Fhl2 (GeneID: 14200) | Mus musculus
Description: four and a half LIM domains 2 [Source:MGI Symbol;Acc:MGI:1338762]
Synonyms: FHL-2, SLIM3, SLIM-3
Other ID(s): ENSMUSG00000008136, MGI:1338762
Protein Accession Numbers: NP_034342, NP_001276462, XP_011236736
Statistics: ClinVar(704) gnomAD(1374) COSMIC(1003) PTM(40)
ClinVar Pathogenicity of Variations help

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000322142 You are here now! ENST00000336660 ENST00000344213 ENST00000358129 You are here now! ENST00000393352 You are here now! ENST00000393353 You are here now! ENST00000408995 You are here now! ENST00000409177 ENST00000409807 You are here now! ENST00000447958 ENST00000452732 ENST00000530340 ENST00000607522 NP_001034581 You are here now! NP_001305823 You are here now! NP_001305824 You are here now! NP_001305825 You are here now! NP_001305826 NP_001305827 NP_001305828 NP_001361328 You are here now! NP_001441 You are here now! NP_963849 You are here now! NP_963851 You are here now!


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00412 LIM LIM domain 101-158 CL0167 Zn_Beta_Ribbon Homo sapiens
PF00412 LIM LIM domain 162-217 CL0167 Zn_Beta_Ribbon Homo sapiens
PF00412 LIM LIM domain 40-97 CL0167 Zn_Beta_Ribbon Homo sapiens
PF00412 LIM LIM domain 221-278 CL0167 Zn_Beta_Ribbon Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Malignant neoplasm of breast Neoplasms ; Skin and Connective Tissue Diseases ; 0.588 0.517
Cardiomyopathy, Dilated Cardiovascular Diseases ; 0.588 0.517
Cardiomegaly Cardiovascular Diseases ; Pathological Conditions, Signs and Symptoms ; 0.588 0.517
Leukemia, Myelocytic, Acute Neoplasms ; 0.588 0.517
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.588 0.517
Acute Myeloid Leukemia, M1 Neoplasms ; 0.588 0.517
Conduction disorder of the heart Cardiovascular Diseases ; 0.588 0.517
Familial dilated cardiomyopathy Cardiovascular Diseases ; 0.588 0.517
Breast Carcinoma Neoplasms ; Skin and Connective Tissue Diseases ; 0.588 0.517
Mammary Neoplasms, Human Neoplasms ; Skin and Connective Tissue Diseases ; 0.588 0.517
Cardiac Hypertrophy Cardiovascular Diseases ; Pathological Conditions, Signs and Symptoms ; 0.588 0.517
Mammary Neoplasms Neoplasms ; Skin and Connective Tissue Diseases ; 0.588 0.517
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.588 0.517
NO RESULT FOUND
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