Busch Lab

ZMP

ENSDARG00000069029

Ensembl ID:
ENSDARG00000069029
Human Orthologue:
ACSS2
Human Description:
acyl-CoA synthetase short-chain family member 2 [Source:HGNC Symbol;Acc:15814]
Mouse Orthologue:
Acss2
Mouse Description:
acyl-CoA synthetase short-chain family member 2 Gene [Source:MGI Symbol;Acc:MGI:1890410]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa15837 Essential Splice Site Available for shipment Available now
sa13730 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15837
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100103 Essential Splice Site 67 515 1 15
Genomic Location (Zv9):
Chromosome 2 (position 55225984)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 54909107
GRCz11 2 54639803
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGACGCATATCTGGCTTTATATAAAAAGTCMATTGAAGAGCCTGAAGG[T/A]ACGTCTGATAGTACTGAAGACAAACAGTTACGCAATCMMCATTATATGCA
Long Flanking Sequence:
TTAATGTATCTTTGAGTGTGTGTTTGTGTGTCTGTGTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATCATCCGTCAGGCTCGTGCGTCCCCGCCCCCTGCAGTGGGATCAGCAGCCGAGCAGCTGCTCATCCAACCAGAAAAGAGGAGTGTAGAATGCGGCGCTCTGATTGGTGGAGGCGGAGCCGAGCAGACTGAGCAGGATTAAAAACAGGGTACCACATGCTCAGACACAATAAAGAGCTTCATCCACAGACTGACATCCATCCTAAGAATGTCTCCCGTTTCAGACTCCACCAACACGGCTCTTTCAAGCCCAAAGGAGCCCGAGGAGAAGATTTACCATCCACCCGACGGCATTTTCACTGACGCGCACGTGCCTGACTTTGACGCATATCTGGCTTTATATAAAAAGTCCATTGAAGAGCCTGAAGG[T/A]ACGTCTGATAGTACTGAAGACAAACAGTTACGCAATCAACATTATATGCAATGTAGTCATGTTACTATTATATAGTAAAACAGGATGCTTTAAAAGTATAAGTCATGGTGCTGTATATCTTTATTGGTCACACTTTACAATAAGGTCTCATTAGTGAATGTATTTACTAACATGGACATTTACTGTACATTTATTAAAATTTAATTCCTTTGTTAAAGTTAGTTAATTGAAATAAAGTAATTCATTGTTAGTTCTTGTTAACCCAGTGCATTATGTGAATTCGGATGTTAATAATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACACTAGAACTATACTATAAGAGCAACAATGAATAAATGCTGTAGGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGAAAGTATTAGTAAATTTTATTTATTTATTTTTTTTGGGTACAGTTAGTGTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13730
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100103 Nonsense 445 515 13 15
Genomic Location (Zv9):
Chromosome 2 (position 55188107)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 54871230
GRCz11 2 54601926
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTGTTTTGGGAACGGTTGGTGAACCCATTAACCCAGAGGCTTGGCTTTG[G/A]TATTATRATGTTGTGGGTCAGCAGCGCTGTCCGGTTATCGACACCTTCTG
Long Flanking Sequence:
CTTTTCTTCAGACAGCACAGATCTGCTTGATTTGACTGTCTCCTGCCATTTTATTTGTTCTGAAAGCAGGAATTATCAGACTGAAATGGGCTTATGAAGGAATAATGTAACGGGGCTCTATTACATTTAACATTTTCTTAAAACCCGACATTTCCACTACCGATTAAGGTCATATGCAGTCTATATGCAGTCATATGCTGACTGGAGTAGTGTTTGGAGGTGGGCAGAGAAGCCAGCATGTTGCCTGTCACGTCATTTGGGATGTCTGAATTATTCGATTTGTAATGCGCACCTGATCCGAAAGTCTCGTACCAAACAGTATATATATACACATATACACACACACACACACACACACACACACACACACACACACACACACACTATTATTGTTGTATTTTTACCAGTTGTTTGTCTTGGATGTGTCTCAGGTATGATCTGTCCAGCTTGCGTGTTTTGGGAACGGTTGGTGAACCCATTAACCCAGAGGCTTGGCTTTG[G/A]TATTATGATGTTGTGGGTCAGCAGCGCTGTCCGGTTATCGACACCTTCTGGCAAACAGAGACGGTAAAACATTCACTACAATCAAACAAACCCAGTTTCTTGAACCAAAGTTGCCTAAAACCTGCTTAAAGGCACAGATCACCCAAAAAAGAAAACTTTATCATTTACAAACCTGATTGATTTCTTCTGTTGAACACAAAAGGAATATATTTTAAACTATGTTGTTGTTGGTTTCCATTGACCTTAAAAGTACTTTTTCCCTACTATTATGTAAGGAATTCACTATAGCACTATTGAGTCTTTCTTTTCTTTTTTAAGACCTGTTTTAATCATTTGTATTCTTTGTTGTTTTTATTTCTTATACTTCTTTCTTTTATTCTTGTTTATGTAAAGCACTTTAAATTACCAGTGTGTCTTAAATGTGCCATATAATTTAATTATTATATTATTTAATTATAATATAAATTGCCTATTATTGAAAAAGACCAAAATAAGTTGTT
Associated Phenotype:
Not determined