ZMP
si:ch211-239h19.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phosphoinositol 3-phosphate-binding family protein [Source:UniPr
Human Orthologue:
PLEKHA5
Human Description:
pleckstrin homology domain containing, family A member 5 [Source:HGNC Symbol;Acc:30036]
Mouse Orthologue:
Plekha5
Mouse Description:
pleckstrin homology domain containing, family A member 5 Gene [Source:MGI Symbol;Acc:MGI:1923802]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20181 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa38416 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40204 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20181
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 > T
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000067414 | Essential Splice Site | 127 | 1136 | 7 | 30 |
| ENSDART00000112210 | Essential Splice Site | 202 | 1237 | 7 | 26 |
| ENSDART00000127894 | Essential Splice Site | 131 | 1166 | 5 | 24 |
| ENSDART00000135701 | Missense | 83 | 84 | 5 | 5 |
| ENSDART00000141952 | Essential Splice Site | 129 | 1138 | 4 | 27 |
Genomic Location (Zv9):
Chromosome 4 (position 2873452)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 3072331 |
| GRCz11 | 4 | 3002442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAAGAGATGGTTCGTTCTGTCTGATATGTGCCTCTTCTACTACAGAG[G/T]TGAGTTCAGCATCTCTGTTTACACTTACACACTCATTTTATCAATGCACC
Long Flanking Sequence:
AGCTTAAACCCCTCACAAGTGTCATTTCTCTAAATAATAATGTGCTCTCTGTGTGTCTGCAGCCATCCCGGTCCTCAAAGAAAGTGCACAACTTTGGGAAAAGGTCCAACTCCATCAAGAGGAACCCCAATGCACCTGTGATCAAAAACGGCTGGCTTCACAAACAGGTACTTATCAGTGGGAAACATCCATATGCACTCATTCACACACACAAATGGACAATTTAGCCTATAGCGCATGTCTTTTGGAAACAGGAGCACCCAGAGGAAACCCATGCCAACACGGGGAGAACATGCAAACTCCACACTAACATATTGATACAAACACTCCAAAAACCCTTGAGTGCATTGTTTGGGGGAGGGCTTTCTGTACTTGTGATTGGCTGGCTGATTTGATTGACAGTTCTTGTGCTGCTGGTGTTTTTCAGGACAGCACTGGGATGAAGATGTGGAAGAAGAGATGGTTCGTTCTGTCTGATATGTGCCTCTTCTACTACAGAG[G/T]TGAGTTCAGCATCTCTGTTTACACTTACACACTCATTTTATCAATGCACCGTATATCTGATGTTTGTGTTTGAGGATTAATGTTCAGTCGCAGGCCGTGACCAAACGTTCATCTCAGAGACGTTTCTGTTCAGTATGATCAAGTGGCACATTTGCACTGTTATTCATTGGTTTTACTCTGTGTGTTTTCCAAATAACAGCCCTGTAAATGTGGAAAACATACTGAACGAGTAGTTATAAGTGTAATGTGCTCTTGAACGATCTTGCTAGTGCTTTGAATCAACTTTGTGCACAGTATCAGGATTCGCAAATGAATGATTCTGAGTCTGCATAGTTATTTGATTCACTTAAGATTCAGTTTGTGATTCTTTTGAGTCTTTTGAATCATTTTCCCGTGGGTCATTATTCATGCTGTCAACAATTTGTATGTCATTTATTTGTTTTGATTCAATAAATCAAGTGGTTCATTCAATCATATTTAAATTATAAACCTAAATAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38416
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000067414 | Nonsense | 513 | 1136 | 13 | 30 |
| ENSDART00000112210 | Nonsense | 704 | 1237 | 12 | 26 |
| ENSDART00000127894 | Nonsense | 633 | 1166 | 10 | 24 |
| ENSDART00000135701 | None | None | 84 | None | 5 |
| ENSDART00000141952 | Nonsense | 515 | 1138 | 10 | 27 |
Genomic Location (Zv9):
Chromosome 4 (position 2851037)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 3049916 |
