ZMP
mat2a
Ensembl ID:
ZFIN ID:
Description:
methionine adenosyltransferase II, alpha [Source:RefSeq peptide;Acc:NP_997802]
Human Orthologue:
MAT2A
Human Description:
methionine adenosyltransferase II, alpha [Source:HGNC Symbol;Acc:6904]
Mouse Orthologue:
Mat2a
Mouse Description:
methionine adenosyltransferase II, alpha Gene [Source:MGI Symbol;Acc:MGI:2443731]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14309 | Nonsense | Available for shipment | Available now |
| sa16647 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14309
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112201 | Nonsense | 4 | 309 | 1 | 8 |
| ENSDART00000121531 | Nonsense | 4 | 395 | 1 | 9 |
The following transcripts of ENSDARG00000040334 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 6849894)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 7862694 |
| GRCz11 | 10 | 7821394 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTAGAAACAGATTTAGAAGAGCGTAACAATACAATCAATATGAACGGA[C/T]AACTGAACGGCTTTCACAACTCYCTGATTGATGAAGACTGYTTTTTGTTC
Long Flanking Sequence:
GTTACACTGTCTATCATCTGGACTAACGTTGTTTAGACGCCTATATTAGACATCTTTAAAAAAAATGCTTTCAACAAAGTAATCCCAGTCTTTTTTTATATGTGCGGTTTTATTTTCGCTTTTTTATTTAGTAAATTTCTCAGAAATTCCTATCTAAATGTATACATTTAACGCAGTATATATAAGCTGGGCCTTCTTTGTCTCCTCCTTGCCGTTGTAGGGCCCTGGCGTCCTTTCTTATTGGCTTAATGGAAGACGGACGGGGGCGCGCCCGAGTGACGCTTGAGTTTGGAGTGAAGTAGGAGGGATAAAACCTTGAAGACCGGCTGGCGTGAGCATTTGAGGTCAAGTCTACGCAGCGTGTTCGAGACAGAGAAACATCAGAAACATCTATTTAACACCGACGTTAGAAAAGCAGAAACTGACACGCTAGACCGGCGAAACAAACCCGATTAGAAACAGATTTAGAAGAGCGTAACAATACAATCAATATGAACGGA[C/T]AACTGAACGGCTTTCACAACTCTCTGATTGATGAAGACTGCTTTTTGTTCACGTCGGAGTCTGTCGGCGAAGGACACCCTGGTATGTATCATAACACATATATTTAAAGGTTTTTTTTTTATTTTACAAGGTCGCGCGGGAGGTAAACACGATCAGGCACGAGAGCCATTGGCTAACACGTGCTAATAACTGCTGATCTGTATTATTTTTTTTTTGTGTAAATGCGCAGAATTTTCTTATTCTTGCAGTTGATTTAATCCGCGTTTTTAGATGTACGTAAAATGTGGTGTTTGTAAATATATGGTTGGTTAATCTGTGTTTGTAATCCCAGGCCACGCGCGGCGGCCTCGTCGTGTTTGAAGCCCAAAGCGTCATAAAATTATAGATCGTGAATGCATTAAATGGGCCATTTATAATTTTAGTATGTTTTTTATATAACAGAATGGGTAAAATAAGTATTAGACGCGCTATAGTGGCTCCTTGTGACCATTTCCGTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16647
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112201 | Essential Splice Site | 30 | 309 | 1 | 8 |
| ENSDART00000121531 | Essential Splice Site | 30 | 395 | 1 | 9 |
The following transcripts of ENSDARG00000040334 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 6849812)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 7862612 |
| GRCz11 | 10 | 7821312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGACTGYTTTTTGTTCACGTCGGAGTCTGTCGGCGAAGGACAYCCTG[G/A]TATGTATCATAACACANNNTATATTTAAAGGTTTTTTTTNNATTTTACAAGGT
Long Flanking Sequence:
TCCCAGTCTTTTTTTATATGTGCGGTTTTATTTTCGCTTTTTTATTTAGTAAATTTCTCAGAAATTCCTATCTAAATGTATACATTTAACGCAGTATATATAAGCTGGGCCTTCTTTGTCTCCTCCTTGCCGTTGTAGGGCCCTGGCGTCCTTTCTTATTGGCTTAATGGAAGACGGACGGGGGCGCGCCCGAGTGACGCTTGAGTTTGGAGTGAAGTAGGAGGGATAAAACCTTGAAGACCGGCTGGCGTGAGCATTTGAGGTCAAGTCTACGCAGCGTGTTCGAGACAGAGAAACATCAGAAACATCTATTTAACACCGACGTTAGAAAAGCAGAAACTGACACGCTAGACCGGCGAAACAAACCCGATTAGAAACAGATTTAGAAGAGCGTAACAATACAATCAATATGAACGGACAACTGAACGGCTTTCACAACTCTCTGATTGATGAAGACTGCTTTTTGTTCACGTCGGAGTCTGTCGGCGAAGGACACCCTG[G/A]TATGTATCATAACACATATATTTAAAGGTTTTTTTTTTATTTTACAAGGTCGCGCGGGAGGTAAACACGATCAGGCACGAGAGCCATTGGCTAACACGTGCTAATAACTGCTGATCTGTATTATTTTTTTTTTGTGTAAATGCGCAGAATTTTCTTATTCTTGCAGTTGATTTAATCCGCGTTTTTAGATGTACGTAAAATGTGGTGTTTGTAAATATATGGTTGGTTAATCTGTGTTTGTAATCCCAGGCCACGCGCGGCGGCCTCGTCGTGTTTGAAGCCCAAAGCGTCATAAAATTATAGATCGTGAATGCATTAAATGGGCCATTTATAATTTTAGTATGTTTTTTATATAACAGAATGGGTAAAATAAGTATTAGACGCGCTATAGTGGCTCCTTGTGACCATTTCCGTTTGAAGCCTGTGCGCGCGCGTGGTGGCCATGTTGTCGGCGGGCTCGCGGAACATGTGTTCTTGTGCAATGCGGACCCGCGCAATAA
Associated Phenotype:
Not determined