Human Gene TRMU (uc011ara.2)
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Sequence and Links to Tools and Databases
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Primer design for this transcript
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Genetic Association Studies of Complex Diseases and Disorders
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Genetic Association Database (archive): TRMU
CDC HuGE Published Literature: TRMU
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MalaCards Disease Associations
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MalaCards Gene Search: TRMU
Diseases sorted by gene-association score: liver failure, transient infantile* (1675), deafness, mitochondrial, modifier of* (477), mitochondrial myopathy, infantile, transient* (247), mitochondrial non-syndromic sensorineural deafness* (11), myopathy, lactic acidosis, and sideroblastic anemia (8) * = Manually curated disease association
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Comparative Toxicogenomics Database (CTD)
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RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
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Microarray Expression Data
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Press "+" in the title bar above to open this section.
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Orthologous Genes in Other Species
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Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
Mouse | Rat | Zebrafish | D. melanogaster | C. elegans | S. cerevisiae |
No ortholog | No ortholog | No ortholog | No ortholog | No ortholog | No ortholog |
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Descriptions from all associated GenBank mRNAs
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AY927424 - Homo sapiens mRNA sequence. AY927428 - Homo sapiens mRNA sequence. BC069212 - Homo sapiens G-2 and S-phase expressed 1, mRNA (cDNA clone IMAGE:4871934). JD522667 - Sequence 503691 from Patent EP1572962. JD050305 - Sequence 31329 from Patent EP1572962. JD077802 - Sequence 58826 from Patent EP1572962. JD486755 - Sequence 467779 from Patent EP1572962. JD346823 - Sequence 327847 from Patent EP1572962. JD493990 - Sequence 475014 from Patent EP1572962. JD526359 - Sequence 507383 from Patent EP1572962. JD337857 - Sequence 318881 from Patent EP1572962. JD318757 - Sequence 299781 from Patent EP1572962. JD532545 - Sequence 513569 from Patent EP1572962. BC021234 - Homo sapiens cDNA clone IMAGE:4138335, partial cds. JD136652 - Sequence 117676 from Patent EP1572962. JD151275 - Sequence 132299 from Patent EP1572962. JD202424 - Sequence 183448 from Patent EP1572962. JD263348 - Sequence 244372 from Patent EP1572962. JD084812 - Sequence 65836 from Patent EP1572962. JD132438 - Sequence 113462 from Patent EP1572962. JD350246 - Sequence 331270 from Patent EP1572962. JD421739 - Sequence 402763 from Patent EP1572962.
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Other Names for This Gene
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Alternate Gene Symbols: BC069212 UCSC ID: uc011ara.2 Representative RNA: BC069212
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GeneReviews for This Gene
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GeneReviews article(s) related to gene TRMU: trmu-def (TRMU Deficiency)
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Gene Model Information
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category:
| noncoding
| nonsense-mediated-decay:
| no
| RNA accession:
| BC069212.1
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exon count:
| 2 | CDS single in 3' UTR:
| no
| RNA size:
| 1492 |
ORF size:
| 0 | CDS single in intron:
| no
| Alignment % ID:
| 99.80 |
txCdsPredict score:
| 196.50 | frame shift in genome:
| no
| % Coverage:
| 98.86 |
has start codon:
| no
| stop codon in genome:
| no
| # of Alignments:
| 1 |
has end codon:
| no
| retained intron:
| no
| # AT/AC introns
| 0 |
selenocysteine:
| no
| end bleed into intron:
| 0 | # strange splices:
| 0 |
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Click here
for a detailed description of the fields of the table above.
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Methods, Credits, and Use Restrictions
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Click here
for details on how this gene model was made and data restrictions if any.
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