ZMP
zgc:123224
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phosphatase and actin regulator family [Source:UniProtKB/TrEMBL;
Human Orthologue:
PHACTR4
Human Description:
phosphatase and actin regulator 4 [Source:HGNC Symbol;Acc:25793]
Mouse Orthologue:
Phactr4
Mouse Description:
phosphatase and actin regulator 4 Gene [Source:MGI Symbol;Acc:MGI:2140327]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23485 | Nonsense | Available for shipment | Available now |
sa11544 | Essential Splice Site | Available for shipment | Available now |
sa14744 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23485
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 |
---|---|---|---|---|---|
ENSDART00000048151 | None | None | 265 | None | 3 |
ENSDART00000055619 | Nonsense | 462 | 1014 | 4 | 11 |
ENSDART00000065861 | Nonsense | 207 | 693 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 19 (position 14601165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15264769 |
GRCz11 | 19 | 15169131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATCCTCTGCTCCACCCATTGCTAAGCCTCCACCTAGGACTGTGTCTT[T/A]GAATGTAGACGACTCCTCGCGCACTATTCTCATTCCTTCCTTAATAGCAG
Long Flanking Sequence:
ATCTTTAAAGGCATTTAAAAGTTTAAAAAAAATGATTCAGAGTTTTCAAAAAATGTCTTTAATGCAAAGTAAAGGACTCATCACATTTGTGAATTCATGTGGTCTTTAGAGCGCTTCTGCACCTCATTGCTGCTCCATTCACATGCTTCCCTAAGCTTTTCCATTGACTCTTGCTTGTCATTGTGACTATACTGTGCACTTGTGTGTTTCATTTGTGCTTATGTGTGTTTGTGCATGTGTCTTGTGCTCACTCTTAGGATCAGTGGGTGTGCAGTTTGTTCCTGAGCCCAAACCTGCAAGTACTTCCACTAAAGAGTCACAGCCACCCCCTAAACAGGCCATTCTCCCTCCCAAAAGGGTGATTGCTGCTCCTTCCTCCGCTGAGCCTGCTCCAGTCCCACCCTCATTTTCCTCTTTGTCATCATCATCATCCTCATCTTCTTCATCATCCTCATCCTCTGCTCCACCCATTGCTAAGCCTCCACCTAGGACTGTGTCTT[T/A]GAATGTAGACGACTCCTCGCGCACTATTCTCATTCCTTCCTTAATAGCAGGTGACCGTGAGGTGCCGCCAACTGTTCCCGCCCACACAACCCCAGCCACTGTTTCCACCCACAAGACCCTACCCACTGTTCCTGCCCACATGACACCACCTACTGTTCCTGCTCACGTGACAACGCCAGCTGCCCCTGCACACTCAAACCCACCTGCTGTTCTACCTCACTCCACCCCACCCACTGTCCCCAAACACCCCACCCCTGCAGCCCCTGTTCCCCTTAAACAGCCGCCAATGCCCCCTCCCAAACCAGTCCATCACAGCAGCAACACAGCACTGCAAGGTGAGTCATTTTTTGTCCTGTTGCTTTTAAGCTTCAAAGCTGCACCTGCTAGTATGTGGAACTTTATGCTGCTTTTGTGATAGACTTTAGCTGGAGTAGACAGTGGTGCAGGGTAATGAAAGTATGTAAAATGTTTAGTTTTTTATGTTTATTGGGGTTCTCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11544
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048151 | None | None | 265 | None | 3 |
ENSDART00000055619 | Essential Splice Site | 899 | 1014 | 8 | 11 |
ENSDART00000065861 | Essential Splice Site | 597 | 693 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 19 (position 14582041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15245645 |
GRCz11 | 19 | 15150007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCAGAGGCCCACCGCTCAAGAACTGGAGCAGAGAAACATYCTACTAGG[T/G]CAGTGTTGCAATTCCTTTTCACTAGTTCTCCACTYAACTTATKTGTAGTC
