ZMP
acaca
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate acetyl-Coenzyme A carboxylase alpha (ACACA) [Source:UniProtKB/Tr
Human Orthologue:
ACACA
Human Description:
acetyl-CoA carboxylase alpha [Source:HGNC Symbol;Acc:84]
Mouse Orthologue:
Acaca
Mouse Description:
acetyl-Coenzyme A carboxylase alpha Gene [Source:MGI Symbol;Acc:MGI:108451]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa26588 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33724 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40568 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa20542 | Essential Splice Site | Available for shipment | Available now |
| sa2214 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa26588
Status:
Mutation detected in F1 DNA
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:
Not yet available
Founder:
SL4_05_C10
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083079 | Nonsense | 734 | 2356 | 16 | 52 |
| ENSDART00000146773 | Nonsense | 734 | 1190 | 16 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 57793745)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 55714344 |
| GRCz11 | 5 | 56384561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTATTTGTTAGAAATCATTTGAGTGTGTTTTATTTCATTCTCTAGGTA[T/A]CGCATCATTATCGGGAATAAGACGTGTGTGTTTGAAAAGGAGAACGACCC
Long Flanking Sequence:
TGTTGCTCTCGTATGATGGCAGCAGCTACACCACCTACATGAAGGAGGAGGTAGACAGGTAGGAGTCTGGGTGGAATTACGGGATAGAGGATACAGGGACATATTGTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAGGGGGGGCCCTTGGATTTGTTATAGCCCCAGGGCCCAGTGTGTTCTTAATACGGCCCTGCTTTCAGCCATTATAAATCAGTTTTTCATTTCTGATGCTCTGTTTGCTAAATTAAACAAGAAACATCAATTATTAAGGTCATGAATAAATTAACATTATTTTTTACACCCTTAAATAATAAAACATTTTCTATATTATAAATAATTAAACTTAAAATGAAATTAATCCTAATTCATTTAAGAGACTGCAATAAGGGAATAATGCTAAAACACGTATTTGTTAGAAATCATTTGAGTGTGTTTTATTTCATTCTCTAGGTA[T/A]CGCATCATTATCGGGAATAAGACGTGTGTGTTTGAAAAGGAGAACGACCCTTCAGTCCTTCGCTCTCCTTCTGCTGGGAAACTCATCCAGTATACAGTGGAGGATGGAGGACATGTGTTTGCTGGACAATGTTATGCAGAGATAGAGGTTTGAAAGGCAGCTTTAATCACTTTTCAGATTGACAAAGTGAGCATTAGCTATATTAGTGATGTAACAGACATTTTGGCAAAGACATTAAATGTCAGGAATAATGTAAAAAGTAAAAATTGATTTAGCTATAATTATATTAACATTCCATATAAACAAATAGTTTATCGTAAGTGCTGCTTAAATACATAATGATTGTTTTTGTTGTTTATCAGCTAGCAAAAATTTAAAAAGTGATTCCAATGATATTGTTTCTCTGTGTCATTATTGTTGTTGTCAACAACAATGCGATAACAACAATGGTCTTGTTTTTGTTTTGTGGACTTTTTGTGGACTTCGCTGTTCGTTAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33724
Status:
Mutation detected in F1 DNA
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:
Not yet available
Founder:
SL6_08_F11
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083079 | Essential Splice Site | 1351 | 2356 | 31 | 52 |
| ENSDART00000146773 | None | None | 1190 | None | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 57769794)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 55690393 |
| GRCz11 | 5 | 56360610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGGATTTCAGAAAGCAAATCAACTGTGAGGTGGACCAGAGGTTCCATG[T/A]AAGTCATTGTGGAATGTTTTAGACATTGGTACTGTTCCACAACCTACTGA
Long Flanking Sequence:
