ZMP
slc6a19b
Ensembl ID:
ZFIN ID:
Description:
sodium-dependent neutral amino acid transporter B(0)AT1 [Source:RefSeq peptide;Acc:NP_956030]
Human Orthologue:
SLC6A19
Human Description:
solute carrier family 6 (neutral amino acid transporter), member 19 [Source:HGNC Symbol;Acc:27960]
Mouse Orthologue:
Slc6a19
Mouse Description:
solute carrier family 6 (neurotransmitter transporter), member 19 Gene [Source:MGI Symbol;Acc:MGI:19
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22803 | Nonsense | Available for shipment | Available now |
sa15801 | Nonsense | Available for shipment | Available now |
sa22804 | Essential Splice Site | Available for shipment | Available now |
sa36095 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22803
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079248 | Nonsense | 42 | 651 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 20931828)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19168583 |
GRCz11 | 16 | 18974222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGTGGAGGAGGCTGGAGACAGACCCAAGTGGGACAACAAAGCCCAATA[C/A]ATGCTGACCTGCGTGGGCTTCTGTGTGGGGTTGGGCAATGTCTGGCGGTT
Long Flanking Sequence:
TCATTGAAAACAATACATGCAGAGTCAAAATGTTCTTTTCCCTATTCTGTTTGTGATGTTCAAACTGTTAAGGATCTTTGACACCGACTTACCTCTAAAGTCCCATAAAGATCATTATCTTTAGTTATTAACCACAAGAATGGGTAGGAAAACACAAGTGCATGTCATCCGATTCTCAATCTCTGATAAGACATTAATTATTGCCATGCGCAGAGTCTTCTTTCCACATTATTCAGCTGACGAGACATTTTCTGCATCTTCATAGATGGACTGGTGGGATGATGCCAAAGTCCACTACATATACCCGTCCCTTTCAGACAGAGAGTCCTTATCTCTGTGCAGTCTAGCCCATCAGAGACTGAGCCACCGGAGATCATGAAGCTGAAGCTGGTGCTGCCGAACCCGGGTCTTGAGGAGCGGATCTTGAACCATGAGGCGCTGGAGAGGCTGGAGGTGGAGGAGGCTGGAGACAGACCCAAGTGGGACAACAAAGCCCAATA[C/A]ATGCTGACCTGCGTGGGCTTCTGTGTGGGGTTGGGCAATGTCTGGCGGTTCCCCTACTTGTGCCAGAGCCATGGAGGAGGTGAGGGGTTTAACCTTCATTAAAATTCTCATTGGAAAAAACATGGAGTGTCAGTACAAGGGGTTATTACAAGACCTTTCGACTTTTATGTTTAAGTGATCTGCACCAATTTAAATATTTTTGATTTGACGTGTTTTATATATTTTATTATTTTATATTTTACTTTATTTTATCTGCATTCAGCTGAAAAGTTTGTCTTATTTCCCAAAGAATGTAAAATTACAAACCTCAAAATTAAAATATTTATATGAGTGCAGGTATTTTTATTTATATGTTTTTTATCATTTGGGGAAACAATATGACGAATGTTTCAGCTCAACCCCGATAAAATAAAGTTGAGCTGAAATGTTTGTGGTTTTGTTTCCCAAAGAATGTAAAATAAAAAACGTCAAAATGTTAAGATTTAAATGAGCACAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15801
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079248 | Nonsense | 197 | 651 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 20942107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19178862 |
GRCz11 | 16 | 18984501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCTGAACACTTCAGCGGCTATAGATGATACGGGTGGTCTGCAGGTGTG[G/A]ATGGTCCTCTGTTTGAWCTCTGCATGGGCAGTGCTGTATGTCTGCTGCAT
Long Flanking Sequence:
CATCATTCTTTTTCAAATGTCTAATTCTTTCGTTTTGATCTTCACATGGAGATTTGTGCAGCATTACATATTACTTTGTTCATCAGATTCCATTCTGTGTAGAAGCTAAGCATGTGTTGTGTTTCACAGGCATTGCATCTATGTGTGTGTCTTTTCTGGTCAGTCTGTACTACAACACCATCATAGCCTGGGTTATGTGGTATTTCTTCAACTCCTTCCAGGATCCTTTGCCCTGGAGCCAGTGCCCCATCAATGAAAACAGAACAGGTATAATATGAGCATGCTGAGGAGGAGGATTTTATTATTATTTTGATTTCATTTCTATGTCTATTTCTATGATATTTTGGGTTTACTCAAGGTTTGTTTCATCTTCAATGTTATTGTTAATGGTCAGGACCGATTCCAGAGTGTGGGAAGAGCTCACCAGTGGATTATTTCTGGTATCGTGAGACTCTGAACACTTCAGCGGCTATAGATGATACGGGTGGTCTGCAGGTGTG[G/A]ATGGTCCTCTGTTTGATCTCTGCATGGGCAGTGCTGTATGTCTGCTGCATCCGTGGAATAGAAACCACTGGGAAGGTAAAGCTGCTTAAATAAAGGAGGCGATAGGACAGGAATATTTCAGAATCTGAATCAGTTTTTAATTAATTAAGCGAGTCTCAGTTCACAGTAATAATAAAAAAAAAAGTTTAACATGCATAAAGGAACAGTTCATCAAAAAGGAAATTCTGTCTGTCATCATCTGTTCACCCTGTACTTGTTTCAAACATGTTTGAGTTTTTTGTTCTGTCAAGCACAGAGAATATTGGAAACGTAACCACTGACTACCAAAGTCCTTGTTTTTTCTATGGATGTCAGTAATTAATGTTTTCTAAACATTCTGCAAAATATCTTTTGTGTTTAATACAAAAACTCAAACTGGTTTGTAACAATTCAAGGGTGAGTAAATTAACAGAATTTTACTTTGTGCGAGAACTACCTTTTTAAGGATGCGTTTATAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22804
