ZMP
si:dkey-24n17.8
Ensembl ID:
ZFIN ID:
Human Orthologue:
ZFYVE16
Human Description:
zinc finger, FYVE domain containing 16 [Source:HGNC Symbol;Acc:20756]
Mouse Orthologue:
Zfyve16
Mouse Description:
zinc finger, FYVE domain containing 16 Gene [Source:MGI Symbol;Acc:MGI:2145181]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21637 | Nonsense | Available for shipment | Available now |
sa13367 | Nonsense | Available for shipment | Available now |
sa45386 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21637
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111830 | Nonsense | 82 | 1381 | 2 | 17 |
ENSDART00000147918 | Nonsense | 82 | 1384 | 3 | 18 |
The following transcripts of ENSDARG00000075747 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 3010664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2956301 |
GRCz11 | 10 | 2983472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTATGGACTTACATCGCAAAGTATTGACTCAAACCAAAAAGATTCCTA[T/A]TCAAATGAATGGCCCCTCACAGGTGTGGACCTCTTGTCGTCCGTTGATAG
Long Flanking Sequence:
TGTGGCTAAGTAATAACTAAAGTTATTTTTCTTGGAAGGGACAATTGAAAATCTTTCCTCTTGCCATTATTTATAATAAGATTTATAATAATATTATAAAATATTATACATTTTGCCCTGTATAAGGCTGAAATTACATTCATAATTTTCTTGTAAAGGTCTTAAAAAGTCTTGGATTTGACTTGGTGAAACCTACAGACACCCTGTTTAAATTTATGTAGAAAAGTTTATCATATGTTTGTTATATTTTTGTTGCTGCTTTGAAATGTGATCTAATTTAATTTGACTCAAAATAATGCCATTTTTTATGTGATTTTGTTTTTAGAAGAGCTTGAGAGCAAACCGGGCACGTATGTAAGCCCTCCTTGTCCGGACTCTACGCTCATCCCTGGTCGCTTTATACCAGAGCAGCACACAGTCCCACAAACACTCCCAGATGTCAACGCACTGCACTATGGACTTACATCGCAAAGTATTGACTCAAACCAAAAAGATTCCTA[T/A]TCAAATGAATGGCCCCTCACAGGTGTGGACCTCTTGTCGTCCGTTGATAGTAGAGGCATCAAAAGTTCAGCTCCTCCTTGTCCTGACCGCTCGCTGAAGCCTGTGTGTGACCTGGTGAACGATACTGGTTCTGCAAACCTCCAGCAAGCTGATAGTCAGGAAGACTTTAAAGAGCTGGACATTCCAGACGTACAATCGACTGAGGGGCTGCTTGTGGACTTTGAGAGTCCAGAAGATCTTTCCAAACCCAGCCACAGTGAAATACTCAAACGTGACTCTGAGATTAATTGCAATTCCCTCAGTTTGCTGGATGTCATATTACCGGTTGTTGGCGAGCCTTATACTTCGAGTAGCATTACACTTTTGGAGACTGAAAGTTCCTGTCCTGAAGCCTCTAACTCAAACGGGCAGAATGATCGTCCGTGGAGTCAGATGGACGAAGATGATGTTTGTAACACATGTCCTAGTACTACAGAGGAAAATATTTCAGCATTCAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13367
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111830 | Nonsense | 383 | 1381 | 2 | 17 |
ENSDART00000147918 | Nonsense | 383 | 1384 | 3 | 18 |
The following transcripts of ENSDARG00000075747 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 3011567)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2957204 |
GRCz11 | 10 | 2984375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGAAAGAAACTTCAAAYGCACCTTATCGCCAACGGACAAATTAACTTG[T/A]AGAGATTTGGGTGCAAGCAATCCGTCTCCATCCTATTCAGAAAGTCCAAA
Long Flanking Sequence:
AACGGGCAGAATGATCGTCCGTGGAGTCAGATGGACGAAGATGATGTTTGTAACACATGTCCTAGTACTACAGAGGAAAATATTTCAGCATTCAGTGAAGAGCATGCTGTGTCGCTCCAGCCCGACTCAACATCTGAAGATGTCAGAAATCCAGAGGATTTAACTGGAAGTCCCACTTCGGAGAAGGAATCTTCTCTGTCTTGCTTGCCAATGGCTGTATCTATGTGTGGTTCCCTTGTGGCGACTTTAGACCCTCAAAAGGCAGCAGTGGTCGAAACCAAAGATGAGGCTGAACTAGAAACAAAATCAGCAATTCAAGAAGCTGAAGAGTTAACTCTTCCATTAGAAGAGCCAGTGCCTCCATTCTCCTCCAGCAGGCCTGATTCTTCACCTGAGGATGAACCTGAGATTGTCCAGATCATGTCGAACCCTGCTGCTGCAGGCCACTACCCTGAAAGAAACTTCAAACGCACCTTATCGCCAACGGACAAATTAACTTG[T/A]AGAGATTTGGGTGCAAGCAATCCGTCTCCATCCTATTCAGAAAGTCCAAATTATTCGTACGAGTTCGGTATTGCCAACGATTACCTACCTGAAAGCGACCAGACAGTGATGATGGTCACGGACGAGGAACTTGATGCCTTTCTAATGGGTCAAGGTGTGAAAATCAACCCCGATGCAGCGGTGGAAAAATTCAGTGATGACGGCTTTTCAGAATTTAATGGAAATGCTGAAAGAGATGGCTTCTTGGATGAGGAGTTGCAGAGTTGTAAAGTCGAGACTTTTGCCTCACCTGAGAGTGATGGCTCACAGTATCTGGAGGAGAGCGAAGGGTCAAACGTTTCCTCTTCATCTCAAGACAGCAGCCCGCTGAGAGCAGACTCTACTCAAACAATTACTCATGAAACCGTAACCAGCCCTGTTGAGATTCAATCCGTTTGCTCCCCGAACCAAGAGTCAACTTACGGTGGTGCAAGACCAAAGCAGTTGTCCAACCAAACCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45386
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111830 | Essential Splice Site | 801 | 1381 | 5 | 17 |
ENSDART00000147918 | Essential Splice Site | 804 | 1384 | 6 | 18 |
The following transcripts of ENSDARG00000075747 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 3034293)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2979930 |
GRCz11 | 10 | 3007101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAAGATCTTCTCAGGAGTCGAGCCCAGTAACGCCAGACCCGCCGGCGG[T/A]GAGACTGCTAAATCCTCTTAACCGATGCTGCAGATAACTGATGATGACAA
Long Flanking Sequence:
GGGTGTGGTTAAGTATGTTAGCCACACCCAAAACTTTAGATATACCTAATTTAAGAATTTAACTGAAAACAAACAGGAAGTGCATTTTCAGATTTAGATTAAAGATTACAAGAGCAAATCTTTTTTTTTTTTTGGTCTTAATGACATGTGCAGATGAATTGTTCACCACAAAACTAGCAACGTGAGCTAACAAAATCAATATGGTTACTTTTGATTTCATTTTAAACAGTCTGGTATCTAGATGTAATCGTAGAAAGATCCACATCATTCCATAGTTCAAGCTAAGTTTATATAGTACATCATTTGCAGGCTGATCCTAATGAAGCTGTTGTTTTGTCTTTTTGTTGTTGCTGTTGTAGGTTTTCCACGCGAGCAGAAGCATGTGTGGTTTGCCGATGGCATCCTGCCGAACGGTGAGGTAGCCGACACGACCAAACTCTCTGTGCAAACACGAAGATCTTCTCAGGAGTCGAGCCCAGTAACGCCAGACCCGCCGGCGG[T/A]GAGACTGCTAAATCCTCTTAACCGATGCTGCAGATAACTGATGATGACAATTGAAGGCCTTCATTGATTTGCTGCCTTTTCAGCCTGACGATAAGTTTCCGGATGAGCGTGAGGAGAGTGTTGGAGGCAGATCTGACAGCCCTGTGGAGGCGAGCCGTCCACCCGTCAGAGGCCCGTGGGATTACGGTCTGCTGTGCGGCGTGGGCAACTGTGTGCAGAGAGATGCCAGTCTGGTGCCAGAGGATGATGACGGTCTGCCGCCACTTCTCATTATCACCGGAGAGGAGGAAGAAGGGGGTAATGGCTTGTTATGTCTCCATGAAAGCTTGAAAAAAGAAACATTTTAATAATCTGTAGGGAGTTCATGAATCTGGGAGTTGGTACCAAAATAATTCCTAACCTACATTTGTTCTGCTGTATGTTTACATCTTTACAAGCTCTATTTTAACGATCTAGGCACAAAGTCTAAAGCTTGTGGCGCTAAAGCATTAAGGACGTGT
Associated Phenotype:
Not determined