LILRB4 (leukocyte immunoglobulin like receptor B4) - Rat Genome Database

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Gene: LILRB4 (leukocyte immunoglobulin like receptor B4) Homo sapiens
Analyze
Symbol: LILRB4
Name: leukocyte immunoglobulin like receptor B4
RGD ID: 1347745
HGNC Page HGNC:6608
Description: Enables several functions, including apolipoprotein binding activity; fibronectin binding activity; and transmembrane receptor protein tyrosine kinase inhibitor activity. Involved in several processes, including negative regulation of cytokine production; regulation of leukocyte activation; and regulation of signal transduction. Located in cell surface.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: B4; CD85 antigen-like family member K; CD85K; HM18; ILT-3; ILT3; immunoglobulin-like transcript 3; leucocyte Ig-like receptor B4; leukocyte immunoglobulin-like receptor 5; leukocyte immunoglobulin-like receptor subfamily B member 4; leukocyte immunoglobulin-like receptor subfamily B member 4 soluble isoform; leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 4; leukocyte immunoglobulin-like receptor, subfamily B, member 4; LILRB5; LIR-5; LIR5; monocyte inhibitory receptor HM18
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Pig
Green Monkey
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
GRCh381954,662,985 - 54,668,718 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1954,643,889 - 54,670,359 (+)EnsemblGRCh38hg38GRCh38
GRCh371955,174,437 - 55,180,169 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361959,865,936 - 59,871,660 (+)NCBINCBI36Build 36hg18NCBI36
Build 341959,866,263 - 59,873,621NCBI
Celera1952,214,265 - 52,220,001 (+)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1951,497,246 - 51,504,797 (+)NCBIHuRef
CHM1_11955,167,838 - 55,175,378 (+)NCBICHM1_1
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
adaptive immune response  (IEA)
cytokine-mediated signaling pathway  (IBA)
Fc receptor mediated inhibitory signaling pathway  (IDA)
immune system process  (IEA)
interleukin-10-mediated signaling pathway  (IEP)
mast cell activation  (ISO)
negative regulation of activated T cell proliferation  (IMP)
negative regulation of chemokine production  (IMP)
negative regulation of cytokine production involved in inflammatory response  (IMP)
negative regulation of cytotoxic T cell differentiation  (IMP)
negative regulation of I-kappaB kinase/NF-kappaB signaling  (IMP)
negative regulation of interleukin-1 beta production  (IMP)
negative regulation of interleukin-10 production  (IDA)
negative regulation of interleukin-2 production  (IDA)
negative regulation of interleukin-5 production  (IDA)
negative regulation of interleukin-6 production  (IMP)
negative regulation of IP-10 production  (IMP)
negative regulation of MAPK cascade  (IMP)
negative regulation of miRNA transcription  (IDA)
negative regulation of monocyte activation  (IDA,IMP)
negative regulation of osteoclast differentiation  (IDA)
negative regulation of protein localization to nucleus  (IDA)
negative regulation of protein tyrosine kinase activity  (IDA,IMP)
negative regulation of signaling receptor activity  (IDA)
negative regulation of T cell costimulation  (IMP)
negative regulation of T cell cytokine production  (IDA)
negative regulation of T cell proliferation  (IMP)
negative regulation of T cell receptor signaling pathway  (IDA,IMP)
negative regulation of tumor necrosis factor production  (IDA)
negative regulation of type II interferon production  (IDA)
positive regulation of CD8-positive, alpha-beta T cell differentiation  (IDA)
positive regulation of regulatory T cell differentiation  (IDA)
positive regulation of T cell anergy  (IMP)
receptor internalization  (IMP)
tolerance induction  (IDA)

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9079806   PMID:9151699   PMID:9278324   PMID:9548455   PMID:9786947   PMID:9862332   PMID:10781084   PMID:10940079   PMID:10941837   PMID:11491530   PMID:11875462   PMID:12477932  
PMID:15489334   PMID:15670976   PMID:16406677   PMID:16433759   PMID:16493035   PMID:17161342   PMID:17163451   PMID:17266150   PMID:17513794   PMID:17923119   PMID:17993722   PMID:17998301  
PMID:18420485   PMID:18486764   PMID:18802077   PMID:19010139   PMID:19380766   PMID:19535644   PMID:19561330   PMID:19658091   PMID:19833736   PMID:19860908   PMID:20007427   PMID:20237496  
PMID:20935202   PMID:21454581   PMID:21844884   PMID:21873635   PMID:22387553   PMID:22664025   PMID:22767507   PMID:22904259   PMID:23018130   PMID:23027709   PMID:23039892   PMID:23128233  
PMID:23376485   PMID:23533145   PMID:23607934   PMID:23616249   PMID:23666960   PMID:25187353   PMID:25551576   PMID:26678451   PMID:27725776   PMID:27742834   PMID:28005267   PMID:28409541  
PMID:28514442   PMID:28931525   PMID:30126665   PMID:30131301   PMID:30333625   PMID:30581005   PMID:31138763   PMID:31700117   PMID:32036728   PMID:32918786   PMID:33152402   PMID:33372059  
PMID:33644029   PMID:33961781   PMID:33974041   PMID:34089617   PMID:34425800   PMID:34712735  


Genomics

Comparative Map Data
LILRB4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381954,662,985 - 54,668,718 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1954,643,889 - 54,670,359 (+)EnsemblGRCh38hg38GRCh38
GRCh371955,174,437 - 55,180,169 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361959,865,936 - 59,871,660 (+)NCBINCBI36Build 36hg18NCBI36
