ZMP
si:dkey-97i18.2
Ensembl ID:
ZFIN ID:
Description:
Wu:fi20g04 protein [Source:UniProtKB/TrEMBL;Acc:Q7ZVG2]
Human Orthologue:
PHF20L1
Human Description:
PHD finger protein 20-like 1 [Source:HGNC Symbol;Acc:24280]
Mouse Orthologue:
Phf20l1
Mouse Description:
PHD finger protein 20-like 1 Gene [Source:MGI Symbol;Acc:MGI:2444412]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39110 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa13222 | Essential Splice Site | Available for shipment | Available now |
| sa36181 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39110
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002930 | Essential Splice Site | None | 1116 | 1 | 24 |
| ENSDART00000105158 | Essential Splice Site | None | 673 | 1 | 18 |
| ENSDART00000115266 | None | None | 1114 | None | 24 |
| ENSDART00000137311 | Essential Splice Site | None | 209 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 33926890)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 31664790 |
| GRCz11 | 16 | 31622717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAATACACTATAGGAATTAATTGCTATTCTCTCAATGAATTTGCAAAG[G/A]TAAATCTACATGTCACGCATACAGCGGAGGTCAGAAAGCAACTGTCATTC
Long Flanking Sequence:
TCAGCTAATTCTATTTATTATGTGCTAGTTAAATAATTAAAATGAAAGACAAAGCAGAAACCAAGGTTCTTATATAGAGAACTGAACACTAAAATATACTTTTTTTCACTGTTTATGATTTAACACAACTGAATATTTTCCAAAAACAGAAATACACTTGACTTTTTTTGAGGTGAGCTTTTAAGTTTAGAATTTAACATTGACCACTTTCTTTGTATCTGTATAACTTGATAGCAGTTCGAAGATGTCGCACAGAAGATCTACTCCACTTCAACTTCAAGCGAAAGTAAGACTGCTACTGTCTCTTTTACAACAAAACAAAACAAACACAAAAGCGTCTGCTTATTGGTCACGTGTCGGTCTGCGGTGCGCGTGCCCTCGGGCATTTTGTACGTCGCGTGCGTGCGCGCACACGTTCAGTTTGGTTAAAACTAACTGAGCTGGAATGAACACAATACACTATAGGAATTAATTGCTATTCTCTCAATGAATTTGCAAAG[G/A]TAAATCTACATGTCACGCATACAGCGGAGGTCAGAAAGCAACTGTCATTCTTCGAGTCGTGTTAACAAAGACACTGTCCTGTCATTTTTTTTTTCATCTTTTTTTGCACATAGTTTTATCCCCTCGGAACGGTTTAGCTAGTCAGCTGGTACAGCATTAGCTGTTTGCTAGCTCTGCTGTGCTAACTGGACAATGAGAGGTTTGACCTAAAGTTTTGTCTTTTAAATATTGATATGTATCGTGTATGCTCACGGGTTTACTAGTGTTTTCAAGAAAACCTTGACAAATGTATTCAAGCTGGAAAATATTTACAAGAAGCTCGTTACTCTGTACCTAGCATTAGCGAGCTATGGTAATCCAGTAAAAAGAGCAAACTGCCCTCCTAATATTATCATTTGTTTTTTTCAGGATTAAATTTGCATCAGGTTTTTTTAGAGAGTTCGGTTTTATATATGTGGTTGCAGTAGTTTAAAATGGGGATTTATTTCGTGTGCCAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13222
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002930 | Essential Splice Site | None | 1116 | None | 24 |
| ENSDART00000105158 | Essential Splice Site | None | 673 | None | 18 |
| ENSDART00000115266 | None | None | 1114 | None | 24 |
| ENSDART00000137311 | Essential Splice Site | None | 209 | None | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 33926889)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 31664789 |
| GRCz11 | 16 | 31622716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAATACACTATAGGAATTAATTGCTATTCTCTCAATGAAWTTGCAAAGG[T/A]AAATCTACWTGTCACKCATACAGCGGAGGTCAGAAAGCAACTGTCATTCT
