LILRB1 (leukocyte immunoglobulin like receptor B1) - Rat Genome Database

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Gene: LILRB1 (leukocyte immunoglobulin like receptor B1) Homo sapiens
Analyze
Symbol: LILRB1
Name: leukocyte immunoglobulin like receptor B1
RGD ID: 1349645
HGNC Page HGNC:6605
Description: Enables several functions, including MHC protein binding activity; SH2 domain binding activity; and immune receptor activity. Involved in several processes, including negative regulation of leukocyte mediated cytotoxicity; regulation of T cell activation; and regulation of cytokine production. Located in cytoplasm and external side of plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CD85; CD85 antigen; CD85 antigen-like family member J; CD85J; FLJ37515; Ig-like transcript 2; ILT-2; ILT2; immunoglobulin heavy chain variable region; immunoglobulin-like transcript 2; leucocyte Ig-like receptor B1; leukocyte Ig-like receptor-1; leukocyte immunoglobulin-like receptor 1; leukocyte immunoglobulin-like receptor subfamily B member 1; leukocyte immunoglobulin-like receptor subfamily B member 1 soluble isoform; leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 1; LIR-1; LIR1; MIR-7; MIR7; monocyte/macrophage immunoglobulin-like receptor 7; myeloid inhibitory receptor 7; PIR-B; PIRB
RGD Orthologs
Bonobo
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
GRCh381954,616,322 - 54,638,022 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1954,617,158 - 54,638,022 (+)EnsemblGRCh38hg38GRCh38
GRCh371955,127,776 - 55,149,473 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361959,820,441 - 59,840,819 (+)NCBINCBI36Build 36hg18NCBI36
Build 341959,820,440 - 59,840,814NCBI
Celera1952,169,103 - 52,189,488 (+)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1951,451,468 - 51,472,091 (+)NCBIHuRef
CHM1_11955,121,949 - 55,142,575 (+)NCBICHM1_1
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
adaptive immune response  (IEA)
cell surface receptor signaling pathway  (IEA)
cellular response to lipopolysaccharide  (IEP)
cytokine-mediated signaling pathway  (IEA)
defense response to virus  (IDA)
dendritic cell differentiation  (IEP)
Fc receptor mediated inhibitory signaling pathway  (IDA)
immune response-inhibiting cell surface receptor signaling pathway  (NAS)
immune response-regulating signaling pathway  (IBA)
interleukin-10-mediated signaling pathway  (IBA)
negative regulation of alpha-beta T cell activation  (IDA)
negative regulation of calcium ion transport  (IDA)
negative regulation of CD8-positive, alpha-beta T cell activation  (IDA)
negative regulation of cell cycle  (IDA)
negative regulation of cytokine production involved in immune response  (IDA)
negative regulation of dendritic cell apoptotic process  (IDA)
negative regulation of dendritic cell differentiation  (IMP)
negative regulation of endocytosis  (IDA)
negative regulation of interferon-beta production  (IDA)
negative regulation of interleukin-10 production  (IDA)
negative regulation of interleukin-12 production  (IDA)
negative regulation of mononuclear cell proliferation  (IDA)
negative regulation of natural killer cell mediated cytotoxicity  (IDA)
negative regulation of osteoclast development  (IDA)
negative regulation of serotonin secretion  (IDA)
negative regulation of T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell  (IDA)
negative regulation of T cell mediated cytotoxicity  (IDA)
negative regulation of T cell proliferation  (IDA)
negative regulation of transforming growth factor beta production  (IDA)
negative regulation of tumor necrosis factor production  (IDA)
negative regulation of type II interferon production  (IDA)
positive regulation of apoptotic process  (IDA)
positive regulation of gamma-delta T cell activation involved in immune response  (IDA)
positive regulation of gene expression  (IDA)
positive regulation of macrophage cytokine production  (IDA)
positive regulation of transcription by RNA polymerase II  (NAS)
positive regulation of type II interferon production  (IDA)
receptor internalization  (TAS)
response to virus  (IDA)
signal transduction  (IDA)
T cell proliferation involved in immune response  (IDA)

Cellular Component

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:8125298   PMID:8258145   PMID:9079806   PMID:9259559   PMID:9285411   PMID:9382880   PMID:9548455   PMID:9842885   PMID:9933109   PMID:10591185   PMID:10941837   PMID:11114384  
PMID:11169396   PMID:11491530   PMID:11751964   PMID:11907092   PMID:12130517   PMID:12390682   PMID:12477932   PMID:12847262   PMID:12853576   PMID:12874224   PMID:12897781   PMID:14662864  
PMID:14702039   PMID:15100307   PMID:15304001   PMID:15474475   PMID:15489334   PMID:15585844   PMID:15670976   PMID:15905516   PMID:16014635   PMID:16210603   PMID:16305801   PMID:16344560  
PMID:16455647   PMID:17056715   PMID:17400057   PMID:17567994   PMID:17601702   PMID:17869268   PMID:17998301   PMID:18094328   PMID:18398485   PMID:18538388   PMID:18550825   PMID:18632577  
PMID:18684926   PMID:18802077   PMID:18821690   PMID:18946352   PMID:19124746   PMID:19136885   PMID:19304799   PMID:19583775   PMID:19658091   PMID:19841038   PMID:19913121   PMID:20139023  
PMID:20194892   PMID:20580616   PMID:20600445   PMID:20628086   PMID:20631139   PMID:20702625   PMID:21092455   PMID:21213105   PMID:21233315   PMID:21242521   PMID:21270408   PMID:21551166  
PMID:21559424   PMID:21817101   PMID:21873635   PMID:22028331   PMID:22242197   PMID:22296096   PMID:22574131   PMID:22623953   PMID:22802125   PMID:22844324   PMID:22965785   PMID:23103378  
PMID:23208495   PMID:23228398   PMID:23348966   PMID:23404538   PMID:23415844   PMID:23476104   PMID:23514593   PMID:23552990   PMID:23666960   PMID:23685425   PMID:23756160   PMID:23955630  
PMID:23997222   PMID:24018270   PMID:24038602   PMID:24052308   PMID:24156302   PMID:24162774   PMID:24453251   PMID:24550301   PMID:24909369   PMID:25070049   PMID:25187353   PMID:25726929  
PMID:25853899   PMID:25855135   PMID:26186194   PMID:26314621   PMID:26739048   PMID:26776460   PMID:26874236   PMID:26973020   PMID:27109306   PMID:27129285   PMID:27417393   PMID:27764812  
PMID:27901488   PMID:28514442   PMID:28636952   PMID:28646700   PMID:28987961   PMID:29069223   PMID:29158814   PMID:29180808   PMID:29186116   PMID:29234882   PMID:29528338   PMID:29531171  
PMID:30610047   PMID:30853664   PMID:30892832   PMID:30925324   PMID:31451484   PMID:31501273   PMID:32390601   PMID:32534335   PMID:32650338   PMID:32918786   PMID:32973812   PMID:33342344  
PMID:33505397   PMID:33790470   PMID:33961781   PMID:34054869   PMID:34160005   PMID:34186161   PMID:34396443   PMID:34659215   PMID:35041051   PMID:35347579   PMID:35754199   PMID:35917968  
PMID:36004818   PMID:36104364   PMID:36389667   PMID:36713400   PMID:36812290   PMID:36831297   PMID:36925435   PMID:37079240   PMID:37142967   PMID:37686397  


Genomics

Comparative Map Data
LILRB1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381954,616,322 - 54,638,022 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1954,617,158 - 54,638,022 (+)EnsemblGRCh38hg38GRCh38
GRCh371955,127,776 - 55,149,473 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361959,820,441 - 59,840,819 (+)NCBINCBI36Build 36hg18NCBI36
Build 341959,820,440 - 59,840,814NCBI
Celera1952,169,103 - 52,189,488 (+)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1951,451,468 - 51,472,091 (+)NCBIHuRef
CHM1_11955,121,949 - 55,142,575 (+)NCBICHM1_1
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBIT2T-CHM13v2.0
LOC103783591
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22060,636,638 - 60,654,622 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11962,560,398 - 62,578,236 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01951,561,376 - 51,578,564 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11960,401,854 - 60,412,716 (+)NCBIpanpan1.1PanPan1.1panPan2

Variants

.
