Homo sapiens otogelin like (OTOGL), transcript variant 4, mRNA

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.
Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...
Show in Genome Data Viewer
Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

[Phenotype and genotype analysis of recessive hereditary moderate sensorineural hearing loss caused by new mutations in OTOGL gene]. [Zhonghua Yi Xue Za Zhi. 2021]
[Phenotype and genotype analysis of recessive hereditary moderate sensorineural hearing loss caused by new mutations in OTOGL gene].
Feng ML, Huang SS, Tang FZ, Zhang X, Li XH, Qiu SW, Yuan YY. Zhonghua Yi Xue Za Zhi. 2021 Jan 12; 101(2):115-121.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains. [Cell Rep. 2020]
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Haenig C, Atias N, Taylor AK, Mazza A, Schaefer MH, Russ J, Riechers SP, Jain S, Coughlin M, Fontaine JF, et al. Cell Rep. 2020 Aug 18; 32(7):108050.
Novel biallelic OTOGL mutations in a Chinese family with moderate non-syndromic sensorineural hearing loss. [Int J Pediatr Otorhinolaryngol...]
Novel biallelic OTOGL mutations in a Chinese family with moderate non-syndromic sensorineural hearing loss.
Gu X, Sun S, Guo L, Lu X, Mei H, Lai C, Li H. Int J Pediatr Otorhinolaryngol. 2015 Jun; 79(6):817-820. Epub 2015 Mar 18.

RefSeq protein product
See the reference protein sequence for otogelin-like protein isoform 1 precursor (NP_001365539.2).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
BioSystems
BioSystems
CCDS
Link to Consensus CDS
Components (Core)
Links to Core components
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

Homo sapiens otogelin like (OTOGL), transcript variant 4, mRNA
Homo sapiens otogelin like (OTOGL), transcript variant 4, mRNA
gi|1917882158|ref|NM_001378610.3|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide