ZMP
zgc:162925
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC567809 [Source:RefSeq peptide;Acc:NP_001103944]
Human Orthologues:
SLC6A15, SLC6A17
Human Descriptions:
solute carrier family 6 (neutral amino acid transporter), member 15 [Source:HGNC Symbol;Acc:13621]
solute carrier family 6, member 17 [Source:HGNC Symbol;Acc:31399]
solute carrier family 6, member 17 [Source:HGNC Symbol;Acc:31399]
Mouse Orthologues:
Slc6a15, Slc6a17
Mouse Descriptions:
solute carrier family 6 (neurotransmitter transporter), member 15 Gene [Source:MGI Symbol;Acc:MGI:21
solute carrier family 6 (neurotransmitter transporter), member 17 Gene [Source:MGI Symbol;Acc:MGI:24
solute carrier family 6 (neurotransmitter transporter), member 17 Gene [Source:MGI Symbol;Acc:MGI:24
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32499 | Nonsense | Available for shipment | Available now |
sa24554 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32499
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 |
---|---|---|---|---|---|
ENSDART00000018010 | Nonsense | 367 | 676 | 7 | 11 |
ENSDART00000076558 | Nonsense | 367 | 676 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40141806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38740727 |
GRCz11 | 24 | 38628490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCTACCTGTCCTTTCCATCAATGCTTCAGATGTAGAGAGCATCTCAT[T/A]GGACGAGTATGCAAACTGGTACTCGACTCAAGGGATGGAGCTCAGTATCT
Long Flanking Sequence:
ACACATGAAATTCACAAGCGGATTCACAAGCGGAAAAGAGAGAAGAGAACGCAAACAGAAAACAAACAACAAAACATACGTGGAACGTAACAATATTAATAAAAACATTATTCTTCAGCCAATGTAGTTCCTCAGAATCTGTTGTGGTTGAAGCAAAGTGCTTGCCGAGCAACACAGATCCAGCAATAATAAAGTAATGAGGTCACGGGTGTACATTTATTGTGTATTTTACAACTGTTTCAAACGCAACTCCTGCAGCCACAATCTGTTTTATAATGCCTCATAATACACTGTTTGATTTGTACAGTGTTTTCACAATTTCATTCACTAGTTTTTTTTTTTTAACTATGGTAGCATTACTTCACATAACTTTTGAGTTGCTTTAAGATGCTTGGATGTGTCTTTATGTTGCAGTAATCTGAAGGCCCTGCTTAAGGTGACGTCCAGCGCTCCTCTACCTGTCCTTTCCATCAATGCTTCAGATGTAGAGAGCATCTCAT[T/A]GGACGAGTATGCAAACTGGTACTCGACTCAAGGGATGGAGCTCAGTATCTCTGACTACAACATCACAGCCTGCAGCCTGGAGGATGAACTCAGACAGGTACAGTTACTGCAGATTTAATGGAAATAAATGTAGGGCCTGCGCATAAGGTCTAAGGGCGTACTCACACTATGTACAGTTGCCTTTACCGTGCCGAAGCGCGCTTGTCCCCCACTCCCCTCTGCCCCAACAGCCTGCACTCACATTGCATCCGAGCCTGAGCATGCTTGCGTCAGTGATGCGCTGTTCAGTTTAATAGTAGAGAAGTGCTCTCGCTCTGCACAGTAAACATTTCTTTAGTTATATCATTTTGGTCGTTTAAGATCCAGTCACACAAAGTCAAATATTTCGCTGAACAGATCAGCCACTTTGGTTGCTCATAAACAATCATAAAGTCCTTGTGCTGCAGGTATTAGGAGGTTTGCTGAAGGTGCAGCTGATGAGGGGTTTGTGTCTTTAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24554
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018010 | Essential Splice Site | 520 | 676 | 9 | 11 |
ENSDART00000076558 | Essential Splice Site | 520 | 676 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40136404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38735325 |
GRCz11 | 24 | 38623088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTCATCTTTCAGACCATCAGTGTTTCATGGGTTTATGGAGCAGACAG[G/A]TAAAACACACACACACACACACAATTCCATGCAAATGTCAACCTTCCCAT
Long Flanking Sequence:
ATTACTATAATAAATATTACTTGAAAAGATTTACAATGATGAGGACCCTGTTATTTTACTTTTGATTGTTCCAGAAACCCTTATTATTTTTGATCTGTTGTATTTATTTTTTGATCTGTTGTATTTATTCATGCCTTTTATTCTAATTTATGCAGATCTACAATAATGAAATCGTTCCCAATAGAGCTATTCAAAGCATCAGAAGAAATTATTTTATAATAGCAATATATATCTCCGCAAAACAAAATAGCCCAGTGTCAGATTTTTTTCTCTAAAATAGATGAATGTTGTCATCTGGATGTAGCTGTAATATTGTCATTATCCTCTTTCCATTTCTCAGTCTGCAGCTGTACAGTGGGCTTTCTGATCGGTCTGGTGTTCACTCAGCGCTGTGGAAACTACTTTGTGACGATGTTTGATGATTATTCTGCCACTCTTCCTCTGATCATCGTTGTCATCTTTCAGACCATCAGTGTTTCATGGGTTTATGGAGCAGACAG[G/A]TAAAACACACACACACACACACAATTCCATGCAAATGTCAACCTTCCCATGAGAAAAATAAAGTTTTCACCAGAATAGTGAAGTGCTTTCTACGAGTATTTTGCAGTACTGTAAAATAGAACAAGCCTCTGTCAGTGTTTTCAAACAATTATAATTGATTTACCAAAGACACACAAGTGCCAATTTCACATCAGTCACATCCATAACAGAGAGGTGTCACATTAATAAACAAGCTTGTTGCTCATCAATGGAAAAGTAATTTAAAATTAATAATTTTTGTTGTATAGTGAGCAATTCTTACCCTTTTAATTTTTGGGTTGTGCGGTTTAATTCACAGAATTTCTACAAAGTATGTTGTCCACTGTAAACTTGCACTTTTTTGGCCACATCCATAATGCATTAGGGATGTGACGAGATCTCTGGCTACGAAATCTTGCGAAAGTAAATGGTGGCGAGATTTGTCACCAAGGTTAAAAGTTGTCTTGTGAGTTTTGATGGTA
Associated Phenotype:
Not determined