Build 341959,866,263 - 59,873,621NCBI
Celera1952,214,265 - 52,220,001 (+)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1951,497,246 - 51,504,797 (+)NCBIHuRef
CHM1_11955,167,838 - 55,175,378 (+)NCBICHM1_1
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBIT2T-CHM13v2.0
Lilrb4b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391051,356,708 - 51,362,425 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1051,356,728 - 51,362,799 (+)EnsemblGRCm39 Ensembl
GRCm381051,480,612 - 51,486,329 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1051,480,632 - 51,486,703 (+)EnsemblGRCm38mm10GRCm38
MGSCv371051,200,485 - 51,206,025 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361051,169,094 - 51,174,634 (+)NCBIMGSCv36mm8
Celera1052,324,193 - 52,329,733 (+)NCBICelera
Cytogenetic Map10B3NCBI
Lilrb4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2169,805,020 - 69,810,628 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl169,805,250 - 69,810,660 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx175,164,131 - 75,169,435 (-)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.0183,728,450 - 83,733,754 (-)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.0176,872,043 - 76,877,344 (-)NCBIRnor_WKY
Rnor_6.0173,393,854 - 73,399,448 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl173,393,850 - 73,399,579 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0175,149,247 - 75,154,729 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4169,165,498 - 69,170,800 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1169,243,608 - 69,248,911 (-)NCBI
Celera167,336,070 - 67,340,685 (+)NCBICelera
Cytogenetic Map1q12NCBI
LILRB4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11960,392,690 - 60,453,555 (+)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v01951,606,681 - 51,612,751 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
LOC484306
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11102,779,562 - 102,786,924 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1102,843,014 - 102,849,207 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01103,426,664 - 103,432,846 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.11103,068,755 - 103,074,937 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01102,827,945 - 102,834,107 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01103,541,899 - 103,548,063 (-)NCBIUU_Cfam_GSD_1.0
LOC100517285
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1658,996,449 - 59,001,088 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2653,920,421 - 53,925,036 (+)NCBISscrofa10.2Sscrofa10.2susScr3
LILRB4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1647,299,764 - 47,333,711 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366607327,574,619 - 27,579,928 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in LILRB4
1 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3 copy number gain See cases [RCV000050883] Chr19:50191219..58535818 [GRCh38]
Chr19:50694476..59047185 [GRCh37]
Chr19:55386288..63738997 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain See cases [RCV000052925] Chr19:49907832..58557889 [GRCh38]
Chr19:50411089..59069256 [GRCh37]
Chr19:55102901..63761068 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:51141518..58539965 [GRCh38]
Chr19:51644775..59051332 [GRCh37]
Chr19:56336587..63743144 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
NM_001278426.3(LILRB4):c.-99G>A single nucleotide variant Malignant melanoma [RCV000072351] Chr19:54662935 [GRCh38]
Chr19:55174387 [GRCh37]
Chr19:59866199 [NCBI36]
Chr19:19q13.42		 not provided
NM_001278426.3(LILRB4):c.656G>A (p.Gly219Glu) single nucleotide variant Malignant melanoma [RCV000072352] Chr19:54664799 [GRCh38]
Chr19:55176250 [GRCh37]
Chr19:59868062 [NCBI36]
Chr19:19q13.42		 not provided
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3 copy number gain See cases [RCV000134174] Chr19:52612432..58581203 [GRCh38]
Chr19:53115685..59092570 [GRCh37]
Chr19:57807497..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3 copy number gain See cases [RCV000134139] Chr19:52955056..58581203 [GRCh38]
Chr19:53458309..59092570 [GRCh37]
Chr19:58150121..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh37/hg19 19q13.42(chr19:55028722-55683018)x3 copy number gain See cases [RCV000137053] Chr19:55028722..55683018 [GRCh37]
Chr19:59720534..60374830 [NCBI36]
Chr19:19q13.42		 uncertain significance
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain See cases [RCV000135843] Chr19:50152520..58581203 [GRCh38]
Chr19:50655777..59092570 [GRCh37]
Chr19:55347589..63784382 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3 copy number gain See cases [RCV000142008] Chr19:52143873..58445521 [GRCh38]
Chr19:52647126..58956888 [GRCh37]
Chr19:57338938..63648700 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh37/hg19 19q13.42(chr19:54710237-55648526)x1 copy number loss Ductal breast carcinoma [RCV000207190] Chr19:54710237..55648526 [GRCh37]
Chr19:19q13.42		 uncertain significance
chr19:55143156-55294969 complex variant complex Ductal breast carcinoma [RCV000207228] Chr19:55143156..55294969 [GRCh37]
Chr19:19q13.42		 uncertain significance
