ZMP
si:dkeyp-68a7.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
TTYH1
Human Description:
tweety homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:13476]
Mouse Orthologue:
Ttyh1
Mouse Description:
tweety homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1889007]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12432 | Essential Splice Site | Available for shipment | Available now |
sa11736 | Essential Splice Site | Available for shipment | Available now |
sa42682 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28607 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12432
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 |
---|---|---|---|---|---|
ENSDART00000115173 | Essential Splice Site | 273 | 514 | 4 | 14 |
ENSDART00000136994 | None | None | 132 | None | 8 |
ENSDART00000138540 | Essential Splice Site | 152 | 470 | 2 | 12 |
ENSDART00000138772 | None | None | 119 | None | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 15494505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13852964 |
GRCz11 | 16 | 13743084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCTCCTGGATGGGCRGCAAACACCCTCATGGTGAATGAAGACTACAG[G/A]TGAGGAAGACTAGGGAAGATAATGAGATTYTGTAGGYTAAAGGGGACCTA
Long Flanking Sequence:
GCAGCCCTAATATAAACTCTACATTGTAAAAAATAGTCTGGGCTTGCGAGTTTATATTGGGTCAACCAGTCTAAAATCACTTCTTAATTTAACGGTTGCAGTTTACCATTTCTTACATTGTACATTTAAATGAAGTACTTTCCCCATGATCCTCCCCAGGTTTCAGACACTATTTCCGGCCTCCAGCGGTCAGTCTCAGGGCCCTTGACCTCTATGGAGGATGTGTTTGGAGGACACAAACCAGCGCTGGTGCCCACGCGCTCTTGCAGGCGTCTGTCAGAGCGGGTCGTGTCTCTGCTCTCCAACCTGACACTGGGAAGAGGCCTGATCCCCATCGCAGATGGCTTTTACAGGACAAACGGAAGTGAAAGTATAGTGGGAGCCCTCACTCCTGCTCCACCTTCTGTAGCGCCAACCCTCAGTCCATCCGCCAACAGCATTCCTGCACCATTCTCTCCTGGATGGGCAGCAAACACCCTCATGGTGAATGAAGACTACAG[G/A]TGAGGAAGACTAGGGAAGATAATGAGATTCTGTAGGTTAAAGGGGACCTATTTTGCAAAAATGACTTTTATAAGGGCTTTAAACACAGATATGTGGAAACAGTGTGTAGATATTGCCAGCCTGTAATAAACATTAATTGATTTTATTTTTTATTATCACACTTCATGAAAACAGTCTGCACTTTGATTGACATTCTCCCTTTGTACATGTCATCATAGGGGGAAAGTCCAACCTATTAGTGACTATCTTTCTCTCATTAGCATAGACAGCCCTGAGTGAGAAGCAGCTGTCAGCCATTACAGTTATAGCACTGTAATAGCCAAAGATAATGTCAGCGACTATGAGGCATTAAAAATGTGGATTTTTAGAATGTACAAATGAACACTGTAGTTTCCATAAACGGCCTTCTTCTGAGACGCTTCTTTTGACTATCACTTCACTTCTCTGTTTTTTTCAGAGGTAATGTTAGAATATTAATAAAATATTATATGAATGTTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11736
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 |
---|---|---|---|---|---|
ENSDART00000115173 | Essential Splice Site | 305 | 514 | 5 | 14 |
ENSDART00000136994 | None | None | 132 | None | 8 |
