ZMP
zgc:152769
Ensembl ID:
ZFIN ID:
Description:
Methyltransferase-like protein 13 [Source:UniProtKB/Swiss-Prot;Acc:A5WVX1]
Human Orthologue:
METTL13
Human Description:
methyltransferase like 13 [Source:HGNC Symbol;Acc:24248]
Mouse Orthologue:
Mettl13
Mouse Description:
methyltransferase like 13 Gene [Source:MGI Symbol;Acc:MGI:1918699]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10291 | Nonsense | Available for shipment | Available now |
sa29323 | Missense | Mutation detected in F1 DNA | Not yet available |
sa15174 | Nonsense | Available for shipment | Available now |
sa9568 | Nonsense | Available for shipment | Available now |
sa43401 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10291
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 |
---|---|---|---|---|---|
ENSDART00000021394 | Nonsense | 89 | 690 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 14853276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15042522 |
GRCz11 | 20 | 14938502 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCAGCTGACCAACATTGACATCAGCGAGACGGTGGTCTCCCATATGAAC[C/T]AGAGGAATGCAGAGCGCCGTCCAGACCTCTCCTTCCAGCAGCTGGATGCC
Long Flanking Sequence:
ATTTATAATGTGGTAAAATAATATCTATAATAAAAATATAGATGTTCATGATTGATATTTACAGACTTAAATGGTCATGAAATGGCCTCTACAGAGTCCAGACCTTACTATAGTGTTATAGAGGCAGTATGGGATTGCGTGGACAGAGGGAAAAAAGCAGAAAAAAACTCATAAATTAGAAGATGAACTTGCGTCTGGTATATGGACTCATACTAAATACTGTCTTTTACTAGCAGAAGCCGTTGCATTCTGAAAAGAGGGTTTTATTTTTCTCAATTTTGTATGCATATTTCTTTTCTATCTGTTTAAATCTTAATCTGAATTTAGTTTTTTAGTCCATAATGGATGAAGTGCTAATTTTTTGTGTGTAATAATCTGTTGTTGTGCAGGTATTGGTGGTGGGCTGTGGTAACTCTGAACTCAGTGAACAGCTCTATGATGTTGGCTACCGTCAGCTGACCAACATTGACATCAGCGAGACGGTGGTCTCCCATATGAAC[C/T]AGAGGAATGCAGAGCGCCGTCCAGACCTCTCCTTCCAGCAGCTGGATGCCACCCAGACCGGCTTCGAGAGCGGGAGCTTTCAGGTGACTCTGGATAAAGGCACTCTGGACGCCATGGCTTCAGAAGAGGATGGTGCTCTTGCAGGCCGGATGCTGGCAGAGGTTGGCAGAGTTTTGGCTGTGGGCGGGAGGTATGTCTGCATAACGTTAGCCCAGGAGCATGTCATAAAGTTAGCAGTGGAGCATTTTGTTAAGGGATGGGCAGTGAGAGTACATTGTCTAACCGGACAACAGAACGAAGAGTCCGATTCCTCCTTTGCACTCCCCGTTTTTGTGTTGGTTTGCACTAAGTTTCGACAAGCCCCTCCATTTGCTGTTCTTGAGCTGTGCCAGGGGGAGGATGGCGCTCCGGCTAGACTGGCATCAGTAGAGGAGCTGCTGTCTGCAGTCAAGGAGAGGCAGGCTTATAATCTAATGCTGCATAAACTCAGAGGAGGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29323
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:
T > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021394 | Missense | 153 | 690 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 14853084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15042330 |
GRCz11 | 20 | 14938310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCCGGATGCTGGCAGAGGTTGGCAGAGTTTTGGCTGTGGGCGGGAGG[T/G]ATGTCTGCATAACGTTAGCCCAGGAGCATGTCATAAAGTTAGCAGTGGAG
Long Flanking Sequence:
