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Protein-coding gene in the species Homo sapiens
motif-containing protein, mitochondrial is a protein that in humans is encoded by the LRPPRC gene. Transcripts ranging in size from 4.8 to 7.0 kb which result from alternative
LRPPRC
Metabolic disease
Saguenay–Lac-Saint-Jean region of Quebec is caused by a mutation in the LRPPRC gene, located on the small ('p') arm of chromosome 2. Both compound heterozygosity
Leigh_syndrome
Protein family
encoding proteins containing this repeat include: DENND4A, DENND4B, DENND4C LRPPRC PTCD1, PTCD2, PTCD3 MRPS27 Mingler MK, Hingst AM, Clement SL, Yu LE, Reifur
Pentatricopeptide_repeat
Aerobic respiration enzyme
COX assembly factors: SURF1, SCO1, SCO2, COX10, COX15, COX20, COA5 and LRPPRC. Mutations in these proteins can result in altered functionality of sub-complex
Cytochrome_c_oxidase
Protein-coding gene in the species Homo sapiens
cap-binding ability, the CRM1/XPO1 export pathway, and the adaptor protein LRPPRC, which bridges eIF4E and 4ESE-containing transcripts. Nuclear eIF4E also
EIF4E
Muscle disorders caused by mitochondrial dysfunction
cytochrome c oxidase deficiency; COX deficiency) SURF1, SCO2, COX10, SCO1, LRPPRC, COX15, COX6B1, TACO1, COX14, COX20, PET100, COA6, COA3, COX8A, COX4I1,
Mitochondrial_myopathy
Protein-coding gene in the species Homo sapiens
the UCSC Genome Browser. Liu L, McKeehan WL (2002). "Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal
URI1
Protein-coding gene in the species Homo sapiens
PMC 139241. PMID 12477932. Liu L, McKeehan WL (2002). "Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal
HEBP2
Mitochondrial disorder
difficulties. This disorder is caused by an autosomal recessive mutation in the LRPPRC gene in chromosome 2p16. To be more specific, it is caused by a base pair
Leigh syndrome, French Canadian type
Leigh_syndrome,_French_Canadian_type
Q86VZ4 8874 LRP12 HGNC:31708; Q9Y561 8875 LRPAP1 HGNC:6701; P30533 8876 LRPPRC HGNC:15714; P42704 8877 LRR1 HGNC:19742; Q96L50 8878 LRRC1 HGNC:14307; Q9BTT6
List of human protein-coding genes 4
List_of_human_protein-coding_genes_4
Protein-coding gene in the species Homo sapiens
Library of Medicine. Liu L, McKeehan WL (Feb 2002). "Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal
MAP1S
Protein-coding gene in the species Homo sapiens
PMC 155318. PMID 11799066. Liu L, McKeehan WL (2002). "Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal
UXT
deficiency; 256000; SURF1 Leigh syndrome, French-Canadian type; 220111; LRPPRC Leigh syndrome, X-linked; 308930; PDHA1 Leiomyomatosis and renal cell cancer;
List_of_OMIM_disorder_codes
Protein-coding gene in the species Homo sapiens
(NDUFS1, SDHA, ATP5F1A, ETFA, ETFB); Mitochondrial RNA processing proteins (LRPPRC, DHX30, PNPT1); and Mitochondrial translation proteins (TUFM, GFM1, IARS2
FASTKD3
LRPPRC
LRPPRC
LRPPRC
LRPPRC
Boy/Male
Indian
One of the kauravas
Female
English
Anglicized form of Hebrew Miykal, MICHAL means "who is like God." In the bible, this is the name of a daughter of king Saul. Compare with masculine Michal.
Boy/Male
Indian
One who gives protection, The giver of might and glory
Boy/Male
Arabic, German, Muslim
Shining
Girl/Female
Australian, Christian, Hebrew
Gives Joy
Boy/Male
Arthurian Legend
Various names for Arthur's sword.
Girl/Female
Bengali, Gujarati, Hindu, Indian, Kannada, Tamil, Telugu
Graceful Lady; Goddess Saraswati
Boy/Male
Arabic, Muslim
Wisdom
Female
Hebrew
(×ַדִּירָה) Hebrew name ADIRA means "noble; powerful."
Girl/Female
Greek
Iyrical.
LRPPRC
LRPPRC
LRPPRC
LRPPRC
LRPPRC