ENSDART00000138540 | Essential Splice Site | 184 | 470 | 3 | 12 |
ENSDART00000138772 | None | None | 119 | None | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 15492950)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13851409 |
GRCz11 | 16 | 13741529 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTCATTCTCCTGGGTTTAGCCAAACAGTCCCGCTGGCTACTTATTCTG[T/A]RAGTAACACTMATTACTGATCWGCTCTGTGCAAGCAAGTGCTGATATCCA
Long Flanking Sequence:
CATCATTTATTTAAAAATGTAGTTATCTTTTGTGGCATTCCTGATTTCTAACTTCTTAAGCAATGACTGGTGTAGAGAATTAATGAAAACAACAAACAAACAAACATAAATACAATAGAATTAAATGAAATATCTTTGGTTTCTAGGAAGGTGAATATCAAATAATTCAATATCATTTATGGGCACATTAGCAAAATTTCAGCCTTCAAGTCTTTAATTTAATTTAATTTTATTTAATTTTATTTAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTAAATGGTTACTGGGCAGTGAATTTTATGTTTTTATTTGTCATTTAAAAGTCTGACAACAGTTACTCTGGGTCTAGGATTTGAATCTAGCATTTATTATGTTCTGAAAATGTGGTTTAGGTGGCTGTCATATGTGCTGCTGCTTTTGGTGGATCTGGTGGTGTGTTTCTTCATTCTCCTGGGTTTAGCCAAACAGTCCCGCTGGCTACTTATTCTG[T/A]GAGTAACACTCATTACTGATCTGCTCTGTGCAAGCAAGTGCTGATATCCATACATCATTGCTTTTGTTGTGTATGTTTTGCGTCCGAATTCCCCAAGATAGGAAATGCTTACAGAAAAAAAGTCAATTTATTTTTGCTTACTGACTCCCACTCAGGCACAGAGGGGCAGATGGTATAAATGTGTGTGTGTTTGCAGGATGACAGTGCTGGCCTGGTTGTCTCTGTTTATGAGCTGGGGTTCTCTGGGTCTGGAAACACCCACTGTGGTGGTGAGTATTCAGGCAACGTCTTCCCCGACACAAAAACAACAGCTCTCCGAGAGCGGACGTCCAGCACAGAAAAACCACCATCTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAGAGCTTTTGGAGAAAAATCCAGCCAAAGCTCTGTGAATGTGACTTTTTACATTTTAAAAGGTCACAACAGCCAAGATGCAGTCACTTATTGTGTTCTTATGAAAGAGCGAGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42682
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 |
---|---|---|---|---|---|
ENSDART00000115173 | Essential Splice Site | 435 | 514 | 10 | 14 |
ENSDART00000136994 | None | None | 132 | None | 8 |
ENSDART00000138540 | Essential Splice Site | 314 | 470 | 8 | 12 |
ENSDART00000138772 | Essential Splice Site | 40 | 119 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 15481335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13839794 |
GRCz11 | 16 | 13729914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTTCCATCAGCTGGTTGCTCTTCTCAACTGTCGAGGCCTGAACAAGG[T/C]AAACATGGCAGCCTGGTTTTTACCTCAGCCAAGCAGTTTTCATGTCGCAA
Long Flanking Sequence:
