Busch Lab

ZMP

slc6a6

Ensembl ID:
ENSDARG00000058440
ZFIN ID:
ZDB-GENE-030131-3077
Description:
solute carrier family 6, member 6 [Source:RefSeq peptide;Acc:NP_001032750]
Human Orthologue:
SLC6A6
Human Description:
solute carrier family 6 (neurotransmitter transporter, taurine), member 6 [Source:HGNC Symbol;Acc:11
Mouse Orthologue:
Slc6a6
Mouse Description:
solute carrier family 6 (neurotransmitter transporter, taurine), member 6 Gene [Source:MGI Symbol;Ac

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa24206 Essential Splice Site Available for shipment Available now
sa37556 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa8569 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24205 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24206
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064082 Essential Splice Site 204 500 4 11
Genomic Location (Zv9):
Chromosome 22 (position 34312087)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 31596636
GRCz11 22 31513550
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTGCGAACGCCACTAACTTCACGTCCCCCGTCACTGAGTTCTGGGAG[T/C]AAGTATATGTTAATCAAGTACACATTTGTAAGTCATCCCGAAAAGTTGTG
Long Flanking Sequence:
AAGATCAGACTCTGAACCAGTGACTTACATCATTTTCCTCCAACCTTGGATAAGATTGTTCTATGTTTATATTACAAGGACAAGAAGGTCTCATATAAATTTGTGACTTATTTAACCATTCTCGCGCTCTGCTGGAGCACAACTTATTTCATTGCTTTCATTGAGGTTATAATAAAATAACTCAATGATCACAATGATCTACCACACACTGAGGCAGGTCAGTGTGGCATTGGCTTAATGTCGGCACTCCTGTCTTTGTACCAGGTATTGGCTATGCATCCATCGTGATCGTTTCTCTGCTGAACATCTACTACATTGTGATCCTGGCCTGGGGCTTGTACTACCTGTTCCAGTGCTTTCAGCCCGAGCTCCCCTGGGCAAGCTGCAACAACAAGTGGAACACAGAAAACTGTGTTGAGGATACTCTCCGCAGGAACAAGACACTCTGGGCAGCTGCGAACGCCACTAACTTCACGTCCCCCGTCACTGAGTTCTGGGAG[T/C]AAGTATATGTTAATCAAGTACACATTTGTAAGTCATCCCGAAAAGTTGTGGAGTTATGAACCAAAGACATTGCCACATTTATTAATACAGTTGTCCTCTATCACTTCAAATAACTTTGGAGCTCATACCCTTTTGGTGACATTCTCAAATTAAATACATATTAATTTTTTAGATGGACCATATTTTCTTGAGATAGATTAAGCACACTGATCCTGGAACTCCGTCGTCCTAAGGGCTTTAGATAAGGGGTGTTCAAATCTGGACTGCACTGCATTGTACTGTACTTTATTGTACTGTACTGCACAGTTGAGCTCCTACCCTAATTAGACACACATGAACAAGTTAATCAAGGTCTTCTGACTTAGTAGAAACTGCTGAAACTGATTGGGTGAAAATCTGAAGGATGTTCAACCTTTTGGAACTGAAGCTTTTCTTCTATTTAATGACAGTGGTTTCAGCCAAAAATATTATGTTTTATGTATTTTTTTTGAAAAGTGGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37556
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064082 Essential Splice Site 293 500 6 11
Genomic Location (Zv9):
Chromosome 22 (position 34308019)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 31592568
GRCz11 22 31509482
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCAAATTTTATCTGTACCCAAATGTGACTCGCCTCGGAGACCCAGAGG[T/G]AAGATCTCATGGCTATTAACATGTCTCCTCAAGATGCTTTACAATATTAC
Long Flanking Sequence:
GTTGACATGGCTATTTTAAATCTACTTGAGGATAAGTAATGTTTTGACATTCAACACTGTGTTCAAAATAAAATCTGCAGCCAAACCAAACATTACAAGATGGGAGAAAAACAGCACATTATTTCCTCACTGTCTGACCAAAAATTACATTGAGTCAGAGAAGTTAATCTGTAAATTGCATGTTAGCCTAGAAAACTGTTGGATGGTGTCGTTTCAGAATGTGGAAAGTTTGACATGTCTTTCAAAGACCTTGTGAAAAAACTCTGCTTTTTTAGTTTTGTCAAATCTCAAACACAACTTAGTGAGATTTTCATAGAAAAACAGCATTCATTTTAACCTCAGTGTTTTTGGCTCTTCTACTTAGGTTGTGTACGTCACAGCAACATTCCCATTTGTCATGTTAATTGTCCTGCTAGTACGTGGTGTCACACTTCCTGGGGCAGCCGAGGGCATCAAATTTTATCTGTACCCAAATGTGACTCGCCTCGGAGACCCAGAGG[T/G]AAGATCTCATGGCTATTAACATGTCTCCTCAAGATGCTTTACAATATTACCAACCACTGAAACTCAATTCCACAATATCTCAAGTGCTTCTAACACATGTATTGGGTCACTAAAGCCATCGTTCTTACTATAAAGACCATCATAGTTGGTTCCTGGCATAAGTTGAATGAGGTTTTAAAAGGCTTCTTGGCCGGCTAACTTTAACATAAGGACCAACTATTGCTTGACCAAAGTCAAAACATAGGTTAACGACTTGGCAATCTAAAATGGATTTTTCAGCAGTAAAAGTGCTGTTTACAGTTGTTGACATAATGTAAACCAATTACCCTTCGCAACTTAAAAACAGAATAAACTTCGGATGTACAGTTTACAGACAGAAACCCAAGATGTGCAAAAGAGTCGACATAAATAAAGCTTGTGATGGCTTCGGTCAGAAAGCTACAAATCTAAACATGACATGTAGTCGTTGAAACAATTTATATAAGTCCTTAATGGTGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8569
