ZMP
trip4
Ensembl ID:
ZFIN ID:
Description:
thyroid hormone receptor interactor 4 [Source:RefSeq peptide;Acc:NP_001071043]
Human Orthologue:
TRIP4
Human Description:
thyroid hormone receptor interactor 4 [Source:HGNC Symbol;Acc:12310]
Mouse Orthologue:
Trip4
Mouse Description:
thyroid hormone receptor interactor 4 Gene [Source:MGI Symbol;Acc:MGI:1928469]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41030 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13764 | Essential Splice Site | Available for shipment | Available now |
| sa34195 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41030
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 |
|---|---|---|---|---|---|
| ENSDART00000030273 | Nonsense | 234 | 515 | 6 | 12 |
| ENSDART00000126674 | Nonsense | 234 | 564 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 56063931)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52990579 |
| GRCz11 | 7 | 53260231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCAGGGTCGTTTTTTTGTGTGGTCCCAGAGGGAACCGAGCGAGAGTA[T/A]CTGCCCCACCAAGAGTCCAAGATGAAGGCTGGTCTGGAAAAAGCTGTGAA
Long Flanking Sequence:
CGACCCCGGATGAATAAAGGACTGAGCCAAAGGAAAATGAATGAATATTTATTCATGCTTGTAGATTGCATATTATATTTTATGCATGATTCACTCCCCTACAGAGTCACCCCAATAAATCTAAAATGATTAGTTCTTTTCGAATAGAGATATTCAAGTCATCTGCTGAAATTGTAGTCACATAGCAATACTTATCTAGAATAAAAAAACATTGCAATTTTAGATTTTTCTTATATTGTGTAGCCCTGATTGAGACTGATGGACAGCTGTGAAAGTAGCCTTCATAATCAAGGTTAAACTTGTTTGCACATCATTCAGGTGTGCACCAATGAGGAGCAAGAGATATTGCAGAGGGACTCCAACAAGAGCCAAAAGCTCCGCAAAAAACTGATGGGAGGTAAGAAATTAAATGATTCCATGCACCTTAACTTGACCTTCGCAGCATTTTTGTGATCAGGGTCGTTTTTTTGTGTGGTCCCAGAGGGAACCGAGCGAGAGTA[T/A]CTGCCCCACCAAGAGTCCAAGATGAAGGCTGGTCTGGAAAAAGCTGTGAAGCACAAAGATAAGCTACTGGAGTTTGACAAGAACAGGTCAGCCTTTCTAAATACAGTGTTGGTTTAACTGTCAGGATTCATCTAAATAAATACACATTAATGAGTTTAAAGCACAAACAAATATTATTGTTAAAATTATGACCGCTACAGAATTATTAGCCCCCTATTAATAATTTCCCCAAGTTCTGTTTAACAGAAAAAAAAATCAACACATTTTTAAACATTATAGTTTTATAATAACTGATTTCTTTTATCTTTGCCATGATGACAGTACATACTATTTTACAAATTTTTGGTGCAACATGCTTTTATCAAATTAAAAAAATAGCATTTTTATTTAACTTAAACATGAATCATCTACAGTATGTATTCTATGTGTCACACATTCTAAAGTCTCTTAGTTTTATTTGAAGTTATCCTAAATGATATAAAAAAGGCCATTTTAAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13764
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 |
|---|---|---|---|---|---|
| ENSDART00000030273 | Essential Splice Site | 377 | 515 | 8 | 12 |
| ENSDART00000126674 | Essential Splice Site | 377 | 564 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 56059462)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52995048 |
| GRCz11 | 7 | 53264700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAYTTCAGAGAGYTCGTCAACCCCAATATTCTACAGTCTGCACCAGAGG[T/C]ACATGCAAACTCTCAAGTGCATRTAAGATCAGTGCCATTCATATTCGAGA
