ZMP
zgc:193796
Ensembl ID:
ZFIN ID:
Description:
polyhomeotic-like protein 1 [Source:RefSeq peptide;Acc:NP_991270]
Human Orthologues:
PHC1, PHC1B
Human Descriptions:
polyhomeotic homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:3182]
polyhomeotic homolog 1B (Drosophila) [Source:HGNC Symbol;Acc:34502]
polyhomeotic homolog 1B (Drosophila) [Source:HGNC Symbol;Acc:34502]
Mouse Orthologue:
Phc1
Mouse Description:
polyhomeotic-like 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:103248]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14378 | Nonsense | Available for shipment | Available now |
sa22883 | Nonsense | Available for shipment | Available now |
sa18402 | Nonsense | Available for shipment | Available now |
sa22884 | Nonsense | Available for shipment | Available now |
sa31005 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22885 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14378
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 |
---|---|---|---|---|---|
ENSDART00000058496 | Nonsense | 54 | 901 | 3 | 15 |
ENSDART00000128810 | Nonsense | 54 | 828 | 3 | 15 |
ENSDART00000129536 | Nonsense | 54 | 897 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34258055)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31989555 |
GRCz11 | 16 | 31943585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTTATAGGCRCTGCAGGCCTTACAGAGGCAGCCCAATGCAGCTCAGTA[T/A]TTCCAGCAGCTGATGCTGCAGCAGCAGATCAACRGCGCAACCTGTCAACT
Long Flanking Sequence:
ATACAGATTTGAACAGACTAGAGCGCTCCTGCAAGTTTACAAGTGTGTCTGAGAGAAAGTGTTCAAACTGTTTGATTGTATTTGTTATAACTAGCCGTTTTAATTCACATTTAATGAATGAGAACAGCGTTTAATCTCTTCTAAATCGTTTGTTTATGCATATTTTTCTCTGGTATTCAGTTACAAAGTTTGATTGACTGGTCGTCCATCCAGTGAGCATGGAGGCAGGAGAAGACCAGACCAACTCCAGCTCAACCAATAGCAGCGCAGCTTCAGGGGGAAACTCCCGCCCTCCTCAGATAGCTCAAATGTCTCTCTATGAAAGGCAAGCTGTTCAGGTGGGTCAGAAAGCCTGCAGTCTGAACTAATAGCCAGATTGAAGTGTAATTTAAATCACTTGTTCACATTCGTGTGTTAAATTGAGGGAAACATAGTTGTTTGTGCTTCTCAATGTTATAGGCACTGCAGGCCTTACAGAGGCAGCCCAATGCAGCTCAGTA[T/A]TTCCAGCAGCTGATGCTGCAGCAGCAGATCAACAGCGCAACCTGTCAACTCCACAACCTGGCTGCTGTGCAACAGGTGAGACTCTTTAGACCAGGGGTGCCCAAACTTTTATTATGAAGGGCCAAAAACAAACTTTATTGAGGCTAGTGGGCCGAATTTGTTTAATAATATTTAAAAAATATATATAAAACATTGCTTTATATTAACTAAAAGGGTATATATTTTTTACATTTTATAATGAACTTATTACAGTAAAAACAAAAACAATCTCATTTATAATAGAGTTGCACTGTTTTTTGCCTTGATTTGCTCTGACTTGTTGAGTGACAGTATTTACATTTTAAAAACACAGATTAATTTACATTTAATTGAAACATTTCATTTCAGTTTGCTTTTTTGTTGCTCGGTAACAAAACAAACACACAAAAAAGGTTACATCAAATTAGAAATGAAAATCTCTATTAAAGGCATTCTCCCCAATCCTCTTATTCTCAAATGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22883
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058496 | Nonsense | 260 | 901 | 8 | 15 |
