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FGFR2 IIIa TM [extracellular region]
Stable Identifier
R-MMU-8851701
Type
Protein [EntityWithAccessionedSequence]
Species
Mus musculus
Compartment
extracellular region
External Reference Information
External Reference
UniProt:P21803 Fgfr2
Gene Names
Fgfr2, Bek, Ect1
Chain
signal peptide:1-21, chain:22-821
Reference Genes
BioGPS Gene:14183 Fgfr2
KEGG:mmu:14183 Fgfr2
Monarch:14183 Fgfr2
NCBI Gene:14183 Fgfr2
UCSC:P21803 Fgfr2
Reference Transcript
RefSeq:NM_010207.2 Fgfr2
RefSeq:NM_201601.2 Fgfr2
Participates
as a component of
FGFR2 IIIa TM:FGF1,2:FGFR2b,c:HS [plasma membrane] (Homo sapiens)
as an input of
Mouse FGFR2 IIIa TM binds FGF1,2 and full-length receptors (Homo sapiens)
as an output of
Aberrant alternative splicing generates a soluble disease variant FGFR2 IIIa TM (Mus musculus)
Other forms of this molecule
phospho-Fgfr2 [plasma membrane]
phospho-Fgfr2 [plasma membrane]
phospho-Fgfr2 [plasma membrane]
phospho-Fgfr2 [plasma membrane]
Fgfr2 [plasma membrane]
Fgfr2 [plasma membrane]
Fgfr2 [plasma membrane]
Fgfr2 [plasma membrane]
Disease
Name
Identifier
Synonyms
acrocephalosyndactylia
DOID:12960
Apert syndrome
Cross References
RefSeq
NP_034337.2
,
NP_963895.2
Mondo
0019796
PRO
P21803
MGI
95523
GlyGen
P21803
PDB
4HWU
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