Regulator interaktivne ćelijske polarizacije porodice 2RHO jest protein koji je kod ljudi kodiran genom RIPOR2.[5]

RIPOR2
Identifikatori
AliasiRIPOR2
Vanjski ID-jeviOMIM: 611410 MGI: 2444879 HomoloGene: 9284 GeneCards: RIPOR2
Lokacija gena (čovjek)
Hromosom 6 (čovjek)
Hrom.Hromosom 6 (čovjek)[1]
Hromosom 6 (čovjek)
Genomska lokacija za RIPOR2
Genomska lokacija za RIPOR2
Bend6p22.3Početak24,804,282 bp[1]
Kraj25,042,170 bp[1]
Lokacija gena (miš)
Hromosom 13 (miš)
Hrom.Hromosom 13 (miš)[2]
Hromosom 13 (miš)
Genomska lokacija za RIPOR2
Genomska lokacija za RIPOR2
Bend13|13 A3.1Početak24,685,508 bp[2]
Kraj24,917,799 bp[2]
Ontologija gena
Molekularna funkcija GO:0001948, GO:0016582 vezivanje za proteine
14-3-3 protein binding
vezivanje identičnih proteina
Ćelijska komponenta ćelijska membrana
projekcija ćelije
membrana
citoplazma
apical plasma membrane
citoskelet
Filopodija
stereocilium
stereocilium membrane
Biološki proces multicellular organism development
Ćelijska diferencijacija
muscle organ development
sluh
skeletal muscle fiber development
positive regulation of myoblast differentiation
positive regulation of myoblast fusion
negative regulation of establishment of T cell polarity
negative regulation of T cell migration
negative regulation of T cell proliferation
regulation of mitotic spindle assembly
Hemotaksija
Ćelijska adhezija
negative regulation of signal transduction
negative regulation of cell adhesion
negative regulation of Rho protein signal transduction
positive regulation of filopodium assembly
positive regulation of neutrophil chemotaxis
negative regulation of protein localization to cell leading edge
cellular response to chemokine
regulation of establishment of cell polarity
positive regulation of neutrophil extravasation
negative regulation of Rho guanyl-nucleotide exchange factor activity
establishment of protein localization
protein homooligomerization
auditory receptor cell stereocilium organization
cellular response to mechanical stimulus
Izvori:Amigo / QuickGO
Ortolozi
VrsteČovjekMiš
Entrez
Ensembl
UniProt
RefSeq (mRNK)
NM_001286445
NM_001286446
NM_001286447
NM_014722
NM_015864

NM_001346031
NM_001346032

NM_001080381
NM_001286100
NM_001286101
NM_029679
NM_178658

RefSeq (bjelančevina)
NP_001273374
NP_001273375
NP_001273376
NP_001332960
NP_001332961

NP_055537
NP_056948

NP_001073850
NP_001273029
NP_001273030
NP_083955
NP_848773

NP_001389841
NP_001389842
NP_001389843
NP_001389844
NP_001389845
NP_001389846
NP_001389847
NP_001389848

Lokacija (UCSC)Chr 6: 24.8 – 25.04 MbChr 13: 24.69 – 24.92 Mb
PubMed pretraga[3][4]
Wikipodaci
Pogledaj/uredi – čovjekPogledaj/uredi – miš

Aminokiselinska sekvenca

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Dužina polipeptidnog lanca je 1.068 aminokiselina, а molekulska težina 118.519 Da.[6]

1020304050
MLVGSQSFSPGGPNGIIRSQSFAGFSGLQERRSRCNSFIENSSALKKPQA
KLKKMHNLGHKNNNPPKEPQPKRVEEVYRALKNGLDEYLEVHQTELDKLT
AQLKDMKRNSRLGVLYDLDKQIKTIERYMRRLEFHISKVDELYEAYCIQR
RLQDGASKMKQAFATSPASKAARESLTEINRSFKEYTENMCTIEVELENL
LGEFSIKMKGLAGFARLCPGDQYEIFMKYGRQRWKLKGKIEVNGKQSWDG
EETVFLPLIVGFISIKVTELKGLATHILVGSVTCETKELFAARPQVVAVD
INDLGTIKLNLEITWYPFDVEDMTASSGAGNKAAALQRRMSMYSQGTPET
PTFKDHSFFRWLHPSPDKPRRLSVLSALQDTFFAKLHRSRSFSDLPSLRP
SPKAVLELYSNLPDDIFENGKAAEEKMPLSLSFSDLPNGDCALTSHSTGS
PSNSTNPEITITPAEFNLSSLASQNEGMDDTSSASSRNSLGEGQEPKSHL
KEEDPEEPRKPASAPSEACRRQSSGAGAEHLFLENDVAEALLQESEEASE
LKPVELDTSEGNITKQLVKRLTSAEVPMATDRLLSEGSVGGESEGCRSFL
DGSLEDAFNGLLLALEPHKEQYKEFQDLNQEVMNLDDILKCKPAVSRSRS
SSLSLTVESALESFDFLNTSDFDEEEDGDEVCNVGGGADSVFSDTETEKH
SYRSVHPEARGHLSEALTEDTGVGTSVAGSPLPLTTGNESLDITIVRHLQ
YCTQLVQQIVFSSKTPFVARSLLEKLSRQIQVMEKLAAVSDENIGNISSV
VEAIPEFHKKLSLLSFWTKCCSPVGVYHSPADRVMKQLEASFARTVNKEY
PGLADPVFRTLVSQILDRAEPLLSSSLSSEVVTVFQYYSYFTSHGVSDLE
SYLSQLARQVSMVQTLQSLRDEKLLQTMSDLAPSNLLAQQEVLRTLALLL
TREDNEVSEAVTLYLAAASKNQHFREKALLYYCEALTKTNLQLQKAACLA
LKILEATESIKMLVTLCQSDTEEIRNVASETLLSLGEDGRLAYEQLDKFP
RDCVKVGGRHGTEVATAF

Funkcija

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Protein kodiran ovim genom stimulira stvaranje nemitotskog multijedarnog sincicija iz proliferativnih citotrofoblasta tokom diferencijacije trofoblasta. Alternativna prerada ovog gena dovodi do više varijanti transkripta (prema RefSeq, nov 2013).

Klinički značaj

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Mutacije u RIPOR2 povezane su s gubitkom sluha.[7]

Reference

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000111913 - Ensembl, maj 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000036006 - Ensembl, maj 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.
  5. ^ "Entrez Gene: Family with sequence similarity 65, member B".
  6. ^ "UniProt, Q9Y4F9" (jezik: engleski). Pristupljeno 4. 10. 2021.
  7. ^ Diaz-Horta O, Subasioglu-Uzak A, Grati M, DeSmidt A, Foster J, Cao L, Bademci G, Tokgoz-Yilmaz S, Duman D, Cengiz FB, Abad C, Mittal R, Blanton S, Liu XZ, Farooq A, Walz K, Lu Z, Tekin M (juli 2014). "FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing". Proceedings of the National Academy of Sciences of the United States of America. 111 (27): 9864–8. Bibcode:2014PNAS..111.9864D. doi:10.1073/pnas.1401950111. PMC 4103326. PMID 24958875.

Dopunska literatura

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