ZMP

ywhabl

Ensembl ID:

ENSDARG00000040287

ZFIN ID:

ZDB-GENE-030131-448

Description:

tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide like [Sour

Human Orthologues:

YWHAB, YWHAQ, YWHAZ

Human Descriptions:

tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide [Source:HGN
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta polypeptide [Source:HG
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide [Source:HGN

Mouse Orthologues:

Ywhab, Ywhaq, Ywhaz

Mouse Descriptions:

tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide Gene [Sourc
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta polypeptide Gene [Sour
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide Gene [Sourc

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa6430	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6430

Status:

Mutation detected in F1 DNA
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
ENSDART00000058956	Essential Splice Site	187	238	3	5
ENSDART00000114304	Essential Splice Site	194	245	4	6

Genomic Location (Zv9):

Chromosome 16 (position 26932010)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	24777685
GRCz11	16	24692717

KASP Assay ID:

554-4272.1 (used for ordering genotyping assays)

KASP Sequence:

CTACGAGATTCTCAACTCRCCCGAACAGGCCTGCAAGCTCGCCAAAACAG[T/C]AAGTTTAACAGATTAACAGACWCCCACACAAGCTAATCAACAAACTATGA

Long Flanking Sequence:

TTGTGTTTTGTGGGTGGTTTATTTGTTGTGTAACTCCCCCTAGCGTCAAATGTCATTTCACTGCTTTAGAGCAGAATGTGATTGTTCATGTCAACTGAAAATACTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGATACTTTTTTAATGTTTTTAAATAAAACAGTTTCACAGTATTTATTAAATCAGCTCGAATATTGAATTGTGAAAATTGCTTCAATACAACACTTCAATTTAAATGGTTTCAAAAGTTTAATTGGAGTTACTGACTAACTACAGAGTTTGTCAAAGTTAAACGTTCTTTACACATGTTCTCTCTATCTCCAGCTATCATTGGCAATTCGCAGGAGGCCTACAAGGATGCGTTTGAAATCAGTAAGGCAGAGATGCAGCCCACACACCCCATTCGTTTGGGTCTCGCTCTCAATTTCTCCGTATTCTACTACGAGATTCTCAACTCACCCGAACAGGCCTGCAAGCTCGCCAAAACAG[T/C]AAGTTTAACAGATTAACAGACACCCACACAAGCTAATCAACAAACTATGAAAGTGTTAGTCGTGGAGTATGTTGTGAATATAGAATATCTACATTAAACTTCTACCATTTTTGTTGGATGTCTTTCTCCCAGGCTTTTGATGAGGCCATTGCAGAGCTCGATTCACTGAATGAAGAATCCTACAAAGACAGCACATTGATCATGCAGCTACTGCGGGACAACTTGACAGTCAGTTTTTTTCTTTTAAAGCAGATGAAGACAAATGAGTACATTTTATTTATTATGAAATAAAAGTAACTTTTTGTAAGGTTTAACTAAAAAATAATAGCTTTACATTGTAAAATAGGCAAAATAGAATACAAATTGGCAAATAGTATAATCTAAAAAAGATTGTTATAATAATTTTAAAAAACAATAAGGATTTAATGCCACAATGTAATTATTACCTTAAATGTATAATAAAATATATATATAAACTGAGGGGGTAGGTGGGCATTCGG

Associated Phenotype:

Not determined