ZMP
slc1a2a
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 1 (glial high affinity glutamate transporter), member 2a [Source:RefSeq pepti
Human Orthologue:
SLC1A2
Human Description:
solute carrier family 1 (glial high affinity glutamate transporter), member 2 [Source:HGNC Symbol;Ac
Mouse Orthologue:
Slc1a2
Mouse Description:
solute carrier family 1 (glial high affinity glutamate transporter), member 2 Gene [Source:MGI Symbo
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34174 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30892 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41004 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa729 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34174
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073932 | Nonsense | 19 | 548 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 51322094)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49592330 |
| GRCz11 | 7 | 49865106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCAAGTGGAGATCAGAATGCATGAGAATCATCTGGATCCTCTTCCA[G/T]AGCCTGAAGAGTCCATATGTGGAAGCTGCTGTGACAAACTCATGAAGAAC
Long Flanking Sequence:
ATCATGACATTTCCAGTAAACCTGGGTCTGCTGATGTGATCTATACACTATCTTCACATTCTTCTTAATTTCATCAGATCTTATTTTGGATTTTTATCACTGTGGCTATTGCTTTATATCAAATTTGAACTCTGAAAACACATTTTTAGTATCTGGAACTGCGTATTTTCATTCCATTCTGGTTCACGAACATTGATTGCATCAGTTAGATTAAAACTGCACTGTCATTCAGTGTTGTTGTGTCTGCAGCACATCATACACAAACATGTTTTTGTCACACGTACTGGAATACAACGGTTTGTATTGATGACAATGAATGGATTTTACTTGGTGGTTTACAGAAGCTTGTGTAAAATCACAACCAAAGCTGGTAGTGTATGCCAGATCATTTATATTGACATAGTTTACTGTATGCTTCGCTTTTGTTGTCCTCCAGTGCCAAGAAGATGCAGAAGCAAGTGGAGATCAGAATGCATGAGAATCATCTGGATCCTCTTCCA[G/T]AGCCTGAAGAGTCCATATGTGGAAGCTGCTGTGACAAACTCATGAAGAACCTGCTTCTAACGCTCACTGTTCTGGGCAAGTCTTTCTTCATGTTTGTATAATCAGTGTGTATTAGTTTGTTTTGTACTTAATAAATGTTGCTAACAGGCAAAAAACAAACAAACAAACAAACAAAAAAACTTATTACTGTTTGTGCTAAATTATGCACTTTTTAAATGATGTGTTATATGACACCACATTTAGGTTAACCATGCATTGTAAAACACTACTGTAAAATTTAAAGTATTACAGGCAGTTTTGGTTGCCATTAAAATTATACAGTCTACAAGTTCACTGTAAAATAACAATAACAATTGTTATTGTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30892
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073932 | Essential Splice Site | 224 | 548 | 5 | 10 |
| ENSDART00000073932 | Essential Splice Site | 224 | 548 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 51327058)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49597294 |
| GRCz11 | 7 | 49870070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATCATTAACGTACATCGCATTAAGATGATGTGTTATGTGTTCTTGTA[G/A]GTATCATTGGTTTCTTTGTGGCATTTGGGATTTGCATGGGAAAGATGGGA
Long Flanking Sequence:
TTCTGGTGCTCCTCATCCACCCTGGAAACCCCAAACTCAAGGCAAACCTGGGCGAGGGCAAAAAGAATGACGAAGTGTCCAGTTTAGATGCCTTCTTTGATCTCATCCGAAATCTGTTTCCAGAAAATCTCGTTCAGGCTTGTTTCCAGCAGGTTTGTGTTCCTAGAGTGCTTTGTTTTTTTATTTAATCTCATTCTTTAAACTTATTCTGTAAATTTTATAACAGTTAATGGTCTCTCGTTAATATTCAATGTCTTAATGATTCATATAAAATGTCTTTTAGATCCAGACTGTTACTACTAAGGTGGAAATCGCTCCTCCTCCCCCTCCAACTCGGTTTGGACGAAACGCTACCAAGGGTGCAGCGAAATATGTGATCAAGAAATCTCTTCAGTTCAAGAGCGGCATGAATGTGTTAGGTATCAAATGGCTTCATGATATATGCATGAAAAGATCATTAACGTACATCGCATTAAGATGATGTGTTATGTGTTCTTGTA[G/A]GTATCATTGGTTTCTTTGTGGCATTTGGGATTTGCATGGGAAAGATGGGAGAGAAGGCCAAACTGATGGTTGATTTCTTCAACACTCTCAATGAGATCGTTATGAGGCTTGTCGGCATGATCATGTGGTCAGTATTCATGATTTTAATCCCATTGATCACATTTCATACTATTTTTTGACTGATTTATTTACTGTGCAGATAAAGTACACTGTAAAAAGCAATTAGTTGACTTTACTAAATAAAAACATGTCAACTAAATATGTCGCCTTATGATTATTAGGTAAACAAATTAAAAGTTAAGTCAATGTATGCCTTTTTGTAAGTCAAATTAATTTGTTGCCTTTTAAGCAGCAAGTTTACTTCACTTTTTGGAGTGCATATAGTAGTCAACATTTCAAGTGGATCAACAAGTTCTAAAACTTTTAAACAACACTCATTACTACGGAGACCCGGAAAGGACATGAATGAGGTGGAAAAAATGGATGGGAGAAAAAAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41004
