ZMP
tfb2m
Ensembl ID:
ZFIN ID:
Description:
dimethyladenosine transferase 2, mitochondrial [Source:RefSeq peptide;Acc:NP_001107089]
Human Orthologue:
TFB2M
Human Description:
transcription factor B2, mitochondrial [Source:HGNC Symbol;Acc:18559]
Mouse Orthologues:
AC122891.1, Tfb2m
Mouse Description:
transcription factor B2, mitochondrial Gene [Source:MGI Symbol;Acc:MGI:107937]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10078 | Nonsense | Available for shipment | Available now |
sa2933 | Nonsense | F2 line generated | Not yet available |
sa36345 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10078
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110058 | Nonsense | 219 | 437 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 17 (position 11927598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 11910120 |
GRCz11 | 17 | 12064186 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCCCCCGTCATGTACTCAGAAAAGCTCTTCTCTGACCTTGCCATCTCW[G/T]AAGTACCGTGGACAGCAGGTTAGTGAACCAAACATTCAGAATAATATGAG
Long Flanking Sequence:
ATTATGTAGGAAATAAGACCTACATTTTTTTGTTCTCATGAACACATGGGATGGAAGTATTGTTGTATTTACAAATAATTTATGCAATATTACATATTTATGTTTGAGAAAATCTTGCAACAAATATCCAAGGATGTTTCTAACATCCTTGACAACCTCAACCTCTTTTGAATCCAGTTGGTCAAAAGACCAAGAGGGGAATTTAGATTTCTTAGTTTGTGACATCTTTAATGTTAGTTAAATCATTAAAAAAACGCTACAAAATGTACACAATAGCAACAATCTCACTGTAAAGGCAAACTTTTCTGTGATTTACAGTCTAATATGGTCATCTTCCACACCCATAAACTGTTTTAATTTTAAAGGAACTGGAGAGCAGACTGGAGGGGCAGCTGGATGTGGTTCATTGTGATTTCTTCAAACTGGACCCCATTGGCAACGGCATCATGAAACCCCCCGTCATGTACTCAGAAAAGCTCTTCTCTGACCTTGCCATCTCT[G/T]AAGTACCGTGGACAGCAGGTTAGTGAACCAAACATTCAGAATAATATGAGCAGATAATAACAAGAAGATTAGATGGATTTGCTCTTCAGTGTTTGGACTTTCAGCAGTGAAATTTAAACCAGACTGAACTGAACTTCAACTCTGAAAACTGGACTGACAGTTTCGATTTACTTAAACTTCTTTCTTAAGCTGCTTTGATACAATCTACATTGTAAAAGCGCTACAGAAATAAAGATTAATTGAATTGAATTAGCACAACAATATATAACGGTTATTTTACATTGTAAAACTACTCAAATAGTAAAGCATGATAATTGTAACACCTAAGTTGCTTGTTTCATTTCCAACAAGAACTAAATATAAAAAACCAATGTCACTTTTGCTGAAAATGTCTGCCAAATTCATAAATGTGATCCTGGAGTCTTATGTTGCACAGGTATATTTGTAGAAATTGCCAACAATACGTTGTTATGAGTCTCTTTCGCTTATGACTAAGGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2933
Status:
F2 line generated
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110058 | Nonsense | 333 | 437 | 8 | 10 |
ENSDART00000110058 | Nonsense | 333 | 437 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 17 (position 11935696)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 11918218 |
GRCz11 | 17 | 12072284 |
KASP Assay ID:
554-3434.1 (used for ordering genotyping assays)
KASP Sequence:
ATTATATACTTTTTTTTTTTTGAACAGCTATCCCAGAGTGAAAACCTTTG[T/A]CTGGTGCGKATCACCCCACGCGAGGACTTGTTTAGCTCTCATTTAACTCC
