Incidental Mutation 'IGL02119:Acsbg2'
ID 280533
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Acsbg2
Ensembl Gene ENSMUSG00000024207
Gene Name acyl-CoA synthetase bubblegum family member 2
Synonyms Bgr
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL02119
Quality Score
Status
Chromosome 17
Chromosomal Location 57150103-57181447 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 57175459 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000042352 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043062]
AlphaFold Q2XU92
Predicted Effect probably benign
Transcript: ENSMUST00000043062
SMART Domains Protein: ENSMUSP00000042352
Gene: ENSMUSG00000024207

DomainStartEndE-ValueType
Pfam:AMP-binding 53 519 7e-93 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Phenotypic analysis of mice homozygous for a gene trap allele indicates this mutation has no notable phenotype in any parameter tested. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 T A 2: 69,158,344 (GRCm39) probably null Het
Ap3b1 T C 13: 94,598,911 (GRCm39) V495A probably benign Het
Astn1 T C 1: 158,338,724 (GRCm39) probably benign Het
Bora A G 14: 99,290,974 (GRCm39) D94G probably damaging Het
Bpifb9b G T 2: 154,155,544 (GRCm39) V348L possibly damaging Het
Cd160 A T 3: 96,716,139 (GRCm39) I17N possibly damaging Het
Cyp2d11 A C 15: 82,274,265 (GRCm39) I372S probably damaging Het
Dennd2c T A 3: 103,044,559 (GRCm39) V380D probably damaging Het
Fat4 C T 3: 39,037,088 (GRCm39) A3580V probably benign Het
Filip1 A G 9: 79,725,548 (GRCm39) S1024P probably benign Het
Flnc G A 6: 29,447,511 (GRCm39) E1105K probably damaging Het
Gbp4 T A 5: 105,268,908 (GRCm39) E415V probably benign Het
Gdap1l1 T A 2: 163,295,588 (GRCm39) F224Y probably damaging Het
Gm11146 A T 16: 77,385,498 (GRCm39) probably null Het
Gsn G T 2: 35,192,507 (GRCm39) R485L probably damaging Het
Havcr1 A G 11: 46,666,320 (GRCm39) Y261C probably damaging Het
Maneal A T 4: 124,752,960 (GRCm39) I229N probably benign Het
Med24 A T 11: 98,619,661 (GRCm39) M27K probably benign Het
Nipsnap2 T A 5: 129,825,056 (GRCm39) probably benign Het
Noa1 T A 5: 77,455,426 (GRCm39) Q430L probably benign Het
Or1l4 C A 2: 37,091,281 (GRCm39) S9R possibly damaging Het
Or5d47 T A 2: 87,804,754 (GRCm39) N85I probably benign Het
Or7g12 T C 9: 18,899,908 (GRCm39) V208A probably benign Het
Or8h9 T C 2: 86,789,527 (GRCm39) I92V probably benign Het
Pde3a T A 6: 141,405,529 (GRCm39) S460R probably damaging Het
Pdzd8 T C 19: 59,288,922 (GRCm39) Q826R possibly damaging Het
Pfkfb4 C T 9: 108,854,178 (GRCm39) R351W probably damaging Het
Pikfyve T A 1: 65,311,730 (GRCm39) I1989N probably damaging Het
Poldip2 T A 11: 78,408,734 (GRCm39) F200I probably damaging Het
Prodh2 T C 7: 30,205,929 (GRCm39) V208A probably damaging Het
Ranbp10 T C 8: 106,553,635 (GRCm39) D89G probably damaging Het
Rbm33 T A 5: 28,544,015 (GRCm39) S90R probably damaging Het
Slc44a4 A C 17: 35,147,637 (GRCm39) D441A probably damaging Het
Slc4a10 A T 2: 62,059,014 (GRCm39) I174F probably damaging Het
Smim17 T C 7: 6,430,160 (GRCm39) probably benign Het
Tln1 T C 4: 43,546,760 (GRCm39) E872G probably damaging Het
Tmem214 G A 5: 31,030,090 (GRCm39) A296T probably benign Het
Top2b T C 14: 16,406,733 (GRCm38) L625S probably damaging Het
Vmn2r59 A G 7: 41,695,593 (GRCm39) V273A probably benign Het
Vmn2r9 G A 5: 108,991,502 (GRCm39) L620F probably damaging Het
Whrn T G 4: 63,353,724 (GRCm39) K348Q probably damaging Het
Zc3h14 T C 12: 98,730,154 (GRCm39) V399A probably benign Het
Other mutations in Acsbg2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01474:Acsbg2 APN 17 57,168,621 (GRCm39) missense possibly damaging 0.90
IGL02418:Acsbg2 APN 17 57,156,730 (GRCm39) missense probably benign
R0023:Acsbg2 UTSW 17 57,154,710 (GRCm39) missense probably damaging 0.98
R0023:Acsbg2 UTSW 17 57,154,710 (GRCm39) missense probably damaging 0.98
R0149:Acsbg2 UTSW 17 57,160,924 (GRCm39) splice site probably benign
R1542:Acsbg2 UTSW 17 57,156,791 (GRCm39) missense probably damaging 1.00
R2014:Acsbg2 UTSW 17 57,160,855 (GRCm39) missense possibly damaging 0.52
R4170:Acsbg2 UTSW 17 57,160,846 (GRCm39) missense probably benign 0.00
R4465:Acsbg2 UTSW 17 57,168,580 (GRCm39) missense probably damaging 1.00
R4867:Acsbg2 UTSW 17 57,169,914 (GRCm39) missense possibly damaging 0.93
R5169:Acsbg2 UTSW 17 57,156,913 (GRCm39) missense probably benign 0.07
R5524:Acsbg2 UTSW 17 57,157,197 (GRCm39) missense probably damaging 1.00
R6521:Acsbg2 UTSW 17 57,168,565 (GRCm39) missense probably benign 0.00
R6531:Acsbg2 UTSW 17 57,153,617 (GRCm39) missense probably damaging 1.00
R7126:Acsbg2 UTSW 17 57,153,633 (GRCm39) missense probably damaging 0.99
R7167:Acsbg2 UTSW 17 57,164,000 (GRCm39) missense probably benign 0.44
R7423:Acsbg2 UTSW 17 57,175,257 (GRCm39) missense probably benign
R7970:Acsbg2 UTSW 17 57,156,728 (GRCm39) missense probably benign 0.43
R8023:Acsbg2 UTSW 17 57,152,448 (GRCm39) missense probably damaging 1.00
R8104:Acsbg2 UTSW 17 57,152,443 (GRCm39) missense probably benign 0.27
R8887:Acsbg2 UTSW 17 57,175,285 (GRCm39) missense probably benign 0.25
Z1177:Acsbg2 UTSW 17 57,160,898 (GRCm39) missense probably benign 0.02
Posted On 2015-04-16