mutLBSgeneDB |
Gene summary for FGF12 |
Gene summary |
Basic gene Info. | Gene symbol | FGF12 |
Gene name | fibroblast growth factor 12 | |
Synonyms | FGF12B|FHF1 | |
Cytomap | UCSC genome browser: 3q28 | |
Type of gene | protein-coding | |
RefGenes | NM_004113.5, NM_021032.4, | |
Description | FGF-12FHF-1fibroblast growth factor 12Bfibroblast growth factor FGF-12bfibroblast growth factor homologous factor 1myocyte-activating factor | |
Modification date | 20141207 | |
dbXrefs | MIM : 601513 | |
HGNC : HGNC | ||
Ensembl : ENSG00000114279 | ||
HPRD : 03303 | ||
Vega : OTTHUMG00000156132 | ||
Protein | UniProt: P61328 go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_FGF12 | |
BioGPS: 2257 | ||
Pathway | NCI Pathway Interaction Database: FGF12 | |
KEGG: FGF12 | ||
REACTOME: FGF12 | ||
Pathway Commons: FGF12 | ||
Context | iHOP: FGF12 | |
ligand binding site mutation search in PubMed: FGF12 | ||
UCL Cancer Institute: FGF12 | ||
Assigned class in mutLBSgeneDB | C: This gene just belongs to mutLBSgenes. |
Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez |
GO ID | GO Term | PubMed ID | GO:0008543 | fibroblast growth factor receptor signaling pathway | 12815063 |
Top |
Ligand binding site mutations for FGF12 |
Lollipop-style diagram of mutations at LBS in amino-acid sequence. We represented ligand binding site mutations only. (You can see big image via clicking.) : non-synonymous mutation on LBS, Circle size denotes number of samples. |
Cancer type specific mutLBS sorted by frequency |
LBS | AAchange of nsSNV | Cancer type | # samples | Y134 | Y136H | LUAD | 1 | Y134 | G133D | LUAD | 1 | K148 | K148N | LUSC | 1 | S195 | S196L | SKCM | 1 | R188 | R188K | SKCM | 1 | S195 | S195L | SKCM | 1 |
cf) Cancer type abbreviation. BLCA: Bladder urothelial carcinoma, BRCA: Breast invasive carcinoma, CESC: Cervical squamous cell carcinoma and endocervical adenocarcinoma, COAD: Colon adenocarcinoma, GBM: Glioblastoma multiforme, LGG: Brain lower grade glioma, HNSC: Head and neck squamous cell carcinoma, KICH: Kidney chromophobe, KIRC: Kidney renal clear cell carcinoma, KIRP: Kidney renal papillary cell carcinoma, LAML: Acute myeloid leukemia, LUAD: Lung adenocarcinoma, LUSC: Lung squamous cell carcinoma, OV: Ovarian serous cystadenocarcinoma, PAAD: Pancreatic adenocarcinoma, PRAD: Prostate adenocarcinoma, SKCM: Skin cutaneous melanoma, STAD: Stomach adenocarcinoma, THCA: Thyroid carcinoma, UCEC: Uterine corpus endometrial carcinoma. |
Top |
Protein structure related information for FGF12 |
Relative protein structure stability change (ΔΔE) using Mupro 1.1 Mupro score denotes assessment of the effect of mutations on thermodynamic stability. (ΔΔE<0: mutation decreases stability, ΔΔE>0: mutation increases stability) |
: nsSNV at non-LBS: nsSNV at LBS |
nsSNVs sorted by the relative stability change of protein structure by each mutation Blue: mutations of positive stability change. and red : the most recurrent mutation for this gene. |
LBS | AAchange of nsSNV | Relative stability change | Y134 | Y136H | -1.0686617 | R188 | R188K | -0.91182391 | K148 | K148N | -0.89818707 | S195 | S196L | -0.62796969 | Y134 | G133D | -0.57295974 | S195 | S195L | -0.24881199 |
(MuPro1.1: Jianlin Cheng et al., Prediction of Protein Stability Changes for Single-Site Mutations Using Support Vector Machines, PROTEINS: Structure, Function, and Bioinformatics. 2006, 62:1125-1132) |
Structure image for FGF12 from PDB |
Top |
Differential gene expression and gene-gene network for FGF12 |
Differential gene expression between mutated and non-mutated LBS samples in all 16 major cancer types |
Differential co-expressed gene network based on protein-protein interaction data (CePIN) |
Top |
Top |
Phenotype information for FGF12 |
Gene level disease information (DisGeNet) |
Disease ID | Disease name | # PubMed | Association type |
Mutation level pathogenic information (ClinVar annotation) |
Allele ID | AA change | Clinical significance | Origin | Phenotype IDs |
Top |
Pharmacological information for FGF12 |
Gene expression profile of anticancer drug treated cell-lines (CCLE) Heatmap showing the correlation between gene expression and drug response across all the cell-lines. We chose the top 20 among 138 drugs.We used Pearson's correlation coefficient. |
Drug information targeting mutLBSgene (Approved drugs only) |
Drug status | DrugBank ID | Name | Type | Drug structure |
Gene-centered ligand-gene interaction network |
Ligands binding to mutated ligand binding site of FGF12 go to BioLip |
Ligand ID | Ligand short name | Ligand long name | PDB ID | PDB name | mutLBS |
Top |
Conservation information for LBS of FGF12 |
Multiple alignments for P61328 in multiple species |
LBS | AA sequence | # species | Species | K148 | PECKFKESVFE | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | K185 | EGQIMKGNRVK | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | K193 | RVKKTKPSSHF | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | P194 | VKKTKPSSHFV | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | Q81 | RLFSQQGYFLQ | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | R114 | IPVGLRVVAIQ | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | R188 | IMKGNRVKKTK | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | S150 | CKFKESVFENY | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | S195 | KKTKPSSHFVP | 3 | Homo sapiens, Mus musculus, Rattus norvegicus | Y134 | MNGEGYLYSSD | 3 | Homo sapiens, Mus musculus, Rattus norvegicus |
Copyright © 2016-Present - The University of Texas Health Science Center at Houston |