ZMP
zgc:113074
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC541437 [Source:RefSeq peptide;Acc:NP_001013580]
Human Orthologue:
PTBP2
Human Description:
polypyrimidine tract binding protein 2 [Source:HGNC Symbol;Acc:17662]
Mouse Orthologue:
Ptbp2
Mouse Description:
polypyrimidine tract binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:1860489]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37918 | Essential Splice Site | Available for shipment | Available now |
| sa14689 | Essential Splice Site | Available for shipment | Available now |
| sa24524 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37918
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000046928 | None | None | 183 | None | 9 |
| ENSDART00000123275 | Essential Splice Site | 36 | 512 | 4 | 14 |
The following transcripts of ENSDARG00000015230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 31685365)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 30918458 |
| GRCz11 | 24 | 30855669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTCTCTCTATTCCCTGTATAATGTCCTCTTTCTGACCACTTTTGAC[A/T]GATACAACATCCAATGGCAGTGACAGCAAAAAACTCAGAGTTGAAGAGAG
Long Flanking Sequence:
TGGTCAGTCAATAAATACTAATACCGTTTTATCGGCCCAGCCCTATGTTCAGCTGTTGAGCATGTGAATACAATGGCCAATTCGCATTGTTTAGGAACGTGCTCAGAATGCATTTAAATATTAGCGGGAAATGGATGTTTTAAAAATATCAGTAAATATTGGTACCTAATTCGATACTTTTGAAGCCGTATTAAACATCAATAAACCATGCTAGATTTAATTTAGGTTTTATTCACATATAAACATTGATTTAGTGAAATGAACAGAAGTTCCACCATACCATCTTTACATATACCAACAAACCTCTTTAATTCATGTGAAAGATCAAAATTTACACATGCATGAAGTTTGAATAGCGGGTGAATGGCCTTTCAGTGGAGAAACAGAAATATTACATCGTTTTATTTGTGTTCTAGATGTAATGTTTTCTTTTTTCCCTGTATAGCGATAAATGTTCTCTCTATTCCCTGTATAATGTCCTCTTTCTGACCACTTTTGAC[A/T]GATACAACATCCAATGGCAGTGACAGCAAAAAACTCAGAGTTGAAGAGAGAGTCGGCGACGCCCCGCCATCCCGTGTTCTCCACATCAGAAAGTTACCTAACGATGTGTCTGAAGCAGAGATCATTGCTCTGGGGCTTCCTTTCGGAAAGGTCACCAATATTCTCACACTGAAAGGCAAAAACCAGGTGCGTGGGCCAGCTGAAACCTTTTTGCTTTTACTTTAGTGAGAGATGATGAGTCTTTAGAAGGAGATGCTATTTCTGGATGGACTAACAGCTTTGAGTTGATCGTCTTTGTCTTCAGGCGTTTCTGGAGCTCAGCACGGAGGAAGCTGCTATGACAATGGTCAATTATTACTCCGCTGTGACGCCTCATGTCCGTAGTGTGCCTGTCTACATACAGTATTCCAATCACAAAGAACTCAAGACTGACAATTCAAGCCAGGTAACAAATGACCTAATTGGTCCAGTTTAAAACATGTTTGATTTTTCAAATCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14689
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 |
|---|---|---|---|---|---|
| ENSDART00000046928 | Essential Splice Site | 12 | 183 | 5 | 9 |
| ENSDART00000123275 | Essential Splice Site | 341 | 512 | 10 | 14 |
The following transcripts of ENSDARG00000015230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 31697819)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 30906004 |
| GRCz11 | 24 | 30843215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCTCCTCTAAAGATGGTTACGCCCCACAGTCTGTTTACCCTCTTCGG[T/C]ATGTTCTCGTTAGCTCTACCTTTTTTTCATTTGGTTTCTCTTATTGTTCT