GTCTGGTATATGGACTCATACTAAATACTGTCTTTTACTAGCAGAAGCCGTTGCATTCTGAAAAGAGGGTTTTATTTTTCTCAATTTTGTATGCATATTTCTTTTCTATCTGTTTAAATCTTAATCTGAATTTAGTTTTTTAGTCCATAATGGATGAAGTGCTAATTTTTTGTGTGTAATAATCTGTTGTTGTGCAGGTATTGGTGGTGGGCTGTGGTAACTCTGAACTCAGTGAACAGCTCTATGATGTTGGCTACCGTCAGCTGACCAACATTGACATCAGCGAGACGGTGGTCTCCCATATGAACCAGAGGAATGCAGAGCGCCGTCCAGACCTCTCCTTCCAGCAGCTGGATGCCACCCAGACCGGCTTCGAGAGCGGGAGCTTTCAGGTGACTCTGGATAAAGGCACTCTGGACGCCATGGCTTCAGAAGAGGATGGTGCTCTTGCAGGCCGGATGCTGGCAGAGGTTGGCAGAGTTTTGGCTGTGGGCGGGAGG[T/G]ATGTCTGCATAACGTTAGCCCAGGAGCATGTCATAAAGTTAGCAGTGGAGCATTTTGTTAAGGGATGGGCAGTGAGAGTACATTGTCTAACCGGACAACAGAACGAAGAGTCCGATTCCTCCTTTGCACTCCCCGTTTTTGTGTTGGTTTGCACTAAGTTTCGACAAGCCCCTCCATTTGCTGTTCTTGAGCTGTGCCAGGGGGAGGATGGCGCTCCGGCTAGACTGGCATCAGTAGAGGAGCTGCTGTCTGCAGTCAAGGAGAGGCAGGCTTATAATCTAATGCTGCATAAACTCAGAGGAGGAACAGACTCAAGCAGCACACCCTCACTCACGCTGTGCCACGCAGCCAGCGGACGCCCACGGTACACTCTGACCATACAGGACGGCCCACCTTCTGCTAAGACCCCGCGGAGCAATCACTTCGCCATCTTTATTGGTGAGCGTTAGGTTTTATTTTATAGAGTGCAACATAGTGGTCCATATTGTATCATTTCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15174
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 |
---|---|---|---|---|---|
ENSDART00000021394 | Nonsense | 336 | 690 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 14850380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15039626 |
GRCz11 | 20 | 14935606 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTCCAGTGCAAAATTCAGACGTCTTGTCATTGTGGCAATGCATCGAGAC[C/T]AAGAATAWGAAGACATGCAGGCTGTCCAATCAGAGCTCTCGCCAGTGGTC
Long Flanking Sequence:
GACGTCAACTATGTATATGTATGTATTATGTATGGTTTGTTAGGATAGACTGATGTTAGGCTGATAATATATGATTATAGTTCAAAACAAAAAAAAATATGGAGAAATTCAGCTTTAAAATAGTCTAAATTAAGTTCTTATCGATGTGTATTGCTAATCTAAAATTAGGTGCTAATGAATTTGTGGAAGGACACTTACAAAATGTATATAAATAAATAAAGAATAAAAAGAAAAAAAATAATAGAAAAGACAATCATTTTCACACCTGTACAGTGTATTTTTGGCTCTTCCCTCAAATATATTTGTGCAACTTAACACACAAGTCATTTTATGTTTGGTTCAAAAGATGAAATAATGCAGTTTAATGGCATTTATTCTGTTTACGTTTAGTTCCTCAGGGTCGTGAGTCTGATTGGTTATATGGTTCAGCTGAAGGTCGAGCTCAGTTAGCGTCCAGTGCAAAATTCAGACGTCTTGTCATTGTGGCAATGCATCGAGAC[C/T]AAGAATATGAAGACATGCAGGCTGTCCAATCAGAGCTCTCGCCAGTGGTCATGGAACTCGCCCCTCCTGGAATGCCAGCCAATCAGCAGGTACACTAAAATAACAAACAAAGTGAGAGTGGTTGAGTTTAAAGATGTTTATATCAGGTTTATTTTTTCTAAATGCACAACAGCTAATCGCTAGTAGTTAATAGATATCCTTAAAACTAACATCTACGTTTTTTATTTAATTTCACGGGACCCTTAAGAAGCAGATGTCTCTAATGTTCATCCTTCATGGTCCTCATTCCTCTCTCTTTCCCATGCCCTCTGTTTAAGGTGCCGTTTCTGTCAGTGGGAGGAGATCTAGGCTGGAGGGAAGTGATTGGACGAGGGCTCAGTGCTTTGACTGGAGAGTATTCAGTGGAGGATGTGAGAGGAGAGGACGGTTACCTCTATCGCAGGCTTATCTTTATGAATAATTCTCAGCTGGTGCAGTCAGAGAGCAGACTCCAATCTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9568
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 |
---|---|---|---|---|---|
ENSDART00000021394 | Nonsense | 338 | 690 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 14850372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15039618 |
