Busch Lab

ZMP

slc18a3a

Ensembl ID:
ENSDARG00000006356
ZFIN ID:
ZDB-GENE-060929-990
Description:
Probable vesicular acetylcholine transporter-A [Source:UniProtKB/Swiss-Prot;Acc:Q08C75]
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
sa16779 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16779
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
ENSDART00000026765 Nonsense 16 513 1 1
Genomic Location (Zv9):
Chromosome 13 (position 29647696)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 29293644
GRCz11 13 29424094
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATCATGGCTACGGAGGAATCAGGTGGCTTGGCGCAAACCGYCGCCGTT[A/T]AACTTTCGGAGATGGGGGAAAGAACTAAACAGTTAGGAAATGCGATCCAG
Long Flanking Sequence:
TCACATCCTTGGGAAAAAAGAGAGGAGTGATTCCAATGGAATCAACATGTAAGCGCATCTGCATTGGGTGGCATCAATAAGAAGACGGCTGAGGGGAAATGATGACACTGCGCTACAGGTGAATTCATCCATTGACGCTCATTCAGGCTCCGCGCGTCCAGCCACAATGACAGCGTGAAGAAGGAGGGAAAGCGAGAAGGCTATTTTTTGACCTGACTGTGAGTTTTTGACCCGAATACGATGAAACAACACTGCGTGGCAGCAGTCGCGAGAGAGGAAATGCACGCGCAAAGAAGGACTGCAAGGTAAAGCAGGAAAAGTTGCTCTGCGCGCCGAGGCTTCACTATTCAGTGAGTGCTGGGCAACCCGGTGCGCGCAGACTTTCTCGGGGAGAGAAGCACAGCGTAGAAGCGAGTTAAGAGCATTTTTCCTGAAGCGACCAAAGTGTGTGGATCATGGCTACGGAGGAATCAGGTGGCTTGGCGCAAACCGCCGCCGTT[A/T]AACTTTCGGAGATGGGGGAAAGAACTAAACAGTTAGGAAATGCGATCCAGGACCCCGAGCGACAAAGAAGGATTATTCTAGTCATTGTGTGCGTGGCACTTCTGCTAGACAATATGCTTTACATGGTCATCGTGCCAATTGTGCCCGACTACTTAGCGCACTTAGAGAGCGAATCGGAGCAGGCGCATGTAAAAGGTAATTCCTCAATTAACATCACGCAAAACGAGAACTTTGACCTGCAGATCGGCGTGCTTTTCGCTTCAAAAGCCATTTTGCAGCTCCTTGTCAATCCTTTGACTGGAACTTTCATAGACCGAGTCGGCTACGACATCCCACTTTTAATTGGACTCAGTATCATGTTCGTCTCAACGTGCATTTTTGCCTTCGCCGAGAACTACGCGACCCTGTTCATGGCGCGCAGTCTGCAAGGGCTCGGCTCGGCGTTCGCAGACACTTCAGGAATTGCCATGATCGCGGACAAGTACGCGGAGGAGTCGGAG
Associated Phenotype:
Not determined