LUC7L (LUC7 like) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: LUC7L (LUC7 like) Homo sapiens
Analyze
Symbol: LUC7L
Name: LUC7 like
RGD ID: 1316796
HGNC Page HGNC:6723
Description: Enables identical protein binding activity. Predicted to be involved in mRNA splice site recognition. Predicted to act upstream of or within negative regulation of striated muscle tissue development. Predicted to be located in nucleus. Predicted to be part of U1 snRNP and U2-type prespliceosome.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ10231; hLuc7B1; Luc7; LUC7-LIKE; LUC7B1; putative RNA-binding protein Luc7-like 1; putative SR protein LUC7B1; sarcoplasmic reticulum protein LUC7B1; SR+89
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3816188,990 - 229,449 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl16188,969 - 229,463 (-)EnsemblGRCh38hg38GRCh38
GRCh3716238,989 - 279,448 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3616178,971 - 219,450 (-)NCBINCBI36Build 36hg18NCBI36
Build 3416178,974 - 219,450NCBI
Celera16437,860 - 478,332 (-)NCBICelera
Cytogenetic Map16p13.3NCBI
HuRef16156,536 - 196,987 (-)NCBIHuRef
CHM1_116238,912 - 279,378 (-)NCBICHM1_1
T2T-CHM13v2.016182,837 - 223,275 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
nucleus  (IEA)
U1 snRNP  (IBA,IEA)
U2-type prespliceosome  (IBA,IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:11157797   PMID:11170747   PMID:12477932   PMID:14702039   PMID:15383276   PMID:15489334   PMID:15840729   PMID:16169070   PMID:16712791   PMID:17081983   PMID:17207965  
PMID:17353931   PMID:17568003   PMID:19615732   PMID:19913121   PMID:20139978   PMID:20467437   PMID:20508642   PMID:20628086   PMID:21081503   PMID:21555454   PMID:21653829   PMID:21873635  
PMID:21988832   PMID:22365833   PMID:22990118   PMID:23263863   PMID:23414517   PMID:23455924   PMID:23602568   PMID:23940030   PMID:24457600   PMID:24711643   PMID:24981860   PMID:25921289  
PMID:26167880   PMID:26170170   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26673895   PMID:26687479   PMID:26760575   PMID:26777405   PMID:27025967   PMID:27248496   PMID:27684187  
PMID:27926873   PMID:28514442   PMID:28515276   PMID:28561026   PMID:28611215   PMID:28977666   PMID:29128334   PMID:29298432   PMID:29346117   PMID:29509190   PMID:29511261   PMID:29802200  
PMID:29845934   PMID:30110629   PMID:30209976   PMID:30463901   PMID:30804502   PMID:30833792   PMID:30940648   PMID:31048545   PMID:31076518   PMID:31091453   PMID:31253590   PMID:31365120  
PMID:31586073   PMID:31665637   PMID:31980649   PMID:32296183   PMID:32687490   PMID:32707033   PMID:32807901   PMID:32814053   PMID:32877691   PMID:33301849   PMID:33658012   PMID:33742100  
PMID:33852859   PMID:33961781   PMID:34133714   PMID:34185411   PMID:34349018   PMID:35013218   PMID:35256949   PMID:35271311   PMID:35819319   PMID:35850772   PMID:35944360   PMID:36114006  
PMID:36215168   PMID:36244648   PMID:36273042   PMID:36537216   PMID:36574265   PMID:36912080   PMID:36931259   PMID:37689310   PMID:38113892  


Genomics

Comparative Map Data
LUC7L
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3816188,990 - 229,449 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl16188,969 - 229,463 (-)EnsemblGRCh38hg38GRCh38
GRCh3716238,989 - 279,448 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3616178,971 - 219,450 (-)NCBINCBI36Build 36hg18NCBI36
Build 3416178,974 - 219,450NCBI
Celera16437,860 - 478,332 (-)NCBICelera
Cytogenetic Map16p13.3NCBI
HuRef16156,536 - 196,987 (-)NCBIHuRef
CHM1_116238,912 - 279,378 (-)NCBICHM1_1
T2T-CHM13v2.016182,837 - 223,275 (-)NCBIT2T-CHM13v2.0
Luc7l
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391726,471,874 - 26,504,484 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1726,471,870 - 26,504,478 (+)EnsemblGRCm39 Ensembl
GRCm381726,252,899 - 26,285,510 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1726,252,896 - 26,285,504 (+)EnsemblGRCm38mm10GRCm38
MGSCv371726,389,855 - 26,422,449 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361725,980,551 - 26,009,568 (+)NCBIMGSCv36mm8
Celera1726,787,083 - 26,820,005 (+)NCBICelera
Cytogenetic Map17A3.3NCBI
cM Map1713.09NCBI
Luc7l
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81015,777,837 - 15,811,586 (+)NCBIGRCr8
mRatBN7.21015,273,340 - 15,307,131 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1015,273,348 - 15,303,112 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1020,017,433 - 20,048,112 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01019,506,315 - 19,536,997 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01015,001,288 - 15,031,087 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01015,538,878 - 15,572,651 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1015,538,872 - 15,568,638 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01015,434,018 - 15,467,745 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41015,522,334 - 15,549,100 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11015,523,381 - 15,550,147 (+)NCBI
