FCGR1BP (Fc gamma receptor Ib, pseudogene)

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Gene: FCGR1BP (Fc gamma receptor Ib, pseudogene) Homo sapiens

Analyze

No known orthologs.

Symbol:

FCGR1BP

Name:

Fc gamma receptor Ib, pseudogene

RGD ID:

1349361

HGNC Page

HGNC:3614

Description:

Predicted to enable IgG receptor activity. Predicted to be involved in antibody-dependent cellular cytotoxicity and cell surface receptor signaling pathway. Predicted to be located in clathrin-coated endocytic vesicle membrane; early endosome membrane; and plasma membrane. Predicted to be active in external side of plasma membrane.

Type:

pseudo (Ensembl: transcribed_unprocessed_pseudogene)

RefSeq Status:

REVIEWED

Previously known as:

CD34; CD64; CD64b; Fc fragment of IgG receptor Ib; Fc fragment of IgG, high affinity Ib, receptor (CD64); Fc fragment of IgG, high affinity Ib, receptor for (CD64); Fc gamma receptor I; Fc gamma receptor Ib; Fc-gamma receptor I B2; Fc-gamma RI; Fc-gamma RIA; fc-gamma RIB; FCG1; FcgammaRIa; FCGR1; FCGR1A; FCGR1B; FcRI; fcRIB; hFcgammaRIB; High affinity immunoglobulin gamma Fc receptor I; high affinity immunoglobulin gamma Fc receptor IB; IGFR1; IGFRB; IgG Fc receptor I; igG Fc receptor IB

RGD Orthologs

Alliance Orthologs

More Info

homologs ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Other homologs ²				less info ...
Sus scrofa (pig):	FCGR1A (Fc fragment of IgG, high affinity Ia, receptor (CD64))	HGNC	EggNOG
Alliance orthologs ³
Mus musculus (house mouse):	Fcgr1 (Fc receptor, IgG, high affinity I)	Alliance	DIOPT (OrthoFinder\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Fcgr1a (Fc gamma receptor 1A)	Alliance	DIOPT (OMA\|OrthoFinder\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	zgc:154125	Alliance	DIOPT (InParanoid\|PANTHER\|PhylomeDB)
Xenopus tropicalis (tropical clawed frog):	fcgr1	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PhylomeDB)
Xenopus tropicalis (tropical clawed frog):	XB5960289 [provisional:fcrl4]	Alliance	DIOPT (Hieranoid\|InParanoid\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus tropicalis (tropical clawed frog):	fcrl3	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PhylomeDB)

Related Functional Gene:

FCGR1A

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	1	121,087,345 - 121,097,161 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	1	121,087,395 - 121,096,152 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh38.p14 Ensembl	1	121,042,602 - 121,103,109 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	1	120,926,128 - 120,935,944 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	120,728,657 - 120,737,417 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Cytogenetic Map	1	p11.2	NCBI
HuRef	1	118,453,001 - 118,453,262 (-)	NCBI		HuRef
CHM1_1	1	121,745,435 - 121,755,251 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	1	121,096,728 - 121,106,544 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

all-trans-retinoic acid (EXP)

antirheumatic drug (EXP)

bisphenol A (EXP)

cisplatin (EXP)

Dibutyl phosphate (EXP)

maleic acid (EXP)

nickel atom (EXP)

paracetamol (EXP)

triphenyl phosphate (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

adaptive immune response (IEA)

antibody-dependent cellular cytotoxicity (IBA)

cell surface receptor signaling pathway (IBA)

Fc receptor signaling pathway (IEA)

Fc-gamma receptor signaling pathway (IEA)

immune response (NAS)

Cellular Component

clathrin-coated endocytic vesicle membrane (TAS)

early endosome membrane (TAS)

external side of plasma membrane (IBA)

plasma membrane (IEA,NAS,TAS)

Molecular Function

IgG binding (IEA)

IgG receptor activity (IBA)

immunoglobulin receptor activity (NAS)