chr19:54754752-55624113 complex variant complex Ductal breast carcinoma [RCV000207291] Chr19:54754752..55624113 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42(chr19:55017416-55602115)x3 copy number gain not provided [RCV000752784] Chr19:55017416..55602115 [GRCh37]
Chr19:19q13.42		 benign
GRCh37/hg19 19q13.42(chr19:55148430-55176347)x3 copy number gain See cases [RCV000449450] Chr19:55148430..55176347 [GRCh37]
Chr19:19q13.42		 benign
GRCh37/hg19 19q13.42(chr19:55148430-55176347)x1 copy number loss See cases [RCV000447039] Chr19:55148430..55176347 [GRCh37]
Chr19:19q13.42		 benign
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:54344821-58956888)x3 copy number gain See cases [RCV000448186] Chr19:54344821..58956888 [GRCh37]
Chr19:19q13.42-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.42(chr19:53867570-55833460)x3 copy number gain not provided [RCV000684091] Chr19:53867570..55833460 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3 copy number gain not provided [RCV000684095] Chr19:54196216..58759679 [GRCh37]
Chr19:19q13.42-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3 copy number gain not provided [RCV000740208] Chr19:50740074..59097160 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.42(chr19:54474844-55181741)x3 copy number gain not provided [RCV001007058] Chr19:54474844..55181741 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42(chr19:54701333-55536206)x3 copy number gain not provided [RCV001007059] Chr19:54701333..55536206 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54334195-56434037)x3 copy number gain not provided [RCV001259948] Chr19:54334195..56434037 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
NC_000019.9:g.(?_54297303)_(55678016_?)dup duplication not provided [RCV001981426] Chr19:54297303..55678016 [GRCh37]
Chr19:19q13.42		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2854
Count of miRNA genes:1014
Interacting mature miRNAs:1220
Transcripts:ENST00000270452, ENST00000391733, ENST00000391734, ENST00000391736, ENST00000430952, ENST00000434286, ENST00000461262, ENST00000461839, ENST00000470943, ENST00000494796
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.

Markers in Region
ECD03210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,178,980 - 55,179,782UniSTSGRCh37
Build 361959,870,792 - 59,871,594RGDNCBI36
Celera1952,219,133 - 52,219,935RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,501,967 - 51,502,769UniSTS
ECD03234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,175,818 - 55,176,619UniSTSGRCh37
Build 361959,867,630 - 59,868,431RGDNCBI36
Celera1952,215,971 - 52,216,772RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,498,805 - 51,499,606UniSTS
ECD03985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,177,363 - 55,178,141UniSTSGRCh37
Build 361959,869,175 - 59,869,953RGDNCBI36
Celera1952,217,516 - 52,218,294RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,500,350 - 51,501,128UniSTS
ECD04074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,174,976 - 55,175,751UniSTSGRCh37
Build 361959,866,788 - 59,867,563RGDNCBI36
Celera1952,215,122 - 52,215,904RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,497,956 - 51,498,738UniSTS
ECD14330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,174,074 - 55,174,570UniSTSGRCh37
Build 361959,865,886 - 59,866,382RGDNCBI36
Celera1952,214,215 - 52,214,711RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,497,048 - 51,497,545UniSTS
RH47724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,179,444 - 55,179,588UniSTSGRCh37
Build 361959,871,256 - 59,871,400RGDNCBI36
Celera1952,219,597 - 52,219,741RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,502,431 - 51,502,575UniSTS
GeneMap99-GB4 RH Map19281.76UniSTS
NCBI RH Map19589.4UniSTS
REN93748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,216 - 55,172,465UniSTSGRCh37
Build 361959,864,028 - 59,864,277RGDNCBI36
Celera1952,212,357 - 52,212,606RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,495,190 - 51,495,439UniSTS
REN93749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,463 - 55,172,722UniSTSGRCh37
Build 361959,864,275 - 59,864,534RGDNCBI36
Celera1952,212,604 - 52,212,863RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,495,437 - 51,495,696UniSTS
REN93750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,713 - 55,172,966UniSTSGRCh37
Build 361959,864,525 - 59,864,778RGDNCBI36
Celera1952,212,854 - 52,213,107RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,495,687 - 51,495,940UniSTS
REN93751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,829 - 55,173,077UniSTSGRCh37
Build 361959,864,641 - 59,864,889RGDNCBI36
Celera1952,212,970 - 52,213,218RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,495,803 - 51,496,051UniSTS
REN93752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,996 - 55,173,220UniSTSGRCh37
Build 361959,864,808 - 59,865,032RGDNCBI36
Celera1952,213,137 - 52,213,361RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,495,970 - 51,496,194UniSTS
REN93753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,173,197 - 55,173,437UniSTSGRCh37
Build 361959,865,009 - 59,865,249RGDNCBI36
Celera1952,213,338 - 52,213,578RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,496,171 - 51,496,411UniSTS
REN93754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,173,407 - 55,173,660UniSTSGRCh37
Build 361959,865,219 - 59,865,472RGDNCBI36
Celera1952,213,548 - 52,213,801RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,496,381 - 51,496,634UniSTS
