ZMP

acsbg2

Ensembl ID:

ENSDARG00000004094

ZFIN ID:

ZDB-GENE-030131-7099

Description:

long-chain-fatty-acid--CoA ligase ACSBG2 [Source:RefSeq peptide;Acc:NP_001119851]

Human Orthologue:

ACSBG2

Human Description:

acyl-CoA synthetase bubblegum family member 2 [Source:HGNC Symbol;Acc:24174]

Mouse Orthologues:

1700061G19Rik, Acsbg2

Mouse Descriptions:

RIKEN cDNA 1700061G19 gene Gene [Source:MGI Symbol;Acc:MGI:1925875]
acyl-CoA synthetase bubblegum family member 2 Gene [Source:MGI Symbol;Acc:MGI:3587728]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44683	Nonsense	Mutation detected in F1 DNA	Not yet available
sa34372	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa27178	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44683

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012120	None	None	752	None	15
ENSDART00000123926	None	None	752	None	15
ENSDART00000124809	Nonsense	36	794	1	15

Genomic Location (Zv9):

Chromosome 8 (position 20695921)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	20125818
GRCz11	8	20157903

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGAAGCTGGCATTTTAAAACCTCTTGATTCGGAAAAGCCAAAGACAAGG[C/T]AGCGTTTTTCATCCGTGACGATGCACTGTAAGTTTGTGTTTTTGTATTTA

Long Flanking Sequence:

GCAAGCCAGCACAAAATGCTCTTATTACCCCAGCGTATAAATGGGACAGATGTGTGTTGGTGGGTTACATGTCTATCGCCTGATGTCAGTGCAGCTGTGCTGGCTTTTTCTAGGCTGATATATCACTCAAGGTTGCACTGTAATAACCTCCCAGCATCTGCACTGGTTAGTATGTATGAGAGTGTCAGTGGTGCGTGTGTTTTTTGGCCCCTCCCCTTCCTCTCTCCTTCAGTGGGCTGGTATGCCCATATATGGAGGATGAGTCTTGTGGTGTGAGTGATTTTAGCCAATCGGAGCACGAATGTGTTTCTGGGGGGGTTTTGAGGATTCTGCTGTCGTGGAGGGTGTGGTTTTTGGAGGAGGGGAAAGCCTCTCTGTTTGAAAATGAATGTACTACATGCACAGTTGTAGGGTGTGAGAAAGCCGCCATCATTTTGAAGTCTGACGATAAGGAAGCTGGCATTTTAAAACCTCTTGATTCGGAAAAGCCAAAGACAAGG[C/T]AGCGTTTTTCATCCGTGACGATGCACTGTAAGTTTGTGTTTTTGTATTTAATGTGTGAGGTGATGATTTAATAGCATTTGCAGTTGATATGGGTGATCTCACAAGCTGGGAGTTTAAGATGTATTTTAAGCAACAGATTTGTGTATGTGGTCATCAGTGTTTTATGTGTTTATGTTGATAATGGATTTGAGTTTAAATGATATTAATGATGATATTATATTATATCAGAGGCGTGGTCCTGTTTGTGCTGGGTGAGATGATTCTAGCATATGAATGATTGGGTTTCAGTGAGCATTTGCATGCATGTGTTCCTCACACACAGATAGGTTCTCTTTTTAAATGAGCAATGGAAAGTTCCTCCTGTTATTGCGAGAGGGATTTCAGCTTTCCATAGCTGTATACAGATGGTAATTTTTCGGGTGGGGGCTGATCGTGGCCGTCAGTTGCTGCCAGCATCTGCTGTGTAACCCCCCCCCCATCCTTATTATTCTCCTGTTGAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34372

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012120	Essential Splice Site	48	752	2	15
ENSDART00000123926	Essential Splice Site	48	752	2	15
ENSDART00000124809	Essential Splice Site	90	794	2	15

Genomic Location (Zv9):

Chromosome 8 (position 20704602)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	20134499
GRCz11	8	20166584

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGACAGTCTCGCCTCTCTGGAAGACGCTGCCGCAGAGTCTACAGCAAAG[T/G]CAGTCCCTGTCCAGTACACTTTTGTTTCTTTTTTACTTGGTCAGGCATAG

Long Flanking Sequence:

GTATAGTCCAATTTGTGTGTCTTAGTTCCACACTCTCATGACACAAAAAAAAAAAAACAACTTGAATAAAACTATTGATGCTGGACATTACAGAATGTCAATTGTACTTGTGACACTACTGTATTAATAGTATGTCAATAGTAAATGAATCTTGATTATATGTATTACATAAACATTTAATGGCAGTTTTTAAATATATTATTAATTATGTATTTATTAAGTTGATGTCTCTTAGCATGTTGTGTCATTCAATTAATAGTACTGTATATATTTATAGGTCACCTTGCTCTCTAGATATTGACATTAGGCATTAAGGGGATGTCATTTGAGTGCTACTCCTAACACTGCATCTGTTCTCATTAGTGACCGCGTGTGAACCCACGGCCATGTCCACAGCTGTAGTGATGGAGCATCCAGGAGATGAGAGCCTCCTTCAGTCCTGTGGAACTGCAGACAGTCTCGCCTCTCTGGAAGACGCTGCCGCAGAGTCTACAGCAAAG[T/G]CAGTCCCTGTCCAGTACACTTTTGTTTCTTTTTTACTTGGTCAGGCATAGGTAACTAAATTCCCACAGGTAATTTATATTTTACAGTCATGAAATGTAGGTCACATGAGCTTGTGTTTGTAAACATAAGTGATGACATGTTGGAATGTGGTCATTGTGTCAAAAACTGGTTGTGCAAATGCCATGCCAGGTTCATGAATGAAGATACATGCCATCATAATATATTGCATAAAGATTCATTACAGCGTAAAATATTAACATGAGTTGTGTAAACAAATTTACCTTCTTACATTTTTCATTGTTTTCAAACGTACAGGGAATCTGCAGGGTCTTCAATTCTTAAAATGTATTAGCTAAGTGTCAAAACCCAAATTTTAGACCTTAAAAAGTCTTAAATCTACTGAAATATTGTGTTGTAGGTTTTAAATCTTTTTTTAACAGGTCTTAATTTTTTCTTTGTTCAGGAATAGCTGCCCAATCTCATCATTAACACTCATACAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa27178

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012120	Essential Splice Site	631	752	13	15
ENSDART00000123926	Essential Splice Site	631	752	13	15
ENSDART00000124809	Essential Splice Site	673	794	13	15

Genomic Location (Zv9):

Chromosome 8 (position 20724504)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	20154401
GRCz11	8	20186486

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTTATAGGAGACAAGAGAAAATTCCTCTCCATGCTGCTTACCGTTAAG[G/A]TACCTTTTCAGATTTGTGTGTTTATGCGTAGAAAACCTGCTGTCAATCTT

Long Flanking Sequence:

TTAACTTAATAGAATTATTTTTATCAAAAATGTCCCAAATATTGGGACCAAATATCACAGAGAGTCAAGTGCAAAATAGGTTAAGACATGCTTTTTTGGGGTAATAAATAATTGCATAAATACCAGTGAATGGTTTCCCGCGAGCTCGAGTAAACATACAGTACAATTCATATAAATATGCTACTTTTTCATTCCTTTAAAACCTGTTTGAACACATTATAATCTGCTTTTATTCATTTTTGATCTTTGTTTTTGTATTTCTTGTATTTTATGTTTCTTTTAAGTTTATGCAAAAGCACTTTGAATTACCATTGTGTATAGTATATGGGCTGTCTAATGAAGCTTATATTTGTATTCCAGAATTGATCATCACAGCTGGAGGTGAAAATATTCCCCCGGTCCCTATTGAAGACGCGGTTAAAGAGGCCATTCCCCTCATCAGTAATGCCATGCTTATAGGAGACAAGAGAAAATTCCTCTCCATGCTGCTTACCGTTAAG[G/A]TACCTTTTCAGATTTGTGTGTTTATGCGTAGAAAACCTGCTGTCAATCTTCTTTCATGTTCAAATTTAAAAAAAGTCATATCTAAACTACCTGACTTTTGTCTGAATCACTCAACAAGTGACACATTTTTGTCAGATGTTTATATTTCTTTGTCTTTTTACTCTGTTACACGTTCACTCAAAATCTGCTCAAATTAAATTGACCACATATTGTAGTAAATTGCATTGTACCAGTCTAACTGAAGAACAAAAGTGCAGAGCTTTGATTATTCTTCATTATTGATTAGTGTTTATTGCCCTTGTTGTGCAATCTGCACCGATATCGTGTTCTTCTAAAACTGAAAGGTGTAAATCTAATCTGAACATCTCATCCGAGGCCTCTTTCACAAGGCGGGTAGGCTTATGTAAGCTTACTGGGAGATAACATTCATTTTAAAGATGCATGAGAATTTTTTTAAACTACACACTAATGAGATCCTATCAGAAGGATCAGGTGATAAC

Associated Phenotype:

Not determined