ZMP
zgc:64103
Ensembl ID:
ZFIN ID:
Description:
flotillin 2 [Source:RefSeq peptide;Acc:NP_956933]
Human Orthologue:
FLOT2
Human Description:
flotillin 2 [Source:HGNC Symbol;Acc:3758]
Mouse Orthologue:
Flot2
Mouse Description:
flotillin 2 Gene [Source:MGI Symbol;Acc:MGI:103309]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15634 | Essential Splice Site | Available for shipment | Available now |
| sa35840 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15634
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101157 | Essential Splice Site | 116 | 177 | 4 | 7 |
| ENSDART00000101789 | Essential Splice Site | 116 | 428 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 15414675)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 16459638 |
| GRCz11 | 15 | 16395660 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGCTGTGGTTCTGCAAACCCTTGAGGGACATTTGCGTTCAATCTTAGG[T/C]TAATACATCACCAAGAATTACAATAACCTYATTAAAACTAACASTTCCTT
Long Flanking Sequence:
TAAAAGCATAAAATCTAAAAAAAAAATTTATAATAAGATTTATTAATATTAATATTTTTAAGTCCTTCATTAATCTTCAGGACACAAATTAAGATATTGTAGATGAAATCTGAGAGCTCCCTCATCCTCCATAGACAGCAACACTCCCAACTTATTCAAAGTTCAGAAATTAAAAACAAAATTACATGTTATGGGTAAACTGAACCATTAATGAGCGATGGAAACAACTTATCCAAAACAACTAATTCAGTAATAAACACAGGAAGTGTAAACAAAGGAGCTTCATCAATGTATCATTAAACAATGCACACCCCCTATTTCAAGTTATTTTTGAAGAGTTCAAAATGTGGATAACTGGTGCATTCTGTTTTCCAGGTCAAGGTTATGACTGACAAAGACTTGCTGGCTATTGCTTGTGAGCAGTTTCTGGGAAAGTCTGTCATGGAAATCAAAGCTGTGGTTCTGCAAACCCTTGAGGGACATTTGCGTTCAATCTTAGG[T/C]TAATACATCACCAAGAATTACAATAACCTTATTAAAACTAACACTTCCTTCTATGATTTTTAATGTTGTGTTGCTGTTCAACAACAGGCACATTAACCGTGGAGCAGATCTACCAGGACAGAGATCAGTTTGCTCGGCTGGTGAGAGAGGTGGCAGCTCCTGACGTGGGCCGCATGGGCATCGAGATCCTCAGCTTCACTATCAAAGTAAGTTATGAGGGTTTTGAATGCAAAATCACTCAAGATGCAGAATAGATGTGCATTAGCCGTCATGCATTTTGCAATAAACAAATAAAAGCACATTTTGAGAACAAACAAAACCCATCCAGAGATATTGTTTGTTTTTATAAATGTAATTATATGTTCATTCTAACTGCCTTCTAACTGGCTTCATCATGCAGTTGATTCCTTTAGACCAAGGGTATCCAATTTCTGTCCTAGAGGGTCGGTGTTCTGTTGAGTTTAGCTCCAACTTGCTTCAACGCACTTGCCAGGAAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35840
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101157 | None | None | 177 | None | 7 |
| ENSDART00000101789 | Essential Splice Site | 233 | 428 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 15417574)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 16462537 |
| GRCz11 | 15 | 16398559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCTTGAGCTGCAAAAAGCCGCTTTTAACCAAGAAGTAAACACTAAGG[T/G]CAGATTCAATGTAATTCCAGTGCCTGGCCATCTTTTTTAGTCATGGTCAT
Long Flanking Sequence:
CCACAAAAATATTGAGCAATATTTCAGCATTGATGGATATTTTGAATTATAGTTAATAAAATATTCTTCATCTAATAATGTATCTATAAATCAACCATAAAGTATCATTTCCTAACACATTTACCTCCTATCAGGTTATTTACTTTACTATACTCTGACACTTGTCTCTCCAAACAGGATGTTTACGATAAGCTGGACTACTTGAGTTCTCTTGGAAAGACGCAGACAGCTGCTGTACAAAGAGACGCAGACATCGGAGTGGCCGAGGCAGAGAGGGATGCTGGGATTAGAGTAAGAGGCTTCTGTCTTAGTTTTCTTTACGGCTAATGCATTATCCATTAGATACACGGTCTTCAAAGCTGCTGTTTTCTCCCATCAGGAAGCTGAATGCAAGAAAGAAATGATGGATGTGAAGTTCTTGGCCGACACTAAAATGGCCGACTCCAAACGAGAGCTTGAGCTGCAAAAAGCCGCTTTTAACCAAGAAGTAAACACTAAGG[T/G]CAGATTCAATGTAATTCCAGTGCCTGGCCATCTTTTTTAGTCATGGTCATTGGGTTAGTGATGTTTGCGTTTGTCCACCTCGCAGAAAGCCGAGTCTCAACTGGCCTATGAGCTGCAAGCCGCTAAAGAGCAGCAGAAGATCCGATTGGAGGAGATCGAAATCGAGGTTGTGCAGAGGAAAAAACAAATCTCCATAGAGGAGAGGGAGATTGAGAGGACAGAGAAGGAGCTCATCGCTACGGTCAAGCGGCCGGCTGAAGCCGAGGCTTACAAGATGGAGCAGCTCGCTGAAGGATACAAGTGAGTCCTGTATCTTATCAACTCTTTATAAAGCTCACATCTGTCTATCCATATTTTTTAGAGATCTTTTTATCATTTTTGTACCACATAGTGTTAAATTTAGAGGTGCCATAAAATGAAAGTCTACATGTATCTAGGGATAGCTGAATAATAAGAGAATAATAAGAACATAGTAATGACACTGTGAACATCAAGCATGG
Associated Phenotype:
Not determined