Variants in LILRB1
65 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_001081637.2(LILRB1):c.1745C>T (p.Pro582Leu) single nucleotide variant Malignant melanoma [RCV000072350] Chr19:54636585 [GRCh38]
Chr19:55148036 [GRCh37]
Chr19:59839848 [NCBI36]
Chr19:19q13.42
not provided
NM_001081637.2(LILRB1):c.1259C>T (p.Ser420Leu) single nucleotide variant Malignant melanoma [RCV000063629] Chr19:54633316 [GRCh38]
Chr19:55144767 [GRCh37]
Chr19:59836579 [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(chr19:55116560-55164779)x1 copy number loss See cases [RCV000134636] Chr19:55116560..55164779 [GRCh37]
Chr19:59808372..59856591 [NCBI36]
Chr19:19q13.42
benign
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 Breast ductal adenocarcinoma [RCV000207190] Chr19:54710237..55648526 [GRCh37]
Chr19:19q13.42
uncertain significance
chr19:55143156-55294969 complex variant complex Breast ductal adenocarcinoma [RCV000207228] Chr19:55143156..55294969 [GRCh37]
Chr19:19q13.42
uncertain significance
chr19:54754752-55624113 complex variant complex Breast ductal adenocarcinoma [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(chr19:55028722-55148430)x1 copy number loss See cases [RCV000449455] Chr19:55028722..55148430 [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
NM_001081637.3(LILRB1):c.1463G>C (p.Arg488Pro) single nucleotide variant Inborn genetic diseases [RCV003277037] Chr19:54634740 [GRCh38]
Chr19:55146191 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.872A>G (p.Tyr291Cys) single nucleotide variant Inborn genetic diseases [RCV003270024] Chr19:54632674 [GRCh38]
Chr19:55144125 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.805G>A (p.Ala269Thr) single nucleotide variant Inborn genetic diseases [RCV003284542] Chr19:54632607 [GRCh38]
Chr19:55144058 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1744C>T (p.Pro582Ser) single nucleotide variant Inborn genetic diseases [RCV003289723] Chr19:54636584 [GRCh38]
Chr19:55148035 [GRCh37]
Chr19:19q13.42
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
NM_001081637.3(LILRB1):c.1047G>T (p.Gln349His) single nucleotide variant Inborn genetic diseases [RCV003267087] Chr19:54633104 [GRCh38]
Chr19:55144555 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.42(chr19:55017885-55157759)x1 copy number loss not provided [RCV001007060] Chr19:55017885..55157759 [GRCh37]
Chr19:19q13.42
likely benign
NM_001081637.3(LILRB1):c.1508A>G (p.Gln503Arg) single nucleotide variant Inborn genetic diseases [RCV003273950] Chr19:54635125 [GRCh38]
Chr19:55146576 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1879G>A (p.Glu627Lys) single nucleotide variant not provided [RCV001530746] Chr19:54636798 [GRCh38]
Chr19:55148249 [GRCh37]
Chr19:19q13.42
benign
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
NM_001081637.3(LILRB1):c.425= (p.Thr142=) single nucleotide variant not provided [RCV001641647] Chr19:54632001 [GRCh38]
Chr19:55143452 [GRCh37]
Chr19:19q13.42
benign
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
GRCh37/hg19 19q13.42(chr19:55029433-55157759)x1 copy number loss not provided [RCV001834174] Chr19:55029433..55157759 [GRCh37]
Chr19:19q13.42
likely benign
NC_000019.9:g.(?_54297303)_(55678016_?)dup duplication not provided [RCV001981426] Chr19:54297303..55678016 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1666G>A (p.Asp556Asn) single nucleotide variant Inborn genetic diseases [RCV003299887] Chr19:54636506 [GRCh38]
Chr19:55147957 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1415T>C (p.Leu472Pro) single nucleotide variant Inborn genetic diseases [RCV003303904] Chr19:54634692 [GRCh38]
Chr19:55146143 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1786G>A (p.Glu596Lys) single nucleotide variant Inborn genetic diseases [RCV003261074] Chr19:54636626 [GRCh38]
Chr19:55148077 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.995C>T (p.Pro332Leu) single nucleotide variant Inborn genetic diseases [RCV002990545] Chr19:54633052 [GRCh38]
Chr19:55144503 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1059A>C (p.Gln353His) single nucleotide variant Inborn genetic diseases [RCV002969622] Chr19:54633116 [GRCh38]
Chr19:55144567 [GRCh37]
Chr19:19q13.42
likely benign
NM_001081637.3(LILRB1):c.1895C>A (p.Pro632His) single nucleotide variant Inborn genetic diseases [RCV002992237] Chr19:54636814 [GRCh38]
Chr19:55148265 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1289C>T (p.Thr430Ile) single nucleotide variant Inborn genetic diseases [RCV002778097] Chr19:54633665 [GRCh38]
Chr19:55145116 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1816G>A (p.Ala606Thr) single nucleotide variant Inborn genetic diseases [RCV002841210] Chr19:54636735 [GRCh38]
Chr19:55148186 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.871T>C (p.Tyr291His) single nucleotide variant Inborn genetic diseases [RCV002684395] Chr19:54632673 [GRCh38]
Chr19:55144124 [GRCh37]
Chr19:19q13.42
likely benign
NM_001081637.3(LILRB1):c.266C>T (p.Thr89Ile) single nucleotide variant Inborn genetic diseases [RCV002776728] Chr19:54631695 [GRCh38]
Chr19:55143146 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1213C>T (p.Pro405Ser) single nucleotide variant Inborn genetic diseases [RCV002686976] Chr19:54633270 [GRCh38]
Chr19:55144721 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.874G>A (p.Gly292Arg) single nucleotide variant Inborn genetic diseases [RCV002864258] Chr19:54632676 [GRCh38]
Chr19:55144127 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1669G>A (p.Glu557Lys) single nucleotide variant Inborn genetic diseases [RCV002752197] Chr19:54636509 [GRCh38]
Chr19:55147960 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.284G>A (p.Arg95Gln) single nucleotide variant Inborn genetic diseases [RCV002946672] Chr19:54631713 [GRCh38]
Chr19:55143164 [GRCh37]
Chr19:19q13.42
likely benign
NM_001081637.3(LILRB1):c.1148C>G (p.Pro383Arg) single nucleotide variant Inborn genetic diseases [RCV002707043] Chr19:54633205 [GRCh38]
Chr19:55144656 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1051T>G (p.Trp351Gly) single nucleotide variant Inborn genetic diseases [RCV002952106] Chr19:54633108 [GRCh38]
Chr19:55144559 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.953T>A (p.Ile318Asn) single nucleotide variant Inborn genetic diseases [RCV002704240] Chr19:54632755 [GRCh38]
Chr19:55144206 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.780C>G (p.Asp260Glu) single nucleotide variant Inborn genetic diseases [RCV002952262] Chr19:54632582 [GRCh38]
Chr19:55144033 [GRCh37]
Chr19:19q13.42
likely benign
NM_001081637.3(LILRB1):c.629T>C (p.Leu210Pro) single nucleotide variant Inborn genetic diseases [RCV002757530] Chr19:54632205 [GRCh38]
Chr19:55143656 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.536G>A (p.Arg179His) single nucleotide variant Inborn genetic diseases [RCV002956157] Chr19:54632112 [GRCh38]
Chr19:55143563 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1800G>T (p.Gln600His) single nucleotide variant Inborn genetic diseases [RCV002763118] Chr19:54636640 [GRCh38]
Chr19:55148091 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1397T>A (p.Ile466Asn) single nucleotide variant Inborn genetic diseases [RCV002742181] Chr19:54634674 [GRCh38]
Chr19:55146125 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1265C>G (p.Pro422Arg) single nucleotide variant Inborn genetic diseases [RCV003003824] Chr19:54633641 [GRCh38]
Chr19:55145092 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.176G>A (p.Arg59His) single nucleotide variant Inborn genetic diseases [RCV002941639] Chr19:54631605 [GRCh38]
Chr19:55143056 [GRCh37]
Chr19:19q13.42
likely benign
NM_001081637.3(LILRB1):c.866G>C (p.Arg289Pro) single nucleotide variant Inborn genetic diseases [RCV002769900] Chr19:54632668 [GRCh38]
Chr19:55144119 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.854G>A (p.Gly285Asp) single nucleotide variant Inborn genetic diseases [RCV002832512] Chr19:54632656 [GRCh38]
Chr19:55144107 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.703A>G (p.Ile235Val) single nucleotide variant Inborn genetic diseases [RCV002898324] Chr19:54632505 [GRCh38]
Chr19:55143956 [GRCh37]
Chr19:19q13.42
likely benign
NM_001081637.3(LILRB1):c.934G>A (p.Asp312Asn) single nucleotide variant Inborn genetic diseases [RCV002959894] Chr19:54632736 [GRCh38]
Chr19:55144187 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1454G>A (p.Arg485Gln) single nucleotide variant Inborn genetic diseases [RCV002670561] Chr19:54634731 [GRCh38]
Chr19:55146182 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.401T>A (p.Val134Glu) single nucleotide variant Inborn genetic diseases [RCV002921637] Chr19:54631977 [GRCh38]
Chr19:55143428 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1931G>A (p.Ser644Asn) single nucleotide variant Inborn genetic diseases [RCV002944838] Chr19:54636850 [GRCh38]
Chr19:55148301 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1476C>G (p.His492Gln) single nucleotide variant Inborn genetic diseases [RCV003295919] Chr19:54634753 [GRCh38]
Chr19:55146204 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1484C>T (p.Ser495Leu) single nucleotide variant Inborn genetic diseases [RCV003184422] Chr19:54634761 [GRCh38]
Chr19:55146212 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1175C>T (p.Ala392Val) single nucleotide variant Inborn genetic diseases [RCV003184092] Chr19:54633232 [GRCh38]
Chr19:55144683 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.196A>G (p.Thr66Ala) single nucleotide variant Inborn genetic diseases [RCV003196237] Chr19:54631625 [GRCh38]
Chr19:55143076 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.781G>A (p.Gly261Arg) single nucleotide variant Inborn genetic diseases [RCV003284674] Chr19:54632583 [GRCh38]
Chr19:55144034 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1751C>G (p.Ser584Cys) single nucleotide variant Inborn genetic diseases [RCV003209431] Chr19:54636591 [GRCh38]
Chr19:55148042 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.386C>T (p.Ala129Val) single nucleotide variant Inborn genetic diseases [RCV003215905] Chr19:54631962 [GRCh38]
Chr19:55143413 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1654C>A (p.Gln552Lys) single nucleotide variant Inborn genetic diseases [RCV003206961] Chr19:54636494 [GRCh38]
Chr19:55147945 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.236A>G (p.Lys79Arg) single nucleotide variant Inborn genetic diseases [RCV003219519] Chr19:54631665 [GRCh38]
Chr19:55143116 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1877G>A (p.Arg626Gln) single nucleotide variant Inborn genetic diseases [RCV003344857] Chr19:54636796 [GRCh38]
Chr19:55148247 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.101A>G (p.Glu34Gly) single nucleotide variant Inborn genetic diseases [RCV003366618] Chr19:54631530 [GRCh38]