Long Flanking Sequence:
CAGCTAATTCTATTTATTATGTGCTAGTTAAATAATTAAAATGAAAGACAAAGCAGAAACCAAGGTTCTTATATAGAGAACTGAACACTAAAATATACTTTTTTTCACTGTTTATGATTTAACACAACTGAATATTTTCCAAAAACAGAAATACACTTGACTTTTTTTGAGGTGAGCTTTTAAGTTTAGAATTTAACATTGACCACTTTCTTTGTATCTGTATAACTTGATAGCAGTTCGAAGATGTCGCACAGAAGATCTACTCCACTTCAACTTCAAGCGAAAGTAAGACTGCTACTGTCTCTTTTACAACAAAACAAAACAAACACAAAAGCGTCTGCTTATTGGTCACGTGTCGGTCTGCGGTGCGCGTGCCCTCGGGCATTTTGTACGTCGCGTGCGTGCGCGCACACGTTCAGTTTGGTTAAAACTAACTGAGCTGGAATGAACACAATACACTATAGGAATTAATTGCTATTCTCTCAATGAATTTGCAAAGG[T/A]AAATCTACATGTCACGCATACAGCGGAGGTCAGAAAGCAACTGTCATTCTTCGAGTCGTGTTAACAAAGACACTGTCCTGTCATTTTTTTTTTCATCTTTTTTTGCACATAGTTTTATCCCCTCGGAACGGTTTAGCTAGTCAGCTGGTACAGCATTAGCTGTTTGCTAGCTCTGCTGTGCTAACTGGACAATGAGAGGTTTGACCTAAAGTTTTGTCTTTTAAATATTGATATGTATCGTGTATGCTCACGGGTTTACTAGTGTTTTCAAGAAAACCTTGACAAATGTATTCAAGCTGGAAAATATTTACAAGAAGCTCGTTACTCTGTACCTAGCATTAGCGAGCTATGGTAATCCAGTAAAAAGAGCAAACTGCCCTCCTAATATTATCATTTGTTTTTTTCAGGATTAAATTTGCATCAGGTTTTTTTAGAGAGTTCGGTTTTATATATGTGGTTGCAGTAGTTTAAAATGGGGATTTATTTCGTGTGCCAAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36181
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002930 | Essential Splice Site | 871 | 1116 | 21 | 24 |
| ENSDART00000105158 | None | None | 673 | None | 18 |
| ENSDART00000115266 | Essential Splice Site | 869 | 1114 | 20 | 24 |
| ENSDART00000137311 | None | None | 209 | None | 8 |
Genomic Location (Zv9):
Chromosome 16 (position 33912352)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 31650252 |
| GRCz11 | 16 | 31608179 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAAACTGAAATGTCTCCAGATTTGTTACTAAAATATGCTCTTTTCTCA[G/T]GTCAGAGGTGGAGCGCAAAGTACCGCCATGATAAAGACTGGCTTCAAAAA
Long Flanking Sequence:
CAAGATATTCGGAAGAATGCTTTAAGTTGTATTTAGTTGACATCCATAATAGAAAGAAAATAATACTGTAGAAGTTAATGGCTTTTTTACAACAGTTTCAGTATGTCTTCCGTTGTATTCAACAGAATGAAGAAGTGAGGGATTAGCATGATGACAATTAAAAATAATGGGTTAACTGTCACTTTAAATGTGTTGAAATAGTGCCTGAAAATGTGTATTTGTCTTTTTGCGTATCACTTTACAGTGTGAAGAATGTATGTGCTGGCAGCACAGTGTATGTATGGGGCTTTTGGAGGACAGCATCCCTGAACAGTACATCTGTTACATCTGTAGAGACCCTCCAGGTAACAATCATGCAACAGTTGAAAATTGTTAGCAGGATCTTTAACTGTATCCTGCTATTACAAATGTCTGTTTTTATTCCTTAAATGAATAAAATTAATTCTAAATATTAAACTGAAATGTCTCCAGATTTGTTACTAAAATATGCTCTTTTCTCA[G/T]GTCAGAGGTGGAGCGCAAAGTACCGCCATGATAAAGACTGGCTTCAAAAAGGCCACATGTACGGCCTGTCTTTCCTCGCCGAGAACTACTCGCATCAGAATGCCAAGAAAATCGTGTCCACTCACCAGCTGCTGGCTGATGTTTACAGTGTTAAAAACCTGCTCCATGGCCTTCAGCTAAAGATGGATATTTTACAGTAAGAGCAATTACCAGAAGCCTGCTTAATCCTTTAAATTAGATGTTAACTAATTAACTGTCACTAGATATTTTATGTATAGAATTTGTAGCGCACAGTTGTTACGCTTGAAAAACCTAAGAATTTTAAAGCGTTTTAAAGGGCTTCTTTTATGCTCTTGTTGTCATAAAAATAAGTCTGTGACATTTTAATTGGAAAATTGATCAGTTGTTATATCATGCTTTCCCAACTTTTTGGTTGGAAGCACACACACCGTTTTCGTGGACTAGACACAGCACTACAGTTAAGGTGTTTGAGTTTAGAA
Associated Phenotype:
Not determined