ZMP
slc7a3
Ensembl ID:
ZFIN ID:
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
solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 Gene [Source:MGI Symb
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23972 | Nonsense | Available for shipment | Available now |
| sa43672 | Nonsense | Mutation detected in F1 DNA | Not yet available |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
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
Mutation Details
Allele Name:
sa43672
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000043727 | Nonsense | 129 | 644 | 3 | 12 |
The following transcripts of ENSDARG00000020645 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 29263973)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30483217 |
| GRCz11 | 21 | 30519912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAATTGCTGGTGTGTGTGCTTTTTTTTTTTAGGTACAGCTAGCGTGGCT[C/T]GAGCTTGGAGCTCTACGTTTGATAACTTGATTGAGCAGAAGATCTCCAAC
Long Flanking Sequence:
TGTTTAAAACCAAACTGCAAATCTCCAGCTGCAATTCAGCAGAGATTTGCCACTCACACCACCAGTGACAAAGACAGACACACACAGTCACACATTCACTTACCAACACTTACAGATTTTTGGAATTTCATTTCATTATCGTCATGATGGTGATGATCCTGATAGTGTTTTTGCTATTTATTTAAAGCCACTTAATAATTAAACTGAGTGAGTTTAGCTGTTAAGTTACCTCATATGTATACCCCTGTTAAACTAATATTTTGTTGACTAATATATTAATTGATAGGTATTCTAATAATCATGGCACACAAATATTTGATCCTTGATAAAACTAAGTTTGCAATAGTGAGATGTACAGTTGAGTTGTTGAGTATGAGTAGTTTTAGTTTTTATTACATTTTAAGGACAGTGTATTTGATGCACATTTGAAAGATATTCAGAGTTTAAATGAAAATTGCTGGTGTGTGTGCTTTTTTTTTTTAGGTACAGCTAGCGTGGCT[C/T]GAGCTTGGAGCTCTACGTTTGATAACTTGATTGAGCAGAAGATCTCCAACTTCTTCAGGGCATCGATGGCCATGAAAGTTCCTGGGAAAGTCCTTGCTGAATATCCAGACTTGTTTGCCCTCATTCTCATCTTGCTACTGACTGGTGAGCAGTCGGAGAACAGACATTATCAGTTAAATGTGTTTTGAATGAACAAATGATGAAAGGAAAGTATATATTTACAAAGGGATAGATAGACAGATAGACAGACAGACAGATAGATAGATAGACAGACAGATAGAGAGACAGATAGAGAGACAGACAGATAGACAGGCAGATAGATAGACAGATAGATAGACAGGCAGATAGACAGATAGACAGATAGATAGATAGATAGATAGATTGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAAAATGTTCAATATTTTT
Associated Phenotype:
Not determined