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073932 | Essential Splice Site | 224 | 548 | 5 | 10 |
| ENSDART00000073932 | Essential Splice Site | 224 | 548 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 51327058)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49597294 |
| GRCz11 | 7 | 49870070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATCATTAACGTACATCGCATTAAGATGATGTGTTATGTGTTCTTGTA[G/A]GTATCATTGGTTTCTTTGTGGCATTTGGGATTTGCATGGGAAAGATGGGA
Long Flanking Sequence:
TTCTGGTGCTCCTCATCCACCCTGGAAACCCCAAACTCAAGGCAAACCTGGGCGAGGGCAAAAAGAATGACGAAGTGTCCAGTTTAGATGCCTTCTTTGATCTCATCCGAAATCTGTTTCCAGAAAATCTCGTTCAGGCTTGTTTCCAGCAGGTTTGTGTTCCTAGAGTGCTTTGTTTTTTTATTTAATCTCATTCTTTAAACTTATTCTGTAAATTTTATAACAGTTAATGGTCTCTCGTTAATATTCAATGTCTTAATGATTCATATAAAATGTCTTTTAGATCCAGACTGTTACTACTAAGGTGGAAATCGCTCCTCCTCCCCCTCCAACTCGGTTTGGACGAAACGCTACCAAGGGTGCAGCGAAATATGTGATCAAGAAATCTCTTCAGTTCAAGAGCGGCATGAATGTGTTAGGTATCAAATGGCTTCATGATATATGCATGAAAAGATCATTAACGTACATCGCATTAAGATGATGTGTTATGTGTTCTTGTA[G/A]GTATCATTGGTTTCTTTGTGGCATTTGGGATTTGCATGGGAAAGATGGGAGAGAAGGCCAAACTGATGGTTGATTTCTTCAACACTCTCAATGAGATCGTTATGAGGCTTGTCGGCATGATCATGTGGTCAGTATTCATGATTTTAATCCCATTGATCACATTTCATACTATTTTTTGACTGATTTATTTACTGTGCAGATAAAGTACACTGTAAAAAGCAATTAGTTGACTTTACTAAATAAAAACATGTCAACTAAATATGTCGCCTTATGATTATTAGGTAAACAAATTAAAAGTTAAGTCAATGTATGCCTTTTTGTAAGTCAAATTAATTTGTTGCCTTTTAAGCAGCAAGTTTACTTCACTTTTTGGAGTGCATATAGTAGTCAACATTTCAAGTGGATCAACAAGTTCTAAAACTTTTAAACAACACTCATTACTACGGAGACCCGGAAAGGACATGAATGAGGTGGAAAAAATGGATGGGAGAAAAAAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa729
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 |
|---|---|---|---|---|---|
| ENSDART00000073932 | Essential Splice Site | 344 | 548 | 6 | 10 |
| ENSDART00000073932 | Essential Splice Site | 344 | 548 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 51329922)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49600158 |
| GRCz11 | 7 | 49872934 |
KASP Assay ID:
554-0636.1 (used for ordering genotyping assays)
KASP Sequence:
TCATGGGACTTTTCCAAGCTTGGGTCACCGCCTTAGGAACAGCTTCCAGG[T/C]TAGTCACTTTCCTTTAATTATGTTTTCCCTTAGATATTTGTATGACACAC
Long Flanking Sequence:
TTTAGGTTTAGATATTGGGTAGGACTAGAGATGTAGAATAAGATCATTCTTTATGAGTACTAATAAAAAGCCAGTATCATAATAATAAACATGTAATAAGCTAGCAGTTAATTGTGTGAATACTGAAACTAAGGTGTTCCCATTTCCTTGTGTAGTGTGTTTTTGTTTACTGTATTTGTTTCCTTTAACTTTATTAAACTGACCAACTATATTTCCTGTTGAAGGTGTAGTTTAGCTATTAATTTGTTTTTCTGTCCTGTCACAGGTATTCCCCCATTGGTATTGCGTGTTTGATCTGTGGGAAGATCATCTCCATTAATGATCTGGAAATGGTGGCCAAACAACTGGGCATGTACATGGTCACGGTCATCGTTGGACTCATTATTCATGGAGGCATATTTCTTCCCTTAATATATTTTGTAATCGTTCGGAAAAACCCATTCAAATTCTTCATGGGACTTTTCCAAGCTTGGGTCACCGCCTTAGGAACAGCTTCCAGG[T/C]TAGTCACTTTCCTTTAATTATGTTTTCCCTTAGATATTTGTATGACACACGTTGAACTAAAGAGTTTAGTTTGTTATGTTTGGTTGTGTCTCAATTTTTGATATGCAATTTTTGTAGTGCTGGCACATTACCTGTCACTTTCCGCTGCTTGGAAGAAAATCTGGGTATCGACAAGAGAGTGACGCGATTCGTGTTACCTGTTGGAGCAACCATCAACATGGACGGTACTGCACTTTATGAGGCCGTAGCTGCCATTTTTATTGCCCAGATGAATGGAATCGAACTTGATCCTGGTCAGATCGTGACAGTCAGGTAAGAGCAAATTTCTAGACAAAAAAAATAAACAATTTAGTATAAATTTACAATACATTGTTTGTACCACAACATTATTTTTGTTGCTCATTCATTGCTCATGCTCATTGTAAACACTGCCAACACATGCTTCAGTCCAACTTCTATATACTACACTCTCAGAAATAAAAGTATGCAAGCTTTCACTG
Associated Phenotype:
Not determined