Chr19:55142981 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.486T>G (p.Asp162Glu) single nucleotide variant Inborn genetic diseases [RCV003349253] Chr19:54632062 [GRCh38]
Chr19:55143513 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1507C>G (p.Gln503Glu) single nucleotide variant Inborn genetic diseases [RCV003385098] Chr19:54635124 [GRCh38]
Chr19:55146575 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_001081637.3(LILRB1):c.1375C>T (p.His459Tyr) single nucleotide variant Inborn genetic diseases [RCV003369581] Chr19:54634652 [GRCh38]
Chr19:55146103 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43
likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:6160
Count of miRNA genes:1047
Interacting mature miRNAs:1280
Transcripts:ENST00000324602, ENST00000396315, ENST00000396317, ENST00000396321, ENST00000396327, ENST00000396331, ENST00000396332, ENST00000418536, ENST00000421584, ENST00000427581, ENST00000434867, ENST00000448689, ENST00000462628, ENST00000473412, ENST00000480257, ENST00000480375, ENST00000487425
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
ECD00782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,144,602 - 55,145,492UniSTSGRCh37
Build 361959,836,414 - 59,837,304RGDNCBI36
Celera1952,185,083 - 52,185,973RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,467,687 - 51,468,577UniSTS
ECD01260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,681 - 55,142,552UniSTSGRCh37
GRCh371954,804,146 - 54,805,020UniSTSGRCh37
Build 361959,495,958 - 59,496,832RGDNCBI36
Celera1952,182,162 - 52,183,033UniSTS
Celera1951,827,732 - 51,828,606RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,427,942 - 51,428,837UniSTS
HuRef1951,464,766 - 51,465,637UniSTS
ECD04689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,804,263 - 54,805,020UniSTSGRCh37
GRCh371955,141,681 - 55,142,434UniSTSGRCh37
Build 361959,496,075 - 59,496,832RGDNCBI36
Celera1952,182,162 - 52,182,915UniSTS
Celera1951,827,849 - 51,828,606RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,464,766 - 51,465,519UniSTS
ECD10050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,147,831 - 55,148,443UniSTSGRCh37
Build 361959,839,643 - 59,840,255RGDNCBI36
Celera1952,188,312 - 52,188,924RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,470,916 - 51,471,527UniSTS
ECD11182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,768 - 55,147,348UniSTSGRCh37
GRCh371954,779,517 - 54,780,097UniSTSGRCh37
Build 361959,471,329 - 59,471,909RGDNCBI36
Celera1952,187,249 - 52,187,829UniSTS
Celera1951,820,174 - 51,820,754RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,107,156 - 51,107,736UniSTS
HuRef1951,469,853 - 51,470,433UniSTS
ECD12015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,793 - 55,147,348UniSTSGRCh37
GRCh371954,779,517 - 54,780,072UniSTSGRCh37
Build 361959,471,329 - 59,471,884RGDNCBI36
Celera1952,187,274 - 52,187,829UniSTS
Celera1951,820,174 - 51,820,729RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,107,156 - 51,107,711UniSTS
HuRef1951,469,878 - 51,470,433UniSTS
ECD12535  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,204 - 55,146,745UniSTSGRCh37
GRCh371954,780,120 - 54,780,671UniSTSGRCh37
Build 361959,471,932 - 59,472,483RGDNCBI36
Celera1952,186,685 - 52,187,226RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,107,759 - 51,108,310UniSTS
HuRef1951,469,289 - 51,469,830UniSTS
ECD16466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,131 - 55,141,570UniSTSGRCh37
Build 361959,832,943 - 59,833,382RGDNCBI36
Celera1952,181,612 - 52,182,051RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,464,216 - 51,464,655UniSTS
ECD18786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,136,454 - 55,136,801UniSTSGRCh37
GRCh371954,789,391 - 54,789,741UniSTSGRCh37
Build 361959,481,203 - 59,481,553RGDNCBI36
Celera1952,176,935 - 52,177,282RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,117,029 - 51,117,379UniSTS
HuRef1951,459,538 - 51,459,885UniSTS
ECD19993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,138,188 - 55,138,489UniSTSGRCh37
Build 361959,830,000 - 59,830,301RGDNCBI36
Celera1952,178,669 - 52,178,970RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,115,554 - 51,115,850UniSTS
HuRef1951,461,273 - 51,461,574UniSTS
ECD22004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,136,569 - 55,136,801UniSTSGRCh37
GRCh371954,789,391 - 54,789,623UniSTSGRCh37
Build 361959,481,203 - 59,481,435RGDNCBI36
Celera1952,177,050 - 52,177,282RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,117,029 - 51,117,261UniSTS
HuRef1951,459,653 - 51,459,885UniSTS
REN92192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,683 - 55,146,926UniSTSGRCh37
GRCh371954,779,939 - 54,780,182UniSTSGRCh37
Build 361959,471,751 - 59,471,994RGDNCBI36
Celera1952,187,164 - 52,187,407UniSTS
Celera1951,820,596 - 51,820,839RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,107,578 - 51,107,821UniSTS
HuRef1951,469,768 - 51,470,011UniSTS
REN92194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,967 - 55,146,227UniSTSGRCh37
GRCh371954,780,648 - 54,780,908UniSTSGRCh37
Build 361959,472,460 - 59,472,720RGDNCBI36
Celera1952,186,448 - 52,186,708RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,108,287 - 51,108,547UniSTS
HuRef1951,469,052 - 51,469,312UniSTS
REN92195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,763 - 55,145,987UniSTSGRCh37
GRCh371954,780,888 - 54,781,112UniSTSGRCh37
Build 361959,472,700 - 59,472,924RGDNCBI36
Celera1952,186,244 - 52,186,468RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,108,527 - 51,108,751UniSTS
HuRef1951,468,848 - 51,469,072UniSTS
REN92212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,142,140 - 55,142,406UniSTSGRCh37
GRCh371954,784,494 - 54,784,759UniSTSGRCh37
Build 361959,476,306 - 59,476,571RGDNCBI36
Celera1952,182,621 - 52,182,887RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,112,132 - 51,112,397UniSTS
HuRef1951,465,225 - 51,465,491UniSTS
REN92217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,979 - 55,141,249UniSTSGRCh37
GRCh371954,785,635 - 54,785,899UniSTSGRCh37
Build 361959,477,447 - 59,477,711RGDNCBI36
Celera1952,181,460 - 52,181,730RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,113,273 - 51,113,537UniSTS
HuRef1951,464,064 - 51,464,334UniSTS
REN92218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,741 - 55,141,002UniSTSGRCh37
GRCh371954,785,876 - 54,786,137UniSTSGRCh37
Build 361959,477,688 - 59,477,949RGDNCBI36
Celera1952,181,222 - 52,181,483RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,113,514 - 51,113,775UniSTS
HuRef1951,463,826 - 51,464,087UniSTS
REN92219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,511 - 55,140,764UniSTSGRCh37
GRCh371954,786,114 - 54,786,367UniSTSGRCh37
Build 361959,477,926 - 59,478,179RGDNCBI36
Celera1952,180,992 - 52,181,245RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,113,752 - 51,114,005UniSTS
HuRef1951,463,596 - 51,463,849UniSTS
REN92234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,136,168 - 55,136,404UniSTSGRCh37
GRCh371954,789,791 - 54,790,027UniSTSGRCh37
Build 361959,481,603 - 59,481,839RGDNCBI36
Celera1952,176,649 - 52,176,885UniSTS
Celera1951,831,067 - 51,831,303RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,117,429 - 51,117,665UniSTS
HuRef1951,459,252 - 51,459,488UniSTS
REN92235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,135,952 - 55,136,186UniSTSGRCh37
GRCh371954,790,009 - 54,790,242UniSTSGRCh37
Build 361959,481,821 - 59,482,054RGDNCBI36
Celera1952,176,433 - 52,176,667UniSTS
Celera1951,831,285 - 51,831,519RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,117,647 - 51,117,880UniSTS
HuRef1951,459,036 - 51,459,270UniSTS
REN92236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,135,850 - 55,136,106UniSTSGRCh37
GRCh371954,790,088 - 54,790,344UniSTSGRCh37
Build 361959,481,900 - 59,482,156RGDNCBI36
Celera1952,176,331 - 52,176,587RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,117,726 - 51,117,982UniSTS
REN92238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,135,206 - 55,135,459UniSTSGRCh37
GRCh371954,790,735 - 54,790,988UniSTSGRCh37
Build 361959,482,547 - 59,482,800RGDNCBI36
Celera1952,175,687 - 52,175,940UniSTS
Celera1951,832,012 - 51,832,265RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,118,373 - 51,118,626UniSTS
HuRef1951,458,290 - 51,458,543UniSTS
REN92239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,134,944 - 55,135,221UniSTSGRCh37
GRCh371954,790,973 - 54,791,247UniSTSGRCh37
Build 361959,482,785 - 59,483,059RGDNCBI36
Celera1952,175,425 - 52,175,702UniSTS
Celera1951,832,250 - 51,832,524RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,118,611 - 51,118,885UniSTS
HuRef1951,458,028 - 51,458,305UniSTS
REN93455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,139,995 - 55,140,236UniSTSGRCh37
GRCh371955,103,244 - 55,103,484UniSTSGRCh37
Build 361959,795,056 - 59,795,296RGDNCBI36
Celera1952,180,476 - 52,180,717UniSTS
Celera1952,143,714 - 52,143,954RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,426,344 - 51,426,584UniSTS
HuRef1951,463,080 - 51,463,321UniSTS
REN93456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,217 - 55,140,453UniSTSGRCh37
GRCh371955,103,465 - 55,103,702UniSTSGRCh37
Build 361959,795,277 - 59,795,514RGDNCBI36
Celera1952,180,698 - 52,180,934UniSTS
Celera1952,143,935 - 52,144,172RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,426,565 - 51,426,802UniSTS
HuRef1951,463,302 - 51,463,538UniSTS
REN93557  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,126,681 - 55,126,913UniSTSGRCh37
Build 361959,818,493 - 59,818,725RGDNCBI36
Celera1952,167,155 - 52,167,387RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,449,765 - 51,449,997UniSTS
REN93558  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,126,940 - 55,127,164UniSTSGRCh37
Build 361959,818,752 - 59,818,976RGDNCBI36
Celera1952,167,414 - 52,167,638RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,450,024 - 51,450,248UniSTS
REN93559  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,127,139 - 55,127,366UniSTSGRCh37
Build 361959,818,951 - 59,819,178RGDNCBI36
Celera1952,167,613 - 52,167,840RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,450,223 - 51,450,450UniSTS
REN93560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,127,288 - 55,127,550UniSTSGRCh37
Build 361959,819,100 - 59,819,362RGDNCBI36
Celera1952,167,762 - 52,168,024RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,450,372 - 51,450,634UniSTS
REN93561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,127,526 - 55,127,788UniSTSGRCh37
Build 361959,819,338 - 59,819,600RGDNCBI36
Celera1952,168,000 - 52,168,262RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,450,610 - 51,450,872UniSTS
REN93562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,127,787 - 55,128,023UniSTSGRCh37
Build 361959,819,599 - 59,819,835RGDNCBI36
Celera1952,168,261 - 52,168,497RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,450,871 - 51,451,107UniSTS
REN93563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,127,996 - 55,128,246UniSTSGRCh37
Build 361959,819,808 - 59,820,058RGDNCBI36
Celera1952,168,470 - 52,168,720RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,451,080 - 51,451,330UniSTS
REN93564  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,128,223 - 55,128,488UniSTSGRCh37
Build 361959,820,035 - 59,820,300RGDNCBI36
Celera1952,168,697 - 52,168,962RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,451,307 - 51,451,572UniSTS
REN93565  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,128,456 - 55,128,707UniSTSGRCh37
Build 361959,820,268 - 59,820,519RGDNCBI36
Celera1952,168,930 - 52,169,181RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,451,540 - 51,451,791UniSTS
REN93566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,128,685 - 55,128,910UniSTSGRCh37
Build 361959,820,497 - 59,820,722RGDNCBI36
Celera1952,169,159 - 52,169,384RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,451,769 - 51,451,994UniSTS
REN93567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,128,876 - 55,129,125UniSTSGRCh37
Build 361959,820,688 - 59,820,937RGDNCBI36
Celera1952,169,350 - 52,169,599RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,451,960 - 51,452,201UniSTS
REN93568  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,129,114 - 55,129,356UniSTSGRCh37
Build 361959,820,926 - 59,821,168RGDNCBI36
Celera1952,169,588 - 52,169,830RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,452,190 - 51,452,432UniSTS
REN93569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,129,244 - 55,129,499UniSTSGRCh37
Build 361959,821,056 - 59,821,311RGDNCBI36
Celera1952,169,718 - 52,169,973RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,452,320 - 51,452,575UniSTS
REN93570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,129,477 - 55,129,706UniSTSGRCh37
Build 361959,821,289 - 59,821,518RGDNCBI36
Celera1952,169,951 - 52,170,187RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,452,553 - 51,452,790UniSTS
REN93571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,129,671 - 55,129,932UniSTSGRCh37
Build 361959,821,483 - 59,821,744RGDNCBI36
Celera1952,170,152 - 52,170,413RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,452,755 - 51,453,016UniSTS
REN93572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,129,739 - 55,129,986UniSTSGRCh37
Build 361959,821,551 - 59,821,798RGDNCBI36
Celera1952,170,220 - 52,170,467RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,452,823 - 51,453,070UniSTS
REN93573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,130,055 - 55,130,284UniSTSGRCh37
Build 361959,821,867 - 59,822,096RGDNCBI36
Celera1952,170,536 - 52,170,765RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,453,139 - 51,453,368UniSTS
REN93574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,130,139 - 55,130,378UniSTSGRCh37
Build 361959,821,951 - 59,822,190RGDNCBI36
Celera1952,170,620 - 52,170,859RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,453,223 - 51,453,462UniSTS
REN93575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,130,352 - 55,130,593UniSTSGRCh37
Build 361959,822,164 - 59,822,405RGDNCBI36
Celera1952,170,833 - 52,171,074RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,453,436 - 51,453,677UniSTS
REN93576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,130,567 - 55,130,824UniSTSGRCh37
Build 361959,822,379 - 59,822,636RGDNCBI36
Celera1952,171,048 - 52,171,305RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,453,651 - 51,453,908UniSTS
REN93577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,130,795 - 55,131,044UniSTSGRCh37
Build 361959,822,607 - 59,822,856RGDNCBI36
Celera1952,171,276 - 52,171,525RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,453,879 - 51,454,128UniSTS
REN93578  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,131,041 - 55,131,295UniSTSGRCh37
Build 361959,822,853 - 59,823,107RGDNCBI36
Celera1952,171,522 - 52,171,776RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,454,125 - 51,454,379UniSTS
REN93579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,131,272 - 55,131,510UniSTSGRCh37
Build 361959,823,084 - 59,823,322RGDNCBI36
Celera1952,171,753 - 52,171,991RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,454,356 - 51,454,594UniSTS
REN93580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,131,471 - 55,131,721UniSTSGRCh37
Build 361959,823,283 - 59,823,533RGDNCBI36
Celera1952,171,952 - 52,172,202RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,454,555 - 51,454,805UniSTS
REN93581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,131,711 - 55,131,969UniSTSGRCh37
Build 361959,823,523 - 59,823,781RGDNCBI36
Celera1952,172,192 - 52,172,450RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,454,795 - 51,455,053UniSTS
REN93582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,131,967 - 55,132,212UniSTSGRCh37
Build 361959,823,779 - 59,824,024RGDNCBI36
Celera1952,172,448 - 52,172,693RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,455,051 - 51,455,296UniSTS
REN93583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,132,095 - 55,132,319UniSTSGRCh37
Build 361959,823,907 - 59,824,131RGDNCBI36
Celera1952,172,576 - 52,172,800RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,455,179 - 51,455,403UniSTS
REN93584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,132,616 - 55,132,854UniSTSGRCh37
Build 361959,824,428 - 59,824,666RGDNCBI36
Celera1952,173,097 - 52,173,335RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,455,700 - 51,455,938UniSTS
REN93585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,132,850 - 55,133,104UniSTSGRCh37
Build 361959,824,662 - 59,824,916RGDNCBI36
Celera1952,173,331 - 52,173,585RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,455,934 - 51,456,188UniSTS
REN93586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,133,039 - 55,133,293UniSTSGRCh37
Build 361959,824,851 - 59,825,105RGDNCBI36
Celera1952,173,520 - 52,173,774RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,456,123 - 51,456,377UniSTS
REN93587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,133,274 - 55,133,504UniSTSGRCh37
Build 361959,825,086 - 59,825,316RGDNCBI36
Celera1952,173,755 - 52,173,985RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,456,358 - 51,456,588UniSTS
REN93588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,133,480 - 55,133,741UniSTSGRCh37
Build 361959,825,292 - 59,825,553RGDNCBI36
Celera1952,173,961 - 52,174,222RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,456,564 - 51,456,825UniSTS
REN93589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,133,713 - 55,133,938UniSTSGRCh37
Build 361959,825,525 - 59,825,750RGDNCBI36
Celera1952,174,194 - 52,174,419RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,456,797 - 51,457,022UniSTS
REN93590  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,133,818 - 55,134,067UniSTSGRCh37
Build 361959,825,630 - 59,825,879RGDNCBI36
Celera1952,174,299 - 52,174,548RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,456,902 - 51,457,151UniSTS
REN93591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,134,051 - 55,134,318UniSTSGRCh37
Build 361959,825,863 - 59,826,130RGDNCBI36
Celera1952,174,532 - 52,174,799RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,457,135 - 51,457,402UniSTS
REN93592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,134,282 - 55,134,533UniSTSGRCh37
Build 361959,826,094 - 59,826,345RGDNCBI36
Celera1952,174,763 - 52,175,014RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,457,366 - 51,457,617UniSTS
REN93593  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,134,508 - 55,134,746UniSTSGRCh37
Build 361959,826,320 - 59,826,558RGDNCBI36
Celera1952,174,989 - 52,175,227RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,457,592 - 51,457,830UniSTS
REN93594  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,134,727 - 55,134,972UniSTSGRCh37
Build 361959,826,539 - 59,826,784RGDNCBI36
Celera1952,175,208 - 52,175,453RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,457,811 - 51,458,056UniSTS
REN93595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,134,928 - 55,135,160UniSTSGRCh37
Build 361959,826,740 - 59,826,972RGDNCBI36
Celera1952,175,409 - 52,175,641RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,458,012 - 51,458,244UniSTS
REN93596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,135,137 - 55,135,406UniSTSGRCh37
Build 361959,826,949 - 59,827,218RGDNCBI36
Celera1952,175,618 - 52,175,887RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,458,221 - 51,458,490UniSTS
REN93597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,135,284 - 55,135,523UniSTSGRCh37
GRCh371954,790,671 - 54,790,910UniSTSGRCh37
Build 361959,482,483 - 59,482,722RGDNCBI36
Celera1952,175,765 - 52,176,004UniSTS
Celera1951,831,948 - 51,832,187RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,118,309 - 51,118,548UniSTS
HuRef1951,458,368 - 51,458,607UniSTS
REN93598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,135,935 - 55,136,183UniSTSGRCh37
GRCh371954,790,012 - 54,790,259UniSTSGRCh37
Build 361959,481,824 - 59,482,071RGDNCBI36
Celera1952,176,416 - 52,176,664UniSTS
Celera1951,831,288 - 51,831,536RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,117,650 - 51,117,897UniSTS
HuRef1951,459,019 - 51,459,267UniSTS
REN93599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,136,167 - 55,136,404UniSTSGRCh37
GRCh371954,789,791 - 54,790,028UniSTSGRCh37
Build 361959,481,603 - 59,481,840RGDNCBI36
Celera1952,176,648 - 52,176,885UniSTS
Celera1951,831,067 - 51,831,304RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,117,429 - 51,117,666UniSTS
HuRef1951,459,251 - 51,459,488UniSTS
REN93600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,136,906 - 55,137,277UniSTSGRCh37
GRCh371955,136,906 - 55,137,137UniSTSGRCh37
Build 361959,828,718 - 59,828,949RGDNCBI36
Celera1952,177,387 - 52,177,758UniSTS
Celera1952,177,387 - 52,177,618RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,459,990 - 51,460,221UniSTS
HuRef1951,459,990 - 51,460,361UniSTS
REN93602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,137,298 - 55,137,551UniSTSGRCh37
Build 361959,829,110 - 59,829,363RGDNCBI36
Celera1952,177,779 - 52,178,032RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,460,382 - 51,460,635UniSTS
REN93603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,137,468 - 55,137,692UniSTSGRCh37
Build 361959,829,280 - 59,829,504RGDNCBI36
Celera1952,177,949 - 52,178,173RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,460,552 - 51,460,776UniSTS
REN93604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,137,666 - 55,137,938UniSTSGRCh37
Build 361959,829,478 - 59,829,750RGDNCBI36
Celera1952,178,147 - 52,178,419RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,460,750 - 51,461,022UniSTS
REN93605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,137,910 - 55,138,134UniSTSGRCh37
Build 361959,829,722 - 59,829,946RGDNCBI36
