Busch Lab

ZMP

mycbp2

Ensembl ID:
ENSDARG00000001220
ZFIN ID:
ZDB-GENE-030616-132
Description:
probable E3 ubiquitin-protein ligase MYCBP2 [Source:RefSeq peptide;Acc:NP_001012247]
Human Orthologue:
MYCBP2
Human Description:
MYC binding protein 2 [Source:HGNC Symbol;Acc:23386]
Mouse Orthologue:
Mycbp2
Mouse Description:
MYC binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2179432]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa21455 Essential Splice Site Available for shipment Available now
sa17311 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21455
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039157 Essential Splice Site 388 4574 None 82
ENSDART00000044835 Essential Splice Site None 3118 None 83
ENSDART00000124901 Essential Splice Site 388 4648 None 83
ENSDART00000126745 Essential Splice Site None 631 None 81
Genomic Location (Zv9):
Chromosome 9 (position 17736413)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 17212483
GRCz11 9 17220195
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTTCATCATTGTGTTTGTGTGGGTGCTAATAACAGTCTATTGATTCC[A/T]GGGCCATGTATACAACTCCACATCACGTATCAGGAACCGTAAGGAGAAAA
Long Flanking Sequence:
AATTAAACATGATTCTGAGAAACATATTACATTTAAAAGGAATAATCACCTAAATATTTTATTTTGTCATCATTTACTTACCCTTTACTTCTTTCCAGACCTGTTAGTTTTTTTTTTTCATTCTGTTAAGCACAAAAGAAGATATTTTAAAGAATGTTAGAACATGGAAACTTTTAACAATTGACATCCATAATAGGAAAAACACCATGGAAGTCAATGCCAATGTTCTTTAGTATACCTTCCTTTGGGTTCTACAAAGCAAACATTTCAAATTGTTTTGGTGCAAGTAAACAGTATTAAATAAAAGCATAATTAAAATTTTTCGGGTGAATGATGCCTTTAAATTATTATTATTATTTTTTTAAGTTTTAACTTACCTTCATTTCAATTGTTGTTCATTTACTTTTTGATGATTTGAGTTGTAGATATGATGTAGTGCTAACACAGCAGGTTGTTCATCATTGTGTTTGTGTGGGTGCTAATAACAGTCTATTGATTCC[A/T]GGGCCATGTATACAACTCCACATCACGTATCAGGAACCGTAAGGAGAAAAGGTCATGGCTGGGATTCGCCCAGGTATTGACCTCTTGCCTTATAACAATGTTTCTTTTTCATCAACTGCCTGCTTTTATAATGTCAGCATACTTGTATAGATGTTATAAAAGTTGAATTGATACATTTTTATCTCTTAAATGTAACCTTTTAACCTCTTCGAACTACAAAAATGTGATTCTGTGTTTCTAACAGCCTTGATTTATTTACAGGGTTGTTTGCTATATCGAGACATGAACAGTCACAACATGGCAGCCATAAAGATCAACCCAGAGACTCTGGAGCAGGAGGGCACTATCACAGTGCCTGGTACAAACACCTTTCTTACTTGATAGTGCTTGCTAAAGGCAGGGCAAATTTTTTTTTTTCATTCAAATAATGAATTAATGAATTTGAATAGCTACTGGACTTCATTTTATGTTATGTAAATAGAAATAGATAAGTTAATGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17311
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039157 Nonsense 2720 4574 55 82
ENSDART00000044835 Nonsense 2431 3118 56 83
ENSDART00000124901 Nonsense 2794 4648 56 83
ENSDART00000126745 None None 631 54 81
Genomic Location (Zv9):
Chromosome 9 (position 17600587)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 17076657
GRCz11 9 17084369
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAKGGCAGAACCTCAGGAYTTAGGGCTGAGTCTCCAAACCCTGGCTCC[C/T]GATCCTCCTCACCAAAACAAAAGACCTTCACTTCAGGGAGATCTAGCCCT
Long Flanking Sequence:
TGTCAGTGGAGTCTTTATGTTTTTTTCATCTACCATTTTACATTTTGTTCCTTACGTTACTGTTGTGTTTTCCCCTTACATTTTCAGGTGCCATGTTTATTTTATTGTCTTTTTATACACATGTAAATGAGGCCTTACAGGCCTTTGTGAGGGTGCCCTTTGTATTAATGCTTTGCAAATTGGTAACTCTTGATGTGTTACAATACGCAGGTGACAGAGATAACATGGCCAGTTGGTCTGTGTCTCCAGGCAGCAAACATCGTCAAGAGAGCCGATCCTCCAAAACCGACAGCCACTCAAACCGATCTGTTGACCAGGTGAAGAGCAAGAACAACGAGAGTCTGTCTGCCAGCGAAGCCCTCATTCTGAAATCAGATACAGGCAAATTGCGGTCTGACTCTCACAGCCGCTCCCATTCTCCTAACCACAACACTCTTCAAGCCCTGAAAGCTGATGGCAGAACCTCAGGACTTAGGGCTGAGTCTCCAAACCCTGGCTCC[C/T]GATCCTCCTCACCAAAACAAAAGACCTTCACTTCAGGGAGATCTAGCCCTTCTAGCACCAGTTCCCCACGCTCATCATCTCCTCATGATAAGAACCTGCCCGCCAAAGTTAGTCCCTCTAAAGTTCACCTGGATCCACCACGCGAGAGATCCAAATCGGACTCTTATACACTAGATCCTGACACTCTTAGAAAGAAGAAGGTCCCTCTTATGGAACCTCTAAGGGGCAGGTCTACATCCCCAAAGCCAAAACTCCCACCCAAAGAGAGCAAAGGAGGTAGCAGCAATGCAGAAAACCGAGCCCCTTCTCCCCATGTAGTTCAGGAAAATCTCCACAGTGAAGTAGTGGAGGTATGTCGGTCTAGCGCCTTGCTATCCAACGATGAAGGCAATGATGAGAATTCAGAGTTGCACAATGCTGAAGAAGGCTCCTCCAAGGTCCATTTTAGCATTGGAAAAGCACCAGTCAAGGAAGAACTTGAAAGTCGCTCTTCACCCAAA
Associated Phenotype:
Not determined