ZMP
mettl2a
Ensembl ID:
ZFIN ID:
Description:
Methyltransferase-like protein 2-A [Source:UniProtKB/Swiss-Prot;Acc:A8KBL7]
Human Orthologues:
METTL2A, METTL2B
Human Descriptions:
methyltransferase like 2A [Source:HGNC Symbol;Acc:25755]
methyltransferase like 2B [Source:HGNC Symbol;Acc:18272]
methyltransferase like 2B [Source:HGNC Symbol;Acc:18272]
Mouse Orthologue:
Mettl2
Mouse Description:
methyltransferase like 2 Gene [Source:MGI Symbol;Acc:MGI:1289171]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13444 | Nonsense | Available for shipment | Available now |
sa19983 | Nonsense | Available for shipment | Available now |
sa13383 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13444
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007857 | Nonsense | 97 | 353 | 3 | 9 |
The following transcripts of ENSDARG00000008105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 19561586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19524621 |
GRCz11 | 3 | 19674361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TWTCTAGAGGAGTTTGACRACAGGGCCAATGAATACTGGAATGACTTTTA[C/A]ACCATTCACGAGAACCGCTTCTTYAAGGATCGTCACTGGCTCTTTACAGA
Long Flanking Sequence:
TTATTGCTGCAACCTTGTATATTTTAGAATGGTTTACTTGGAATACATTTTGTTGGATAGTTTGTTTATTTTTTATTTAGCATTTCCTGGTATTTTAAATTGGTGTATGGATGTAATTTCTGCATTAATTCAATCTTGGTATTGCCATGCAAAAAAACAATAAACTTTAAATTTGTATTTATAAATTTATCAACATATTTGGAATTTATTTATCTACTTTATGGCCATCCATTTAAGCCTGTTACTCAAATATAAAGAAAAATGTCATCAGCACAGACAGTCAAAAACACTTAAGGTTATCTAAACATAGCATATTTAACCGGTATTTTAATAAGGATGTGTGAACATTATCATACTATTAAAAACATGTATTTACTAGTAAAGTCAAACCTGCTTGCTTACTAAGTATTTTTTTCCTTATGGTAAATCATCTCTTTATTTGCTTCTCTATTTCTAGAGGAGTTTGACGACAGGGCCAATGAATACTGGAATGACTTTTA[C/A]ACCATTCACGAGAACCGCTTCTTCAAGGATCGTCACTGGCTCTTTACAGAGTTCCCCGAGCTTGCACCTCAGCAAAAGCATTTACGGGGTGCTGAGGAGAAGGAAAGCCTGGAACACATGTTAAATGGTGAAGATGTTTCCTCGAATCACACACATGATGAATTTCCTGGAGCCTCTGCATCCTATCGCATCCTGGAGGTGAGTTTTGCAATGCAGCAGACACATTTAAAAATTTTAATCGGTCAACCAAAAATCTGCTGCTGTTTAATAGTCTTGCAAAGAACTAAAAAATAAATATTTTGAAAAATGTTCCAGTTGCCTTTTTTTTTCATTCAGTGAAAGTCAATGGAGCCCAGTGTCATCTAGCTGTGTTTTCATCCATGTATTTTGGGATGTTGCATTAAAAACATTCTGGATGTAAATGTCAGGAATCATTCAATTTAATTCAGCTTTATTTGTATAGCGCTTTTACAATGTGGATTGTGTCAAAGCAGCTTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19983
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 |
---|---|---|---|---|---|
ENSDART00000007857 | Nonsense | 273 | 353 | 7 | 9 |
The following transcripts of ENSDARG00000008105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 19565598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19528633 |
GRCz11 | 3 | 19678373 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATTGCTGAAACCCGGAGGAGTGTTGTTATTGAGAGACTATGGCCGATA[T/A]GACATGGCACAGCTACGTTTCAAAAAAGGTAAATGTTTTGACCTTGTGAA