ENSDART00000128810 | Nonsense | 187 | 828 | 8 | 15 |
ENSDART00000129536 | Nonsense | 256 | 897 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34265920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31997420 |
GRCz11 | 16 | 31951450 |
KASP Assay ID:
2260-9915.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGTACATTCCCACTTAACCAGCAGACTCAGACTCCACAACAGTTTGGT[C/T]AATCAACCCAGCAGGTCCAACCACAAACTCAACCCCTTGCCAACGCCAAA
Long Flanking Sequence:
TTTTGTTGTATCTCCTTATTTTGTGATGTAATATTATGCTTTGTTTCTGTATGTTTGTTTTGAATATGTAAGTCGTATAACTTATAAATGTGTATTTTTTTTCAGTTTTTCTTGTTGTGAGATAATGTATGAGATTATGTGATCCTGGAGTGTACAAAAAGGAGCAACATACCGTGATGAACAATGATGAAGAGCTGTTTGCTCAATGTTACACACCTTCTATCAGCCTTTTTATTTTAATAAATTGCCATTTTTAGAGCTTTGGTTTTGTCGCTTTTTTGAATAAATATTTTACAGAAAATAAATGTAAATTTGAAAGTTGTAACAATGATTGTACACATTCATTACTTTCAGTGTTTCCTCTTTGACTTTAATGTCAAATTTCTACATATTGTTTATTTTCCAGTGCACTGACTATTTGATCATTTATATTCCTGTCTCTCTGACCTAAAGGTACATTCCCACTTAACCAGCAGACTCAGACTCCACAACAGTTTGGT[C/T]AATCAACCCAGCAGGTCCAACCACAAACTCAACCCCTTGCCAACGCCAAACTCCAGAGCTTCTCCAACACCGCCAATCCCAGCGTGCCTGCCCTCAACGTAAAGCCCACTAACCAATCCGCTGTTGCCCCACAGCAAGCAGGAGCTTCCTCCAACCCCCCGTCCTCCTCGCCCACTCCCTCACTCCCTCTCTCCCAGCTTCTCCTTTCTCAATCTGGCTTGCACCAAACTCGAGGTGTACCAGGTTCTACAGCCACCGTTACCCACATCCTGGTACCCACTTCTAACGTCCCCACATCTACTCAAGGTTATCCACTGGGAACGGTGGCGACCAAATCCAACATGACTGCCCAGACATTGGTGGTGCAGCCACTCCAGCAAACGGGGGCAAATCTGAGCACGGAGAAGCTAGCTCATGGTACAGGGCATGTGCCAATTCAGCCTAAAACGGCTCAGGGCCATCGGGTGCCAGTACAGATGTCCCCTCGCCACCCACCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18402
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058496 | Nonsense | 522 | 901 | 8 | 15 |
ENSDART00000128810 | Nonsense | 449 | 828 | 8 | 15 |
ENSDART00000129536 | Nonsense | 518 | 897 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34266706)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31998206 |
GRCz11 | 16 | 31952236 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTTAAAACAGCCCAAAGTGCCCTCCCTATCTCTCAGATGCAGACCAAT[C/T]AGAGTGCAGTATTGASTCAGGGTAATCCCGCTTCAGTCACACACKCCATG
Long Flanking Sequence:
ACGTCCCCACATCTACTCAAGGTTATCCACTGGGAACGGTGGCGACCAAATCCAACATGACTGCCCAGACATTGGTGGTGCAGCCACTCCAGCAAACGGGGGCAAATCTGAGCACGGAGAAGCTAGCTCATGGTACAGGGCATGTGCCAATTCAGCCTAAAACGGCTCAGGGCCATCGGGTGCCAGTACAGATGTCCCCTCGCCACCCACCTCCCATTCTCCCAGCACCACCCAACAACGGCCAGGCCACCGCAGGTCTTCACCCTCCCCACGTCCCAGTTCAGCTGGTCGGAGCAAGGCAGAGCACTCTGGGAAACTCACAAGCGTTAGCATTGGCCCAGGCTCGAACTTGTTGCTCCCAGCAGGACGGAACAGCTGCCGTGGGAGTCAATAACCCGGGCAATGTTGTTACCATGGTTACTGCTATGGATACAAGTGGAGCTGGCATGTGCCTTAAAACAGCCCAAAGTGCCCTCCCTATCTCTCAGATGCAGACCAAT[C/T]AGAGTGCAGTATTGAGTCAGGGTAATCCCGCTTCAGTCACACACTCCATGGATGGACAGAATAACTCTGGAGACTCTTTGTTTGTTCAGTCTGCACAAGCGCAGGTTAGTGGATAATGGGTGAACTCTGATTCTTCATTTGCCATGTCTATTGTGAGACTCATGCACTTATTTTTATCTTGTAGATAAAGCCTGCTATTGGTCCAATAAAAAGGAAGTCAGAGTCAGATTTGACCCATGAGATTTCGAATGAGCCAATCAGTGGAAGTCCCTCAATGCAAGACTCCGCCCCTCCTCTCTCGCCTGCTCCTTCACTGGATACAGGTCAGCCTTGTGTAGTGAAAGATTGACTGTTTTGGTTGTGCTGGAGCCCCTCAGATCAGGGCTGGGCGATATGGCACAATTTCAGTCTCGATAATTATTTGTCCATATTAAACGATAATGATATATATTTCAATGCAAGTTGTTAATACTTCCATATTTAAGAGTACCCCAACAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22884
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 |
---|---|---|---|---|---|
ENSDART00000058496 | Nonsense | 577 | 901 | 9 | 15 |
ENSDART00000128810 | Nonsense | 504 | 828 | 9 | 15 |
ENSDART00000129536 | Nonsense | 573 | 897 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34266952)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31998452 |
GRCz11 | 16 | 31952482 |
KASP Assay ID:
2260-9917.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTGGTCCAATAAAAAGGAAGTCAGAGTCAGATTTGACCCATGAGATTT[C/A]GAATGAGCCAATCAGTGGAAGTCCCTCAATGCAAGACTCCGCCCCTCCTC
Long Flanking Sequence:
CCACCGCAGGTCTTCACCCTCCCCACGTCCCAGTTCAGCTGGTCGGAGCAAGGCAGAGCACTCTGGGAAACTCACAAGCGTTAGCATTGGCCCAGGCTCGAACTTGTTGCTCCCAGCAGGACGGAACAGCTGCCGTGGGAGTCAATAACCCGGGCAATGTTGTTACCATGGTTACTGCTATGGATACAAGTGGAGCTGGCATGTGCCTTAAAACAGCCCAAAGTGCCCTCCCTATCTCTCAGATGCAGACCAATCAGAGTGCAGTATTGAGTCAGGGTAATCCCGCTTCAGTCACACACTCCATGGATGGACAGAATAACTCTGGAGACTCTTTGTTTGTTCAGTCTGCACAAGCGCAGGTTAGTGGATAATGGGTGAACTCTGATTCTTCATTTGCCATGTCTATTGTGAGACTCATGCACTTATTTTTATCTTGTAGATAAAGCCTGCTATTGGTCCAATAAAAAGGAAGTCAGAGTCAGATTTGACCCATGAGATTT[C/A]GAATGAGCCAATCAGTGGAAGTCCCTCAATGCAAGACTCCGCCCCTCCTCTCTCGCCTGCTCCTTCACTGGATACAGGTCAGCCTTGTGTAGTGAAAGATTGACTGTTTTGGTTGTGCTGGAGCCCCTCAGATCAGGGCTGGGCGATATGGCACAATTTCAGTCTCGATAATTATTTGTCCATATTAAACGATAATGATATATATTTCAATGCAAGTTGTTAATACTTCCATATTTAAGAGTACCCCAACAATGACTGAAGCCACAAAATGTAGAGGGTCCATTAAATGGCATGATATTTTCTGTGGCGGTAAATTTGGTACATCTTTAACATCAACACACTTTTAGATTGCCATTGTTGCACATTTCTGCTGTGTGATTGGCTCTTAGATCAATTTAGGGTGCTTTCACACCTGTGAATCGATTCAGTTGTTTCGAAACAGAGATTACAAATGTTACATTGTTGCTCTTTGCTCTTGGAGCGGTTCGCTTTCACATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31005
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 |
---|---|---|---|---|---|
ENSDART00000058496 | Essential Splice Site | 603 | 901 | 10 | 15 |
ENSDART00000128810 | Essential Splice Site | 530 | 828 | 10 | 15 |
ENSDART00000129536 | Essential Splice Site | 599 | 897 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34269645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32001145 |
GRCz11 | 16 | 31955175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTTTTGCTTTGTCTTCACCTTGCTTATTTTCTTTATTTCTCATTTA[G/A]TCCCAGAGATAGCATTCTCCTCTCCTCCTACATTGTCCCTCTCTCTGCCT
Long Flanking Sequence:
CAAAAGGATACGTTTTTTTTTTTTTTTTTGCAGAGATCAGCCCATATAAACAAACTGTTGTTGAACTTGTGTAAGTCTCAGAAATTCTTCGGAAACTTCAAATATAATTAACACAGGATTTGGTTTAATCAGAATGTCTACTGTATCTGAAAAAAAACTTTTGTTCCAGTAACTCTGTAATCTGGGACATATAACAAGAATGAGACAGGTTGGAAACTGACATTTGTCACACAATGGCGACACTTCTGGAAATGTTTGATTCAATTTACACTTGGAATAGTGAAGCCTATGAAGCACTTTAAACTGAAAGAGACAATGTCTTGAATAATGGAACATCTGTGAACCAGTTCAAGACTTTGTTCCCAAATTTCACTTTTACATAATGTAATTTGTATTAAATATAATATTTACTGTTTTAATTGTTTATTTGTATTATTATGTAATATAGTTAATGTTTTTGCTTTGTCTTCACCTTGCTTATTTTCTTTATTTCTCATTTA[G/A]TCCCAGAGATAGCATTCTCCTCTCCTCCTACATTGTCCCTCTCTCTGCCTCTTCCTCTCCCTCGTGGAGCAGGACAGGGCGATCGAGCACCTGTTCCACAGGCTGTGGTCAAACCTCAGGTTCTCACTCACCTCATCGAGGGCTTTGTCATCCAGGAGGGAGCTGAACCTTTCCCTGTGAGTCTTTCTAGTTTAGTCCGTCTAGTGCAGTGTTTCTCAACCACAATCTTGAAGGACCACCAACACTGCATGTTTTGTATGTCTCCTTTGTCTGGCACACCTATTACAGGTCTTTCAGTCTCTGCTGATGAGCTGATGATCTAAATCAGGTGTGTTTGGTTAAGAAGTCATTGAAAGTGTGCAGAGCTGTTGATCTACTAGGCACGTGGTTGAGAAACACTGATCTAGTGTTTCATAGAAAGGCAGAATGTGTTTTCAAAAATAAAGTTTAGCCAGCATTAAACGTTCATTAAGTAGTGAACTGATTGCTTTGTGATTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22885
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 |
---|---|---|---|---|---|
ENSDART00000058496 | Nonsense | 724 | 901 | 13 | 15 |
ENSDART00000128810 | Nonsense | 651 | 828 | 13 | 15 |
ENSDART00000129536 | Nonsense | 720 | 897 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 34270735)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32002235 |
GRCz11 | 16 | 31956265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGAATCTTTTTTTTTTTTTAGGTACAATGTGAGCTTTAGAAACCACT[T/A]ACGGGCCAGTAGAGGTCTTGAGGGTGCAGAACGGCCAGCAGGGGGCCCCG
Long Flanking Sequence:
CACGAAGATGAATGGAAGAATGTTTCCTATAGTCTAAGTGGTTCTTTGCTCTCTCCATATTCGCATATGTGTCTGTCATTTACAGAGTTAAAGTGTGAATACTGTCTTAATTTTGCACCAGCCAGCCAGTTCAGAAGATCCAAGCGCTTTTGCACCATTAGCTGCTCAAAGAGGTGAGCCCAAAATCAGCGTTGATAAATTTGTCAAATGTTTCTGAAATATGTATCGTATTTTCTGGTAGATAATCTCACATGATGGTATCTTGTACAGAATTACATTACTGAAAACTGGAAAAACACATTTATTAAACACATAATTAACATAGGTGTGTATCAGGAGTCGCCTTCCTGCAGATTTCAGTTGCCTCTGGTGTATGCTGTGGTTGTGGATCAAAACGATATGACTAATAAAGAATGAACCTGAATGATTATGGGGTGTCTTGTTTTTTACATCTGAATCTTTTTTTTTTTTTAGGTACAATGTGAGCTTTAGAAACCACT[T/A]ACGGGCCAGTAGAGGTCTTGAGGGTGCAGAACGGCCAGCAGGGGGCCCCGTGGTCCAGGATGTTATTGCCAGACGCCGGGCTCCTCGCAGAAGCAGCTCTGAGATCGCTTGTGCTAAAATAACAGGAAGGCATCTTCCTGTAAAGGTAAGATGATGGACATTGATAATCAAAATTATTATTTTGTGTTATTTACCAGTCTGTGGTTGGCTAGATTTTTAAAAGAATTAAAATTAAAAACTAAATGATGTTCTTTTTTCATGAAAAAATCTACTATGGTCCCCTATAATGAAAACCATCTTTTCTAAGCAGTTTGGGCAGAACTGTGTGTAGGTATAGTGTGTCCACTGTCATACCGGACTGATATAAAGACAATAAGTCTATTTTTTTTTTTTTTTTTTTTTTTTTAACGTTAAAATAGGATTCAAATCCCTCCCATTTTGAGGTCCACCTCAGTGTGAAGTAGGAGTTTGGTTTCTGCACCCACCAAATTAATTGATAA
Associated Phenotype:
Not determined