ZMP

acss2

Ensembl ID:

ENSDARG00000037781

ZFIN ID:

ZDB-GENE-040718-388

Description:

acetyl-coenzyme A synthetase, cytoplasmic [Source:RefSeq peptide;Acc:NP_001002641]

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
sa37622	Nonsense	Mutation detected in F1 DNA	Not yet available
sa24258	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa37622

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
ENSDART00000055054	None	None	415	None	11
ENSDART00000125122	Nonsense	263	698	8	19
ENSDART00000138745	None	None	269	None	9
ENSDART00000141235	Nonsense	263	422	8	11

Genomic Location (Zv9):

Chromosome 23 (position 9367175)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	9325316
GRCz11	23	9260286

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTCTTTCAGTGTGAGTAACCTCTCCATTAACCCCCTTTAGCAGGAGAAA[C/T]AGAAAGAAAGAGTAAGGAAGGTCCGTCCCCCTCCACAGGTATTTCATGTC

Long Flanking Sequence:

GACTTTGTAATAAAAGTTAATAAGAAGCCTCACTCTTTGCTTATGAAATTCGTAGTGTTTCACGCACAATACTACAACACCTGAATCGGTGGAGAGTTCAGTGGAGCAGTTCAGACGAAATGCATTATCCCTTTCATTCTAATCTTTTAATGTTAACACTTGTCCTGTGCATCTTCTGCAGTGTTTAGTCTCTTTCATCGTCCCATACTTTAAAGATATCTCTGGTTATTTAACAAAGGCTTTGCATTACTGTTGTAAATCCATAAAGGTCTGGCATGATTTCTCTTGAGCTGTTGTGCTGAAGACCTTTGAAACTTTCAACGTATTATGTGTGACATTCATTAATGCAGGCTGACCCATTTTAATTTTAATGTTGTCAATGTGACCTTAATCCAAGAGATCTTTGCCATTTATTCCCCCTTCAGTGTGAGTCCATTTCTGTGTCCTTCTCCTCTTTCAGTGTGAGTAACCTCTCCATTAACCCCCTTTAGCAGGAGAAA[C/T]AGAAAGAAAGAGTAAGGAAGGTCCGTCCCCCTCCACAGGTATTTCATGTCTCCTTTGTGTTTTTGTTTTTCTGATTAACACCAGTTTGTCTGCTCTCTTTCTCGTTCTCTTGGGGATGGTTTGAAAACTTTAGCACAACCCTCACTTTTTCACACAACTCTGTTTTTTACACTGTTGTGTGTGTATGTGTGTCACTCTCTGTGTTTGCTTTTGCAAATGCAATTCACTATTTACGCACTCATCAGACTTGGCATTTAAGCTATTAATTAAAGGCACATTCTGGCTTATTAACAACTTCTAGCTTTCCCAGTGCATGACAAACATCCAACACATTTTGTAAAAGTAAACAATTGAATTTTTAAAAACCGTTAATACTATTTTAAACACAAGCTGAGCAGTTACTAGCAGGGTTCATACGGTCATGAAAAACCTGGAAAGGTCATGGATTTTTGACATTGCATTTTCTAGACCTTGAAAAGTTTTGGCAAAGCAGAAAAACC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24258

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

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000055054	Essential Splice Site	95	415	2	11
ENSDART00000125122	Essential Splice Site	378	698	10	19
ENSDART00000138745	None	None	269	None	9
ENSDART00000141235	Essential Splice Site	378	422	10	11

Genomic Location (Zv9):

Chromosome 23 (position 9379658)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	9337799
GRCz11	23	9272769

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCATACATCACGTATGGGCCCTTGGCCAATGGGGCGACCAGTGTGTTGG[T/C]AAGGGGAACACCCTGATAAGCATTATTTGTGTCAGATTTTTGCATAATGC

Long Flanking Sequence:

AAAACATCAAAAGGGGGCTAATAATTCCGACTTCAACTGTATAACAATCATTTGTTCTGTAGACAGTCGAGAAAAAAAAAAAATATTGCTTAAGAGGTCTAATAATTTTGCCCTAAAATGGTTTTTAAAAACTCTAAACTGCTTTTATTCTAGCAGGAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAAAATATTATAGGAAACACTGAAAAAATCAGTGCTCTGTTAAACATCATCATTCCAATACAGATTCCCCTTGAACTGTGCAATGTTTGCTTTTCATTTATATCTGTTATTTGGTCCTCATGCTCTGTCACTCCTCTAGGGTGTATTGCACACAGTGAGTGGATACATGCTCTACACCGCCTCCACCTTCAAGATGGTGTTTGATTATCACTCTGACGATGTTTACTGGTGCACCGCTGACATCGGCTGGATCACCGGCCACTCATACATCACGTATGGGCCCTTGGCCAATGGGGCGACCAGTGTGTTGG[T/C]AAGGGGAACACCCTGATAAGCATTATTTGTGTCAGATTTTTGCATAATGCCCTGTGATGTCACTTTTATTGTGTAATTAAAAGTATATTGACTCATTTACATTGGCACTTGTTGTTGTATATGAATACAAACTTGTAATATTCTGTCTCTAGTTTGAGGGTCTTCCAACGTACCCAGATGTGAGCCGAATGTGGGAGATTGTTGATAAATATCATGTCTCAAAGTTCTACACGGCACCCACTGCCATCCGGCTCCTGATGAAGTATGGCAGTGATCCCGTTCACAAGTGAGTTTGGGCTCTGTCTTTAAAGAACTTAAAGCATAACTTGTCTTTAAATACACACTTATATATTTTTACAAACTCCTTTAGTATTATTATTATTTTTAATCTTTTTTTAATCTTTCATATGATTAAAGTTCAATATTAATAGAGGTAAACAGTATTGTATTGTAGTTTTGTACAGGTTAATCCCATCCCCTGAGCCCTTGTTCATGAACTC

Associated Phenotype:

Not determined