Long Flanking Sequence:
TGCTTTTTTTAATCAACGATCAAATAAATATTATACATGCAAATAGCATTTAAAGCACAAATGTGGCAGTATTTATATTTCTGTCTAAATCTAGTTATGAAATTGTGTTTTAATTACTCCAATTTGCTATTGAAATATATTCCTCACAGTGGCTTTCATAACTTGATTTCATGACAGATTAATTTAAATGTATACATTAATTAAGATATAAGAGATAACGACTATATATAGGATAAGATGCAAATATGTACACAAAAAAACTTGTAACTTGGAATGGTCCAGAAGTGTGTTTTGTGACTAAAGTGTGACTAAAATTTTGATCTTGGGATTTATTTCATAAAGTTAATTAATTAATTAATTGTATATTAAATATAGAGCTATAATTATTGTGTATAGAACTATATTTATCAAATTTAGTCCTATACATGCATGCCCAACCAAAAGACTCTCATTATATACTTTTTTTTTTTTGAACAGCTATCCCAGAGTGAAAACCTTTG[T/A]CTGGTGCGTATCACCCCACGCGAGGACTTGTTTAGCTCTCATTTAACTCCCTTGAACGGCAGCACACTGGTCCTGATGGTGAAACAATGCCTTGCCAAGAGAAAAGGCAAACTGATTCAACAAATTAAGTAAGTTTATGCATTTTTGGACCTCTTAATGCGTCTTACTCCTGTTATTGCATGCATTTTTGGTTGATCGAATGACAAGTTGTAGACAGGAGGACACCTGTCTATACCTGCTGTTTAAATCCCTTATCATTGTCCACTTTTCGGATTAGAGATTTCTGATTATGGTGTGTGTATAGGCCACTTCCCATAGCTCATAGTAGCACAGTACTGTATAGTAATATAGTAAGGCTTGTAATCTGACTTTTTTTTTGTCTTCTGTCTTCATAAGCTCATGGAGTCCTGGCATGGGATCGGAGTTGATCTCAAATCTTGGTTTTCTTGACGACACACTGACAGGTGACGTTTACCCTGATGAGTACAAGCGTCTCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36345
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110058 | Nonsense | 425 | 437 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 17 (position 11936240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 11918762 |
GRCz11 | 17 | 12072828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTTGAGCTGATGGAACAGTCTGGAAGCTTCGCTGAGAGCTGGCTTTA[T/A]CAGGAGACGCTGGAAACCACAAAAATAGGCCACGGTTAACACCACCAGAG
Long Flanking Sequence:
TAACTCCCTTGAACGGCAGCACACTGGTCCTGATGGTGAAACAATGCCTTGCCAAGAGAAAAGGCAAACTGATTCAACAAATTAAGTAAGTTTATGCATTTTTGGACCTCTTAATGCGTCTTACTCCTGTTATTGCATGCATTTTTGGTTGATCGAATGACAAGTTGTAGACAGGAGGACACCTGTCTATACCTGCTGTTTAAATCCCTTATCATTGTCCACTTTTCGGATTAGAGATTTCTGATTATGGTGTGTGTATAGGCCACTTCCCATAGCTCATAGTAGCACAGTACTGTATAGTAATATAGTAAGGCTTGTAATCTGACTTTTTTTTTGTCTTCTGTCTTCATAAGCTCATGGAGTCCTGGCATGGGATCGGAGTTGATCTCAAATCTTGGTTTTCTTGACGACACACTGACAGGTGACGTTTACCCTGATGAGTACAAGCGTCTCTTTGAGCTGATGGAACAGTCTGGAAGCTTCGCTGAGAGCTGGCTTTA[T/A]CAGGAGACGCTGGAAACCACAAAAATAGGCCACGGTTAACACCACCAGAGACATTCGCCTTCACAACTGATCATGGAGAAAACAGAAAAAAAAAAGTGTTGTTTTATATGGAAGAAAGACAACTAGTGAAGAAAAACACTATCTTGCTTTACAAACAAACTCTTAATGATGGCTAATATGTAGACAGACTTGTCTATAACAGACTTTACATATTGATAAAGTTATATTTAGTCAAATGACGGGGACTGGAGAAGCTGGTGTTGGAGACATGAATGATACTGAACTCATGAAGCCAATAACTATTATGTGTGTACTGCATATACACCGAATACTTCCTTAATCTCTTTGATTCGAATAGGAGATCTTAAATATGAATAGAATTAAGCGACTTGTAATCCTAATGATTGCATTAGCACAGCCAGTTGAGATGTACATTTGCAAAGTGCTCATGTTTTTGTGTTTTCATATTTAAATGTTTGCTGTATTTAATAAGATGATTT
Associated Phenotype:
Not determined