ZMP

slc7a3

Ensembl ID:

ENSDARG00000020645

ZFIN ID:

ZDB-GENE-041114-206

Description:

solute carrier family 7, member 3 [Source:RefSeq peptide;Acc:NP_001007330]

Human Orthologue:

SLC7A3

Human Description:

solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 [Source:HGNC Symbol;A

Mouse Orthologues:

AU018091, Slc7a3

Mouse Descriptions:

expressed sequence AU018091 Gene [Source:MGI Symbol;Acc:MGI:2142124]
solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 Gene [Source:MGI Symb

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa23972	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa23972

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000043727	Nonsense	83	644	2	12

The following transcripts of ENSDARG00000020645 do not overlap with this mutation:

ENSDART00000101021

Genomic Location (Zv9):

Chromosome 21 (position 29260953)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	30480197
GRCz11	21	30516892

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTATGCTTCCTCGTGGCCGCTCTTTCCTCCATGCTGGCTGGATTGTGCTA[T/A]GCAGAATTCGGCGCTCGAGTCCCGAAGACTGGATCTGCATACTTGTATAG

Long Flanking Sequence:

AAATCACAAAATGGTGCATTCACTGAAGTCTGGAAATGATTTGTAGTGAACACTATGTTCAGCAGTAAAAAAAAAAACACTGTGAAAAAACAAGTCCTAACTAGATCAGTTAGATTAAAACTAGACGTACTGTCTTGTGTAACCGACTTTTACACACCCAGATGTGTCTAATTCTTCCTTCCTCTTTTCTGGGCTCTTCTAGGCAAATAAAAACCAGCACAACCAACAACCTCACCAGATCTGGAATTAACCATGGTGGACAAGATGGCCTCTTTCGGACACATCCTGCTGCGGCGGCGGGCGCTAGATTTTTCAGGAGAGGAGACGCGGTTTGCTCGGTGTTTGTCCACACTGGACCTGGTGGCTCTCGGCGTGGGATCAACACTGGGTGCTGGAGTTTACGTTCTGGCTGGAGAAGTTGCAAGAGAGAAGGCTGGTCCTGCTATAGTGTTATGCTTCCTCGTGGCCGCTCTTTCCTCCATGCTGGCTGGATTGTGCTA[T/A]GCAGAATTCGGCGCTCGAGTCCCGAAGACTGGATCTGCATACTTGTATAGCTACGTAACAGTTGGCGAAATCTGGGCCTTCATCACTGGTTGGAACCTCATCCTCTCATATGTTATAGGTAAGTTTAGTACTAGAGTGCCCTCCATTGATATTGGTACTTTTGGTTAAAATGAGCAAAGTGTTTATTGATTAGTGTGTTTATTGATTGAATGAATGTAAATTACCTTATTTTCTCCTCCTCATGTTGTTTTAAACCTTTATGAGTGTCTTCTGAAGAAAACAAGATTCTGAAGAACACCGGTTGTCGGGGGGTTGTCAGCATTTTTGCTATAATTAATATATCTTCTTTTATATTCAACAGAAGAGTTATGCTTTGCTTGAAAGGGGTGATCGTTAGACTGTCACAACAAATTTAGAATTATGACATGACACTTGTCATAAGCACCTATAAAATCTCATTTTTATTTATGACACATTTTATTAAGTGTCATTCGCTCAGT

Associated Phenotype:

Not determined