GRCz11 | 20 | 14935598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAAATTCAGACGTCTTGTCATTGTGGCAATGCATCGAGACCAAGAATA[T/A]GAAGACATGCAGGCTGTCCAATCAGAGCTCTCGCCAGTGGTCATGGAACT
Long Flanking Sequence:
CTATGTATATGTATGTATTATGTATGGTTTGTTAGGATAGACTGATGTTAGGCTGATAATATATGATTATAGTTCAAAACAAAAAAAAATATGGAGAAATTCAGCTTTAAAATAGTCTAAATTAAGTTCTTATCGATGTGTATTGCTAATCTAAAATTAGGTGCTAATGAATTTGTGGAAGGACACTTACAAAATGTATATAAATAAATAAAGAATAAAAAGAAAAAAAATAATAGAAAAGACAATCATTTTCACACCTGTACAGTGTATTTTTGGCTCTTCCCTCAAATATATTTGTGCAACTTAACACACAAGTCATTTTATGTTTGGTTCAAAAGATGAAATAATGCAGTTTAATGGCATTTATTCTGTTTACGTTTAGTTCCTCAGGGTCGTGAGTCTGATTGGTTATATGGTTCAGCTGAAGGTCGAGCTCAGTTAGCGTCCAGTGCAAAATTCAGACGTCTTGTCATTGTGGCAATGCATCGAGACCAAGAATA[T/A]GAAGACATGCAGGCTGTCCAATCAGAGCTCTCGCCAGTGGTCATGGAACTCGCCCCTCCTGGAATGCCAGCCAATCAGCAGGTACACTAAAATAACAAACAAAGTGAGAGTGGTTGAGTTTAAAGATGTTTATATCAGGTTTATTTTTTCTAAATGCACAACAGCTAATCGCTAGTAGTTAATAGATATCCTTAAAACTAACATCTACGTTTTTTATTTAATTTCACGGGACCCTTAAGAAGCAGATGTCTCTAATGTTCATCCTTCATGGTCCTCATTCCTCTCTCTTTCCCATGCCCTCTGTTTAAGGTGCCGTTTCTGTCAGTGGGAGGAGATCTAGGCTGGAGGGAAGTGATTGGACGAGGGCTCAGTGCTTTGACTGGAGAGTATTCAGTGGAGGATGTGAGAGGAGAGGACGGTTACCTCTATCGCAGGCTTATCTTTATGAATAATTCTCAGCTGGTGCAGTCAGAGAGCAGACTCCAATCTGCTGCTGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43401
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021394 | Essential Splice Site | 554 | 690 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 14847634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15036880 |
GRCz11 | 20 | 14932860 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTACACTGGGAGACGGACTGGAGCACATCACAACCCTGGAGAGTGAAGG[T/A]GAGAAAGCATCTAGATCAGAGGCCGGCCGTACACTGTGCATCTTTGTTTA
Long Flanking Sequence:
GATTAGATAACATGAACAACACAGTTAATGAGCAACTGTTAATAAGGCATAGATAATGGTGGCGTAGTGTTTGCTTTACAATAATTCAATGAACAAATGCTTTGTTAATGATAAATCATGTTAGGAAAGCGTTAACAAACATGTGACAGACGTGATTTTATACTTTTAAGTTAACATTGAGTGAGATATGTCAGATATTTGTACTTTGCACATCCATTCTTCTCAATAATATGCATAATTCAAAGATGAACCTGTTCTGATCAGTCTGTCATGTGTTCTCCAACAGATCAGCCAGTGTCTGTGTTGCTGGTGGGTCTAGGTGGTGGCGGCCTGCCTCAGTTTGTGCGGGACTTTGTGCCATGTGCTCGGGTGGAGGTGGTTGAACTGGATCCGGTGGTGCTGGATGTCGCTCAGACCTGGTTTGGATTTCAGATTGACGACAGGCTAAAAGTTACACTGGGAGACGGACTGGAGCACATCACAACCCTGGAGAGTGAAGG[T/A]GAGAAAGCATCTAGATCAGAGGCCGGCCGTACACTGTGCATCTTTGTTTAAGGCATAGTTCAACCAAAAATGTATAGGGCTGCACAATATATCGTTACTGCATCGATATCGCAATGTGTGTATCATTCATTCATTCATTCATTCAAATAATCATTCATTTTCCTTCAGCTTAGTCTCTTATATATCAGCGGATTGAACCGCCAACTATTTCATCATATGTTTTACACAGCGGATGCCCTTCCAGCCGCAACCCAGTAATATAAAAAAACTTCCATACACGTTCACATTTACACAGTATGGCCAACTTAGTTTACCAAATTCACCTATAGGGCATATCTTTGGACTTTGAGGGAAATCGGAGCACCCGGAGTAAATCCACATGCACACAGGGAGAACATGCAAACTCCACAAAGAAATGCTAGCTAACTCAGCTAAGACTCGAACGAGCGACTTTCTTGCTGTGAGGCGACAGTGCTAACTACTGAGCCTTTGTGCCACCC
Associated Phenotype:
Not determined