ZMP
si:ch211-149p5.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate thyrotropin-releasing hormone degrading ectoenzyme (TRHDE) [Sour
Human Orthologue:
TRHDE
Human Description:
thyrotropin-releasing hormone degrading enzyme [Source:HGNC Symbol;Acc:30748]
Mouse Orthologue:
Trhde
Mouse Description:
TRH-degrading enzyme Gene [Source:MGI Symbol;Acc:MGI:2384311]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45176 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40298 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45176
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 |
---|---|---|---|---|---|
ENSDART00000112301 | Nonsense | 332 | 994 | 3 | 19 |
ENSDART00000133056 | Nonsense | 332 | 947 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 22178548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23521883 |
GRCz11 | 4 | 23242858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTGTGTTGTTGTTGTAGATTCGGCTGTACGCCAGACCTGATGCCATC[C/T]AGAGCGGATCGGGTGACTACGCTCTGCGCATCACCAAGAGACTCCTGCAG
Long Flanking Sequence:
ATATTATTTGATTTGCTAAAGATCATGAGACACAAATGAATGGAGTTATGGTGGTAAAAATAACATACATAAGTTGCAAAAAAATAAATAAATATAGATATTTAAACCATATATTTATAAATATTTAACCAGTGGTAAAAGCAACTTTTCTTACTTTTCTGGTGAATCTTTTTTTTAAGATTTATGGGTAGCAGTTCTTCATAATTCAATAATAACATTGCAATCATGGTTGCCCTGCTTAAAAAAAAAAAGGTTCTTGGGTGAAAATTACTGATTTTTAATTTTGTGGCACTCTAGTTTTGAATGTTTTGCATAATAGATGGCGGATGCACTTGAAAGATGAATGAAATATTCAGCCAGATGAAGGCGTTTGGTAGATAAATTCACCATGGCTTACTCTACATTTCTCCTCAAGGGAGACGAATAAGAGTCCATTTTGACTTCTGTTTTCTGTTGTGTTGTTGTTGTAGATTCGGCTGTACGCCAGACCTGATGCCATC[C/T]AGAGCGGATCGGGTGACTACGCTCTGCGCATCACCAAGAGACTCCTGCAGTTTTACCAGGATTACTTCAAAGTCAAATATTCCCTCCCCAAATTAGGTAAGCCGGCCGGTGAAATGTCTTCATCTTTATCTGGCTTCAGTGACGCTGCTGAAACTGGTGATAAATGTTCTTCTCATCAGATTTTTCATTGTTCCTTCTGTCGGTTCTGTGTGAATTCATGTTTCGTTTTGGTGTAAAGAAGTGAAGAGTGTCGATATCAACACAGTTCTTGAGTTTATTGATCCTCAAAGTGCTGCAGGCGTGTGCGCCTGTGTTTGGTCTTGGGAATCAGAGCACGCACCTTGCGTGTGTTGTGAAAGTGTGTGTTTGTGGCTGTATTGACTTGTGTGTGTGCTGTATGTAGTTGTAAGTGTGAGTGTGTTTGTTCTGGACGACTCGTTTCGCTCCATTGGGTTCCTGTCAGCTCTCTGTATTCATTTGAATGTAGGCATCAATCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40298
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112301 | Essential Splice Site | 364 | 994 | 3 | 19 |
ENSDART00000133056 | Essential Splice Site | 364 | 947 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 22178646)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 23521981 |
GRCz11 | 4 | 23242956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTTTACCAGGATTACTTCAAAGTCAAATATTCCCTCCCCAAATTAGG[T/C]AAGCCGGCCGGTGAAATGTCTTCATCTTTATCTGGCTTCAGTGACGCTGC
Long Flanking Sequence:
TATTTAAACCATATATTTATAAATATTTAACCAGTGGTAAAAGCAACTTTTCTTACTTTTCTGGTGAATCTTTTTTTTAAGATTTATGGGTAGCAGTTCTTCATAATTCAATAATAACATTGCAATCATGGTTGCCCTGCTTAAAAAAAAAAAGGTTCTTGGGTGAAAATTACTGATTTTTAATTTTGTGGCACTCTAGTTTTGAATGTTTTGCATAATAGATGGCGGATGCACTTGAAAGATGAATGAAATATTCAGCCAGATGAAGGCGTTTGGTAGATAAATTCACCATGGCTTACTCTACATTTCTCCTCAAGGGAGACGAATAAGAGTCCATTTTGACTTCTGTTTTCTGTTGTGTTGTTGTTGTAGATTCGGCTGTACGCCAGACCTGATGCCATCCAGAGCGGATCGGGTGACTACGCTCTGCGCATCACCAAGAGACTCCTGCAGTTTTACCAGGATTACTTCAAAGTCAAATATTCCCTCCCCAAATTAGG[T/C]AAGCCGGCCGGTGAAATGTCTTCATCTTTATCTGGCTTCAGTGACGCTGCTGAAACTGGTGATAAATGTTCTTCTCATCAGATTTTTCATTGTTCCTTCTGTCGGTTCTGTGTGAATTCATGTTTCGTTTTGGTGTAAAGAAGTGAAGAGTGTCGATATCAACACAGTTCTTGAGTTTATTGATCCTCAAAGTGCTGCAGGCGTGTGCGCCTGTGTTTGGTCTTGGGAATCAGAGCACGCACCTTGCGTGTGTTGTGAAAGTGTGTGTTTGTGGCTGTATTGACTTGTGTGTGTGCTGTATGTAGTTGTAAGTGTGAGTGTGTTTGTTCTGGACGACTCGTTTCGCTCCATTGGGTTCCTGTCAGCTCTCTGTATTCATTTGAATGTAGGCATCAATCTCTCTGGGCTTCTGTCTGTCGCTCTTCTGCCGTCTGCTCACTCATCTCCAAATGTGTGTGTGTGTGTGTTTCAGCAGGCATGTAATATTAATCATGTGCTTT
Associated Phenotype:
Not determined