ZMP
zgc:165571
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC335309 [Source:RefSeq peptide;Acc:NP_001092702]
Human Orthologue:
AGR2
Human Description:
anterior gradient homolog 2 (Xenopus laevis) [Source:HGNC Symbol;Acc:328]
Mouse Orthologue:
Agr2
Mouse Description:
anterior gradient 2 (Xenopus laevis) Gene [Source:MGI Symbol;Acc:MGI:1344405]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa27478 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa27479 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27478
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085763 | Essential Splice Site | 98 | 168 | None | 8 |
| ENSDART00000139019 | Essential Splice Site | 98 | 105 | None | 7 |
| ENSDART00000085763 | Essential Splice Site | 98 | 168 | None | 8 |
| ENSDART00000139019 | Essential Splice Site | 98 | 105 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 46665737)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 45797017 |
| GRCz11 | 9 | 45597496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCTAAAACAGCACAGATATTCACAAGAGTTTTGTGATTGTGAATTTC[A/C]GCATGAGACCACCGATACCCACTTGGCCCCAGATGGCTTCTACGTTCCCA
Long Flanking Sequence:
CAGAGTGAACACCTTCATGAACACGGGGAGAACATGCAAACTCCACACAGTAATGTCAACTGACTCAGCTGGGGCGCAAACCAGCAACCTTCTTGCTGTGAGGCAACAGTGCTAACCACTGAGCCACTGTGCCACACCATCTGCTAATTTGTGTACTTCAAGTGCTAAAATCTACTTTAAAAGTGCTAAAATATGGGTTTAATAAGGTACGAAAGTGTAGCTTTTGCGTTTTCATTCCTGAGAGTAAAGAGTAACGTGTCTGTATTATATAGAAAGTTCTGTTGCACTTCAATTGATTTATTTCCTCCAATACTCTATTTGTAGCTCTGAAAAAGGCATTTTCTGAACATCAGTCAATTCAACGGATGGCCAAATCAGAATTCATCATGCTCAATTTAGTGGTAAAGTAGAACTATTGTCATACTTTCAGCAGACTTTAACAAGAAATATGTGTCTAAAACAGCACAGATATTCACAAGAGTTTTGTGATTGTGAATTTC[A/T]GCATGAGACCACCGATACCCACTTGGCCCCAGATGGCTTCTACGTTCCCAGGATCATGTTTGTTGGTAAGTTTTTACGCTTTTGATTAAATACTACATTTTTATAATTGATCTGGTTACAAATACCTAAGTCTCTGGTACGGAGGATTTATTTATTTAAGTTTAATGCCATATCAGGAGCTTTGGCTATATTCATGACAAAACTAAATATACAAGATATACCATGCAATCATATCAGTACATATCAGTACAAACATACAAATAACAAAAACACAGAAGAGTCAAATACAATCTTTTAGTTTAATAATGATAAATATTCTAAAATTTCCCGTAAAATATTTCCTGAATAAAAACATTTTCTTAAATCATTTAAAAATACACATTCTATTAAAATATGTTTTATTGTCAGCATTTTCTTACACAAGTCACAAATAGGTTTTTCTTCCTTTATCAATACATATGAGTGTGTAAGTCTTGAGCATAGATATATACACTAGATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27479
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085763 | Essential Splice Site | 98 | 168 | None | 8 |
| ENSDART00000139019 | Essential Splice Site | 98 | 105 | None | 7 |
| ENSDART00000085763 | Essential Splice Site | 98 | 168 | None | 8 |
| ENSDART00000139019 | Essential Splice Site | 98 | 105 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 46665737)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 45797017 |
| GRCz11 | 9 | 45597496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCTAAAACAGCACAGATATTCACAAGAGTTTTGTGATTGTGAATTTC[A/C]GCATGAGACCACCGATACCCACTTGGCCCCAGATGGCTTCTACGTTCCCA
Long Flanking Sequence:
CAGAGTGAACACCTTCATGAACACGGGGAGAACATGCAAACTCCACACAGTAATGTCAACTGACTCAGCTGGGGCGCAAACCAGCAACCTTCTTGCTGTGAGGCAACAGTGCTAACCACTGAGCCACTGTGCCACACCATCTGCTAATTTGTGTACTTCAAGTGCTAAAATCTACTTTAAAAGTGCTAAAATATGGGTTTAATAAGGTACGAAAGTGTAGCTTTTGCGTTTTCATTCCTGAGAGTAAAGAGTAACGTGTCTGTATTATATAGAAAGTTCTGTTGCACTTCAATTGATTTATTTCCTCCAATACTCTATTTGTAGCTCTGAAAAAGGCATTTTCTGAACATCAGTCAATTCAACGGATGGCCAAATCAGAATTCATCATGCTCAATTTAGTGGTAAAGTAGAACTATTGTCATACTTTCAGCAGACTTTAACAAGAAATATGTGTCTAAAACAGCACAGATATTCACAAGAGTTTTGTGATTGTGAATTTC[A/C]GCATGAGACCACCGATACCCACTTGGCCCCAGATGGCTTCTACGTTCCCAGGATCATGTTTGTTGGTAAGTTTTTACGCTTTTGATTAAATACTACATTTTTATAATTGATCTGGTTACAAATACCTAAGTCTCTGGTACGGAGGATTTATTTATTTAAGTTTAATGCCATATCAGGAGCTTTGGCTATATTCATGACAAAACTAAATATACAAGATATACCATGCAATCATATCAGTACATATCAGTACAAACATACAAATAACAAAAACACAGAAGAGTCAAATACAATCTTTTAGTTTAATAATGATAAATATTCTAAAATTTCCCGTAAAATATTTCCTGAATAAAAACATTTTCTTAAATCATTTAAAAATACACATTCTATTAAAATATGTTTTATTGTCAGCATTTTCTTACACAAGTCACAAATAGGTTTTTCTTCCTTTATCAATACATATGAGTGTGTAAGTCTTGAGCATAGATATATACACTAGATAT
Associated Phenotype:
Not determined