Human Gene MYRIP (uc010hhu.3)
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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): MYRIP
CDC HuGE Published Literature: MYRIP
Positive Disease Associations: Body Composition
, Body Mass Index
, Echocardiography
, Natriuretic Peptide, Brain
, Neurobehavioral Manifestations
, Sleep
, sleep duration
Related Studies: - Body Composition
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[PubMed 0]
- Body Composition
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[PubMed 0]
- Body Composition
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[PubMed 0]
  more ... click here to view the complete list
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MalaCards Disease Associations
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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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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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AK312412 - Homo sapiens cDNA, FLJ92749. BC092512 - Homo sapiens myosin VIIA and Rab interacting protein, mRNA (cDNA clone MGC:104940 IMAGE:3093499), complete cds. AK126013 - Homo sapiens cDNA FLJ44025 fis, clone TESTI4026700, highly similar to Rab effector MyRIP. AF396687 - Homo sapiens rab effector MYRIP (MYRIP) mRNA, complete cds. BC109311 - Homo sapiens myosin VIIA and Rab interacting protein, mRNA (cDNA clone MGC:130034 IMAGE:40036096), complete cds. BC109312 - Homo sapiens myosin VIIA and Rab interacting protein, mRNA (cDNA clone MGC:130035 IMAGE:40036097), complete cds. AK310972 - Homo sapiens cDNA, FLJ18014. AB083783 - Homo sapiens slac2-c mRNA for Slp homologue lacking C2 domains-c, complete cds. KJ905446 - Synthetic construct Homo sapiens clone ccsbBroadEn_15029 MYRIP gene, encodes complete protein. AK125334 - Homo sapiens cDNA FLJ43344 fis, clone NT2RI3008162, highly similar to Rab effector MyRIP. AK316068 - Homo sapiens cDNA, FLJ78967 complete cds, highly similar to Rab effector MyRIP. AK294714 - Homo sapiens cDNA FLJ56979 complete cds, highly similar to Rab effector MyRIP. JD345037 - Sequence 326061 from Patent EP1572962. AL050090 - Homo sapiens mRNA; cDNA DKFZp586F1018 (from clone DKFZp586F1018). JD244100 - Sequence 225124 from Patent EP1572962. JD099701 - Sequence 80725 from Patent EP1572962. JD248171 - Sequence 229195 from Patent EP1572962. JD052206 - Sequence 33230 from Patent EP1572962. JD313425 - Sequence 294449 from Patent EP1572962. JD465910 - Sequence 446934 from Patent EP1572962. JD158182 - Sequence 139206 from Patent EP1572962. JD445561 - Sequence 426585 from Patent EP1572962. JD205872 - Sequence 186896 from Patent EP1572962. JD067336 - Sequence 48360 from Patent EP1572962. JD362597 - Sequence 343621 from Patent EP1572962. JD311015 - Sequence 292039 from Patent EP1572962. JD278573 - Sequence 259597 from Patent EP1572962. JD218610 - Sequence 199634 from Patent EP1572962. JD453983 - Sequence 435007 from Patent EP1572962. JD351610 - Sequence 332634 from Patent EP1572962. JD355030 - Sequence 336054 from Patent EP1572962. JD258057 - Sequence 239081 from Patent EP1572962. JD467645 - Sequence 448669 from Patent EP1572962. JD074448 - Sequence 55472 from Patent EP1572962. JD281897 - Sequence 262921 from Patent EP1572962. JD046208 - Sequence 27232 from Patent EP1572962. JD092195 - Sequence 73219 from Patent EP1572962.
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Other Names for This Gene
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Alternate Gene Symbols: BC109312 UCSC ID: uc010hhu.3 RefSeq Accession: NM_015460
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Gene Model Information
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category:
| nearCoding
| nonsense-mediated-decay:
| yes
| RNA accession:
| BC109312.1
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exon count:
| 17 | CDS single in 3' UTR:
| no
| RNA size:
| 3245 |
ORF size:
| 0 | CDS single in intron:
| no
| Alignment % ID:
| 99.94 |
txCdsPredict score:
| 3593.50 | frame shift in genome:
| no
| % Coverage:
| 99.97 |
has start codon:
| yes
| stop codon in genome:
| no
| # of Alignments:
| 1 |
has end codon:
| yes
| 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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