ZMP
si:dkey-252h13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate pleckstrin homology-like domain, family B, member 1 (PHLDB1) [So
Human Orthologue:
PHLDB1
Human Description:
pleckstrin homology-like domain, family B, member 1 [Source:HGNC Symbol;Acc:23697]
Mouse Orthologue:
Phldb1
Mouse Description:
pleckstrin homology-like domain, family B, member 1 Gene [Source:MGI Symbol;Acc:MGI:2143230]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20452 | Essential Splice Site | Available for shipment | Available now |
| sa40463 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33627 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20452
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 |
|---|---|---|---|---|---|
| ENSDART00000086734 | Essential Splice Site | 873 | 1424 | 12 | 25 |
| ENSDART00000138464 | Essential Splice Site | 873 | 1365 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 5 (position 32091055)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29851885 |
| GRCz11 | 5 | 30452038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAAGAATGGCCAAAGATAGAACCCTGGCCCTGCAGATGCTCCACAAG[G/A]TTGAGTATAAGGATTAACATCTGTCTACACTGATGTTTGACACTTAAAGG
Long Flanking Sequence:
GAGGAACATTTGTCTGTCTGCTTGTTTGTTTTTCCCATCTGTTCGTCTGCCTCTGTCTTCCCCTCTCTGTCTCTCTGTCCATCTGTGCATGTGTGTGTGTGTGTGTGTAGAAGGTGGAGGCACTGGAGTCGGCCACTAAGCGCTTTGAGGATTTGGAGTTTCGCCAGTTGGAGCGGGAGAGTGGCATTGAGGAGGAGAAGGAGACGGTTGGCAGGCAGCTGTTGCAGGAGAAGGCAGAGTATCACCGGAATGTGGCCAAAAGGAAGGTAATAGCACTGATCTCATGTCAGGTCTATTATAGGTCTCATAATGTCAGTATTGAGCTGCAAATCTTGGGTCAGGCTAAAGCATAGACACTTTTTGGTATGAAATTTTTTTTGGTGATGCAGGAGAAAATGGCAGCTTTGGAGATCCAGGCTAACCAACTTGGACTTCAGGCAGCTCAGGATTGTGAAAGAATGGCCAAAGATAGAACCCTGGCCCTGCAGATGCTCCACAAG[G/A]TTGAGTATAAGGATTAACATCTGTCTACACTGATGTTTGACACTTAAAGGAATATTGCAGGTTTGGTTGAAGTTAAGATCAGCTGGCAATATTTGTGATAATGGTAAAAAAACACCACTTTTTTTGGAAATGGGCTCTTTTTACTACTCCCCTAGTGTTAAACAGATGAGTTTTACCATATTTAAATCCACTCGCTTTTTAGGGGTCTGGCGGGAGCACGTTTAGCTTAGCTTAGCTTTGCATAGATTATTGAATCGGATTAGACCAGTGCTTCTCAACCACATTCCTGTAGGACCACCAACACTGCATGGTTTTAATGTCGCATCCATTACAGGTCTTTCAGTCTCTGCTAATGAGTTGAAGATCTGAATCAGGTGTGTTTGGTTAAGGAGACATAGATAATGTGCAGAGCTGGTGGTCCTTCAGGGACATGGTTGAGAAACACTGGATTAGACCATTAGCACCTCGCTCAAAATGACCAGAGTTTCCTGTTCATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40463
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086734 | Essential Splice Site | 1227 | 1424 | None | 25 |
| ENSDART00000138464 | Essential Splice Site | 1168 | 1365 | None | 23 |
Genomic Location (Zv9):
Chromosome 5 (position 32076738)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29837568 |
| GRCz11 | 5 | 30437721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCTGAAGGAGGCCCAGCAGGAGAAAGCCAGACTGGTGGAGAGTCGAG[T/C]GAGCGCCATTAAACTTTAATTGTCTGTGAAATATAATCTATCTTTCTCCC
