ZMP
phf8
Ensembl ID:
ZFIN ID:
Description:
Histone lysine demethylase PHF8 [Source:UniProtKB/Swiss-Prot;Acc:P0CH95]
Human Orthologue:
PHF8
Human Description:
PHD finger protein 8 [Source:HGNC Symbol;Acc:20672]
Mouse Orthologues:
4921501E09Rik, Phf8
Mouse Descriptions:
PHD finger protein 8 Gene [Source:MGI Symbol;Acc:MGI:2444341]
RIKEN cDNA 4921501E09 gene Gene [Source:MGI Symbol;Acc:MGI:1921292]
RIKEN cDNA 4921501E09 gene Gene [Source:MGI Symbol;Acc:MGI:1921292]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7309 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9816 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7309
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026314 | Essential Splice Site | 33 | 1032 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 23 (position 27847323)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27680145 |
GRCz11 | 23 | 27606686 |
KASP Assay ID:
554-4740.1 (used for ordering genotyping assays)
KASP Sequence:
CCCGATTCATGATTGAGTGTGATGTTTGTCAGGACTGGTTTCATGGCAGG[T/G]GAGGTTGCAAAATTTTTAAATGACTGTTAAAAGCTAAATCTTGTACTTNN
Long Flanking Sequence:
ACTAATTCTTTTGTATTATTTTGAACACATTTCCAAAGTTTAATATTTTAAATAATTTACACATTCTATTTGAATTGTAGTTTGGCTATAATACGTTGAATTGTTCATTTGACAAATTTTTCTTACTTTCTCAACAGGTGTCGAGCCATGGTATGCACCTATTGCCCGGTTTGACTGCAACGGCTGAAGCATATTGATCTACAGTTGTCTGAAAGCTGTTGACACTGCCAACAAAATTTACTGTGAATCTGGTCTTTTCAACACCTCAACGGAATTGCTGACCTTTGTAAAGAAAATTGACACTCCACAGAGACAAATAAATAAACTGTGGTGCTTGGAAAAGAAGCAATACCATATTAAAAGACTTTTTTACATTAAGATAGTAGGCCGGAGGCTTTAGAATGGCATCTGTTCCGGTTTACTGCCTGTGTCGTCTCCCTTATGATGTCACCCGATTCATGATTGAGTGTGATGTTTGTCAGGACTGGTTTCATGGCAGG[T/G]GAGGTTGCAAAATTTTTAAATGACTGTTAAAAGCTAAATCTTGTACTTCTTATGAATGTGTTTTTTGTGAATGTAATAATATATGTTTTTTCTTTTTGTGTAGTTGTGTTGGTGTGGAGGAGGACAAAGCAGCAGAAATTGATCTGTATCATTGTCCTAACTGTCAGGTGACACATGGACCATCTGTCAGTAAGTGTCACAAATGGTGTAATAAATGTCAATTCTGACTATTTCTTAGTAAGTCTTTTTGTGGATTAAAAATAAATGTTTTCAGAGTATCTGTACCTATATTCATCTATTTTAAATCTCTGTTCATAGTCAATACAACCTTTATATAATCATGTTCATAGTACATCCATCTGTAAATATCACCCATAGTTTTTCTTTAATTGCACTTTATAACTTATACCTGTATCCTGCACTTGCTGCTGTTGCACTCCTGTTTAGACCTAAACTGCATTTCCTGGCCTCGTACTTGTGCATATTTAATGACAATAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9816
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 |
---|---|---|---|---|---|
ENSDART00000026314 | Essential Splice Site | 839 | 1032 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 23 (position 27836634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 27669456 |
GRCz11 | 23 | 27595997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAATGAAAAGGAAGCGAAACTGGGATGATACCCCTTGGAGTCCCAAAG[G/A]TAAATAACATGTATGAAATAMATTTTTGCAGACTTTNNTTTTTTTTCTAA
Long Flanking Sequence:
ACTTCCATCATCCAGGTTAAGTCTCTGGAGGAGTTTATGAGTTCACAGAGCTGGGTGCACCTCTGAATGGATCTAGTGGACTCAGCTCGGCTCGGCTCCAAATGGCTCAATGCTGTTTTTAGCCTTTCTAAAGCATATAAACACAGTTATTCTCTCTATAAAATCCATGTTAGCCATTTAGCAATGAAGCTACAGTCACCGGGCTGACAGAAGCCCTGCCCATCACGCGAATCCGCGTCTGTTCTGAACCGGATTTGACGTGCGAACGAAGCGAGTAAACTCAAATGTTCACACGTTTATTTACGCACGAATAGCAAGATTTATCCACTCATTCCGCGCCTGGACACAGTATAAGAATGAAAATACTCTGGGTGATTTCACCACGTTTGCACCCTCTTTTTCAGTGTATCCATCACTAGAGTCTGATGAGGAGGATCACGTAAGCAAGTCCAAAATGAAAAGGAAGCGAAACTGGGATGATACCCCTTGGAGTCCCAAAG[G/A]TAAATAACATGTATGAAATACATTTTTGCAGACTTTATTTTTTTTTCTAAACGGTTCTAATCATTGTTTGTTTAAATGCCTTTAGCCCGTGTAACCCCTACATTGCCGAAGCAGGAGCGACCGGTGAGAGAGGGTGCCAGGGTTGCATCTGTAGAAACCGGGCTGGCAGCTGCGGCAGCCAAACTGGCACAACAGGTGAGCTTCTGTTTCATTGTGCCAGAATTTCTATCTACATGAACCATTACATACAATTTTGCCTCATTTCCACTAGGCTTGTGTTTCCACTGCCAATTAAGTTAAGCAATTAAGCACAGCCATACACACAAAGTACCCTTAATCAGTAGGCATGGTATATGCCAGAAAGTTGCAATTAATTCATTTTCAATCATAAAAGAACCCAATACAGGCAGTTCACATATCGTGTCTTTTGTGAACTCAAGTTTATTTTTTCGAATGTAGATGCGTGTAGATAGAGAGAGGAATCTGCACACTTTGCACAC
Associated Phenotype:
Not determined