Misplaced Pages

MYO1C

Article snapshot taken from[REDACTED] with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Protein-coding gene in the species Homo sapiens
MYO1C
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

4BYF

Identifiers
AliasesMYO1C, MMI-beta, MMIb, NMI, myr2, myosin IC, MyoIC
External IDsOMIM: 606538; MGI: 106612; HomoloGene: 32046; GeneCards: MYO1C; OMA:MYO1C - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)
Chromosome 17 (human)Genomic location for MYO1CGenomic location for MYO1C
Band17p13.3Start1,464,186 bp
End1,492,686 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for MYO1CGenomic location for MYO1C
Band11 B5|11 45.92 cMStart75,541,330 bp
End75,564,736 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lung

  • tibial nerve

  • subcutaneous adipose tissue

  • popliteal artery

  • tibial arteries

  • gastric mucosa

  • buccal mucosa cell

  • right coronary artery

  • sural nerve

  • abdominal fat
Top expressed in
  • right lung

  • right lung lobe

  • left lung

  • submandibular gland

  • lacrimal gland

  • parotid gland

  • tunica media of zone of aorta

  • left lung lobe

  • ascending aorta

  • endothelial cell of lymphatic vessel
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

4641

17913

Ensembl

ENSG00000197879

ENSMUSG00000017774

UniProt

O00159

Q9WTI7

RefSeq (mRNA)

NM_033375
NM_001080779
NM_001080950
NM_001363855

NM_001080774
NM_001080775
NM_008659
NM_001370611

RefSeq (protein)

NP_001074248
NP_001074419
NP_203693
NP_001350784

NP_001074243
NP_001074244
NP_032685
NP_001357540

Location (UCSC)Chr 17: 1.46 – 1.49 MbChr 11: 75.54 – 75.56 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Myosin-Ic is a protein that in humans is encoded by the MYO1C gene.

This gene encodes a member of the unconventional myosin protein family, which are actin-based molecular motors. The protein is found in the cytoplasm, and one isoform with a unique N-terminus is also found in the nucleus. The nuclear isoform associates with RNA polymerase I and II and functions in transcription initiation. The mouse ortholog of this protein also functions in intracellular vesicle transport to the plasma membrane. Multiple transcript variants encoding different isoforms have been found for this gene. The related gene myosin IE has been referred to as myosin IC in the literature, but it is a distinct locus on chromosome 19.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000197879Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000017774Ensembl, 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. Crozet F, el Amraoui A, Blanchard S, Lenoir M, Ripoll C, Vago P, Hamel C, Fizames C, Levi-Acobas F, Depetris D, Mattei MG, Weil D, Pujol R, Petit C (Apr 1997). "Cloning of the genes encoding two murine and human cochlear unconventional type I myosins". Genomics. 40 (2): 332–41. doi:10.1006/geno.1996.4526. PMID 9119401.
  6. ^ "Entrez Gene: MYO1C myosin IC".

Further reading

External links

  • Overview of all the structural information available in the PDB for UniProt: O00159 (Unconventional myosin-Ic) at the PDBe-KB.
Proteins of the cytoskeleton
Human
Microfilaments
and ABPs
Myofilament
Actins
Myosins
Other
Other
Intermediate
filaments
Type 1/2
(Keratin,
Cytokeratin)
Epithelial keratins
(soft alpha-keratins)
Hair keratins
(hard alpha-keratins)
Ungrouped alpha
Not alpha
Type 3
Type 4
Type 5
Microtubules
and MAPs
Tubulins
MAPs
Kinesins
Dyneins
Microtubule organising proteins
Microtubule severing proteins
Other
Catenins
Membrane
Other
Nonhuman
See also: cytoskeletal defects
Stub icon

This article on a gene on human chromosome 17 is a stub. You can help Misplaced Pages by expanding it.

Categories: