ZMP
zgc:110348
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC100126119 [Source:RefSeq peptide;Acc:NP_001103317]
Human Orthologue:
TSTA3
Human Description:
tissue specific transplantation antigen P35B [Source:HGNC Symbol;Acc:12390]
Mouse Orthologue:
Tsta3
Mouse Description:
tissue specific transplantation antigen P35B Gene [Source:MGI Symbol;Acc:MGI:98857]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15220 | Nonsense | Available for shipment | Available now |
| sa16508 | Essential Splice Site | Available for shipment | Available now |
| sa29465 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15220
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 |
|---|---|---|---|---|---|
| ENSDART00000062578 | None | None | 241 | 2 | 11 |
| ENSDART00000100262 | Nonsense | 66 | 354 | 2 | 10 |
| ENSDART00000100267 | Nonsense | 32 | 320 | 2 | 10 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 49138937)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 48914345 |
| GRCz11 | 20 | 48745562 |
KASP Assay ID:
2261-4946.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGTGGGCTGGTGGGGCGAGCCATAKAGCGGGTGGTGAAAGAGGAGGGC[A/T]GAGRAGGAGAAGAATGGACATTCCTSTCATCCAAAGAWGCCAATCTTTTG
Long Flanking Sequence:
GAGTGCTATCCTGCTGGAGAATTTGCCCTCTCCTGTGGTTTGTAATGTAATGGGCAGCACAAATGTCTTGATACCTCAGGCTGTTATTGTTGCAGTCCACTCTGCAGATCTCTCGCAAGACTGAATCTAATCCCAAACCATGATTTTTCCTTCACCAAACTTGACTGATTTCCATGAGAATCTTGAGTCCATGCGGGTTCCAATAAGTCTTCTGCAGTATTTGTGATGATTGGGATGCAGTTCAACAGACGATTCATCTGAAAAATCCACCTGATGCTACTTTTCCAAATTATCAACTAGAAGTTGCTCTTACAACTGGGATCCACGACAAGACTTTTGTCAGGTAGCGTATTACACATTAACACCTGTAATGTTGATCAAACCTCTTTCCTCTCTCTCTCTGTCAGATGAACGGGACGGTCGAGCCAATGCGTGTGCTAGTGACGGGCGGCAGTGGGCTGGTGGGGCGAGCCATAGAGCGGGTGGTGAAAGAGGAGGGC[A/T]GAGGAGGAGAAGAATGGACATTCCTCTCATCCAAAGAAGCCAATCTTTTGTAAGAACTCCAAAAAAAAAAAACACAAATCATTTGTCAGACAAATTACACAACAGAGTAATTAAAATGTCAAGCCATCACACCCCTCGCATTAATATAATTATTTGCTCTTTAACCCTGAGTGCTACCTGATGAAGTGAACTGCAGATGAATTATGCTTTAATGTTTGTGTCCAGTTCAAATTAACTACCCTTTCATTATGTTGGCGGCTGTTTTTGCCCCATTGACTTCCATTATAATTACAATTTTAAAGCCATGACAGCTTATAATCATGCATTATTGCTTGTTGGTGGCTTTCCCAGTGTATTTTTTTTTTACAGTCGATCATCAGTTCGCAGCGTTAAACCTTTAAATCTGCCTGTATAAAATGTCTCTAGCTCTTATATAGAGGTATATGGAGTAAAACAGCAGATTATAGTGGGTGCATAAATACACTTACTATGTTTCGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16508
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 |
|---|---|---|---|---|---|
| ENSDART00000062578 | Essential Splice Site | 84 | 241 | 5 | 11 |
| ENSDART00000100262 | Essential Splice Site | 188 | 354 | 5 | 10 |
| ENSDART00000100267 | Essential Splice Site | 154 | 320 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 49119346)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 48933936 |
| GRCz11 | 20 | 48765153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAATTTYGGTTATGCCTTYGCCAARCGCATGATTGATGTCCAAAACAGG[T/C]YAGAAACAGGTTTAAAGCATGTATGCCYCACATGAAAGCATATCTGGRTC
