Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
23529 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Cardiotrophin like cytokine factor 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
CLCF1 |
SynonymsGene synonyms aliases
|
BSF-3, BSF3, CISS2, CLC, NNT-1, NNT1, NR6 |
ChromosomeChromosome number
|
11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
11q13.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
|
This gene is a member of the glycoprotein (gp)130 cytokine family and encodes cardiotrophin-like cytokine factor 1 (CLCF1). CLCF1 forms a heterodimer complex with cytokine receptor-like factor 1 (CRLF1). This dimer competes with ciliary neurotrophic facto |
miRNAmiRNA information provided by mirtarbase database.
|
|
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
|
|
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|
Protein
|
UniProt ID |
Q9UBD9 |
Protein name |
Cardiotrophin-like cytokine factor 1 (B-cell-stimulating factor 3) (BSF-3) (Novel neurotrophin-1) (NNT-1) |
Protein function |
In complex with CRLF1, forms a heterodimeric neurotropic cytokine that plays a crucial role during neuronal development (Probable). Also stimulates B-cells. Binds to and activates the ILST/gp130 receptor. {ECO:0000269|PubMed:10448081, ECO:000026 |
PDB |
8D7H
,
8D7R
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF06875 |
PRF |
40 → 213 |
Plethodontid receptivity factor PRF |
Domain |
|
Sequence |
|
Sequence length |
225 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
|
|
Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Cold-induced sweating syndrome |
COLD-INDUCED SWEATING SYNDROME 1, COLD-INDUCED SWEATING SYNDROME 2, Cold-induced sweating syndrome |
rs104894198, rs104894203, rs761746361, rs137853143, rs137853144, rs2145329741, rs137853145, rs367543004, rs137853929, rs137853932, rs137853934, rs137853935, rs768727082, rs137853928, rs879255557, rs879255558, rs780705654, rs879255556, rs1555758035, rs1600650861 |
1678282, 20400119, 16782820 |
Crisponi syndrome |
Crisponi syndrome |
rs1600651228 |
1678282, 20400119 |
Scoliosis |
Scoliosis, unspecified |
rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085 |
|
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Cubitus valgus |
Acquired cubitus valgus |
|
|
Clinodactyly |
Clinodactyly of fingers, Clinodactyly |
|
|
Facial paralysis |
Facial paralysis |
|
|
High palate |
Byzanthine arch palate |
|
|
Hypohidrosis |
Hypohidrosis |
|
|
Impaired cognition |
Impaired cognition |
|
|
Micrognathism |
Micrognathism |
|
|
Microstomia |
Microstomia |
|
|
Sensorimotor neuropathy |
Sensorimotor neuropathy |
|
|
Syndactyly of the toes |
2-3 toe syndactyly |
|
|
Thoracolumbar scoliosis |
Thoracolumbar scoliosis |
|
|
|