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 |
sa36500 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36499 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
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
Mutation Details
Allele Name:
sa36500
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085124 | Nonsense | 711 | 971 | 9 | 15 |
ENSDART00000139980 | Nonsense | 717 | 975 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 43620273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43584948 |
GRCz11 | 17 | 43575486 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTAGTTGCACCCTTCAGGACACAGGATGCCGAACGCAACATAATGCCT[C/A]AGTAAAAGGGAAATCGGAATGTTTTGGAAAACAGTCCAAAGATGATAACC
Long Flanking Sequence:
TCATTCTCCAAGCTTGAGTGATCTGGCTGTGGTCTTACCTCAATCAGCTGATGCTCCTGAAGCTGGCGAAGGCGGGGCTTTGGTCGCCACTCAGTGCCTGCTTAACTCCTGTGTGTGCTGTGCTGGTGGCTGCGTCGACAACCATGAGGATGCCATGGAACCTGCTGGCAGGAGCATGGCACTGGGATTCGAGAAGCACAAGTTGACCATCACAAGCTCCGTCATCCAATCGGCTGTAGCTGCTGGCAGCCCAGGGAAGGGAAATGGACATTTGCCGCTCACCCTGCCCCCGTCTCAGGGCCACCTTACCCATTCTGTGCCAAACTGCTCAGTGCAAAACCAAGCGAGAGAAGATGAGGGCAGTCAGGATGGTATCCACTATCCCTGCTGTGAGAAATGCAGCCCAGGGGTACTTCTGGCTCAGGACAGAGGCTCAGGACAGGAGGGAGGACCTAGTTGCACCCTTCAGGACACAGGATGCCGAACGCAACATAATGCCT[C/A]AGTAAAAGGGAAATCGGAATGTTTTGGAAAACAGTCCAAAGATGATAACCGGAAGATCAATAGGTTTGTTTAATTTGCAGGAAGCATGTATTAAGCTTTCACATTTAAAGAGATAGTTTAGCCAAAAAAGAACGTTCTGACATCATTTACTTGTTTCAGACCGGTTTGAATTTCCTTCTTCTGTTGCGCACATGTTAAAGAATGTCAGAAAAAGCAGCCGTTGACTTCCATAGTATTTTTGTTCCTACTTTGGATGTCAGCAGTTGCTTTTTTCCAACATTGTTCAACCGAGGAAAGAAATTCGTAAACATTTAGAACCACTCGAGTGTCAGTAAATGGTGAGGAAATGTTCATTTTTCGGTGACTTATAGCTTTAAGTTTTAACTCCTCCCCCTCGCCCCATTTTGAAAATGTTTTGTTTGTTACCATCTTTTTTAAATATATGAGTTTATTTCATTCTGAAGGTTGTCATGCTTTTAAGTTCTACTATTTCCCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36499
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085124 | Essential Splice Site | 732 | 971 | 10 | 15 |
ENSDART00000139980 | Essential Splice Site | 738 | 975 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 43619731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43584406 |
GRCz11 | 17 | 43574944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTTTCTTTTGTTGCCGCCTCATGTTTTTTGTTTTGGAATGGTCCACA[G/T]CAGTTCTCAGGAGTCCCCCCTCAGTTCTGTACCCAGCAGTGACATTGATG
Long Flanking Sequence:
ATGATAACCGGAAGATCAATAGGTTTGTTTAATTTGCAGGAAGCATGTATTAAGCTTTCACATTTAAAGAGATAGTTTAGCCAAAAAAGAACGTTCTGACATCATTTACTTGTTTCAGACCGGTTTGAATTTCCTTCTTCTGTTGCGCACATGTTAAAGAATGTCAGAAAAAGCAGCCGTTGACTTCCATAGTATTTTTGTTCCTACTTTGGATGTCAGCAGTTGCTTTTTTCCAACATTGTTCAACCGAGGAAAGAAATTCGTAAACATTTAGAACCACTCGAGTGTCAGTAAATGGTGAGGAAATGTTCATTTTTCGGTGACTTATAGCTTTAAGTTTTAACTCCTCCCCCTCGCCCCATTTTGAAAATGTTTTGTTTGTTACCATCTTTTTTAAATATATGAGTTTATTTCATTCTGAAGGTTGTCATGCTTTTAAGTTCTACTATTTCCCTTTCTTTTGTTGCCGCCTCATGTTTTTTGTTTTGGAATGGTCCACA[G/T]CAGTTCTCAGGAGTCCCCCCTCAGTTCTGTACCCAGCAGTGACATTGATGGTGTTTCTGTTACTACATGCAGTTTGTCAAGTTCATATGCACCCAGGTAAACCTTTGTCTGATATTTAGAACTAGACTATGTAAGCACTGTTTTTGTAGAATGCATCAGGGATGAGATTTTTCTTTTGTTAGACCAACCCAAAAGTTAGCATGGCCTGGCTAAGATGTTCAGAAAAAGCACAGCCATGTTTTATTGGCTCACGTTTAGCGTGTGCGGAGTATGATGTTAAGAGTGTTGGATTCTATGGAAATGCATGAGCTGACTAAGGCCAAGTCCCAGTTCTATATTCTGCTTGACCCTTGAAACAGAATGATAGGGTGGGGATGAAAATATTCCCAGAAGAAACAGGACACCACTACTACACATGCAAACGTCATCAGGTTAAGCTCATACATCACACAAGATGTCACCTGCATTATTTATTCTAGAAAGAACAAGCACATTAACGT
Associated Phenotype:
Not determined