ZMP
zfyve28
Ensembl ID:
ZFIN ID:
Description:
Lateral signaling target protein 2 homolog [Source:UniProtKB/Swiss-Prot;Acc:A0JMD2]
Human Orthologue:
ZFYVE28
Human Description:
zinc finger, FYVE domain containing 28 [Source:HGNC Symbol;Acc:29334]
Mouse Orthologue:
Zfyve28
Mouse Description:
zinc finger, FYVE domain containing 28 Gene [Source:MGI Symbol;Acc:MGI:2684992]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14866 | Essential Splice Site | Available for shipment | Available now |
| sa11552 | Nonsense | Available for shipment | Available now |
| sa32170 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14866
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085124 | Essential Splice Site | 174 | 971 | 5 | 15 |
| ENSDART00000139980 | Essential Splice Site | 174 | 975 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 43626838)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 43591513 |
| GRCz11 | 17 | 43582051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGTGTATACATTAACATKTTGTAATGATATCCCATATCTGTTTGCTGT[A/T]GTTATGTGTCRGCCATGGTGCCTGTGAAGTCTCCTAASGAGTATTACATC
Long Flanking Sequence:
TATCATGCAAAATCAGCAGGCTACAAGACATATACTTGTTGCATAACATGTATGTACAGAACAATGCATTTTTAATTATTCCATTCTAGTGCAACCATAAAGAGTAAAAAAATATTGCCCCACAGTATGAGAAATAAACTGCTCATGACAGGGACGTGGTGGTGGTAAGAAAGCAGTTCATCGAGTAATCTAATGCATTAATAAAGGGAACTTTTATCAGGTACATAGTTCTGTTTTATATTCAGACAAGCATGAGTGGAATGAAAAATAATAAAGTTTATTATTTATTTATTTATTTATGAATTGTTTGTTTGTGTATATTATCACTAAAAATTTTATTATATAGAAAGTATAAAAAAATTTCACGCACTACAAACGCTTCTGCTATGCATACTCTTGAGTCTGCAGCTGGTCATGTATGCTGGTCACTTGCTGTGTGAAGCTGGCCTGAGTGTGTATACATTAACATGTTGTAATGATATCCCATATCTGTTTGCTGT[A/T]GTTATGTGTCAGCCATGGTGCCTGTGAAGTCTCCTAAGGAGTATTACATCCAGCAGGAAGTGATTGTGCTCTTCTGTGAAACAGTCGAGAGGTAAATCTTTAAATCTAGCCCTGGGTATTGACAACTAGCGCGAAATGCATTGCACAGCATAATACATTTATAGTGCTACAAGTGTTTATCAATTAAATTACGTTAATTTAAACTGTATTAATAAGCCAATGTGTTGTGTTCCCATTTTAAGGGCCCTGAAGCTTGAATATCTTACTCAAGACATGATCGACGACTATGAACCAGCTCTCATGTTTACAATTCCTAGACTTGCCATTGTCTGGTAGGTGATTCACCTCTCTAATGATCTGTTTTTAAGTATTTATTTTCCTTACGCTGTATATGTCATACATCTATTTGTTTCTGCTCATTTGGTAATGCTATGCTTTGTAATGTTTTCTTGCATTAGTGGCCTTGTTATTTACTCCGAAGGGCCTCTTAACCTCGACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11552
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085124 | Nonsense | 477 | 971 | 9 | 15 |
| ENSDART00000139980 | Nonsense | 483 | 975 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 43620974)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 43585649 |
| GRCz11 | 17 | 43576187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATCCCCYGAGGGATCANNNNNNNNNNNNNNNNNNTCCTGTAATGGTTG[G/A]TTGACAGTCTGCCAATCGAGCGACGYCACCAATTTGGGTTGTCAGCGCAA
