FCER1A (Fc fragment of IgE receptor Ia) - Rat Genome Database
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Gene: FCER1A (Fc fragment of IgE receptor Ia) Homo sapiens
Analyze
Symbol: FCER1A
Name: Fc fragment of IgE receptor Ia
RGD ID: 736318
HGNC Page HGNC
Description: Predicted to have IgE receptor activity. Predicted to be involved in several processes, including leukotriene biosynthetic process; positive regulation of leukocyte mediated immunity; and positive regulation of macromolecule metabolic process. Localizes to cell surface. Biomarker of asthma and rhinitis.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: alpha polypeptide; Fc epsilon receptor Ia; Fc epsilon RI alpha-chain; Fc fragment of IgE, high affinity I, receptor for; Fc IgE receptor, alpha polypeptide; fc receptor, ige, high affinity i, alpha polypeptide; Fc-epsilon RI-alpha; FCE1A; FcERI; high affinity immunoglobulin epsilon receptor alpha-subunit; high affinity immunoglobulin epsilon receptor subunit alpha; igE Fc receptor subunit alpha; immunoglobulin E receptor, high-affinity, of mast cells, alpha polypeptide
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1159,289,714 - 159,308,224 (+)EnsemblGRCh38hg38GRCh38
GRCh381159,283,575 - 159,308,202 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371159,253,365 - 159,277,992 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh371159,253,678 - 159,278,014 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361157,526,128 - 157,544,638 (+)NCBINCBI36hg18NCBI36
Build 341156,072,576 - 156,091,086NCBI
Celera1132,329,745 - 132,348,256 (+)NCBI
Cytogenetic Map1q23.2NCBI
HuRef1130,610,827 - 130,635,025 (+)NCBIHuRef
CHM1_11160,649,107 - 160,673,443 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
asthma  (IEP)
drug allergy  (EXP)
Drug Eruptions  (EXP)
rhinitis  (IEP)
urticaria  (EXP)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:1472946   PMID:1533243   PMID:1535625   PMID:2146219   PMID:2964640   PMID:2967464   PMID:8125119   PMID:8245459   PMID:8613143   PMID:8752908   PMID:9103201   PMID:10917520  
PMID:11409901   PMID:11531339   PMID:11776381   PMID:12070183   PMID:12200378   PMID:12217383   PMID:12270716   PMID:12477932   PMID:12646639   PMID:12671054   PMID:12855579   PMID:12897750  
PMID:12902495   PMID:13129935   PMID:14655898   PMID:14746805   PMID:15140034   PMID:15217825   PMID:15373772   PMID:15489334   PMID:15562891   PMID:15696081   PMID:15743766   PMID:16081836  
PMID:16237063   PMID:16339523   PMID:16459334   PMID:16563391   PMID:16581830   PMID:16709862   PMID:17125826   PMID:17165285   PMID:17192395   PMID:17267694   PMID:17430357   PMID:17521040  
PMID:17541278   PMID:17686114   PMID:17703412   PMID:17883736   PMID:17903293   PMID:17965580   PMID:17993265   PMID:18036650   PMID:18179824   PMID:18187193   PMID:18321309   PMID:18356810  
PMID:18382690   PMID:18394141   PMID:18523286   PMID:18680511   PMID:18726713   PMID:18846228   PMID:19082920   PMID:19141351   PMID:19150851   PMID:19164348   PMID:19245427   PMID:19258923  
PMID:19359220   PMID:19372141   PMID:19385959   PMID:19423540   PMID:19494509   PMID:19514647   PMID:19555572   PMID:19685047   PMID:19697153   PMID:19748979   PMID:20028371   PMID:20117843  
PMID:20126404   PMID:20141544   PMID:20163202   PMID:20237496   PMID:20406964   PMID:20410486   PMID:20438785   PMID:20503287   PMID:20523060   PMID:20603037   PMID:20664273   PMID:20691829  
PMID:21209833   PMID:21216468   PMID:21516097   PMID:21622859   PMID:21725845   PMID:21738338   PMID:21873635   PMID:21903095   PMID:21958156   PMID:21988832   PMID:22075330   PMID:22173243  
PMID:22222815   PMID:22384272   PMID:22800345   PMID:22939635   PMID:23251661   PMID:23621092   PMID:23725541   PMID:23980848   PMID:24354852   PMID:24361879   PMID:24569373   PMID:24610015  
PMID:24623722   PMID:25412950   PMID:25713122   PMID:25923080   PMID:26136426   PMID:26613553   PMID:26626992   PMID:26707911   PMID:26774660   PMID:27417022   PMID:29243845   PMID:29295972  
PMID:30144948   PMID:30685572   PMID:30972912   PMID:32296183  


