ZMP

mybl2

Ensembl ID:

ENSDARG00000032264

ZFIN ID:

ZDB-GENE-041007-1

Description:

myb-related protein B [Source:RefSeq peptide;Acc:NP_001003867]

Human Orthologue:

MYBL2

Human Description:

v-myb myeloblastosis viral oncogene homolog (avian)-like 2 [Source:HGNC Symbol;Acc:7548]

Mouse Orthologue:

Mybl2

Mouse Description:

myeloblastosis oncogene-like 2 Gene [Source:MGI Symbol;Acc:MGI:101785]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14950	Essential Splice Site	Available for shipment	Available now
sa35002	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14950

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
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Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000040577	Essential Splice Site	94	633	4	16
ENSDART00000121489	Essential Splice Site	94	633	4	15
ENSDART00000137479	None	None	240	None	5

Genomic Location (Zv9):

Chromosome 11 (position 1519739)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	1527879
GRCz11	11	1554467

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

RGATCCTGATCTTGTYAAAGGACCCTGGACYAAGGAGGAGGACGAGAAGG[T/C]AAAATNNNNGTAGAGACTGCAGTGGAGTTAATGGATTATATCACWACAGTYWAG

Long Flanking Sequence:

CTCATACTTTTATTAATTAGACTAAATGATTGTATGAGACTCTTTTCAGTGTTGATGTTTTTTGTACAATGAATGTTTATTAAGAAACTTATATGATTGCTTGTTATATATTGTATTTTTAGTTTAGGTTTTGTCATGAATGCTGCTGATATGGCATTAAAACATAAATAAATATTGCATATCTCTAATTTCATGTTCATTGGCATATCCCAGGATGATAAGCTGCGTAAACTGGTGCTGAATGTTGGATCAAATGACTGGAAATACATCGCTGGATTTTTACCTGTAAGTGTGTTTATCATGCATTCAGAAAACGCACATCAGATGTTATTTATGCTTTGATCTATTGAACATTTGAGTGTCTGATTAAAGTTGAAATGCTGTAAGAGTGTGTTTGTTGTTGAAGAATCGATCGGAGCATCAGTGTCAGCATCGCTGGTTCAAAGTTTTAGATCCTGATCTTGTCAAAGGACCCTGGACCAAGGAGGAGGACGAGAAGG[T/C]AAAATGTAGAGACTGCAGTGGAGTTAATGGATTATATCACTACAGTCTAGGTTAAGTCATTATTTTTGTAGTATATATTTTATTCTGTTCTATTAAATAAATTAAAGTTTGTGGCCTGATATATGAATATAGGACACTTATGATGTACACGTTTTAGATAAACAATTGTTTACCTATTGCTAATTAAGTAATAAATTATTACTAATTTATTTTCTGATTATTTTACATTTTTACAGACTCCCCCACTTCATCATCATCATAGTAATAATAATAATAGTAATACATTTTATTTATAATGCACTTTTCAAAAACCCAAAGCGCTACAACTGAGAAATCAAACATGCATTGAACTACAAAGATTCAACATAGAAAAAGTATACAATATATATACAGTTGAAGTCAGAATTATTAGCCCCCCTTTGAATTTTTGTTGCTTTTTTAAATATTTCTTTTATTATATTTAAAAGAGCAAGGAAATTTTCACAGTATGTCTAATAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35002

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
ENSDART00000040577	Nonsense	316	633	9	16
ENSDART00000121489	Nonsense	316	633	9	15
ENSDART00000137479	None	None	240	None	5

Genomic Location (Zv9):

Chromosome 11 (position 1527108)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	1535248
GRCz11	11	1561836

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACCATGTCGGACTTCGACCTGCCGGAGGAGAGCCAGAGCTCGGAGCTCT[T/A]GCAGTTTCGTCTGGAGGGCAGTGCACTGCAAGAGCTCAGCAAGGGCAGTA

Long Flanking Sequence:

GGAGCTGATGGATGGGGTGAGTCAAGCCTGATTTACCTGAATCACTATTAGGATTACAACCGGTTGCTAATTGTGCATGAAATGTAGTCAACAATAGTGTGAGACTGATAACGGCAGCCAGAAGAGAGAGTAATGTTGAATGTTGTTACTGTCCTGCCCCCTTATACTCTGCATTACACATCCCTCGCATGAGAGGTAGTTAGTTTTTTGCAATTGAATACAAAGATGATGCTATACATATAAATGTTTTACATGTTTTAAAAAAATGTAAATCTTTTAAGGATTTAAGATGCCGATGAGCGTTAACGTCTTGTGAAAAGGGTCTAATGCAAGTGCACACACTGCAAAATCGATGCGTAAATGATATATTGTGCAGCCCTACATCATGGGACTATTAAGTGTGTGTTGGACTGATCAGAGTGTGTGTGTGCAGGATCTGGAGGGCTGGTGTACCATGTCGGACTTCGACCTGCCGGAGGAGAGCCAGAGCTCGGAGCTCT[T/A]GCAGTTTCGTCTGGAGGGCAGTGCACTGCAAGAGCTCAGCAAGGGCAGTAAAGGAGAGCTGATCCCCATCTCGCCCGGCGGAGCCACTCCTCCATCCATCCTGAGTCGCCGCAGCCGTCGACGCATCGCCCTCTCGCCAGACCCCAATGACTCCATGACCCCAAAGAGCACGCCGGTCAAGATCCTGCCCTTTTCCCCCTCACAGGTGGGAAAACGCAACACAACACTAGCCATGTTTCCATCCAAAGATGCAAATTAAATGTATGCGCAAAACTGGAGTATAGCATAAAAGATTTGAGAATAAAGCAGCGTTTCCATCCAACGAGTCTAAGATAACAAAATCATCACTTCCTCATAAACTGCAGCCAAATATCAAAAGAAAAACAGAAGTTACAGTGTTGGGCTTTTTTTTCAGGGTTCCCACTGGTCCTTAATAAGTCTTAAAATGTCTTAAATTAAAATCCGGGAAATTAAGGTCTTAAATTGTCTTAAATTTTACC

Associated Phenotype:

Not determined