References

References - curated

#	Reference Title	Reference Citation
1.	Localization of FCGR1 encoding Fcgamma receptor class I in primates: molecular evidence for two pericentric inversions during the evolution of human chromosome 1.	Maresco DL, etal., Cytogenet Cell Genet 1998;82(1-2):71-4.
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1379234	PMID:1402657	PMID:1430234	PMID:1830050	PMID:8697799	PMID:8889548	PMID:9232445	PMID:9490697	PMID:9881690	PMID:9933095	PMID:11802953	PMID:12477932
PMID:12766061	PMID:17124586	PMID:19330030	PMID:21135020	PMID:21832933	PMID:21873635	PMID:32073518	PMID:34373451	PMID:35381635	PMID:35906200

Genomics

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 1p12-q21.2(chr1:120836007-149583533)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051844]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051844]\|See cases [RCV000051844]	Chr1:120836007..149583533 [GRCh38] Chr1:145425395..153212501 [GRCh37] Chr1:144136752..151479125 [NCBI36] Chr1:1p12-q21.2	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1428
Count of miRNA genes:	537
Interacting mature miRNAs:	600
Transcripts:	ENST00000369178, ENST00000369383, ENST00000369384, ENST00000466915, ENST00000471609, ENST00000472543
Prediction methods:	Microtar, 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.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1300021	BP45_H	Blood pressure QTL 45 (human)	1.77	0.00218	Blood pressure	systolic	1	103389009	129389009	Human

Markers in Region

GDB:190043

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	149,370,603 - 149,370,937	UniSTS	GRCh37
GRCh37	1	149,755,559 - 149,755,893	UniSTS	GRCh37
Build 36	1	147,637,227 - 147,637,561	RGD	NCBI36
Cytogenetic Map	1	q21.2-q21.3	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	1	p11.2	UniSTS

D1S3356

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	1	q21.2-q21.3	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	1	p11.2	UniSTS
Whitehead-RH Map	1	570.4	UniSTS
Whitehead-YAC Contig Map	1		UniSTS

RH69162

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	1	q21.2-q21.3	UniSTS
Cytogenetic Map	1	p11.2	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1190	2138	2358	2134	4338	1656	2144	5	565	1387	410	1710	6130	5691	6	3639	773	1606	1474	163

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_045213	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_164758	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_164759	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_164760	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC244453	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH002811	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH007343	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307244	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK308886	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK311502	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL357493	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW134502	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC110416	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM992325	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ030076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU682943	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CD677904	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L03419	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	L03420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000369178 ⟹ ENSP00000481411

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,322 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000369383 ⟹ ENSP00000358390

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,300 - 121,097,161 (+)	Ensembl

Ensembl Acc Id:

ENST00000369384 ⟹ ENSP00000358391

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,295 - 121,097,161 (+)	Ensembl

Ensembl Acc Id:

ENST00000453173

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,262 - 121,096,304 (+)	Ensembl

Ensembl Acc Id:

ENST00000466915

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,304 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000471609

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,345 - 121,095,642 (+)	Ensembl

Ensembl Acc Id:

ENST00000472543 ⟹ ENSP00000479641

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,301 - 121,096,322 (+)	Ensembl

Ensembl Acc Id:

ENST00000615565

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,362 - 121,093,801 (+)	Ensembl

Ensembl Acc Id:

ENST00000616817 ⟹ ENSP00000478655

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,345 - 121,095,642 (+)	Ensembl

Ensembl Acc Id:

ENST00000623603 ⟹ ENSP00000485498

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,345 - 121,095,642 (+)	Ensembl

Ensembl Acc Id:

ENST00000697334

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,395 - 121,096,152 (+)	Ensembl

Ensembl Acc Id:

ENST00000697335

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,311 - 121,091,051 (+)	Ensembl

Ensembl Acc Id:

ENST00000697336

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,372 - 121,096,308 (+)	Ensembl

Ensembl Acc Id:

ENST00000700794

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,328 - 121,096,389 (+)	Ensembl

