protein fantom isoform X12 [Homo sapiens]

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.
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.

Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family. [Reprod Sci. 2022]
Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family.
Zhang P, Wu B, Wang Y, Ren Y, Li G, Qan Y, Lei C, Wang H. Reprod Sci. 2022 Aug; 29(8):2200-2207. Epub 2022 Mar 1.
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS). [Genet Epidemiol. 2019]
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS).
Javanrouh N, Soltanian AR, Tapak L, Azizi F, Ott J, Daneshpour MS. Genet Epidemiol. 2019 Apr; 43(3):342-351. Epub 2018 Dec 30.
Rs3213758 in the RPGRIP1L Gene Associated with Susceptibility to Segmental Vitiligo in a Chinese Han Population. [Chin Med J (Engl). 2018]
Rs3213758 in the RPGRIP1L Gene Associated with Susceptibility to Segmental Vitiligo in a Chinese Han Population.
Hu M, Wang TM, Dong YY, She QY, Gao S, Liu DX, Deng YH. Chin Med J (Engl). 2018 Dec 20; 131(24):3022-3024.

RefSeq genomic sequence
See the genomic reference sequence for the RPGRIP1L gene (NG_008991.2).
RefSeq mRNA
See reference mRNA sequence for the RPGRIP1L gene (XM_011522973.4).

BioProject
Proteins related to BioProjects
Nucleotide
Nucleotide sequence from coding region
Taxonomy
Taxonomy sequences associated with protein record
BioSystems
BioSystems
CDD Search Results
Display conserved domains within a protein
Conserved Domains (Concise)
Link to a concise list of conserved domains in a protein
Conserved Domains (Full)
Link to conserved domains within a protein
Domain Relatives
Display proteins with similar conserved domain architecture
Encoding mRNA
Link from protein to encoding mRNA
Gene
Link to related Genes
Genome
Genome record encoding protein sequence
Identical Structures
3D structures for identical protein sequences
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed
SNP
Related SNPs

protein fantom isoform X12 [Homo sapiens]
protein fantom isoform X12 [Homo sapiens]
gi|767989665|ref|XP_011521275.1|

Protein
Mus musculus multiple endocrine neoplasia 1 (Men1), transcript variant 1, mRNA
Mus musculus multiple endocrine neoplasia 1 (Men1), transcript variant 1, mRNA
gi|270309146|ref|NM_001168488.1|

Nucleotide
PREDICTED: prolyl 3-hydroxylase 2 [Haliaeetus leucocephalus]
PREDICTED: prolyl 3-hydroxylase 2 [Haliaeetus leucocephalus]
gi|729749645|ref|XP_010571370.1|

Protein

Your browsing activity is empty.

Activity recording is turned off.

Protein