ZMP
slc18a2
Ensembl ID:
ZFIN ID:
Description:
Slc18a2 protein [Source:UniProtKB/TrEMBL;Acc:Q5CZP4]
Human Orthologue:
SLC18A2
Human Description:
solute carrier family 18 (vesicular monoamine), member 2 [Source:HGNC Symbol;Acc:10935]
Mouse Orthologue:
Slc18a2
Mouse Description:
solute carrier family 18 (vesicular monoamine), member 2 Gene [Source:MGI Symbol;Acc:MGI:106677]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36403 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36404 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6475 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12325 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36403
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025466 | Nonsense | 130 | 561 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 23614392)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23764541 |
GRCz11 | 17 | 23784565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACCCCTCTTTCTCCATCGAGCACCTTTCAGAGCATTGTGTCTTTGTA[T/A]GACAACACCACACGTGTGACAGGCTTCAGCCCGCAGATGAGCACAGCTGG
Long Flanking Sequence:
GTGTTAAACAGCGTTTCTAGCTGTCTAAATCTGATCTGTGGTTTTCTGAACAGGTTATGAACAAGTCGAATGAATACAATAATGATTAAAACAAACACAGAAGAGGCTCTAATGGTTTAAAAATGCTATTAAATACATTAAAAACCACCAGACTTCAATCAATAAAACATGTTAATGGTATCTTGTGCGCTTAAGACACATTCCTTAAAATTAATTAGCTTTAACATGTCGCCAATAAGGTAAAACTAGGGACTCATTATTTTTCCATTAAAACCAATGTAACTTCCATTTGAACCATTGAAAGAAATACAAATTCTTGAATGGTTTCTAATGTTTTTTTCAGCACGGTGGTTATGTTGTTTCCTCTATTTCATCTCTCTAGTGCCTATTATCCCAAGTTACCTGTACACGGTGGACGACGAGGCTGCTCAGATGGTTAAGAATCACTCCATGACCCCTCTTTCTCCATCGAGCACCTTTCAGAGCATTGTGTCTTTGTA[T/A]GACAACACCACACGTGTGACAGGCTTCAGCCCGCAGATGAGCACAGCTGGTCCAATGAGCCTGGCTCCTACTTTTGTGAGCCCTCAAAACCAGTCCGACTGTCCCAAAGCAGATGACCAGCTTCTGAACGAGAATGTGAAAGTGGGTCTGTTGTTTGCCTCTAAAGCAACAGTACAGCTAATCACTAACCCCTTCATAGGACCACTAACCAACAGGTACAGCCGCTAGTTTAACTTAAAAAAAAAAACACAGCAGTGTTTCTCTTAAAAGCAGGATGGGATTGCATGACATTTGTGTGTGTGTGTTGAGTGTAAATGGAGTGTAAGTAAGTTGAATATTGCTGTGCTATTCTGCTACAGCTCTATCTATTCAAGGATCAGCAGTAGTGTGATCACTCGTGCATGTGCCGTCATATCTTCACATGCTCAGATTTGGCCAATCCAGCTAAATTTGGCACCACAGCACTGAATGGATCCCACTAGAGCAAACCGGTGGCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36404
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025466 | Essential Splice Site | 222 | 561 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 23615580)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23765729 |
GRCz11 | 17 | 23785753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATCCCAATGTTTGCTGGTTTCTGCATCATGTTTGTTTCTACGATCAG[T/C]GAGTACATAAAACATATATATTTTTAATGCTGCTTTTAACATTAATCTAA
Long Flanking Sequence:
TAATCAATATTTTGTCAGTAAATTTTACATCCACAGCTACAAAAAACAGCAACACACTGAATTGAACATAAATTTTAAAGTAAATAAAAACTTCAATATTTTAAAATACTTAAATTTTCAACTCTAAAAACTGGTCTAACAGTTTCAATTTACTATAACTTTTATGTTGAGCTGCTTTGACACACAGTCTATATTGTGAAAACTATAGAAATAAACATGAATTGAATTGATTTAAAATAGTTTTTCATATAAATATTCCAAAAAACTTTTCATCCAGTCTTTACAACTTAATCACAACATATTTCTTTTCAGTGAAACACTGCAACATGTAACAAAACATTTCACTTCAAAATGTTTGTGAAAAAAAAAATGCTGATGCACTTTAAAGTTTTGCGTTTTATTCGATACATCCCTGAAGCATTTCTTATCTGTAATTGCAGAATAGGATACCAGATCCCAATGTTTGCTGGTTTCTGCATCATGTTTGTTTCTACGATCAG[T/C]GAGTACATAAAACATATATATTTTTAATGCTGCTTTTAACATTAATCTAATTTCTAAGAGAAAGCAGTTGAGAAGATCTTGCAGATGTGCAATGCATGATTTTAAAGTATGATAACAGCAGCTAAACTCTCTGGTGTGTCATATTCATACGATAAATGGATCTACTTTTCCTCTTTCTTCTGTCTGGGTTTTATTCTGTGTGAAGTGTTTGCCTTTTCATCAAGCTACACGCTGCTGTTTTTGGCCAGATCTCTGCAAGGTGTTGGCTCGTCCTGTTCTTCTGTGGCAGGTAACATGTTTTGTGCAATGTTATGTTAGAATTTAAAAAAAACCTGTCAAATGCTGCAATGAAATTCTTTATGATGCCTTATTTAGCATATTTTGCAAACCTGAGTGCACTGAATTGCATTTGACTTTGGTTTTCTTTGAATTCTGTATGCAAACATCTGCTGATAATGACAGTAGTGTAAAATGGATCCCATTCTCATTTAACCCTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6475