Celera1014,942,376 - 14,969,587 (+)NCBICelera
Cytogenetic Map10q12NCBI
Luc7l
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544216,965,788 - 16,997,329 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495544216,965,788 - 16,997,329 (+)NCBIChiLan1.0ChiLan1.0
LUC7L
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v218403,094 - 443,370 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1164,196,025 - 4,236,318 (-)NCBINHGRI_mPanPan1
PanPan1.116177,857 - 217,524 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl16177,857 - 217,519 (-)Ensemblpanpan1.1panPan2
LUC7L
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1640,274,290 - 40,310,084 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl640,273,801 - 40,309,921 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha641,537,095 - 41,572,894 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0640,616,502 - 40,652,360 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl640,616,511 - 40,652,360 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1640,304,768 - 40,340,566 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0640,265,757 - 40,301,559 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0640,744,252 - 40,780,083 (+)NCBIUU_Cfam_GSD_1.0
Luc7l
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344112,589,490 - 112,624,860 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936501687,036 - 722,919 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936501687,352 - 722,720 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LUC7L
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl341,449,002 - 41,470,977 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1341,442,127 - 41,473,115 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2340,960,784 - 40,991,229 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LUC7L
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.15132,018 - 176,060 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl5128,232 - 176,020 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366606831,010,060 - 31,053,221 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Luc7l
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249131,045,658 - 1,075,538 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249131,047,942 - 1,075,588 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in LUC7L
24 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3 copy number gain See cases [RCV000052367] Chr16:23141..11296695 [GRCh38]
Chr16:73141..11390552 [GRCh37]
Chr16:13141..11298053 [NCBI36]
Chr16:16p13.3-13.13		 pathogenic
GRCh38/hg38 16p13.3(chr16:29941-2560460)x3 copy number gain See cases [RCV000052368] Chr16:29941..2560460 [GRCh38]
Chr16:79941..2610461 [GRCh37]
Chr16:19941..2550462 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:46566-1800860)x3 copy number gain See cases [RCV000052369] Chr16:46566..1800860 [GRCh38]
Chr16:96566..1850861 [GRCh37]
Chr16:36566..1790862 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:46766-3214623)x3 copy number gain See cases [RCV000052370] Chr16:46766..3214623 [GRCh38]
Chr16:96766..3264623 [GRCh37]
Chr16:36766..3204624 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:23141-1773349)x1 copy number loss See cases [RCV000053251] Chr16:23141..1773349 [GRCh38]
Chr16:73141..1823350 [GRCh37]
Chr16:13141..1763351 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:23141-1712523)x1 copy number loss See cases [RCV000053252] Chr16:23141..1712523 [GRCh38]
Chr16:73141..1762524 [GRCh37]
Chr16:13141..1702525 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:46766-1997582)x1 copy number loss See cases [RCV000053253] Chr16:46766..1997582 [GRCh38]
Chr16:96766..2047583 [GRCh37]
Chr16:36766..1987584 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:105429-1499893)x1 copy number loss See cases [RCV000053267] Chr16:105429..1499893 [GRCh38]
Chr16:155427..1549894 [GRCh37]
Chr16:95427..1489895 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3 copy number gain See cases [RCV000133780] Chr16:46766..11525516 [GRCh38]
Chr16:96766..11619372 [GRCh37]
Chr16:36766..11526873 [NCBI36]
Chr16:16p13.3-13.13		 pathogenic
GRCh38/hg38 16p13.3(chr16:46766-1544014)x1 copy number loss See cases [RCV000134917] Chr16:46766..1544014 [GRCh38]
Chr16:96766..1594015 [GRCh37]
Chr16:36766..1534016 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:46766-4247185)x3 copy number gain See cases [RCV000136687] Chr16:46766..4247185 [GRCh38]
Chr16:96766..4297186 [GRCh37]
Chr16:36766..4237187 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:46722-1867327)x1 copy number loss See cases [RCV000137826] Chr16:46722..1867327 [GRCh38]
Chr16:96722..1917328 [GRCh37]
Chr16:36722..1857329 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:46766-882211)x1 copy number loss See cases [RCV000137979] Chr16:46766..882211 [GRCh38]
Chr16:96766..932211 [GRCh37]
Chr16:36766..872212 [NCBI36]
Chr16:16p13.3		 pathogenic|uncertain significance
GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3 copy number gain See cases [RCV000139166] Chr16:43732..13326806 [GRCh38]
Chr16:93732..13420663 [GRCh37]
Chr16:33732..13328164 [NCBI36]
Chr16:16p13.3-13.12		 pathogenic
GRCh38/hg38 16p13.3(chr16:43722-308914)x3 copy number gain See cases [RCV000141393] Chr16:43722..308914 [GRCh38]
Chr16:93722..358914 [GRCh37]
Chr16:33722..298915 [NCBI36]
Chr16:16p13.3		 uncertain significance
GRCh38/hg38 16p13.3(chr16:59980-1221651)x1 copy number loss See cases [RCV000141384] Chr16:59980..1221651 [GRCh38]
Chr16:109978..1271651 [GRCh37]
Chr16:49978..1211652 [NCBI36]
Chr16:16p13.3		 pathogenic
GRCh38/hg38 16p13.3(chr16:35880-605262)x1 copy number loss See cases [RCV000143709] Chr16:35880..605262 [GRCh38]
Chr16:85880..655262 [GRCh37]
Chr16:25880..595263 [NCBI36]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:102839-28327676)x3 copy number gain See cases [RCV000203445] Chr16:102839..28327676 [GRCh37]
Chr16:16p13.3-11.2		 pathogenic
GRCh37/hg19 16p13.3(chr16:97494-323799)x3 copy number gain Breast ductal adenocarcinoma [RCV000207213] Chr16:97494..323799 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:97494-1257060)x3 copy number gain Breast ductal adenocarcinoma [RCV000207237] Chr16:97494..1257060 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:216724-340009)x3 copy number gain See cases [RCV000240006] Chr16:216724..340009 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:88165-1715454)x1 copy number loss See cases [RCV000239415] Chr16:88165..1715454 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:72769-1511716)x1 copy number loss See cases [RCV000240294] Chr16:72769..1511716 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:239130-841725)x3 copy number gain See cases [RCV000240506] Chr16:239130..841725 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:113746-240243)x3 copy number gain See cases [RCV000449423] Chr16:113746..240243 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-754083)x1 copy number loss See cases [RCV000446474] Chr16:85880..754083 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-13.2(chr16:78801-9169448) copy number gain See cases [RCV000446555] Chr16:78801..9169448 [GRCh37]
Chr16:16p13.3-13.2		 pathogenic
GRCh37/hg19 16p13.3(chr16:97133-5122974)x3 copy number gain See cases [RCV000445663] Chr16:97133..5122974 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:106859-735154)x3 copy number gain See cases [RCV000511218] Chr16:106859..735154 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-643107)x1 copy number loss See cases [RCV000510746] Chr16:85880..643107 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-12.2(chr16:85880-22442007)x3 copy number gain See cases [RCV000511360] Chr16:85880..22442007 [GRCh37]
Chr16:16p13.3-12.2		 pathogenic
GRCh37/hg19 16p13.3-13.2(chr16:85880-9883129)x3 copy number gain See cases [RCV000510698] Chr16:85880..9883129 [GRCh37]
Chr16:16p13.3-13.2		 pathogenic
GRCh37/hg19 16p13.3-12.3(chr16:85880-19806921)x3 copy number gain See cases [RCV000512194] Chr16:85880..19806921 [GRCh37]
Chr16:16p13.3-12.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85880-546267)x3 copy number gain See cases [RCV000512217] Chr16:85880..546267 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-1875694)x1 copy number loss not provided [RCV000683741] Chr16:85880..1875694 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85880-294656)x1 copy number loss not provided [RCV000683739] Chr16:85880..294656 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:236050-252479)x0 copy number loss not provided [RCV000738944] Chr16:236050..252479 [GRCh37]
Chr16:16p13.3		 benign
GRCh37/hg19 16p13.3(chr16:61451-1593645)x1 copy number loss not provided [RCV000751445] Chr16:61451..1593645 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:109978-4316797) copy number gain Chromosome 16p13.3 duplication syndrome [RCV000767731] Chr16:109978..4316797 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:232111-378473)x3 copy number gain not provided [RCV000847636] Chr16:232111..378473 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-2053328)x1 copy number loss not provided [RCV000849039] Chr16:85880..2053328 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:259506-401213)x3 copy number gain not provided [RCV000848602] Chr16:259506..401213 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-830613)x1 copy number loss not provided [RCV000846660] Chr16:85880..830613 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85880-1468459)x1 copy number loss not provided [RCV000848130] Chr16:85880..1468459 [GRCh37]
Chr16:16p13.3		 pathogenic
NM_201412.3(LUC7L):c.1111A>G (p.Ile371Val) single nucleotide variant not specified [RCV004305223] Chr16:189203 [GRCh38]
