Busch Lab

ZMP

si:dkeyp-89d7.1

Ensembl ID:
ENSDARG00000061458
ZFIN ID:
ZDB-GENE-030131-1796
Description:
PHD finger protein 14 [Source:RefSeq peptide;Acc:NP_001038252]
Human Orthologue:
PHF14
Human Description:
PHD finger protein 14 [Source:HGNC Symbol;Acc:22203]
Mouse Orthologue:
Phf14
Mouse Description:
PHD finger protein 14 Gene [Source:MGI Symbol;Acc:MGI:1923539]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa23576 Nonsense Available for shipment Available now
sa3007 Splice Site, Nonsense F2 line generated Not yet available
sa5650 Splice Site, Nonsense F2 line generated Not yet available
sa43328 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23576
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087662 Nonsense 563 900 9 18
ENSDART00000103114 None None 507 None 12
Genomic Location (Zv9):
Chromosome 19 (position 39765289)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 38629272
GRCz11 19 38216392
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTGGACACATCTGATATCAGTGCAAGCGTGGATGGACGACGCAAACAT[A/T]AGCAGCCTGCTCTCACTGCAGACTTTGTGAACTACTACCTTGGTATGTGG
Long Flanking Sequence:
TAGAAATTAGTTGCTAAAACTATTATGTTTAGAAATGTATTGAAAAAAATCTCAGTTGAACAGAAATTGAGAAAAAAAATAAAGGGGGGTTAATGATTCTGTTTGTGTTGAACTTTACAATCTTGTTTATTCTCAAACAGCAATATTATACACTAACTAAATTTAAAGCGTAAACTCATAATCAAGGGCATCTAAAAATGCTGCTCTGGATATTATTGACATCTGTTTTGCTCATCAATCAAACAAAGCCTCTGTAATTTTTCAACATCTAGGCTCGTATAACCACGAGGCTCCAGCAGTACAGGGCAAAAGCAGAGCTGTCTCGAAACACTCGGCCGCAGGCATGGGTGCCCCGAGAGAAGCTTCCCCGACCTCTCACCTCCAGTGCTTCAGCCATCCGGAAGCTGATGAGGAAAGCCGAGCTCATGGGAATCAGCACAGACATCTTCCCCGTGGACACATCTGATATCAGTGCAAGCGTGGATGGACGACGCAAACAT[A/T]AGCAGCCTGCTCTCACTGCAGACTTTGTGAACTACTACCTTGGTATGTGGATTTGGTTTCTCACTTGATAATTAAAATTATTAAGTTTAGTTAACTCATCAGGTGTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCATTTGAGTCATTTATTTTTATTTCAATGAATAAACAAACATTGATGCATTTTTACCTTGTAGCTTTGGGCCATTTGACTTTAAAGAGCACATGTTTAAAGCAGCAGACGACATACAAGGGATGACTACATTGCCTCGCAATCCTGTCCTAAAGTGTCTTTTGAGAGAGAGAGAGGGGACCTCACGTTCTTATTTCTACGGATGTTCACAACTATACCAGCTATGTTTGAATCACATTCAACTTTAAAGAATGCGTGTTGTTTTCGTTTTTAGTGCAAAATCATCAGAAATTTACATTGAGTAATAAGATCATTTCTATCACGCATATCATTTAAATCCTGACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3007
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087662 Splice Site, Nonsense 725 900 14 18
ENSDART00000103114 Splice Site, Nonsense 332 507 8 12
