Busch Lab

ZMP

LOC565776

Ensembl ID:
ENSDARG00000016141
Human Orthologue:
SLC6A2
Human Description:
solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 [Source:HGNC Symbol;A
Mouse Orthologue:
Slc6a2
Mouse Description:
solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 Gene [Source:MGI Symb

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa13869 Nonsense Available for shipment Available now
sa21005 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa13869
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000012580 Nonsense 562 637 12 14
Genomic Location (Zv9):
Chromosome 7 (position 36809467)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 35083310
GRCz11 7 35354787
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCTTTTCTGTGCAGTTAGTGGTGATCGCCAGCATTGTTACCTCCGGA[C/T]GACTGACATATGATGAATATGTTTTCCCAYACTGGGCAGATATGCTGGGC
Long Flanking Sequence:
ATGAAATCTCAAGAATTGTTTCCTTTCAGCTCATTTTAAATAAGTGAACAAGTAAAAAAACCATGTTAGTTTTTATAAATATGCAAAGATGTCAAATAAACTTCTTTACATTGTCATTGTGACCTATTGTTTGTAGACTTTTGAGAATTTTTTATTAATTTTAGAATAAAGCTATATAAGATAAAAATGTAAAGGGCTCTGATAGCTTTCCAAATGCACTGTACTGTATGTAACCTAACCTAAAACAATAGTACTTACAGAATGGCTGGGAACTGTTTTACTCATTGTTCATATAGAACAGTCACCTCATTTGAACTGGAAATACAGCTCAGACTATTGAGTTTTATTATTCATTTAGTCTCAGCAAATAAAAACTGCTTTCCTATGCTGACAATTTTACTCAATTTGCAATATAGCGAACTATTCCTTATTGTTTCTGTACTTCCTGAATTCTCTTTTCTGTGCAGTTAGTGGTGATCGCCAGCATTGTTACCTCCGGA[C/T]GACTGACATATGATGAATATGTTTTCCCATACTGGGCAGATATGCTGGGCTGGAGCATAGCATTGTCTTCTATGCTGTTTGTACCATTTTACGCCATCTACAAATTCTTTAGTGTGCCAAGCAGTTTTAAAGAGGTTAGTAAACCCACACACACATTGACAATTACTTACTGATATTTTTACATACAGCAATTTATAAGAACTATGCATTTTACAATATTAATATGTATCTCACTTCTATGTACAAGTTTGTCCCCACTACACCTTCATTTACCCCCAAATACACACATTCAGACATAAAATACTGGGTAGTCCACATTTTCATCTGAAAACAGAAATGATAGGTATACTGTAGTTCTAAACATTCAGCTCTTGAAGACAAATTCACTTGGTCCTCCATTAGTGGAGAGGCTCTTATTGCTTATTTCACATATACCCTTCATTGGGGGCTGCAGACTGATCCAAAGCTGCCTTTCCACTGTACACGACAAGCGACAGACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21005
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
ENSDART00000012580 Essential Splice Site 630 637 13 14
Genomic Location (Zv9):
Chromosome 7 (position 36806641)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 35080484
GRCz11 7 35351961
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACATGAACATCACTTGGTGGCGGAGGGCAATGTCAGACAGTTCAAGG[T/C]AAGACCTGGGTACAGTGTTAAAAGTCTCAATATATCTATGCAATCTGAAA
Long Flanking Sequence:
TTTTGTTTTCATGCATCAGTAAGAACACTTGGCCAATGAACTTCCAAGCTTCAGTAGATTTCATAAAGGCCATCAAGTGTTCAATGTCCTCAATAAATCTCTCCATGACTTAAATCTGTTTCATGACTCGGTGTGGTCCAAGAAATGTGAGATGTTTTCATCTATAAATGTGTCACTTCCCAAAGCCACAAGCACGCTACTGACATCTGGCTCACTTACTGTTCACACTCATATTTTCCACAAGCAGCAATCAAGCTTAAATGGCTTCAGAGATCATCTATCATACGATATGGAGAATATAATGCCACATTGCCATCTGTTTCTATGCAGATAATTAAGTTACTGTTTAGATTTGTTGTTTATTATTGTGGTGTGTTTATGCCTGGAAAAGTAGTTCACTTTGTGTGTTCGATGTCCTTTATTTCAGAGGTTAGCGTATTGTGTTACTCCAGAACATGAACATCACTTGGTGGCGGAGGGCAATGTCAGACAGTTCAAGG[T/C]AAGACCTGGGTACAGTGTTAAAAGTCTCAATATATCTATGCAATCTGAAAACACCAAATCAACTTTCCAAATCTAAGTTGATACAACTCTGCATTTTTACGGTGTAGTAAAGAGATTGAAGCCTATTTGCCAAGAAACAGAATTCTTACATGTTTTATTGTTCATTTTGTCTTATTTTTGCAGCTCAAACATTGGTTAACCATCTGATGAAGCAGTCAGGTGGGAATGACCTCTCTAATGCTACTTGAATGCTGGAGAAGATGTGGTGTGTGTGAAAGAGAAAGGTTTCAGCAAAGGTCTCATGCCATGTGAAAGTATCCCCTGAGAAAAGGACAGAGCGATGCGATGGCTTTGTGCGTTTCCCAACCACACACTATACTGTCCGGTCTGCTCCATTTGTGTTCAGTGGTTGACTTGACTTTTTTATATTGTAAAGCAAAATAAATGTTACGCCTATACTTTTTTAAAATCATACAATTGCATTTTAGTGTTAACATCTC
Associated Phenotype:
Not determined