Long Flanking Sequence:
AAAATTAAAGTTTTTTTTTTAGATGTTATCAGTATTATTTGTATTTATCTAGAGTATAATGGTGCGCCCGCTTCTAATGTTATCACTTGATTAAATGGGCATTATCAGTGGCTATCAGCTGATAGATATGGGAAAGCAGGGCCAAGTGTCAGTGTTGCAGTTTGACAAGTGTGAGTGCTCCAAATCAAGGCCAGGTGTGGTTCAATTAAATTCAACTTTATTTCTATAGTGTTTTACAATAGATTGTGTCAAAGCAGCTTAACATAGAAGTGTAAATTGAAACTGTTTCAGTCCAGTTAAAGTTATCACTTTTCATGAACCAGACTATTTTTATTGTGTCAATGGAATTAAAAGTGAGTGTACTTTCTTTTTCACAAGGCCGTATGTTTATGATCATTTATTTGTAACTGCTTGGTTTGTTTCAGATCCACAATGGTCCACCACATGACTCTAATTTCGGTTATGCCTTCGCCAAGCGCATGATTGATGTCCAAAACAGG[T/C]TAGAAACAGGTTTAAAGCATGTATGCCCCACATGAAAGCATATCTGGGTCACATTTCAATGCACTGCAATACATCAATATTTCTGTAGTGTTTTTTATAATAAAGATTGTATCAAGGAAGCGTAACATAAATAAAGAAAAAGAGAATAAAAAGCCATAATATTTTAAATTGTGGAACATTCCAGCAATTCTCGCAGCCTGGAAAGTAGTGTAGTATATAAAGAAGATTTAGTATTCTCCAAAAGTATGCAGTAGTGTCTCTAAAAGTGTACAGACATGCAACTTAAAGAAAGTCAAGCATGTATTGAAGAAGAAATGAGCCAGGCTAAAATTGTGCTATGTGTGAAAGATGAGCAGCCTGCAGAAGAGCAGAAGCAACTATGAGAGGCAAGAGAATAACTGAATATGTAAAATTATGCAACATGTAAAGAATTATGCAGCACGGTGGCACAGTGGGTAGCACAATCGCCTCACAGTAAGAAGGTTGCTGGTTCGAGCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29465
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062578 | Essential Splice Site | 129 | 241 | None | 11 |
| ENSDART00000100262 | Essential Splice Site | 233 | 354 | None | 10 |
| ENSDART00000100267 | Essential Splice Site | 199 | 320 | None | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 49114970)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 48938312 |
| GRCz11 | 20 | 48769529 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGCTGAGCTCTCTTTTTGATACTAACCATTTGTGCCTGTGTGTCTTGT[A/G]GAGGAAGGTAAACCTCTGCAGGTCTGGGGTTCAGGGAAACCTCTGCGTCA
Long Flanking Sequence:
TATACTGTTCCTTTTACAGCATTGATTATGTAATGTGATTAAAATACAATCAGTTAAATAAACTTAAGCATTCATTAAGTTTTTCAAGAGTAAAACGAGATGAAAAACCATGTAAACTATAGTGCCGTCAGTAGCAGCAGGCTAAAAACACAGAAAATACTGGGGTGAAATACACTTCCATATTTTAAAGACATGATAGAATTGCATTAAATTTCATTGTAATGCAGCGCTTCTTTTCCGGCCTGAGACCCACTTTATATCATATATTAATCAATAAGACAGTAAAGATCACTGATATTTAAAGAAATCAGATCTTAAACATGGCGATTTTAGAATGGCATGACCATTCACTGGATGCGCTTGAGCTGACTGACAGATAAAAAAAGTCTGTGTGCATGCATAAACCCCATCAAAATCAAATACACATTATGAAAGGCTTAAAATCTCATTTAAGCTGAGCTCTCTTTTTGATACTAACCATTTGTGCCTGTGTGTCTTGT[A/G]GAGGAAGGTAAACCTCTGCAGGTCTGGGGTTCAGGGAAACCTCTGCGTCAGTTCATCTATTCTTTGGATCTGGCTCGTCTGTTCCTGTGGGTTTTAAGGGAATACGATGAAGTGGATCCAATCATTCTCTCAGGTAGAAAAAAAATCAACTTTTTTTGTCAATACACGTGTACAAGTACAAGGCAATGAAATACAGTTTCGGTCTGACCAGGCGTCTAACCATTATATATATTATAGTATATTTTTCCTCCAATTTCTGTTCAACGGAAAGAAGATTGTTTCAGCACATTTCTAAACATAATAGTTTTAATAACTCATTCATAAAAACTGATTTATTTTATCTTTGCCATGATGACAACAAATAATATTTGACTAGATATTTTACAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAAATAGGTTATAGGCAAGTTGAGGTAATTAGGCAAATCATTGCATAAGATGGTTTGTTCTGTAGAAAATTGAAAA
Associated Phenotype:
Not determined