ZMP
ttyh2
Ensembl ID:
ZFIN ID:
Description:
tweety homolog 2 [Source:RefSeq peptide;Acc:NP_001002490]
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 |
---|---|---|---|
sa38903 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16459 | Nonsense | Available for shipment | Available now |
sa35361 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38903
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009172 | Essential Splice Site | 102 | 535 | 2 | 14 |
ENSDART00000081046 | Essential Splice Site | 102 | 316 | 2 | 8 |
ENSDART00000134670 | Essential Splice Site | 102 | 483 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 12 (position 40148327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38430633 |
GRCz11 | 12 | 38605054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCTTGCTGTGTGACTTGGGCTGCTGTTGCTGCCGGGCTCATCTGCTGG[T/A]ACGTACCACCCACCGTTCACATGCTGAGAGGATAAACCTGCTCAAGATGC
Long Flanking Sequence:
ATTATTTTTTTGTAAATATAGTTTTAATAACATTTTAATTACGTTTATTATAATATATTTTATAATCAAATTCAATATGCAGCATATGTAAAAATCCGGTTGGTCATTTGTTAAAAGTAAATCAAACATTACAATGCCTGTCTCTGAACATATTCCAGAATTCTGTTTCTCATAACTAGGCTGTTGAATGCTAAGGGAAATGTTTCATTATGAATGCCAAACATACTACATCAAACCATTTCATTTTAAGAGCGCAGGATTTTTCCCTCTCATGTCTCTTTCAATAAAGAAACCCATATCTCATGTTTTTTCCCCCCATGCAGTCGCTCATCTTCCTGGGCTGTGTAGCAGCGGCTGGGCTCGGTGTGAACCTGCTGTGTTTGGCCATATACCTGAGCTGCCTGTGCTGCTGTCGGAAAGATGAGGAGGAAGAGGAAAGTAAGAAATCCAACTCTTGCTGTGTGACTTGGGCTGCTGTTGCTGCCGGGCTCATCTGCTGG[T/A]ACGTACCACCCACCGTTCACATGCTGAGAGGATAAACCTGCTCAAGATGCAGACTGCATAGTTAAGCAGTCAAGCGCATGAGTGTGTGTGTAAGTGAAAATTGTAAGAATGATGTGGTTACATTTCTATTGTGGCTGTCATTGGTGTCTGGCATTAAGCAGAATTTAACACTTTAGGATTTGATGTTTGGAAATTGTACTCTTTTGTTTCATTGGAATGGGATGATGCTTTTGTCACATTAGCTATGTTAAAGGGCACCTAGGATAAAAATCATCTTTAGTTAGCTGTTTGGACAGAACTGTGTGGAAGTATAGTGTGTCCACAGTTATATTGGGGTTATAGAAACACAATAAGTCTCTTTTTTTAATTTCCTGACGTTAAAATAAGATCCAAATCCTTCCCATTTGCAGATTCACTGCAATGTGACGTAGGAGTGCGGTTTCCGAGTTGATTAACAGCCACGTATCAACATGTCTCTATAGTAACAAGTATAATCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16459
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009172 | Nonsense | 238 | 535 | 5 | 14 |
ENSDART00000081046 | Nonsense | 238 | 316 | 5 | 8 |
ENSDART00000134670 | Nonsense | 238 | 483 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 12 (position 40198575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38480881 |
GRCz11 | 12 | 38655302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATCTTGGATCTGATCATCTGTCTTGCTGCTTGTCTGGGTCTGGCCAAA[C/T]AATCTCGMTGGTTGCTGACTACGTGAGTACAAACCTTSAGTACATCTMAT
Long Flanking Sequence:
