ZMP
ywhaba
Ensembl ID:
ZFIN ID:
Description:
14-3-3 protein beta/alpha-A [Source:UniProtKB/Swiss-Prot;Acc:Q5PRD0]
Human Orthologues:
YWHAB, YWHAZ
Human Descriptions:
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide [Source:HGN
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide [Source:HGN
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide [Source:HGN
Mouse Orthologues:
Ywhab, Ywhaz
Mouse Descriptions:
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide Gene [Sourc
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide Gene [Sourc
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide Gene [Sourc
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16229 | Essential Splice Site | Available for shipment | Available now |
sa11447 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16229
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 |
---|---|---|---|---|---|
ENSDART00000025940 | Essential Splice Site | None | 244 | 1 | 6 |
ENSDART00000143458 | None | None | 226 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 52163531)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 52212713 |
GRCz11 | 6 | 52212712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTCCCATCGTTAACAGAYACAAATCAGGACTCGAAATATATTCCAATG[T/C]GAGTTACACTACCCGCGAAGGCMGCTCGTGTGATAGTATGAATATTAGGG
Long Flanking Sequence:
TTTTTATGTGTTAGAAATGTTATAAGGCCTTCATAGAACGAGACAAATATTTACATACATAACCCATACCTAATATATAATAATAATAAACGAGAAATGTCAGTTATCTTCACATAATCAGTTTTATCCACTGAGTTTTCTCAGTATGTGTTGTATATATGAGCATTTGAGCTGCATTTGAGATTTCCAAACCTGATTCTTCTCACTCGAGCTGTCGAGCGCCTCCTGGCAACGGTCGCTATGGTGACTGCCGACGTCACGCACGACTTCGGTTGCCATGGCCCTCGTGACGTTAGCGACCGTGTCAAACAGTGTAGGAAACCCCGCGCGGCGGTCGCCATGGATACTGGCGGGGGGGAGGGGTGGAGTTTAGAGGAAGCGGAAGTGTCAGCGCAAGCGGAAGTGGTACTGCCCTGAATACCCCGAGCAGCGAAACGGAGGACAGCTTGATACTCCCATCGTTAACAGACACAAATCAGGACTCGAAATATATTCCAATG[T/C]GAGTTACACTACCCGCGAAGGCCGCTCGTGTGATAGTATGAATATTAGGGGTGTGTTTTGCTGTATTGTTGCTCATGTAAGCCCCCCTCATCATTGTCAATGGCGGAAGGTGTCTATTGTGGTTTGGGGCTGGGTACAAGGACTTAGGCCGAGGCGGGCGATGAGTAGCGATTATTGCCGAATTATTCCCGATTACATCCGATTTCTGTTTGAACCGCGCTGTTCTTTGTGTAAGCGCGTTATCAAGCGAGCATCGCGCCAAACAACCCTCTCCCCGTGCGGGAGCAACGGCCAGCGGCGTCCCGCGTCTATTCAGCGCCTGCCCGTCGCGAAAGCTAACCGGCTAACCAGTCGATAGACAAATTAACCAGACGAGTAAATCATGTACGTCGGCATCAGTAACGGACTAATTTAATTTGTCTCAAACAATCGACTCGCCTGATTAAATTCCACTAGGGAATGTGAGTGAGAGGGCGTTGCATTGGTGGCTAAAACTGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11447
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 |
---|---|---|---|---|---|
ENSDART00000025940 | Essential Splice Site | 194 | 244 | 4 | 6 |
ENSDART00000143458 | Essential Splice Site | 194 | 226 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 52171206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 52220388 |
GRCz11 | 6 | 52220387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATGAAATCCTCAACACCCCAGAGCAGGCCTGCAGTTTGGCAAAGACGG[T/C]CAGAYGTTTTACTATCTGCTTGTTTAAANTTTTTTTACAACTTAATAGTT
Long Flanking Sequence:
ATAGCTTGACATTGGTCTTGCCTCCTCTCTCTCAGGGTCTCCTGGAGAAGTACCTCATTCCCAACGCTAGCCAGGCAGAGAGCAAAGTCTTCTACCTGAAAATGAAAGGAGATTATTACAGATACCTGTCCGAGGTGGCATCCGGGGACTCAAAGAGAAGTGAGTTTGTTTGATTTGAAATGCTGCCTAAAAATGTCAGGTTTAAATGGCTGAAACAAAAACTAAGGCTCTGAAATAAACAGTTAGATGCTAGCCTGAAGAAACTGCATCAGGACATTCAGGCGGTGATGTTACGCTCATGAAATTGATTTTTGTGTTTTTCTATCGAATTACAGCCACAGTGGAGAACTCTCAGAAGGCCTACCAGGATGCATTTGAGATCAGCAAGAAGGAAATGCAGCCAACACACCCCATCAGGCTGGGACTAGCGCTGAACTTCTCCGTCTTTTACTATGAAATCCTCAACACCCCAGAGCAGGCCTGCAGTTTGGCAAAGACGG[T/C]CAGACGTTTTACTATCTGCTTGTTTAAATTTTTTTTACAACTTAATAGTTCTGTTCTGAGTATATTCAGTGTACCGTTTGTTTTTATAACTCAATTATAACTTCTATTCATTCATCAAAAAGATTATTCTGTTTATTCTGAATACTAAGATGTATATTTGCAGTGTGCAGGCACAGTGCACCTGACCTTCATTTTTACTTTTACCATAGGCTTTCGATGAGGCAATTGCTGAGCTGGACACCTTGAATGAGGACTCTTACAAAGACAGCACCCTCATCATGCAGTTACTAAGGGACAACCTCACTGTAAGTGTTAGCTTTCTGCTTTCTTGTTTACTTTTTTTTTTATAGATGTAGAAAGACATCAAATTGAATGAATTCAATGCAAAATTATTATAGGGTGGACAGTTTACACATGGTTTAAGAATATTAGTACGAGTTGGCTAAAGTACATGCACTACCTTACATAAGTCTTGTCGTTGATCCCAGTTGTATGAGCAA
Associated Phenotype:
Not determined