Long Flanking Sequence:
AAATCACTTTTATTGTCACATCATCAGCAGAACGTGTGCTATGACGAGTGAAAAGCTTAGGAAATTGTGTGTACATCTAGCACCAAAAACGACAAAAATACAAGTAAAACACACAAAACACAACAAAGATTGCTGGGAGCTCGCAACACGGCGGCCATGCTCGACACCATCTTGATTTCGATTGTGTAATTATTTTTAACAGCATTTTACTAATGTCTTGTGAGGTCAGTTCACCTATTAGATAACTTATGATTTGTTGTTACTATTCTATGTTATTTTCTATAGAACTCACTCAGTATGTTATGAACGACTGCAGCTGTGGTCTGTCTAGAGTAAGCAGTCAGGATCAGTGTCGTCTTCTGCCGCTAGAAACTCCTCAGCAACAGTAACGCTGTGTTTCTCCCTCAGCAGCAACGGGCTGGCAGGACTGAGACTGGAGGAGATGGAGAAGATGCTGAAGGAGGCCCAGCAGGAGAAAGCCAGACTGGTGGAGAGTCGAG[T/C]GAGCGCCATTAAACTTTAATTGTCTGTGAAATATAATCTATCTTTCTCCCTGTCTCCCATATAAAAGAGATCTTTTTCATGAATTTAAAAAGGAAGCCCCTGGTCCCTTTGGCATTACTGCATTAAAGATTGTTTCTTACCTACAAAGAGTGATAGACATGAAAGGCTGGATCTTAACAAGCTCTCCGACAGTAATACTCGCTCTGACAATCTCTTGCTGAATGATTTTTTCATGCATCCCCAGTCACTCCGCGCTGTGTATTTTATGTATTTGTATGTGTTTTTTTCCCTATTGTCTATTAAAGCGTCTCTCACGATACATTTGAAGCCCCTCTGTGTCCTAATCTGTCCGCCTGTCTTTATGTCAGGAGAGGGAAGTCCAGGCAAGAAAGCAGATGCTGGAGGCTGAGAGACGGAGGAGAGAGGAGGTGGAGAGGAGGCTGCTGGATGAAACCGCTCACAGACAGAGGCTCGTGGAGGAAGAGGTCAAGATGAGGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33627
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 |
|---|---|---|---|---|---|
| ENSDART00000086734 | Essential Splice Site | 1378 | 1424 | 24 | 25 |
| ENSDART00000138464 | Essential Splice Site | 1319 | 1365 | 22 | 23 |
Genomic Location (Zv9):
Chromosome 5 (position 32066630)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29827460 |
| GRCz11 | 5 | 30427613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGGCCATAGAAGAGGTGTATTACGATCACCTGCGCAGCGCCACGAAG[G/A]TAAAAACCGAAAAGCCCTCCTGTTTACCATCAACAGCTCCAGCTCGCACT
Long Flanking Sequence:
AAAAATCGCCATTTAAAAAAGAATAAAAATGACAAAATCAGTAAAACTTAATCAAATTAAAGTAAAAATGGTGAAATATAATAAAAACTAAACTGTTTTTTAAAATCTAATGATACAAGATAGAAAGAGAACACTGATTCAAAACATTTTTCAACTGAAATAAAATGGAAATAGGGTTATACTGTATAAATCTGCAAAAATATTTAAAGTCTAATATTTCTTATTTAGTTTTAACTTCATATATTAAAAACCAATCACTAAATACTCTGTAGACATTTTTTTAAATCTAATAAAATAACTCAAATTCAAATAATAAAATAAAATCAAACTTTTAAAGGATCTCAGTGATTCTAAAACAATATGTTTCTCAGTTTTTCCTCACGGTTTATTTATTTTTTTTTTTGTCATTCTCAGATAAACACGAGACCAAACTGAAGGGTGTCATCTACTTCCAGGCCATAGAAGAGGTGTATTACGATCACCTGCGCAGCGCCACGAAG[G/A]TAAAAACCGAAAAGCCCTCCTGTTTACCATCAACAGCTCCAGCTCGCACTCCAGCAGCGACTCTGGTGAAAGTTTAAACAGACAGGCGTCTCTTCATAAAGAGAATTTCTTACAGCACAAGCCAAAAGAGATCAAAGCAGCTTCATGTTCATGTACATTTCGTCATGCTTTCTTTTTTTTCCCACTTCAGCGACATGCCTTCCCCCCCCTGCCCTGCTGTTCTCCATCTTCTCGCACTTTAACACACACTTTATCTTTTTTTCTGCCCCTACAGAGTCCGAATCCTTCGCTGACCTTCTGCGTGAAGACTCATGATCGACTTTATTTCATGGTGGCTCCGTCTCCAGAGGCCATGCGCATCTGGATGGACGTCATAGTAACAGGTGCTGAAGGCTACACACAGTTTATGACCTGAAGGAGCCATCAGCTATGAGAGACATATACAAATTGCCAAAAAAAGCCAGCACTGATAGATTTCTGTCATCGTGACTAGAGAAGAA
Associated Phenotype:
Not determined