ZMP

si:ch211-158b22.2

Ensembl ID:

ENSDARG00000078825

ZFIN ID:

ZDB-GENE-041014-120

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:A5PEY7]

Human Orthologue:

BUB1B

Human Description:

budding uninhibited by benzimidazoles 1 homolog beta (yeast) [Source:HGNC Symbol;Acc:1149]

Mouse Orthologue:

Bub1b

Mouse Description:

budding uninhibited by benzimidazoles 1 homolog, beta (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MG

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23826	Essential Splice Site	Available for shipment	Available now
sa29477	Nonsense	Mutation detected in F1 DNA	Not yet available
sa29478	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23826

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114313	Essential Splice Site	175	722	5	20
ENSDART00000138976	Essential Splice Site	207	753	6	21

Genomic Location (Zv9):

Chromosome 20 (position 53840671)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	53685450
GRCz11	20	53490867

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTGTGATTCAGTAGCAGTTCAGTGAGTCGAGAGGACGATATGAATCAAA[G/A]TGAGTTTCTGCAAGTGATTCGTTTGTTTAATATACATTTTTACATTGTTT

Long Flanking Sequence:

AGTTCAACTGTATATCGAAAATCAGAAATGATATCAGCACAAAACACACTCTCCAAAATAGTGTTGACTTTTCATTATATTGTGCATGCATATTTTGCTGTAATAAAGAGCTGGATTAAGGGTGGAAAAGGTTGATTTATTTAGATGTTTTTCACTCTTTTGTGATTCAGTAGCAGATTGGTGATTCGGTTTATGAACAAATCATTTGAGTCAATTGATTCATTGATTCATTCATACCTGCAGCCACTTCTCTTATTTCCAAATGAATCACCCGTTTTGAACAAATCATTTGAATAAAACTGATTATTTGGTGTCATGTTTATGTATTGCACGCCTTAACCAGGAAAGAGACCAGCACAGAAATGTTAATTATTGTTTTCATTTATGCATGCTTTGCAAAGATCAGTGATTAAGATATTTCATTTGTTTTATTGATGTCGCTTTTTCCTCTGTGTGATTCAGTAGCAGTTCAGTGAGTCGAGAGGACGATATGAATCAAA[G/A]TGAGTTTCTGCAAGTGATTCGTTTGTTTAATATACATTTTTACATTGTTTTTATTAGTGCAGCTGCTGCTGTTTGATATTAGGCAATAAAAGCAGAGATGCTCATGAATATGGTGACTGATTGTGTGTTTTTAAGGTGGAAGTGATGCAAAACTGCAGAAAACAGCAAAACCTTTCACCATTTATGATGAGAGTACACAGACGAACAAAATGTAAGACTGATTTTCTTTGTTAATTCTTTTTGATAGTGTTTTCATTCATTCTTTATCATTCGTTAATCAATTTTTTTGTCTCACAGGGTTTATATTTTTATTTTTTTTTATTTAATTATTTATTTATTTATTTATTATTATTATTATTATTTATATTTATTTTTTTTATTTTTTTATTTATTTATTTAAGTATTTATTTATTATTATAATAATAATTTTTTTAAATATTTTTTATTTAATTATTTACTTATTTATTTTTAATTTTTTTTATTAATCAATTAATTAATAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29477

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114313	Nonsense	411	722	13	20
ENSDART00000138976	Nonsense	442	753	14	21

Genomic Location (Zv9):

Chromosome 20 (position 53850976)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	53695755
GRCz11	20	53501172

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGTCAGGAGTGGGGCGGCTCTACTTTTTGTCAGGATCCCACGAAACGCT[T/A]GAATGATGCAGAGAGCAGCCGATCTGCGGAGAGACCAGAGACTGAGCTGG

Long Flanking Sequence:

GTTTTAAAATATCCAGGTCATTCTAACATAGAAGAAATCAGGCTATACTTTTCTGTTTCTTTGATTGTGTTTAATAAGCAATAAAATCATTGTGGGCTGGTTTGCAATGGCAATACTCCGCTATTTAGAGCAAGGTAGGGCCCCAAAATGATTCAGCTTAGCGCACCCAAAAGTACAGGGCCGGCCCTGATGATATGTGCATTTATTTTCAAGTCCTAAAAAAGTGGTGTACTCTCATTGTAAACATGTGTCTGGTTGTTAGACGCTTTCTAAAATGTTTGAGTTTTTATGTTTATTTGTCATTTAATTCAGCTCAAGACTTTGACTCTGTGTGAACTAGTCTAATACTTCATGTTTCATTCAGTACATTATAACACATGTTATGGAAAGCCTTGTTCTTAAATCTCATGTGTGTTTTGTGTGTGTATACTGTAGTCCTATCCTGGAGATCAGTCAGGAGTGGGGCGGCTCTACTTTTTGTCAGGATCCCACGAAACGCT[T/A]GAATGATGCAGAGAGCAGCCGATCTGCGGAGAGACCAGAGACTGAGCTGGAGAACGGTGGGAAATTTACATCACTGATCATTCACTCTGTCTGCCGAACTGGACATGTGTGATTTTGATACTAAATGACTAATAAAAAAAGATATTAAAAAATTAATTAAATTAATTAAAAAATTAATTAAATTAATTAAAAAATAATATTTATAGGTTTATATTTAATATTTTAAGGGGTGGTCCACTATGATATCATATTTTAAACTTTAGTTGATGTGTAATGTAGCTGTGTGAACATAAACAGCATCTCTGAATGTCAAATGCTCAAAGTTCAATGCAAAGGGAGACCTTGGTTTTACAGAGTTACCTTAGCAAAGCCTACAATGAACGAATTTTGGGGACTACAAAAAATAAGAGGTCGCTGTGAACTCTGAGCCATGCCCTGTAAGTGTTTTTATTTGTTAAAATTGATCATCACATGTACAGTGTCTAGCCTTAACGGTATGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29478

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
ENSDART00000114313	Essential Splice Site	474	722	14	20
ENSDART00000138976	Essential Splice Site	505	753	15	21

Genomic Location (Zv9):

Chromosome 20 (position 53853355)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	53698134
GRCz11	20	53503551

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACAGGAAAGCTGGACTTCTGCCTGACACCAGCGATGATCTGCATCTCGG[T/C]ATCCAGAAAACTCCTGCACACATTCAATTCAATCAATGCTTATTTCTATA

Long Flanking Sequence:

GTGTGTGTGTGTTTCAGTTTCAGCTCAAAATAGCACACAGATATTGTTTCTAACTCTCTGCAGCTGACCCTTTTAGGTTTTGATCTTATTGTGGTGTTTTGGTGACTGTCGCTTCAAATTCAAATGAGCTCTTTTCAGAAGAGGGCGGAGCTGCAAAAGACTGTGTGTCAGCATAGTGGCAGATTCAAAAACAAGACTAAAGTCCTATGCTAATGAGGCAGGGATTGTCTCTGATGGGCGGGGATTTTTTTAAAATCTAATATAAAATACAAATATTATTTTATTATATTATATTGTACAAAAAGTTGATAGCAGGATAAATAATGTTATCTTGTTGTATTTTCAACGTGTGTTTGTGTTTTCTCAGTCAGTAAATGGCAGGATGTCTGCAGTCTGCATGTGAGATCCAGGATCTTCGACCAATCAGATGTGACGTCCTTGCCCAACTTCCACAGGAAAGCTGGACTTCTGCCTGACACCAGCGATGATCTGCATCTCGG[T/C]ATCCAGAAAACTCCTGCACACATTCAATTCAATCAATGCTTATTTCTATAGAGCTTTTACTATGTAGATTGTGTCAAAGCAGCTGAACACAGAGACATATTTAAATTTAATTACATTTAATTACATCTCAGACATGTGTATTCAAGGCCTGGAAATGACTTAAAAACAAACTTAGCTTCTTGAACGTGCTTCAATTAAGTATTAAATACAACAAATGGTGTCATTTCAACAACTGCACTGTGCTGCGGTCACATACACAACAAAACAAATGGAGAAGCTATTCATTTAAAAATGTTACAATACAATAACAATGACAAATAATGCATACTTTATCAATAATTATGAGTGCGTTTGGATATTACCAGTATTGAATTCAACACATCTTATTAAAGTTCTTTCTGGACAAAATTACTCTGACATGTTTAACATAACTATTAAGTGTAAGGGAAATGTTATGTAGGGAGGCACGGTGGCTCAGTGGGTTGGCACAGTTGACTCAC

Associated Phenotype:

Not determined