Genomics

Comparative Map Data
FCER1A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1159,289,714 - 159,308,224 (+)EnsemblGRCh38hg38GRCh38
GRCh381159,283,575 - 159,308,202 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371159,253,365 - 159,277,992 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh371159,253,678 - 159,278,014 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361157,526,128 - 157,544,638 (+)NCBINCBI36hg18NCBI36
Build 341156,072,576 - 156,091,086NCBI
Celera1132,329,745 - 132,348,256 (+)NCBI
Cytogenetic Map1q23.2NCBI
HuRef1130,610,827 - 130,635,025 (+)NCBIHuRef
CHM1_11160,649,107 - 160,673,443 (+)NCBICHM1_1
Fcer1a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391173,048,836 - 173,054,799 (-)NCBIGRCm39mm39
GRCm381173,221,269 - 173,227,232 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1173,221,284 - 173,227,214 (-)EnsemblGRCm38mm10GRCm38
MGSCv371175,151,402 - 175,157,360 (-)NCBIGRCm37mm9NCBIm37
MGSCv361175,057,959 - 175,063,889 (-)NCBImm8
Celera1176,073,170 - 176,079,126 (-)NCBICelera
Cytogenetic Map1H3NCBI
cM Map180.33NCBI
Fcer1a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21385,686,099 - 85,692,394 (-)NCBI
Rnor_6.0 Ensembl1391,730,925 - 91,737,053 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01391,727,253 - 91,737,106 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01396,245,261 - 96,251,522 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41389,429,982 - 89,436,507 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11389,618,865 - 89,625,338 (-)NCBI
Celera1385,289,763 - 85,295,958 (-)NCBICelera
RH 3.4 Map13566.1RGD
Cytogenetic Map13q24NCBI
Fcer1a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495546811,094,788 - 11,101,173 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495546811,094,792 - 11,101,191 (+)NCBIChiLan1.0ChiLan1.0
FCER1A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11138,439,921 - 138,458,258 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1138,439,921 - 138,458,258 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01134,655,230 - 134,660,961 (+)NCBIMhudiblu_PPA_v0panPan3
FCER1A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl3822,683,477 - 22,690,763 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.13822,683,478 - 22,688,842 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Fcer1a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_0049367401,201,370 - 1,206,871 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FCER1A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl491,118,879 - 91,125,437 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1491,118,867 - 91,125,448 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2499,069,615 - 99,075,656 (+)NCBISscrofa10.2Sscrofa10.2susScr3
FCER1A
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1204,635,316 - 4,640,787 (-)NCBI
ChlSab1.1 Ensembl204,635,328 - 4,640,590 (-)Ensembl
Fcer1a
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247942,003,031 - 2,008,930 (-)NCBI

Position Markers
SHGC-132100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371159,277,781 - 159,278,011UniSTSGRCh37
Build 361157,544,405 - 157,544,635RGDNCBI36
Celera1132,348,023 - 132,348,253RGD
Cytogenetic Map1q23UniSTS
HuRef1130,634,792 - 130,635,022UniSTS
TNG Radiation Hybrid Map171850.0UniSTS
D1S2397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371159,277,739 - 159,278,013UniSTSGRCh37
Build 361157,544,363 - 157,544,637RGDNCBI36
Celera1132,347,981 - 132,348,255RGD
Cytogenetic Map1q23UniSTS
HuRef1130,634,750 - 130,635,024UniSTS
GeneMap99-GB4 RH Map1589.3UniSTS
Whitehead-RH Map1709.4UniSTS
NCBI RH Map11426.2UniSTS
GeneMap99-G3 RH Map16034.0UniSTS
FCER1A_3020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371159,277,495 - 159,278,087UniSTSGRCh37
Build 361157,544,119 - 157,544,711RGDNCBI36
Celera1132,347,737 - 132,348,329RGD
HuRef1130,634,506 - 130,635,098UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:108
Count of miRNA genes:84
Interacting mature miRNAs:84
Transcripts:ENST00000368114, ENST00000368115
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 3
Medium 120 301 62 40 169 21 1239 64 110 68 77 189 20 152 702
Low 1864 1631 1032 364 854 234 1956 1040 1048 217 941 1005 133 1 824 1278 1
Below cutoff 325 894 524 179 445 166 778 874 1975 73 284 184 12 218 676 2 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001387280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide A21606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB059236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL513323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP002535 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC005912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS544001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  J03605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L14075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X06948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z29585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000368114   ⟹   ENSP00000357096
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1159,302,336 - 159,307,993 (+)Ensembl
RefSeq Acc Id: ENST00000368115   ⟹   ENSP00000357097
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1159,289,714 - 159,308,224 (+)Ensembl
RefSeq Acc Id: NM_001387280   ⟹   NP_001374209
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381159,302,336 - 159,308,202 (+)NCBI
RefSeq Acc Id: NM_001387281   ⟹   NP_001374210
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381159,302,336 - 159,308,202 (+)NCBI
RefSeq Acc Id: NM_001387282   ⟹   NP_001374211
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381159,302,336 - 159,308,202 (+)NCBI
RefSeq Acc Id: NM_002001   ⟹   NP_001992
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381159,283,575 - 159,308,202 (+)NCBI
GRCh371159,253,678 - 159,278,014 (+)NCBI
Build 361157,526,128 - 157,544,638 (+)NCBI Archive
HuRef1130,610,827 - 130,635,025 (+)NCBI
CHM1_11160,649,107 - 160,673,443 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001992   ⟸   NM_002001
- Peptide Label: isoform 1 precursor
- UniProtKB: P12319 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000357096   ⟸   ENST00000368114
RefSeq Acc Id: ENSP00000357097   ⟸   ENST00000368115
RefSeq Acc Id: NP_001374209   ⟸   NM_001387280
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001374211   ⟸   NM_001387282
- Peptide Label: isoform 2 precursor
RefSeq Acc Id: NP_001374210   ⟸   NM_001387281
- Peptide Label: isoform 3 precursor
Protein Domains
Ig-like

