ZMP
agxt2l1
Ensembl ID:
ZFIN ID:
Description:
Alanine--glyoxylate aminotransferase 2-like 1 [Source:UniProtKB/Swiss-Prot;Acc:Q7SY54]
Human Orthologue:
AGXT2L1
Human Description:
alanine-glyoxylate aminotransferase 2-like 1 [Source:HGNC Symbol;Acc:14404]
Mouse Orthologue:
Agxt2l1
Mouse Description:
alanine-glyoxylate aminotransferase 2-like 1 Gene [Source:MGI Symbol;Acc:MGI:1919010]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41056 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21106 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41056
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 |
|---|---|---|---|---|---|
| ENSDART00000051524 | Nonsense | 299 | 492 | 8 | 13 |
| ENSDART00000135167 | Nonsense | 107 | 125 | 3 | 8 |
The following transcripts of ENSDARG00000035544 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60563622)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 59782587 |
| GRCz11 | 7 | 60087824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAAATGGCCATCCAATGTCATGCGTGATCACCAGCAGAGAGATTGCT[G/T]AAAGCTTCATGTCTTCTGGAATGGAGTACTTCAACACAGTGAGGACAGCA
Long Flanking Sequence:
GCTCTCAATGCTTTTGAGCCATTTGCTTTACACTTTGCACCTAGATTGTTAAAATAGAGCCCGAAGACTGAAAATGACACAGGCTTCTCTCAAAAGCTAATAAGACAATATACAGAAGGCATTGTTGTTGGAAAAAATGCTCATGCCATAACTTCTTATTTAAGTATTATATACTTCTTATATAAGTATTTGAATTGTGTTTAATGTTTACATTCATGTGTGCTGATAATATGTTGTTTCTAAATCAAAAGACATATTATAATTAGTTAAGAATGTACCATGAATGTACCATATCTCTGACACTGTACCACAGGCATGTGAGAAACGCTGGAGGCATTTTCATTGCTGATGAGGTCCAGGTGGGCTTTGGAAGGGTGGGGACTCACTTCTGGGGCTTTCAGCTACAGGGAGAAGATTTTGTACCAGATATTGTTACAATGGGCAAACCTATTGGAAATGGCCATCCAATGTCATGCGTGATCACCAGCAGAGAGATTGCT[G/T]AAAGCTTCATGTCTTCTGGAATGGAGTACTTCAACACAGTGAGGACAGCATGTTGTTAATGGCAGGCAGGCACAAACTAATATGAAAAATATTCTTATTGTAAATAATGTTCCTATTGTACTTTATCATCAGCTGGCTATATAATCTAAACACACACACACACACACACACACACACACACACATATATATATATATAGTAATACACTATTAAACTATTAAATTATTAGTATTATTTTAAAAAAGCTTGTTAAATACACTATTACTTTTTTTTTTTTTTTGCAGCTTAGTCACAGTAATAATAATGTATAATGTGATAAAAGCAGTATTTAATTGCAACAAGAAAAAAATATATACCAGCATTAGCTATAGACCCCATAGAATAATGATTTATTAAACAAAAGCAAAAAGTAAAAGAAGAACATCTGTCTTTGTGCTATCTAGTTTGGCGGTAACCCTGTATCATGTGCTATTGGGTTGGCGGTGCTTAATGTAATTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21106
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:
C > A
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051524 | Splice Site, Nonsense | 392 | 492 | 10 | 13 |
| ENSDART00000135167 | Splice Site | None | 125 | 5 | 8 |
The following transcripts of ENSDARG00000035544 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60564778)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 59783743 |
| GRCz11 | 7 | 60088980 |
KASP Assay ID:
2259-9643.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAGAGTAAAAGGACCCCTGCTACAGCTGAAGCTCAGGAGGTTATTTA[C/A]AGGTAAGAATAAGTTTGTAAAGAGTAATTCATATTGCACTGCCAGACATA
Long Flanking Sequence:
TGCATAAAGTTTGACCTGGCCTTGTTATGTTAGTTTGAAGTAAATAATTTCCCTAGGGTTGTTTGTGACATGTACGCTTGGAATAGTGCTGTAAAAAAGTATGTCTGATCTCAAGAAAAAAAACGTAAGTATTTTACGTTTTGCCAGTTTAGTGGCTAATTCGTACAAATTCTTACGAGTTCAGTCGTACGAAATGGTACGATTTTAAAAAGGAGGCGTGGCACCTGACTCCACCCCTAACCCCAACCGTCATTGGGGGATAAGCAAATCGTACTAAATTGTACGAATTAGATCGTACGAATTCATACGAATTAGCCACTAAATGAAAAAGTTACGAATTGCCGTGAGATTGTGTTGGAAATACATAAAGCAAGGTGGTTTAAAGCTGCAGATCAAACATTTTATTCTAAAAGGGGACGTGGCCTATTTGTTGGGTTGGAGCTGGTCAGAAATCAGAGTAAAAGGACCCCTGCTACAGCTGAAGCTCAGGAGGTTATTTA[C/A]AGGTAAGAATAAGTTTGTAAAGAGTAATTCATATTGCACTGCCAGACATAAACAGAGGAAATAAAAGACACTTTGTTGGGTTTTGTCAAATTTTGTATTAGGTTAGTGTGATTTCACTAAGCTGGAAATATTCCTGGAATAAGTTGATCCTGGAATGCAATTCATGTTCTATATATTTTGATCCTGGAGCAACAATCCAGTCAGCCAATTAGATATGAGGGATAAGTTTATAGTTTAGGTTAAAAGTAGGCTTACAGTGGAAGTTATGTGTTTCTACATATTTGTTATCCAACTATTAATTATTTTGCAAAAACAAAACAAAACAAAAAAAAAAATGCAGTGAGGGTTAGGTATAGGGGGTTAGATATGGTTTATAAATTATCGAACAGAACTGATATTCCAGGATCAACATACTGTAGGTGTTAACGATCGCGTCCTACTTTCACCCACCATAGGTATCTGTTGGTGTTTGTCATGTCGTGATTTGGTAAATGAACATG
Associated Phenotype:
Not determined