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025466 | Nonsense | 264 | 561 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 23618898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23769047 |
GRCz11 | 17 | 23789071 |
KASP Assay ID:
554-5475.1 (used for ordering genotyping assays)
KASP Sequence:
ATTGTGTAGGTATGGGGATGCTGGCAAGTGTTTAHACAGATGACGAGGAA[C/T]GAGGAAACGCTATTGGGATTGCACTGGGAGGACTAGCAATGGGAGTTTTA
Long Flanking Sequence:
GAAACATCTCAAGAATGATCAGTAGAAACAGAATGTACCTGAGCTCAATTTAGAGCTTTATGGCAAAGACTGCGAATACTTATAAGTACATGTGATTTTTCAGGTTTTTTATATTAATTTGTAACAATTTCTAAAAAAAATTTACATTGTCATTATGGGGTATTGTGTGTACAATTTTGAGGAAATAAATGAATTTAATCCATTTTGGAATAAGTTTATAGCATGAAAATTGTTGGAAAAGTGAAGCACTTTGAATACTTTCCGGATGCACTGTATGTACACAATGTAAAAGCATTGTTTATATGTATGTTGTGTTAGTCATGTTGATTAGTAAATGTATGTTTGTTTGTTTGTTTTTTGGACTATTTAAATAAATCAAAAAGGGTGAAAAGTTTGTATATTTTTTGCTGTACATTCTTCTGTAACTCCTGATAAAGCTGTCTGTTTATTATTGTGTAGGTATGGGGATGCTGGCAAGTGTTTACACAGATGACGAGGAA[C/T]GAGGAAACGCTATTGGGATTGCACTGGGAGGACTAGCAATGGGAGTTTTAGGTGCATGATCTGTTTAAAATTCTTTTCAATATTTTCATTGACAATACTTGTTTGGCACAAGAGAAATTGACAAAGTCCTAGTTTACTTTTTGGAACTCATCCCATGAAGAGAGATATCATACGTCGGCGGGGTGGATATGCATTAAGTGGCTTTGACTTTAAAAAGCCCTGGAGCAGTGGTCAGAAGAACACAGTGCTTCCCGATAATGGCATCATGCTTTAATCTCAGGATGTTTAATCATTAATAGTCCATTATTTTTATTCATAATGTCAAGTGTTTAAAAATATATTTTTGATCTACTGGATAAGAGCCATCTTGCAAAACAGTGATTAAATGTTGCTGTCGTCATACTGTACTTAATCAAATGGAGAGCAACCGGAAAATGGAGCACAATAATTTTGATTAAAACATAAAACTATATTCATCCAGATATTTGTAAAGGTACTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12325
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025466 | Nonsense | 514 | 561 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 23633732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23783881 |
GRCz11 | 17 | 23803905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCTCATGACCATCATCGGTTTAGTGGACATCAKGTTTGCTCCTCTTTG[T/A]TTCTTTCTGCGAAATCCTCCCGCCAACGAGGAAAAGATGGTTAGAATYCA
Long Flanking Sequence:
CATGTTGCTAACATGTTTTAGCTTGTTAGTGTGAAGGGATTGTCTAAACATTTGGTCATTAAATGACATAACAATAAGAGACATTGTCATGAATGGGCATGTGTAATATATTGTTATGTTACTGTTAATGTGCATAATATTCAGTGTCGGTGTAAAATGCGTGTCATAAACAGCCTGTATTTTGTGGTCTGCAGGTATGGTGGACTCTTCAATGATGCCTATCATGGGTTATCTGGTCGATCTGAGGCACGTGTCGGTGTATGGAAGTGTGTACGCCATTGCTGATGTCGCCTTTTGCATGGGTTTTGCTTTAGGTAATGTCTGAAATGAAAATTCAGTCTGTTAGAAATGCCTTCATTCATTTTAATGTGTTTAGCAGCATTTAACACTCGCGTTTATTGTGCAGGTCCATCAGCAGGTGGAGCGATCGCGCGGAGCATCGGCTTCCCCTGGCTCATGACCATCATCGGTTTAGTGGACATCATGTTTGCTCCTCTTTG[T/A]TTCTTTCTGCGAAATCCTCCCGCCAACGAGGAAAAGATGGTTAGAATCCACCATATATACATATACTAACATACATTATACCCATCGCAATCTACACACTCATGAAAAAAGTAATTTTCATCACAAAATGTTTTAGGTGACACAGGTTTCTCTAATTATTTAGAAAATTAGAATTAATTAGAAATTAAAAATTTAGTGGTTTCATCCGTCCGGTATTGATTAGATGATGGCTGTTGCAAATAACAATGGGAGCGTGCAATGTAAAAAGTAATTAGCTACTTTCAGGGCTTGATATTGACATTTTTGATCACCAGCCACTGTGGCTAGTAGTTTTCCAACGTTACATTTTCACTAGCCACAGTTTTGTTGTTTGGAAAATATATTTATATGCAAAAAAATTACTTGATTTAAATTTTATGTTATGTCTACATGCCTCCTCGTTCATTTAACTTTTTTGTGTGTTGTGACCTTGCTCAATGGATTGTTGTTTCATAGTGTCG
Associated Phenotype:
Not determined