Celera1952,178,391 - 52,178,615RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,460,994 - 51,461,219UniSTS
REN93606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,138,106 - 55,138,334UniSTSGRCh37
Build 361959,829,918 - 59,830,146RGDNCBI36
Celera1952,178,587 - 52,178,815RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,461,191 - 51,461,419UniSTS
REN93607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,138,310 - 55,138,580UniSTSGRCh37
Build 361959,830,122 - 59,830,392RGDNCBI36
Celera1952,178,791 - 52,179,061RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,461,395 - 51,461,665UniSTS
REN93608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,138,561 - 55,138,821UniSTSGRCh37
Build 361959,830,373 - 59,830,633RGDNCBI36
Celera1952,179,042 - 52,179,302RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,461,646 - 51,461,906UniSTS
REN93609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,138,792 - 55,139,042UniSTSGRCh37
Build 361959,830,604 - 59,830,854RGDNCBI36
Celera1952,179,273 - 52,179,523RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,461,877 - 51,462,127UniSTS
REN93610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,139,018 - 55,139,257UniSTSGRCh37
Build 361959,830,830 - 59,831,069RGDNCBI36
Celera1952,179,499 - 52,179,738RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,462,103 - 51,462,342UniSTS
REN93611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,139,234 - 55,139,472UniSTSGRCh37
Build 361959,831,046 - 59,831,284RGDNCBI36
Celera1952,179,715 - 52,179,953RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,462,319 - 51,462,557UniSTS
REN93613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,139,632 - 55,139,866UniSTSGRCh37
Build 361959,831,444 - 59,831,678RGDNCBI36
Celera1952,180,113 - 52,180,347RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,462,717 - 51,462,951UniSTS
REN93614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,139,849 - 55,140,115UniSTSGRCh37
Build 361959,831,661 - 59,831,927RGDNCBI36
Celera1952,180,330 - 52,180,596RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,462,934 - 51,463,200UniSTS
REN93615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,139,978 - 55,140,222UniSTSGRCh37
GRCh371955,103,227 - 55,103,470UniSTSGRCh37
Build 361959,795,039 - 59,795,282RGDNCBI36
Celera1952,180,459 - 52,180,703UniSTS
Celera1952,143,697 - 52,143,940RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,426,327 - 51,426,570UniSTS
HuRef1951,463,063 - 51,463,307UniSTS
REN93616  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,217 - 55,140,458UniSTSGRCh37
Build 361959,832,029 - 59,832,270RGDNCBI36
Celera1952,180,698 - 52,180,939RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,463,302 - 51,463,543UniSTS
REN93617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,438 - 55,140,671UniSTSGRCh37
GRCh371954,786,207 - 54,786,440UniSTSGRCh37
Build 361959,478,019 - 59,478,252RGDNCBI36
Celera1952,180,919 - 52,181,152RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,113,845 - 51,114,078UniSTS
HuRef1951,463,523 - 51,463,756UniSTS
REN93618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,659 - 55,140,885UniSTSGRCh37
GRCh371954,785,993 - 54,786,219UniSTSGRCh37
Build 361959,477,805 - 59,478,031RGDNCBI36
Celera1952,181,140 - 52,181,366RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,113,631 - 51,113,857UniSTS
HuRef1951,463,744 - 51,463,970UniSTS
REN93619  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,818 - 55,141,048UniSTSGRCh37
Build 361959,832,630 - 59,832,860RGDNCBI36
Celera1952,181,299 - 52,181,529RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,463,903 - 51,464,133UniSTS
REN93620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,015 - 55,141,278UniSTSGRCh37
Build 361959,832,827 - 59,833,090RGDNCBI36
Celera1952,181,496 - 52,181,759RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,464,100 - 51,464,363UniSTS
REN93621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,238 - 55,141,473UniSTSGRCh37
Build 361959,833,050 - 59,833,285RGDNCBI36
Celera1952,181,719 - 52,181,954RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,464,323 - 51,464,558UniSTS
REN93622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,467 - 55,141,726UniSTSGRCh37
Build 361959,833,279 - 59,833,538RGDNCBI36
Celera1952,181,948 - 52,182,207RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,464,552 - 51,464,811UniSTS
REN93623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,719 - 55,141,950UniSTSGRCh37
GRCh371955,104,880 - 55,105,112UniSTSGRCh37
Build 361959,796,692 - 59,796,924RGDNCBI36
Celera1952,182,200 - 52,182,431UniSTS
Celera1952,145,350 - 52,145,582RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,427,980 - 51,428,212UniSTS
HuRef1951,464,804 - 51,465,035UniSTS
REN93624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,927 - 55,142,171UniSTSGRCh37
Build 361959,833,739 - 59,833,983RGDNCBI36
Celera1952,182,408 - 52,182,652RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,465,012 - 51,465,256UniSTS
REN93625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,142,144 - 55,142,410UniSTSGRCh37
Build 361959,833,956 - 59,834,222RGDNCBI36
Celera1952,182,625 - 52,182,891RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,465,229 - 51,465,495UniSTS
REN93626  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,142,341 - 55,142,593UniSTSGRCh37
Build 361959,834,153 - 59,834,405RGDNCBI36
Celera1952,182,822 - 52,183,074RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,465,426 - 51,465,678UniSTS
REN93627  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,142,570 - 55,142,794UniSTSGRCh37
GRCh371955,105,755 - 55,105,978UniSTSGRCh37
Build 361959,797,567 - 59,797,790RGDNCBI36
Celera1952,183,051 - 52,183,275UniSTS
Celera1952,146,225 - 52,146,448RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,428,855 - 51,429,078UniSTS
HuRef1951,465,655 - 51,465,879UniSTS
REN93628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,142,758 - 55,142,997UniSTSGRCh37
GRCh371955,105,942 - 55,106,176UniSTSGRCh37
Build 361959,797,754 - 59,797,988RGDNCBI36
Celera1952,183,239 - 52,183,478UniSTS
Celera1952,146,412 - 52,146,646RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,429,042 - 51,429,276UniSTS
HuRef1951,465,843 - 51,466,082UniSTS
REN93629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,142,968 - 55,143,197UniSTSGRCh37
Build 361959,834,780 - 59,835,009RGDNCBI36
Celera1952,183,449 - 52,183,678RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,466,053 - 51,466,282UniSTS
REN93630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,143,038 - 55,143,288UniSTSGRCh37
Build 361959,834,850 - 59,835,100RGDNCBI36
Celera1952,183,519 - 52,183,769RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,466,123 - 51,466,373UniSTS
REN93631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,143,198 - 55,143,452UniSTSGRCh37
Build 361959,835,010 - 59,835,264RGDNCBI36
Celera1952,183,679 - 52,183,933RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,466,283 - 51,466,537UniSTS
REN93632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,143,429 - 55,143,670UniSTSGRCh37
Build 361959,835,241 - 59,835,482RGDNCBI36
Celera1952,183,910 - 52,184,151RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,466,514 - 51,466,755UniSTS
REN93634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,143,818 - 55,144,047UniSTSGRCh37
Build 361959,835,630 - 59,835,859RGDNCBI36
Celera1952,184,299 - 52,184,528RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,466,903 - 51,467,132UniSTS
REN93635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,144,036 - 55,144,296UniSTSGRCh37
Build 361959,835,848 - 59,836,108RGDNCBI36
Celera1952,184,517 - 52,184,777RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,467,121 - 51,467,381UniSTS
REN93636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,144,266 - 55,144,495UniSTSGRCh37
Build 361959,836,078 - 59,836,307RGDNCBI36
Celera1952,184,747 - 52,184,976RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,467,351 - 51,467,580UniSTS
REN93637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,144,481 - 55,144,729UniSTSGRCh37
Build 361959,836,293 - 59,836,541RGDNCBI36
Celera1952,184,962 - 52,185,210RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,467,566 - 51,467,814UniSTS
REN93638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,144,699 - 55,144,923UniSTSGRCh37
Build 361959,836,511 - 59,836,735RGDNCBI36
Celera1952,185,180 - 52,185,404RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,467,784 - 51,468,008UniSTS
REN93639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,144,896 - 55,145,163UniSTSGRCh37
Build 361959,836,708 - 59,836,975RGDNCBI36
Celera1952,185,377 - 52,185,644RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,467,981 - 51,468,248UniSTS
REN93640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,068 - 55,145,340UniSTSGRCh37
Build 361959,836,880 - 59,837,152RGDNCBI36
Celera1952,185,549 - 52,185,821RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,468,153 - 51,468,425UniSTS
REN93641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,318 - 55,145,567UniSTSGRCh37
Build 361959,837,130 - 59,837,379RGDNCBI36
Celera1952,185,799 - 52,186,048RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,468,403 - 51,468,652UniSTS
REN93642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,549 - 55,145,794UniSTSGRCh37
Build 361959,837,361 - 59,837,606RGDNCBI36
Celera1952,186,030 - 52,186,275RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,468,634 - 51,468,879UniSTS
REN93643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,763 - 55,145,988UniSTSGRCh37
Build 361959,837,575 - 59,837,800RGDNCBI36
Celera1952,186,244 - 52,186,469RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,468,848 - 51,469,073UniSTS
REN93644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,967 - 55,146,227UniSTSGRCh37
GRCh371954,780,648 - 54,780,908UniSTSGRCh37
Build 361959,472,460 - 59,472,720RGDNCBI36
Celera1952,186,448 - 52,186,708RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,108,287 - 51,108,547UniSTS
HuRef1951,469,052 - 51,469,312UniSTS
REN93645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,204 - 55,146,442UniSTSGRCh37
Build 361959,838,016 - 59,838,254RGDNCBI36
Celera1952,186,685 - 52,186,923RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,469,289 - 51,469,527UniSTS
REN93646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,683 - 55,146,927UniSTSGRCh37
GRCh371954,779,938 - 54,780,182UniSTSGRCh37
Build 361959,471,750 - 59,471,994RGDNCBI36
Celera1952,187,164 - 52,187,408UniSTS
Celera1951,820,595 - 51,820,839RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,107,577 - 51,107,821UniSTS
HuRef1951,469,768 - 51,470,012UniSTS
REN93647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,899 - 55,147,134UniSTSGRCh37
Build 361959,838,711 - 59,838,946RGDNCBI36
Celera1952,187,380 - 52,187,615RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,469,984 - 51,470,219UniSTS
REN93648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,977 - 55,147,219UniSTSGRCh37
GRCh371954,779,646 - 54,779,888UniSTSGRCh37
Build 361959,471,458 - 59,471,700RGDNCBI36
Celera1952,187,458 - 52,187,700UniSTS
Celera1951,820,303 - 51,820,545RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,107,285 - 51,107,527UniSTS
HuRef1951,470,062 - 51,470,304UniSTS
REN93650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,147,428 - 55,147,698UniSTSGRCh37
Build 361959,839,240 - 59,839,510RGDNCBI36
Celera1952,187,909 - 52,188,179RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,470,513 - 51,470,783UniSTS
REN93651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,147,677 - 55,147,921UniSTSGRCh37
Build 361959,839,489 - 59,839,733RGDNCBI36
Celera1952,188,158 - 52,188,402RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,470,762 - 51,471,006UniSTS
REN93652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,148,289 - 55,148,524UniSTSGRCh37
GRCh371954,720,753 - 54,721,002UniSTSGRCh37
Build 361959,412,565 - 59,412,814RGDNCBI36
Celera1952,188,770 - 52,189,005UniSTS
Celera1951,762,428 - 51,762,677RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,036,573 - 51,036,822UniSTS
HuRef1951,471,373 - 51,471,608UniSTS
REN93653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,148,482 - 55,148,706UniSTSGRCh37
Build 361959,840,294 - 59,840,518RGDNCBI36
Celera1952,188,963 - 52,189,187RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,471,566 - 51,471,790UniSTS
REN93654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,149,034 - 55,149,260UniSTSGRCh37
Build 361959,840,846 - 59,841,072RGDNCBI36
Celera1952,189,515 - 52,189,741RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,472,118 - 51,472,344UniSTS
REN93655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,149,238 - 55,149,491UniSTSGRCh37
Build 361959,841,050 - 59,841,303RGDNCBI36
Celera1952,189,719 - 52,189,972RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,472,322 - 51,472,575UniSTS
stSG605928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,146,901 - 55,148,083UniSTSGRCh37
GRCh371954,778,782 - 54,779,964UniSTSGRCh37
Build 361959,470,594 - 59,471,776RGDNCBI36
Celera1952,187,382 - 52,188,564UniSTS
Celera1951,819,439 - 51,820,621RGD
HuRef1951,469,986 - 51,471,168UniSTS
HuRef1951,106,421 - 51,107,603UniSTS
stSG605932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,783,513 - 54,784,712UniSTSGRCh37
Build 361959,475,325 - 59,476,524RGDNCBI36
HuRef1951,465,271 - 51,466,460UniSTS
HuRef1951,111,151 - 51,112,350UniSTS
stSG605937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,135,984 - 55,136,283UniSTSGRCh37
GRCh371954,789,912 - 54,790,210UniSTSGRCh37
Build 361959,481,724 - 59,482,022RGDNCBI36
Celera1952,176,465 - 52,176,764UniSTS
Celera1951,831,188 - 51,831,487RGD
HuRef1951,459,068 - 51,459,367UniSTS
HuRef1951,117,550 - 51,117,848UniSTS
stSG605949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,712 - 55,143,027UniSTSGRCh37
GRCh371954,803,677 - 54,804,989UniSTSGRCh37
Build 361959,495,489 - 59,496,801RGDNCBI36
Celera1952,182,193 - 52,183,508UniSTS
Celera1951,827,263 - 51,828,575RGD
HuRef1951,464,797 - 51,466,112UniSTS
stSG606204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,140,829 - 55,141,831UniSTSGRCh37
Build 361959,832,641 - 59,833,643RGDNCBI36
Celera1952,181,310 - 52,182,312RGD
HuRef1951,463,914 - 51,464,916UniSTS
stSG606205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,141,812 - 55,142,029UniSTSGRCh37
Build 361959,833,624 - 59,833,841RGDNCBI36
Celera1952,182,293 - 52,182,510RGD
HuRef1951,464,897 - 51,465,114UniSTS
stSG606206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,142,073 - 55,143,179UniSTSGRCh37
GRCh371955,105,235 - 55,106,358UniSTSGRCh37
Build 361959,797,047 - 59,798,170RGDNCBI36
Celera1952,182,554 - 52,183,660UniSTS
Celera1952,145,705 - 52,146,828RGD
HuRef1951,465,158 - 51,466,264UniSTS
HuRef1951,428,335 - 51,429,458UniSTS
stSG606208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,144,525 - 55,145,797UniSTSGRCh37
GRCh371954,781,078 - 54,782,358UniSTSGRCh37
Build 361959,472,890 - 59,474,170RGDNCBI36
Celera1952,185,006 - 52,186,278RGD
HuRef1951,467,610 - 51,468,882UniSTS
HuRef1951,108,717 - 51,109,997UniSTS
stSG606209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,145,777 - 55,146,998UniSTSGRCh37
GRCh371954,779,867 - 54,781,098UniSTSGRCh37
Build 361959,471,679 - 59,472,910RGDNCBI36
Celera1952,186,258 - 52,187,479RGD
HuRef1951,468,862 - 51,470,083UniSTS
HuRef1951,107,506 - 51,108,737UniSTS
stSG606211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,148,088 - 55,148,472UniSTSGRCh37
Build 361959,839,900 - 59,840,284RGDNCBI36
Celera1952,188,569 - 52,188,953RGD
HuRef1951,471,173 - 51,471,556UniSTS
RH70709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371955,148,318 - 55,148,460UniSTSGRCh37
Build 361959,840,130 - 59,840,272RGDNCBI36
Celera1952,188,799 - 52,188,941RGD
Cytogenetic Map19q13.4UniSTS
HuRef1951,471,402 - 51,471,544UniSTS
GeneMap99-GB4 RH Map19280.16UniSTS
ECD00082  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.4UniSTS
REN93649  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.4UniSTS
stSG605948  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.4UniSTS


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
Medium 107 703 49 13 1556 12 34 11 70 28 64 434 1 44 13
Low 2007 1613 1550 555 301 403 2009 987 2746 289 1123 901 150 1149 1270 2 2
Below cutoff 207 666 97 37 43 27 2044 1147 834 63 175 74 14 1 11 1496 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001081637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001081638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001081639 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388357 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388358 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_103518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526335 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329623 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054329632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331457 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054331462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001753590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001753591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002958244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_935716 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB204835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204841 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204849 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB204850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC009892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC245036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF009005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF009006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF009007 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF009220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF009221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF189277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF283984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF283985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015731 (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
  CS540228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU024913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU104682 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU234142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CU467612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA263280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA953794 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA991480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU915608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM135402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MT897911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MT897912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MT897913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U82279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000324602   ⟹   ENSP00000315997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,630,484 - 54,638,022 (+)Ensembl
RefSeq Acc Id: ENST00000396315   ⟹   ENSP00000379608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,631,074 - 54,637,076 (+)Ensembl
RefSeq Acc Id: ENST00000396317   ⟹   ENSP00000379610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,631,074 - 54,637,076 (+)Ensembl
RefSeq Acc Id: ENST00000396327   ⟹   ENSP00000379618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,630,410 - 54,637,528 (+)Ensembl
RefSeq Acc Id: ENST00000396331   ⟹   ENSP00000379622
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,617,158 - 54,637,528 (+)Ensembl
RefSeq Acc Id: ENST00000396332   ⟹   ENSP00000379623
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,630,512 - 54,637,528 (+)Ensembl
RefSeq Acc Id: ENST00000421584   ⟹   ENSP00000410165
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,631,074 - 54,637,076 (+)Ensembl
RefSeq Acc Id: ENST00000427581   ⟹   ENSP00000395004
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,630,633 - 54,637,190 (+)Ensembl
RefSeq Acc Id: ENST00000462628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,633,143 - 54,637,528 (+)Ensembl
RefSeq Acc Id: ENST00000473412
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,633,126 - 54,634,183 (+)Ensembl
RefSeq Acc Id: ENST00000480257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,631,262 - 54,632,055 (+)Ensembl
RefSeq Acc Id: ENST00000480375
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,634,893 - 54,636,105 (+)Ensembl
RefSeq Acc Id: ENST00000487425
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1954,634,371 - 54,635,616 (+)Ensembl
RefSeq Acc Id: NM_001081637   ⟹   NP_001075106
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,484 - 54,638,022 (+)NCBI
GRCh371955,128,384 - 55,149,007 (+)NCBI
Build 361959,833,780 - 59,840,819 (+)NCBI Archive
HuRef1951,451,468 - 51,472,091 (+)NCBI
CHM1_11955,135,536 - 55,142,575 (+)NCBI
T2T-CHM13v2.01957,723,992 - 57,731,530 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001081638   ⟹   NP_001075107
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,484 - 54,637,556 (+)NCBI
GRCh371955,128,384 - 55,149,007 (+)NCBI
Build 361959,833,720 - 59,840,819 (+)NCBI Archive
HuRef1951,451,468 - 51,472,091 (+)NCBI
CHM1_11955,135,430 - 55,142,575 (+)NCBI
T2T-CHM13v2.01957,723,992 - 57,731,064 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001081639   ⟹   NP_001075108
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,484 - 54,637,556 (+)NCBI
GRCh371955,128,384 - 55,149,007 (+)NCBI
Build 361959,833,720 - 59,840,819 (+)NCBI Archive
HuRef1951,451,468 - 51,472,091 (+)NCBI
CHM1_11955,135,430 - 55,142,575 (+)NCBI
