ZMP
acbd7
Ensembl ID:
ZFIN ID:
Description:
acyl-CoA-binding domain-containing protein 7 [Source:RefSeq peptide;Acc:NP_001122240]
Human Orthologue:
ACBD7
Human Description:
acyl-CoA binding domain containing 7 [Source:HGNC Symbol;Acc:17715]
Mouse Orthologue:
Acbd7
Mouse Description:
acyl-Coenzyme A binding domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:1925495]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39103 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42740 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39103
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
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046209 | Essential Splice Site | 44 | 88 | None | 4 |
| ENSDART00000141708 | Essential Splice Site | 44 | 67 | None | 3 |
| ENSDART00000046209 | Essential Splice Site | 44 | 88 | None | 4 |
| ENSDART00000141708 | Essential Splice Site | 44 | 67 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 30825627)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 28662765 |
| GRCz11 | 16 | 28597388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTGTACGGCCTCTACAAACAAGCTGTTGTTGGGGATATTAATATTGG[T/C]AGGAACCGATTAATTTGATTTGTTTGGTTTTGTTTTTAAATCCATATTAT
Long Flanking Sequence:
CTTCTGGATGTGCACTCGTCAGTGAGTTACGTCATTCGTCGCTCATCTTTGCTTTAGTATGAAGTTGCGCTATGCGTATCTTATACACAAATTGTTCGTTTTGTATTAGAGTCTTGTGGAGTTGGCCCTCAACATGGCAACCCATAGCTTGTAGGTTTATAATGGTACAAAGGGCACAATGTTGGCAACATGCAACTATTAGTTCATTGTGGCAATAAAACAAAAGGCTTCATACAGTGCGCGAATAATACACGATGCAAAGTGATTAAGGAAGTGCTTAGTGGGGCAAAATGGGTCAGACCTACCAAGCTTTTTGCAGTTGTTACCAGCAGATAAGCATTATGAGAATTAACGCTGAAGTCATGATGTTTGTGGCTACAGGCAGAATTCGATCAATATGCAGAGGATGTGAAGAAAGTCAAGACCAGACCTACAGACCAGGAGCTGCTGGATTTGTACGGCCTCTACAAACAAGCTGTTGTTGGGGATATTAATATTGG[T/A]AGGAACCGATTAATTTGATTTGTTTGGTTTTGTTTTTAAATCCATATTATATAAATCCAAATATTTTAAATTAAACCATCAGTTGCAGATAAACTGAGAATTTTTAAGAGGTCTCATATTTTGCTGTTGTTCCATTTCTACACACACACACACACACACACACACACACACACACACACACACACACACACAGAAAACTATATTTATGTAGTAGTTTATCTCCAATAATTATTTATTTACTCCATTTATAAGTTTATTGTTATGAAAAATACACAAGAATATTATTTTAAAATATTGTAAAAAAACATATACAACAATGTTGTACTTTTGTTGTACAACAAAGTACAATAAATAATAATAATAATTTATGTCAATGTGTAAGTGGGTTTCCAGTTGCAAATTATTGATTATTTTTAATTATTTTATTAATTTAATTATAAATTTTGTTTAATTTAGTTTCCAAATCATTTCTAATGTGCACATTTATAAAGTTGAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42740
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046209 | Essential Splice Site | 44 | 88 | None | 4 |
| ENSDART00000141708 | Essential Splice Site | 44 | 67 | None | 3 |
| ENSDART00000046209 | Essential Splice Site | 44 | 88 | None | 4 |
| ENSDART00000141708 | Essential Splice Site | 44 | 67 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 30825627)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 28662765 |
| GRCz11 | 16 | 28597388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTGTACGGCCTCTACAAACAAGCTGTTGTTGGGGATATTAATATTGG[T/C]AGGAACCGATTAATTTGATTTGTTTGGTTTTGTTTTTAAATCCATATTAT
Long Flanking Sequence:
CTTCTGGATGTGCACTCGTCAGTGAGTTACGTCATTCGTCGCTCATCTTTGCTTTAGTATGAAGTTGCGCTATGCGTATCTTATACACAAATTGTTCGTTTTGTATTAGAGTCTTGTGGAGTTGGCCCTCAACATGGCAACCCATAGCTTGTAGGTTTATAATGGTACAAAGGGCACAATGTTGGCAACATGCAACTATTAGTTCATTGTGGCAATAAAACAAAAGGCTTCATACAGTGCGCGAATAATACACGATGCAAAGTGATTAAGGAAGTGCTTAGTGGGGCAAAATGGGTCAGACCTACCAAGCTTTTTGCAGTTGTTACCAGCAGATAAGCATTATGAGAATTAACGCTGAAGTCATGATGTTTGTGGCTACAGGCAGAATTCGATCAATATGCAGAGGATGTGAAGAAAGTCAAGACCAGACCTACAGACCAGGAGCTGCTGGATTTGTACGGCCTCTACAAACAAGCTGTTGTTGGGGATATTAATATTGG[T/C]AGGAACCGATTAATTTGATTTGTTTGGTTTTGTTTTTAAATCCATATTATATAAATCCAAATATTTTAAATTAAACCATCAGTTGCAGATAAACTGAGAATTTTTAAGAGGTCTCATATTTTGCTGTTGTTCCATTTCTACACACACACACACACACACACACACACACACACACACACACACACACACACAGAAAACTATATTTATGTAGTAGTTTATCTCCAATAATTATTTATTTACTCCATTTATAAGTTTATTGTTATGAAAAATACACAAGAATATTATTTTAAAATATTGTAAAAAAACATATACAACAATGTTGTACTTTTGTTGTACAACAAAGTACAATAAATAATAATAATAATTTATGTCAATGTGTAAGTGGGTTTCCAGTTGCAAATTATTGATTATTTTTAATTATTTTATTAATTTAATTATAAATTTTGTTTAATTTAGTTTCCAAATCATTTCTAATGTGCACATTTATAAAGTTGAACATA
Associated Phenotype:
Not determined