Promoters
RGD ID:6857718
Promoter ID:EPDNEW_H2024
Type:initiation region
Name:FCER1A_1
Description:Fc fragment of IgE receptor Ia
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381159,302,336 - 159,302,396EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q23.1-25.1(chr1:157747246-176021247)x3 copy number gain See cases [RCV000051854] Chr1:157747246..176021247 [GRCh38]
Chr1:157717036..175990383 [GRCh37]
Chr1:155983660..174257006 [NCBI36]
Chr1:1q23.1-25.1
pathogenic
GRCh38/hg38 1q23.1-23.3(chr1:156664483-160727411)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051851]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051851]|See cases [RCV000051851] Chr1:156664483..160727411 [GRCh38]
Chr1:156634275..160697201 [GRCh37]
Chr1:154900899..158963825 [NCBI36]
Chr1:1q23.1-23.3
pathogenic
NM_002001.3(FCER1A):c.15G>A (p.Met5Ile) single nucleotide variant Malignant melanoma [RCV000059944] Chr1:159302379 [GRCh38]
Chr1:159272169 [GRCh37]
Chr1:157538793 [NCBI36]
Chr1:1q23.2
not provided
NM_002001.3(FCER1A):c.114G>A (p.Trp38Ter) single nucleotide variant Malignant melanoma [RCV000059945] Chr1:159303965 [GRCh38]
Chr1:159273755 [GRCh37]
Chr1:157540379 [NCBI36]
Chr1:1q23.2
not provided
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q23.1-23.2(chr1:158685035-159301350)x3 copy number gain See cases [RCV000512504] Chr1:158685035..159301350 [GRCh37]
Chr1:1q23.1-23.2
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_002001.3(FCER1A):c.530C>T (p.Thr177Met) single nucleotide variant not provided [RCV000949233] Chr1:159306186 [GRCh38]
Chr1:159275976 [GRCh37]
Chr1:1q23.2
benign
NM_002001.3(FCER1A):c.324C>T (p.Val108=) single nucleotide variant not provided [RCV000886280] Chr1:159304175 [GRCh38]
Chr1:159273965 [GRCh37]
Chr1:1q23.2
benign
NM_002001.3(FCER1A):c.761C>T (p.Pro254Leu) single nucleotide variant not provided [RCV000967736] Chr1:159307919 [GRCh38]
Chr1:159277709 [GRCh37]
Chr1:1q23.2
benign
NM_002001.3(FCER1A):c.251A>G (p.Lys84Arg) single nucleotide variant not provided [RCV000961103] Chr1:159304102 [GRCh38]
Chr1:159273892 [GRCh37]
Chr1:1q23.2
benign
NM_002001.3(FCER1A):c.302G>A (p.Ser101Asn) single nucleotide variant not provided [RCV000970169] Chr1:159304153 [GRCh38]
Chr1:159273943 [GRCh37]
Chr1:1q23.2
benign
GRCh37/hg19 1q23.1-24.2(chr1:157321299-167391423)x1 copy number loss not provided [RCV000848773] Chr1:157321299..167391423 [GRCh37]
Chr1:1q23.1-24.2
pathogenic
NM_002001.3(FCER1A):c.741C>A (p.Asn247Lys) single nucleotide variant not provided [RCV000954372] Chr1:159307899 [GRCh38]
Chr1:159277689 [GRCh37]
Chr1:1q23.2
benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3609 AgrOrtholog
COSMIC FCER1A COSMIC
Ensembl Genes ENSG00000179639 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000357096 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000357097 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000368114 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000368115 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000179639 GTEx
HGNC ID HGNC:3609 ENTREZGENE
Human Proteome Map FCER1A Human Proteome Map
InterPro Ig-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Immunoglobulin UniProtKB/TrEMBL
KEGG Report hsa:2205 UniProtKB/Swiss-Prot
NCBI Gene 2205 ENTREZGENE
OMIM 147140 OMIM
Pfam Ig_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00047 UniProtKB/TrEMBL
PharmGKB PA28056 PharmGKB
PROSITE IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART IGc2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00409 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt E9PRN1_HUMAN UniProtKB/TrEMBL
  FCERA_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q6GU38_HUMAN UniProtKB/TrEMBL


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-19 FCER1A  Fc fragment of IgE receptor Ia    Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide  Symbol and/or name change 5135510 APPROVED