ZMP
tmpo
Ensembl ID:
ZFIN ID:
Description:
thymopoietin [Source:RefSeq peptide;Acc:NP_851299]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33437 | Essential Splice Site | Available for shipment | Available now |
sa6936 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11203 | Nonsense | Available for shipment | Available now |
sa17619 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33437
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 |
---|---|---|---|---|---|
ENSDART00000016690 | Essential Splice Site | 168 | 685 | 3 | 15 |
ENSDART00000042874 | Essential Splice Site | 168 | 515 | 3 | 11 |
ENSDART00000044005 | Essential Splice Site | 168 | 369 | 3 | 6 |
ENSDART00000125762 | Essential Splice Site | 168 | 657 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 4 (position 15937656)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16880496 |
GRCz11 | 4 | 16869472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATCAGAATGGCAACAATGATTCAGACCAGTACAGCGACAGGGAGGAAG[G/A]TAACACATTACCAAATACCTAAAAAAAAAAAAATCTGACATTGTACTATT
Long Flanking Sequence:
ATGATGAGTTAAATAACTCTATTTGGAAAGAATTCATAATTTTACATCGTGATAATTCACAAAAGTAAATAGTGCATTTATTACAAAGTGTAATAAGCAAATCACACACATGAGTACAATAGAGCAAAGATACATATCAAATAGACGGTGCTTTATTTTCAATTTTACCTCAATACTGTTCGGATTTCCAGAAAACCAAGTGGAAATCAAGTGGAAAATAACACACTAGTCTTAATTGTAATAACAACTATATCTCCTAAATATATGTGTTCTTTAATAAACATTACATTTTGGGCAGGATGATTCTTGTGTAGACCTAATACTGACATTTAATGTCTTCTTCACATCAGCATCCACTAGGAAGGTGTATGAGAAGCGGCTTCAGAAGCTGCTGGATCAGGGTCCTCCTGTAGCTGTGGCTCTTCCCTCAGAGACGTCACAGACTGATGGCAATCAGAATGGCAACAATGATTCAGACCAGTACAGCGACAGGGAGGAAG[G/A]TAACACATTACCAAATACCTAAAAAAAAAAAAATCTGACATTGTACTATTTTATTCTCTTGCGATTTTTATATTTCTATGTGAATACAATTTTTTCTGACATAAAGCTCTACTTGGAATAAAATCATTACCTTTGATTGGAATAATCTTGCAGAGGAGTGAATCAAAGAAATTGCAAGAATGAATATTTAAGATAGAACAAAGACCAAAGTGAAATAATAGTCCGATATTCAGGTACCGTATTACACTACGATATCATCATGATATATTGCCCCTGATAATGACAGGTCACCATATTAGTGATGTATCGCAAGAAAACCATCCACAATATATCATATTTGTAAATCAAGAGGGATAAATGCATTAAAGTCATAAGATATACTACTTTTATTAACATCACATATATTTCTTAGAATTGCAACATTTGATATGAGGTTCAATCTGCCATTTATAGAATAGCCACCTTATGTATATCGCTATTTTGTCCTGCCCCATTTATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6936
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016690 | Nonsense | 410 | 685 | 11 | 15 |
ENSDART00000042874 | Nonsense | 310 | 515 | 8 | 11 |
ENSDART00000044005 | None | None | 369 | None | 6 |
ENSDART00000125762 | Nonsense | 410 | 657 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 4 (position 15930223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16873063 |
GRCz11 | 4 | 16862039 |
KASP Assay ID:
554-4392.1 (used for ordering genotyping assays)
KASP Sequence:
ACATTAATAAATCAGGTGGATGACCAGGGTATGCAGGACGTCCTGAGCTG[T/A]AGATCTGCAAATGGTGGTCTTCTGGTAWGTTTCGCAGTTATGCACTGYTT
Long Flanking Sequence:
TTCATGAACATCATGTCATATTCTAGTGCCACCGTGTTACTTACATTGCTCTTACATTAATAAAGACAGTGCCGAAGGATCCCAAACCCTCTAAGCGCTACTCCATGTCTGCAACAGAATCAACAAAACGCCCAGTATCCAGTCTGAACAACAAGGTGTCAGAGCTATGTTTCTTAAAGCATCCATAAATATAAAAGCCTCGCATTTAACAGTTGAGCTGATTGGTTTGCCTCTTGTGGTTTCTTTTGTAGCATGATGAGAATACTGCTGACATCCCCTCCCCTCCGCATAGACAATCCAGTCGAGAGCCACTAGTTTCTCTGATTAATACTGCTTGTGTTGAGGTGAAGATGCACACATTTACATCTCTAGTTGATGCTTTCAGCTTTTAAGCAATATATTAGATCTATCCAGTCTTCATTTTGGAATTAATTGCATGTTCATTATGCTACATTAATAAATCAGGTGGATGACCAGGGTATGCAGGACGTCCTGAGCTG[T/A]AGATCTGCAAATGGTGGTCTTCTGGTATGTTTCGCAGTTATGCACTGCTTATAACTCTATTAAATATACATTTTGGCAGCTTATGAGGCTCTGTTTATTCTCTAAAGGCCCAGGGTGTCAGATCTGCTGCCGTATCGAAGCTTTCAAAGCCTGTTTTGAGTCAGAGCAAACCTTCCAAACCCTTGGTAGACATGATGTGCTGTCTCTCGCCTTCCAGTGATCGACAAAAAGAGGTTTTCCCATCACATTCACTTCCTTACAAGAACTTCTGTTTGGTTTCTGAGGACTCTCTTACTGTGTCATGTGAACTTTCTCAGGTTTGCAGATTGCAAATTGTGTTTTTTTGAAGTAATGGAGCAGGTTTTAGTAGGGTTGGGTGTGTTATTTTTTATATCATTATTTTTTTTATCAACAGTAATATTGTAAATGTTTCACTTTGTACCATCAAGCAAGCATAACCACAATTCCTAAATATCTTCAAATCATCACAGCTAATATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11203
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016690 | Nonsense | 473 | 685 | 12 | 15 |
ENSDART00000042874 | None | None | 515 | None | 11 |
ENSDART00000044005 | None | None | 369 | None | 6 |
ENSDART00000125762 | None | None | 657 | None | 15 |
Genomic Location (Zv9):
Chromosome 4 (position 15929951)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16872791 |
GRCz11 | 4 | 16861767 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGACAAAAAGAGGTTTTCCCATCACATTCACTTCCTTACAAGAACTTCTG[T/A]TTGGTTTCTGAGGACTCTCTTACTGTGTCATGTGAACTTTCTCAGGTTTG
Long Flanking Sequence:
ATCCCCTCCCCTCCGCATAGACAATCCAGTCGAGAGCCACTAGTTTCTCTGATTAATACTGCTTGTGTTGAGGTGAAGATGCACACATTTACATCTCTAGTTGATGCTTTCAGCTTTTAAGCAATATATTAGATCTATCCAGTCTTCATTTTGGAATTAATTGCATGTTCATTATGCTACATTAATAAATCAGGTGGATGACCAGGGTATGCAGGACGTCCTGAGCTGTAGATCTGCAAATGGTGGTCTTCTGGTATGTTTCGCAGTTATGCACTGCTTATAACTCTATTAAATATACATTTTGGCAGCTTATGAGGCTCTGTTTATTCTCTAAAGGCCCAGGGTGTCAGATCTGCTGCCGTATCGAAGCTTTCAAAGCCTGTTTTGAGTCAGAGCAAACCTTCCAAACCCTTGGTAGACATGATGTGCTGTCTCTCGCCTTCCAGTGATCGACAAAAAGAGGTTTTCCCATCACATTCACTTCCTTACAAGAACTTCTG[T/A]TTGGTTTCTGAGGACTCTCTTACTGTGTCATGTGAACTTTCTCAGGTTTGCAGATTGCAAATTGTGTTTTTTTGAAGTAATGGAGCAGGTTTTAGTAGGGTTGGGTGTGTTATTTTTTATATCATTATTTTTTTTATCAACAGTAATATTGTAAATGTTTCACTTTGTACCATCAAGCAAGCATAACCACAATTCCTAAATATCTTCAAATCATCACAGCTAATATTGATCGAGTTGCATTGTAGACAACATTGTTTGTTTTTCTGTTTTGCCAATGTTAATAGCTCAAGAACCAAAGCAGAATATTTGTACATCTCAGAGAGCAACATTGCAGTAATCATTTGAGTAAACAAAACAGTGATCCTTTCATAAACAGTCACATTATTTCTAAATGAATCAGCTGTTTGAACATATCGTGTGAATGAATCACTCCTTGAACACCACCACCAACCAGCATTCATTCATTCATTTTCTTTTAAGCTTCATCCCTTTATTAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17619
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016690 | Essential Splice Site | 530 | 685 | 13 | 15 |
ENSDART00000042874 | None | None | 515 | None | 11 |
ENSDART00000044005 | None | None | 369 | None | 6 |
ENSDART00000125762 | Essential Splice Site | 502 | 657 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 4 (position 15928702)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16871542 |
GRCz11 | 4 | 16860518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCCGAGGACTCGATAACAAGCTGATGGRTATGAAGGAGACAATGATGG[T/A]AACTTTGAGCTACATGGTGTTTGGCTCCACCGGTGGTTAATTGGGATGAG
Long Flanking Sequence:
AACTCTCCAAAATCACCTTACATAAAGAACTTATTCACCTTGTGTACATGCTCTACAATAAGCTGTCAACGCAACATTTATAATGTTTACTCTTCTGGTCCAAAGTGTTTACTTTCTTTCTCTGGATGATCTTAAAGCCACAGTAAGGATGTTTTTCTGACAGATATCACACATGCACACTTATAAACTCACAGGAAGCAGGTTAATGTGTTTGCATAATGGGCAAATTTGTCTAAGGGGAAGATAACTAGCAGTAAATAACCTTATTCTGATAAAGAAAAACAGGTTAAAATGTTTACTTGTTTATTGTCTGCTTAAAACATGCATGTAAATCTTCTGTTAGTCATCATTAAAGCTTTTATTGGTTTATCAGGAGAGCTGTGGTTCACCACAGACCCATCCCAAATCAAGACATTCCAAAATCACCCCTTTCCTCTCCCAAATCACTCCTGTCCGAGGACTCGATAACAAGCTGATGGATATGAAGGAGACAATGATGG[T/A]AACTTTGAGCTACATGGTGTTTGGCTCCACCGGTGGTTAATTGGGATGAGGACATTTGAATAATGATTTTGGGCTCACTCGTGTTATACTTGGCTGTGATGTTACATAATGTTTTCCCTTTTAGTTTTTTAAAGTGAAAGCTGAAAACATTTTTAGAATCGCAGTGATCTGTGTTCACAATTTTGTGGCTCTTTTGTTCTTGTGCGCAGGTTGAAAAGGTGTCAGCCATTGATCAGACCCCGAGGGCGGTGGAGAGAGACGTGCTTAAAGAAATCTTCCCCACTGAAAACCTCAACACTCCCACTGGAATCAGGTATGGAGCCCAGATCATTCAAACTTTCTGAACATTTTCTGAGAACAAGCTCAAGTCAAAGTGTCTGTTTTTAAAAATGTACTTCAAATGGGACATGAATTATACGGTTTACTTCTATTATTTTAAAATGTTAAACTTGTAACCAATTCGAATTGGCACATTTTCACTTATAAAAAAAAAAAATATG
Associated Phenotype:
Not determined