Human Gene MRFAP1 (ENST00000320912.8) from GENCODE V44
Description: Found in a complex composed of MORF4L1, MRFAP1 and RB1. Interacts via its N-terminus with MORF4L1. Interacts with CSTB and MORF4L2. (from UniProt Q9Y605) RefSeq Summary (NM_001272053): This gene encodes an intracellular protein that interacts with members of the MORF4/MRG (mortality factor on chromosome 4/MORF4 related gene) family and the tumor suppressor Rb (retinoblastoma protein.) The protein may play a role in senescence, cell growth and immortalization. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]. Gencode Transcript: ENST00000320912.8 Gencode Gene: ENSG00000179010.16 Transcript (Including UTRs) Position: hg38 chr4:6,640,091-6,642,729 Size: 2,639 Total Exon Count: 3 Strand: + Coding Region Position: hg38 chr4:6,640,863-6,641,246 Size: 384 Coding Exon Count: 1
ID:MOFA1_HUMAN DESCRIPTION: RecName: Full=MORF4 family-associated protein 1; AltName: Full=Protein PGR1; AltName: Full=Protein associated with MRG of 14 kDa; SUBUNIT: Found in a complex composed of MORF4L1, MRFAP1 and RB1. Interacts via its N-terminus with MORF4L1. Interacts with CSTB and MORF4L2. SUBCELLULAR LOCATION: Nucleus. Cytoplasm, perinuclear region. Note=Colocalizes with MORF4L1 to cell nuclei. SIMILARITY: Belongs to the MORF4 family-associated protein family.
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
Protein Domain and Structure Information
ModBase Predicted Comparative 3D Structure on Q9Y605
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Orthologous Genes in Other Species
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.