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 are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16779	Nonsense	Available for shipment	Available now
sa42217	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16779

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
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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

Mutation Details

Allele Name:

sa42217

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026765	Nonsense	296	513	1	1

Genomic Location (Zv9):

Chromosome 13 (position 29646854)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	29292802
GRCz11	13	29423252

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGCCCACCATCGCAAACTGGATGGAAGAGACCATGAATGCATCCCAATG[G/A]CAGATCGGGATCACCTGGCTGCCAGCCTTCTTCCCTCACATATTAGGCGT

Long Flanking Sequence:

ATTGGACTCAGTATCATGTTCGTCTCAACGTGCATTTTTGCCTTCGCCGAGAACTACGCGACCCTGTTCATGGCGCGCAGTCTGCAAGGGCTCGGCTCGGCGTTCGCAGACACTTCAGGAATTGCCATGATCGCGGACAAGTACGCGGAGGAGTCGGAGAGGAGTCGCGCGCTGGGCATTGCCCTCGCCTTCATCTCCTTCGGAAGCCTGGCGGCTCCCCCGTTTGGAGGGGTACTGTATGAGTTCGCGGGCAAACGCTTCCCGTTCATTGCGCTCGCATGTGTGTGTTTGGCAGACGGTATACTATGCCTGACTGTGCTCAAGCCCTTTTCCAGTAGGACTAGAGAGAACATGCCGGTCGGCACCCCAATTTACAAACTAATGATCGACCCGTACATAGCGGTCGTGGCAGGAGCTTTGACCACATGTAACATTCCCCTTGCTTTTCTGGAGCCCACCATCGCAAACTGGATGGAAGAGACCATGAATGCATCCCAATG[G/A]CAGATCGGGATCACCTGGCTGCCAGCCTTCTTCCCTCACATATTAGGCGTTTATCTCACTGTCAAGCTGGCAGCAAAGTATCCACACTTGCAGTGGTTTTATGGTGCACTTGGCATGGTCATCATTGGTGCCAGCTCGTGCATTGTGCCGGCTTGCAAAAACTTTGAGCAGCTGATAATCCCCCTGTGTGGCGTTTGCTTCGGCATTGCACTGGTAGACACAGCTTTATTACCCACACTCGCTTTTCTAGTAGACGTCCGCCACGTGTCTGTGTATGGTAGTGTATACGCTATTGCAGACATCTCCTACTGTGTTGCCTACGCGCTGGGCCCGATCGTGGCCGGTAAAATAGTGCACGACCTCGGTTTTGTGCAGCTCAATCTGGGCATGGGTCTGGCGAACGTACTTTACGCACCAGCCCTGCTACTGCTGCGCAACGTGAGCTTAATGAAACCATCCCATTCCGAGAGAAACATGCTACTGGAGGAGGGAGCCACAGG

Associated Phenotype:

Not determined