Chr16:239202 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-1166355)x1 copy number loss not provided [RCV001006741] Chr16:85880..1166355 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:106988-735154)x3 copy number gain not provided [RCV001006742] Chr16:106988..735154 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:84485-5251013)x3 copy number gain not provided [RCV001537890] Chr16:84485..5251013 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:205271-589830)x3 copy number gain not provided [RCV001006743] Chr16:205271..589830 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:256384-542814)x3 copy number gain not provided [RCV001259752] Chr16:256384..542814 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-5249457)x3 copy number gain not provided [RCV001259749] Chr16:85880..5249457 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85880-754083) copy number loss not specified [RCV002052499] Chr16:85880..754083 [GRCh37]
Chr16:16p13.3		 pathogenic
NC_000016.9:g.(?_256302)_(5971108_?)dup duplication Familial Mediterranean fever [RCV001877532]|Fanconi anemia [RCV001877533]|not provided [RCV001877531] Chr16:256302..5971108 [GRCh37]
Chr16:16p13.3		 uncertain significance
NC_000016.9:g.(?_256302)_(4852572_?)dup duplication Epilepsy [RCV003113403]|Idiopathic generalized epilepsy [RCV003109446]|Saldino-Mainzer syndrome [RCV003113404] Chr16:256302..4852572 [GRCh37]
Chr16:16p13.3		 uncertain significance
NC_000016.9:g.(?_256302)_(633035_?)del deletion Epilepsy [RCV003113402] Chr16:256302..633035 [GRCh37]
Chr16:16p13.3		 pathogenic
NC_000016.9:g.(?_256302)_(1657267_?)del deletion Saldino-Mainzer syndrome [RCV003116765]|not provided [RCV003116766] Chr16:256302..1657267 [GRCh37]
Chr16:16p13.3		 pathogenic|no classifications from unflagged records
NC_000016.9:g.(?_256302)_(1918176_?)del deletion not provided [RCV003119703] Chr16:256302..1918176 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:111043-6627459)x3 copy number gain See cases [RCV002292215] Chr16:111043..6627459 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85881-1350186)x1 copy number loss not provided [RCV002474576] Chr16:85881..1350186 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:106989-293949)x1 copy number loss not provided [RCV002473487] Chr16:106989..293949 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:204932-313258)x3 copy number gain not provided [RCV002475882] Chr16:204932..313258 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.965C>T (p.Ala322Val) single nucleotide variant not specified [RCV004088666] Chr16:189977 [GRCh38]
Chr16:239976 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.919C>T (p.Arg307Trp) single nucleotide variant not specified [RCV004093121] Chr16:190023 [GRCh38]
Chr16:240022 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.229G>A (p.Glu77Lys) single nucleotide variant not specified [RCV004185492] Chr16:220675 [GRCh38]
Chr16:270674 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.1006T>G (p.Ser336Ala) single nucleotide variant not specified [RCV004085099] Chr16:189308 [GRCh38]
Chr16:239307 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.448G>A (p.Asp150Asn) single nucleotide variant not specified [RCV004219754] Chr16:206066 [GRCh38]
Chr16:256065 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.992C>T (p.Ala331Val) single nucleotide variant not specified [RCV004330927] Chr16:189322 [GRCh38]
Chr16:239321 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.179C>T (p.Thr60Ile) single nucleotide variant not specified [RCV004257951] Chr16:220725 [GRCh38]
Chr16:270724 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:85881-1657611)x1 copy number loss not provided [RCV003483253] Chr16:85881..1657611 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85881-470832)x1 copy number loss not provided [RCV003483254] Chr16:85881..470832 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.360T>A (p.Ser120=) single nucleotide variant LUC7L-related condition [RCV003959126] Chr16:208084 [GRCh38]
Chr16:258083 [GRCh37]
Chr16:16p13.3		 likely benign
NM_201412.3(LUC7L):c.938A>G (p.His313Arg) single nucleotide variant LUC7L-related condition [RCV003964421] Chr16:190004 [GRCh38]
Chr16:240003 [GRCh37]
Chr16:16p13.3		 benign
NM_201412.3(LUC7L):c.941G>A (p.Arg314His) single nucleotide variant LUC7L-related condition [RCV003919448] Chr16:190001 [GRCh38]
Chr16:240000 [GRCh37]
Chr16:16p13.3		 likely benign
NC_000016.10:g.174045_192395del deletion Alpha-thalassemia, zf type [RCV000016969] Chr16:174045..192395 [GRCh38]
Chr16:16p13.3		 pathogenic
NM_201412.3(LUC7L):c.1081C>T (p.Arg361Trp) single nucleotide variant not specified [RCV004410869] Chr16:189233 [GRCh38]
Chr16:239232 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.253G>T (p.Asp85Tyr) single nucleotide variant not specified [RCV004410870] Chr16:220651 [GRCh38]
Chr16:270650 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.426G>T (p.Gln142His) single nucleotide variant not specified [RCV004410871] Chr16:206088 [GRCh38]