Ensembl Acc Id:

ENST00000700943

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,331 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000700986

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,302 - 121,096,318 (+)	Ensembl

Ensembl Acc Id:

ENST00000701453

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,341 - 121,096,322 (+)	Ensembl

Ensembl Acc Id:

ENST00000701628

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,334 - 121,096,312 (+)	Ensembl

Ensembl Acc Id:

ENST00000701713

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,311 - 121,096,381 (+)	Ensembl

Ensembl Acc Id:

ENST00000701949

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,331 - 121,096,381 (+)	Ensembl

Ensembl Acc Id:

ENST00000702526

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,331 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000702760

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,345 - 121,096,307 (+)	Ensembl

Ensembl Acc Id:

ENST00000702854

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,345 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768787

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,042,602 - 121,095,954 (+)	Ensembl

Ensembl Acc Id:

ENST00000768788

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,043,141 - 121,095,993 (+)	Ensembl

Ensembl Acc Id:

ENST00000768789

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,044,011 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,044,098 - 121,096,314 (+)	Ensembl

Ensembl Acc Id:

ENST00000768791

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,044,110 - 121,096,308 (+)	Ensembl

Ensembl Acc Id:

ENST00000768792

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,050,340 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768793

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,043,125 - 121,088,030 (+)	Ensembl

Ensembl Acc Id:

ENST00000768794

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,364 - 121,103,109 (+)	Ensembl

Ensembl Acc Id:

ENST00000768795

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,369 - 121,102,514 (+)	Ensembl

Ensembl Acc Id:

ENST00000768796

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,311 - 121,096,425 (+)	Ensembl

Ensembl Acc Id:

ENST00000768797

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,364 - 121,096,317 (+)	Ensembl

Ensembl Acc Id:

ENST00000768798

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,364 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768799

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,369 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768800

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,372 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768801

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,372 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768802

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,369 - 121,096,304 (+)	Ensembl

Ensembl Acc Id:

ENST00000768803

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,399 - 121,095,992 (+)	Ensembl

Ensembl Acc Id:

ENST00000768804

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,769 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,802 - 121,095,982 (+)	Ensembl

Ensembl Acc Id:

ENST00000768806

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,044,121 - 121,051,846 (+)	Ensembl

Ensembl Acc Id:

ENST00000768807

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,328 - 121,094,068 (+)	Ensembl

Ensembl Acc Id:

ENST00000768808

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,364 - 121,096,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000768810

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,050,270 - 121,051,926 (+)	Ensembl

Ensembl Acc Id:

ENST00000768811

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	121,087,345 - 121,088,552 (+)	Ensembl

RefSeq Acc Id:

NR_045213

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	121,087,345 - 121,097,161 (+)	NCBI
GRCh37	1	120,926,128 - 120,935,944 (-)	NCBI
HuRef	1	118,453,001 - 118,453,262 (-)	NCBI
CHM1_1	1	121,745,435 - 121,755,251 (+)	NCBI
T2T-CHM13v2.0	1	121,096,728 - 121,106,544 (+)	NCBI

Sequence:

show sequence

AATATCTTGCATGTTACAGATTTCACTACTCCCACCAGCTTGGAGACAACATGTGGTTCTTGAC
AACTCTGCTCCTTTGGGTTCCAGTTGATGGGCAAGTGGACACCACAAAGGCAGTGATCACTTTG
CAGCCTCCATGGGTCAGCGTGTTCCAAGAGGAAACCATAACCTTGCACTGTGAGGTGCTCCATC
TGCCTGGGAGCAGCTCCACACAGTGGTTTCTCAATGGCACAGCCACTCAGACCTCGACCCCCAG
CTACAGAATCACCTCTGCCAGTGTCAATGACAGTGGTGAATACAGGTGCCAGAGAGGTCTCTCA
GGGCGAAGTGACCCCATACAGCTGGAAATCCACAGAGGCTGGCTACTACTGCAGGTCTCCAGCA
GAGTCTTCATGGAAGGAGAACCTCTGGCCTTGAGGTGTCATGCGTGGAAGGATAAGCTGGTGTA
CAATGTGCTTTACTATCGAAATGGCAAAGCCTTTAAGTTTTTCCACTGGAATTCTAACCTCACC
ATTCTGAAAACCAACATAAGTCACAATGGCACCTACCATTGCTCAGGCATGGGAAAGCATCGCT
ACACATCAGCAGGAATATCACAATACACTGTGAAAGAGCTATTTCCAGCTCCAGTGCTGAATGC
ATCTGTGACATCCCCACTCCTGGAGGGGAATCTGGTCACCCTGAGCTGTGAAACAAAGTTGCTC
TTGCAGAGGCCTGGTTTGTAGCTTTACTTCTCCTTCTACATGGGCAGCAAGACCCTGCGAGGCA
GGAACACATCCTCTGAATACCAAATACTAACTGCTAGAAGAGAAGACTCTGGGTTATACTGGTG
CGAGGCTGCCACAGAGGATGGAAATGTCCTTAAGCACAGCCCTGAGTTGGAGCTTCAAGTGCTT
GGCCTCCAGTTACCAACTCCTGTCTGGTTTCATGTCCTTTTCTATCTGGCAGTGGGAATAATGT
TTTTAGTGAACACTGTTCTCTGGGTGACAATACGTAAAGAACTGAAAAGAAAGAAAAAGTGGAA
TTTAGAAATCTCTTTGGATTCTGGTCATGAGAAGAAGGTAATTTCCAGCCTTCAAGAAGACAGA
CATTTAGAAGAAGAGCTGAAATGTCAGGAACAAAAAGAAGAACAGCTGCAGGAAGGGGTGCACC
GGAAGGAGCCCCAGGGGGCCACGTAGCAGCGGCTCAGTTGGTGGCCATCGATCTGGACCGTCCC
CTGCCCACTTGCTCCCCGTGAGCACTGCGTACAAACATCCAAAAGTTCAACAACACCAGAACTG
TGTGTCTCATGGTATATAACTCTTAAAGCAAATAAATGAACTGACTTCAACTGGGATACATTTG
GAAATGTGGTCATCAAAGATGACTTGAAATGAGGCCTACTCTAAAGAATTCTTGAAAAACTTAC
AAGTCAAGCCTAGCCTGATAATCCTATTACATAGTTTGAAAAATAGTATTTTATTTCTCAGAAC
AAGGTAAAAAGGTGAGTGGGTGCATATGTACAGAAGATTAAGACAGAGAAACAGACAGAAAGAG
ACACACACACAGCCAGGAGTGGGTAGATTTCAGGGAGACAAGAGGGAATAGTATAGACAATAAG
GAAGGAAATAGTACTTACAAATGACTCCTAAGGGACTGTGAGACTGAGAGGGCTCACGCCTCTG
TGTTCAGGATACTTAGTTCATGGCTTTTCTCTTTGACTTTACTAAAAGAGAATGTCTCCATACG
CGTTCTAGGCATACAAGGGGGTAACTCATGATGAGAAATGGATGTGTTATTCTTGCCCTCTCTT
TTGAGGCTCTCTCATAACCCCTCTATTTCTAGAGACAACAAAAATGTTGCCAGTCCTAGGCCCC
TGCCCTGTAGGAAGGCAGAATGTAACTGTTCTTTTTGTTTAACGATTAAGTCCAAATCTCCAAG
TGCGGCACTGCAAAGAGACGCTTCAAGTGGGGAGAAGCGGCGATATCATAGAGTCCAGATCTTG
CCTCCAGAGATTTGCTTTACCTTCCTGATTTTCTGGTTACTAATTAGCTTCAGGATACGCTGCT
CTCATACTTGGGCTGTAGTTTGGAGACAAAATATTTTCCTGCCACTGTGTAACATAGCTGAGGT
AAAAACTGAACTATGTAAATGACTCTACTAAAAGTTTAGGGAAAAAAAACAGGAGGAGTATGAC
ACACACAGCAA

hide sequence

RefSeq Acc Id:

NR_164758

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	121,087,345 - 121,097,161 (+)	NCBI
T2T-CHM13v2.0	1	121,096,728 - 121,106,544 (+)	NCBI

Sequence:

show sequence

AATATCTTGCATGTTACAGATTTCACTACTCCCACCAGCTTGGAGACAACATGTGGTTCTTGAC
AACTCTGCTCCTTTGGGGCTGGCTACTACTGCAGGTCTCCAGCAGAGTCTTCATGGAAGGAGAA
CCTCTGGCCTTGAGGTGTCATGCGTGGAAGGATAAGCTGGTGTACAATGTGCTTTACTATCGAA
ATGGCAAAGCCTTTAAGTTTTTCCACTGGAATTCTAACCTCACCATTCTGAAAACCAACATAAG
TCACAATGGCACCTACCATTGCTCAGGCATGGGAAAGCATCGCTACACATCAGCAGGAATATCA
CAATACACTGTGAAAGGCCTCCAGTTACCAACTCCTGTCTGGTTTCATGTCCTTTTCTATCTGG
CAGTGGGAATAATGTTTTTAGTGAACACTGTTCTCTGGGTGACAATACGTAAAGAACTGAAAAG
AAAGAAAAAGTGGAATTTAGAAATCTCTTTGGATTCTGGTCATGAGAAGAAGGTAATTTCCAGC
CTTCAAGAAGACAGACATTTAGAAGAAGAGCTGAAATGTCAGGAACAAAAAGAAGAACAGCTGC
AGGAAGGGGTGCACCGGAAGGAGCCCCAGGGGGCCACGTAGCAGCGGCTCAGTTGGTGGCCATC
GATCTGGACCGTCCCCTGCCCACTTGCTCCCCGTGAGCACTGCGTACAAACATCCAAAAGTTCA
ACAACACCAGAACTGTGTGTCTCATGGTATATAACTCTTAAAGCAAATAAATGAACTGACTTCA
ACTGGGATACATTTGGAAATGTGGTCATCAAAGATGACTTGAAATGAGGCCTACTCTAAAGAAT
TCTTGAAAAACTTACAAGTCAAGCCTAGCCTGATAATCCTATTACATAGTTTGAAAAATAGTAT
TTTATTTCTCAGAACAAGGTAAAAAGGTGAGTGGGTGCATATGTACAGAAGATTAAGACAGAGA
AACAGACAGAAAGAGACACACACACAGCCAGGAGTGGGTAGATTTCAGGGAGACAAGAGGGAAT
AGTATAGACAATAAGGAAGGAAATAGTACTTACAAATGACTCCTAAGGGACTGTGAGACTGAGA
GGGCTCACGCCTCTGTGTTCAGGATACTTAGTTCATGGCTTTTCTCTTTGACTTTACTAAAAGA
GAATGTCTCCATACGCGTTCTAGGCATACAAGGGGGTAACTCATGATGAGAAATGGATGTGTTA
TTCTTGCCCTCTCTTTTGAGGCTCTCTCATAACCCCTCTATTTCTAGAGACAACAAAAATGTTG
CCAGTCCTAGGCCCCTGCCCTGTAGGAAGGCAGAATGTAACTGTTCTTTTTGTTTAACGATTAA
GTCCAAATCTCCAAGTGCGGCACTGCAAAGAGACGCTTCAAGTGGGGAGAAGCGGCGATATCAT
AGAGTCCAGATCTTGCCTCCAGAGATTTGCTTTACCTTCCTGATTTTCTGGTTACTAATTAGCT
TCAGGATACGCTGCTCTCATACTTGGGCTGTAGTTTGGAGACAAAATATTTTCCTGCCACTGTG
TAACATAGCTGAGGTAAAAACTGAACTATGTAAATGACTCTACTAAAAGTTTAGGGAAAAAAAA
CAGGAGGAGTATGACACACACAGCAA

hide sequence

RefSeq Acc Id:

NR_164759

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	121,087,345 - 121,097,161 (+)	NCBI
T2T-CHM13v2.0	1	121,096,728 - 121,106,544 (+)	NCBI

Sequence:

show sequence

AATATCTTGCATGTTACAGATTTCACTACTCCCACCAGCTTGGAGACAACATGTGGTTCTTGAC
AACTCTGCTCCTTTGGGTTCCAGTTGATGGGCAAGTGGACACCACAAAGGCAGTGATCACTTTG
CAGCCTCCATGGGTCAGCGTGTTCCAAGAGGAAACCATAACCTTGCACTGTGAGGTGCTCCATC
TGCCTGGGAGCAGCTCCACACAGTGGTTTCTCAATGGCACAGCCACTCAGACCTCGACCCCCAG
CTACAGAATCACCTCTGCCAGTGTCAATGACAGTGGTGAATACAGGTGCCAGAGAGGTCTCTCA
GGGCGAAGTGACCCCATACAGCTGGAAATCCACAGAGGCTGGCTACTACTGCAGGTCTCCAGCA
GAGTCTTCATGGAAGGAGAACCTCTGGCCTTGAGGTGTCATGCGTGGAAGGATAAGCTGGTGTA
CAATGTGCTTTACTATCGAAATGGCAAAGCCTTTAAGTTTTTCCACTGGAATTCTAACCTCACC
ATTCTGAAAACCAACATAAGTCACAATGGCACCTACCATTGCTCAGGCATGGGAAAGCATCGCT
ACACATCAGCAGGAATATCACAATACACTGTGAAAGGCCTCCAGTTACCAACTCCTGTCTGGTT
TCATGTCCTTTTCTATCTGGCAGTGGGAATAATGTTTTTAGTGAACACTGTTCTCTGGGTGACA
ATACGTAAAGAACTGAAAAGAAAGAAAAAGTGGAATTTAGAAATCTCTTTGGATTCTGGTCATG
AGAAGAAGGTAATTTCCAGCCTTCAAGAAGACAGACATTTAGAAGAAGAGCTGAAATGTCAGGA
ACAAAAAGAAGAACAGCTGCAGGAAGGGGTGCACCGGAAGGAGCCCCAGGGGGCCACGTAGCAG
CGGCTCAGTTGGTGGCCATCGATCTGGACCGTCCCCTGCCCACTTGCTCCCCGTGAGCACTGCG
TACAAACATCCAAAAGTTCAACAACACCAGAACTGTGTGTCTCATGGTATATAACTCTTAAAGC
AAATAAATGAACTGACTTCAACTGGGATACATTTGGAAATGTGGTCATCAAAGATGACTTGAAA
TGAGGCCTACTCTAAAGAATTCTTGAAAAACTTACAAGTCAAGCCTAGCCTGATAATCCTATTA
CATAGTTTGAAAAATAGTATTTTATTTCTCAGAACAAGGTAAAAAGGTGAGTGGGTGCATATGT
ACAGAAGATTAAGACAGAGAAACAGACAGAAAGAGACACACACACAGCCAGGAGTGGGTAGATT
TCAGGGAGACAAGAGGGAATAGTATAGACAATAAGGAAGGAAATAGTACTTACAAATGACTCCT
AAGGGACTGTGAGACTGAGAGGGCTCACGCCTCTGTGTTCAGGATACTTAGTTCATGGCTTTTC
TCTTTGACTTTACTAAAAGAGAATGTCTCCATACGCGTTCTAGGCATACAAGGGGGTAACTCAT
GATGAGAAATGGATGTGTTATTCTTGCCCTCTCTTTTGAGGCTCTCTCATAACCCCTCTATTTC
TAGAGACAACAAAAATGTTGCCAGTCCTAGGCCCCTGCCCTGTAGGAAGGCAGAATGTAACTGT
TCTTTTTGTTTAACGATTAAGTCCAAATCTCCAAGTGCGGCACTGCAAAGAGACGCTTCAAGTG
GGGAGAAGCGGCGATATCATAGAGTCCAGATCTTGCCTCCAGAGATTTGCTTTACCTTCCTGAT
TTTCTGGTTACTAATTAGCTTCAGGATACGCTGCTCTCATACTTGGGCTGTAGTTTGGAGACAA
AATATTTTCCTGCCACTGTGTAACATAGCTGAGGTAAAAACTGAACTATGTAAATGACTCTACT
AAAAGTTTAGGGAAAAAAAACAGGAGGAGTATGACACACACAGCAA

