ZMP
zgc:113405
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate astrotactin 1 (ASTN1, zgc:113405) [Source:UniProtKB/TrEMBL;Acc:B
Human Orthologue:
ASTN1
Human Description:
astrotactin 1 [Source:HGNC Symbol;Acc:773]
Mouse Orthologue:
Astn1
Mouse Description:
astrotactin 1 Gene [Source:MGI Symbol;Acc:MGI:1098567]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19808 | Nonsense | Available for shipment | Available now |
sa16944 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19808
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077216 | Nonsense | 437 | 1319 | 6 | 23 |
ENSDART00000098764 | Nonsense | 387 | 424 | 5 | 5 |
ENSDART00000134926 | None | None | 177 | None | 4 |
ENSDART00000141796 | None | None | 114 | None | 4 |
ENSDART00000145451 | None | None | 714 | None | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 34440926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 34737636 |
GRCz11 | 2 | 34720093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGATCGGCCTGGTCTGTGCGTCTCACCTTTCCTGTAGCCTGAACGTC[A/T]GAGTGATCCTTCACGTACCGGAGCATCTCATTGCAGACGGTAATCTCATC
Long Flanking Sequence:
CAATGTTGTGTGCCTAGATTTGACATGTAACAGATGTACGGCACAGCACTACACCAAACCAGCTTGGCTGTATCACACAAAAATTGATAAAAAACAACTTACCCCCCCACACCCCAAAAAAATATTGCCATTTGCAGTATTTAGCATAAAAGCAGCATGCATCAAAAGGTAAACCGTTATCTCCCCACTGCTCTATTCGTGCCAGAGCTACTGGCGCTCTCCGAGTTTGGCTGGCTGGTTTGATCCAGTGCTCCTTTCATGGACCACCAACCCTGATGTGGTCTGTTTTTTAACCGTCTCCCTTGTGCCTTCCCGACATGCACATAAAAATGTGAACTTTCTAGACTTGTAGCATCGCTTGTTTATTGCTTCCTCTTTCTGTCTTCTCCTCAGGTTCCCCACGGAGTCCTATCAATAAGACCACCCTCACTTTGATCAGCGTGGTGAGCTGTGTGATCGGCCTGGTCTGTGCGTCTCACCTTTCCTGTAGCCTGAACGTC[A/T]GAGTGATCCTTCACGTACCGGAGCATCTCATTGCAGACGGTAATCTCATCACCCGCTCCGCTTCCCGTCCGGCCCCTGAACAGTGGGGCTCCTCGGCCCCCCGTCTACCACCATAACTATTACTGCACTAAAGCAAATGTCACACCGACTCCTGCTTTGTCTCTGGTGAAAAGCACAGATGTGTTTTGAAAGCATCAAAGCACAATCGGACATGAATGCATAGTCTCTAGTTGTGTGTCAAACGATGCACTATACACCGTGTGCTTGTACTGCACACTGTGTACCAGTTAATACATTTTTAAATGTGATGGTCTCACATTAAATACTAATGTTTATTTTATTTTTAACACAGCATTCCCTCAATTTGGTTGTTGTTAGCTTTAGCGTGTTAGCTAAACTACAGTGAGCCTGGTGCGTAACCTGTAATGTGTTGTTAGAACTTTATCTTTCTGTTGTTACAAGTAATAGAATAAAAAGATGCTGCAGTGAACTTTGTACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16944
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077216 | Essential Splice Site | 1101 | 1319 | 19 | 23 |
ENSDART00000098764 | None | None | 424 | None | 5 |
ENSDART00000134926 | None | None | 177 | None | 4 |
ENSDART00000141796 | None | None | 114 | None | 4 |
ENSDART00000145451 | Essential Splice Site | 496 | 714 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 34647072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 34943782 |
GRCz11 | 2 | 34926239 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTCAGGAGAAGGTGACAGAGCGGACTGATCACTCCAAAGTTGAGACGG[G/A]TAAGCTTGAATAATRTACACATTCCCATCRGTGACCATAGAATAAACACA
Long Flanking Sequence:
GAAAGTAGTCCTAGTTATTTAAAATTTACATATTTTTCATAATTGTTATTAATAATTGTAAACTTTTAACATGTTCTTCATCTTTGTCTTCTCGTGCAGGCTCTGCAGGAGGCCATGATGAGTGTTTTATGGTGCTCTGCTAAAGGGGATGTTATTGATGACTGGTGCAGATGTGACTCCAATGCTTTTGGCACAGATGGACTGCCAACCTGTGCTCCGCTGCCTCAACCTATGTGAGTTCAAGCAATATCCTCAGTTTAAATGTCCGAAGTAAGGCCTTAAAGTTCAGATCTTGATCAATCAATTAGTCATGAATGGTAGTAAAAGTTGATTTCATGCTCTTGCCAGGCTCAAACTGTCCCATTCGTATGAGCCCAGCAGCTCATTGGTCATCATAGAATGGAATCACACAGAGCCACCAATTGGAGTGAGGATTGCTGATTACCTCATCAGTCAGGAGAAGGTGACAGAGCGGACTGATCACTCCAAAGTTGAGACGG[G/A]TAAGCTTGAATAATGTACACATTCCCATCGGTGACCATAGAATAAACACACACACTCATACACAGAGTAGGAACAATACTTAAAGCTCACTTATATTAGCGGCTGTATAACAAGTGGGATAATGAATATTTAGCCAGTCATTATCAAAAATTAAACCCCTTCAGGGTGAAACAGGAGACCGCTGCCTCATGCTGGAGTCCTGATCATCCTGCCAGGGAATTAATTTGTGATAATGACAACTGTCTGCAAATGAATGCACTGAGACTAAACCACAAAAAATTTAATAATCTAACCATATATTATGTTGAAAAAATACAATTAAAAGGCATTAACATAAAGATGGCAGCGGCTCAGTGGTCGCACTCACAGCACAAAGGTCGTTGGTCCGAATTTCGACTGGGCATTTTTGTGTGAAGTCTGTGTGTTCTCCCCAAGTTGGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAACTCCAAAGACATATGCTATAGTAT
Associated Phenotype:
Not determined