| GRCz11 | 4 | 2980027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGCTCTCCTGACTGCTGTGCTTTCCTCTTTCTCTGTCAGTACTCCTA[T/A]CCTGCGGAACGCAGAGCTGCTCCTCCCGCACAGAACATCACTGCACAGTC
Long Flanking Sequence:
ATGGATGGGAGGATAGAAAGAGTTATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATTAAGAGAGAGCGATGATGGATAGAGCGATGCATGGATGGATGATAGATGGATGAAGAGCGTGATGGATTGATGGAGAGAGGTATGGATGGATGGATGGATGGAAAGATAGAAAGATAATTTCAGCCTCTGTAAGCAGAAGTGACTTCTTTCAAAGACAGTAATACAATCGTAAGATGGAAGAGCATTGGCAATACTGTATAGCGTTGGTCAAGTCATACTCATCTGTCTTCACATCTGAATCCTGCTCAAAGACGTTCATCAATGAATATGCAGTAAACCAGTCGTTTTTAAGAGCTGATAATGTTATTTTTGCTTTAAATGACTGAGCCTTTAAGAGTTTCTAATTCTCAGCGTTTAATGCAGTTTTGAGCAGAACTCTTTGTTGCAGCTCTCCTGACTGCTGTGCTTTCCTCTTTCTCTGTCAGTACTCCTA[T/A]CCTGCGGAACGCAGAGCTGCTCCTCCCGCACAGAACATCACTGCACAGTCTCTTCAAGGCAAAACGGTACGTGCTCCCACTTCTCCACCCACCACTTCCTCTGTGCAAAGGAAACGCTTGTAACTCTCAGAGCCAAAACTTTGCTTTCCTGTCAAACTCTTTGCATTTTTTTTCAGTTTCCAGCCACTAAGGATTCGTTCGGGCTTTGGTTTGCAAATTAGGCTTTTTCGGAGTGAATATTTCACATGCGGAGGTTGAGTCAACATGAATTGTTGCTTTCTTGAAGTGCCCCTGTTATGCTTTTTCAGATACTACCTTTCGGTTTTGTAGCTGTTTGTGGATGCAAAAGATCTGAAAAGTTTCAACGATCACATTAAATAGTTTCACACAGTTCTGCACAAGCCTATTGTTGTTTCTAATATATTTGCATAATGTTATTCTGTAGTGCTTATTGGCTGCCTAGGAATAACAAGTATAGAGCAGAATAGTGCCATCTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40204
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000067414 | Essential Splice Site | 669 | 1136 | 19 | 30 |
| ENSDART00000112210 | Essential Splice Site | 776 | 1237 | 15 | 26 |
| ENSDART00000127894 | Essential Splice Site | 705 | 1166 | 13 | 24 |
| ENSDART00000135701 | None | None | 84 | None | 5 |
| ENSDART00000141952 | Essential Splice Site | 671 | 1138 | 16 | 27 |
Genomic Location (Zv9):
Chromosome 4 (position 2835748)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 3034627 |
| GRCz11 | 4 | 2964738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATTAAAACAGCTTGTGTCTCACTCCTGCATGCTTGTGTGCTTGTTTTT[A/C]GCACACACTGGAGACGGCGCTGCTCTCCGCCAGTCAGGAGATCGAGATGA
Long Flanking Sequence:
TTTTATGAATTCACAAGCATTTTCAGACTACCTGAGATATTATTACATAAAGAATAAAGTTGCTTAATAAAACATCCTCGGCTTTATTGTCTGCAGGCGAAGTTAAGTCGGCTCTGTGAGCAGGACAAAGTAGTGCGAACTCAAGAAGAGAAACTGCAGCAGCTCCACAGAGAAAAGGTGAAGTCCATCAGCAAGTTCAGCATCTTTAGCTGTGTTTCCATCCAAAAATATGAATTAGAAAAAATATAAAGATATAAATCACATGACTTTACTGATGCTCATGCTGGAGTTTATTCAGTAAATGTGTTTCCCTCTTAGTTTATGTCCATTTTTACTTATCTAATTAATATTTATTCATTATTAATGCACATTTTCAAAATCTATGCTTATTTTGTTGCTTTCATTAAGCACTTTTATGCGATATTGTAATAAATGCACATTAGAATAGCTGGATTAAAACAGCTTGTGTCTCACTCCTGCATGCTTGTGTGCTTGTTTTT[A/C]GCACACACTGGAGACGGCGCTGCTCTCCGCCAGTCAGGAGATCGAGATGAGCTCTGAAAACCCAGCGGCGGTCCAGAGCGTGGTCCAGCAGAGGGACGTCCTGCAGAGTGGCCTGCTGAGCACCTGCAGAGAGCTGAGCCGCGTCAGCACTGTACGACAACACACACTCACAATACATTCAACAGAGCAGAGCAATTCCGTGCAAATTTCAACCTTGCCATGAAAAAAAAATTATGTTTTCACCAAAATATTGAAAGCCTTTTTAGGTTTTTTGTGTAAGCAAGTATTTTACAGTAGTGTAAATATACTCATAAATGTCTGTCAGTGTTCTCAAACTATTATATTTAATTTACCAAAGTCACATAAGTGCCAATTTCACATCTGCCACATCCATAACAGAGAGATGTCACATCCATAATGCAAAATCTAATCAAATCAATGATGTTTGCTCTATAGAGAGCAGCTCTTCTCCTTTTGATGATCCATATTTCTTTTGTGTC
Associated Phenotype:
Not determined