Incidental Mutation 'IGL02119:Acsbg2'
ID280533
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Acsbg2
Ensembl Gene ENSMUSG00000024207
Gene Nameacyl-CoA synthetase bubblegum family member 2
SynonymsBgr
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.079) question?
Stock #IGL02119
Quality Score
Status
Chromosome17
Chromosomal Location56843103-56874447 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 56868459 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000042352 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043062]
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: 69,328,000 probably null Het
Ap3b1 T C 13: 94,462,403 V495A probably benign Het
Astn1 T C 1: 158,511,154 probably benign Het
Bora A G 14: 99,053,538 D94G probably damaging Het
Bpifb9b G T 2: 154,313,624 V348L possibly damaging Het
Cd160 A T 3: 96,808,823 I17N possibly damaging Het
Cyp2d11 A C 15: 82,390,064 I372S probably damaging Het
Dennd2c T A 3: 103,137,243 V380D probably damaging Het
Fat4 C T 3: 38,982,939 A3580V probably benign Het
Filip1 A G 9: 79,818,266 S1024P probably benign Het
Flnc G A 6: 29,447,512 E1105K probably damaging Het
Gbp4 T A 5: 105,121,042 E415V probably benign Het
Gdap1l1 T A 2: 163,453,668 F224Y probably damaging Het
Gm11146 A T 16: 77,588,610 probably null Het
Gsn G T 2: 35,302,495 R485L probably damaging Het
Havcr1 A G 11: 46,775,493 Y261C probably damaging Het
Maneal A T 4: 124,859,167 I229N probably benign Het
Med24 A T 11: 98,728,835 M27K probably benign Het
Nipsnap2 T A 5: 129,747,992 probably benign Het
Noa1 T A 5: 77,307,579 Q430L probably benign Het
Olfr1099 T C 2: 86,959,183 I92V probably benign Het
Olfr365 C A 2: 37,201,269 S9R possibly damaging Het
Olfr74 T A 2: 87,974,410 N85I probably benign Het
Olfr834 T C 9: 18,988,612 V208A probably benign Het
Pde3a T A 6: 141,459,803 S460R probably damaging Het
Pdzd8 T C 19: 59,300,490 Q826R possibly damaging Het
Pfkfb4 C T 9: 109,025,110 R351W probably damaging Het
Pikfyve T A 1: 65,272,571 I1989N probably damaging Het
Poldip2 T A 11: 78,517,908 F200I probably damaging Het
Prodh2 T C 7: 30,506,504 V208A probably damaging Het
Ranbp10 T C 8: 105,827,003 D89G probably damaging Het
Rbm33 T A 5: 28,339,017 S90R probably damaging Het
Slc44a4 A C 17: 34,928,661 D441A probably damaging Het
Slc4a10 A T 2: 62,228,670 I174F probably damaging Het
Smim17 T C 7: 6,427,161 probably benign Het
Tln1 T C 4: 43,546,760 E872G probably damaging Het
Tmem214 G A 5: 30,872,746 A296T probably benign Het
Top2b T C 14: 16,406,733 L625S probably damaging Het
Vmn2r59 A G 7: 42,046,169 V273A probably benign Het
Vmn2r9 G A 5: 108,843,636 L620F probably damaging Het
Whrn T G 4: 63,435,487 K348Q probably damaging Het
Zc3h14 T C 12: 98,763,895 V399A probably benign Het
Other mutations in Acsbg2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01474:Acsbg2 APN 17 56861621 missense possibly damaging 0.90
IGL02418:Acsbg2 APN 17 56849730 missense probably benign
R0023:Acsbg2 UTSW 17 56847710 missense probably damaging 0.98
R0023:Acsbg2 UTSW 17 56847710 missense probably damaging 0.98
R0149:Acsbg2 UTSW 17 56853924 splice site probably benign
R1542:Acsbg2 UTSW 17 56849791 missense probably damaging 1.00
R2014:Acsbg2 UTSW 17 56853855 missense possibly damaging 0.52
R4170:Acsbg2 UTSW 17 56853846 missense probably benign 0.00
R4465:Acsbg2 UTSW 17 56861580 missense probably damaging 1.00
R4867:Acsbg2 UTSW 17 56862914 missense possibly damaging 0.93
R5169:Acsbg2 UTSW 17 56849913 missense probably benign 0.07
R5524:Acsbg2 UTSW 17 56850197 missense probably damaging 1.00
R6521:Acsbg2 UTSW 17 56861565 missense probably benign 0.00
R6531:Acsbg2 UTSW 17 56846617 missense probably damaging 1.00
R7126:Acsbg2 UTSW 17 56846633 missense probably damaging 0.99
R7167:Acsbg2 UTSW 17 56857000 missense probably benign 0.44
Posted On2015-04-16