Long Flanking Sequence:
ATATGAATGTATCCTTACCCTGGTACCTGGGTAACTACATTTGGCACAATTATTTGCTCGTATAATGTAGAAATACATAAAGCAGCCATTCTCCTGCATTTCCTGTGTACTGACCTGTTTTATATATTTTTTGTTCCCCCTTTTTGCTTATACTCCATTTGCTTCTCCATTTTTGATTTTGTCCCACTCTGTCTCTCTTTATAATTTTTTTTTACCCTCATTTATATGGTTTTGTTGTTTCTCACCACACTTTTATCACACCTCGCTGTTCATGCTCTTGTTTTTTATTTTTGTTCTTATTTTTTTGCTTGACCAAAACTTCGGACCCCCAATTAACCGCCCCGAACCATGATCCATGACCACTTCACCATTCTGCGGGAAACCACCCTCCGTTATGGATGATCTGTTCATCTCTGCTCTTCCTCGACTCTTCTCTCTGTCCGCTTGCTCCTCTCTCCTCTAAAGATGGTTACGCCCCACAGTCTGTTTACCCTCTTCGG[T/C]ATGTTCTCGTTAGCTCTACCTTTTTTTCATTTGGTTTCTCTTATTGTTCTCTTTATTATTATTATTATTATTCATGTACTTTTGGTTTCTTTATCCAAAGTCAGCATGAAATGGACATTTCAGATATTGGCCAGTAGATTTACTTAATGTCCATTGAAAATAATTGACTACTTGTGTGTCTCTGATTTAAATTTTTGTTAACGTTTTTGCTTGTAAACTTCTAGAGTCGCATGTACTCGACTGCTAATTCATTTAAACGACATAGTTCACCCCTAAAAATTGACAATTACCTCATTATTTACTTTTTCTCATGTGGTTATAAATCATAAGAGTTTCTTCTTTTAAATACAAAAGAAGATATTTTGAAGAATGTAGGTTGCACACATTGACTTGTAATATGACAACAATTAATATGGAAGTTAATGAGTGCCAGCATTTTTCAAAATATCTTCTTTTGTGTTTAACAGAAGAAATAAAAACTCAAATAGGTTTTGAAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24524
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 |
|---|---|---|---|---|---|
| ENSDART00000046928 | Nonsense | 151 | 183 | 9 | 9 |
| ENSDART00000123275 | Nonsense | 480 | 512 | 14 | 14 |
The following transcripts of ENSDARG00000015230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 31704770)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 30899053 |
| GRCz11 | 24 | 30836264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCATTTCTTTTCTCTGCAGAGATCATAAAATGGCCCTGATTCAGATGT[C/A]GACCATCGAAGAAGCCATTCAATGCCTGATCGACCTCCACAATTACAACA
Long Flanking Sequence:
TAAAAGGCAGATTTTTTTTTAACAAAATTTCTCTTTAGAAATAGTACAAAAATGTCAACCGATTCTGTCTGTCATGGCTTTACTGAAAGAATCTTTCTTATATTATTAAAAACAGGGTTCTCACAGTTAAAAGAACTTGGATTTCAGACATTTGGATTAGGCCTGTGGACCATTCCTCGTACATAGTTTACTTAATTAGCTGGATTTGGTTATTGAAAATTTGACACAATACAGGATTGTTTCGTTCTTCAGATTCTGACATGTGGCACAATTATATATTGTGAATAATATTAACCTTAATTATTTTATGAAAAAAAAAAGCTTTTATTCCAGCCAAACTAAAAAAATGAGACATTCTCAGAAGAAAAATGTATAGAAGAAAAATTCCACATTTTAACACCTCATCAAAAGAAGCCCCCCCCCCCCCCCCCCCCCCCCTCTTTCATGCGTGACCATTTCTTTTCTCTGCAGAGATCATAAAATGGCCCTGATTCAGATGT[C/A]GACCATCGAAGAAGCCATTCAATGCCTGATCGACCTCCACAATTACAACATGGGTAATAACCACCACCTGAAGGTCTCCTTTTCCAAATCCACCATCTGAAACGTAACCCGAGAGGTCTCGATCTCAACCTTTTTTTCTATCGTCGCCTGTTGACTGTTTCAATACACTGGGGACCATGCGTTTCTTTTTCCAAGATTCATTCCTAAAGAAGATGTCTAAAGAAAGAAATATTGTGACTGATTTTCCAAGGACCTTTTTTTTTTTTAACACCGTTTCCCTATCGTGGGCACTCTGATGTGCTAGAAAGCTGTTGTGGTGTAAAGTCCTGATCCCCTTATAATAAAAAAAGCAGAAAAGAATGTGCCTTACAAAACTTTTCAGAATTATTGTTTTTCTCAAACCCATGCTTTTGTTTGAGGGTAATATTACACTAAGTGTCATGTTTTTATTTTCTTCTCCTCGTGTTGAGTCTGTATAGTGTATAAAATCCATCAATCTT
Associated Phenotype:
Not determined