ZMP
si:dkeyp-51b7.1
Ensembl ID:
ZFIN ID:
Description:
PHD finger protein 19 [Source:RefSeq peptide;Acc:NP_001121998]
Human Orthologue:
PHF19
Human Description:
PHD finger protein 19 [Source:HGNC Symbol;Acc:24566]
Mouse Orthologue:
Phf19
Mouse Description:
PHD finger protein 19 Gene [Source:MGI Symbol;Acc:MGI:1921266]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21215 | Nonsense | Available for shipment | Available now |
sa1129 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa21215
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 |
---|---|---|---|---|---|
ENSDART00000113286 | Nonsense | 125 | 563 | 4 | 14 |
ENSDART00000142150 | Nonsense | 125 | 562 | 5 | 15 |
The following transcripts of ENSDARG00000078050 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12908423)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12353186 |
GRCz11 | 8 | 12390891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTCCTTCCTCATGCTTGTCTTGCATCTTCAGGCTTTCATCAGCTCTG[C/A]CACTTGCCCACGGTGGAGAGCTCAGCTGACCCATCGCCTTGGTTCTGCAG
Long Flanking Sequence:
AGGACCAGAGCCTTTTTTGATAAGTAGAAAATAGAACAGCACTCTTCAAAAAAAAAAAGTGGAAATGGAGTTATATAGATGTTGCCATGACTTCTTGCATGACGCAATGACTGGGGAACTCTTCTGCCTGTGGACAAAACTGATTAGCATGTGCTTGTGATAATGTATTTTAAAAGACTGGAGTGGAAAATGCGCTGTGATTTGCATTATAAACGCCGTGGCGTCTACAAAGCAAATAGAGAACTATTCTGGGTGTCTTTGATGGTGTTTGGTAAGACTGCATTACAGTAATGACTCGCTGGGGACGCAGAAGTGGCTCTCTGAAGTCTCAAGGATTAGTGTCGACTTCATCTCTGCTGATCATATTTACACATCTGATTGGCTTTGAGTAGATCTGTTGGGTTTTTTTTTCTTTTGGTTTGTGTGTGTGTGTGTGTGTGTGTGCTAACATTTGTCCTTCCTCATGCTTGTCTTGCATCTTCAGGCTTTCATCAGCTCTG[C/A]CACTTGCCCACGGTGGAGAGCTCAGCTGACCCATCGCCTTGGTTCTGCAGAAGGTGCATTTTTGCCTTGGCTGTGAGAGTAAGTACTTCAAATTCTTGTGTGTGTGTGTGTGTATATATTTTTTGCAGGATTTCTACATCTCCTGGAAAACCTGGGAATCCTTAAGAATTATTAAGTGTGTTTACATGCATATTCTAAACTCAGTTATGCTTTTTTTTTTTTTTTTTGCATTCATTTATTTTCCTTCGGCTTAGTCTCTTTATTTATAAGGTTTCGCCACAGTGCAATGAACTGACAACTTATCACGCATATTTTACACAGCGTATGCCCTTCCAGCCTCAACCCATCCTTTTGAAACAAATCATACACACTTATTCACACATATACACTATGGCCAATTTAGCTTATTAGATTCACCTATAGCGCATGTCTTTGGACTCTAGGGGAAACCAGAGCACCTGGAGGAAACCAACACAGGGATAACATGCAAAATCCACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1129
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113286 | Nonsense | 367 | 563 | 10 | 14 |
ENSDART00000142150 | Nonsense | 366 | 562 | 11 | 15 |
The following transcripts of ENSDARG00000078050 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12892490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12337253 |
GRCz11 | 8 | 12374958 |
KASP Assay ID:
554-1040.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAGGCCCAAAAAAGTGATGCACATAGGGGACGCAAAAAAGCAGTCAGC[A/T]GAAGCAGGTTAGTTTCACAATCTCTGAGCATTTCTGACAACCTTTTGTTT
Long Flanking Sequence:
GCTCAAGGCTACAGAATCTCACTGGAAGAAGTAGGTCATGTAGGTACTTCTTGCATATTGTTTCTCGAATTCTATGAATTCCGACTACTCAGCTTGCGTACTATATAGTAGGGAAGTATTTGACTTTGGACGCAGCCAACAACTTTTTTACTTGTCTAGAAAATTCTTATTGATATGAGAATTTTTTTATTTTTGAAGTAGAAACATGCAATAACCTTGATTTTTCAGTGACAACAAAAATAAGTATTATTTTGATTAACTAGCATTTGAAAAAAAAAGACAAAATGTTTTTGGGGGGGTCTAAACTTTTTTTTAAAATTTATTATTATTAAGACATTTTGTTTTCTTTTTGTTTTAGGTTTCTCTGCGGCAAGGAGATCAAGAAGAGGAAATGCATTTTCCGACTAAGAACGAGGGTCCCTCCTAACCCTCCATCTAAGTTGTACCCAGAGAAGGCCCAAAAAAGTGATGCACATAGGGGACGCAAAAAAGCAGTCAGC[A/T]GAAGCAGGTTAGTTTCACAATCTCTGAGCATTTCTGACAACCTTTTGTTTTCTTTCTAGTGCCTCTTTTTTATTAACTGTGCTTCTAGTTGATGGAAACAAACTCATCCATGAGACTGGTCATCAAGACATCTATCACAATAAAATTGAAATTAATTGGCTTTTTGTGTATTATCCAGTCGGCTGATCATAAATAAAAGCTTTTATTATTTTACCAAGGGACTTAAAGGAACACTTTGTTTGGAAATAGAGTTAAACAGTTTCTATTTACCATTAGTATGAATCTTGTCAAATTATCTCTAGGTCTGGTGGGAGCACTTGTAGCTTAGCTTAGCATAGATCATTGAATCTGATTAGACCATTACCGTCTTTCGGATGAGACGTTAAACCGAGGTCCTGACTCTCTGTGGTCATTAAAAATCCCATGGCACTTCTAGTGAAAGAGCAGGGGTGTAACCCCGGTGTCCTGGCCAAAGTCCCTCTATCGGCCCTTACGATCAT
Associated Phenotype:
Not determined