hide sequence

RefSeq Acc Id:

NR_164760

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	121,087,345 - 121,095,642 (+)	NCBI
T2T-CHM13v2.0	1	121,096,728 - 121,105,025 (+)	NCBI

Sequence:

show sequence

AATATCTTGCATGTTACAGATTTCACTACTCCCACCAGCTTGGAGACAACATGTGGTTCTTGAC
AACTCTGCTCCTTTGGGTTCCAGTTGATGGGCAAGTGGACACCACAAAGGCAGTGATCACTTTG
CAGCCTCCATGGGTCAGCGTGTTCCAAGAGGAAACCATAACCTTGCACTGTGAGGTGCTCCATC
TGCCTGGGAGCAGCTCCACACAGTGGTTTCTCAATGGCACAGCCACTCAGACCTCGACCCCCAG
CTACAGAATCACCTCTGCCAGTGTCAATGACAGTGGTGAATACAGGTGCCAGAGAGGTCTCTCA
GGGCGAAGTGACCCCATACAGCTGGAAATCCACAGAGGCTGGCTACTACTGCAGGTCTCCAGCA
GAGTCTTCATGGAAGGAGAACCTCTGGCCTTGAGGTGTCATGCGTGGAAGGATAAGCTGGTGTA
CAATGTGCTTTACTATCGAAATGGCAAAGCCTTTAAGTTTTTCCACTGGAATTCTAACCTCACC
ATTCTGAAAACCAACATAAGTCACAATGGCACCTACCATTGCTCAGGCATGGGAAAGCATCGCT
ACACATCAGCAGGAATATCACAATACACTGTGAAAGAGCTATTTCCAGCTCCAGTGCTGAATGC
ATCTGTGACATCCCCACTCCTGGAGGGGAATCTGGTCACCCTGAGCTGTGAAACAAAGTTGCTC
TTGCAGAGGCCTGGTTTGTAGCTTTACTTCTCCTTCTACATGGGCAGCAAGACCCTGCGAGGCA
GGAACACATCCTCTGAATACCAAATACTAACTGCTAGAAGAGAAGACTCTGGGTTATACTGGTG
CGAGGCTGCCACAGAGGATGGAAATGTCCTTAAGCACAGCCCTGAGTTGGAGCTTCAAGTGCTT
GGTGAGAATGACGGGAAGCCACTGGCACAGAAGAAGGGACTCCCTTATCTCCCATGGGACTGAG
GTTTGTTCAAGGGTTTTTGGCCCAGACAAGAGGGGAAAGTCTCTTCAGGAAAAGCCCACAAGCA
GGCCTTTCCATCCTTGATTCACAACATCACTCTTCTCCTCGCAAACTGTTAAATTTCCTTTCCT
TTCTTTTTCTTTTTCCTTTGCCTTTCCTTCCTCTATTTCTTTCCTTCCTCCATTTCTTTCCTTC
ATTTTCTCCTCTGTCCTTCTTTTCTTCTCCTTCATTTTATTTTCCCCTCCCTCCCACTCTTCCC
TCCACTCCATGACCCCTCCTTCTCTCTCTCTCTCTCTCCCTGCTTCCCTGCCTCCCTCCTCCTC
ACCAACAATCTCACCAACAATTTATCAAGTTCTTCCTATCTGTTGTCATACGTCTGGGGATATA
AAGACATTTGAGTATAGTTCTTGCTTCAAGGAGCTCACAAGGTGGATTTATCAGACAGTGATTT
TGTAAACTGCAAATCACCACCTCCCCAAGTATCTCTGTTTAACTGAGGCAGAGGGATTGTGAGC
TCTAGAACAAAGTCTCCTTGGGGGGGAAAAAAGTTCATCTTCAACCCAAATTCATTTCAAGTAT
TAAATGGCACAGAGATATCAGTTGTCTCTGGAACTAGGGAGTAAG