Chr16:256087 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.470T>C (p.Met157Thr) single nucleotide variant not specified [RCV004410872] Chr16:206044 [GRCh38]
Chr16:256043 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.700G>A (p.Glu234Lys) single nucleotide variant not specified [RCV004410873] Chr16:193003 [GRCh38]
Chr16:243002 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.854G>A (p.Arg285Gln) single nucleotide variant not specified [RCV004410874] Chr16:190088 [GRCh38]
Chr16:240087 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.892A>G (p.Arg298Gly) single nucleotide variant not specified [RCV004410875] Chr16:190050 [GRCh38]
Chr16:240049 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.959G>A (p.Arg320Gln) single nucleotide variant not specified [RCV004410876] Chr16:189983 [GRCh38]
Chr16:239982 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.618G>A (p.Leu206=) single nucleotide variant LUC7L-related condition [RCV003933825] Chr16:199131 [GRCh38]
Chr16:249130 [GRCh37]
Chr16:16p13.3		 likely benign
GRCh37/hg19 16p13.3(chr16:85880-1498731)x1 copy number loss not provided [RCV000683740] Chr16:85880..1498731 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85880-3216551)x3 copy number gain not provided [RCV000683742] Chr16:85880..3216551 [GRCh37]
Chr16:16p13.3		 pathogenic
GRCh37/hg19 16p13.3-13.13(chr16:85880-11209288)x3 copy number gain not provided [RCV000683743] Chr16:85880..11209288 [GRCh37]
Chr16:16p13.3-13.13		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3(chr16:85880-1468828) copy number loss not specified [RCV002052500] Chr16:85880..1468828 [GRCh37]
Chr16:16p13.3		 pathogenic
NC_000016.9:g.(?_256302)_(1843653_?)del deletion Idiopathic generalized epilepsy [RCV003109815] Chr16:256302..1843653 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.773G>A (p.Arg258Lys) single nucleotide variant not specified [RCV004202492] Chr16:192930 [GRCh38]
Chr16:242929 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.281T>C (p.Ile94Thr) single nucleotide variant not specified [RCV004238355] Chr16:208163 [GRCh38]
Chr16:258162 [GRCh37]
Chr16:16p13.3		 uncertain significance
NM_201412.3(LUC7L):c.1043A>C (p.Asp348Ala) single nucleotide variant not specified [RCV004352914] Chr16:189271 [GRCh38]
Chr16:239270 [GRCh37]
Chr16:16p13.3		 uncertain significance
GRCh37/hg19 16p13.3(chr16:254059-306243)x1 copy number loss not provided [RCV003483255] Chr16:254059..306243 [GRCh37]
Chr16:16p13.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5147
Count of miRNA genes:1225
Interacting mature miRNAs:1554
Transcripts:ENST00000293872, ENST00000337351, ENST00000397780, ENST00000397783, ENST00000418978, ENST00000419516, ENST00000426094, ENST00000428363, ENST00000429378, ENST00000430864, ENST00000442701, ENST00000443357, ENST00000464711, ENST00000467552, ENST00000468732, ENST00000469109, ENST00000490762, ENST00000494366, ENST00000494545, ENST00000495349
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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
RH46576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,022 - 239,206UniSTSGRCh37
Build 3616179,023 - 179,207RGDNCBI36
Celera16437,912 - 438,096RGD
Cytogenetic Map16p13.3UniSTS
HuRef16156,588 - 156,772UniSTS
ECD00759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,677 - 240,568UniSTSGRCh37
Build 3616179,678 - 180,569RGDNCBI36
Celera16438,567 - 439,458RGD
Cytogenetic Map16p13.3UniSTS
HuRef16157,243 - 158,134UniSTS
ECD02455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716238,622 - 239,451UniSTSGRCh37
Build 3616178,623 - 179,452RGDNCBI36
Celera16437,512 - 438,341RGD
Cytogenetic Map16p13.3UniSTS
HuRef16156,188 - 157,017UniSTS
ECD02786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716258,065 - 258,882UniSTSGRCh37
Build 3616198,066 - 198,883RGDNCBI36
Celera16456,955 - 457,772RGD
Cytogenetic Map16p13.3UniSTS
HuRef16175,629 - 176,446UniSTS
ECD03567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,999 - 278,790UniSTSGRCh37
Build 3616218,000 - 218,791RGDNCBI36
Celera16476,882 - 477,673RGD
Cytogenetic Map16p13.3UniSTS
HuRef16195,537 - 196,328UniSTS
ECD03807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,096 - 277,879UniSTSGRCh37
Build 3616217,097 - 217,880RGDNCBI36
Celera16475,979 - 476,762RGD
Cytogenetic Map16p13.3UniSTS
HuRef16194,634 - 195,417UniSTS
ECD03922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716278,817 - 279,597UniSTSGRCh37
Build 3616218,818 - 219,598RGDNCBI36
Celera16477,700 - 478,480RGD
Cytogenetic Map16p13.3UniSTS
HuRef16196,355 - 197,135UniSTS
ECD06789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716255,917 - 256,616UniSTSGRCh37
Build 3616195,918 - 196,617RGDNCBI36
Celera16454,807 - 455,506RGD
Cytogenetic Map16p13.3UniSTS
HuRef16173,480 - 174,179UniSTS
ECD06973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716244,446 - 245,140UniSTSGRCh37
Build 3616184,447 - 185,141RGDNCBI36
Celera16443,336 - 444,030RGD