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079248 | Essential Splice Site | 340 | 651 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 20947142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19183897 |
GRCz11 | 16 | 18989536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATAATTGGTTTCAGAGCCACAGAGAGATTTGATGACTGTATGAATGGG[T/C]AAGTATTTAGCTGTGTCACAACACATCATTTGACCTTCTGTTTTGGTAGA
Long Flanking Sequence:
ACAAAAGAAATGATAAGAAAACACAATAAATCCAATATTTAATAGTAATAACAAAGATTTATCAGCATTTTTATTTTTATTTTTTTTGGCTAGTAACTTTTGACGAGAAACAAAATAATTGTGAATAAAAGAGAAAAAAAGACTAGTATGCCCTGTGGGAGGAACGTAGTTTTTAGATCAATGTGATATACATTTCAGATATAAGAGAAAATCACTTCTTGAGCATAGTATTAGGCATATGGGCTAGTAACATTTTTCTTTCGCTTGCAGAGTTTTTGTGTGAGATTCATTCTTACAATCAGTTTTCAAGAACAGCAGAAACCCAGTACAAATTCTTCAGTCAAATATGTATTCTCTCTCTTCCCAACAGCAATAACTGTGAGCAAGATGCAGTAATCATCTCTGTCATTAATGCGTTCACTTCCATCTATGCGGCCACTGTCATTTACAGCATAATTGGTTTCAGAGCCACAGAGAGATTTGATGACTGTATGAATGGG[T/C]AAGTATTTAGCTGTGTCACAACACATCATTTGACCTTCTGTTTTGGTAGAAAATTGTGGTTCATGACATTCCACACAGATAAGTGTGACGACTTGAGTGACTCAGTTGTTGTTACCATGAAGGGGCATCTTATCAAAGGATTAATTCAGTATCTCTCAGCTCCAAGTTTTTAAATGTCACCACCAGAGTTATCGCATAGATGGTGTGTACAATCTATGAACAACACTTTTGATTCATTTGTAAATGTTGGGTTACTTTATGTTATGGATGCAATAAAGTTTCAAGAGTTAACTACATTAACTAAAAATGAAAGATGCAGTATTTCTAAACCATTAATTATCTTTGCTAAGCTTAGCTTTTGCTCCAACATTACAATTTTTTTTATAAATATTTATAAATACTTCATAATTAGTGGCCTTATTTAAATCAGGAATGCCCAAACTAGTGTCCACAAGCCAAAGTTGGCCCATAATAAACTTTGACCGCCATCCCATCTAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36095
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 |
---|---|---|---|---|---|
ENSDART00000079248 | Nonsense | 417 | 651 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 20950139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19186894 |
GRCz11 | 16 | 18992533 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTGTGTTCACTGAGGCAATCACCAAGATGCCACTGTCTCCACTCTG[G/A]TCCGTCCTGTTCTTCATTATGCTCTTCTGCCTTGGCTTGTCCTCCATGTT
Long Flanking Sequence:
AACTTGCATTGTGTATCAATTCTCATTACTAACTGGTAGCCTGCCCCTTTAGATATTGCCTGCTCATTTAGATATTGGCTGTTTATTTGTAATTAGAAAGCATATACACTGATTATTATTCTTTATGCCTAATTCTACCTATATCCTAACCACATTTAGAACTATTAATCAGCAGCAAGTTGGGTGTTTGATGCAAAAATAATAGTTAGAAGTGTATTAATAACAATAATTGTACCTTTAAAAAAGCGTGACAGAATAATAGGTTAGAATAAAACCATTAGTTTAGAAATGAACACATGGGGTCTTCTTAATCTCACATGAGTTTAGATAGTATAAAAAATTCAATAACTAAACAAACATCATTTCTGTATTTGTATAGTTATATGTTAAATGTAAATAAAGCTGTAAATTTGGACACTTTCACAGGGTGTAGAAGGAACGGGTCTTGCCTTTATTGTGTTCACTGAGGCAATCACCAAGATGCCACTGTCTCCACTCTG[G/A]TCCGTCCTGTTCTTCATTATGCTCTTCTGCCTTGGCTTGTCCTCCATGTTTGGCAACATTGAGGGTGTTCTGGTTCCCCTGCAGGACCTAGGGGTCTTCCCCAAAAGCTGGCCTAAGGAAATTATTTCAGGTAATAAACCAATGCTGAACCTAGGTTATTAAGCTGGAATTAAATTGGCCATATTGGCCTAGAAATGTCTTACTACACAATGTAACTGCAGAATTATCATACTTTTGATTATTTTGAATACTATTTTTGAGCAAGATGCTAATATTCTTATCTGATTCAGTGATCTATGTTAAGCTAAGCTAAAAGTGCACCCACCAGGCAGAGATCGGCTGAATGGATTAAAGAGCCCATATTATACATGAAATAGGGTCATATCTTGGTTGTAAGAGTCTCCAACAACAGTCTAATATGCATGCAAGGTCAAAAAACACTTTCATGGTCTTATAATCTGCATTTATTTTTACCTAATTATCCCAGCGACTCCTGTATG
Associated Phenotype:
Not determined