Long Flanking Sequence:
TCACCAGGACATGCTTACTTCATATTGAAGTGGTCTATTTTTAGAAATATTTACAGACATCAGTCCTGTTTTTTATTTTTTTATGTACAGCACTGTTTTACATTTATTAAATTGGCAAATTCTATGAATTCATCGATTCTGTTCACATTTACTGCATTCTGTATCATTTTCTTTGGCCAAACTGATGTTTCTTATGTCTAGTTGTTCCACATACTGTAATAACATTTTTAACTGAAGCCACAATTTCATGACCATTTATTTTTTTATTTGAAAAGTAACGAATCATAAAAAAAGATAATCAGGGAAGGAACAGTCAGCCAGTTGTTATCAAATAAGTATAACAGAGCGATCTGTCCACATCTTTCATTAAATATCACTGCCTGCCCTCTTCATGCTTTAACTTCTTAATCCATGTTTTCCAGGATGCAAAAGTCTATCAATAGATTGGGACGATTGCTGAAACCCGGAGGAGTGTTGTTATTGAGAGACTATGGCCGATA[T/A]GACATGGCACAGCTACGTTTCAAAAAAGGTAAATGTTTTGACCTTGTGAAAAGAAAATCACAAAGGAACCTTGAGTTATCTTGCATTTTATTCTTTCATTTAAAAGTGTAAAATCTTAAATCCTAGTTTAAGATACATATTTTCGTATTTGTAGTGTCAGTGCCTTTGACTATTAACATTTTTTGACTTCGACTTTGATGATATGGTCCATTTCAGTTTGGTACAGATCTTCTTTTTTTTTCCACTCGGTATAGATCCAGGGGTCGGATTTATAAAATTTGCATAGAAACTCTCCTAAAGGTTTTTTTTTTTTTAAAGTGTTTTTTAATTAGTCACATGACCTAGTAGTTACGTCACAGAGTACTGACCCAAGAGAACTGGGTTCGGATCCATCTTCGGCAAAGATTGTTTCTTTTGGTTAATTTTTTTCGTCATTGTTTATACAATTCCAAGACTTATACTGAACTGTACACCGCCGTTGTTAAAGGATGTATACCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13383
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 |
---|---|---|---|---|---|
ENSDART00000007857 | Nonsense | 326 | 353 | 9 | 9 |
The following transcripts of ENSDARG00000008105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 19569678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 19532713 |
GRCz11 | 3 | 19682453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTGTTCTCCAGTGCKGGTCTGGAGAAGCTGCAGAATTTGGTGGATCGA[C/T]GWTTGCAGGTGAACAGAGGAAAGCAGCTTACAATGTACAGAGTCTGGGTT
Long Flanking Sequence:
TAAACGTGTACCTTGCTATTTTTCTGAAAAAAAATGAAGCTGTAGTAAATTTTTAGTATTTTGATGCTTGAAAATGATTTTTCATCTTTAGTACAAAACTGTTTTGTAATTATTTATTACTTGAATTTATTGCTGCTATTGATTGACTTTTCAATCTGTATCTATCATGACAGAATTTAATGCGTATGTGATGATAAGCTGCCTGTTTTTGCTCAATCAGGGAGGTGCTTGTCTGAAAACTTCTATGTTCGAGGTGATGGAACCCGCGTCTACTTTTTCACACAAGGTAAATGCATGTTCAGACTTGCCTTTTCTTAAGAAACAAGAAAACCACTATTTCATAAACAAGCTTTGGTTGCAGACCTGAATATAATAAAAAGAGATAACACTTTTATAGATGTATCTATTTATTTCTTACCTATGTGGTTTTCCCTTTAGATGAGCTGCATGATCTGTTCTCCAGTGCGGGTCTGGAGAAGCTGCAGAATTTGGTGGATCGA[C/T]GATTGCAGGTGAACAGAGGAAAGCAGCTTACAATGTACAGAGTCTGGGTTCAGTGCAAGTATCGCAAGGTCCTGGCACCCACTTAACATCAAAACCGCTTGTTTGGAGAGAAGGAGAACATCTGGATTGCTGTACCATGACAAATCTGTGACGTAGTTTTACAGATGATGGACAGACTGCAGGAGCTTCAAGGTTACGGTGCTTATGTTTGCTCAAAGTGGTATCTGATGTATCCTGCTTGGGAATAAGAGGACAAGAGTTCCCATGATGCACCTGAGGGCTTTAAACTGTTTGTCCATCACATTGAGTGATGTTTTTTTAAGGACAATTTTTTAGTAGGAATAAACCAGATGAAATGAAGGCAAATTCCCTTTCTGACTATCGGCTTTTTCATTGTTTGTTTTTACCAATCAGCAGGTACAAACATGAGACATAGACTAATAACTACAAAACTATAAATTTGCGTTCAATCATAAATGTTTTTATTAATATTGTTTTTT
Associated Phenotype:
Not determined