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064082 Essential Splice Site 328 500 7 11
Genomic Location (Zv9):
Chromosome 22 (position 34307314)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 31591863
GRCz11 22 31508777
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCATGACGTCACTGGGAAGCTACAACAAGTACAAATACAACTGCTACAG[G/A]TGGGTTTCGATACCCCGGGGCTGGGAGGGGGGCTTAGTCMAGTCAATGGG
Long Flanking Sequence:
CATAAGGACCAACTATTGCTTGACCAAAGTCAAAACATAGGTTAACGACTTGGCAATCTAAAATGGATTTTTCAGCAGTAAAAGTGCTGTTTACAGTTGTTGACATAATGTAAACCAATTACCCTTCGCAACTTAAAAACAGAATAAACTTCGGATGTACAGTTTACAGACAGAAACCCAAGATGTGCAAAAGAGTCGACATAAATAAAGCTTGTGATGGCTTCGGTCAGAAAGCTACAAATCTAAACATGACATGTAGTCGTTGAAACAATTTATATAAGTCCTTAATGGTGTATACAGTTCTGAAGGACCTTCGAGAGGCAGAACGCATGCAAATATTTGAGTTTGCTCTATTCATGTTGTCAGTCAGTGAATGGTTTGGCGTCTTGTGTACAGGTTTGGATTGATGCTGGGACGCAGATTTTCTTCTCTTACGCAATCTGTCTGGGAGCCATGACGTCACTGGGAAGCTACAACAAGTACAAATACAACTGCTACAG[G/A]TGGGTTTCGATACCCCGGGGCTGGGAGGGGGGCTTAGTCCAGTCAATGGGCAAAGTGGGAACACAGGGAACCTGTGTTTTAATTAACAAACTCCATGACATATGTGTGACATAGGGACTGTTTGCTGCTGGGAGGCCTGAACAGCGCTACCAGTTTTGTGTCTGGCTTCGCAATATTTTCCGTCCTGGGCTTCATGGCACAAGAGCAAGGGGTGGACATTGCCGATGTGGCAGAGTCAGGTACGAGGGTCTAGTAGCAGTGATGGTGGGCACTGCTGCAGCAAATAACATGAAAAAACTTCGGCAAAAAAATACGACAATAACATTTTCGGAGCCAGTAAAATAAGTTTCGGGATCTAAACCCATAAAATTTGGAACCTTCACCATCATTGAGCAGATTAAAACCATTCAAAGTGTTGATGCATAAGGCGGGCTCAGCGAGAACTGGAATTCGCTTGGAATCGTCTGTAGAACTTAATGGAGAGAACTTTCTTGGAGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24205
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
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064082 Nonsense 496 500 11 11
Genomic Location (Zv9):
Chromosome 22 (position 34300392)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 31584941
GRCz11 22 31501855
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATTGCTGTAGCCTGGGTTTATGGTGAGTACAAGACTTGCACAACTTA[T/A]AATGGGGTTATGTAGTTGTAGCATCTCTTGAAATGGGTGTTTCATTACTT
Long Flanking Sequence:
GAGCAGTGAAAATTCCACAGAGGAATCAAACTGCTAAACTAGGAGATCCGGCCTGCTCTGACAATGCACATCTAGGATTCCTCTGGCCCCCTTCAAATCTCGGCCCCTGATTGCTAAGCCCCCGGAACAGCGATAAACTGAGAATGCTATTATGCGGCTGGAGCCACACAGTGTCCCATTTTTTTTCCATGACATAATGTCTTATGTCACCCCTGAATGCATTGTGCAACAAGTCTAAAAGAAAACTAGTCAAGTGTTTAGCCAACCCCTGGTCACAACAGTCCCCCATTGTGACAGCCTTTAGCAATTACAGCATGAACTAGAGCCTGAGCGCTTTCTCATTTGCTTTTGTCTTTTATTTTTGTTTTGCAGGGTGGCATGTATGTGTTTCAACTCTTTGACTACTATGCAGCCAGTGGCGTGTGCCTTTTATGGGTTGCATTCTTTGAATGTATTGCTGTAGCCTGGGTTTATGGTGAGTACAAGACTTGCACAACTTA[T/A]AATGGGGTTATGTAGTTGTAGCATCTCTTGAAATGGGTGTTTCATTACTTTAAAGTAATGAATCCATTTAGGCTTGATACTGCATGATGTTTACTGTATAACACGTATAACAATTCACTACCTGACAAAATTCTTGTCACCTATCCAACAAATAATAAATTGACTTCTAGTTGATCATTTGGTGTTAAAAATACATTTTATTTAAAGGCGCCTTTCTAGCAACTCAAGGACACCGTACAATCAACAAGAATAATAAAACAACTAGAGAAATAATAAAATATACACAGCAATAGTGCAAATAAAATTAAGTATTAAAAGCCATCTTAAATAAGTGGGGTTTAAGTTTTGATTTGAACAATGTAAGGGAGTCAATGTTTCTGGTAATGAGCAGGGGCGCAACTGCACATTTACTGATGGGTATGCGGCTTCAACTTTTGCGCGCCCCCCTTTAATCCAACTATATTTTATAACAGGCAAGTGATAAAATGTGGAAAATATTT
Associated Phenotype:
Not determined