ZMP
phf16
Ensembl ID:
ZFIN ID:
Description:
Protein Jade-3 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVP1]
Human Orthologue:
PHF16
Human Description:
PHD finger protein 16 [Source:HGNC Symbol;Acc:22982]
Mouse Orthologue:
Phf16
Mouse Description:
PHD finger protein 16 Gene [Source:MGI Symbol;Acc:MGI:2148019]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16861 | Essential Splice Site | Available for shipment | Available now |
sa18542 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16861
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023163 | Essential Splice Site | 96 | 795 | 5 | 13 |
ENSDART00000147826 | Essential Splice Site | 96 | 795 | 5 | 12 |
The following transcripts of ENSDARG00000019614 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37446732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37520490 |
GRCz11 | 6 | 37498384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGTGCAAGTGCTGGCCAGTCCAGACACTATCCCTCAGCCCTCTGTGAG[G/A]TATGTCACTTTGAGTATAAACTGGGNNNNNNNNNAGTATTGGACGTGYAC
Long Flanking Sequence:
TATTTTAAAATAATTGTTAAGTTAAAATGTCGTCCAAGTTACCGGTTAAAACCTGATGAGGCAAATCTGGCAATGAGATCTTAAAATGTATGGAAAAAGTCTTAAAATGTCTTAAAAGGTGTTGAATTTAACTCCATGATCCTTGTATAAAGGTCCCTCGACGTCCTTTTCCTCTAACAAGTATGGAAGCAAACCAGGCACCCCCGCCTCTGCTCAGAAGAAACCAGCAGAGGTAAACACTAAAAAATAACACCTCAACATGTTAACATAATTTTAAGTAGTCTTACGAATGTTAAAGTTCAATGGTCAAATCACTTATTTACATTTTTTCCTTCTTTTTAGGTGTTCAGAAAAGACCTGATCAGTGCGATGAAGCTGCCAGACTCTCACCATATTTCTTCAGAGGATTATTACCTGTTGGCAGACACATGGAAGCAGGAATGGGAGAAAGGAGTGCAAGTGCTGGCCAGTCCAGACACTATCCCTCAGCCCTCTGTGAG[G/A]TATGTCACTTTGAGTATAAACTGGGGGGAAGAAAAGTATTGGACGTGCACGCTCTTGCATATGGTTTAAGGGGGTCTGGTTATGTTTTTATTCTTTCAGCTTTGCAGTTTTTGCATGAAAGAGATCTTCAACAAAACCTGAATTGAACTGAAATGCATTGAACTCAACGAACAAGCCAGTATTGTGCGGTGAACCAGTCCATGTAAATATAAAATGAGCTTAAATTAACTATTTCTAACAAAGAAAAAAGGAGAAGACATAATTACAATTATAAATGAAAAAAAGAATGAAATAATAAAATAAAACCAATAAAATCATAAGAAGTAGTAAAACTTAAGCTCCTCCTGGGTTATTATTGACATCAGTTGGGCATTTAGTGTTTTAATGTCCTCACAGGTCTAATAATATGGATATGTTATATGAATAATGTTTGTGTTATATAGAAATATTTGAGAATTATCCAAAAATCAAACAAAAAGAGCTCAGGGTTAGCCTAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18542
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 |
---|---|---|---|---|---|
ENSDART00000023163 | Nonsense | 782 | 795 | 12 | 13 |
ENSDART00000147826 | Nonsense | 782 | 795 | 12 | 12 |
The following transcripts of ENSDARG00000019614 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 37427676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37501434 |
GRCz11 | 6 | 37479328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAGGAAGGACTCAAAACCAGAGAGGAGATTATGTCAAGTCTGCCAGT[C/T]GAGCAAAACACTCTTATGGCTCTAGGAYATCGGTGCAAAGGTGACAATCT
Long Flanking Sequence:
CGGTAAAACAATCAGGCAAACCATTAGCTCTGCACGCCGCCCTTCACGGTCAGTCATCCAACGGGAAGACCAAAAATGAAGCGGAAAAAACGCGGCAAATTAAATCCAACGGCATTCTAGACAAACCCATTCTCCAAAGAGACACTTCCTGCCTGGCGGCCAGCGAGAAAGACCCCCGCAGTGAGATTTCAGGGAAAAGTCAGCCATCGGGATTCCACAAAACCTCTCTTGAGCACTTCAGTCGATCTCTCAAGGAGGCCACTGTGAGTTTAGTACGGACCGAGGACCTTCGGACCTTTGAAAAGAACTCACGCAAGTCCTCCGGATTCTCAAAACCTCTTTCCACCGAGCGGCCGCAAGGGGGCGGCAGAGCGTCTCAGGAAAGCGATGGTTACTGTCCGGATGCAGAGCTCAGTGATTCTGAACCCGAAGCCAAAGGGAAGTGCAGGCAAGGAGGAAGGACTCAAAACCAGAGAGGAGATTATGTCAAGTCTGCCAGT[C/T]GAGCAAAACACTCTTATGGCTCTAGGACATCGGTGCAAAGGTGACAATCTTCAAAAAGCATTACAAACATCCCACTGCCACAAGTTATTATGGTTTCTTAGACTTCTGGTGGTACATCGGAAGTGCCAGATTCTAGTTTTCCTCTGTTGAGGATCATTTGTTTGCTTTTTGTTGAGTGCCAAAACATGGCTGGCTGGTTGGGGAAGTGAAGTTAGTCTATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGGGACTGATTTATCACTGTGTTTTCTATCCTGCCGATGTGTTTCTGCTGCCCTTGGACTCATGAGAGTATTATGGGTGGTGAAGCAGTGTTGTACATAAAAAGCAAGGTCGTTTTTTTAGACTGTACATAGTAGTTCGTGTTGAGACGTGGAAAACATTGAGGTGTTTTCCACGTACAGAAACATCA
Associated Phenotype:
Not determined