meis4.1a

Ensembl ID:
ENSDARG00000002937
ZFIN IDs:
ZDB-GENE-020122-3, ZDB-GENE-020122-4, ZDB-GENE-020122-4
Description:
myeloid ecotropic viral integration site 4.1a [Source:RefSeq peptide;Acc:NP_571972]
Human Orthologue:
MEIS1
Human Description:
Meis homeobox 1 [Source:HGNC Symbol;Acc:7000]
Mouse Orthologue:
Meis1
Mouse Description:
Meis homeobox 1 Gene [Source:MGI Symbol;Acc:MGI:104717]

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa25673 Essential Splice Site Mutation detected in F1 DNA During 2017
sa16771 Essential Splice Site Available for shipment Available now
sa44514 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa25673
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028018 Essential Splice Site 4 380 None 13
ENSDART00000145313 Essential Splice Site 4 285 None 8

The following transcripts of ENSDARG00000002937 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 51988334)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 50835695
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CGCGTTGAGAAAAGCGAGTCGGTGACGCGGAGTCCTCATGGCGCAACGGG[T/A]GCGTAAAATCAACCAAAGGAGAGAAAAAAACTCAAACGTGGCCGTCAAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16771
Current 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:
G > T
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028018 Essential Splice Site 72 380 2 13
ENSDART00000145313 Essential Splice Site 72 285 2 8

The following transcripts of ENSDARG00000002937 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 51989480)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 50836841
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CCGCCGCCCGTTAACGACGCGCTCAAGCGGGACAAAGACGCCATTTACGG[G/T]TATGTGCTGKGATTAAAATTATGTGYCATCACAAAGCTTGATTGCWGGRC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44514
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028018 Essential Splice Site 285 380 None 13
ENSDART00000145313   285 285 None 8

The following transcripts of ENSDARG00000002937 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 52005773)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CAAAGTGGCAACCAATATCATGAGAGCATGGCTGTTCCAGCACCTCACGG[T/C]AAAACACGTCTCTGCTTTCCCAATGATTACACTTTTAAGGTCTTAATTGA
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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