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Gene: FERMT1 (fermitin family member 1) Homo sapiens
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Symbol: FERMT1
Name: fermitin family member 1
Description: Predicted to have actin filament binding activity. Involved in several processes, including establishment of epithelial cell polarity; keratinocyte migration; and keratinocyte proliferation. Localizes to the cell junction and cytosol. Implicated in Kindler syndrome; telangiectasis; and vesiculobullous skin disease.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: C20orf42; chromosome 20 open reading frame 42; DTGCU2; fermitin family homolog 1; FLJ20116; FLJ23423; KIND1; kindlerin; kindlin 1; kindlin syndrome protein; unc-112-related protein 1; UNC112 related protein 1; UNC112A; URP1
Orthologs:
Mus musculus (house mouse) : Fermt1 (fermitin family member 1)  MGI  Alliance
Rattus norvegicus (Norway rat) : Fermt1 (fermitin family member 1)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Fermt1 (fermitin family member 1)
Pan paniscus (bonobo/pygmy chimpanzee) : FERMT1 (fermitin family member 1)
Canis lupus familiaris (dog) : FERMT1 (fermitin family member 1)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Fermt1 (fermitin family member 1)
Sus scrofa (pig) : FERMT1 (fermitin family member 1)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38206,074,845 - 6,123,609 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37206,055,492 - 6,104,191 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36206,003,492 - 6,052,191 (-)NCBINCBI36hg18NCBI36
Build 34206,003,492 - 6,052,191NCBI
Celera206,126,766 - 6,175,354 (-)NCBI
Cytogenetic Map20p12.3NCBI
HuRef206,012,168 - 6,061,355 (-)NCBIHuRef
CHM1_1206,055,497 - 6,104,189 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
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References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FERMT1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1315645
Created: 2005-01-12
Species: Homo sapiens
Last Modified: 2019-11-26
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.