GTTTTTTTCTTCTCTCTTTTTCGCTGTAGAGCATTCAAGATGAGCCCATTCATATTCTTAATGTGGCAATAAAGACGGACAGTGATATTGATGATGATGGGCTGGCGGCCATGTTTCGTGAGTTTACACAGTCTAAGGTGAAGGAAGTTGTTCTGCTCTCTATGGGTTGCCTGTTTTTATTGGACATGTTAAAGTAATGTCTGACTCAGTAAGTTCAATTCTGATTATTTCTACTACAGAAATCTCTGCTGTTTGACCACGGCATCCGAAGACTTACCTTCCTGGTTGCTCAGAAGGTAAGCTTTCAAAGATGACTTTTGAGCATGCTTCTGATCTCCTGAAATCAGATTATATAATCTGCAATCGGTTAATTTGAATGACAGTAAATGATTGACTTCAGTTCTGCTCTGCTAACTGCATGTATGTGTGTTTGTCTTGGTACCGTTATTAACAGGATTTCAGAAAGCAAATCAACTGTGAGGTGGACCAGAGGTTCCATG[T/A]AAGTCATTGTGGAATGTTTTAGACATTGGTACTGTTCCACAACCTACTGAGCTGTTTTGCTGTCAACCTTTTTGGCAGCATCTTAACCAATATAGAACTTCACAAATGACTTAACTGAAACACTCATTCAAGCATACACTAGCAGTGTTGCTCTGCTAATGATTCATTTTTCATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTCATTTTAAACAATATGGAACTTCACAAATTACTTAACTGAAGCACTCATTCTAGTATATACTAACAAAGCTACTTCTCTGCAGAGTGTGATTAAACATTGCTAACAGTTCATTCTAGTAGAGGTCAATAAGTGTTGCTATGCTAATGATTCACTTCTTATTTTCATTATATTGGATTATATTATATTTTATTATATTACTCTATATTATATTATATTATATTATAATATATTATAATATATTACTCTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40568
Status:
Mutation detected in F1 DNA
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:
Not yet available
Founder:
SL7_02_G3
KASP Assay Location:
Unknown
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083079 | Essential Splice Site | 1437 | 2356 | 33 | 52 |
| ENSDART00000146773 | None | None | 1190 | None | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 57764443)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 55685042 |
| GRCz11 | 5 | 56355259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCTTCTTTGTGCGGGCAATCATCCGTCACTCAGATTTGGTCACCAAG[G/T]TAGGAGAGTCTCTGCTGTCTGAGATCACCTTCAAAAATCTGATTAGGTGT
Long Flanking Sequence:
ATTTTATTTTAAAATTTTATTTTACTTTAAATTTTATTTAGTTTTTTTAAATTTTTTATTAGTTTTTTTATTTTATTTTACTTTAATTTTTTTTATTTTATTTTTTATTTGACATACATGTGCATGCAAATAGAAATTAATCTTTGCACAAGGCTAGAGCAAACCACTGCGTTTATGAAAATATTTTTTCTAAGGAGTACATTTTGAGTTCTAGTACTTAATTAATACTAGTTAATATTTTAGATATTTTTCCAATTGTCAATTTGTTTATTTGTTTTTTTTAGTTTGAGGAAGACCGTATCTACAGACACTTGGAACCTGCATTAGCTTTCCAGCTGGAGCTCAACCGCATGCGTAATTTTGCACTGACAGCCATCCCCTGTGCCAATCATAAGATGCACCTGTACTTGGGAGCTGCCCGTGTGGAAGTAGGCACTGAGGTCACAGATTACCGCTTCTTTGTGCGGGCAATCATCCGTCACTCAGATTTGGTCACCAAG[G/T]TAGGAGAGTCTCTGCTGTCTGAGATCACCTTCAAAAATCTGATTAGGTGTTTGATACTGTTTGGTTCTATGCCGTGTAGGAAGCATCATTTGAGTACCTGCACAACGAGGCAGAACGCTTGCTGCTGGAGGCCATGGATGAACTGGAAGTGGCTTTCAACAACACCACTGTGCGAACCGACTGCAATCACATCTTCCTCAACTTCGTTCCAACAGTCATCATGGACCCTTCAAAGGTTTTAATAAGTTTGATTGGATTTTCTTGTTTCGTTGGTATACTGTATACAGTACTGAGAGAAAGTTTTTTGAGAAAAAACAAAAGAAAAAATAACTTTTTCACAGTACTCTATATATCAATACTTTATTTTCGGTGTCTTTATTAAGATACAAACAGAAAATATGGGAAGTATGTACACACACACACACACACAAACACATACACAGACACAGACAAAAAAGAAACAACAGCACAATTTTCACAATAGAATTACTTTAAATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20542
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:
Founder:
SL6_04_B9
KASP Assay Location:
Project 554.60, Plate 4, Well C01
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083079 | Essential Splice Site | 1986 | 2356 | 44 | 52 |
| ENSDART00000146773 | None | None | 1190 | None | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 57734291)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 55654890 |
