ZMP

msi2a

Ensembl ID:

ENSDARG00000033901

ZFIN ID:

ZDB-GENE-030826-25

Description:

musashi homolog 2a [Source:RefSeq peptide;Acc:NP_997961]

Human Orthologue:

MSI2

Human Description:

musashi homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:18585]

Mouse Orthologue:

Msi2

Mouse Description:

Musashi homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1923876]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12004	Essential Splice Site	Available for shipment	Available now
sa34961	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12004

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099473	Essential Splice Site	21	388	None	16
ENSDART00000132096	Essential Splice Site	21	388	None	15

The following transcripts of ENSDARG00000033901 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 10 (position 38833560)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	37556575
GRCz11	10	37500333

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGAGTCAAGTCACCTCTGGAAGCCTGAACGATTCGCAACACGACCCGGGG[T/C]AAGAAGACAGGACGAGTTTGTGTTTGGAGTTTGATTGTGTCCGTGCTCGC

Long Flanking Sequence:

CATATAAATAGTTTGCAACCAGTTACCTTACAAACTCAATGAATGTTATCAGTGTGTTACAAAGATTTTAGTTTAGATTTTAAACATCACTTATATTTTTCAGAGCGCTTCTCGGCTGTGTTTATTCAGAAGGTGGCGCAAATGTAAACTTTATAAGTGTTAAGAGCTTACTAGAAGAACTGAATGTACTCTCGAGGCTCCTGTCAAACGCTGCTAACCAACAGGGGGCGTCGTTTCCTTTGATAGGTGAGCGCAGAGCTCCGCTGGATTGGCCGGCTCACGTTATGAGCCACGCCTCCTCCGGAGAGGGGCGGGAGCCGCGCGCAGATCCCACGTGTGACGCTAGCGCTCCCGGTTCGGTAATATTCCTTGAGCTGGGGCTGCAGTGCCCGTGTGTGTGTGTATGCATGTGTTTGGAGTTGGTTGGGCTTTGAGCAATGGAAGCGGACGCGAGTCAAGTCACCTCTGGAAGCCTGAACGATTCGCAACACGACCCGGGG[T/C]AAGAAGACAGGACGAGTTTGTGTTTGGAGTTTGATTGTGTCCGTGCTCGCGCAGTTCTGCTGATGTTTTTGATTGACAGGTCATTTCTAACGGTTCCTTTCAGCTCCGGTTGCTCGTAGGTCGCTGCTTAAACGAGCCGTTTACGCGGATAATGGCCGTTTTGACATCTGGAGTCACTTATTCCTTGTTTTCTCTTTACAGTAAAATGTTTATCGGTGGACTCAGCTGGCAAACCTCACCAGGTAAGGACATTTCCTTGTGTTTCAGAGTTGTTTCGCGTCGTAATTCTCTGTCGGACGCGATGAGACTGCGTGCGTGTGTGTTGTGATTGTGTCGCTGCGCACAAGGTTATTGTGATTTCTAGTCATCTGACACTAAAAGCGAGCGACGCGACAAAACTTGAACGCTCTCATTATAATCAACGAAGTGTGAAGCCCGCGACCTTCGCTGATTATAACGACAGCTCCGCAGGCTTCATCGCGTCGCTCACTTGCGGTGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34961

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
ENSDART00000099473	Nonsense	182	388	9	16
ENSDART00000132096	Nonsense	182	388	9	15

The following transcripts of ENSDARG00000033901 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 10 (position 39062366)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	37785381
GRCz11	10	37729139

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GACGCTTAGCTTTTCTCTTCTTCTCTGTGTGTCTGTCTGCAGGTAGAATG[T/A]AAGAAGGCTCAACCAAAGGAGGTGATGTTTCCTCCAGGCACGAGGGGGAG

Long Flanking Sequence:

TTTGTTAGCTCACATTGCTAGTTTTATGCATGGTGAACAATTGATCTGTGCATATCATTTGGAAAAAAAAAATTAGCTCTTGGATTCTAAAATCTGAAAATGCTCTTCCTGTTTGTTTTCAGTTAAATTCTCAGATTATGTCTGTCTTGGGTATTGGGCGTGGCTAATATAGTAAACCACGCCCCTACAACTCTCTGTATTGACAACAAACCAAAATGTTGAGCAGGTGGTGCCGGTTAGGTTGTAATAACTCATCTAAAACCTCTTTCCCCGTATTTATGAATAGAATGTCTACTTTACTACATCCAGTCAGCTCACAGGAGAAAAACTATTCAATTTCCATTTCTCTGTAACTGTAACAATATGAACAAAAGGTGTTTGCAGCTTCTGGTTTGTGTGGACTTTAAGTCTGCCATGATCATTTTAATGTCTTGGTTAGTCTGAAATGTTGACGCTTAGCTTTTCTCTTCTTCTCTGTGTGTCTGTCTGCAGGTAGAATG[T/A]AAGAAGGCTCAACCAAAGGAGGTGATGTTTCCTCCAGGCACGAGGGGGAGGGCGAGAAGTCTTCCCTACACCATGGACGCCTTCATGTTGGGCATGGGCATGTTGAGTAAGTCTAACACACACACTTGCACGCTTGCTTACTAACCGGTGGACTGATGAACAATAGGCGGGGCTTTTGGTTATAACTCTGCTGGACCAGAGGCAAGTGTGTGATGTTAGTCTAGTTGAGGTGCTGTGGGGTTCATCAGACCTGATGAGCAGATAAGCGTCTGTATTAATGGCTCAAATGAAGAGGAAAATGAGACTAATGTTGAGTGCAGCCATCTGCCTGACCTCTGCCTTCACTAATGACAGCAGAACACCTCAGCTGCACTCGTCATACACAGCACACCCATGCCTCATCCTATTATCTGCTGATTGTTTATGTTGTCTATGAGTAGCTGTAAAGGGAGCTTTGTTCAGGGTTGTGCTTTATCATGAATAAACTGACCAATCAGCAC

Associated Phenotype:

Not determined