ZMP
phactr4
Ensembl ID:
ZFIN ID:
Description:
Phosphatase and actin regulator 4 [Source:UniProtKB/Swiss-Prot;Acc:Q6PEI3]
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 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22898 | Nonsense | Available for shipment | Available now |
| sa13740 | Nonsense | Available for shipment | Available now |
| sa14374 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22898
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044235 | Nonsense | 51 | 754 | 4 | 15 |
| ENSDART00000081066 | Nonsense | 51 | 810 | 2 | 13 |
| ENSDART00000145017 | None | None | 282 | None | 3 |
| ENSDART00000145485 | Nonsense | 65 | 75 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 36651493)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 34280114 |
| GRCz11 | 16 | 34234144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCTCTACCCTGGGGAAGATCTTCAAACCCTGGAAGTGGAGGAAGAAG[A/T]AAAGCAGCGAGAAGTTTAAGGAAACTTCAGAAGGTCCTTTGTTCTTTTCT
Long Flanking Sequence:
TGAATTGCCTCTTGTTACAGTTATGAAATAGTTTGATAACAAGCAGAAAATGTTCATGACCACACTGAAATGGTCTATATATAATGGATGATAAAATCCTTTAACTTTCACTCTTAAGCATTTTTTCTGTTTGCATCTATATGTTGAACAAAATGTCTTTGGATTCAGAGCAGTGCCCAGGACGCAGATGTATATATAGGACAGTGTGTTTGGTCCATTTCATATGATGTTACAATTCATTCTGATGTGGCACGCTATGTCTAATATGCTTGCATAAACATGAAGTTACGTAAACCATCTGACCCAAGGCCTGTTGGAGCCATTGATACGGCTGTGTTTGACGTGTCCCTGTCTCTCCTCCAGATGATGAAGTCGAGCACCAGCACAGCACCATGGGCAGTGAAGGGGGCACGGCAGGGGATGGCACTCCTCCTCCCAAACGCAAGGGAAAGTTCTCTACCCTGGGGAAGATCTTCAAACCCTGGAAGTGGAGGAAGAAG[A/T]AAAGCAGCGAGAAGTTTAAGGAAACTTCAGAAGGTCCTTTGTTCTTTTCTCTGCATGTTTGTGTTGGAAAATGGCTTTCCTTCACTTTTTTCCTAAATCACACCCTGTTTGTGAACGTTTACTTTCCGTTGCTGCTGATATGAATGTTGTTTTCTCAGATGTTTGGAGGAATATTGTTACAGTTTCAATATCCCTTTGCATAGTTGTTCTCAAGAGGTCTTATAATATTTTGTTCCAAGTTTAAAGTGAAAATAGTGTCATTTAGAGAATTGAGTTAATATTATTTAATTAATTTATTATTATTATTATTATTATTATTTTTCATTTTCATTACTACGCAGATGACACCCAGCTCTACCTATCAACCAAACCCAACCACAAACTCCACAAACTTTCTGAAATTTAATGACAATAAAACTGAAATTCTACTTATAGGTACATGATCCACTTTAAACAAATCACATAACTTTTCTATTCCTACAGATGATTCTGTCACCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13740
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 |
|---|---|---|---|---|---|
| ENSDART00000044235 | Nonsense | 68 | 754 | 5 | 15 |
| ENSDART00000081066 | Nonsense | 68 | 810 | 3 | 13 |
| ENSDART00000145017 | None | None | 282 | None | 3 |
| ENSDART00000145485 | None | None | 75 | None | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 36647525)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 34276146 |
| GRCz11 | 16 | 34230176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAGATWTATATTGTTTTTGTTCCCTCCACAGTTTTGGAAAGAAAGATGT[C/A]RATGAGGAGGCCAAGACAGGAACTGATTGAGCAGGGAGTGCTCAAGGAGC
Long Flanking Sequence:
CCGTTGAATTTGCCAATATGTTTATTATGTTTGTCAATATTTACATGAATCAACGTTGTCAAAAGACAAACTTGATGTTTGACCATGGAAATCTGTATCTATATATCTATATATTAAAGTGGTCTCTTAGTTTTCCCCCAAACTTAAGCATAAAAACATACTTTGGCCTGAAATGCTCTTATTGTCCAATAGTTCAAATTATATAATTCAGTTATAAGCATGGATTTTTATAATGTAAGTTTGTCCAGTGGTCCTTGGCTGGTTTTACTTTAGGACTTGATATCTCGTATATCAAATGTTGACCTAACTCTGTACTTAAAATATAAGTCTAAAAAAATATTATCCTGAATCCATGAGCACTGATTGTATTTGTCATGTAATGTCTTTGCAAGAAATCTAATAATCATTGTTTCAAAACCTTTGAGTTATAGAAAACCATGTTTTTTTTTTTTAGATATATATTGTTTTTGTTCCCTCCACAGTTTTGGAAAGAAAGATGT[C/A]GATGAGGAGGCCAAGACAGGAACTGATTGAGCAGGGAGTGCTCAAGGAGCTTCCTGACAATGGTAGGAAAGAAAAGTTTGTCTGTGTTTCTGTGTGTGCCTACTAAAGCATATTTAAATATGCTTTTTTTTGTCATATCCACCATTACAAAAAACTTCATAATGATGATTTGTAAAATGTTAATAAATGGAGCAAGATTTCTTGTAAGGTTACTGTTTGGAGACCGTATTTGGTTTTAGCTGCTACTAAGAAACACTTTTTAAACACTGCCAATTTTAAAACATTTTGGAAGTTTTATGTATTTTTTTCACCATGCCCAGAATACTTTACAAAAATACAATAACATTTTTAATGTTTGAGAATTATTTCTACAATTTCCAACAAAACCAACAGTTGTGCCATAATATATATTTTTATCTGCCATTTGTTGTAATATTAAGTCAAACCATGCAGTGAATACATCAAATTCTGTTTTAATACGTAAAATTCCTTATATTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14374
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044235 | Essential Splice Site | 368 | 754 | 7 | 15 |
| ENSDART00000081066 | Essential Splice Site | 368 | 810 | 5 | 13 |
| ENSDART00000145017 | None | None | 282 | None | 3 |
| ENSDART00000145485 | None | None | 75 | None | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 36639738)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 34268359 |
| GRCz11 | 16 | 34222389 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MTGCCTCCACCCAAACCCATCAACCGCAGCAACAACCCTGCCATTATGGG[T/C]GAGTGAATAWAAGATATAATGTGACCTCTGTAAATGTCAGAGAAATTACA
Long Flanking Sequence:
TTTGACCTTAAAAGTAACAACCCTTCCCTAAGTCCAGCTTAAGTTACTATGAAGCACAAACTAAATATCAAATTTAAACTTTTCTAACTTAATATTATATCTTCCCTCACAGAATCCGACAGCAGTCAGTACCTCCCCAACTCCGAGATGATGAGGGACACCCTGCGTGAGCCTCTGCCCCCAAAACAATCCATCATGCCCCCCAAATGGCTAATGACCTCCACCCCTGAACCTGGATCTGACAGCTTGCCCCGCACTCCCGTCCACAACCCAGCAGCACCTTCCTTCTGCTCCTCCAACTCCTCCTCTTCCTCCTCAGCTGGGAAACCTCTCCGTAACGTGTCTTCGGCGGGTGCAAACACAGCGCCCCCCGGCGGTGCCCCCCTCACCACCTCCTCAGCGCCATGCTCGATGGGTACCATCCCGAATCATCCCTCTAAACAGCCCCCTATGCCTCCACCCAAACCCATCAACCGCAGCAACAACCCTGCCATTATGGG[T/C]GAGTGAATATAAGATATAATGTGACCTCTGTAAATGTCAGAGAAATTACACAATTCACAATTCATTCCCTTCCTCAATCAGGCTCAATGATAAACTGCTCCGGATTAATAGGTGAAGGGATGTTTCTGTAGAAGTTAATTATTATATTAACTAAAGAACAACTAAAACATTTTATTATTATATAATTAAAGAAGTATATTAATGTGTAAACACAAAAATACACATTGAATATTTCAATACATACATACATAGAATACTATAGATTTTTATCCTTTATGTTTTAATTAAAATCATTTAAAAATTCGAATTTGTCATTTTTAAAACTCATTGTACTTGACCATTATAAATTAAATTCTTAGTTTTTTTTAATTATGCATTTTTTGTCGGCAAGTTTATGCATCTCATTTCCTAAAAATGGTAATTCAAAGTGCTTTACATAAACACGAATAAAACAAACTCAAAATACAACTACACTACCTGTGAAACTTGTTGCCTATTCA
Associated Phenotype:
Not determined