Busch Lab

ZMP

LOC100006023

Ensembl ID:
ENSDARG00000062077
Human Orthologue:
ACSBG1
Human Description:
acyl-CoA synthetase bubblegum family member 1 [Source:HGNC Symbol;Acc:29567]
Mouse Orthologue:
Acsbg1
Mouse Description:
acyl-CoA synthetase bubblegum family member 1 Gene [Source:MGI Symbol;Acc:MGI:2385656]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa38089 Nonsense Mutation detected in F1 DNA Not yet available
sa38088 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa38089
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
ENSDART00000089332 Nonsense 318 674 8 13
Genomic Location (Zv9):
Chromosome 25 (position 27027573)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 25901284
GRCz11 25 25996362
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGACATGAAATTTTATGGTAAATTTTAGGGGACTTTGGTGGACTCACTA[C/T]GAGAGGTGACTCCCACAGCCCACATGGGTGTTCCCCGTGTTTGGGAGAAA
Long Flanking Sequence:
AACATGCAATTATTTATACTGAGATATGTTGTTACATTGGATGAGTGTCATCTGTGTATGTAGATGCTGCACGCAGTGGCATTGGGCAAATCTGTGAATTAACCTACTCAAGATATATAATGATTTTCTCTGAAAGTAGAAAGCAATTAACACTTTTTTTAGAGACTCTCTCAACTGGAACATTTCTGCATGAACCTTTGGTTATATTAATTGGGTGTTTTGAATAAAAGAGACATGCAAAATATGCAAAGAGGTGACTTGTAAGTACTGAAATTGACAGTCACTGGTTTAAGCAACCATAACACACATTATGAAGGGTTACAAACTTTATTTTGTTAAAATGTATTGCTTGGGCAAATTTTTTACTTAGTGATGGTTGGCAGTATTGATGGTTTATCTGAAGTTACAAATATAAAATATTGCAAAGGATATAAATACATTCATCTGATGTTGACATGAAATTTTATGGTAAATTTTAGGGGACTTTGGTGGACTCACTA[C/T]GAGAGGTGACTCCCACAGCCCACATGGGTGTTCCCCGTGTTTGGGAGAAAATTATGGAAAAGATCAAAGAAGGCATTTCAAGGTGTGGATATATGAAAAGGAAAATGGTAACCTGGGCCATGTCAGTTAGCTTGGATGCTAATCAAAGGCTTAAAAAGTATGTCCGTTGTTTTACAGCATTTTGTTTTTTATATGCTGCATTCAGGATTTATGGACATTTATTGTAATTAAATTTTATTTTATTTGTCTTTATATCAGGGATGAAGAGAAGTCTTTTCTCTTTACTCTTGCTGAAAAATTAATTTTGCAGAAGCTTCGTGCCGAGCTTGGTTTCTCCAGTTGTGTGAAGTTCTTTTCAGGTGCAGCACCTATTGGAAGGGAAACCCTTCAATTTTTTCTTGGCCTTAACATTCGGCTTTATGAAGCCTATGGAATGAGTGAAACCTCAGGACCCCATTTTATGTCTGGACCAGAAGCTTACCAGTTTCTAAGGCAAGACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38088
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089332 Essential Splice Site 567 674 11 13
Genomic Location (Zv9):
Chromosome 25 (position 27024991)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 25898702
GRCz11 25 25993780
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTAATTGGTGACGAAAGGAAATTTTTGTCCATGCTGCTAACACTAAAGG[T/A]ATATTATGCTTTAAAAAAGTTCTTGCTTTAACACTTCCAAAACCACTTAG
Long Flanking Sequence:
ATGTACAGCTGTTTACTTTGGCTTTAGCCTGTATAGGTTCTGTTTAGAACATGATGTTATCTGTTCTGACATACTGTGTGAAAGCATTGGTAAATTGGACGGTAAAATTACATTGTTTTGGTTTTGGTAGAGTTTGTGTGTAAAAGAAGTTCAAGCATTTTAAATTTGTGTTAACTGGATGCATTTTGTGTCAAAGCAACAAGAAATGTGTAAATTGTATAGCCCACGGAGACGGATGTTGTGCTAACCGTGTTAAGAGTTTAGGAAACTTGTTAAATGTATTGAAAAAAGAGTCATAGCAATTGTAAAAAACTGTAAAAGAGTACCTTTCAATGACCATGAAATGTCTTTACATTCAGAACTCATTATTACTGCCGGAGGAGAAAATATTCCACCACTACCCATTGAGGATGCTGTGAAACAGGAGTTGTCAATCATTAGCAACGCCATGCTAATTGGTGACGAAAGGAAATTTTTGTCCATGCTGCTAACACTAAAGG[T/A]ATATTATGCTTTAAAAAAGTTCTTGCTTTAACACTTCCAAAACCACTTAGGTCAATTTTTTTCCCTTCCTTTCTTAGTGTACAGTCAATCCAGAGACCACTGAGCCCACTGACATTCTTAGCTTGGAGGCTGTAGAATTCTGTCAGCGGATTGGTAGCCAATCAACAAAATTGTCAGATATCACTGGAGGAAAAGACAAGTTAGTTTACAAGTCCATTGAAGATGGTATTGGACAGGTCAATTCCAAAGCAACCTCAAATGCTCAGCGTATACAAAAATGGACCATATTAGATAAAGATTTCTCAGTTGCTGGAGGAGAACTAGGTGGGTGGTGCAACACTTAAGCATTGACCCAATTTGACCTTTTTTTAAACAGGGAGATTAAAAAAGTATTAATTTTTTTTCTCATAGATCTCAGCAATTTTGAATTACAAGAGATGACAAAAACTAAATTTCTTTTCAGGTCCTACAATGAAGCTACGCCGGCCAGTGGTTTTGCA
Associated Phenotype:
Not determined