Busch Lab

ZMP

phf17

Ensembl ID:
ENSDARG00000033707
ZFIN ID:
ZDB-GENE-030131-5648
Description:
Protein Jade-1 [Source:UniProtKB/Swiss-Prot;Acc:Q803A0]
Human Orthologue:
PHF17
Human Description:
PHD finger protein 17 [Source:HGNC Symbol;Acc:30027]
Mouse Orthologue:
Phf17
Mouse Description:
PHD finger protein 17 Gene [Source:MGI Symbol;Acc:MGI:1925835]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa10671 Nonsense Available for shipment Available now
sa10070 Essential Splice Site Available for shipment Available now
sa45609 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa1499 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10671
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042060 Nonsense 134 829 5 11
ENSDART00000121706 Nonsense 134 829 4 10

The following transcripts of ENSDARG00000033707 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 26674645)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 26814564
GRCz11 17 26832955
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCTTGGGTACGTGGGTATTCAGACAYTGGCTGATGGCATGTGTCGCTA[T/A]GACCTGAATGAGGAGGACGTAGCTTGGCTGCAGATCACTAATGAAGAGTT
Long Flanking Sequence:
CGAAATCGCATTATTGTTCAGGAAAATTGTGATGGGTTTCTTTTGCCCATATCGCACAGCCCTGCGTATGACTGTTGTAGATGTTTGTCATTTAGTACATATTCTTTTGCACAATTTCTTTTCTTTTCCACAGGTGTTCAGGACAGACCTGATCACAGCTATGAAGCTGCATGATTCACACCAGCTTAATCCTGAGGACTATTATGAGCTGGCCGATCCCTGGCGGCAGGAGTGGGAGAAAGGGGTTCAAGTTCCTGTCAGTCCAGAGTCTATACCGCAGTGTACAGTGCGGTATAATATGTTTTTCCTCTTCCCTATCAAACTATTCTCCTTAAGTAGTTCCCATTGATTCATTGTTCTTTTTCTTTTTTTTGCAGCACTGTAGCTGAGAAAAGCACCGCTCCTCTGTTCATCAAGCCCAAGAAGCTGATTCGCTCATCTGAGTCATCGATGCTTGGGTACGTGGGTATTCAGACACTGGCTGATGGCATGTGTCGCTA[T/A]GACCTGAATGAGGAGGACGTAGCTTGGCTGCAGATCACTAATGAAGAGTTCAGTAAAATGGGTGAGCAAATACTGTCTGGAGTTTTCATTTTGCTCTTTATGCAAACAAATTTCTTCACTCTGTGGGAAAAAAAGCACTTACAGCTAAATAATTTGCTTGTAGGCATGCAACCCCTGGATGAGCTTACAATGGAGCGGGTCATGGAGGAGTTTGAGCGCCGTTGCTATGACAACATGAGCCACGCCATGGAAACAGAGGAGGGGCTTGGTATCGAGTATGATGAGGATGTGGTCTGCGATGTCTGTCAGTCTCCTGACGGCGAGGACGGCAACGAGATGGTGTTCTGTGACAAGTGCAACATCTGCGTGCATCAGGTGTGTGTGTGTTGCTAATGTTGTCAAAAAGAACAATATTTCAATACTGAAATACTTAAAGTGAAACATAACTTTTTTTTACAATGCCTGCTGTATTCTTCCTCTCAAGTTCAAGTCTCTTTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10070
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042060 Essential Splice Site 155 829 None 11
ENSDART00000121706 Essential Splice Site 155 829 None 10

The following transcripts of ENSDARG00000033707 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 26674708)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 26814627
GRCz11 17 26833018
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGACGTAGCTTGGCTGCAGATCACTAATGAAGAGTTCAGTAAAATGGG[T/C]GAGCAAATACTGTCTGGAGTTTTCATTTTGCTCTTTATGCWAACAAATTW
Long Flanking Sequence:
GCGTATGACTGTTGTAGATGTTTGTCATTTAGTACATATTCTTTTGCACAATTTCTTTTCTTTTCCACAGGTGTTCAGGACAGACCTGATCACAGCTATGAAGCTGCATGATTCACACCAGCTTAATCCTGAGGACTATTATGAGCTGGCCGATCCCTGGCGGCAGGAGTGGGAGAAAGGGGTTCAAGTTCCTGTCAGTCCAGAGTCTATACCGCAGTGTACAGTGCGGTATAATATGTTTTTCCTCTTCCCTATCAAACTATTCTCCTTAAGTAGTTCCCATTGATTCATTGTTCTTTTTCTTTTTTTTGCAGCACTGTAGCTGAGAAAAGCACCGCTCCTCTGTTCATCAAGCCCAAGAAGCTGATTCGCTCATCTGAGTCATCGATGCTTGGGTACGTGGGTATTCAGACACTGGCTGATGGCATGTGTCGCTATGACCTGAATGAGGAGGACGTAGCTTGGCTGCAGATCACTAATGAAGAGTTCAGTAAAATGGG[T/C]GAGCAAATACTGTCTGGAGTTTTCATTTTGCTCTTTATGCAAACAAATTTCTTCACTCTGTGGGAAAAAAAGCACTTACAGCTAAATAATTTGCTTGTAGGCATGCAACCCCTGGATGAGCTTACAATGGAGCGGGTCATGGAGGAGTTTGAGCGCCGTTGCTATGACAACATGAGCCACGCCATGGAAACAGAGGAGGGGCTTGGTATCGAGTATGATGAGGATGTGGTCTGCGATGTCTGTCAGTCTCCTGACGGCGAGGACGGCAACGAGATGGTGTTCTGTGACAAGTGCAACATCTGCGTGCATCAGGTGTGTGTGTGTTGCTAATGTTGTCAAAAAGAACAATATTTCAATACTGAAATACTTAAAGTGAAACATAACTTTTTTTTACAATGCCTGCTGTATTCTTCCTCTCAAGTTCAAGTCTCTTTATTTGCATGATTTTTGCACAGTATTGCCAAAGCATTTTATATATGTATAAAATATGTAATATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45609
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042060 Essential Splice Site 281 829 7 11
ENSDART00000121706 Essential Splice Site 281 829 6 10