GAACACTTGTGGTGCTTTTGAGTTGGGATAGAGGTTGGGTTATGGATAGATTTAGTGGCATGGGTAGGTTTTAGGGTGGGTTAAGGTTTAAGGGATGGTCAACAGTGTATTTACAAATGGAATTACAAAAGTTAATTACAGATGTAATTACATAAAGGTATTTAATCAAGCATAAGTACACAGTAAATACATGTATTTACACAATAAGTACAATGTGCCACTTAATATAAAGTGGGACCAAAAACTCAAACTGGAGATATTTTTAAAAAAGTTTTCTTCATTTTGGCTCCCCAAAATTCTTTTCTCTTATTTCCTTTATTTATGTCACATCTTGATTAACATTTTTTAAGCCTGGCAATAGATTCAGTGAATTCTCAGATCATGTATGTATTTATTCATTCAGTGCTGACTTTTCTTTCTTCTAAAGGTGGTTGACGTACCTTTTGATACTGATCTTGGATCTGATCATCTGTCTTGCTGCTTGTCTGGGTCTGGCCAAA[C/T]AATCTCGCTGGTTGCTGACTACGTGAGTACAAACCTTGAGTACATCTCATTACCATGAAAAGATTTGAGAACTTTGAGTCATATCTGTTATATTAGATTTTTAAATAGATGTGTCTCAGCCAAATATTGTCAACCCAGGCTTATTATGGATGCATACCCTTGCATACATTTCTGGAGAGTGCGAAATACATCCCAAGAGCTACGTTTTTTTGCAGCTTTTGTTTTCGCAAATCCACCAGAGGCCACTTGGTATGCTTTTTCAGGTCTCAAATTTCTCTTGCGAGTGCCATTCATGCCTGCTCTTCTCACGTAAATCGACCAGAGGCTGCTGTCGACTGACTGACTGACTGACTGACTGACCGACCGACCGACCGACCGACCGACCGACCGACCGACCGACCGACCGACCGACCGACTGACTGACTGACTGACCGACCGACCGACCACCAACTCACCCACCCAGAACATTTTCTACACCCAACCGATTGTGTTTTCAAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35361
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 |
---|---|---|---|---|---|
ENSDART00000009172 | Nonsense | 303 | 535 | 8 | 14 |
ENSDART00000081046 | Nonsense | 303 | 316 | 8 | 8 |
ENSDART00000134670 | Nonsense | 303 | 483 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 12 (position 40215732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38498038 |
GRCz11 | 12 | 38672459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTTGTTCTTGTTTTCTAGATATCGTCCATTATTACCTGTACTGCAGC[C/T]AGACTCTCCCAAACCCCTTTCAGCAGGTACTATGTTCAATATAAATGACT
Long Flanking Sequence:
CATTTGGTCTGCATTTACAGTTCCTGTATCTTTGGAATGAAGACACTTTGGGCTTTGATATCCTTCATCTAGCTCAAAACAAAAAAGTTATAGATGCTTAAGTTATGTAAAATTAATTGCACAACTTAATACTAGTATCTCACAAAATAACTAGTAAAAATGTATCTACTGTCATGATAGCAAAGAAAAAAAGTTGTAAAAAAAGCAAAAGAAGACGTCACTTGGGAAATATTTGAAAAAGTTCACAGGAAGGCTAATTATTTTGCCTTCAGGTCAAAATAAGTCAAGTTATTACTTAACTCGTAATGACTTTTAATTTCTTTTAATGACTTTTCATAATTATGACATACCAATTCAACATTATGACATACAGTAATTCCAGTTGATGCATGTTTTTTTCTTCTTCTCATAAGCCTGAAACAAGCGTCCATAATGTCATGCTGATCATTCATTTTTGTTCTTGTTTTCTAGATATCGTCCATTATTACCTGTACTGCAGC[C/T]AGACTCTCCCAAACCCCTTTCAGCAGGTACTATGTTCAATATAAATGACTGAGTGCACTACTTTACTCTTTCATTCCTTTAATATGTCAAAGGTAATGAGCAAAGATGTGAATTATAAGGAATTTGAGGCTATTTTCAAGGTGTTTATATGTACTTAAAGTGATAGTTGACTCAAAAATGTTTATTTTGCTCACTGTTTACTCTCCTTCAAGAGTTTTTTCCTTAATTTTTAAAGTTTTTTTTACTTTTACACTTATAATGTATTTTGAAATGACACCATTTAGTTTAAATCCAAGCACTGAAAATGCATTAAAATGATTTGTACAGTATTTTGATTTTAAAAGGCCGATACAAATCCCCGAACTGCATCTGGCTTTATCAGTCTGTCTCTCCTCCTGTACTCAGTGTCTTTCTCCTTCACTCCTCCAGTATCTCTGGGGTTTTTAGGTCAGCCAGTAAAAGGCCAGTGTCCTACATCTCTGCTCACTGCAGCTCGGCAA
Associated Phenotype:
Not determined