Long Flanking Sequence:
AAAGAGAAAGGAGTGGAGGAGGTTGTGGATCTCACACTGTTTGTCACTCAGGAAGATTCTGTATGGAAGGAGGAGGAGGAGAAGCAGGTGCTGCCCGAGTCCTCCAGCGAGAGCGAGGAGGAGGAGCCCATCGATGCTGACTTGGCTTGCTCCATGCAGTATGATGAAGAAGAGATCGAGCAACTTAATATGATGGTGCATCAAGTAGGAGACGAAATGTCTACACTGCTTTCCCCTCCAAGTCAGAATCAGTCCCCAGCTCACCGGCCTCGACCCTACAATGGAAGCAGTCTCGAAGGTTCCAGTGCCACCTCCAGCACACAGGCGTCTCCTAGGAGAGCCCCGGGATCGTACCATGATGATGACCGGGTGTTCTTCATGGACGATCTGGAGTCTGGCCTTAGTAGTGAGCTCTGCCGTGGACAGCTTCCTCTTCCTACCGTATGCCTCAGATCCCCTGAGGGATCACACTGTAGACCCGACGCATCCTGTAATGGTTG[G/A]TTGACAGTCTGCCAATCGAGCGACGCCACCAATTTGGGTTGTCAGCGCAAACTGAGCCAATCAACTGAGTCTGTTGGAAACTCAGACAGGATGGTGAACGGATGGGAAGGATTGCAGGATGAGGATAGCGTACAGACTGCTGAAGAAATCGCCAATCGTACTGGTGGAATGAAGCTGTCCGCCACCGTTATTTTTAACCCTCATTCTCCAAGCTTGAGTGATCTGGCTGTGGTCTTACCTCAATCAGCTGATGCTCCTGAAGCTGGCGAAGGCGGGGCTTTGGTCGCCACTCAGTGCCTGCTTAACTCCTGTGTGTGCTGTGCTGGTGGCTGCGTCGACAACCATGAGGATGCCATGGAACCTGCTGGCAGGAGCATGGCACTGGGATTCGAGAAGCACAAGTTGACCATCACAAGCTCCGTCATCCAATCGGCTGTAGCTGCTGGCAGCCCAGGGAAGGGAAATGGACATTTGCCGCTCACCCTGCCCCCGTCTCAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32170
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085124 | Nonsense | 483 | 971 | 9 | 15 |
| ENSDART00000139980 | Nonsense | 489 | 975 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 43620957)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 43585632 |
| GRCz11 | 17 | 43576170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTGTAGACCCGACGCATCCTGTAATGGTTGGTTGACAGTCTGCCAAT[C/A]GAGCGACGCCACCAATTTGGGTTGTCAGCGCAAACTGAGCCAATCAACTG
Long Flanking Sequence:
GGAGGTTGTGGATCTCACACTGTTTGTCACTCAGGAAGATTCTGTATGGAAGGAGGAGGAGGAGAAGCAGGTGCTGCCCGAGTCCTCCAGCGAGAGCGAGGAGGAGGAGCCCATCGATGCTGACTTGGCTTGCTCCATGCAGTATGATGAAGAAGAGATCGAGCAACTTAATATGATGGTGCATCAAGTAGGAGACGAAATGTCTACACTGCTTTCCCCTCCAAGTCAGAATCAGTCCCCAGCTCACCGGCCTCGACCCTACAATGGAAGCAGTCTCGAAGGTTCCAGTGCCACCTCCAGCACACAGGCGTCTCCTAGGAGAGCCCCGGGATCGTACCATGATGATGACCGGGTGTTCTTCATGGACGATCTGGAGTCTGGCCTTAGTAGTGAGCTCTGCCGTGGACAGCTTCCTCTTCCTACCGTATGCCTCAGATCCCCTGAGGGATCACACTGTAGACCCGACGCATCCTGTAATGGTTGGTTGACAGTCTGCCAAT[C/A]GAGCGACGCCACCAATTTGGGTTGTCAGCGCAAACTGAGCCAATCAACTGAGTCTGTTGGAAACTCAGACAGGATGGTGAACGGATGGGAAGGATTGCAGGATGAGGATAGCGTACAGACTGCTGAAGAAATCGCCAATCGTACTGGTGGAATGAAGCTGTCCGCCACCGTTATTTTTAACCCTCATTCTCCAAGCTTGAGTGATCTGGCTGTGGTCTTACCTCAATCAGCTGATGCTCCTGAAGCTGGCGAAGGCGGGGCTTTGGTCGCCACTCAGTGCCTGCTTAACTCCTGTGTGTGCTGTGCTGGTGGCTGCGTCGACAACCATGAGGATGCCATGGAACCTGCTGGCAGGAGCATGGCACTGGGATTCGAGAAGCACAAGTTGACCATCACAAGCTCCGTCATCCAATCGGCTGTAGCTGCTGGCAGCCCAGGGAAGGGAAATGGACATTTGCCGCTCACCCTGCCCCCGTCTCAGGGCCACCTTACCCATTCTG
Associated Phenotype:
Not determined