A G 18: 58,043,358 (GRCm39) I601V possibly damaging Het
Slc25a42 A T 8: 70,644,519 (GRCm39) I60N probably benign Het
Slc2a3 C T 6: 122,713,694 (GRCm39) G173S probably damaging Het
Slc46a3 G A 5: 147,823,404 (GRCm39) T146M probably damaging Het
Specc1 C A 11: 61,920,120 (GRCm39) P7T possibly damaging Het
Sptbn4 T C 7: 27,123,235 (GRCm39) D229G probably benign Het
Sspo T C 6: 48,427,984 (GRCm39) I154T probably benign Het
Stx5a T C 19: 8,726,254 (GRCm39) probably null Het
Stxbp6 A T 12: 44,902,640 (GRCm39) C210* probably null Het
Tagap1 C T 17: 7,224,285 (GRCm39) R137Q probably benign Het
Tbc1d9 A G 8: 83,997,932 (GRCm39) Y1163C probably damaging Het
Tex14 T G 11: 87,440,296 (GRCm39) L1367R probably damaging Het
Tnnt3 C T 7: 142,065,262 (GRCm39) R131C possibly damaging Het
Tpx2 T A 2: 152,732,544 (GRCm39) M606K probably benign Het
Trim46 A T 3: 89,145,008 (GRCm39) Y489N probably damaging Het
Ttc28 C T 5: 111,424,188 (GRCm39) S1485L probably benign Het
Txnl1 T C 18: 63,812,585 (GRCm39) T70A probably benign Het
Unc80 T C 1: 66,731,708 (GRCm39) L3053P probably damaging Het
Wars1 G T 12: 108,854,359 (GRCm39) N18K possibly damaging Het
Wnt8a A G 18: 34,677,937 (GRCm39) D115G probably damaging Het
Xndc1 T A 7: 101,722,398 (GRCm39) V21E probably damaging Het
Zfp493 T A 13: 67,934,388 (GRCm39) C114S probably damaging 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
R0595:Apob UTSW 12 8,058,369 (GRCm39) missense probably benign 0.01
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
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'- TTTGCATAACCTCACAGTACCC -3'
(R):5'- TGTCCAGCTGAGTATGAGCC -3'

Sequencing Primer
(F):5'- CTCTTTCAGGAGTGCAGCAGTC -3'
(R):5'- CCAGCTGAGTATGAGCCAAGGG -3'
Posted On 2014-08-25