hide sequence

Protein Sequences


GenBank Protein	AAA35825	(Get FASTA)	NCBI Sequence Viewer
	AAA35826	(Get FASTA)	NCBI Sequence Viewer
	AAA58414	(Get FASTA)	NCBI Sequence Viewer
	AAD13842	(Get FASTA)	NCBI Sequence Viewer
	CAI14143	(Get FASTA)	NCBI Sequence Viewer
	CAI14144	(Get FASTA)	NCBI Sequence Viewer
	CAI14145	(Get FASTA)	NCBI Sequence Viewer
	Q92637	(Get FASTA)	NCBI Sequence Viewer

Ensembl Acc Id:

ENSP00000485498 ⟸ ENST00000623603

Ensembl Acc Id:

ENSP00000478655 ⟸ ENST00000616817

Ensembl Acc Id:

ENSP00000479641 ⟸ ENST00000472543

Ensembl Acc Id:

ENSP00000358390 ⟸ ENST00000369383

Ensembl Acc Id:

ENSP00000358391 ⟸ ENST00000369384

Ensembl Acc Id:

ENSP00000481411 ⟸ ENST00000369178

Protein Domains

Ig-like C2-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q92637-F1-model_v2	AlphaFold	Q92637	1-280	view protein structure

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:3614	AgrOrtholog
COSMIC	FCGR1BP	COSMIC
Ensembl Genes	ENSG00000198019	Ensembl
	ENSG00000291135	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000369383	ENTREZGENE
	ENST00000369384	ENTREZGENE
	ENST00000471609	ENTREZGENE
Gene3D-CATH	2.60.40.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000198019	GTEx
	ENSG00000291135	GTEx
HGNC ID	HGNC:3614	ENTREZGENE
Human Proteome Map	FCGR1BP	Human Proteome Map
InterPro	Ig-like_dom	UniProtKB/Swiss-Prot
	Ig-like_dom_sf	UniProtKB/Swiss-Prot
	Ig-like_fold	UniProtKB/Swiss-Prot
	Ig_Fc_receptor	UniProtKB/Swiss-Prot
	Ig_sub	UniProtKB/Swiss-Prot
	Ig_sub2	UniProtKB/Swiss-Prot
NCBI Gene	2210	ENTREZGENE
OMIM	601502	OMIM
PANTHER	HIGH AFFINITY IMMUNOGLOBULIN GAMMA FC RECEPTOR I-RELATED	UniProtKB/Swiss-Prot
	IMMUNOGLOBULIN FC RECEPTOR	UniProtKB/Swiss-Prot
Pfam	Ig_2	UniProtKB/Swiss-Prot
	Ig_3	UniProtKB/Swiss-Prot
PROSITE	IG_LIKE	UniProtKB/Swiss-Prot
SMART	IGc2	UniProtKB/Swiss-Prot
	SM00409	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF48726	UniProtKB/Swiss-Prot
UniProt	FCGRB_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary	Q7KZ13	UniProtKB/Swiss-Prot
	Q92638	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2021-11-08	FCGR1BP	Fc gamma receptor Ib, pseudogene	FCGR1B	Fc fragment of IgG receptor Ib	Symbol and/or name change	19259463	PROVISIONAL
2016-01-19	FCGR1B	Fc fragment of IgG receptor Ib	FCGR1B	Fc fragment of IgG, high affinity Ib, receptor (CD64)	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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