ZMP

LOC559395

Ensembl ID:

ENSDARG00000051730

Human Orthologue:

SLC7A10

Human Description:

solute carrier family 7, (neutral amino acid transporter, y+ system) member 10 [Source:HGNC Symbol;A

Mouse Orthologue:

Slc7a10

Mouse Description:

solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 Gene [Source:MGI Sym

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15382	Essential Splice Site	Available for shipment	Available now
sa17817	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa15382

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
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Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000073398	Essential Splice Site	302	517	7	11

Genomic Location (Zv9):

Chromosome 25 (position 37308342)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	35721988
GRCz11	25	36271707

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACAGTGTTACTCTTACAAAGCTTTCYTAGCAGCTTTGTTTCGTTTGCTGT[A/T]GACGTTCGGTGAGAAGCTTCTCGGGAWGTTTTCCACACTCATGCCCATTT

Long Flanking Sequence:

ATTTATTTGCTTATGTTAATGTGTGAAAATGAATTTAGTTTTTATAATAATGTCATTAATATCATCGACTAATATGCAAATGTTTATAGGATTTATTTACAATACAGTTTGTGATGTAATAAATATTATATGAGAGACTTACCCCAAAAAATGGTAAATATTTATATTTATCTTATGTTTAAATCTTAATTTCATAAATGTATAACTGGTTTTGTGATGCTATGTGGCTGCATATGCAAATGTGTATATTACATTTTTTATTTCTCTCACACTCTCTCTCACTCTCTCTTAGAAATCTGCCCCGGGCCATCTACATCTCCATTCCACTGGTGACATGTGTGTACACCCTCACAAACATCGCCTACTTCTCCTCCATGTCTCCTGAGGAGCTGCTGTCCTCAAACGCAGTGGCTGTCGTAAGTGCTATTTTTTTTTACTACCAGATTATTAACAGTGTTACTCTTACAAAGCTTTCTTAGCAGCTTTGTTTCGTTTGCTGT[A/T]GACGTTCGGTGAGAAGCTTCTCGGGATGTTTTCCACACTCATGCCCATTTCTGTGGCTCTGTCAACTTTCGGGGGCATCAATGGTTACCTGTTCACCTCCTCCAGGTCAGTGCATTTCAATATACCTTTACCTTGCATCAGGAGGACTTGGGAAACTTATAAAATCCAAAAATGTGAATTATTTATTTTCACTTTTTTCTAAGAAAAAAATAACTTTGTTTTAAGCAATGTGTGCTTTAATTTCAGTTGTTCAACATTGATGTTCAATAAATAATCACCGATAGCTGATAGTGTGTGTTTCCTTCAGTTATTTTAAAATCAAGTGATGCACCCTTCATTCAATAATCTCTGACTGGTCTTATGTGAGCACATTTACTGGACATAACTTCTCAGTTAACTATGAGGGCAAAAAAATTAAATAAATAAACAAAATAATCGTTCATTATTCCTAATCAAAATGTTTCCTATTATTTACTCTATTATTATTATTATTATTATTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17817

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:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000073398	Nonsense	474	517	10	11

Genomic Location (Zv9):

Chromosome 25 (position 37306287)

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCGGTTTATTTCCTGGGGGTTTACTGGAAAGACAAGCCCAGATGCATATA[T/G]GACTTCACAGGTAAGGGGACTCGATGTGAATGCCGTCTGCTGTTAAAAAC

Long Flanking Sequence:

ACTATTCTCATGTGCATTTTGACATATTGCATACAGTTGAAGTCACAATTATTCGCCCTCCTGTGAATTATTTTTTTTAATATTTCCCAAAGGATGATTAACAGGGCAAGGAATTGTTCACAGTGTTTACTATAATATTTGTTTTATTTTGGCTGGAATAAAAGCAGTTTAAAAAAAAACATTTTAAGCTCAGTATTATTACCCCCTTAAGCAATATTTGTTTTGGATTGTTTACAGAACAATCACCCTAAAAATCATGAGATCTGCAATCAACATCTGCTGTCAGATCATGTTTTGGTATTTGAGCATGTGTGTGCTTCTCTGTGCGCTCAGGTGAGTCTGCTCGTGCCTGTGTGTTACCTGCTCTTCTGGGCTCTCCTGCTGGCCTTCAGTTTGCACTCGGAGCCGCTGGTGTGTGGAGTGGGTTTGGTCATTATGCTCACTGGAGTACCGGTTTATTTCCTGGGGGTTTACTGGAAAGACAAGCCCAGATGCATATA[T/G]GACTTCACAGGTAAGGGGACTCGATGTGAATGCCGTCTGCTGTTAAAAACTAGCCTAGATTATCGTCTGCTGTTAATAAACTAGCATAGAGCGCCGTCTGCTGTTAAAAACTAGCCTAGATCACTGTCTGCTGTTAATAAACTAGCCTAGAGCGCTGTCTGCTGTTAATAACTAGCCTAGAGCGTAGTCTGATGTTAATAAACTAGCCTAGCGCACTGTCTGCTGTTGATAAACTAGCCTAGAGTGCAGTCTGCTGTTAATAAACTAGCCTAGAGTGCTGTCTGCTGTTATTAAACTAGCCTAGAGCGTCGTCTGCTGTTAATAAACTAGCCTGGAGCACCGTCTGCTGTTAATAACCTAGCCTAGAGCGACGTCTGATGTTAATAACCTAGCCTAGAGCGTTGTCTGCTGTTAATAAACTAGCATAGAGCGCTGTCTGATGTTAATAACCTAGCCTAGAGCACCGCCAGCTGTTATTAATCTAGCCTAGAGCATCATCT

Associated Phenotype:

Not determined