| GRCz11 | 5 | 56325107 |
KASP Assay ID:
2259-6585.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGATCATGCAGCCATGGGCACAGAGTGTTGTCGTAGGACGGGCCAG[G/A]TAAGCACTGATTGATGCATACAACAGACACAAAAAGTATTTGAACTCAAG
Long Flanking Sequence:
CTAGTTTTGTATTAAACCATTTTTTACTGTTGACCTTTTTATATCTTGTGCTTTGTGGATGCGTTTTAGTGTCCAGTAATGGATGACTGTAGTTGGAGGGTTTATGTTTGAGGTACACACTAGGTCTCTCCACAAAGAGATAAGGCACTCTTGGATATATGGAGTGTTTTTTTATTGACTAGACTGATTACACATCACTGTAATTGCCACAGTGAGGTTGGGAGATATCGGGAGCGGGTGGCAGAGAGAGGAATCTTTGTCTCAGTGCTCAGACAGGTCTCAGTGTAATTGAACGGTAACCTCTTCTACAGCGAGCATATGCTTCTCTTCAGCTGAAGTCTGCATATGTCTGACAAAGAGAGGGTGCTAATGCTACTCTGATGGTCTCTTTTTCTGTAAACAGACATTAAGGGTGCATGGGTGAGTGGGTTCTTCGACCAGGGCTCTTTTCTGGAGATCATGCAGCCATGGGCACAGAGTGTTGTCGTAGGACGGGCCAG[G/A]TAAGCACTGATTGATGCATACAACAGACACAAAAAGTATTTGAACTCAAGTCTTATTACCATATGAATGCCTTTGTTTTGAGTCACAAAACAGGCATATAATGTCTTTGTATATATATATATTTTTTTTTTTTTTGAAAACTGTGCTTGTGGTATCATTCTTTTAAATAAATGGCACATCCAATATCATGCATTCACAAAATACAGATCTTTGTAATGATTAATCACACTCATCCGTGAACTTGTGTTGACCCCCTTTCCTGAATGCTTAAAGGGCTGCACTTGTCGATTGGAAAGGTCCTGCACTGATAAATGCACTTTGAAAGCTCCTTTGGGGAACATTAGCTCTATATGTCTTCTTGTGTTCTCTTTTAGTTGTTTGACACAATACAAACTGACATCGAATATGTCGATTTTGTTGAACTTGGTATTATCTGTCCACCTGATAAAGCCAGATATATATGTTTTGTTTTATTATGTTTGCATTTAAAATAAGTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2214
Status:
F2 line generated
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:
Not yet available
Founder:
mrf259
KASP Assay Location:
Project 554.26, Plate 19, Well E01
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083079 | Nonsense | 2188 | 2356 | 49 | 52 |
| ENSDART00000146773 | None | None | 1190 | None | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 57726582)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 55647181 |
| GRCz11 | 5 | 56317398 |
KASP Assay ID:
554-2696.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCTGGAGAGTAAACTAAAAGAGAGAGAAGAGTTCCTGCTGCCCATATA[T/A]CATCAAGTAGCTGTTCAGTTYGCTGACCTTCATGACACACCGGGCCGCAT
Long Flanking Sequence:
TCTGTCCAAACAGCTTACAAAACTTGACATTTTCATAGGTGCTCTTTAATAAAAGTGCTCTTAATGTTATTTAAATACTTTACAATTGTTTCTTTCAATTTTAATTTTTTTTTCAATGAATTAGTAGATGTAAGTTAATAACTATTAACAGTAACGTTGCAACTTACTTATTGTTTACCCATTTAACAATGTAATACTGTTTACAATTTTACAATTTAAAAACATGAGCCACAATAATGGCAATTAAGATTTACCATTTCTTATGGATTGATCTTTCTTCCGCAAACAAAAAAATCTCATTAAAAGGTTGTTGCTAAATATTATATCACAGGGTGGCCTTACTGATATAAGGTGCATATGTTTATATACATTCTCCACACTATTAAATTTGTTCATTTGTTTTCCTCTGTGTAATCAGGAACCCCAGAGTTGAGTGTGTCTGAGCGTAAAGAGCTGGAGAGTAAACTAAAAGAGAGAGAAGAGTTCCTGCTGCCCATATA[T/A]CATCAAGTAGCTGTTCAGTTCGCTGACCTTCATGACACACCGGGCCGCATGCAGGAGAAAGGAGTCATCACTGTCAGTACACTTCAATGCATTTCAATAACTCCCAAATACGTTTCTATTCATCTTTCTCCATACTGAACAATCTGAAGTTCATTTTATCTGTAATTGTCATGAATTTATGTGTACTCGATGTTCGCTTGTATTGTGCGTGTTCAGGATATCCTTGAGTGGAGCACGTCTCGGCAGTTTTTCTACTGGCGTTTGCGGAGGTTATTGCTGGAGGAAACGGTGAAGAGGAAGATCCAGTGTGCTAACAGTGAGCTGACGGACGGACAGGTTCAGGCTATGCTTCGCCGTTGGTTCGTGGAAGCAGAGGGAGCTGTGAAAGTACGTTACCCCAAACCTTTTTTTCCCCTCCAGATTATCAAAAATACTTTTTCAGAAATATTTTCCTTATCACTCAAACTATTTGTATATGTTTGAAAGAAGGATTTTGAGTA
Associated Phenotype:
Not determined