Cytogenetic Map16p13.3UniSTS
HuRef16162,013 - 162,707UniSTS
ECD08617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716240,899 - 241,549UniSTSGRCh37
Build 3616180,900 - 181,550RGDNCBI36
Celera16439,789 - 440,439RGD
Cytogenetic Map16p13.3UniSTS
HuRef16158,465 - 159,115UniSTS
ECD11249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716271,727 - 272,305UniSTSGRCh37
Build 3616211,728 - 212,306RGDNCBI36
Celera16470,610 - 471,188RGD
Cytogenetic Map16p13.3UniSTS
HuRef16189,276 - 189,854UniSTS
ECD12651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716270,462 - 271,000UniSTSGRCh37
Build 3616210,463 - 211,001RGDNCBI36
Celera16469,352 - 469,890RGD
Cytogenetic Map16p13.3UniSTS
HuRef16188,023 - 188,561UniSTS
ECD13143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716276,383 - 276,908UniSTSGRCh37
Build 3616216,384 - 216,909RGDNCBI36
Celera16475,266 - 475,791RGD
Cytogenetic Map16p13.3UniSTS
HuRef16193,921 - 194,446UniSTS
ECD14191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716261,505 - 262,004UniSTSGRCh37
Build 3616201,506 - 202,005RGDNCBI36
Celera16460,396 - 460,895RGD
Cytogenetic Map16p13.3UniSTS
HuRef16179,069 - 179,568UniSTS
ECD14273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716275,866 - 276,363UniSTSGRCh37
Build 3616215,867 - 216,364RGDNCBI36
Celera16474,749 - 475,246RGD
Cytogenetic Map16p13.3UniSTS
HuRef16193,405 - 193,901UniSTS
ECD16017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716259,510 - 259,966UniSTSGRCh37
Build 3616199,511 - 199,967RGDNCBI36
Celera16458,401 - 458,857RGD
Cytogenetic Map16p13.3UniSTS
HuRef16177,074 - 177,530UniSTS
ECD16771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716260,307 - 260,733UniSTSGRCh37
Build 3616200,308 - 200,734RGDNCBI36
Celera16459,198 - 459,624RGD
Cytogenetic Map16p13.3UniSTS
HuRef16177,871 - 178,297UniSTS
ECD17042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716249,011 - 249,426UniSTSGRCh37
Build 3616189,012 - 189,427RGDNCBI36
Celera16447,900 - 448,315RGD
Cytogenetic Map16p13.3UniSTS
HuRef16166,577 - 166,992UniSTS
ECD19005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716247,626 - 247,964UniSTSGRCh37
Build 3616187,627 - 187,965RGDNCBI36
Celera16446,516 - 446,854RGD
Cytogenetic Map16p13.3UniSTS
HuRef16165,193 - 165,531UniSTS
ECD19256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716274,842 - 275,170UniSTSGRCh37
Build 3616214,843 - 215,171RGDNCBI36
Celera16473,725 - 474,053RGD
Cytogenetic Map16p13.3UniSTS
HuRef16192,390 - 192,718UniSTS
ECD19625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716242,834 - 243,149UniSTSGRCh37
Build 3616182,835 - 183,150RGDNCBI36
Celera16441,724 - 442,039RGD
Cytogenetic Map16p13.3UniSTS
HuRef16160,400 - 160,715UniSTS
ECD19785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716248,333 - 248,642UniSTSGRCh37
Build 3616188,334 - 188,643RGDNCBI36
Celera16447,222 - 447,531RGD
Cytogenetic Map16p13.3UniSTS
HuRef16165,899 - 166,208UniSTS
ECD20248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716263,101 - 263,392UniSTSGRCh37
Build 3616203,102 - 203,393RGDNCBI36
Celera16461,992 - 462,283RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,665 - 180,956UniSTS
ECD20617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716273,389 - 273,667UniSTSGRCh37
Build 3616213,390 - 213,668RGDNCBI36
Celera16472,272 - 472,550RGD
Cytogenetic Map16p13.3UniSTS
HuRef16190,939 - 191,217UniSTS
ECD23676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716273,980 - 274,161UniSTSGRCh37
Build 3616213,981 - 214,162RGDNCBI36
Celera16472,863 - 473,044RGD
Cytogenetic Map16p13.3UniSTS
HuRef16191,528 - 191,709UniSTS
ECD24323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716262,565 - 262,707UniSTSGRCh37
Build 3616202,566 - 202,708RGDNCBI36
Celera16461,456 - 461,598RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,129 - 180,271UniSTS
ECD24375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716268,255 - 268,392UniSTSGRCh37
Build 3616208,256 - 208,393RGDNCBI36
Celera16467,146 - 467,283RGD
Cytogenetic Map16p13.3UniSTS
HuRef16185,818 - 185,955UniSTS
REN95014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716238,613 - 238,867UniSTSGRCh37
Build 3616178,614 - 178,868RGDNCBI36
Celera16437,503 - 437,757RGD
Cytogenetic Map16p13.3UniSTS
HuRef16156,179 - 156,433UniSTS
REN95015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716238,861 - 239,090UniSTSGRCh37
Build 3616178,862 - 179,091RGDNCBI36
Celera16437,751 - 437,980RGD
Cytogenetic Map16p13.3UniSTS
HuRef16156,427 - 156,656UniSTS
REN95016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,067 - 239,316UniSTSGRCh37
Build 3616179,068 - 179,317RGDNCBI36
Celera16437,957 - 438,206RGD
Cytogenetic Map16p13.3UniSTS
HuRef16156,633 - 156,882UniSTS
REN95017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,252 - 239,501UniSTSGRCh37
Build 3616179,253 - 179,502RGDNCBI36
Celera16438,142 - 438,391RGD
Cytogenetic Map16p13.3UniSTS
HuRef16156,818 - 157,067UniSTS