REN93755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,173,638 - 55,173,899UniSTSGRCh37
Build 361959,865,450 - 59,865,711RGDNCBI36
Celera1952,213,779 - 52,214,040RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,496,612 - 51,496,873UniSTS
REN93756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,173,890 - 55,174,144UniSTSGRCh37
Build 361959,865,702 - 59,865,956RGDNCBI36
Celera1952,214,031 - 52,214,285RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,496,864 - 51,497,119UniSTS
REN93757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,174,120 - 55,174,380UniSTSGRCh37
Build 361959,865,932 - 59,866,192RGDNCBI36
Celera1952,214,261 - 52,214,521RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,497,095 - 51,497,355UniSTS
REN93758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,174,366 - 55,174,623UniSTSGRCh37
Build 361959,866,178 - 59,866,435RGDNCBI36
Celera1952,214,507 - 52,214,764RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,497,341 - 51,497,598UniSTS
REN93759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,174,923 - 55,175,183UniSTSGRCh37
Build 361959,866,735 - 59,866,995RGDNCBI36
Celera1952,215,069 - 52,215,329RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,497,903 - 51,498,163UniSTS
REN93760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,175,102 - 55,175,332UniSTSGRCh37
GRCh371954,849,831 - 54,850,058UniSTSGRCh37
Build 361959,541,643 - 59,541,870RGDNCBI36
Celera1951,890,751 - 51,890,978RGD
Celera1952,215,248 - 52,215,478UniSTS
Cytogenetic Map19q13.4UniSTS
HuRef1951,498,082 - 51,498,312UniSTS
HuRef1951,171,705 - 51,171,933UniSTS
HuRef1951,171,706 - 51,171,933UniSTS
REN93761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,175,313 - 55,175,567UniSTSGRCh37
Build 361959,867,125 - 59,867,379RGDNCBI36
Celera1952,215,459 - 52,215,713RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,498,293 - 51,498,547UniSTS
REN93762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,175,548 - 55,175,787UniSTSGRCh37
GRCh371955,086,101 - 55,087,427UniSTSGRCh37
Build 361959,867,360 - 59,867,599RGDNCBI36
Celera1952,215,694 - 52,215,940RGD
Celera1952,126,569 - 52,127,895UniSTS
Cytogenetic Map19q13.4UniSTS
HuRef1951,498,528 - 51,498,774UniSTS
REN93763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,175,761 - 55,175,985UniSTSGRCh37
Build 361959,867,573 - 59,867,797RGDNCBI36
Celera1952,215,914 - 52,216,138RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,498,748 - 51,498,972UniSTS
REN93764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,175,964 - 55,176,201UniSTSGRCh37
Build 361959,867,776 - 59,868,013RGDNCBI36
Celera1952,216,117 - 52,216,354RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,498,951 - 51,499,188UniSTS
REN93765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,176,178 - 55,176,403UniSTSGRCh37
Build 361959,867,990 - 59,868,215RGDNCBI36
Celera1952,216,331 - 52,216,556RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,499,165 - 51,499,390UniSTS
REN93766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,176,366 - 55,176,622UniSTSGRCh37
Build 361959,868,178 - 59,868,434RGDNCBI36
Celera1952,216,519 - 52,216,775RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,499,353 - 51,499,609UniSTS
REN93767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,176,600 - 55,176,827UniSTSGRCh37
Build 361959,868,412 - 59,868,639RGDNCBI36
Celera1952,216,753 - 52,216,980RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,499,587 - 51,499,814UniSTS
REN93768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,176,746 - 55,176,970UniSTSGRCh37
Build 361959,868,558 - 59,868,782RGDNCBI36
Celera1952,216,899 - 52,217,123RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,499,733 - 51,499,957UniSTS
HuRef1951,039,220 - 51,039,443UniSTS
HuRef1951,108,704 - 51,108,928UniSTS
REN93769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,176,946 - 55,177,200UniSTSGRCh37
Build 361959,868,758 - 59,869,012RGDNCBI36
Celera1952,217,099 - 52,217,353RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,499,933 - 51,500,187UniSTS
REN93770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,177,176 - 55,177,400UniSTSGRCh37
Build 361959,868,988 - 59,869,212RGDNCBI36
Celera1952,217,329 - 52,217,553RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,500,163 - 51,500,387UniSTS
REN93771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,177,370 - 55,177,626UniSTSGRCh37
Build 361959,869,182 - 59,869,438RGDNCBI36
Celera1952,217,523 - 52,217,779RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,500,357 - 51,500,613UniSTS
REN93772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,177,591 - 55,177,839UniSTSGRCh37
Build 361959,869,403 - 59,869,651RGDNCBI36
Celera1952,217,744 - 52,217,992RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,500,578 - 51,500,826UniSTS
REN93773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,177,817 - 55,178,070UniSTSGRCh37
Build 361959,869,629 - 59,869,882RGDNCBI36
Celera1952,217,970 - 52,218,223RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,500,804 - 51,501,057UniSTS
REN93774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,177,986 - 55,178,210UniSTSGRCh37
Build 361959,869,798 - 59,870,022RGDNCBI36
Celera1952,218,139 - 52,218,363RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,500,973 - 51,501,197UniSTS
