ZMP
zgc:110283
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC550268 [Source:RefSeq peptide;Acc:NP_001017605]
Human Orthologue:
ANXA1
Human Description:
annexin A1 [Source:HGNC Symbol;Acc:533]
Mouse Orthologue:
Anxa1
Mouse Description:
annexin A1 Gene [Source:MGI Symbol;Acc:MGI:96819]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38522 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
This allele has been removed from public view.
Allele Name:
sa26607
Status:
Less stringent filtering
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:
n/a
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064512 | Essential Splice Site | 153 | 340 | 6 | 13 |
| ENSDART00000073926 | None | None | 283 | None | 11 |
| ENSDART00000131368 | None | None | 35 | None | 4 |
| ENSDART00000133044 | Essential Splice Site | 153 | 198 | 6 | 8 |
| ENSDART00000144620 | Essential Splice Site | 153 | 198 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 67507926)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 64309567 |
| GRCz11 | 5 | 64998564 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGGACAAACAAGGAGATCACGGCGCTGAAGAATAGTTTCAAAGAAGG[T/G]AGCAAAAATCACATAAATACTACATACCAAAGCAGATTTACTGAATGTGT
Long Flanking Sequence:
TTTTCTGTTTAAAAAAGCTGTCCCAAAAAAAAAAATGCTGGGAAATGCTGGAAACCAGTAGCCATTGACATCCTTAATAGGGAAAAAGGGCACTATGTAAATCAATATATACCAGTGTCAAACATTCTTCAAAATATTTTCTTTTGTGTTCAACAGAAGGAACAAAAAAAACTTAAACACGTTTGGATCAGGTTTTTATTTTTGGGTGAACTATTCCTTTTATATTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTGAAAACATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGATTGAATGTTCCTTTTATAAACAAATGTACTTACATGCATACTTAATTGATACTCAGGGTCTTGGGACAAAAGAGAATGTCCTGAGTGAAATTCTGGGGACAAGGACAAACAAGGAGATCACGGCGCTGAAGAATAGTTTCAAAGAAGG[T/G]AGCAAAAATCACATAAATACTACATACCAAAGCAGATTTACTGAATGTGTAAGCTGCTTTACTTTTTCAGTAACACTTTAGTTTAAGTAATAATTCACATCATTTACTAATGGCTTATTAACTGCCTATTATTAAGACATGAACTGTTCATCAGCACTTATTCAGTGATCTTATTTTACTTCCCCAATCCTACCCAATACCTAAACCCAACTACCTTACTTACTATTAAGCAGCTAATTAGTAGTTTATTGAGCTAAAAGTCTTAGTTAATAATGCAACAAAATAAATCTGACCGCTTTTATGTTGTGCAGTCTATAGAGAGACGCTGGAGGAAGATATTAAACATGATGTTAGTGGAAATCTTGAAAATGTCCTGCTTTCCCTTTGCAAGGTAAAAAAGTGCAATATTGGCGGTGAATTTAATTTGTATGAGTATTGCATATAGGTGATTATTATATGAATTGCATAAACAATTACATATTAATGTTTCCTCAGGCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38522
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064512 | Nonsense | 242 | 340 | 10 | 13 |
| ENSDART00000073926 | Nonsense | 185 | 283 | 8 | 11 |
| ENSDART00000131368 | None | None | 35 | None | 4 |
| ENSDART00000133044 | None | None | 198 | None | 8 |
| ENSDART00000144620 | None | None | 198 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 67505758)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 64322723 |
| GRCz11 | 5 | 64996496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAAATCCACAGTTTTCCAATATTATGGTCAATTTAGTAAAGATGGTT[T/A]GGCCAAAGATCTGCAGAGCGAGCTAAGTGGAGACTTTGAAGACTGCATGA
Long Flanking Sequence:
TGTGTCATTATTCAAAACTTCTTCATTAAAATCTTTGTTGTTGAAAACAAATAATATAAAGTTGGAGATGCGAAATGTGACTACAATTATAGAATCACCCATATATAGCAGTTGTGTTGGTGTGTAACAATTAAACAACATGAACTTAGCATAGTTTGTTGCAATTTGCTAAATATCTGACTTCTCAATACCTGGCCAATCACAGTCATTTATTGTAGACTGTTATCAAGTAAGGATTGTACATTAAAACGCATGAATGATATACGTTCTCGTGTTGTTTCAGGCTCTGTTTGAGGCAGGAAAGAATCGGATTGGTACAGTTTGCTCAGTTCTGATTGACATCCTCACAAACAGGAGTGAAGCTCAGCTGTGCAAAAGTAGGATATTTGACTTTCAGTGTGATATAGCGGTGAAGCCCAGCTAATGTTTACTGAGGAGTTAACAGTGTTATTGAAAATCCACAGTTTTCCAATATTATGGTCAATTTAGTAAAGATGGTT[T/A]GGCCAAAGATCTGCAGAGCGAGCTAAGTGGAGACTTTGAAGACTGCATGATGACGCTGGGTAAATATACTGTACACGTTTTCTTTTCTTTGTTTCTGTGTACTGTATTCATGTGGGTGTTAAAAACAGAAACTAGACAAACGCTTCACTGTCCATCTGAATAAAGGAGGCTTCCTAAAATCTGTTAGCAAGACAGGCCTGTTCTTCCAGCTTTGCATGTTCAGTGTGTTTTCATTCAAATGTCCAAAATGGATCGCATCAGATCCAAGAGTGAATAAATGTAAAACATGTATAAACTGCATTCCCAACAGTGTAATCTCTCTCTTATGTTTTAGTGAAGGTTGCTTGGAATAAACCTGCCTACTTTGCAGAAAAGCTCCAACATGCTATGAAGGTAAAGTTGCAAAGGGTTCATTCATTCATTCATTCATATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTTATATAT
Associated Phenotype:
Not determined