REN95018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,485 - 239,713UniSTSGRCh37
Build 3616179,486 - 179,714RGDNCBI36
Celera16438,375 - 438,603RGD
Cytogenetic Map16p13.3UniSTS
HuRef16157,051 - 157,279UniSTS
REN95019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,706 - 239,962UniSTSGRCh37
Build 3616179,707 - 179,963RGDNCBI36
Celera16438,596 - 438,852RGD
Cytogenetic Map16p13.3UniSTS
HuRef16157,272 - 157,528UniSTS
REN95020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,939 - 240,177UniSTSGRCh37
Build 3616179,940 - 180,178RGDNCBI36
Celera16438,829 - 439,067RGD
Cytogenetic Map16p13.3UniSTS
HuRef16157,505 - 157,743UniSTS
REN95021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716240,158 - 240,390UniSTSGRCh37
Build 3616180,159 - 180,391RGDNCBI36
Celera16439,048 - 439,280RGD
Cytogenetic Map16p13.3UniSTS
HuRef16157,724 - 157,956UniSTS
REN95022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716240,359 - 240,604UniSTSGRCh37
Build 3616180,360 - 180,605RGDNCBI36
Celera16439,249 - 439,494RGD
Cytogenetic Map16p13.3UniSTS
HuRef16157,925 - 158,170UniSTS
REN95023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716240,509 - 240,734UniSTSGRCh37
Build 3616180,510 - 180,735RGDNCBI36
Celera16439,399 - 439,624RGD
Cytogenetic Map16p13.3UniSTS
HuRef16158,075 - 158,300UniSTS
REN95024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716240,705 - 240,972UniSTSGRCh37
Build 3616180,706 - 180,973RGDNCBI36
Celera16439,595 - 439,862RGD
Cytogenetic Map16p13.3UniSTS
HuRef16158,271 - 158,538UniSTS
REN95025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716240,939 - 241,185UniSTSGRCh37
Build 3616180,940 - 181,186RGDNCBI36
Celera16439,829 - 440,075RGD
Cytogenetic Map16p13.3UniSTS
HuRef16158,505 - 158,751UniSTS
REN95026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716241,165 - 241,396UniSTSGRCh37
Build 3616181,166 - 181,397RGDNCBI36
Celera16440,055 - 440,286RGD
Cytogenetic Map16p13.3UniSTS
HuRef16158,731 - 158,962UniSTS
REN95027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716241,332 - 241,563UniSTSGRCh37
Build 3616181,333 - 181,564RGDNCBI36
Celera16440,222 - 440,453RGD
Cytogenetic Map16p13.3UniSTS
HuRef16158,898 - 159,129UniSTS
REN95028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716241,856 - 242,084UniSTSGRCh37
Build 3616181,857 - 182,085RGDNCBI36
Celera16440,746 - 440,974RGD
Cytogenetic Map16p13.3UniSTS
HuRef16159,422 - 159,650UniSTS
REN95029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716242,077 - 242,306UniSTSGRCh37
Build 3616182,078 - 182,307RGDNCBI36
Celera16440,967 - 441,196RGD
Cytogenetic Map16p13.3UniSTS
HuRef16159,643 - 159,872UniSTS
REN95030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716242,273 - 242,497UniSTSGRCh37
Build 3616182,274 - 182,498RGDNCBI36
Celera16441,163 - 441,387RGD
Cytogenetic Map16p13.3UniSTS
HuRef16159,839 - 160,063UniSTS
REN95031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716242,754 - 242,980UniSTSGRCh37
Build 3616182,755 - 182,981RGDNCBI36
Celera16441,644 - 441,870RGD
Cytogenetic Map16p13.3UniSTS
HuRef16160,320 - 160,546UniSTS
REN95032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716242,968 - 243,192UniSTSGRCh37
Build 3616182,969 - 183,193RGDNCBI36
Celera16441,858 - 442,082RGD
Cytogenetic Map16p13.3UniSTS
HuRef16160,534 - 160,758UniSTS
REN95033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716243,038 - 243,263UniSTSGRCh37
Build 3616183,039 - 183,264RGDNCBI36
Celera16441,928 - 442,153RGD
Cytogenetic Map16p13.3UniSTS
HuRef16160,604 - 160,829UniSTS
REN95034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716243,522 - 243,778UniSTSGRCh37
Build 3616183,523 - 183,779RGDNCBI36
Celera16442,412 - 442,668RGD
Cytogenetic Map16p13.3UniSTS
HuRef16161,088 - 161,344UniSTS
REN95035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716244,170 - 244,404UniSTSGRCh37
Build 3616184,171 - 184,405RGDNCBI36
Celera16443,060 - 443,294RGD
Cytogenetic Map16p13.3UniSTS
HuRef16161,737 - 161,971UniSTS
REN95036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716244,391 - 244,647UniSTSGRCh37
Build 3616184,392 - 184,648RGDNCBI36
Celera16443,281 - 443,537RGD
Cytogenetic Map16p13.3UniSTS
HuRef16161,958 - 162,214UniSTS
REN95037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716244,626 - 244,877UniSTSGRCh37
Build 3616184,627 - 184,878RGDNCBI36
Celera16443,516 - 443,767RGD
Cytogenetic Map16p13.3UniSTS
HuRef16162,193 - 162,444UniSTS
REN95038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716244,875 - 245,122UniSTSGRCh37
Build 3616184,876 - 185,123RGDNCBI36
Celera16443,765 - 444,012RGD
Cytogenetic Map16p13.3UniSTS
HuRef16162,442 - 162,689UniSTS
REN95039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716244,968 - 245,223UniSTSGRCh37
Build 3616184,969 - 185,224RGDNCBI36
Celera16443,858 - 444,113RGD
Cytogenetic Map16p13.3UniSTS
HuRef16162,535 - 162,790UniSTS
REN95040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716245,160 - 245,407UniSTSGRCh37
Build 3616185,161 - 185,408RGDNCBI36
