Incidental Mutation 'R5608:Apoo-ps'
ID 439404
Institutional Source Beutler Lab
Gene Symbol Apoo-ps
Ensembl Gene ENSMUSG00000049233
Gene Name apolipoprotein O, pseudogene
Synonyms Apoo, EG621156
MMRRC Submission 043272-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.298) question?
Stock # R5608 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 107550644-107551229 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 107550709 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000061241
SMART Domains Protein: ENSMUSP00000132704
Gene: ENSMUSG00000049233

DomainStartEndE-ValueType
Pfam:ApoO 41 177 3.3e-43 PFAM
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.9%
Validation Efficiency 95% (54/57)
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl5 T C 10: 80,178,781 (GRCm39) D199G probably benign Het
Adgrl1 G T 8: 84,663,886 (GRCm39) G1118W probably damaging Het
Adgrv1 T C 13: 81,303,395 (GRCm39) E117G probably damaging Het
Alkbh7 A T 17: 57,305,446 (GRCm39) I88F probably damaging Het
Ankrd26 C A 6: 118,488,583 (GRCm39) D1359Y probably damaging Het
Arfgap2 G A 2: 91,100,547 (GRCm39) R298H probably damaging Het
Birc6 G A 17: 74,920,539 (GRCm39) V2109I probably damaging Het
Blvrb C T 7: 27,158,894 (GRCm39) P98L probably benign Het
Bmpr1b C A 3: 141,563,283 (GRCm39) M220I possibly damaging Het
Bpifa1 T C 2: 153,989,495 (GRCm39) probably benign Het
Capn7 A G 14: 31,092,664 (GRCm39) Y737C probably damaging Het
Cdh13 A T 8: 119,484,213 (GRCm39) D158V probably benign Het
Cenpe C A 3: 134,940,837 (GRCm39) S662* probably null Het
Colec12 T A 18: 9,848,267 (GRCm39) D148E possibly damaging Het
Dennd5a C A 7: 109,518,630 (GRCm39) E480* probably null Het
Dpysl4 T C 7: 138,678,459 (GRCm39) V473A probably damaging Het
Dyrk3 T C 1: 131,056,452 (GRCm39) S574G probably benign Het
Fchsd1 C T 18: 38,092,926 (GRCm39) probably benign Het
H2-Aa T C 17: 34,502,816 (GRCm39) T117A possibly damaging Het
Helq C T 5: 100,938,085 (GRCm39) G454S probably damaging Het
Incenp CGCTGCTGCTGC CGCTGCTGCTGCTGC 19: 9,871,232 (GRCm39) probably benign Het
Ktn1 TTGTTGTCTTTGTGTT TTGTT 14: 47,971,554 (GRCm39) probably benign Het
Lig1 C A 7: 13,039,933 (GRCm39) T715N probably damaging Het
Lrrc31 C A 3: 30,743,994 (GRCm39) probably null Het
Ltbp2 A C 12: 84,834,238 (GRCm39) probably null Het
Marcks A T 10: 37,012,912 (GRCm39) V41E probably damaging Het
Mex3c T A 18: 73,723,014 (GRCm39) M369K possibly damaging Het
Msh6 A G 17: 88,294,329 (GRCm39) D1028G probably damaging Het
Nhlrc3 C T 3: 53,369,732 (GRCm39) probably null Het
Or1n1b A G 2: 36,780,527 (GRCm39) F111S probably damaging Het
Or52s1b T C 7: 102,822,056 (GRCm39) T263A probably damaging Het
Or52z12 G A 7: 103,233,506 (GRCm39) W92* probably null Het
Or8b8 G A 9: 37,809,078 (GRCm39) C126Y probably damaging Het
Pcdhga6 A G 18: 37,840,514 (GRCm39) N78S possibly damaging Het
Plag1 T A 4: 3,905,463 (GRCm39) K76* probably null Het
Ptpn21 T A 12: 98,655,036 (GRCm39) T644S probably benign Het
Qrfpr A G 3: 36,235,114 (GRCm39) V292A possibly damaging Het
Rbbp6 T A 7: 122,596,309 (GRCm39) V617E probably damaging Het
Rnf157 A T 11: 116,287,146 (GRCm39) probably null Het
Serpina5 A C 12: 104,070,003 (GRCm39) Y300S probably damaging Het
Slc41a3 A G 6: 90,617,889 (GRCm39) K279R probably benign Het
Smndc1 A G 19: 53,372,084 (GRCm39) V110A probably benign Het
Spata31e2 T C 1: 26,722,129 (GRCm39) Q1017R probably damaging Het
Tubgcp6 A G 15: 88,995,353 (GRCm39) V419A probably benign Het
Uggt2 C T 14: 119,326,611 (GRCm39) G200D possibly damaging Het
Utrn A T 10: 12,547,581 (GRCm39) S1620T probably benign Het
Xkr4 T C 1: 3,741,603 (GRCm39) probably benign Het
Zscan22 G A 7: 12,640,919 (GRCm39) G388S probably damaging Het
Other mutations in Apoo-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00091:Apoo-ps APN 13 107,551,134 (GRCm39) exon noncoding transcript
IGL01418:Apoo-ps APN 13 107,551,032 (GRCm39) exon noncoding transcript
IGL02732:Apoo-ps APN 13 107,551,123 (GRCm39) exon noncoding transcript
R0388:Apoo-ps UTSW 13 107,551,173 (GRCm39) exon noncoding transcript
R0652:Apoo-ps UTSW 13 107,550,910 (GRCm39) exon noncoding transcript
R2442:Apoo-ps UTSW 13 107,551,140 (GRCm39) exon noncoding transcript
R5141:Apoo-ps UTSW 13 107,550,895 (GRCm39) exon noncoding transcript
R5195:Apoo-ps UTSW 13 107,551,053 (GRCm39) exon noncoding transcript
R5395:Apoo-ps UTSW 13 107,550,993 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- TGGCCTGTAATATGGCATCACC -3'
(R):5'- TCCCAAGACTCGGTGTTATTGG -3'

Sequencing Primer
(F):5'- GTTGTTTTTCCTGAAGAAAGCCAG -3'
(R):5'- CCCAAGACTCGGTGTTATTGGTTTTG -3'
Posted On 2016-10-26