ZMP
si:ch73-119j17.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
PHF1
Human Description:
PHD finger protein 1 [Source:HGNC Symbol;Acc:8919]
Mouse Orthologue:
Phf1
Mouse Description:
PHD finger protein 1 Gene [Source:MGI Symbol;Acc:MGI:98647]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9170 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15490 | Nonsense | Available for shipment | Available now |
sa42809 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22939 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9170
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080059 | Splice Site, Nonsense | 21 | 519 | 1 | 14 |
ENSDART00000134471 | Splice Site, Nonsense | 26 | 326 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 48489728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 45458949 |
GRCz11 | 16 | 45425665 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTTTTGGCCAGGTGGAGCGATGGACTTTTATATCTCGGCAATGTYAAA[C/T]GAGTAAGTTTCTCCAAGTTTGTTCGGAGRAGGGAGCCGGTGGARAGGATG
Long Flanking Sequence:
ACATCTCTTCCCCGTCTCTGTGACCCCAGCAGAGCCGATCACTCCACACAGGTACATCCCGTGCACGTATGATCTGCCATGCGTGTTAATTGATATGTGCGTGCGCGCGCCGTCATGTGTGTCAGCTCTCCTGAGTTGCGCGCATTGATTAGTGCACATCTGGCCGCGCGTTTTGCATGCATTGTTGTGGCATCTGCATATGCATTACGGTCGGTTGCATAAAGCAGCCAGTGTTTTTTTCCCCCTTCTTTTTTCTTTTTGATCATGTGTGGCACTGCAATGTGCATTGACTCTTCATCATTTATCCTACTGTACTGTATACTGTCGCTATGCACAGAGTTTAACCCTTTAGGCTGCTGCTGTTTGCTACTTGATTTGAAAGCCTCTGGATGTTTTGTGCGCTCTTCTTTCCCGCTCTCTTCAGGATGGGGGGAGTCAGTGAAGGAGAGGATGTTTTGGCCAGGTGGAGCGATGGACTTTTATATCTCGGCAATGTCAAA[C/T]GAGTAAGTTTCTCCAAGTTTGTTCGGAGGAGGGAGCCGGTGGAGAGGATGAAAAAGCAAGTTTTGAAAACTGCGACTTGTACTTGTGAAAATGAGTGTGGTGTTGTTTGGGATGTGTTCGTCTTGCAGGTGGACAGTGTCAAGCAGTGCTGTTTGATCAGATTTGAGGATAACTCTGAATTCTGGGTCCTCAGGAAAGACATCCACTCGTGTGAGTTTAAAACTCTGAATTTTAAGTCAAAAACTAAGCGTAAACATCTCGGTGAGCAGCTTGATGTCAAAACGACATCCAATAGACATCAAGTATAATGTCAAAAAACGCATTCAAATTGCAAATCGACTTGATGTCCAAATCTTGCCATCCGCTTGACATCCACACACTGATGCTCTTTGCCACCAAATTAAAAACACCAAAAGTAATATATTAAACGTTTTATTTATTTGAAAGCTTAAGAACAAAATTACAAAATTTATACTTTTAATTTTTTCCCTACCATGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15490
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 |
---|---|---|---|---|---|
ENSDART00000080059 | Nonsense | 272 | 519 | 9 | 14 |
ENSDART00000134471 | Nonsense | 277 | 326 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 48504181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 45473402 |
GRCz11 | 16 | 45440118 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGTCAGACACGCCRAGGCAAGACCGTTGCCAAAACCTGCTCAACGCTT[T/A]AAACTCCCACAAAGACAGGTGAGACAYGGATTACGCTCGGAAAAAGGCTG
Long Flanking Sequence:
GAATTCCGTTATTTACAGGAGGCCTCCAAAATTTCCAGGGGCCCTAAGCAGATGCTTACCTTGCTTATTATTTAAATTCACCCCTGAATATAATGTTGTTTCTAAAATAAAGATTTTTTTCTCTATCAATTATAAATTCCACTTGCTTCAGACTAGCAAAAGAACTCAAATCATTAATTCATATATGTGCTATGAAGTGCGTTAGTGCTTCTGTCGACTTTTTCATAAAAGAAACATCAGCACAGAAAAGAAAACAGCAGTCGTTGAGCGATTTTTGCAAGTTTTTCAGCCTGTAAATGGGGTCATTTTGGATTTTCTGTTGACTTGAATGTATTCCCGAGTGTACTTTTGAATACTCTCTCTTGCAGTTTGTGGTCAATCTGAGCTCTTATCTTTCAAATGCATTTGTTCCACGCCGGCCTTCATTCCTTTCTGTATTTGTGTCTCTCAGCTGTCAGACACGCCGAGGCAAGACCGTTGCCAAAACCTGCTCAACGCTT[T/A]AAACTCCCACAAAGACAGGTGAGACACGGATTACGCTCGGAAAAAGGCTGATTTCCATACACCAGCCCATAGGGGGGTGTACTGCGGCGCACATTTGCAATAATATCAGCAAAAGCATTACTGTAATTGCTTTACATTATAAGTGGTTTTCCCCTCCCCACAAATAGTGTTTTGATAGCTGACGGTGGTTTCGTCTTTCAGAATAAATTATTTAAAGTCCATTTCCATTTTCTTTCTGTCAAGGTTAGTGGTTGATGCCCGCTCATACGCTGGCGCTTAAATAACCGAATCAGATGTTTTAGTTTGGCGGCCAGAAACAAATAAAAATCTGTCAGCGAGGCCTGAGGACAGCAGTTGAATACCAATGCAATCTGATTTGGGTTTATCCTAAAGGTTCGTCTCGGGGAAGGAAATCAAGAAGAAGAAATGTCTCTTCGGGCTCCAGGTTCGAGCTCCTCCCCCTCTGTCATCCGACCAATCACCTTTCATCGCCGAACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42809
