ZMP
ENSDARG00000089192
Ensembl ID:
Mouse Orthologue:
Slc7a15
Mouse Description:
solute carrier family 7 (cationic amino acid transporter, y+ system), member 15 Gene [Source:MGI Sym
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13935 | Essential Splice Site | Available for shipment | Available now |
sa36530 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13935
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 |
---|---|---|---|---|---|
ENSDART00000128764 | Essential Splice Site | 320 | 467 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 50063687)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49437374 |
GRCz11 | 17 | 49537279 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCAGTGGAGGACGAGTRTGTTACGTTGCAGCAAGAGAGGGCCATATGG[T/C]AAGAAAGTGTATTTGARGAYAACAGGAAACNNTATTGGGTTAAAATAGTAGA
Long Flanking Sequence:
TGGCTCCATCAGACAGTCCTTCTGCGCATGTCAAGGCTCCAATTTCAGCAGGCTTTTGCGACAGTTTGTGCCTGTCAAGCAGGCGTTTTGCCCTCAAGGCGTTCAATGGGTCGTGTCGTCCATATTTTTTACAGTCATTGGTGTAATCCATACCTGCCAACACTCCCGTTTTGTTGCTTCTCCCGGAAATCTCCAGTAATTTCACTAGCACCCCTGTGGTTTAGATTAATAAAGGGACTAAGCCGTAAAGAAAATGAATGAATGAAATGATATATTGTATTGTTCTTTCTCATGTTCTTGGTACTCATGTTAGCCACAGATTTTAATTTGATGATGTAAACCCTTAGTTATTTTTCTTTTTTGTGACAGAAATAAGGTGTTAGGAGGATGGGGCTGGGTGATGTCCATTGCTGCAGCACTCTCATCCTTTGGTTCTCTAAATGGATCCTTTTTCAGTGGAGGACGAGTGTGTTACGTTGCAGCAAGAGAGGGCCATATGG[T/C]AAGAAAGTGTATTTGAAGATAACAGGAAACTATTGGGTTAAAATAGTAGACTTTGTAAATGTAAAGAAGCAATGCATTTGCTAAATAATGGGTTCAGGAAAATGCCCCTTACCTGTGATTTGTGTGAATTTTCTTAAGTGCAATCACATTCCATGAAAATGAACTGGACAAGTGCTATAAAATGTATTTCTGTCTTTCAGCCTGACATACTAGCCATGGCTCACATGCACCGGCTTACTCCATCTCCTGCCCTCATTTTCAACACTGTCATTGCTCTTATTGTTCTCATTCCCGGGGACTTCCAGGCAATAGTCAACTTTTTAAGGTACTGCGCCTTATTTGGATAAAACTTTCTGCAAAATCCATCTATGTACTATTTTTGTAATCTTCACTATGCACTAATCATTTGAAATTAAATAATTGGGAAAAAAGTTTGAATGTTTGAAACTCAACTATTTTATAGAATACAGTTAGATCGAGATATCATTGATGATCTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36530
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128764 | Essential Splice Site | 362 | 467 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 50063360)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49437047 |
GRCz11 | 17 | 49536952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTGTTCTCATTCCCGGGGACTTCCAGGCAATAGTCAACTTTTTAAGG[T/G]ACTGCGCCTTATTTGGATAAAACTTTCTGCAAAATCCATCTATGTACTAT
Long Flanking Sequence:
TTGATGATGTAAACCCTTAGTTATTTTTCTTTTTTGTGACAGAAATAAGGTGTTAGGAGGATGGGGCTGGGTGATGTCCATTGCTGCAGCACTCTCATCCTTTGGTTCTCTAAATGGATCCTTTTTCAGTGGAGGACGAGTGTGTTACGTTGCAGCAAGAGAGGGCCATATGGTAAGAAAGTGTATTTGAAGATAACAGGAAACTATTGGGTTAAAATAGTAGACTTTGTAAATGTAAAGAAGCAATGCATTTGCTAAATAATGGGTTCAGGAAAATGCCCCTTACCTGTGATTTGTGTGAATTTTCTTAAGTGCAATCACATTCCATGAAAATGAACTGGACAAGTGCTATAAAATGTATTTCTGTCTTTCAGCCTGACATACTAGCCATGGCTCACATGCACCGGCTTACTCCATCTCCTGCCCTCATTTTCAACACTGTCATTGCTCTTATTGTTCTCATTCCCGGGGACTTCCAGGCAATAGTCAACTTTTTAAGG[T/G]ACTGCGCCTTATTTGGATAAAACTTTCTGCAAAATCCATCTATGTACTATTTTTGTAATCTTCACTATGCACTAATCATTTGAAATTAAATAATTGGGAAAAAAGTTTGAATGTTTGAAACTCAACTATTTTATAGAATACAGTTAGATCGAGATATCATTGATGATCTTTAATTACAGGATTTTTGTTAAATTTAGACCCATAATTTTAGAACAAACAGAATTGAAAATATTAATTCATAGTCTGTATATTAACTGTTTATGCAATTTGTCTGTTCATTTACACAACAGCTTGGAACTGAACATGCTAAATTCTTAAAATGAGTTACAAAGTGTCAATTTGTAAAAATACCACTGTTGTTGTGTCTGTGTAAACACCCGAAAGATTTTTGAAAATGATATGTGTGTGTATGGAAGTTCAGATCATTTTACTGACTCGGATCTTTGGGTCTAGTTCATCGAGACGAATCTTTTTTCGAGTCATTTCGTTCATTTGGTTCA
Associated Phenotype:
Not determined