RNF10

Last updated
RNF10
Identifiers
Aliases RNF10 , RIE2, ring finger protein 10
External IDs OMIM: 615998 MGI: 1859162 HomoloGene: 40990 GeneCards: RNF10
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014868
NM_001330474

NM_016698
NM_001302448
NM_001302449

RefSeq (protein)

NP_001317403
NP_055683

NP_001289377
NP_001289378
NP_057907

Location (UCSC) Chr 12: 120.53 – 120.58 Mb Chr 5: 115.24 – 115.27 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

RING finger protein 10 is a protein that in humans is encoded by the RNF10 gene. [5]

Contents

Function

The protein encoded by this gene contains a ring finger motif, which is known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. EST data suggests the existence of multiple alternatively spliced transcript variants, however, their full length nature is not known. [5]

Model organisms

Model organisms have been used in the study of RNF10 function. A conditional knockout mouse line, called Rnf10tm1a(KOMP)Wtsi [14] [15] was generated as part of the International Knockout Mouse Consortium program — a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists. [16] [17] [18]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion. [12] [19] Twenty two tests were carried out on mutant mice and five significant abnormalities were observed. [12] Homozygous mutant animals displayed increased chromosomal stability in a micronucleus test. Females also had increased body weight, an increased amount of total body fat and an abnormal complete blood count. Males additionally displayed an increase in eating behavior. [12]

Related Research Articles

PRDX6

Peroxiredoxin-6 is a protein that in humans is encoded by the PRDX6 gene. It is a member of the peroxiredoxin family of antioxidant enzymes.

GIT2

ARF GTPase-activating protein GIT2 is an enzyme that in humans is encoded by the GIT2 gene.

24-Dehydrocholesterol reductase

24-Dehydrocholesterol reductase is a protein that in humans is encoded by the DHCR24 gene.

ARID4A

AT rich interactive domain 4A (RBP1-like), also known as ARID4A, is a protein which in humans is encoded by the ARID4A gene.

NCAPH

Condensin complex subunit 2 also known as chromosome-associated protein H (CAP-H) or non-SMC condensin I complex subunit H (NCAPH) is a protein that in humans is encoded by the NCAPH gene. CAP-H is a subunit of condensin I, a large protein complex involved in chromosome condensation

ASXL1

Putative Polycomb group protein ASXL1 is a protein that in humans is encoded by the ASXL1 gene.

RHOBTB3

Rho-related BTB domain-containing protein 3 is a protein that in humans is encoded by the RHOBTB3 gene.

Sodium/hydrogen exchanger 8

Sodium/hydrogen exchanger 8 is a protein that in humans is encoded by the SLC9A8 gene.

Ninein-like protein

Ninein-like protein is a protein that in humans is encoded by the NINL gene. It is part of the centrosome.

ARHGEF4

Rho guanine nucleotide exchange factor 4 is a protein that in humans is encoded by the ARHGEF4 gene.

NPLOC4

Nuclear protein localization protein 4 homolog is a protein that in humans is encoded by the NPLOC4 gene.

TWF1

Twinfilin-1 is a protein that in humans is encoded by the TWF1 gene. This gene encodes twinfilin, an actin monomer-binding protein conserved from yeast to mammals. Studies of the mouse counterpart suggest that this protein may be an actin monomer-binding protein, and its localization to cortical G-actin-rich structures may be regulated by the small GTPase RAC1.

BRDT

Bromodomain testis-specific protein is a protein that in humans is encoded by the BRDT gene. It is a member of the Bromodomain and Extra-terminal motif (BET) protein family.

COQ9

Ubiquinone biosynthesis protein COQ9, mitochondrial, also known as coenzyme Q9 homolog (COQ9), is a protein that in humans is encoded by the COQ9 gene.

PRPSAP2

Phosphoribosyl pyrophosphate synthetase-associated protein 2 is a protein that in humans is encoded by the PRPSAP2 gene.

CRLF3

Cytokine receptor-like factor 3 is a protein that in humans is encoded by the CRLF3 gene.

WDR47

WD repeat domain 47 is a protein that in humans is encoded by the WDR47 gene.

PLEKHM2

Pleckstrin homology domain-containing family M member 2 is a protein that in humans is encoded by the PLEKHM2 gene.

Rtf1, Paf1/RNA polymerase II complex component, homolog is a protein that in humans is encoded by the RTF1 gene.

ARHGAP25

Rho GTPase activating protein 25 is a protein that in humans is encoded by the ARHGAP25 gene. The gene is also known as KAIA0053. ARHGAP25 belongs to a family of Rho GTPase-modulating proteins that are implicated in actin remodeling, cell polarity, and cell migration.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000022840 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000041740 - 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.
  5. 1 2 "Entrez Gene: RNF10 ring finger protein 10".
  6. "Body weight data for Rnf10". Wellcome Trust Sanger Institute.
  7. "Indirect calorimetry data for Rnf10". Wellcome Trust Sanger Institute.
  8. "DEXA data for Rnf10". Wellcome Trust Sanger Institute.
  9. "Haematology data for Rnf10". Wellcome Trust Sanger Institute.
  10. "Salmonella infection data for Rnf10". Wellcome Trust Sanger Institute.
  11. "Citrobacter infection data for Rnf10". Wellcome Trust Sanger Institute.
  12. 1 2 3 4 Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x. S2CID   85911512.
  13. Mouse Resources Portal, Wellcome Trust Sanger Institute.
  14. "International Knockout Mouse Consortium".
  15. "Mouse Genome Informatics".
  16. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (Jun 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMC   3572410 . PMID   21677750.
  17. Dolgin E (Jun 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi: 10.1038/474262a . PMID   21677718.
  18. Collins FS, Rossant J, Wurst W (Jan 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi: 10.1016/j.cell.2006.12.018 . PMID   17218247. S2CID   18872015.
  19. van der Weyden L, White JK, Adams DJ, Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biology. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC   3218837 . PMID   21722353.

Further reading