ZMP
ttyh2l
Ensembl ID:
ZFIN ID:
Description:
Protein tweety homolog 2-like [Source:UniProtKB/Swiss-Prot;Acc:Q6NUZ2]
Human Orthologue:
TTYH2
Human Description:
tweety homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:13877]
Mouse Orthologue:
Ttyh2
Mouse Description:
tweety homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2157091]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17926 | Nonsense | Available for shipment | Available now |
| sa6917 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38411 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17926
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000008607 | Nonsense | 126 | 531 | 3 | 14 |
| ENSDART00000137701 | Nonsense | 126 | 138 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 52228011)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51353419 |
| GRCz11 | 3 | 51608082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAACAGCGAAACCAACGATGGAGTCTACCAGTTGACTTACTCCATTTA[C/A]AATGCCAATCACACACTGGGTGGCATCGGCAGTAYGGTAAGAGTTTYGCT
Long Flanking Sequence:
CATGTGAGGAGTGATTGCATTTTAAAGTTCTTTTGCCCTTTAGAACTCCCAGATCTATCAATTTGTTTTGATAAATGTACATAAAGTACAAAAGCAAGTCATGTTATGGTGTTATAAGCATTTAGCGAGGAAAATATTATTTTTATATTTTCACATTATTTTTTTATCTGTTTTATCTGCTAGTTGTGCAGCTACTTTTGCAGTTTGGTTCAAATGAAGGTGCTTTTGTTTACCTGCGGAGGATGTTTTAAGAATGCTTCAATAACTACTACATTTTTCTCTATCAAGGTCAAGGACCATTTGTATTCTCGTCTGATCTCTTTAAAGTCTCAAATTTTCAACAACACTTTTAAAGCCACATGAAATTGTTGGATTGAAATGAAGCCACATCTGTAACACAAACTGTTGATTTGTTTTCTTCACAGTTCAGCGGTGGGCGTGGGTTTCTATGGAAACAGCGAAACCAACGATGGAGTCTACCAGTTGACTTACTCCATTTA[C/A]AATGCCAATCACACACTGGGTGGCATCGGCAGTATGGTAAGAGTTTCGCTTGCTTCGCCTGTCACTCACCATGCCGTCTCATTTTTATTGGAATAGCCTGAGGAATATTGTGATTAAAACCCAAATCAGAAGCTTTGCCTGTTATATGCTGCATGCAGGAAAAAAAACTAAGAGCTGAAGCCTCAGGGGCTTTTTCACTTCTGCTGCTGGAATATGACTGTATCATGTGATGAGTGACACGCACGCACATACATATATGCAGGAGTGCCACGCTTCTGCCAGGGAGTTGGAGTCATAGTGTCTTTCTTCATTTTAGATTCCAGTTTTTTGAGAAGTCTTGAGTTGGAGACTCTCTCTGGAGATGCAAACACATCCAGCTGGTGTTTATATTCATGTGTGTAAGGAAGCGAAAGCAGAACGCGCACAGACAAGATTGGGATTATCTGTTCATCTGCATTAAAGAGGATTAAAAATCTGTCTGTACATCCACTCGTGCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6917
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 |
|---|---|---|---|---|---|
| ENSDART00000008607 | Essential Splice Site | 292 | 531 | 7 | 14 |
| ENSDART00000137701 | None | None | 138 | None | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 52259841)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51385249 |
| GRCz11 | 3 | 51639912 |
KASP Assay ID:
554-5023.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCCTGACAAGTACATTGTCAATCAAACCAAAGGCACCTTGAGTTCAGG[T/C]AAGTAATATTTTACTGCTCCATATGCCTGTCTTTTGGATGCACCTGCATA
Long Flanking Sequence:
CAGTAGAAGTCTTAGAAATCCTGTCATTCTTTAAAGTCCATGTGAAATTTAAATTTGCAATGTTTATTTTCCTACCACATATTGTTATTATTTAGGTCAAAAAAAAAAAAAGTTTAATTTGGTAATTCAATCAAATTCTGAATGTATTTGGAGTGGCGGTCTTTCTTTGTTGACATCATTTTGACATAATATTCTTAACTACGCCCCTCTTATTGTTAGTTTCCACTACAAAGGAGAATGATATGCATAAAAGCTCCTCCCCTTATTCAATATTCAGCTCCGTTTGAAAGTATATTAACATACCAACATTAAGAATCTCAGAAATTTTCAATTTTCACCTAATTTGCATGAATACTGCAGACACGTCCAAAAATTTTTATTTTGTGTTAGATTTGTAATTATGAGCTTGTTGTTCATCTGTCCTCATAGGGAACCAGTGACTTTTGTGTTTCTCCTGACAAGTACATTGTCAATCAAACCAAAGGCACCTTGAGTTCAGG[T/C]AAGTAATATTTTACTGCTCCATATGCCTGTCTTTTGGATGCACCTGCATATTCTACCATGTATATGTTATTTTATTTACCGTATTGGGCAATGTATAGTAATTATGTTATTGAGTATTTGCTTTGCGGAGTCATGTTTGTGACTTTATTTCGAGAAATCCCTCAGCCATACTTTACACAATAGTTATATGGAAAAATGTGGGGCCGCATTTCTAAAAACATTTCGAACTAAAAAGTACAATTTAGAAAACGTAACATTCGAAAACACATTTTAGATTCCACTTAAAAATTTAGTTTGAATAGATTTTATTTTGTTAAAATGTGTAGTTATTGTAAGTTGCTTGAGTTTTCCAGAACACACTCTGTGGCCCTTATCATATAACCAGCACGATAAGGTGCAAGATGTGTTTGGCACGTTGCTTTGCAAATTTTCATGTTTTGCACCACGTTGTTTAAATAGCAAATCCATTTCCACTACTTTGTGGACTTATGGGCATGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38411
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 > A
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000008607 | Splice Site, Nonsense | 505 | 531 | 13 | 14 |
| ENSDART00000137701 | None | None | 138 | None | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 52273620)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 51399028 |
| GRCz11 | 3 | 51653691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCGCTATGAAAACGTCCCATTAATTGGGAGCGGTTCACCACCACCAT[C/A]GGTATTTTGATTCAAATCCTACATTTAATAAATAATTTATATTCATTATT
Long Flanking Sequence:
AGTTTTAAAATTGTTATGAAAAATAAATTGTTAATGTTTATAGTTACTTGGCACGCCATGAATATAGCCATAGAAGCAGGCATTGTACTAAACACAAACCATCAAGTAATGTCCTGCCTCCTACTGTATCATTGTGGTACCCATTGAGCAGTGTTGCTTTTTTCCTCAGGGACAGGGATTATGATGATATCGATGAAGAGGACCCGTTTAACCCCACAAGGCGCTTTAATGCTTATAACCCCAGCCGAGCTCAAGTCCACAGTTTCTGCAGCTACAGCAGCAGTATGGGCAGCCAGACCAGTCTACAGCCTCCACTGCAGGCCACATCCAGCACACCCGAGTACATGTGAGTGTGTGTAAAAGAAAAATAGAGATGTTGTTTTCTCCACTGTTGACCCACTTATCTTTTCTCCTCTCCTGCAGGAATCAGTCCATGCTGTTTGAAAGAAATCCTCGCTATGAAAACGTCCCATTAATTGGGAGCGGTTCACCACCACCAT[C/A]GGTATTTTGATTCAAATCCTACATTTAATAAATAATTTATATTCATTATTTTTATTTAATTTAATTTTTTTAAATAAATTATAATGATTTAATAAAAAATAATTTGGAAAATAATATTTATATCTATATAATATAGGCTACTAATAATAAATAAGACGCATTTTTAAGTTCAATACATTCATAATATTGATTATTATTATGTGTATTACATCTTCATGTAGCTGCTGATGTTTAGAACTATTTCATTATAGGTTGACAAACTTGCTTCCATATATCATAAAATAAATTCTATATTTAAAAAAGAAAATAGTAATTATGATAATAATAATAATAATAGAATTAAGTATGTTAATATTTAAAGGGCGAGTAAAACATATTTGATGCAATGTTGGCTTACAACAACCTAAAGAATAACCATAACCCTTGTTATGGTTGTTGTGTGTGATTGTGGTGCTCTGCTAAAAACAGAAATGGAGCATTGCTGCCCCCTGTTGTTAAAT
Associated Phenotype:
Not determined