ZMP
slc18a3a
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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