Long Flanking Sequence:
TGTTTACAATGATAATAGAGCTTGTTAAGTTTTAATTATCAATGAAATAATTATAATGTTTTATTTTGTTATTTTATCTTCATTTACAATTAGCAGGGTATTTATAGCCACTGTATATCTCTGTCTGTTCGCATCTCGTCTCTTTGTACCCCATGGCGGTGTAGTCGGAAACTGCTGTTCCACCTAAAAACATGTTTTTAATCCTGTAGTCATGCTGCAGCGCCACATACACCGCGGTAATGGCCAATTTGAAGTGTCGCCCACTGTTGCTGTTTAAATTAATTAAATATGACTTGAAGGTGTTAATTAAAATGCACAATCTGTGTAGCATGACAATAACTTTGTGTATGTGTGTGTGTGTGTGTATTAAAGGTTTGACGAGACTGTCAAGGCCATCAACACTGGTTCTTTTGGCCAGAAGGCAAAACATTCAGCTCCTGCTGATCGACAGCACTTCAGAGAGCTCGTCAACCCCAATATTCTACAGTCTGCACCAGAGG[T/C]ACATGCAAACTCTCAAGTGCATGTAAGATCAGTGCCATTCATATTCGAGAAGTGTTTATGTCTATTGATTCATGTGTGTTTGTGCTGTGTCAGTGGGTTGACGTGGCCAGTAGCAATCCCTCCCGTAAGTCTTCATCAAAGGCAGCGAGCGGTAAAGAGACAAGTGAGCGCAGCCGACTCAGACTGCAGGACAAAGAGCTGCAGGAGATTGCAGACGGCGGCTGGTGTCTCAGCATGCATCAGCCATGGGCTTCACTGCTCGTTAAAGGCATAAAAAGGTACAGTTCACTTGAAGACCCTGTGAGGACTCATAAATGTCCTCTTTATAGGTCTGTCACAATAATCAGTATATCGACATATCACACAACACATGGACATGTTCTCATGTCATCATTTTTTGTAATGCAATATATATCGCCTATACATAACCAATTCCAGCCACATTTTAGCTGATTGCACAGCCTCTCTATCTCCGTATAGTTCCGTATCAGAATGGTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34195
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000030273 | Essential Splice Site | 481 | 515 | 10 | 12 |
| ENSDART00000126674 | Essential Splice Site | 481 | 564 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 56054517)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52999993 |
| GRCz11 | 7 | 53269645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGAAATTGCAGAGGTAGAGGCCATGTACCGCCACCTTTACAAGCATGG[T/G]ATGTTTACTAATATACTAAACCTGTTAAACCTAAATAATCCCTTCATGCA
Long Flanking Sequence:
AGGAAAAACCACCAACAATAAAGAATGCATGACTATTTGTTGTCATGGTTTTGGAATAAAAATAATGTGGTTCTAATGATAGTCAATGTGGCAAAAACAGCAACTAACATAATATGAGGGTAGTCAATTTGAACAATACAGTACAGTTAATGTAATATAAAGGTTACAGGCGAAGGAACAGAAAACAAAATGCATAATATTATGAAGAGAATAGCTTTTTCTTAAACCATTTAAAGTAATCCATTAACTTCATAACTTCTGCCAAGTTTATTGCCCTTTTACAGATCATTTTGATTGTTTATATAGTGTGTGAGTGTGTATATATAACAGCACTCATCTGAATGTGTTTTTCTCCATTTCTTGTGTTTGTGCAGGGTGGAGGGCAGAACATGGTATACATCCCATAGGGGGCGCCTGTGGATTGCAGCAGCAGCTAACAGACCCACTCCTCAAGAAATTGCAGAGGTAGAGGCCATGTACCGCCACCTTTACAAGCATGG[T/G]ATGTTTACTAATATACTAAACCTGTTAAACCTAAATAATCCCTTCATGCACATCTGTATATTTTAGCAACTTCACCTAAATTAGTTATTTTGTTCTTCAGAGCCCCAGTTTCCTGCAGAGTATCCCACTGGCTGTTTGCTGGGCTGCGTGAATGTCTCCGATTGTCTTTCTCAGGAGCAATTCAGAGAACAGGTCAGTAACATTTGCTACTCGCCCATACAAATATTCATTTTTCACTTAAAGTCAGTGTCAAATCAAAATTTAATATGTTATTTTGCTGATCTTCAATTAAAGTCTGACCAATTGTTTTAACTCAACTGAGGAGTTACATAGCAGCTTCATATTAATATCCTCTCATCCATTAGTGTGCTATGAGTGAATACTGTGCAACAGAAAGCCCCACACCCTAATCAGTTTTTAGTTGGAAGTACATCAGCATACAGAAATACAAGTCTCAGCCAGTCCCGGTTTATGTAGATTTCAAACCTTTACTTTTCTCT
Associated Phenotype:
Not determined