ZMP
SPIRE1 (2 of 3)
Ensembl ID:
Description:
spire homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:30622]
Human Orthologue:
SPIRE1
Human Description:
spire homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:30622]
Mouse Orthologue:
Spire1
Mouse Description:
spire homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1915416]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17650 | Nonsense | Available for shipment | Available now |
sa5897 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17650
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074718 | Nonsense | 188 | 206 | 6 | 6 |
ENSDART00000074718 | Nonsense | 188 | 206 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 56398603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 52909294 |
GRCz11 | 16 | 52795037 |
KASP Assay ID:
554-3897.1 (used for ordering genotyping assays)
KASP Sequence:
ATTGCATTTATTCTTTGATAWTTCTGTATTTRMAGTTGTRCTTYTGCTGT[C/T]GAACAAAGCRTTTTTCCCTCTTTACCYGGTCCTACACCTGTCAGTTTTGT
Long Flanking Sequence:
GCATGGAAATGGCCAAAACCCCTCTAAAACCAGCCTGGTCGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGATTTTTCAGCAGGGTGGGCAGCACACTGAACACATTTTATAATTGGTCAGAAACTTGTAAATAACTCATTAAAGAATAAAGTATTTTACATTAAAACCAAGCACATCATTGTTTTTCTTGTGAAATTCCCAATAAGTTTGATGTGTCACATGACCCGCTTCCTTTTGAAAAAACAAAAGTTGGATCCAAGATGGCCGACTTCAAAATGGCCACAATGGTCACCACCTATCTTGAAAGTTTACCCCCTCACATATACTAATGTGCCACAAACAGGACGTTACTATCACCAACCATTCCCATTTTATTAAGGTGTATCCCTATAAATGGCCCACCCTGTATTGTGAATATTAAGTATGACTCTCAATAATTGCATTTATTCTTTGATATTTCTGTATTTACAGTTGTGCTTCTGCTGT[C/T]GAACAAAGCGTTTTTCCCTCTTTACCTGGTCCTACACCTGTCAGTTTTGTAAAAGGTAATAAATAACCTATCATTCAGCTTTGTATTCAATGCATTTTTGTAGATTTATATAGAAAGCAAGACAGAAGACTCATCCTTTCCTGTATTTTTGCAGGCCAGTGTGTTCACAGTGCTGTAAAAAAGTAAGTCACGGTCTGTACAGATTGTTCATGTACGCGTCCTAATTGAAGGCACAATATGTAAATCTTTATTTTGATTATTTGTCTAGATTTGAACATTCTTTGAAACATTTGGGATAATGCAAGTAAATAAGTAAGCAATATGTATAAATATACACTCACCGGCCACTTTATTAGGTACACTTGTCCAACTGCTTGCTAACGCAAATTTCTAATTAGCCAATCACATGGCAGCAACTCAATGCATTTAGACATGTAGACATGGCCAAGACGATCTGCTGCAGGTAGCAGTTACCGAGCATCAGAATGAAGAAGAAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5897
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074718 | Nonsense | 188 | 206 | 6 | 6 |
ENSDART00000074718 | Nonsense | 188 | 206 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 56398603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 52909294 |
GRCz11 | 16 | 52795037 |
KASP Assay ID:
554-3897.1 (used for ordering genotyping assays)
KASP Sequence:
ATTGCATTTATTCTTTGATAWTTCTGTATTTRCAGTTGTGCTTYTGCTGT[C/T]GAACAAAGCGTTTTTCCCTCTTTACCTGGTCCTACACCTGTCAGTTTTGT
Long Flanking Sequence:
GCATGGAAATGGCCAAAACCCCTCTAAAACCAGCCTGGTCGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGATTTTTCAGCAGGGTGGGCAGCACACTGAACACATTTTATAATTGGTCAGAAACTTGTAAATAACTCATTAAAGAATAAAGTATTTTACATTAAAACCAAGCACATCATTGTTTTTCTTGTGAAATTCCCAATAAGTTTGATGTGTCACATGACCCGCTTCCTTTTGAAAAAACAAAAGTTGGATCCAAGATGGCCGACTTCAAAATGGCCACAATGGTCACCACCTATCTTGAAAGTTTACCCCCTCACATATACTAATGTGCCACAAACAGGACGTTACTATCACCAACCATTCCCATTTTATTAAGGTGTATCCCTATAAATGGCCCACCCTGTATTGTGAATATTAAGTATGACTCTCAATAATTGCATTTATTCTTTGATATTTCTGTATTTACAGTTGTGCTTCTGCTGT[C/T]GAACAAAGCGTTTTTCCCTCTTTACCTGGTCCTACACCTGTCAGTTTTGTAAAAGGTAATAAATAACCTATCATTCAGCTTTGTATTCAATGCATTTTTGTAGATTTATATAGAAAGCAAGACAGAAGACTCATCCTTTCCTGTATTTTTGCAGGCCAGTGTGTTCACAGTGCTGTAAAAAAGTAAGTCACGGTCTGTACAGATTGTTCATGTACGCGTCCTAATTGAAGGCACAATATGTAAATCTTTATTTTGATTATTTGTCTAGATTTGAACATTCTTTGAAACATTTGGGATAATGCAAGTAAATAAGTAAGCAATATGTATAAATATACACTCACCGGCCACTTTATTAGGTACACTTGTCCAACTGCTTGCTAACGCAAATTTCTAATTAGCCAATCACATGGCAGCAACTCAATGCATTTAGACATGTAGACATGGCCAAGACGATCTGCTGCAGGTAGCAGTTACCGAGCATCAGAATGAAGAAGAAAGGG
Associated Phenotype:
Not determined