ZMP

LOC100332905

Ensembl ID:

ENSDARG00000090781

Human Orthologue:

SNTA1

Human Description:

syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component) [Source:HGNC Symbol;

Mouse Orthologue:

Snta1

Mouse Description:

syntrophin, acidic 1 Gene [Source:MGI Symbol;Acc:MGI:101772]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa12022	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa12022

Status:

Available for shipment
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Availability:

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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000125816	Nonsense	156	404	2	9

Genomic Location (Zv9):

Chromosome 6 (position 57670519)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	57757286
GRCz11	6	57754150

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AYGATGAAGCTGTTCAGGCCYTGAAGAAAACCGGCAAGGAGGTCATTCTG[G/T]AAGGTAAGACTGGTTTTAAAGAGAAGCTGCGTCTGAAATATATTTTAAAG

Long Flanking Sequence:

CCAAGGCTCAAGGATGAAGGCGATGAAATTTTGATTGGTATTATACAGTGCTGATCATAAATCACACCAAAGAGCACATCAGTCGTCAAGATTTACAGTCGTTGTGTGTTTGGGAATGTGTGCTAGATTAGTTTACAGAGGCGTTTTGTGTCAGTAATTCGTAGTGAGTCTGTGTTTTGCAATGAACAAAACTGATTTACTAATCACATCACTGGACTTTCCTCACATGACGTGCAAGACAATCACAGCTTTTGCTAATTTTATGTCGATTTATTGCTCACGCTTAGTAAGTAATGCATGTTGTGTGCTGTTTTACAGGTGGGAAGGAGAATAAGATGCCCATCCTGATCTCGAAGATCTTCAAAGGACTGGCAGCGGATCAGACGGAGGCTCTTTACGTTGGAGATGCTATTTTATCGGTGAACGGCAACGATCTCAGAGAAGCAACTCACGATGAAGCTGTTCAGGCCCTGAAGAAAACCGGCAAGGAGGTCATTCTG[G/T]AAGGTAAGACTGGTTTTAAAGAGAAGCTGCGTCTGAAATATATTTTAAAGAGCCCCTATTTTGCATTATAAAAGGTCATGTTTTGGTTTTAGGGGTCTCCAACAACAGGCTGATATGTGTGCAAAGTCACTTTCATTGTCTTATAATCTGCATTTATTTTTACCTAATTATCCCAGCGACTCCCATATGAATCGTTCAGTGAATCATTTGTTCCCAAACCCGTCCTTAGCGCGAAGCTAATCTGCGCTGATTGGTCCGATGACCTAGTCTGTTGCGATTGGTCGACTGCGTTCTGCACCAGACAAAGAGAAAAGCCCAACATGGCTATGAAATAGCAGCCAGAGTGTATGTGAGAGCCCAATGCAGGAATGCAATAAAGCAATGCCGTTAAACACCAGCATATACTCTTAACCCTAACCCCAAGTAATAACAACGACACACATTCAGTATTAATCCACACAGTGGCAAAAGCTGAACTATTTTAAACTTGACCACGCCGC

Associated Phenotype:

Not determined