ZMP

si:dkeyp-120h9.1

Ensembl ID:

ENSDARG00000020278

ZFIN ID:

ZDB-GENE-070705-534

Description:

hypothetical protein LOC566469 [Source:RefSeq peptide;Acc:NP_001093492]

Human Orthologues:

SLC7A6, SLC7A7

Human Descriptions:

solute carrier family 7 (cationic amino acid transporter, y+ system), member 6 [Source:HGNC Symbol;A
solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 [Source:HGNC Symbol;A

Mouse Orthologues:

Slc7a6, Slc7a7

Mouse Descriptions:

solute carrier family 7 (cationic amino acid transporter, y+ system), member 6 Gene [Source:MGI Symb
solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 Gene [Source:MGI Symb

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa3008	Essential Splice Site	F2 line generated	Not yet available
sa36866	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa3008

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103636	Essential Splice Site	236	487	4	10
ENSDART00000128391	Essential Splice Site	236	490	4	11

Genomic Location (Zv9):

Chromosome 19 (position 33001392)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	32168681
GRCz11	19	31755994

KASP Assay ID:

554-2643.1 (used for ordering genotyping assays)

KASP Sequence:

GCTGGGATACCCTGAACTTCATCACAGAGGAGATTAAGAACCCAGAGAGG[T/C]ACAAACATCCATGACATTTTGCTTGATATGATAATAATCTRTTAATAATC

Long Flanking Sequence:

AATAATCATTTTTTGAAAAAAAAAAAAAAAAAAACATTATTGTACGTCTGTTTGTAAGACTGTTCTTGAGCATCAAACCAGCATATTGATTTTTGAAGGATATATGAAGGATTATATATTTATATATATATATATATATATATAATATATATAATAATTTTTATTTATTTATTTTTTAATAATACCTTGAAATAGTTTTTTTTTATTTTAGATGTATTTTTAACAGCATTACTATTTGTGCATTTTTAAAATATAATAAATACAACCCTGATAAACCGTAGTGCTACACATTTATATTTTATTAAGTCATTTGCCATTTGTTTCTCATGTTTTTTACAACAATTTGCATTTCAGGAGAAACAAACAACTTTAGGGATTCATTTGAGAATTCTAAACTGGATCCAGGCAACATGTCTTTGGCTCTGTATGCCGCTCTGTACTCTTACTCAGGCTGGGATACCCTGAACTTCATCACAGAGGAGATTAAGAACCCAGAGAGG[T/C]ACAAACATCCATGACATTTTGCTTGATATGATAATAATCTGTTAATAATCATTTAAGTTAATAAGAACCAAATATAATCGAATTGTTTACTACACACTCACTTCTTAGATGCAAATATAATTCATTAAACCATCACAGGGTTGCTCCGGAAAATGTAAACTTTGTAGCTCTTTGCTCGTTTTAAAGGAATAGTTCAACCAAAAAAAAAAGCTTACCTGCCCTCAAGCTCTTCTAAACCTGTTTAAGCTTCTTTCTTCTTTTAAATGCAATAGAAGATAATTTTGAAGATTGCTATTAACCAGTTGTCATTGACTTCCATACCTTTTCCCTACTGTACATTCTTCAAAATTGATTCTACTTTGTTCAACTTCATAATAACAATGAAAACTCATGATGGTTTGGAATCAGTTAAGTAAATTGTGAGTAACTGTTTTTTTAATAAAACAAACTATGTCTTTTTAAAGAGTTAAACCCAAAAATAAAACTTGTTCTATTATTGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36866

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
ENSDART00000103636	Essential Splice Site	277	487	5	10
ENSDART00000128391	Essential Splice Site	277	490	5	11

Genomic Location (Zv9):

Chromosome 19 (position 32999807)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	32167096
GRCz11	19	31754409

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCAGTGCTGGACATGAATACTCTGTTACAGAGTGAAGCCGTGGCTGTGG[T/C]GAGTAAAACTTGGCTTGAAGCTAATCTTTTATCATCGCATCCCAATAACT

Long Flanking Sequence:

AGACCACTAATATACAGCCAGGGATGGTCAAAGTCCAGAAAAGGAACCAAAACATTGTCTAAACAGTCCACATGACTTCAGTAATGTGAACCTCCAAGAACATTTTTGTGTGTGGGGGGAAAATTTTTTTTAAAAAAAGACTTTGTTCACCAGTGTCTACAAGCAATACACTTGTGTGTTGTGTTTCTGACCTTAAATGTTTGAGGTAGGGCCCACACACAAATAAAATTTGTGTTTGGAAACCTGTTTGAAAACGGGAATTTGCAATCCCTTGAGATATAGAAATATATTGAGCTTGATTTACTAATGACTATACAACAGTTTCATTGAATCAAAATAAAGTATTCACATTAAATCTCTATTTCTCTTTTATAGAAATTTGCCGTTGTCAATAGCAATCTCCATGCCCATTGTCACAATAATCTACATCCTAACTAACGTGGCTTATTATGCAGTGCTGGACATGAATACTCTGTTACAGAGTGAAGCCGTGGCTGTGG[T/C]GAGTAAAACTTGGCTTGAAGCTAATCTTTTATCATCGCATCCCAATAACTCTAGCTACTGTATAACCAAACTCAATTTTTTTTAACCACATGATCCTGTATGCCTCGTGCAAGTTAATTGTCTGCGTCTGTTCAGTTTATTTGCTCCAGATTTGATCATGTTTTCATCTCCTGTTACTCTGATCTAGTTAAGCAGAGCAGCTTGAGGCAGGTCCTCTCTCTAGAGATGCTCCATGACATTAGTCCAGAGCCACAGACGTTCTGCTGCCTGCAATTAGGCTAGTTTGCTGCTTCGGAAAGAGTTTTTATGGCTATAATGTCCCATAAACCATGTTTACTGTTTTTGATGCACTGTTTTGTTGCTGATTTGAGGCAGCTGTAAATTACTCCAAAGAATTGTTGTTTTTTCTGTAAGAATCTTAACAGCAGTTCAGCAAATACTAAGCATTTGGAACGACTGCAGCTGCATGAAATATGGAGAAGATGCAAGTAAAATTGTGC

Associated Phenotype:

Not determined