ZMP
zgc:92287
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC436879 [Source:RefSeq peptide;Acc:NP_001002606]
Human Orthologue:
TMPO
Human Description:
thymopoietin [Source:HGNC Symbol;Acc:11875]
Mouse Orthologue:
Tmpo
Mouse Description:
thymopoietin Gene [Source:MGI Symbol;Acc:MGI:106920]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24288 | Essential Splice Site | Available for shipment | Available now |
| sa37661 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24288
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 |
|---|---|---|---|---|---|
| ENSDART00000058742 | Essential Splice Site | 99 | 285 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 18218840)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 18121779 |
| GRCz11 | 23 | 18048122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCAAAGCCAAACTGCTTCAATATGGTGTTAAAGCTGGACCCATTCTAG[G/A]TCAGTCTGTTGAAGTCACGGTTGTTTGGCTTTTAAAACAGTTTATGCAAT
Long Flanking Sequence:
GGATGCAATACTTAATCGCTGGCTTCTTTCATGTGCGTCTTGTTTTTGTTTGATAGCGCAAAGCATTTTTGCTCGATTCTGCTAAAAAGTGAAGTTTCTTCAGCCTGAGGTTGGTTTGTGATGGGGAAACTGCTACAGCAGCTAATATTGGATGTGACCCCTTTTCAGAACGCGTCAGTGCAAGATGCAAAGGCGAGAAAGCCTCAAAACAAGAGTCTATTGAGGATTGCGTGAGCCGAGGTTCACCCTTTGGCAAGCTAGTGTCAGCGTATGTTTATTAGATTATGCTAAAATGTGCTGATTCCTCTCTCCGCCGTGATGAATCGCTATAATTTCACTGCCTCAACAGGATTTTTTTATTAAAATAGTTTGTTGTGTGTATTTCACTGTACAGGCTGAGAAAGAAGAGGCGGCAGAAATGGTAGACCTGGGCTTACTGACTGACGATCAGCTCAAAGCCAAACTGCTTCAATATGGTGTTAAAGCTGGACCCATTCTAG[G/A]TCAGTCTGTTGAAGTCACGGTTGTTTGGCTTTTAAAACAGTTTATGCAATACAATAATCTGGTTCTTCGTGTGTGTGTTTGTTTGTTTGTTTGGAGCAGCGTCTACTAGATTTTTGTATGAAAAGAAGCTAAAGAGGCTGCTGGATTCTTCAGCACAGCACAAGATCAATGGTACAGCAGATGCAGGTCTCTATTCAGACAGTGAAGAAGAGGACGATGAGGAACAGGACTCTGATGAGGAACAGGACTCTGGTAAGGGCCAGCAATGATGCTGAAATACTTGCTTCTCAATCCTGTGCTGGACCCCGCCATCAGTGCACATTGTGTACGTTGTCTTCTAACAGTTCTCAATTCTGGTCCTTAACATGCCTGATTCAGATCATCAGCTCATTAAGAGATCCATGAACTAATCCTTGTTTCAAAGATGATAGACATACAAAATGTGCAGGGCGGGTGGCCCAGAGGACTGGAATTGAGAACCATTGGTTTAAAGGGTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37661
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058742 | Nonsense | 230 | 285 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 18203908)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 18106847 |
| GRCz11 | 23 | 18033190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAATTGCCTCTACTGAGTCCCACTATATTGGAGAGGCAGGAGATTCAG[C/T]AGCGTCTGGTGCCTCTATGGGTTCAGGTCATTGTCTTCCTTATGGTGGTC
Long Flanking Sequence:
ACTAGGGTGCGCTTGATTCGACACATTATTTTAAATATGTGACATTACTATTTGTTTACTAATTTGTTTCTTGATAGGGCAAGTAATTTTTTTTTTGTCTGCTGGGCCATTAAGAAAATCTTTAGCGTTTAACCTTACATTAAGTCTAAAATTTCATTCTGGGGGGTAGAAAGGTCTTAAAGTCTTACGTTTGACTTGGTGAAACCGCAGAAACTCTTGATAAATAAGTCTTTAATGCTCTACTGAAGAAAGAGATTCACCTACATCTTGGATGCCCGTGAGAGTAAATTTACAGTAATTTTTTTCATTTTTGGGTGAACTATCCATTTAAGTACAATTATGTTTCTATTGATTTGTATGCCTCTTATTATGTCCCCTTTTTTGCATACAGTGCTACAAAGAGAAGATCTATAAAGGGAGCTGCAGGCCGTCCCGTGCAGTTTAAATATCCTGAATTGCCTCTACTGAGTCCCACTATATTGGAGAGGCAGGAGATTCAG[C/T]AGCGTCTGGTGCCTCTATGGGTTCAGGTCATTGTCTTCCTTATGGTGGTCTGCCTGCTCTACATCATCTACTCCTGCATGGACGAGCAGCTCTCCAGTCCTTTCACTGCTCTTCTCGATGGTCTGCATGAATCGGCTCTCACATGCATCTCATCCTTCACTGGCGCTTAGCTTTGATGCACTGATGCCAAACGAGGATGTGTCGATTTAATCTCAGGGTCTAGTCCAGCAAATGTCGTTCAAATTATCTTTTATAAACTAGTGTCAGAGGAGATTTTTGTTGAACCGAGTGGAACTAATATACATAACTCCACCATGCTTGCTTTTGAAAGACAGAATAGGGTTTTAAAACTTTAAAAAGGATGTGTTGTCGGCTAGCCCTTTGCATGGATTTTTTTTCTGGTTGATCTTATACAGACGTGTGTTTTATACTGTTTTCTTTACTTGAAAGTTACAGAGGTTATTTATACTCTTGTTGTCCATCCTGATACAGATACCTGA
Associated Phenotype:
Not determined