T2T-CHM13v2.01957,723,992 - 57,731,064 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278398   ⟹   NP_001265327
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,517 - 54,637,556 (+)NCBI
GRCh371955,128,384 - 55,149,007 (+)NCBI
HuRef1951,451,468 - 51,472,091 (+)NCBI
CHM1_11955,135,536 - 55,142,575 (+)NCBI
T2T-CHM13v2.01957,724,025 - 57,731,064 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278399   ⟹   NP_001265328
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,517 - 54,634,183 (+)NCBI
GRCh371955,128,384 - 55,149,007 (+)NCBI
HuRef1951,451,468 - 51,472,091 (+)NCBI
CHM1_11955,135,536 - 55,139,202 (+)NCBI
T2T-CHM13v2.01957,724,025 - 57,727,691 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001388355   ⟹   NP_001375284
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001388356   ⟹   NP_001375285
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,968 - 54,638,022 (+)NCBI
T2T-CHM13v2.01957,710,473 - 57,731,530 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001388357   ⟹   NP_001375286
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,968 - 54,638,022 (+)NCBI
T2T-CHM13v2.01957,710,473 - 57,731,530 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001388358   ⟹   NP_001375287
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,968 - 54,638,022 (+)NCBI
T2T-CHM13v2.01957,710,473 - 57,731,530 (+)NCBI
Sequence:
RefSeq Acc Id: NM_006669   ⟹   NP_006660
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,617,129 - 54,637,556 (+)NCBI
Build 361959,820,441 - 59,840,819 (+)NCBI Archive
HuRef1951,451,468 - 51,472,091 (+)NCBI
CHM1_11955,121,949 - 55,142,575 (+)NCBI
T2T-CHM13v2.01957,710,634 - 57,731,064 (+)NCBI
Sequence:
RefSeq Acc Id: NR_103518
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,517 - 54,637,556 (+)NCBI
GRCh371955,128,384 - 55,149,007 (+)NCBI
HuRef1951,451,468 - 51,472,091 (+)NCBI
CHM1_11955,135,536 - 55,142,575 (+)NCBI
T2T-CHM13v2.01957,724,025 - 57,731,064 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017026192   ⟹   XP_016881681
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,636,636 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047438080   ⟹   XP_047294036
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438081   ⟹   XP_047294037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438082   ⟹   XP_047294038
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438083   ⟹   XP_047294039
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438084   ⟹   XP_047294040
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438085   ⟹   XP_047294041
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438086   ⟹   XP_047294042
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438087   ⟹   XP_047294043
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,638,022 (+)NCBI
RefSeq Acc Id: XM_047438088   ⟹   XP_047294044
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,636,636 (+)NCBI
RefSeq Acc Id: XM_047438089   ⟹   XP_047294045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,322 - 54,633,238 (+)NCBI
RefSeq Acc Id: XM_054319577   ⟹   XP_054175552
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319578   ⟹   XP_054175553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319579   ⟹   XP_054175554
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319580   ⟹   XP_054175555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319581   ⟹   XP_054175556
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319582   ⟹   XP_054175557
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319583   ⟹   XP_054175558
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319584   ⟹   XP_054175559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319585   ⟹   XP_054175560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319586   ⟹   XP_054175561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319587   ⟹   XP_054175562
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319588   ⟹   XP_054175563
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319589   ⟹   XP_054175564
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319590   ⟹   XP_054175565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,731,530 (+)NCBI
RefSeq Acc Id: XM_054319591   ⟹   XP_054175566
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,730,144 (+)NCBI
RefSeq Acc Id: XM_054319592   ⟹   XP_054175567
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,730,144 (+)NCBI
RefSeq Acc Id: XM_054319593   ⟹   XP_054175568
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01957,709,827 - 57,726,746 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001075106 (Get FASTA)   NCBI Sequence Viewer  
  NP_001075107 (Get FASTA)   NCBI Sequence Viewer  
  NP_001075108 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265327 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265328 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375284 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375285 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375286 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375287 (Get FASTA)   NCBI Sequence Viewer  
  NP_006660 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881681 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294036 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294037 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294038 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294039 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294040 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294041 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294042 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294043 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294044 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294045 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175552 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175553 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175554 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175555 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175556 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175557 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175558 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175559 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175560 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175561 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175562 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175563 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175564 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175565 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175566 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175567 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175568 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185597 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185598 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185599 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185600 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185601 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185602 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185603 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185604 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185605 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185606 (Get FASTA)   NCBI Sequence Viewer  
  XP_054185607 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187423 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187424 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187425 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187426 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187427 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187428 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187429 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187430 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187431 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187432 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187433 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187434 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187435 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187436 (Get FASTA)   NCBI Sequence Viewer  
  XP_054187437 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189557 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189558 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189559 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189560 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189561 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189562 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189563 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189564 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189565 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189566 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189567 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189568 (Get FASTA)   NCBI Sequence Viewer  
  XP_054189569 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB63521 (Get FASTA)   NCBI Sequence Viewer  
  AAB63522 (Get FASTA)   NCBI Sequence Viewer  
  AAC51179 (Get FASTA)   NCBI Sequence Viewer  
  AAC51879 (Get FASTA)   NCBI Sequence Viewer  
  AAC51880 (Get FASTA)   NCBI Sequence Viewer  
  AAC51881 (Get FASTA)   NCBI Sequence Viewer  
  AAG08984 (Get FASTA)   NCBI Sequence Viewer  
  AAH15731 (Get FASTA)   NCBI Sequence Viewer  
  AAL36988 (Get FASTA)   NCBI Sequence Viewer  
  AAL36989 (Get FASTA)   NCBI Sequence Viewer  
  ACK56074 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55944 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55945 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55946 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55947 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55948 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55949 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55950 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55951 (Get FASTA)   NCBI Sequence Viewer  
  ADJ55952 (Get FASTA)   NCBI Sequence Viewer  
  BAD97030 (Get FASTA)   NCBI Sequence Viewer  
  BAF84717 (Get FASTA)   NCBI Sequence Viewer  
  BAF84845 (Get FASTA)   NCBI Sequence Viewer  
  CAM90892 (Get FASTA)   NCBI Sequence Viewer  
  EAW72266 (Get FASTA)   NCBI Sequence Viewer  
  EAW72267 (Get FASTA)   NCBI Sequence Viewer  
  EAW72268 (Get FASTA)   NCBI Sequence Viewer  
  EAW72269 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000315997
  ENSP00000315997.7
  ENSP00000379608.1
  ENSP00000379610
  ENSP00000379610.1
  ENSP00000379618
  ENSP00000379618.3
  ENSP00000379622
  ENSP00000379622.1
  ENSP00000379623
  ENSP00000379623.4
  ENSP00000395004.2
  ENSP00000410165
  ENSP00000410165.1
  ENSP00000477838.1
  ENSP00000478282.1
  ENSP00000478831.1
  ENSP00000479156.1
  ENSP00000479753.1