TCTGTACTTTTTCAATCCCTTTAAAACTAAGCAAACTAATTCCAACAGGCTTTCACAAGCCACCATAAAGTTTGCCTTCAATCTTTAATACCTAGTTAAACGTGTGTTGCTCTAGACAAATGCATACAATGAATGCATTCAAATATGTCATTACATGTCTGTTAATCGACATTTTTTTTGTTGAACTGGCATAAGATACTGACCCAGTCCCAGAGAGCACTTTCCAGCATCCACTCTCATCTTTCCAGCCTGGAGAGAGATGCTCTTCCACGCTTCCCAAAAGCAGAGGTATGTCAACACTGCTAAAACTGCTCTCAGTACCAACAACTGACAGCACAGATCAATAGCAGCTGCAGTGAAGCTCTTCTCCACCTGCCGCTGAGCTGCTGTGTTTTCTCTCTTTCAGAGGTCACTCAGGGAGGTTCAGCAGATCCTCAACACCACCGAGGGAAACTTCCATCAGCTGGTTGCTCTTCTCAACTGTCGAGGCCTGAACAAGG[T/C]AAACATGGCAGCCTGGTTTTTACCTCAGCCAAGCAGTTTTCATGTCGCAACAAGTGGACTCATGTGTTGTCCTGTCACTCTCTCAGGATTACGTGGACTCTCTGAAAGGCCTGTGCTATGATGGGATGGAGGGGCTGCTCTATCTGTCTCTCTACTCTTTTCTCTCCGCTTTGGCCTTCACTGCTATTCTTTGCTCCCTCCCTGGAGCCTGGAGGAGCTTCCACAGGTTAGCTGAACTTTATTCCTTCACTTTGGCTAATGCCCCATCTGCTTCTGCTTTTAGGAAAATCTGATTGGATTTATGCTGCAAATTAATTTGATGACAGCAGCAAAATAAAGATGCAAGATAAATAGTAGGGCTGTGCTTTATGTAAATGTGAATTTGGGTCTTCCATATGGTTGTACGGTAAATGATTAGTTGTAAAGTTTATATTATTATTGTTTTTGTTACCGATTTCTATTTTATAAAGCTGTGTTAGAAATGAAGAATCATAGAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28607
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115173 | Essential Splice Site | None | 514 | 14 | 14 |
ENSDART00000136994 | Essential Splice Site | None | 132 | 8 | 8 |
ENSDART00000138540 | Essential Splice Site | 444 | 470 | 12 | 12 |
ENSDART00000138772 | Essential Splice Site | None | 119 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 15465637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13824096 |
GRCz11 | 16 | 13714216 |
KASP Assay ID:
2260-9372.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCCCTTCTCTGCTCTCCTGAACTGCGGATCTGCCCGGTGGTTTCACA[G/A]TACTCTCCCAGCATGCTGACTGGCTACGGCGGCAGTCAATCACACTCCAA
Long Flanking Sequence:
AAATTAAAGTTTGTGCGTCAAGTTTTGCAGTTGGCTTAGTGAACTCTGACCTGCAAAATCGCATCACTTAACTGCGTGAAACCAATCAAGGATCAAAACATGACCTCTCTGGACAGGAATTGTAGCAATCACTCGCTTTTTTATGTCTAATCATATTGTTTAATTCCGCCCCTTTTTGCAAAGCCATACGACAGAGTTTCTCAATTGCAAACTCTAGTTTGACCTTGGCTTCACAGTTCAGTGTATTTTTTACTAAGATACTTCAAATAAATATATGTAAATAAAAATAAATGACTTTGCTTTCTGAAACATGAACAACAGTATCTAAGGGTGGAGCTTAGCGAAGGATTTAAAAGTAATTCTGTAAAAACTGTATGTTTTTATATATACACACATGCATACATACACAGGTATAGATTTAAAAAAAATAATAATATTACTCTCTTTTCTCTTTCCCTTCTCTGCTCTCCTGAACTGCGGATCTGCCCGGTGGTTTCACA[G/A]TACTCTCCCAGCATGCTGACTGGCTACGGCGGCAGTCAATCACACTCCAACCCCTCCCATTCAAGAAACTTGTACTCGCACTAATTATTTTTCTGTATAATAGAAAAGAAAGCTATATAGCCAGGTTTAGTTTTCATATGGATGGACACTTTATGAGACGGGAGACTAATTTAAAACATTACGTGTTAAATATCCGTGCGTAGCGTCAGTACCATTGAGTCATTTGGGTGTAACAGACTTACGAAAACCCCGTCACTTCCTCTCCCTCTAGTGTCAATCTGTACATAGCTGGTGGAAACAAGATGGTATTGACGTTACAGTAGTGCTCTATTTTTAAACGTATAACCACTTTATTTTGGAGTTTTGATATTGTTATATGTAGTCACAGAAACATAGTGGCGATGGCACAATTTCTTTGTATGATTATACAGTTTTCTCTTCACCTTTCTTTTTTAAATATTTGACAGAACCCTATTTTATAAGTGGCGATGCTGTACTAC
Associated Phenotype:
Not determined