ZMP
zgc:152651
Ensembl ID:
ZFIN ID:
Description:
methionyl-tRNA formyltransferase, mitochondrial [Source:RefSeq peptide;Acc:NP_001071010]
Human Orthologue:
MTFMT
Human Description:
mitochondrial methionyl-tRNA formyltransferase [Source:HGNC Symbol;Acc:29666]
Mouse Orthologue:
Mtfmt
Mouse Description:
mitochondrial methionyl-tRNA formyltransferase Gene [Source:MGI Symbol;Acc:MGI:1916856]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41024 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41024
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:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000053814 | Splice Site, Nonsense | 75 | 390 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 54208671)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52478521 |
| GRCz11 | 7 | 52753591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAAGTGATGATTTTGCTCTGGAGTCACTGAAGCGGCTTCATTTGTCT[C/T]GGTAATGACATCCAGGATGTTATTGTATTATTGTCCGTTATGACCTTGCT
Long Flanking Sequence:
CATGGCGCCGCACACATACGCCAGTGTGTACATCTAATTCTTAACCGTAACCTTGCTACTGTCATCTACTGCTTTGGGGAAAAACGGATTAGTATAATGAGCCAACTTTGGAAACGTGATTATAAAAATGCCAAGGTTGTCTCACCTGAAGTTGTCATAGAATATTAGCATGACTTTCTGACTTCTGCGTGCTTAACGTTAATGGAGGACTGATGGTTTTGTAACTTCGCTAGCTGTTAATGGCGGTTTCTGTCATTTATGAAATCTTACATTAAAGTATGTGGAACTTAAACTTCTTAAAGCTCACAGTCCCAGGTCGTTTGCTGTCTCAGAGACTTTGTAGCATCTGTTTCACGCGCCATAGAAGAGGCTTATTTCTCTTGGGCAGAAGCAAATCTTTAGTAACTCAAACACAGTCTGCGTCTAAACCGCCCTGGAGAATACTGTTCTTTGGAAGTGATGATTTTGCTCTGGAGTCACTGAAGCGGCTTCATTTGTCT[C/T]GGTAATGACATCCAGGATGTTATTGTATTATTGTCCGTTATGACCTTGCTGTGTTATTCATGTTATTCATCTGTATTCATTAGAAATGACAATAAAGCTGGAGTCGTCGATGCACTTGAGGTCGTGACGCTGTCCCGTGATGCTCCGGTCAGGAAATATGCAGAGCAGCACAGACTTCCGCTTCACCACTGGCCAGATGTGGACATGAGTACACACTTTGATGTTGGTGTGGTGGTGTCATTTGGCAGCTTAATCAAGGAAAACATCATCAACAAAATGCCATAGTACGTAATAAGGGTTCATCAAACGAATGTTACTTCAGCATGTCCATAATTAGTTTGTTATTATGTTTTGATGAGATTTTTTTCGGAAGTAATTTATTCCAACTTTTCCAAACGTAATTAATGGTCTTAATAATGCTTTTAATTTTGTATGTAGTCTTTAATAAGGGCTGTATAATTGTCATCAAAGCCTGGAGGTGAAGTGCCTTGTATAATTCA
Associated Phenotype:
Not determined