The following transcripts of ENSDARG00000033707 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 26682602)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 26822521
GRCz11 17 26840912
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGGCACCAAGTGGGTCCACGTCAGCTGTGCCCTCTGGATACCTGAAG[T/C]AAGGATGCACGCACAAATGAAGACTTATGTAAAGTGATTCACTTAATGAC
Long Flanking Sequence:
TTACATGGTACAAATGTACAAAACAAATATTTTTTATTTTACTCCTTTAATTACTTTTTTTATCCGGGAGAGTGAAAATTTTGGCAAGGCTAGTGAAAATCTAGAGAACTGGCTTAACTCAACTAATAAAAATGGTTGTCATTGACTCTGACACATTAAAAAACTAAGACATGCATACATATTGTAATTGTGGCATTTTTTTTCCTGTGGTTTTTAAAAAAAAAGAGTGTCATTATATTTAAGGTATCATATTGAAGTTAGAAATTTGTGACCAAATTTTGAAGAAATGTTCCAGCACACATGAATTACATAACCATGTATCTCTCCACAGGCGTGTTATGGTATACTGAAGGTCCCTGAGGGCAGCTGGCTTTGCCGTACCTGTGCGCTGGGTATTTTTCCCAAATGCCACCTGTGCCCTAAAAAAGGCGGAGCCATGAAACCCACCCGCAGTGGCACCAAGTGGGTCCACGTCAGCTGTGCCCTCTGGATACCTGAAG[T/C]AAGGATGCACGCACAAATGAAGACTTATGTAAAGTGATTCACTTAATGACGCAGAAGAGCAGTATGTGTGCTGAGACTGGGCTTTGTTGTGTGCTCTTTATCTCTAGGTAAGCATTGGTAACCCTGAGAAGATGGAGCCTATCACTAATGTGTCTCATATACCCAGCAACAGATGGGCTCTAATATGCTGCCTGTGTAAAGAGAAGACAGGAGCTTGTATTCAGGTATACAGTGCTGATGTTTATCTCTTATTATGTTATGGATACAGTACAGATATGAAGAATGTCCCAGAAATATTGCAAATTTCATTAATGTTTTTAATGAATATTTTCCACATTCTTACAAAAGCATTCATTTTATTTTTTTGTCTTCTGATGTTTTTAGTTCAATTTCAGTTTGTTTATAGCTCTTTTAGGATAGCAATAATTCTCCAATGGCTTTGTTTTTGGTTTTGGATTTCTTTTGCTTTGGTGACTGATTTGTTTACTAATATACAGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1499
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042060 Nonsense 438 829 9 11
ENSDART00000121706 Nonsense 438 829 8 10

The following transcripts of ENSDARG00000033707 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 26684273)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 26824192
GRCz11 17 26842583
KASP Assay ID:
554-1424.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAYGAGTTCTATCGCTTCGTCGCTGCTGATGAGGTTGCCGAACATCTG[C/T]AGCTTCCTCTTGAGATGGTGGACTTCTTGTTTCAATACTGGAAGTTGAAA
Long Flanking Sequence:
GAAAGAAACACTAGCTGTGCAAATACCCTATTTGGGTTAAATGTAACATTTTATCATAATGTATCATGAATCAGAGCACATTTTTCCAGCTTCACATTTCTCCGTCCTCTGTGGTCTAATTCTGACGTCTTGTTTTTCCAAATCCCTAGTGTTCTGCCAAAAGTTGCCGTGTGGCGTTCCACGTGACCTGTGGTCTGCATTGTGGGCTGAAGATGAACACGATCCTCACAGAGGCGGATGAAGTCAAGTTCAAGTCATTTTGTCCCAAGCACTCTGGCCTGGATTGGAACGAGGAAGAGGGCGATGATGACAGACCTGTGAAGGTCCCAACCAGGGAAGACAGAAGCAGAAATAGAGGAATAGATTTCTCTGCTTCTTCCCAAACCAGACTCTCGCAGAACCCAGAGGAGACCAGACTCAGTGAGCGAAAGCTTCGAGTACAGCAGCTGGAGGACGAGTTCTATCGCTTCGTCGCTGCTGATGAGGTTGCCGAACATCTG[C/T]AGCTTCCTCTTGAGATGGTGGACTTCTTGTTTCAATACTGGAAGTTGAAAAGAAAGGTGAACTTTAACCAGCCCCTCATCATGCCGAAGAAAGAGGAGGAAGACAGTCTTGCCCGACGAGAACAGGAAGTGCTTTTAAGGCGACTACGACTCTTTACGCATTTGCGACAGGATCTGGAGAGGGTAAGTTTGCCAGAACCCTTCTATTGTCACATTAGCTCACACGATGGCTTTTTTATCACTCTAAATTAAGGGTGCACGATACTTTGGTACCAGTTGATACTGGAATTTTAAAAACGTCAGTTTTTATTCCTGCTAACATTTGAGCGTTATTGAGCACGTACTTAAACACAGCTTATTTGCCATTGTGTTCACATGCTCAACTGAAATGACTGATTGGCTGTGAAGGTCATCAGTTCACCGAACTCACCGCTGTTTACTGAGTGTAACCACAGATACAGGGACACATTGCAGCATTTTAAAGCTGTGTTTCATCAGCAG
Associated Phenotype:
Not determined