ZMP

myef2

Ensembl ID:

ENSDARG00000059398

ZFIN ID:

ZDB-GENE-051120-114

Description:

myelin expression factor 2 isoform 2 [Source:RefSeq peptide;Acc:NP_001025455]

Human Orthologue:

MYEF2

Human Description:

myelin expression factor 2 [Source:HGNC Symbol;Acc:17940]

Mouse Orthologues:

Gm9833, Myef2

Mouse Descriptions:

myelin basic protein expression factor 2, repressor Gene [Source:MGI Symbol;Acc:MGI:104592]
predicted gene 9833 Gene [Source:MGI Symbol;Acc:MGI:3641855]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa15988	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa15988

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082504	Nonsense	281	553	8	17
ENSDART00000082506	Nonsense	281	557	8	18
ENSDART00000097960	None	None	327	None	10
ENSDART00000123823	Nonsense	281	557	7	16

The following transcripts of ENSDARG00000059398 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 18 (position 4672222)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	5560053
GRCz11	18	5241334

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCTTGACTCGGTGCTCAGCAATGTTCAACGGTCAGATGCTGTTCGACAGA[C/T]AGATGCAYGTRAAGATGGTGAGATGTTACACATGTTATTGAGCAGCCTGT

Long Flanking Sequence:

CATACACAGGGCTTATAGTTCAGCAGAGCTAGTATTTTGACTTTAATTGTGTGTGCCTCTCAGCTGGACTTTAAGGTGGGCTGGAAGAAGCTGAAGGAGGTGTTCGGGATGGCCGGCACCGTGAGGAGAGCCGATGTGAAGGAAGACAAAGATGGAAAGAGTCGTGGGATGGGGACGGTGACCTTCGAGCAGCCACTGGAGGCCGTTCAGGCTATCTGTATCCTCAAACATACACACACACTGAGAGAAGCACTTTGAAGAAGACTTTAAATTATTCACTAATTATATATTTTAAAGTTAAAATGTGGCCAATGTTACCGGTTAAAACAGTCAATGTGGCTTGATAAGGATAAAATGTATTGAAGGAGTCCTAAATAAAGGTTATGACAGTATTGAATTTTATTCTCTGCCTCCTGTATTGTTATGAATGTTATGTACTGATGTTCTGCTCCTTGACTCGGTGCTCAGCAATGTTCAACGGTCAGATGCTGTTCGACAGA[C/T]AGATGCATGTAAAGATGGTGAGATGTTACACATGTTATTGAGCAGCCTGTGTTTCTGTGTTGTGTGTGCTCATTCATTGTGTGTTTTCTTGCAGGATGATAAATCTCTTCCTCCTGATGATTTCCGGCCTGTCGAGAAGTCTCCACAGTTGCCCAGTAAGAGCTCAGTGTGTGCATTGAGAATATTACATTACTGCACAGCCACACTGCAGAGTTATTATTCTCAAAGTCAACACATACCTCTGTAATGCCCCATTTCTAATGTTACAATGAGGGCTTTAAGGTTTAGAATATGCCAAAAGCTTAATAAATGTGAAATGTTTTTATCTCGATTATAACAATGCAGCAGTGAATATGACTTGCTTGTTTGTGTATAATTGTATTTTCGGTGTTTTTGTATTTCAGGGGGTCTGGGTGGTATCGGGATGGGTTTGGGTCCTGGTGGCCAGCCAATAAACGCCAACTGTCTCAGTGGAAGCTCGATGGGACCTGGAGGTGTGT

Associated Phenotype:

Not determined