Incidental Mutation 'R4016:Apold1'
ID 311934
Institutional Source Beutler Lab
Gene Symbol Apold1
Ensembl Gene ENSMUSG00000090698
Gene Name apolipoprotein L domain containing 1
Synonyms LOC381823
MMRRC Submission 040847-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.197) question?
Stock # R4016 (G1)
Quality Score 225
Status Validated
Chromosome 6
Chromosomal Location 134958964-134963799 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 134960869 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 108 (I108V)
Ref Sequence ENSEMBL: ENSMUSP00000132366 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167323]
AlphaFold E9Q0X2
Predicted Effect probably benign
Transcript: ENSMUST00000167323
AA Change: I108V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000132366
Gene: ENSMUSG00000090698
AA Change: I108V

DomainStartEndE-ValueType
Pfam:ApoL 16 143 1.5e-16 PFAM
coiled coil region 192 220 N/A INTRINSIC
Meta Mutation Damage Score 0.0723 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 93.4%
Validation Efficiency 100% (49/49)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] APOLD1 is an endothelial cell early response protein that may play a role in regulation of endothelial cell signaling and vascular function (Regard et al., 2004 [PubMed 15102925]).[supplied by OMIM, Dec 2008]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh8a1 G A 10: 21,271,470 (GRCm39) V399I probably benign Het
Arpc5 G A 1: 152,644,607 (GRCm39) probably benign Het
Capn11 T A 17: 45,964,682 (GRCm39) D45V probably damaging Het
Dctpp1 G A 7: 126,856,285 (GRCm39) R146C probably damaging Het
Dlat C T 9: 50,560,931 (GRCm39) probably null Het
Dock10 T A 1: 80,584,286 (GRCm39) D140V probably damaging Het
Dtx3 A G 10: 127,027,040 (GRCm39) V378A probably benign Het
Ezh2 A G 6: 47,521,516 (GRCm39) I414T probably benign Het
Gm1979 C T 5: 26,209,604 (GRCm39) W41* probably null Het
Igf2bp2 T C 16: 21,882,426 (GRCm39) N425S probably damaging Het
Kdm5a T A 6: 120,371,067 (GRCm39) Y504N probably damaging Het
Map3k21 T A 8: 126,637,924 (GRCm39) I170N probably damaging Het
Mrgpra6 C A 7: 46,838,463 (GRCm39) C245F possibly damaging Het
Nipal2 T G 15: 34,600,207 (GRCm39) K203N possibly damaging Het
Nlrp1b A G 11: 71,063,911 (GRCm39) F621S probably damaging Het
Nos3 G A 5: 24,576,714 (GRCm39) V448M probably damaging Het
Ntrk3 G T 7: 78,112,695 (GRCm39) probably benign Het
Or5b118 A T 19: 13,448,561 (GRCm39) T76S possibly damaging Het
P2rx1 T C 11: 72,900,799 (GRCm39) C190R probably damaging Het
Pdzrn4 T A 15: 92,297,630 (GRCm39) D198E probably benign Het
Ptar1 A G 19: 23,664,824 (GRCm39) M1V probably null Het
Ptch1 T G 13: 63,672,773 (GRCm39) E944A probably benign Het
Purg T A 8: 33,877,019 (GRCm39) L219* probably null Het
Rbp3 G T 14: 33,677,347 (GRCm39) V432L possibly damaging Het
Scnn1b G T 7: 121,513,555 (GRCm39) probably null Het
Sgms1 A G 19: 32,120,192 (GRCm39) V238A possibly damaging Het
Slc16a14 G T 1: 84,890,228 (GRCm39) S359* probably null Het
Smarca2 G A 19: 26,661,327 (GRCm39) probably null Het
Spatc1l A G 10: 76,398,323 (GRCm39) S42G probably benign Het
Stra6 T A 9: 58,042,473 (GRCm39) V34E probably damaging Het
Tex14 A G 11: 87,429,449 (GRCm39) probably null Het
Tox4 T C 14: 52,523,361 (GRCm39) probably null Het
Tyr A G 7: 87,087,148 (GRCm39) S455P probably benign Het
Uggt2 T C 14: 119,263,845 (GRCm39) N1062D possibly damaging Het
Umod A C 7: 119,075,913 (GRCm39) N284K possibly damaging Het
Unc93b1 T C 19: 3,993,572 (GRCm39) I338T probably damaging Het
Vmn2r99 C T 17: 19,598,832 (GRCm39) T172I possibly damaging Het
Whrn G A 4: 63,333,876 (GRCm39) Q415* probably null Het
Other mutations in Apold1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0581:Apold1 UTSW 6 134,960,776 (GRCm39) missense probably benign 0.00
R4013:Apold1 UTSW 6 134,960,869 (GRCm39) missense probably benign
R4017:Apold1 UTSW 6 134,960,869 (GRCm39) missense probably benign
R4599:Apold1 UTSW 6 134,961,032 (GRCm39) missense probably damaging 1.00
R4909:Apold1 UTSW 6 134,960,558 (GRCm39) missense probably benign 0.00
R5154:Apold1 UTSW 6 134,960,636 (GRCm39) missense possibly damaging 0.62
R5275:Apold1 UTSW 6 134,960,763 (GRCm39) missense probably damaging 1.00
R5850:Apold1 UTSW 6 134,961,058 (GRCm39) missense probably damaging 0.99
R5958:Apold1 UTSW 6 134,960,686 (GRCm39) missense probably damaging 1.00
R6802:Apold1 UTSW 6 134,960,693 (GRCm39) missense probably damaging 1.00
R6867:Apold1 UTSW 6 134,961,019 (GRCm39) missense possibly damaging 0.60
R7012:Apold1 UTSW 6 134,961,007 (GRCm39) missense probably damaging 1.00
R8223:Apold1 UTSW 6 134,961,148 (GRCm39) missense probably benign 0.00
R9347:Apold1 UTSW 6 134,960,999 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCCAAGGATTGCTGCTGGAC -3'
(R):5'- TCTGAATCTTGGCCTTCAGG -3'

Sequencing Primer
(F):5'- GAGGCTGGAGCGGCTAC -3'
(R):5'- ACGGCCTGGCTCACTTTG -3'
Posted On 2015-04-29