ZMP
si:dkey-283b15.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
CYTH2
Human Description:
cytohesin 2 [Source:HGNC Symbol;Acc:9502]
Mouse Orthologue:
Cyth2
Mouse Description:
cytohesin 2 Gene [Source:MGI Symbol;Acc:MGI:1334255]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11018 | Essential Splice Site | Available for shipment | Available now |
| sa22743 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11018
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000100848 | Essential Splice Site | 162 | 416 | 5 | 12 |
| ENSDART00000140226 | Essential Splice Site | 162 | 416 | 5 | 12 |
| ENSDART00000100848 | Essential Splice Site | 162 | 416 | 5 | 12 |
| ENSDART00000140226 | Essential Splice Site | 162 | 416 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 6880071)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 5724602 |
| GRCz11 | 16 | 5624228 |
KASP Assay ID:
2260-9159.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTGGATCTTCACGAGTTCACAGATCTGAACTTGGTACAAGCACTTCGG[T/A]AAATCAKTAATTCTTTATTGCATATCTTTAWCCTAAACAATTGTATCTTT
Long Flanking Sequence:
CGCGCTGCAGGTGGTCTGTTTAACTGTTTTCTCGTAGTAAAGTGATCAGTTTTTCCCCTTACAAAGTCCGCCATTTAAATAGCATATGTGCCAGGGCGCGACTGACTCTGATTGGGAGTCTCTGATTTATTTGATGCATGTTATTCTCAAAACACACCCATTACTCATTAAGAGAATAAGCACAAACCTGTTAGACCATGCGCCATGGCGCCAACCGTATTTTTGTCTGTTCTTAAAATAGCAAAAGTGGATTTGGACACGCCCTTAATGCTTTTGTACCATACACTTTAGACAAGGAGCCTTGATCATTAAAATAGAGCCCTAAATGTTTGTACATTGCCACAGTTTTTTAGTCTAGATTTGAAATAATTTAACATTAACATTATTATAATAAAACATTATTCTCCTTTTCTTTCAGAGATGACTTCAATATTAAGGTATTGCAGGCATTTGTGGATCTTCACGAGTTCACAGATCTGAACTTGGTACAAGCACTTCGG[T/A]AAATCATTAATTCTTTATTGCATATCTTTATCCTAAACAATTGTATCTTTGCTACTGTTCTGGATGTTTCTTTAAAGAGCATTTCTAGAAGCCGCTTGCTATTTTAGATTAATTCTGCATCGTCATGGTTAGTTTTGCAGTGTTTACACAGTATCTGTGTGCAGTGGTTGTTTTTATCACACTCTTGTTTTGTGAATGTTCACTACAGGCAGTTTCTGTGGAGTTTCCGCTTGCCAGGCGAAGCTCAAAAAATCGACAGGATGATGGAGGCCTTCGCACAGAGATACTGTCACTGCAATCCTGGAGTCTTCCAGAGCACAGGTCACACACACACACCACTTGTTTTTATACCCCAGTGGGGACTCTCCTGAAGTTGTTATATGTACGCTAGGAGTGTGGGATATTAAGTGTCTATGATAATATGGTAACTGTTGTTTTTATAATGTTCGCACCGATATCATGTCACTCGCAAAAAAATACACACTTCTTGAAAGTCCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22743
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 |
|---|---|---|---|---|---|
| ENSDART00000100848 | Nonsense | 361 | 416 | 11 | 12 |
| ENSDART00000140226 | Nonsense | 361 | 416 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 6889764)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 5734295 |
| GRCz11 | 16 | 5633921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAATAACCGCGGTCAGCTGATTAAAGCCTGTAAGACGGAGGCTGATGGT[C/T]GAGTGGTGGAGGGAAACCACATGGTGTACCGGATCTCTGCTCCCACCCCA
Long Flanking Sequence:
GTGTGTGTGTGTTTGTGTAGGATAAGGAGCCCAGAGGCATCATTCCACTGGAGAATCTGAGCATTCGTGAGGTTGAAGACCCGAGAAAGCCAGTAAGTTTGCTGATCTTTTCATTCATCAATGATAAAAGTGCTGTCACCTAGCTCTACTGTATTATATTTGCTTTATTTATAAGATTTTTTTAAGCAAGACAACCATGTTATTGCTTTCCCGTAAGAACATGTACTGCAGTTCATGTTTTATCTCCAAATGTTAAAAATTCTTAAAAGCATAAATAAATCAGAACATTATAAATCAAAGTTAGAAAGATAGCCTCTAGTTACTGAGTATAAATGACGAAGTTCAAGATAAATGCACCAAAACATTTCAGATCTTTGAGGTAATTTTTCAGTGGTTAAAGTGTCGCCTGCCTCAACGTTTCTGTACAGAACTGCTTTGAGCTCTACATCCCGAATAACCGCGGTCAGCTGATTAAAGCCTGTAAGACGGAGGCTGATGGT[C/T]GAGTGGTGGAGGGAAACCACATGGTGTACCGGATCTCTGCTCCCACCCCAGAGGAGAAGGACGAGTGGATACACAGCATCAAGTGAGGGATTTCTCAGCATCTTGGTTGACTAAACTTGCATTTACGGCAACATCATTCACACCGACCATAGTGCAAACTTTCATTTAGCCTCTGATAGACGTTTGAAATATATTTGCATTTCCTGATGCTGTTATCAGCATATGTGCTGGAGCGGGACAAAGAGGCTCCTTCAGGGTACAAGAACAAAAGATATGCACATTTGAAATGTAAATTTTGGGCTCACAAGAAATCCGATATGGCCTCTCTCAACATAATGCTGAAATACAGTATATTTGGCAAGGAGGAAAAAAAACCTTATAAATTAGCACTGATCATTATAGCATTTAAATTTGTATTTAGACTGAAACAGTTCATTCAACATTTAGTCAAAATATTTTAAAAGTCTAAATTAGCATTTTTGGTTTTTTATTGTTAATGT
Associated Phenotype:
Not determined