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080059 | Splice Site, Nonsense | 368 | 519 | 11 | 14 |
ENSDART00000134471 | None | None | 326 | None | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 48505888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 45475109 |
GRCz11 | 16 | 45441825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAACAGAAATCAAACATCACTGTCAAGAGTTTGTACAAGCACACAGA[C/T]AGTTGAGCTTGTTTTTCTTGTAGTCTTTTAATTATTTTTTGCAAGATGCA
Long Flanking Sequence:
ACTGTTGTATATATATATTATTATTATATTCTATATTATAATTGTTGTTGTTGTATATATACACACAAACACACACACACAACAACAACAACAACAACAATAATAATAATAATAATAATAGTAATAATGACAATAATAATAATAATAACAACAACAACAACAACAACAACAACAACAATAATAATAATAATAATAATAATAATGATAATATTGATATATATATTATTGTTATTACACATTATTATTAAAATATAATATTTCTTTTTTTTTACTATTTAAAATTTCTATAAAAAAAATGAATGAAGTAAAGAGTAAGTACAATTGTAGATGTTGCTGTTGAAGTGAGTGGTTGTCTTATCTTTAGCCCGTCGTCAGTGTCCTGTCAGCGGAGAGCAGTGGCACCGGATGTGCGTAAACCCAAACGTCGGGTCACTGAGACACAGGTCAGTGCAGAAACAGAAATCAAACATCACTGTCAAGAGTTTGTACAAGCACACAGA[C/T]AGTTGAGCTTGTTTTTCTTGTAGTCTTTTAATTATTTTTTGCAAGATGCAGAAAAATCAAGAAGTGTTTACTCCTGCAAGTAGTCATAAAATGCATAGTTTACATAACATTAAAATGATTGCATACGTCTGTTTTGAAGAGATGTACAGTATTTTAAATATAAGAAAACAGCATTTCCTATTTTAGATACCATTTAAAATTAAATAAAATTTTGTATTTTTATTTTATGCACAGGAAAACAATCCATCTATCCATTTGTTTGTCCATCAATCAATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCGTACATTTGTTTGTCCATTCATCTAACCTAAATTATTTATTTTTATTGTAGTATTATTATTAATTTGTATAATCTTTTTAATAAATTTTTGTAGTTTTCTTCTTTTTGTATCCTTGTATCAGTTTTTTATATGTCTATGTAGTTTATTGCAACAAATAATAACTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22939
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 |
---|---|---|---|---|---|
ENSDART00000080059 | Nonsense | 484 | 519 | 14 | 14 |
ENSDART00000134471 | None | None | 326 | None | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 48507703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 45476924 |
GRCz11 | 16 | 45443640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCGGGACGTGCCTCCCTTCCACAGCCCCGTGGGCATGGCTGCACCAT[C/A]GAGCATGGGCTGGGCAGGAGGAGATGCTGTCCGAATCCTTGCCCGACGCG
Long Flanking Sequence:
ATACTGTTTAATGCTTGATTCTGATTGGCTAATGAACATTTATGGAGTGCTCTTATTCCTCAGAAAAACGCACAGCTAAAGTAATTCCAGGCAGATTAGTTAACACAGAAAGTTTTGGATGAGATGTGTAAGAAATTAGTTCTATATTAGGTCTGAGGACAAAAACATTGCTGTATTGTTTGTATTTTTACCAAAACCTGGTTCAATTACGTTTCAACAGCTCCTTTAGAAATATTACTCCCAGGAAAATACGTGATGTGTTGAATACTTTTCCCCCCACTGTATATTTAAAAGGCTTCTGGATGTTTTTTGATGTTTCATCTCTGTTTAAATGTCTGATGTTGTCCTCAGTGCAGAGGACCCTTGTGGACTTCCAGCTCCCTGCCTTCCGTGCTCTGTGTCGTCGGCTCACGCACCGGCGCAGCGCTATGAAAGCTGCCCTTCTCTCTTCCTGCGGGACGTGCCTCCCTTCCACAGCCCCGTGGGCATGGCTGCACCAT[C/A]GAGCATGGGCTGGGCAGGAGGAGATGCTGTCCGAATCCTTGCCCGACGCGTGACGGCCGACGGAAAGCTCCAGTACCTGGTGGAGTGGGGGAACGTGAGCGTCTACTGAAAACACCATCAACAGAGACCCAGGAAAGGGCTACAGACATGCGGATGAACTGCTAGAAAACTGTGAGAGGCTGTTTGGGACAAAACACACTGAAACACTTACAAATATATGTTTGGTCATACACTCACCGGCCACATTATTCAGAACTGTCTTAATCCCTGGAAAACCCTCTGGTACTGCAAATATTCCTTTTTGAAATGGAGATTTTGGTCCATATTGACATGATAGCATCACACAGTTGCTGTAGATTTGTTAGTTGCACATACATGATGTGAATCTCTCGTTCCACCACATCCCAAATGTGCTCTATTGGATTGAGTTCTGGTGACTGTGGAGGCCATTTGAGCACAGTGAACTCATTATCATGTTCAAGAAACAGTCTTAGATGATT
Associated Phenotype:
Not determined