ZMP
zgc:91936
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC445116 [Source:RefSeq peptide;Acc:NP_001003510]
Human Orthologue:
TAPBPL
Human Description:
TAP binding protein-like [Source:HGNC Symbol;Acc:30683]
Mouse Orthologue:
Tapbpl
Mouse Description:
TAP binding protein-like Gene [Source:MGI Symbol;Acc:MGI:2384853]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35890 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42551 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa28451 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35890
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045549 | Essential Splice Site | 82 | 318 | None | 5 |
| ENSDART00000127558 | Essential Splice Site | 82 | 539 | None | 10 |
| ENSDART00000130589 | Essential Splice Site | 104 | 340 | None | 5 |
| ENSDART00000140658 | Essential Splice Site | 104 | 253 | None | 4 |
The following transcripts of ENSDARG00000031814 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 23918651)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 24629838 |
| GRCz11 | 15 | 24565103 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCGTAGTCAAGTACGGGGCGAGGTTGCTGTGGCGCTTGTTAAGAGAG[T/A]GAGATCATTGTCCTTTATTTCTTCACTTAATAATATGTAATGATTGTTGT
Long Flanking Sequence:
CATTTGATTCACCATTTGCGATGTCGGTTTAAGGATTTGATTTATAGTTTGAGCATTTGATTCACCATTTGCGATGTCAGTTTGAGGATTTGATTTATAGTTTGAGCATTTGATTCACCATTTGCAATGTCAGTTTGAGGATTTGATTTATCATTTGCAATGTCAGTTTGAGGATTTGATTTATCATTTGCGATGTCAGTTTGAGGATTTGATTTATCATTTGCAATGTCGGTTTGAGCATTTGATTTATAGTTTGAGCATTGATTTATCATTTGATCTTTTAAGCATTGGAATTTTCATTTTAATTTTGTTAGGAAAAAACTTCCATAAAACAAGGCGCTTGTCGGTCATTTTAAGTATTTCACGTTGGCGATGTGCAGGCAGTAATGTTGGCATCGGAAGAGCCACAGCGGTGGATTTAGCGCGCAGAGGCGCGAGGGTCATTCTGGCTTGCCGTAGTCAAGTACGGGGCGAGGTTGCTGTGGCGCTTGTTAAGAGAG[T/A]GAGATCATTGTCCTTTATTTCTTCACTTAATAATATGTAATGATTGTTGTGTATCTTGTAAACATTCTGCGTTTGTTTGTTTGTATTTAGGAGAGTGGGAGTCAAAATGTGGCGTTCATGCAGCTGGATTTGGCGAGCTTGAAATCAGTGCGCTCCTTCGCTGAAACTTTCCTCAAAACAGAGAAGAGACTTGATATTCTCATCAACAATGCAGGTGCTGTTTTGTTTAACCCATAGGGTTCGTCTGTAATTTATATCTTTTATCTTAATTATATCTATATCTATTTATATCTTAGTTCATTATTATTTACTTTTAGTTATCTTGCTTGTGTTAGTGCAATATTATGTGTTTGGTAAATGTTTAATTTTTCACCCTAACTACCTTTTATTTCTATTTCCATAAATTTTACCTTAGGCTTCTCGATTTTATTGTACGTATGTGTGTGTGTGTGTGTGAATGATATTATGAATGTTTTTAGAAACATCAGTTTTAAAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42551
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045549 | None | None | 318 | None | 5 |
| ENSDART00000127558 | Nonsense | 225 | 539 | 5 | 10 |
| ENSDART00000130589 | None | None | 340 | None | 5 |
| ENSDART00000140658 | None | None | 253 | None | 4 |
The following transcripts of ENSDARG00000031814 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 23927280)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 24638467 |
| GRCz11 | 15 | 24573732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACTGGAGGAATAGTAATGCGCTGGCCTGTTGCAGGAGCACAAGAGTA[T/G]GACGTCTGGTTCACCTGCACATTACGTCATACACAAGGCTTGTTCGTCAT
