ZMP
si:dkeyp-120h9.1
Ensembl ID:
ZFIN ID:
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
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
solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 Gene [Source:MGI Symb
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36866 | Essential Splice Site | Available for shipment | Available now |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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