Homo sapiens TUB like protein 1 (TULP1), transcript variant 1, 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.

Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG. [Acta Ophthalmol. 2023]
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG.
Majander A, Sankila EM, Falck A, Vasara LK, Seitsonen S, Kulmala M, Haavisto AK, Avela K, Turunen JA. Acta Ophthalmol. 2023 Mar; 101(2):215-221. Epub 2022 Sep 21.
TULP1 related retinal dystrophy: report of rare and novel variants with a previously undescribed phenotype in two cases. [Ophthalmic Genet. 2022]
TULP1 related retinal dystrophy: report of rare and novel variants with a previously undescribed phenotype in two cases.
Al-Hindi H, Chauhan MZ, Sanders R, Samarah H, DeBenedictis M, Traboulsi E, Uwaydat SH. Ophthalmic Genet. 2022 Apr; 43(2):277-281. Epub 2021 Dec 5.
A novel homozygous missense mutation p.P388S in TULP1 causes protein instability and retinitis pigmentosa. [Mol Vis. 2021]
A novel homozygous missense mutation p.P388S in TULP1 causes protein instability and retinitis pigmentosa.
Woodard DR, Xing C, Ganne P, Liang H, Mahindrakar A, Sankurathri C, Hulleman JD, Mootha VV. Mol Vis. 2021; 27:179-190. Epub 2021 Apr 2.

RefSeq protein product
See the reference protein sequence for tubby-related protein 1 isoform 1 (NP_003313.3).

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
Full text in PMC
Free full text articles in PMC
Functional Class
Functional class of the sequence domain architecture
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
Probe
Related Probe entry
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

Ensembl [Ensembl]
Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
Order TALEN/CRISPR clone [GeneCopoeia Inc.]
Order TALEN/CRISPR clone
GeneCopoeia Inc.
Order qPCR primer [GeneCopoeia Inc.]
Order qPCR primer
GeneCopoeia Inc.
Order full-length cDNA clone [GeneCopoeia Inc.]
Order full-length cDNA clone
GeneCopoeia Inc.
UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser

Homo sapiens TUB like protein 1 (TULP1), transcript variant 1, mRNA
Homo sapiens TUB like protein 1 (TULP1), transcript variant 1, mRNA
gi|1519244872|ref|NM_003322.6|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide