ZMP

march5

Ensembl ID:

ENSDARG00000032552

ZFIN ID:

ZDB-GENE-070424-47

Description:

E3 ubiquitin-protein ligase MARCH5 [Source:RefSeq peptide;Acc:NP_001076296]

Human Orthologue:

MARCH5

Human Description:

membrane-associated ring finger (C3HC4) 5 [Source:HGNC Symbol;Acc:26025]

Mouse Orthologue:

March5

Mouse Description:

membrane-associated ring finger (C3HC4) 5 Gene [Source:MGI Symbol;Acc:MGI:1915207]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38969	Nonsense	Mutation detected in F1 DNA	Not yet available
sa28189	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38969

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000043069	Nonsense	81	281	2	6

Genomic Location (Zv9):

Chromosome 13 (position 43031490)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	42252449
GRCz11	13	42378509

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACGGGTCGCCTGCCCACAATGCAATGCCGAGTACCTCATTGTGTTCCCT[A/T]AGCTTGGTACGTCAAGTATAAGTGGGTCGATTGTGTCTTGTTTTTATATT

Long Flanking Sequence:

TAAAATGACGCTGCTGTTTAAATCATACATTTATTTTTTACTTCCTTGAAGTGAGTTCATGATCTCATTTCATTTGTGCTTAGTCACTGACCTACATTACTCCACAGTCCTCTCATGCTTTTTCTTTTTTTTGGTTAACTTTCCCTTGATACTTTGAAGAGTTGGTCTGTAAAAATAAATCAGTCTTCTGCTTTGAACTTTACACAATTACTTTCTCCTCAACTTTATGTGTTTACACTTTGTTTGCCCTGAGCTGAACGCAAAGCCAAGCGCCAATTTTTCTGCCCTTCTGTTTGTTTTGTAGGAGTTGTTGGGTTTGTTTTGCCACAGATGAGGATGACCGTACAGCTGAGTGGGTGCGTCCGTGCCGCTGCCGTGGATCTACTAAATGGGTTCATCAGTCGTGTCTTCAGCGCTGGGTGGATGAGAAACAGAGGGGAAACAGCACCGCACGGGTCGCCTGCCCACAATGCAATGCCGAGTACCTCATTGTGTTCCCT[A/T]AGCTTGGTACGTCAAGTATAAGTGGGTCGATTGTGTCTTGTTTTTATATTCAATTCACTTTTAACACATTGTTTATATTAGTTTAACATAGTTACCCGCACTACTATTTAAATGTCAGTTGTGCGCACTAAAGCTGCACTTATTACACGTATCACGCCTTCAAACACCACCCTGAAGTCATTTATTAAATGAAGAAAAGATTCATGCAGTTTCACTTATTGCAGCAAATTCCGTTTTTACTGTTGATATTTGTCGCCAGTTAATCAGAAAGTGACTATTTTGTTCTCTTTGACTCGTTGGATGGAAATGCTGCTTTATTCACACGTCTTTCATGAGATAATCCAGTTTTGCGCATAAAGATAATTCACATTTTTGGATGGAAACATAACTATTGTTAAGCTGTGCTGCTGAATAATTTAGTGGTAACATGATGCTTAGTTTTTAGTAAAGACATTTTCAGTTTGACTAATCTAAAACGTCCTTACTGATTAAAAAAAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28189

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000043069	Essential Splice Site	83	281	3	6

Genomic Location (Zv9):

Chromosome 13 (position 43018403)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	42239362
GRCz11	13	42365422

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGGTTCATGCAGACTTTAAAGGCGGAGTGTGTGTGTGTTTTTGTGTGC[A/T]GGGCCGGTGGTGTATGTGCTGGACCTGGCAGACAGGTTGATCTCGAAGGC

Long Flanking Sequence:

ACATACGGTACAGGTGAATTGGGTTGGCTAAATTGTTCGTATTGTATGAGTGTAAACAAGTGTGTATGGATGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCTGCAGCATAAAACATTCTGGATATGTTGGCGGTTCATTCGGTTGTAGCGACCCCAGATTAATTAAGGGACTAAGCTGAAAAGAAAATGAATGAATGATTGTCTGTGGTATGGGGGGCGTGGCTATCATACTTAACCACGCCTCTCCAATGGTCATTTTTGACAACAAACAGAAATGGTGAGCAGGTCTGTTAGGTTGTTATAACTCTCCTCAAACCCTTTTCCAGATCTTTCTAAATGAAATGCCTACTTTACTACATCCAATGAGCTTGCAGTAGAAAAAACAAGCCACGCCCACTGGAACTGCGTCACAATACGGGGAAAAAAAAAAAAAAACGTTGCAGCTTCTGGTTCATGCAGACTTTAAAGGCGGAGTGTGTGTGTGTTTTTGTGTGC[A/T]GGGCCGGTGGTGTATGTGCTGGACCTGGCAGACAGGTTGATCTCGAAGGCCTGTCCGTTTGCTGCTGCTGGGATCATGGTGGGATCCATTTACTGGACCGCAGTCACATATGGGGCCGTGACAGTCATGCAGGTGAATCATCGCTCGCATTTAAAATTACTTCACAAGAATTCTTTGATCTACACGAATCTCCATCTCTCAGGTTGTAGGTCATAAGGAAGGTCTGGATGTGATGGAAAGAGCCGATCCTCTCTTCTTGCTGATTGGCCTGCCCACCATCCCAGTTATGCTAATTCTGGGAAAGATGATTCGCTGGGAGGATTATGTGCTCCGCCTTTGGAGGAAATACTCCAATAAGCTTCAGATCCTCAACAGTATTTTCCCAGGTCAGTGGTTAAAGGACAGTCACAAAAAAGGGTCGAATTGTAGAGGTATAAAAGAGCTTTAGGCTTTTTCTTCTATAATGCATTTTTAATTATCATTTACTTAAATCACAGACT

Associated Phenotype:

Not determined