IMMT

IMMT
Identifiers
Aliases	IMMT, HMP, MINOS2, P87, P87/89, P89, PIG52, Mic60, PIG4, inner membrane mitochondrial protein, MICOS60, mitofilin
External IDs	OMIM: 600378 MGI: 1923864 HomoloGene: 38234 GeneCards: IMMT
Gene location (Human)
Chr.	Chromosome 2 (human)[1]
End	86,195,770 bp[1]
Gene location (Mouse)
Chr.	Chromosome 6 (mouse)[2]
End	71,877,388 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• GO:0001948 protein binding; • RNA binding;
Cellular component	• integral component of membrane; • mitochondrial inner membrane; • myelin; • MICOS complex; • membrane; • mitochondrion;
Biological process	• cristae formation; • mitochondrial calcium ion homeostasis;
	Sources:Amigo / QuickGO
Orthologs
	10989
	76614
	ENSG00000132305
	ENSMUSG00000052337
	Q16891
	Q8CAQ8
	NM_001100169; NM_001100170; NM_006839
NM_001253681; NM_001253686; NM_001253687; NM_001253688; NM_001253689;
	NM_029673; NM_001362134; NM_001362136; NM_001362137; NM_001362138
	NP_001093639; NP_001093640; NP_006830
NP_001240610; NP_001240615; NP_001240616; NP_001240617; NP_001240618;
	NP_083949; NP_001349063; NP_001349065; NP_001349066; NP_001349067
	Wikidata
View/Edit Human	View/Edit Mouse

Mitochondrial inner membrane protein is a protein that in humans is encoded by the IMMT gene.[5][6][7]

Interactions

IMMT has been shown to interact with BAT2.[8]

References

GRCh38: Ensembl release 89: ENSG00000132305 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000052337 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Gieffers C, Korioth F, Heimann P, Ungermann C, Frey J (Jun 1997). "Mitofilin is a transmembrane protein of the inner mitochondrial membrane expressed as two isoforms". Exp Cell Res. 232 (2): 395–9. doi:10.1006/excr.1997.3539. PMID 9168817.
Icho T, Ikeda T, Matsumoto Y, Hanaoka F, Kaji K, Tsuchida N (Aug 1994). "A novel human gene that is preferentially transcribed in heart muscle". Gene. 144 (2): 301–6. doi:10.1016/0378-1119(94)90394-8. PMID 8039717.
"Entrez Gene: IMMT inner membrane protein, mitochondrial (mitofilin)".
Lehner, Ben; Semple Jennifer I; Brown Stephanie E; Counsell Damian; Campbell R Duncan; Sanderson Christopher M (Jan 2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics. United States. 83 (1): 153–67. doi:10.1016/S0888-7543(03)00235-0. ISSN 0888-7543. PMID 14667819.

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Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
Hillier LD, Lennon G, Becker M, et al. (1997). "Generation and analysis of 280,000 human expressed sequence tags". Genome Res. 6 (9): 807–28. doi:10.1101/gr.6.9.807. PMID 8889549.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Hattori M, Fujiyama A, Taylor TD, et al. (2000). "The DNA sequence of human chromosome 21". Nature. 405 (6784): 311–9. Bibcode:2000Natur.405..311H. doi:10.1038/35012518. PMID 10830953.
Liu J, Akoulitchev S, Weber A, et al. (2001). "Defective interplay of activators and repressors with TFIH in xeroderma pigmentosum". Cell. 104 (3): 353–63. doi:10.1016/S0092-8674(01)00223-9. PMID 11239393.
Bernert G, Fountoulakis M, Lubec G (2003). "Manifold decreased protein levels of matrin 3, reduced motor protein HMP and hlark in fetal Down's syndrome brain". Proteomics. 2 (12): 1752–7. doi:10.1002/1615-9861(200212)2:12<1752::AID-PROT1752>3.0.CO;2-Y. PMID 12469345.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Millar JK, Christie S, Porteous DJ (2004). "Yeast two-hybrid screens implicate DISC1 in brain development and function". Biochem. Biophys. Res. Commun. 311 (4): 1019–25. doi:10.1016/j.bbrc.2003.10.101. PMID 14623284.
Lehner B, Semple JI, Brown SE, et al. (2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics. 83 (1): 153–67. doi:10.1016/S0888-7543(03)00235-0. PMID 14667819.
Goehler H, Lalowski M, Stelzl U, et al. (2004). "A protein interaction network links GIT1, an enhancer of huntingtin aggregation, to Huntington's disease". Mol. Cell. 15 (6): 853–65. doi:10.1016/j.molcel.2004.09.016. PMID 15383276.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
John GB, Shang Y, Li L, et al. (2005). "The Mitochondrial Inner Membrane Protein Mitofilin Controls Cristae Morphology". Mol. Biol. Cell. 16 (3): 1543–54. doi:10.1091/mbc.E04-08-0697. PMC 551514. PMID 15647377.
Stelzl U, Worm U, Lalowski M, et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. hdl:11858/00-001M-0000-0010-8592-0. PMID 16169070.
Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569.
Camargo LM, Collura V, Rain JC, et al. (2007). "Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia". Mol. Psychiatry. 12 (1): 74–86. doi:10.1038/sj.mp.4001880. PMID 17043677.
Xie J, Marusich MF, Souda P, et al. (2007). "The mitochondrial inner membrane protein mitofilin exists as a complex with SAM50, metaxins 1 and 2, coiled-coil-helix coiled-coil-helix domain-containing protein 3 and 6 and DnaJC11". FEBS Lett. 581 (18): 3545–9. doi:10.1016/j.febslet.2007.06.052. PMID 17624330.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000132305 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000052337 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid9168817-5] Gieffers C, Korioth F, Heimann P, Ungermann C, Frey J (Jun 1997). "Mitofilin is a transmembrane protein of the inner mitochondrial membrane expressed as two isoforms". Exp Cell Res. 232 (2): 395–9. doi:10.1006/excr.1997.3539. PMID 9168817.

[pmid8039717-6] Icho T, Ikeda T, Matsumoto Y, Hanaoka F, Kaji K, Tsuchida N (Aug 1994). "A novel human gene that is preferentially transcribed in heart muscle". Gene. 144 (2): 301–6. doi:10.1016/0378-1119(94)90394-8. PMID 8039717.

[entrez-7] "Entrez Gene: IMMT inner membrane protein, mitochondrial (mitofilin)".

[pmid14667819-8] Lehner, Ben; Semple Jennifer I; Brown Stephanie E; Counsell Damian; Campbell R Duncan; Sanderson Christopher M (Jan 2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics. United States. 83 (1): 153–67. doi:10.1016/S0888-7543(03)00235-0. ISSN 0888-7543. PMID 14667819.

IMMT

Interactions

References

Further reading