ENSDART00000087662 Splice Site, Nonsense 725 900 14 18
ENSDART00000103114 Splice Site, Nonsense 332 507 8 12
Genomic Location (Zv9):
Chromosome 19 (position 39793675)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 38657658
GRCz11 19 38244778
KASP Assay ID:
554-2631.1 (used for ordering genotyping assays)
KASP Sequence:
TGAAAAGCAAAAGAGAATACCTGACTCTTTCATCGCTCATCTTTTCCAGG[C/T]AGTGCTCTGAGTGCGACCAGGCCAGCAGTGAYGAGGCTGACATCGCCATG
Long Flanking Sequence:
GATGTGGAGCTCCACAGTTGCGTGCGTGAGCGTTTCTGTGTTTTGTTTATTTGTCAAGCTGAGCCCAATGCTTTCGCTGCTGATTCGAGTAATTCATTTAATCCATGAATAAGAAAGCGTGATGTGGTTCCGCACTGCAGGATGGAAATTAGAAAGCATTTGAAAGATAAAATTGTGTGGGGGGGCCAAGTCGTACCTAATTACTGGCAACTGCCTGCCCCTGAGACAGTAATACTGTATAATCAAAAAGCTTTTGCTCGCTCTAAAGAATTCAGCTATACTTCAATTTTATATATTGTTTTTGAGGGATATTTAACAACCCTTGTGTTTTGATGAATAAGACACATCTGCTTCCTGAGGAGAAAAGGAAAAAAAAACACTGACATGGACCTTGAAAGCCTCTCTCTCATCTCAAAGCGTTCTCCATATTGAGAAATCAATAAGGTCGAATGAAAAGCAAAAGAGAATACCTGACTCTTTCATCGCTCATCTTTTCCAGG[C/T]AGTGCTCTGAGTGCGACCAGGCCAGCAGTGACGAGGCTGACATCGCCATGGAGACACTACCAGATGGAACCAAAAGGTCCAGGAGGCAGATCAAGGGACCAATCAAATTCATCCCTCAAGAAATGAGCCCGGAGCCCAAGAAGCCTCAAGTAAGAGGGACTGTGAGTATGAGCATATCATGACTTGGCTGATCAAATGACATACTTTAGTGCAGTGAGGCTGTGAAGGGGTTTTTCTAAGATGACTTACATCATAAACATCAATTTTAATTCTTCTTTATTTCTATATCGCTGTTGCAATGTTGATTGTGCCAAAGCAGCTTAACATAGAAGTTCTAGTAAATTGAAACTGCGTCAGTCTATTTTTCAGAGTTGGAGTTCATTTTAGTTTAGTTCAGTGTGGTTTAATTTTCACTGCTGAATGGCAAATCCATCGGTGCGCAGCTCCACAAATCTCAAACCGCGCAAGCCAGTGGCAATAGTGGCAAAAAACAAACTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5650
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087662 Splice Site, Nonsense 725 900 14 18
ENSDART00000103114 Splice Site, Nonsense 332 507 8 12
ENSDART00000087662 Splice Site, Nonsense 725 900 14 18
ENSDART00000103114 Splice Site, Nonsense 332 507 8 12
Genomic Location (Zv9):
Chromosome 19 (position 39793675)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 38657658
GRCz11 19 38244778
KASP Assay ID:
554-2631.1 (used for ordering genotyping assays)
KASP Sequence:
TGAAAAGCAAAAGAGAATACCTGACTCTTTCATCGCTCATCTTTTCCAGG[C/T]AGTGCTCTGAGTGCGACCAGGCCAGCAGTGAYGAGGCTGACATCGCCATG
Long Flanking Sequence:
GATGTGGAGCTCCACAGTTGCGTGCGTGAGCGTTTCTGTGTTTTGTTTATTTGTCAAGCTGAGCCCAATGCTTTCGCTGCTGATTCGAGTAATTCATTTAATCCATGAATAAGAAAGCGTGATGTGGTTCCGCACTGCAGGATGGAAATTAGAAAGCATTTGAAAGATAAAATTGTGTGGGGGGGCCAAGTCGTACCTAATTACTGGCAACTGCCTGCCCCTGAGACAGTAATACTGTATAATCAAAAAGCTTTTGCTCGCTCTAAAGAATTCAGCTATACTTCAATTTTATATATTGTTTTTGAGGGATATTTAACAACCCTTGTGTTTTGATGAATAAGACACATCTGCTTCCTGAGGAGAAAAGGAAAAAAAAACACTGACATGGACCTTGAAAGCCTCTCTCTCATCTCAAAGCGTTCTCCATATTGAGAAATCAATAAGGTCGAATGAAAAGCAAAAGAGAATACCTGACTCTTTCATCGCTCATCTTTTCCAGG[C/T]AGTGCTCTGAGTGCGACCAGGCCAGCAGTGACGAGGCTGACATCGCCATGGAGACACTACCAGATGGAACCAAAAGGTCCAGGAGGCAGATCAAGGGACCAATCAAATTCATCCCTCAAGAAATGAGCCCGGAGCCCAAGAAGCCTCAAGTAAGAGGGACTGTGAGTATGAGCATATCATGACTTGGCTGATCAAATGACATACTTTAGTGCAGTGAGGCTGTGAAGGGGTTTTTCTAAGATGACTTACATCATAAACATCAATTTTAATTCTTCTTTATTTCTATATCGCTGTTGCAATGTTGATTGTGCCAAAGCAGCTTAACATAGAAGTTCTAGTAAATTGAAACTGCGTCAGTCTATTTTTCAGAGTTGGAGTTCATTTTAGTTTAGTTCAGTGTGGTTTAATTTTCACTGCTGAATGGCAAATCCATCGGTGCGCAGCTCCACAAATCTCAAACCGCGCAAGCCAGTGGCAATAGTGGCAAAAAACAAACTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43328
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087662 Nonsense 858 900 17 18
ENSDART00000103114 Nonsense 465 507 11 12
Genomic Location (Zv9):
Chromosome 19 (position 39842124)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 38706107
GRCz11 19 38293227
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCGGCTCTGCTACCACTTCGGCTGTCTGGACCCTCCCCTGAAGAAGT[C/A]GCCCAAACAAACAGGTTATGGATGGATCTGTCAGGAATGTGACACCTCTT
Long Flanking Sequence:
AAGGTGGAGGTCTTTTACGGTTTATGTAAAATCAGATAGCTGGAGACGGTGCTTGAGCAGACCTATAACTAAGGACAGGATCTCAGTGTCTTTCTTGACACCTTGACTCCGGAATAAAAATCCTATAGAGATTTATCGACAAGATGAGCTGAAACTCATTTCAGCAGGACCAATCGAGCAGCGTGTTTTATGATGGCTGTACAAGGCCGTGTGAGAGGTTGTGTGCCAATGTGTTTTGAATCTATTAAGCATCTGTTACCTGACAGCAAATGGCTCTGTCACCATCTATCATACCTGCCTGGTTAGGGCCATACTGGCCTCTTGGCAGAGTATCAGCAGATTGTGTGTGTGTGTGTGTGTGTTTCTGTGAAGCGAGCGACGCCACCGCAGCTGCATTTTAATGTATTCTCGCTGCTAATGCGCTGCCTGTTTTCCTCATAGGTGTGATGAGTGTCGGCTCTGCTACCACTTCGGCTGTCTGGACCCTCCCCTGAAGAAGT[C/A]GCCCAAACAAACAGGTTATGGATGGATCTGTCAGGAATGTGACACCTCTTCATCTAAGGTGAGAGTCAACAAGATAAAAACAATCTCCTTCTGCCTGCTTTAGTTAGATTATAATCTTCTCCCAGCATTCCTGGCACATGAGTAATGCCTAAAATGTTTGTTTGATAGTAGTTTGTTAAGTAAAAGTACCATTAGTAGTTCAAAAATGTAGTCCAAGTAGAGTCAAAGTGTCAGCTGTAAATATTACACAAAGTATGAGTAAAAAGTAGCCCTTTTAAAAATACTCAAGAGTAGTGAGTGTTACGCTGGGAAAGGTTGATGCGTTTACATGTCATTTGTGCCTGTGTGTGTGTGTAAACGTAACATTCTGTAGTGCATTTAAGGACATTTCAGTCATCATACAGTCAACATCTGCCATCTTCTCATCAGCGGCATGCAATCACAACTGTCTCTGGTCCATTGCGTGTAAAGCAGGGGTGCCCAAACACGATCATTGATGC
Associated Phenotype:
Not determined