ZMP

SLC18A3 (1 of 2)

Ensembl ID:

ENSDARG00000090189

Description:

solute carrier family 18 (vesicular acetylcholine), member 3 [Source:HGNC Symbol;Acc:10936]

Human Orthologue:

SLC18A3

Human Description:

solute carrier family 18 (vesicular acetylcholine), member 3 [Source:HGNC Symbol;Acc:10936]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa10248	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa10248

Status:

Available for shipment
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Availability:

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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127013	Nonsense	275	431	2	2

Genomic Location (Zv9):

Chromosome 12 (position 50571013)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	48937857
GRCz11	12	48959386

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGCTCGGGATGGTGATCATCGGTGCCAGCTCCTGCACGGTGCCYGCCTGC[A/T]AGACCTTCGGCGAGCTGGTGTTCCCGCTGTGCGGCATCTGCTTCGGCATC

Long Flanking Sequence:

CGCGCGCAGTCTGCAGGGTCTGGGCTCCGCGTTCGCGGACACCTCCGGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGCTGCTGACGGTGGTCAAACCTTTCTCCGACAGGACGCGCGAGAACATGCCCGTCGGGACGCCCATCCACCGGCTCATGGTCGACCCGTACATCGCCGTGGTGGCGGGCGCGCTGACCGTCTGCAACATCCCGCTTGCCTTCCTGGAGCCCACCATCGCCAACTGGATGGAGAGCACGATGGACGCCTCTAAGTGGCAGATGGGGCTGGTGTGGCTGCCGGCGTTCCTGCCGCACGTGCTGGGGGTCTACATCACCGTCCGCCTGGCCGCCCGGTACCCGGAGCGGCAGTGGTTCTACGGCGCGCTCGGGATGGTGATCATCGGTGCCAGCTCCTGCACGGTGCCTGCCTGC[A/T]AGACCTTCGGCGAGCTGGTGTTCCCGCTGTGCGGCATCTGCTTCGGCATCGCGCTGGTGGACACCGCGCTGCTGCCCACGCTGGCGTTCCTGGTGGACGTGCGGCACGTGTCGGTGTACGGCAGCGTTTACGCCATCGCGGACATCTCCTACTCCGTCGCGTACGCCATGGGGCCGGTGGTGGCCGGGCAGATCGTGCACAACCTGGGCTTCGTGCAGCTGAACCTGGGCATGGGGCTGGTGAACGTGCTGTACGCGCCCGCGCTCCTGCTGCTGCGCCCCGTGTGCCAGATCAAGCCCTCCTTCTCGGAGAGGAACGTGCTGCTGGAGGAGGGCCCGAGCGGCCTGTACGACTCTATCCGGCTGGAGGAGCGCGCGCTGCGGCGGAAGGGGCTGAGCGCCGGCGCCGGTACCGAACACGGGCTCCGAGGGCGCTCGGAGGAGGAGGAGGAGTCGGGTCCGGAGAGCGCGTGAGGCGGCCTGCTGTGCTGCTCCTGTAGT

Associated Phenotype:

Not determined