REN93775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,178,187 - 55,178,441UniSTSGRCh37
Build 361959,869,999 - 59,870,253RGDNCBI36
Celera1952,218,340 - 52,218,594RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,501,174 - 51,501,428UniSTS
REN93776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,178,463 - 55,178,689UniSTSGRCh37
Build 361959,870,275 - 59,870,501RGDNCBI36
Celera1952,218,616 - 52,218,842RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,501,450 - 51,501,676UniSTS
REN93777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,178,503 - 55,178,740UniSTSGRCh37
Build 361959,870,315 - 59,870,552RGDNCBI36
Celera1952,218,656 - 52,218,893RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,501,490 - 51,501,727UniSTS
REN93778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,178,760 - 55,179,000UniSTSGRCh37
Build 361959,870,572 - 59,870,812RGDNCBI36
Celera1952,218,913 - 52,219,153RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,501,747 - 51,501,987UniSTS
REN93779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,178,977 - 55,179,250UniSTSGRCh37
GRCh371954,721,182 - 54,721,455UniSTSGRCh37
Build 361959,412,994 - 59,413,267RGDNCBI36
Celera1952,219,130 - 52,219,403UniSTS
Celera1951,762,857 - 51,763,130RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,037,002 - 51,037,275UniSTS
HuRef1951,501,964 - 51,502,237UniSTS
REN93780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,179,228 - 55,179,475UniSTSGRCh37
Build 361959,871,040 - 59,871,287RGDNCBI36
Celera1952,219,381 - 52,219,628RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,502,215 - 51,502,462UniSTS
REN93781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,179,436 - 55,179,687UniSTSGRCh37
Build 361959,871,248 - 59,871,499RGDNCBI36
Celera1952,219,589 - 52,219,840RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,502,423 - 51,502,674UniSTS
REN93782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,179,666 - 55,179,931UniSTSGRCh37
Build 361959,871,478 - 59,871,743RGDNCBI36
Celera1952,219,819 - 52,220,084RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,502,653 - 51,502,918UniSTS
REN93783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,179,928 - 55,180,169UniSTSGRCh37
Build 361959,871,740 - 59,871,981RGDNCBI36
Celera1952,220,081 - 52,220,322RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,502,915 - 51,503,156UniSTS
REN93784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,180,159 - 55,180,387UniSTSGRCh37
Build 361959,871,971 - 59,872,199RGDNCBI36
Celera1952,220,312 - 52,220,540RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,503,146 - 51,503,374UniSTS
REN93785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,180,358 - 55,180,605UniSTSGRCh37
Build 361959,872,170 - 59,872,417RGDNCBI36
Celera1952,220,511 - 52,220,758RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,503,345 - 51,503,592UniSTS
REN93786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,180,579 - 55,180,817UniSTSGRCh37
Build 361959,872,391 - 59,872,629RGDNCBI36
Celera1952,220,732 - 52,220,970RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,503,566 - 51,503,804UniSTS
REN93787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,180,773 - 55,181,026UniSTSGRCh37
Build 361959,872,585 - 59,872,838RGDNCBI36
Celera1952,220,926 - 52,221,179RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,503,760 - 51,504,013UniSTS
REN93788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,180,999 - 55,181,253UniSTSGRCh37
Build 361959,872,811 - 59,873,065RGDNCBI36
Celera1952,221,152 - 52,221,406RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,503,986 - 51,504,240UniSTS
REN93789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,181,232 - 55,181,472UniSTSGRCh37
Build 361959,873,044 - 59,873,284RGDNCBI36
Celera1952,221,385 - 52,221,625RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,504,219 - 51,504,459UniSTS
REN93790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,181,422 - 55,181,664UniSTSGRCh37
Build 361959,873,234 - 59,873,476RGDNCBI36
Celera1952,221,575 - 52,221,817RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,504,409 - 51,504,651UniSTS
stSG606227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,303 - 55,172,543UniSTSGRCh37
Build 361959,864,115 - 59,864,355RGDNCBI36
Celera1952,212,444 - 52,212,684RGD
HuRef1951,495,277 - 51,495,517UniSTS
stSG606228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,544 - 55,172,734UniSTSGRCh37
Build 361959,864,356 - 59,864,546RGDNCBI36
Celera1952,212,685 - 52,212,875RGD
HuRef1951,495,518 - 51,495,708UniSTS
stSG606229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,172,739 - 55,174,101UniSTSGRCh37
Build 361959,864,551 - 59,865,913RGDNCBI36
Celera1952,212,880 - 52,214,242RGD
HuRef1951,495,713 - 51,497,075UniSTS
stSG606230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,174,262 - 55,175,415UniSTSGRCh37
Build 361959,866,074 - 59,867,227RGDNCBI36
Celera1952,214,403 - 52,215,561RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,497,237 - 51,498,395UniSTS
stSG606231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,175,396 - 55,176,574UniSTSGRCh37
Build 361959,867,208 - 59,868,386RGDNCBI36
Celera1952,215,542 - 52,216,727RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,498,376 - 51,499,561UniSTS
stSG606232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,176,555 - 55,177,636UniSTSGRCh37