Long Flanking Sequence:
TCATCATAAAAAAAGAATGCAAGTCTTAAATGTACTTTCATATATATATATATATATATATATATATATATATATATATATATATATATATAGTTAAAGTCAGAATTATTAGCCCCCTTGAATTATTAGAAGACTTTAACCTTCCATGTGCTAGAATCTATACAGTTTGTGAAAACATCAAATGAGAAATCTGAATGCATCTTGTCAGGTGGTCTTGCGAGTCGTGTGAAGCGGAAGGACACTCTGGCACTGAAGCTGGAGCGTCAACAGGAGAAAGAGAAATCACAGGAGGAGGACAGCAGCACCTGGAACAACAAAGAGCAGTGGGAAGCTGTCCGAAACAAGATCGGCACCGCCCTCACAAGGTCTGTGTGTGTTCAGAGGGCTTTTTAGGTGATCTTTGTCCTTTCAGCACTGACACTGCTTGCATTTTGCTCTTTTAGGAGGTTGAGTCAGAGGCCCACCGCTCAAGAACTGGAGCAGAGAAACATCCTACTAGG[T/G]CAGTGTTGCAATTCCTTTTCACTAGTTCTCCACTTAACTTATTTGTAGTCTCAATTTACTGATGCTTCCAAAAAAAATTCCTTGAATATCTTTTTGAATGCTCTTCTGTTTTAGCTAAGAATGAAGAAGTCCGGCGGGCAGAAAGAAGTGAAATTAAACGCAGGCTGACCAGAAAGGTTTGACGGCACACATTTATTACATTTATTTTTTCTGTAATGGATAAATTGAACACTTGTTTTTAGCATTTGCTGTATTTCTTGATCATCCTTTTAACATTTCTCCAACAGCTAATTTTTATTTGTTAAAATGGTCACTATACTTAATGAGTTGCAAAAACTGGAAGCGTTTTTGATGAATACAAATTTAAAACAGCATGCCTTAAAATTAGTGGTCGACCAATGGTGTTTTTTTTTTTTTCTGGCTCATGGCAATATTTAGATTTCAGGGCAGCCAATGGTTGAAATATTTATTAATTTATTGATGAATATGTTTTAGCCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14744
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 |
---|---|---|---|---|---|
ENSDART00000048151 | None | None | 265 | None | 3 |
ENSDART00000055619 | Essential Splice Site | 920 | 1014 | 10 | 11 |
ENSDART00000065861 | Essential Splice Site | 618 | 693 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 19 (position 14579703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 15243307 |
GRCz11 | 19 | 15147669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTTGTAATCCTGCAAAACGTGAAAGTTGTTGTGTTTTTWTGTACGCA[G/A]TWGTCTCAGAGGCCCACAATAGCTGACCTGCAGGCCAGAAAAATTCTGCG
Long Flanking Sequence:
AAGTACAAGTTATCATTGTACGTATGCTCACACGCCTTTATACAATAAACAGATCCATTTTGTAGCAGTCTGTTATGATTAATAAATGCTTGACAAATAGTTCTACCTGGGTCTACACAAAAATTGTACTAATCCCAATTATTTAAATGGTAATTTAAAACTCTTCCATGTATAGTAACAGAATTGGTAATCAGCAATAACGTAAAACTATAATTAAATGTAACTCGAGTAAGATAAATCATTTTAGTTTAGTTTCCAAACATGCATCAAAAATCCCCATTATATTTCAGTTATAGATCTGAAATGCAATCCAAACTGAAACATCTAAACCTATTATTGACATTTGTAGCTTGCTCACTTCTGAACTATCAGTGTAATAGTGGTCCCCAAATACAGCCCTCTGAGCCTCATGATATTCATGCAGCATTCAAGCTTCAAAATGTGTCATTTGTGGTTGTAATCCTGCAAAACGTGAAAGTTGTTGTGTTTTTTTGTACGCA[G/A]TTGTCTCAGAGGCCCACAATAGCTGACCTGCAGGCCAGAAAAATTCTGCGCTTTCACGAGTATGTGGAGTCCACTCATGCTCAAGACTATGACCGGCGCGCAGACAAACCCTGGACCAAACTCACACCTGCTGACAAGGTCTGAGTCAATCATTGGTCTCATCTGACCCCTAGTGGTGACCGATATACCAGCATTCAAATGCTTTCTTATGTAAACTGGAGAGAGTTACATAAAAACATTTGCACGTAATTGAACATGTCTGTACTTTAGCAAAGAAAAAGTTAGGCAAATCTCATTTAAATAGACAAAAGAGAGAGTTTTGGAAGTTTTATATGTAGATTAGACATGCTATCAACGTTACAGTTGAACTCAACACCAGCAGATGTTCTGAGCTTTCAGGGTAGTTCTTCCTATTTCACCTTTTGTTCTTTGTTCTCCTCCAGGCGGCCATAAGAAAAGAGCTGAATGAGTTCAAAAGCTCAGAAATGGAAGTTCACGAG
Associated Phenotype:
Not determined