Long Flanking Sequence:
AGCTGTTTATATGAAGTTGTTTAGATATCGTCTGTTTACTACTATTTTTAGTTGTTTGTGGTTTCATTTAAAATAAATTGCAAATTGGATTTATATTTTCTGATTCAACCAGGTGTAAGTGGATCACAGACTCTTCCTGATGTGCATTGGCCTCATTGCCGTTTTATGGATGAGAAAGTTCATGTAAATAAAGAGGGTCACATAGAAACTGAGTATATCCAGAGAAAGGCTGTAGTTCAGTTTGGTAAAGATGGGGACAGTGCTTTACACCCCGCCATTACCTTCCTCGTCACAGGTGAGCAAAAGTCATTTGAAAATGTTACCTTATTACACTCTTTCCTCTTTAAATAATCAATACATGTTCATTTGCTTCACCTAGGCTCTGAAGTGGATATGAGGCATTATTTAGAGGGACGTGAGAACATGATACAATGTGAGATCCGTAGATACAGCACTGGAGGAATAGTAATGCGCTGGCCTGTTGCAGGAGCACAAGAGTA[T/G]GACGTCTGGTTCACCTGCACATTACGTCATACACAAGGCTTGTTCGTCATCACCACCTTCCTCAGACACACACCTGCAACTCCTGCTCAGGGAAAATTGGACTTTCTACAGTGGATGAAAATCAGTGATGGGGATCTCCTGACAACATCAGGTAACACTGAAGCAGGTGTATTTTCTTCCTAAAAACATGAGAAAAACAACACAATTAAATGTATATGAGATATTAACAATGTTACTGCATTTTTATTGTTTTTATTTAGAAACCTAAATGATGAAAATATATTTCCCTTGAAAAAAATAGAGCATCAGTTACATTTTAAATCTAAATAATGAATTGGTTGTTAATATGAACGATGATTGATATGCAAGTAATTTTATTGATTTATCCTTAAAAAGACAGAAAAATATGTACATTCTTACAGTTTTTACTTTAGAATAAGTATCAACATTTATAAAAAGCTGTTCCGATGAGAAGTATAGTTGGTTTTAATGAACAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28451
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045549 | None | None | 318 | None | 5 |
| ENSDART00000127558 | Essential Splice Site | 386 | 539 | 7 | 10 |
| ENSDART00000130589 | None | None | 340 | None | 5 |
| ENSDART00000140658 | None | None | 253 | None | 4 |
The following transcripts of ENSDARG00000031814 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 23932032)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 24643219 |
| GRCz11 | 15 | 24578484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTGCGCGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTACTCTAC[A/T]GAACAGCCTCGTGTGTCTCTAAATGTGCCCAACACCTTGGCTATGGCAGC
Long Flanking Sequence:
CATGTTTAACAAAATGTTTTTGTTTTTTTTTGATACCACTGCTTTAACATCAAGTTTATATTTACTGTTAGTCACTGCCTTTTACGTTCAATACGGCCTAAATCACCTAGAAGAAAATGCATTTTCGAATATTACAAAATATTTGTTCACCTTTATATATTTCCAAATCTTCTGTGGAACTGAAAAGATATTCAAATCTTTTTCTCCATAGAGTGATGTAGTGCATGGTGAAGCACAGACAAAAAGATCATCCAAATGTCTTATTTCTGTAGAAGATTGTAAGACAGACTGGATTGGAGATTACTGTGTGTACAAGACAACTAAAGTTTATTTTCTGTGTGTGTGTACGTGTGTGTGTACGTGTGTGTGTACGTGTGTGTGTGTACGTGTTTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGCGTGCGCGTGTGCACGTGTGTGCGCGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTACTCTAC[A/T]GAACAGCCTCGTGTGTCTCTAAATGTGCCCAACACCTTGGCTATGGCAGCTGGTCAGGACAAGAAGGTGATCTGTGATGCAGAAAGCTACTATCCCCTGGATGTAAACATTGAGTGGTATCTTGAGAGACACAGAGAAAACCCTATGCCTTCATTCCTGAATGTTCGGCACTCCAGTCATCGGCTTAATCAAGATGGCACATATTCGATCTCAGCCTTCCTCTATCTAGAGCCTGGCTTGGAGAACTCTGGATATCAGTACACCTGCAGTGTTTCCCATAAGTCTTTGCTCAACCCAATCAACAAGAGTTTTTTCCTTGTAGTTACAGGTGAACCTAATTTATTTCCAGAATTATTTGCACAAACATTAAAGTCCATAAATGTTCCTTATCTTAAACAATGAAACCAACCACAAGGCGGTAAATCCACAACCCCAAATCAGAAAAAGTTGGGACAGTATGGAAATTGCAAGTAAAAAAGAAAGTGATTTCTAAATGTACT
Associated Phenotype:
Not determined