Build 361959,868,367 - 59,869,448RGDNCBI36
Celera1952,216,708 - 52,217,789RGD
HuRef1951,499,542 - 51,500,623UniSTS
stSG606234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,178,474 - 55,179,782UniSTSGRCh37
Build 361959,870,286 - 59,871,594RGDNCBI36
Celera1952,218,627 - 52,219,935RGD
HuRef1951,501,461 - 51,502,769UniSTS


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 adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 39 560 36 13 890 14 69 11 112 45 77 272 97 18
Low 2056 1745 1439 470 914 319 2004 1065 2697 242 693 1050 149 1090 1218 2 1
Below cutoff 220 671 215 120 51 108 2013 1064 825 85 578 76 14 17 1544 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001278426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001394939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002958246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB233186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB233206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC009892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC243962 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC245036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF025532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF072099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF189768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF283988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC032342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU175229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX094825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR542048 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU024913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU041368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU234142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU459007 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU467612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU915607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U82979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U91925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000270452   ⟹   ENSP00000270452
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,643,915 - 54,663,955 (+)Ensembl
RefSeq Acc Id: ENST00000391733   ⟹   ENSP00000375613
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,663,020 - 54,668,397 (+)Ensembl
RefSeq Acc Id: ENST00000391734   ⟹   ENSP00000375614
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,662,998 - 54,668,397 (+)Ensembl
RefSeq Acc Id: ENST00000391736   ⟹   ENSP00000375616
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,662,128 - 54,670,359 (+)Ensembl
RefSeq Acc Id: ENST00000430952   ⟹   ENSP00000408995
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,662,995 - 54,668,397 (+)Ensembl
RefSeq Acc Id: ENST00000434286   ⟹   ENSP00000401962
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,663,027 - 54,667,793 (+)Ensembl
RefSeq Acc Id: ENST00000461262
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,666,286 - 54,667,038 (+)Ensembl
RefSeq Acc Id: ENST00000461839
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,643,889 - 54,649,600 (+)Ensembl
RefSeq Acc Id: ENST00000470943
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,665,798 - 54,667,390 (+)Ensembl
RefSeq Acc Id: ENST00000494796   ⟹   ENSP00000483357
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,662,158 - 54,667,699 (+)Ensembl
RefSeq Acc Id: ENST00000695418   ⟹   ENSP00000511897
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1954,662,985 - 54,668,718 (+)Ensembl
RefSeq Acc Id: NM_001278426   ⟹   NP_001265355
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
GRCh371955,174,271 - 55,181,810 (+)NCBI
HuRef1951,497,246 - 51,504,797 (+)NCBI
CHM1_11955,167,838 - 55,175,378 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278427   ⟹   NP_001265356
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
GRCh371955,174,271 - 55,181,810 (+)NCBI
HuRef1951,497,246 - 51,504,797 (+)NCBI
CHM1_11955,167,838 - 55,175,378 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278428   ⟹   NP_001265357
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
HuRef1951,497,246 - 51,504,797 (+)NCBI
CHM1_11955,167,838 - 55,175,378 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278429   ⟹   NP_001265358
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
GRCh371955,174,271 - 55,181,810 (+)NCBI
HuRef1951,497,246 - 51,504,797 (+)NCBI
CHM1_11955,167,838 - 55,175,378 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278430   ⟹   NP_001265359
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,665,207 (+)NCBI
GRCh371955,174,271 - 55,181,810 (+)NCBI
HuRef1951,497,246 - 51,504,797 (+)NCBI
CHM1_11955,167,838 - 55,170,226 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,758,733 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001394933   ⟹   NP_001381862
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001394934   ⟹   NP_001381863
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001394935   ⟹   NP_001381864
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001394936   ⟹   NP_001381865
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001394937   ⟹   NP_001381866
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001394938   ⟹   NP_001381867
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001394939   ⟹   NP_001381868
