ZMP
acsf2
Ensembl ID:
ZFIN ID:
Description:
Acyl-CoA synthetase family member 2, mitochondrial [Source:UniProtKB/Swiss-Prot;Acc:Q0P4F7]
Human Orthologue:
ACSF2
Human Description:
acyl-CoA synthetase family member 2 [Source:HGNC Symbol;Acc:26101]
Mouse Orthologue:
Acsf2
Mouse Description:
acyl-CoA synthetase family member 2 Gene [Source:MGI Symbol;Acc:MGI:2388287]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22107 | Nonsense | Available for shipment | Available now |
sa31878 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22107
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087040 | Nonsense | 153 | 606 | 5 | 17 |
ENSDART00000132737 | Nonsense | 153 | 231 | 4 | 6 |
ENSDART00000138437 | None | None | 135 | None | 4 |
ENSDART00000143213 | Nonsense | 153 | 181 | 5 | 6 |
The following transcripts of ENSDARG00000061201 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 28103625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26441234 |
GRCz11 | 12 | 26532594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGCTAAAGTGGATTGTGATTGAACAGGTTGCGGTGAACCCGGCTTAT[C/T]AATTGCAAGAGGTAGAATTTGCTCTCAGAAAGGTAAGTTAATGTTTATAC
Long Flanking Sequence:
AGCTGCCATCTTGAAACCTGCCCATTTAAACAGTTTCAAGTTACAACGGGTTTGCTCACTTTTTTTTTTAAGTTGTCAGATTTTCACTCTTAAGGTAAAGTAGCTAATGACTTTTTGCAGTGTTTGTACAAAAAGTGGTGATTTTATCAAATGCAAATCTGCAAGAGTGGGTGTCTTAGATTAACCATAAACTTGGAAAATATGATGTGCTAATGTTAAGCAATTGTAATGTCTTTCAGTGTAAAAAATGTGGTATATATTTTGATTTCAGGTGGAAAAGGCTGCTGCGGGTCTGCTGGCGGCTGGGCTGAAGCGGGGAGATCGATTAGGGATGTGGGGACCAAATATCTATGAATGGGTACTGATGCAGTTTGCCACAGCTAAAGCAGGGATCATTTTGGTGAGCGTTTTTCACCGTTTTGACTTTGGTTTATCAATAATATTGAATTAGCCTGCTAAAGTGGATTGTGATTGAACAGGTTGCGGTGAACCCGGCTTAT[C/T]AATTGCAAGAGGTAGAATTTGCTCTCAGAAAGGTAAGTTAATGTTTATACATGCACATAAGAACAACAAACTATCAATGTTCTGGACTGTTTTTGACTTTTTTGGCTTTATTTGCAGTAGATTAAAAACTAGGTCAGATTTATATAGAAGCCTGCGTTTGAGTTTTAAGGTCTGAAATGAAGTGACTGTGAATTAAAAATTAAGAAATTGAGGTAAACTTATGAGAATTAAAGTAATAGTTCACCCAAAATTGAAAATGCTCTCATTATTAACCCAAATTTTTCACAAACCTGTTGAGCACAAAAACAAATGTTGGAAAAATGCTGGTAACCTGTAATCAATGACCTCCATAGTGTTTGTTTTGTTCTTCTATGGAAGGAAACGGTTACAAGTTTCTAACATTTTTCAGAAAATCTTCTTTTGTGTTCAGCAGAAAAAAGAAACTCACAAAAGGTAAGTAAAGTTTCATTTTTGGGTGAACTATCCCTTTAAGATTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31878
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087040 | Nonsense | 351 | 606 | 10 | 17 |
ENSDART00000132737 | None | None | 231 | None | 6 |
ENSDART00000138437 | None | None | 135 | None | 4 |
ENSDART00000143213 | None | None | 181 | None | 6 |
The following transcripts of ENSDARG00000061201 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 28097791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26435400 |
GRCz11 | 12 | 26526760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAACTGTTTAACCAGGTGTACATTTGTCTACGGTACCCCCACTATGTA[T/A]ATCGACATGCTCGGACAGCCAGACCTGGCCAAGTTTGATTTGTCATCAGT
Long Flanking Sequence:
TTTAAAATCTATTCTGAATGTAACTGGCAGCCAGTGTAGAGACCTGAGGACAGGTGTGATGTGCTCTGATTTCCTGGTCCTGGTCAGAATTCTGGCTGCAGCATTCTGGATGAGCTGCAAGTGTCTGACTGTCTTTTTGGGAAGGCCAGTGAGGAGTCCATTACAGTAATCCACCCTGCTACTGATAAAAGCATGAACAAGTTTCTCTAAATCTTCACTAGAAACAAAGCATCTGATTCTTGCTATGTTTAGACAATAATGATAAATCTTGGTACTTTGTTCCACGTCTATCGGACATACTGTACTGTACTGAATATATATTGTCATAACTAAATTACAAGGAACATAAAGAAGACAGCAGTGTATAATTTAGGTAATGTTTAAATGTCATATATGACATGCATAAACGAAGTGTATACAATTGAATACAATTCATTTAATACCATTGACACAAACTGTTTAACCAGGTGTACATTTGTCTACGGTACCCCCACTATGTA[T/A]ATCGACATGCTCGGACAGCCAGACCTGGCCAAGTTTGATTTGTCATCAGTTCGGGGTGGTGAGTCAATAAAATGTTTTTATAAAATCTAAAGTGTTGCTAAATGAAAGTTATCAATTAACTTATACACATTTGTCAAGGAGTACATTGTGCACTTCCATCAGTATTTTGCTAAGATGTAATTTTGTGTACTGTCAGGTATTGCGGCTGGATCTCCTTGTCCTCCTGAGGTCATGCGTAAAATCCTAAATGTCATGGGTATTAAGGAAATGGTGGTAAGTAGTTATTTATAATAAAAAAATGATTTCAAATTCTCTGATAATGATTGTCCAAATCACTAGAGGGAGACAGAGGTTTCCACATTACTGGTTTAGCAGCAGTTTTGGCAATATTTTCTGTTATGAATTGAACGAGCTCAGATCCACTCAGTTTATGGAACTTTTATTCTAGCTTTCATAAACGCATTCATTCTCTTCTGATAAAATCAGTGTGTTTAGTTGAC
Associated Phenotype:
Not determined