ZMP

B0R025_DANRE

Ensembl ID:

ENSDARG00000054343

Description:

Novel protein similar to human solute carrier family 7 (Cationic amino acid transporter, y+ system),

Human Orthologue:

SLC7A8

Human Description:

solute carrier family 7 (amino acid transporter, L-type), member 8 [Source:HGNC Symbol;Acc:11066]

Mouse Orthologue:

Slc7a8

Mouse Description:

solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 Gene [Source:MGI Symb

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa10837	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa10837

Status:

Available for shipment
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Availability:

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Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076523	Essential Splice Site	471	501	10	11

Genomic Location (Zv9):

Chromosome 2 (position 38020986)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	38335900
GRCz11	2	38318228

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTTGGCATCTATTGGGAAAATAAGCCCAAGAGCTTCAGTTCTTTTGTTGG[T/A]ATGAAGAAATCTTAAATCTTATGTGATAATGTTAAARAKGATTTACAAAT

Long Flanking Sequence:

TATCTACTCTGCTGATGCTGTGTGTCAGTGACATATACACCCTCATCAACTACGTTGGCTTCATCAACTACCTGTTTTATGGGGTCACTGTTGCCGGGCAGATTGTGCTTCGCATCAGAGAGCCAGACATATATCGGCCAATCAAAGTAAGACTCAATCCTATTGACTATTTGTTAGTTATGACTTGGCAGCAAACCCTGAGAACTGTCAGATCCCAGCAGTTGCTATGAACAGCAATTATGCATAATTATAGATTTCTGTGTTTGGTGTTGCGCATTTTGTAGTTCTCCACAGAAAAAATCAACAAGTTTCACTCCACAGGTGAGCTTGGCATGGCCGGCAGTTTTCCTGATTTTCTGGGCTTTCCTGCTGATCTTCTCTCTGTACTCGGAGCCTGTGGTGTGCTGTATTGGTCTGGCCATCATGCTATCTGGGGTTCCTGTGTATCTGTTTGGCATCTATTGGGAAAATAAGCCCAAGAGCTTCAGTTCTTTTGTTGG[T/A]ATGAAGAAATCTTAAATCTTATGTGATAATGTTAAAAATGATTTACAAATGTCAGTCACATTCGCTTAAGACTCAACAGACTGTAAATGAGGGCCACTAAAAACACTCCATCTGCCATTGTATGTACACACAGCCAGACTGACACACTTGGGGCAGAAGTTGTGCCTGGTGGTTTACCCTGGCGAGGACAGAGAAGATGGAAATGAAGACAGAGAGGAAGATGGATAGGATTACAGCAAGAAGTAAATTTTATGGTTATATTGATGGGTATTCATGCGTCAACTTTCAGTAATATAATTCTTGATAGATTTTGAAAATGCAAATATGCACACAGTTAAGAGACTAATTTAATACAGGGTGTCCACCGGGTCTTACAAAGTCTTAAAATGTCATAAATTTCAAAACAAATTATATATATATTATTAGATAACTTTTATATATATTTATATATTTTATATATTTTATATATATTTTTTATATATATTTTAACAAATTATATA

Associated Phenotype:

Not determined