  ENSP00000479887.1
  ENSP00000480259.1
  ENSP00000480365.1
  ENSP00000481605.1
  ENSP00000481700.1
  ENSP00000481701.1
  ENSP00000481891.1
  ENSP00000481949.1
  ENSP00000481972.1
  ENSP00000482054.1
  ENSP00000482125.1
  ENSP00000482978.1
  ENSP00000483139.1
  ENSP00000484046.1
  ENSP00000484746.1
  ENSP00000484936.1
  ENSP00000484938.1
GenBank Protein Q8NHL6 (Get FASTA)   NCBI Sequence Viewer  
  QTU69487 (Get FASTA)   NCBI Sequence Viewer  
  QTU69488 (Get FASTA)   NCBI Sequence Viewer  
  QTU69489 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_006660   ⟸   NM_006669
- Peptide Label: isoform 1 precursor
- UniProtKB: Q8NHK0 (UniProtKB/Swiss-Prot),   Q8NHJ9 (UniProtKB/Swiss-Prot),   O75025 (UniProtKB/Swiss-Prot),   O75024 (UniProtKB/Swiss-Prot),   A8MXT0 (UniProtKB/Swiss-Prot),   A2IXV4 (UniProtKB/Swiss-Prot),   Q8NHL6 (UniProtKB/Swiss-Prot),   A0A0B4J1W1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001075107   ⟸   NM_001081638
- Peptide Label: isoform 3 precursor
- UniProtKB: A0A087WSX8 (UniProtKB/TrEMBL),   A0A0G2JQ44 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001075108   ⟸   NM_001081639
- Peptide Label: isoform 4 precursor
- UniProtKB: D9IDM5 (UniProtKB/TrEMBL),   D9IDM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001075106   ⟸   NM_001081637
- Peptide Label: isoform 2 precursor
- UniProtKB: A0A087WSV6 (UniProtKB/TrEMBL),   A0A0G2JNQ6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265327   ⟸   NM_001278398
- Peptide Label: isoform 5 precursor
- UniProtKB: A8MVE2 (UniProtKB/TrEMBL),   A0A0G2JQ46 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265328   ⟸   NM_001278399
- Peptide Label: isoform 6 precursor
- UniProtKB: F6RVM3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881681   ⟸   XM_017026192
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: ENSP00000395004   ⟸   ENST00000427581
RefSeq Acc Id: ENSP00000315997   ⟸   ENST00000324602
RefSeq Acc Id: ENSP00000410165   ⟸   ENST00000421584
RefSeq Acc Id: ENSP00000379610   ⟸   ENST00000396317
RefSeq Acc Id: ENSP00000379608   ⟸   ENST00000396315
RefSeq Acc Id: ENSP00000379618   ⟸   ENST00000396327
RefSeq Acc Id: ENSP00000379623   ⟸   ENST00000396332
RefSeq Acc Id: ENSP00000379622   ⟸   ENST00000396331
RefSeq Acc Id: NP_001375284   ⟸   NM_001388355
- Peptide Label: isoform 3 precursor
- UniProtKB: A0A087WSX8 (UniProtKB/TrEMBL),   A0A0G2JQ44 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375287   ⟸   NM_001388358
- Peptide Label: isoform 2 precursor
- UniProtKB: A0A087WSV6 (UniProtKB/TrEMBL),   A0A0G2JNQ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375286   ⟸   NM_001388357
- Peptide Label: isoform 3 precursor
- UniProtKB: A0A087WSX8 (UniProtKB/TrEMBL),   A0A0G2JQ44 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375285   ⟸   NM_001388356
- Peptide Label: isoform 4 precursor
- UniProtKB: D9IDM5 (UniProtKB/TrEMBL),   D9IDM8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294036   ⟸   XM_047438080
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047294037   ⟸   XM_047438081
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047294038   ⟸   XM_047438082
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047294039   ⟸   XM_047438083
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047294040   ⟸   XM_047438084
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047294041   ⟸   XM_047438085
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047294042   ⟸   XM_047438086
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047294043   ⟸   XM_047438087
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047294044   ⟸   XM_047438088
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047294045   ⟸   XM_047438089
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054175552   ⟸   XM_054319577
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175553   ⟸   XM_054319578
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054175554   ⟸   XM_054319579
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054175555   ⟸   XM_054319580
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054175556   ⟸   XM_054319581
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054175557   ⟸   XM_054319582
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054175558   ⟸   XM_054319583
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054175559   ⟸   XM_054319584
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054175562   ⟸   XM_054319587
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054175563   ⟸   XM_054319588
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054175565   ⟸   XM_054319590
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054175561   ⟸   XM_054319586
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175560   ⟸   XM_054319585
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054175564   ⟸   XM_054319589
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054175566   ⟸   XM_054319591
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054175567   ⟸   XM_054319592
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054175568   ⟸   XM_054319593
- Peptide Label: isoform X11
Protein Domains
Ig-like   Ig-like C2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NHL6-F1-model_v2 AlphaFold Q8NHL6 1-650 view protein structure

Promoters
RGD ID:13205633
Promoter ID:EPDNEW_H26396
Type:initiation region
Name:LILRB1_3
Description:leukocyte immunoglobulin like receptor B1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26397  EPDNEW_H26398  EPDNEW_H26399  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,616,968 - 54,617,028EPDNEW
RGD ID:13205631
Promoter ID:EPDNEW_H26397
Type:initiation region
Name:LILRB1_2
Description:leukocyte immunoglobulin like receptor B1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26396  EPDNEW_H26398  EPDNEW_H26399  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,617,131 - 54,617,191EPDNEW
RGD ID:13205635
Promoter ID:EPDNEW_H26398
Type:initiation region
Name:LILRB1_1
Description:leukocyte immunoglobulin like receptor B1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26397  EPDNEW_H26396  EPDNEW_H26399  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,484 - 54,630,544EPDNEW
RGD ID:13205637
Promoter ID:EPDNEW_H26399
Type:initiation region
Name:LILRB1_4
Description:leukocyte immunoglobulin like receptor B1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26397  EPDNEW_H26396  EPDNEW_H26398  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381954,630,975 - 54,631,035EPDNEW
RGD ID:6795746
Promoter ID:HG_KWN:30985
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000396315,   ENST00000396321,   ENST00000396327,   ENST00000396332,   NM_001081639,   OTTHUMT00000140843,   UC010ERQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361959,833,796 - 59,834,296 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6605 AgrOrtholog
COSMIC LILRB1 COSMIC
Ensembl Genes ENSG00000104972 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
  ENSG00000274669 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000276452 UniProtKB/TrEMBL
  ENSG00000277134 UniProtKB/TrEMBL
  ENSG00000277807 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000324602 ENTREZGENE
  ENST00000324602.12 UniProtKB/TrEMBL
  ENST00000396315.5 UniProtKB/TrEMBL
  ENST00000396317 ENTREZGENE
  ENST00000396317.5 UniProtKB/TrEMBL
  ENST00000396327 ENTREZGENE
  ENST00000396327.7 UniProtKB/TrEMBL
  ENST00000396331 ENTREZGENE
  ENST00000396331.5 UniProtKB/TrEMBL
  ENST00000396332 ENTREZGENE
  ENST00000396332.8 UniProtKB/TrEMBL
  ENST00000421584 ENTREZGENE
  ENST00000421584.5 UniProtKB/TrEMBL
  ENST00000427581.6 UniProtKB/TrEMBL
  ENST00000610532.4 UniProtKB/TrEMBL
  ENST00000610641.4 UniProtKB/TrEMBL
  ENST00000610752.4 UniProtKB/TrEMBL
  ENST00000610815.4 UniProtKB/TrEMBL
  ENST00000611295.4 UniProtKB/TrEMBL
  ENST00000612335.3 UniProtKB/TrEMBL
  ENST00000612636.4 UniProtKB/Swiss-Prot
  ENST00000613145.4 UniProtKB/TrEMBL
  ENST00000613400.4 UniProtKB/TrEMBL
  ENST00000615004.3 UniProtKB/TrEMBL
  ENST00000615841.4 UniProtKB/TrEMBL
  ENST00000616408.4 UniProtKB/Swiss-Prot
  ENST00000616565.4 UniProtKB/TrEMBL
  ENST00000616890.4 UniProtKB/TrEMBL
  ENST00000617686.4 UniProtKB/Swiss-Prot
  ENST00000618055.4 UniProtKB/Swiss-Prot
  ENST00000618681.4 UniProtKB/Swiss-Prot
  ENST00000619093.4 UniProtKB/TrEMBL
  ENST00000619118.1 UniProtKB/TrEMBL
  ENST00000619395.4 UniProtKB/TrEMBL
  ENST00000620471.4 UniProtKB/TrEMBL
  ENST00000620642.4 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000104972 GTEx
  ENSG00000274669 GTEx
  ENSG00000276452 GTEx
  ENSG00000277134 GTEx
  ENSG00000277807 GTEx
HGNC ID HGNC:6605 ENTREZGENE
Human Proteome Map LILRB1 Human Proteome Map
InterPro A1B_glyco/leuk_Ig-like_rcpt UniProtKB/TrEMBL
  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/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10859 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 10859 ENTREZGENE
OMIM 604811 OMIM
PANTHER LEUKOCYTE IMMUNOGLOBULIN-LIKE RECEPTOR SUBFAMILY A MEMBER 1-RELATED 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 PA30379 PharmGKB
PIRSF Alpha_1B_glycoprot_prd UniProtKB/TrEMBL
PROSITE IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROKAR_LIPOPROTEIN UniProtKB/TrEMBL
SMART IGc2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00409 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WSV6 ENTREZGENE, UniProtKB/TrEMBL
  A0A087WSX8 ENTREZGENE, UniProtKB/TrEMBL
  A0A0B4J1W1 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JLS4_HUMAN UniProtKB/TrEMBL
  A0A0G2JMG0_HUMAN UniProtKB/TrEMBL
  A0A0G2JNK9_HUMAN UniProtKB/TrEMBL
  A0A0G2JNM2 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JNQ6 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JNR3_HUMAN UniProtKB/TrEMBL
  A0A0G2JP64 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JP80_HUMAN UniProtKB/TrEMBL
  A0A0G2JQ15 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JQ44 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2JQ46 ENTREZGENE, UniProtKB/TrEMBL
  A2IXV4 ENTREZGENE
  A8MVE2 ENTREZGENE, UniProtKB/TrEMBL
  A8MXT0 ENTREZGENE
  D9IDM4_HUMAN UniProtKB/TrEMBL
  D9IDM5 ENTREZGENE, UniProtKB/TrEMBL
  D9IDM6_HUMAN UniProtKB/TrEMBL
  D9IDM7_HUMAN UniProtKB/TrEMBL
  D9IDM8 ENTREZGENE, UniProtKB/TrEMBL
  D9IDM9_HUMAN UniProtKB/TrEMBL
  D9IDN1_HUMAN UniProtKB/TrEMBL
  F6RVM3 ENTREZGENE, UniProtKB/TrEMBL
  F6TER3_HUMAN UniProtKB/TrEMBL
  LIRB1_HUMAN UniProtKB/Swiss-Prot
  O75024 ENTREZGENE
  O75025 ENTREZGENE
  Q8NHJ9 ENTREZGENE
  Q8NHK0 ENTREZGENE
  Q8NHL6 ENTREZGENE
UniProt Secondary A2IXV4 UniProtKB/Swiss-Prot
  A8MXT0 UniProtKB/Swiss-Prot
  O75024 UniProtKB/Swiss-Prot
  O75025 UniProtKB/Swiss-Prot
  Q8NHJ9 UniProtKB/Swiss-Prot
  Q8NHK0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-19 LILRB1  leukocyte immunoglobulin like receptor B1  LILRB1  leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 1  Symbol and/or name change 5135510 APPROVED