Busch Lab

ZMP

LOC568699

Ensembl ID:
ENSDARG00000040610
Human Orthologue:
SLC7A11
Human Description:
solute carrier family 7, (cationic amino acid transporter, y+ system) member 11 [Source:HGNC Symbol;
Mouse Orthologue:
Slc7a11
Mouse Description:
solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 Gene [Source:MGI Sym

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa20198 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa20198
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000059440 Essential Splice Site 238 476 7 12
Genomic Location (Zv9):
Chromosome 4 (position 5678146)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 5796327
GRCz11 4 5804897
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTCTTTAAATATTTGTCATTATTTTTTATATTTCATATATTGTTCTC[A/C]GGACCGTCCCATTGGCCATCATTTTCTCCATGGTGACTGTTACTGTGTTC
Long Flanking Sequence:
TGATCCGTTTAATTAAAAACATTGATTTGATACATTAAATTAATTTGAATTAAAATGTTTAATTTAAAAAATAACAATTTTTTTGGCATTTGTAAAACATTTCCAAGGTTTGGTTCCCATAAATAAAAAATTGCACATTGAAATGAATCCAAATGCGAGAACAGAGGTGGGAAATTTTATTTCTGCTTTCAGGGAACACCAAAAACTTCCAGAATGCCTTTGAATCTGATTCTGTATCTCTGACTAAACTACCCCTGGCCTTTTACTCAGGTCTTTATGCATACGGTGGATGGTCAGTATCATCACATTCAAATATATCAAAAAATCTAAATCAAAGGACTAAAGTAAATGACGTGTTTGTTTTTGCTTGCAGGTTTTATTTAAATTTTATAACCGAAGAGGTAATTAACCCCAACAGGTAATCAGTCCTCTATGCTGTACAATATTGTTATCTTCTTTAAATATTTGTCATTATTTTTTATATTTCATATATTGTTCTC[A/C]GGACCGTCCCATTGGCCATCATTTTCTCCATGGTGACTGTTACTGTGTTCTATGTGCTGGTCAATGTGGCTTATTACACAATGATGACCGCAAATGAGTTGCTGGTATCAGATGCAGTGGCAGTGGTGGGTACAGCTGGATTGCACACTTTTTAAATAGGTTTCATTTGAGAATAAATATCATGATTTTGCTGTCTTTAATGCATCACAGACGTTTGCAAATCGGGCTCTTCAAGGTGTCGCTCCTGCAATACCTGTATTAGTGGCTCTTTCCTGCCTTGGAGCTCTGAATGGAGGGTTTTTTGGCTCACCAAGGTGGGATTTAAGAGATCTAAATTGGTTTGTAATAACTCTGACAGGTTAAAAGTGATGTTTTTATGACTCTGTTTATGCAGGATGTTGTTTGTGGGAGCCAGAGAGGGTCATTTACCGGCGATCTTCTCCATGATCCATATTCGCAGACAAACACCACTGCCAGCCGTGCTGTTTCTGGTACAGTCT
Associated Phenotype:
Not determined