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
T2T-CHM13v2.01957,756,498 - 57,762,244 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017026216   ⟹   XP_016881705
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047438100   ⟹   XP_047294056
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
RefSeq Acc Id: XM_047438101   ⟹   XP_047294057
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
RefSeq Acc Id: XM_047438102   ⟹   XP_047294058
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,666,730 (+)NCBI
RefSeq Acc Id: XM_047438103   ⟹   XP_047294059
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,662,985 - 54,668,718 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001265355 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265356 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265357 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265358 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265359 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381862 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381863 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381864 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381865 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381866 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381867 (Get FASTA)   NCBI Sequence Viewer  
  NP_001381868 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881705 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294056 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294057 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294058 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294059 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB68665 (Get FASTA)   NCBI Sequence Viewer  
  AAB87666 (Get FASTA)   NCBI Sequence Viewer  
  AAC51355 (Get FASTA)   NCBI Sequence Viewer  
  AAC99761 (Get FASTA)   NCBI Sequence Viewer  
  AAG02024 (Get FASTA)   NCBI Sequence Viewer  
  AAH26309 (Get FASTA)   NCBI Sequence Viewer  
  AAL36992 (Get FASTA)   NCBI Sequence Viewer  
  ACK56073 (Get FASTA)   NCBI Sequence Viewer  
  BAF84771 (Get FASTA)   NCBI Sequence Viewer  
  CAG46845 (Get FASTA)   NCBI Sequence Viewer  
  EAW72270 (Get FASTA)   NCBI Sequence Viewer  
  EAW72271 (Get FASTA)   NCBI Sequence Viewer  
  EAW72272 (Get FASTA)   NCBI Sequence Viewer  
  Q8NHJ6 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001265357   ⟸   NM_001278428
- Peptide Label: isoform 3 precursor
- UniProtKB: Q8NHJ6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001265355   ⟸   NM_001278426
- Peptide Label: isoform 1 precursor
- UniProtKB: Q8NHJ6 (UniProtKB/Swiss-Prot),   A0A8Q3SHR1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265356   ⟸   NM_001278427
- Peptide Label: isoform 2 precursor
- UniProtKB: Q8NHJ6 (UniProtKB/Swiss-Prot),   A0A0A0MSZ8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265358   ⟸   NM_001278429
- Peptide Label: isoform 4
- Sequence:
RefSeq Acc Id: NP_001265359   ⟸   NM_001278430
- Peptide Label: isoform 5 precursor
- UniProtKB: Q8NHJ6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016881705   ⟸   XM_017026216
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000483357   ⟸   ENST00000494796
RefSeq Acc Id: ENSP00000270452   ⟸   ENST00000270452
RefSeq Acc Id: ENSP00000375616   ⟸   ENST00000391736
RefSeq Acc Id: ENSP00000375613   ⟸   ENST00000391733
RefSeq Acc Id: ENSP00000375614   ⟸   ENST00000391734
RefSeq Acc Id: ENSP00000408995   ⟸   ENST00000430952
RefSeq Acc Id: ENSP00000401962   ⟸   ENST00000434286
RefSeq Acc Id: NP_001381862   ⟸   NM_001394933
- Peptide Label: isoform 6 precursor
- UniProtKB: A0A0A0MS20 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001381868   ⟸   NM_001394939
- Peptide Label: isoform 12 precursor
- UniProtKB: A8MUE1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001381863   ⟸   NM_001394934
- Peptide Label: isoform 7 precursor
RefSeq Acc Id: NP_001381864   ⟸   NM_001394935
- Peptide Label: isoform 8 precursor
RefSeq Acc Id: NP_001381865   ⟸   NM_001394936
- Peptide Label: isoform 9
RefSeq Acc Id: NP_001381867   ⟸   NM_001394938
- Peptide Label: isoform 11
RefSeq Acc Id: NP_001381866   ⟸   NM_001394937
- Peptide Label: isoform 10
RefSeq Acc Id: ENSP00000511897   ⟸   ENST00000695418
RefSeq Acc Id: XP_047294056   ⟸   XM_047438100
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047294057   ⟸   XM_047438101
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047294059   ⟸   XM_047438103
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047294058   ⟸   XM_047438102
- Peptide Label: isoform X4
Protein Domains
Ig-like   Ig-like C2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NHJ6-F1-model_v2 AlphaFold Q8NHJ6 1-448 view protein structure

Promoters
RGD ID:13205641
Promoter ID:EPDNEW_H26401
Type:initiation region
Name:LILRB4_1
Description:leukocyte immunoglobulin like receptor B4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26400  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,663,000 - 54,663,060EPDNEW
RGD ID:6795754
Promoter ID:HG_KWN:30991
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000391734,   ENST00000391735,   ENST00000391736,   NM_006847,   OTTHUMT00000141131,   OTTHUMT00000141132,   UC002QGR.1,   UC010ERS.1,   UC010ERT.1,   UC010ERU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361959,864,446 - 59,866,167 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6608 AgrOrtholog
