Busch Lab

ZMP

mat1a

Ensembl ID:
ENSDARG00000039605
ZFIN ID:
ZDB-GENE-030131-6127
Description:
S-adenosylmethionine synthase isoform type-1 [Source:RefSeq peptide;Acc:NP_956165]
Human Orthologue:
MAT1A
Human Description:
methionine adenosyltransferase I, alpha [Source:HGNC Symbol;Acc:6903]
Mouse Orthologue:
Mat1a
Mouse Description:
methionine adenosyltransferase I, alpha Gene [Source:MGI Symbol;Acc:MGI:88017]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa35458 Nonsense Mutation detected in F1 DNA Not yet available
sa2678 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa35458
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057869 Nonsense 56 390 3 9
Genomic Location (Zv9):
Chromosome 13 (position 18684216)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 18504251
GRCz11 13 18635243
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGTCGTTTGGCTAATTATTGTTGTTCTAATCATCAGAGACTGTCTGC[A/T]AAACTGGTATGGTGCTTCTCTGTGGTGAGATCACATCTCGGGCCAATGTG
Long Flanking Sequence:
GTGTCAGATTTAGTGAGTCTTAACTATAGGGGAGGCATTGAAACTCTTACACTAAACTGAAACATACACTTGAACCTTAATCAGAGTCCTTACATAACTTTGTTTTATAATAGTGTGCTTATGTTTACAGATAAAATCTGTGACCAAATCAGTGATGCAGTTCTTGACGCACACTTAAAGCAGGACCCGGATGCTAAAGTAGCCTGTGGTGAGTGAACAGTTTAATTGCAAACTAAATAAACACGTTTATGTTTTTATTTTTTGTATAAACATTGATATATTTGAAAGTCCACAGTCCAACAGTTGGTCAATCTTCACTTGGTTATCGAGTGACCATTTTTAGCACTTTCTATCTGTTAAGTTTAACGGCATTTAAATGAATAACATCTCTATTTCCAAATTCAATCTAGCAATGGGTTACACAGTGACAGTTTTTTTAATTTTTTTTTTATGGGTCGTTTGGCTAATTATTGTTGTTCTAATCATCAGAGACTGTCTGC[A/T]AAACTGGTATGGTGCTTCTCTGTGGTGAGATCACATCTCGGGCCAATGTGGACTACCAGAAGATTGTGCGAGACACCATAAAACACATTGGTTATGACAACTCTGAAAAAGGTCAGGATCGATACATATTTTGTTTTTCCGTGCATCATCCGTTAAATCTATTCACCAATTTTTATCACTTTTCACTCTTTTCTCTTCCCTGTTCAGGTTTCGACTATAAAACTTGCAATGTGCTGGTAGCTCTCGAGCAGCAGTCTCCTGATATAGCTCAGGGTGTCCATGTTGACAGGCATGAGGAAGATATTGGAGCTGGAGATCAGGTCTGTACACAAAAGAAATTCAAATGTGTTCAAATGGTTCATTTGTGATCAACCTGTTCATGTTGGATTTCTGTTCTGTTTTAGGGGCTCATGTTTGGCTACGCCACTGATGAGACAGAAGAGTGCATGCCTCTCACCATTGTCCTTGCTCACAAACTCAATTCAAAAATGGCTGAGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2678
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057869 Nonsense 260 390 7 9
Genomic Location (Zv9):
Chromosome 13 (position 18680163)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 18500198
GRCz11 13 18631190
KASP Assay ID:
554-2509.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGTAAAATAATCTCTTTTTNCCAGGGAGATGCTGGTGTTACAGGAAGG[A/T]AGATTATTGTGGACACATATGGTGGATGGGGAGCTCATGGTGGTGGYGCC
Long Flanking Sequence:
ATCCACTGCATAAAACATATACTGGAAAAGTTGGTGGTTCATTCAGCTGGGGTGACCCCAGATTAATAACGAGACTAAGCCGAAAAGAAGATGAATGAATGAAGAACTTGATTAGATTGTTCGGGTGTTTAAAACTGTTGAAATTGAACCCAGTAGGACTTTGGACCTCAGGGAACAGATTTAGGGACTAGGGCAGGAGGTTTGCAAAATAAATTAATTCATCCTTTTAAAATTTCACAGAATTAATCATTTATTTTATTCATGCTTGTGCATAGTGATTGGAAGTTGTAAGTTTCCTTTGGACGTTTCAATCTAGTCCACTTTTTTTTTTATTAAATGCCACTGCATATTTACATCAGCGGAACATATTTAACAGCTGGTTGGAAATATTTAACTCAGAACTGCAAAAAGATTGCAGTTTACCAGTATTGTTGGAAACCATTGATTTAAAGAGTAAAATAATCTCTTTTTTCCAGGGAGATGCTGGTGTTACAGGAAGG[A/T]AGATTATTGTGGACACATATGGTGGATGGGGAGCTCATGGTGGTGGCGCCTTCTCTGGAAAGGACTACACTAAGGTGGATCGTTCTGCTGCCTATGCTGCTCGCTGGGTAGCGAAGTCTCTGGTGAAGTCCAAACTGTGCAGAAGAGTGCTGGTTCAGGTGAGACAAAATAATTTTGAGCCATTGCCTTGTGTCTGGACAAAAATGTTGATTCAAGCAACACACCAAATTACTGTCCAATTTTATCTGACTTGGTTAAACTGGAATGGGTGAGCTGGTTTCTGGTAAGGGTCACGAATAATATATTTGCTGTGTAGGTGTCTTACGCCATTGGAGTCGCCCACCCACTCTCAATCTCCCTCTTCACCTACGGCTCATCGGAAAAAACAGAGAAGGAGTTGCTACATATTGTCAACAAGAACTTTGACCTCCGACCAGGTGTCATTGTTAGGTAATCAATTAATAAGATAATATGTTCTTTTAATGTTCTCCAAATTCAGG
Associated Phenotype:
Not determined