COSMIC LILRB4 COSMIC
Ensembl Genes ENSG00000186818 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000275730 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000276042 UniProtKB/TrEMBL
  ENSG00000278279 UniProtKB/TrEMBL
  ENSG00000278555 UniProtKB/TrEMBL
Ensembl Protein ENSP00000270452.3 UniProtKB/TrEMBL
  ENSP00000375613 ENTREZGENE
  ENSP00000375613.3 UniProtKB/TrEMBL
  ENSP00000375614 ENTREZGENE
  ENSP00000375614.3 UniProtKB/TrEMBL
  ENSP00000375616.1 UniProtKB/Swiss-Prot
  ENSP00000401962 ENTREZGENE
  ENSP00000401962.1 UniProtKB/TrEMBL
  ENSP00000408995 ENTREZGENE
  ENSP00000408995.2 UniProtKB/TrEMBL
  ENSP00000478077.1 UniProtKB/TrEMBL
  ENSP00000478476.1 UniProtKB/TrEMBL
  ENSP00000478511.1 UniProtKB/TrEMBL
  ENSP00000478542.1 UniProtKB/Swiss-Prot
  ENSP00000478584.1 UniProtKB/TrEMBL
  ENSP00000478727.1 UniProtKB/TrEMBL
  ENSP00000479289.1 UniProtKB/TrEMBL
  ENSP00000479497.1 UniProtKB/TrEMBL
  ENSP00000479829.1 UniProtKB/Swiss-Prot
  ENSP00000480977.1 UniProtKB/TrEMBL
  ENSP00000481233.1 UniProtKB/TrEMBL
  ENSP00000481609.1 UniProtKB/TrEMBL
  ENSP00000482234.1 UniProtKB/Swiss-Prot
  ENSP00000482694.1 UniProtKB/TrEMBL
  ENSP00000483171.1 UniProtKB/TrEMBL
  ENSP00000483296.1 UniProtKB/TrEMBL
  ENSP00000483357.1 UniProtKB/TrEMBL
  ENSP00000483376.1 UniProtKB/TrEMBL
  ENSP00000483708.1 UniProtKB/TrEMBL
  ENSP00000484286.1 UniProtKB/TrEMBL
  ENSP00000484348.1 UniProtKB/TrEMBL
  ENSP00000484515.1 UniProtKB/TrEMBL
  ENSP00000484720.1 UniProtKB/TrEMBL
  ENSP00000484809.1 UniProtKB/TrEMBL
  ENSP00000511897 ENTREZGENE
  ENSP00000511897.1 UniProtKB/TrEMBL
Ensembl Transcript ENST00000270452.6 UniProtKB/TrEMBL
  ENST00000391733 ENTREZGENE
  ENST00000391733.7 UniProtKB/TrEMBL
  ENST00000391734 ENTREZGENE
  ENST00000391734.7 UniProtKB/TrEMBL
  ENST00000391736.5 UniProtKB/Swiss-Prot
  ENST00000430952 ENTREZGENE
  ENST00000430952.6 UniProtKB/TrEMBL
  ENST00000434286 ENTREZGENE
  ENST00000434286.1 UniProtKB/TrEMBL
  ENST00000494796.5 UniProtKB/TrEMBL
  ENST00000611165.4 UniProtKB/TrEMBL
  ENST00000612454.4 UniProtKB/Swiss-Prot
  ENST00000613090.4 UniProtKB/TrEMBL
  ENST00000613131.1 UniProtKB/TrEMBL
  ENST00000614214.4 UniProtKB/TrEMBL
  ENST00000614340.4 UniProtKB/TrEMBL
  ENST00000614699.4 UniProtKB/Swiss-Prot
  ENST00000615614.4 UniProtKB/TrEMBL
  ENST00000616137.4 UniProtKB/TrEMBL
  ENST00000616806.1 UniProtKB/TrEMBL
  ENST00000617098.4 UniProtKB/TrEMBL
  ENST00000617426.4 UniProtKB/TrEMBL
  ENST00000618034.1 UniProtKB/TrEMBL
  ENST00000618480.4 UniProtKB/TrEMBL
  ENST00000619525.1 UniProtKB/TrEMBL
  ENST00000619910.4 UniProtKB/TrEMBL
  ENST00000620735.4 UniProtKB/TrEMBL
  ENST00000621149.4 UniProtKB/TrEMBL
  ENST00000621368.4 UniProtKB/TrEMBL
  ENST00000621555.4 UniProtKB/TrEMBL
  ENST00000621693.4 UniProtKB/Swiss-Prot
  ENST00000621985.4 UniProtKB/TrEMBL
  ENST00000622693.1 UniProtKB/TrEMBL
  ENST00000695418 ENTREZGENE
  ENST00000695418.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000186818 GTEx
  ENSG00000275730 GTEx
  ENSG00000276042 GTEx
  ENSG00000278279 GTEx
  ENSG00000278555 GTEx
HGNC ID HGNC:6608 ENTREZGENE
Human Proteome Map LILRB4 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
  Immunoglobulin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:11006 UniProtKB/Swiss-Prot
NCBI Gene 11006 ENTREZGENE
OMIM 604821 OMIM
PANTHER LEUKOCYTE IMMUNOGLOBULIN-LIKE RECEPTOR SUBFAMILY B MEMBER 4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MHC CLASS I NK CELL RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ig_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00047 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30382 PharmGKB
PROSITE IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087X0F8_HUMAN UniProtKB/TrEMBL
  A0A0A0MQW7_HUMAN UniProtKB/TrEMBL
  A0A0A0MS20 ENTREZGENE, UniProtKB/TrEMBL
  A0A0A0MSZ8 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JM38_HUMAN UniProtKB/TrEMBL
  A0A0G2JM43_HUMAN UniProtKB/TrEMBL
  A0A0G2JM57_HUMAN UniProtKB/TrEMBL
  A0A0G2JM84_HUMAN UniProtKB/TrEMBL
  A0A0G2JMH7_HUMAN UniProtKB/TrEMBL
  A0A0G2JML1_HUMAN UniProtKB/TrEMBL
  A0A0G2JNA7_HUMAN UniProtKB/TrEMBL
  A0A0G2JNE9_HUMAN UniProtKB/TrEMBL
  A0A0G2JNL1_HUMAN UniProtKB/TrEMBL
  A0A0G2JP25_HUMAN UniProtKB/TrEMBL
  A0A0G2JP84_HUMAN UniProtKB/TrEMBL
  A0A0G2JPA9_HUMAN UniProtKB/TrEMBL
  A0A0G2JPC7_HUMAN UniProtKB/TrEMBL
  A0A0G2JPI0_HUMAN UniProtKB/TrEMBL
  A0A0G2JPU4_HUMAN UniProtKB/TrEMBL
  A0A0G2JPV4_HUMAN UniProtKB/TrEMBL
  A0A0G2JPX5_HUMAN UniProtKB/TrEMBL
  A0A0G2JQ10_HUMAN UniProtKB/TrEMBL
  A0A0G2JQ20_HUMAN UniProtKB/TrEMBL
  A0A8Q3SHR1 ENTREZGENE, UniProtKB/TrEMBL
  A8MUE1 ENTREZGENE, UniProtKB/TrEMBL
  C9JST2_HUMAN UniProtKB/TrEMBL
  LIRB4_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary A8MVL8 UniProtKB/Swiss-Prot
  O15468 UniProtKB/Swiss-Prot
  O75021 UniProtKB/Swiss-Prot
  Q6FGQ9 UniProtKB/Swiss-Prot
  Q8N1C7 UniProtKB/Swiss-Prot
  Q8NHL5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-19 LILRB4  leukocyte immunoglobulin like receptor B4    leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 4  Symbol and/or name change 5135510 APPROVED
2011-08-16 LILRB4  leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 4  LILRB4  leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 4  Symbol and/or name change 5135510 APPROVED