Celera16444,050 - 444,297RGD
Cytogenetic Map16p13.3UniSTS
HuRef16162,727 - 162,974UniSTS
REN95041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716245,303 - 245,537UniSTSGRCh37
Build 3616185,304 - 185,538RGDNCBI36
Celera16444,193 - 444,427RGD
Cytogenetic Map16p13.3UniSTS
HuRef16162,870 - 163,104UniSTS
REN95042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716245,514 - 245,766UniSTSGRCh37
Build 3616185,515 - 185,767RGDNCBI36
Celera16444,404 - 444,656RGD
Cytogenetic Map16p13.3UniSTS
HuRef16163,081 - 163,333UniSTS
REN95043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716245,744 - 245,984UniSTSGRCh37
Build 3616185,745 - 185,985RGDNCBI36
Celera16444,634 - 444,874RGD
Cytogenetic Map16p13.3UniSTS
HuRef16163,311 - 163,551UniSTS
REN95044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716245,894 - 246,137UniSTSGRCh37
Build 3616185,895 - 186,138RGDNCBI36
Celera16444,784 - 445,027RGD
Cytogenetic Map16p13.3UniSTS
HuRef16163,461 - 163,704UniSTS
REN95045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716246,114 - 246,370UniSTSGRCh37
Build 3616186,115 - 186,371RGDNCBI36
Celera16445,004 - 445,260RGD
Cytogenetic Map16p13.3UniSTS
HuRef16163,681 - 163,937UniSTS
REN95046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716246,309 - 246,535UniSTSGRCh37
Build 3616186,310 - 186,536RGDNCBI36
Celera16445,199 - 445,425RGD
Cytogenetic Map16p13.3UniSTS
HuRef16163,876 - 164,102UniSTS
REN95047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716246,452 - 246,685UniSTSGRCh37
Build 3616186,453 - 186,686RGDNCBI36
Celera16445,342 - 445,575RGD
Cytogenetic Map16p13.3UniSTS
HuRef16164,019 - 164,252UniSTS
REN95048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716246,648 - 246,872UniSTSGRCh37
Build 3616186,649 - 186,873RGDNCBI36
Celera16445,538 - 445,762RGD
Cytogenetic Map16p13.3UniSTS
HuRef16164,215 - 164,439UniSTS
REN95049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716247,234 - 247,491UniSTSGRCh37
Build 3616187,235 - 187,492RGDNCBI36
Celera16446,124 - 446,381RGD
Cytogenetic Map16p13.3UniSTS
HuRef16164,801 - 165,058UniSTS
REN95050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716247,299 - 247,523UniSTSGRCh37
Build 3616187,300 - 187,524RGDNCBI36
Celera16446,189 - 446,413RGD
Cytogenetic Map16p13.3UniSTS
HuRef16164,866 - 165,090UniSTS
REN95051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716247,503 - 247,749UniSTSGRCh37
Build 3616187,504 - 187,750RGDNCBI36
Celera16446,393 - 446,639RGD
Cytogenetic Map16p13.3UniSTS
HuRef16165,070 - 165,316UniSTS
REN95052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716247,728 - 247,966UniSTSGRCh37
Build 3616187,729 - 187,967RGDNCBI36
Celera16446,618 - 446,856RGD
Cytogenetic Map16p13.3UniSTS
HuRef16165,295 - 165,533UniSTS
REN95053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716247,865 - 248,090UniSTSGRCh37
Build 3616187,866 - 188,091RGDNCBI36
Celera16446,755 - 446,980RGD
Cytogenetic Map16p13.3UniSTS
HuRef16165,432 - 165,657UniSTS
REN95054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716248,070 - 248,344UniSTSGRCh37
Build 3616188,071 - 188,345RGDNCBI36
Celera16446,960 - 447,233RGD
Cytogenetic Map16p13.3UniSTS
HuRef16165,637 - 165,910UniSTS
REN95055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716248,331 - 248,582UniSTSGRCh37
Build 3616188,332 - 188,583RGDNCBI36
Celera16447,220 - 447,471RGD
Cytogenetic Map16p13.3UniSTS
HuRef16165,897 - 166,148UniSTS
REN95056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716248,509 - 248,737UniSTSGRCh37
Build 3616188,510 - 188,738RGDNCBI36
Celera16447,398 - 447,626RGD
Cytogenetic Map16p13.3UniSTS
HuRef16166,075 - 166,303UniSTS
REN95057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716248,612 - 248,842UniSTSGRCh37
Build 3616188,613 - 188,843RGDNCBI36
Celera16447,501 - 447,731RGD
Cytogenetic Map16p13.3UniSTS
HuRef16166,178 - 166,408UniSTS
REN95058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716248,816 - 249,048UniSTSGRCh37
Build 3616188,817 - 189,049RGDNCBI36
Celera16447,705 - 447,937RGD
Cytogenetic Map16p13.3UniSTS
HuRef16166,382 - 166,614UniSTS
REN95059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716249,034 - 249,290UniSTSGRCh37
Build 3616189,035 - 189,291RGDNCBI36
Celera16447,923 - 448,179RGD
Cytogenetic Map16p13.3UniSTS
HuRef16166,600 - 166,856UniSTS
REN95060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716249,233 - 249,489UniSTSGRCh37
Build 3616189,234 - 189,490RGDNCBI36
Celera16448,122 - 448,378RGD
Cytogenetic Map16p13.3UniSTS
HuRef16166,799 - 167,055UniSTS
REN95062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716250,473 - 250,698UniSTSGRCh37
Build 3616190,474 - 190,699RGDNCBI36
Celera16449,362 - 449,587RGD
Cytogenetic Map16p13.3UniSTS
HuRef16168,038 - 168,263UniSTS
REN95063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716250,639 - 250,894UniSTSGRCh37
Build 3616190,640 - 190,895RGDNCBI36
Celera16449,528 - 449,783RGD
Cytogenetic Map16p13.3UniSTS
HuRef16168,204 - 168,459UniSTS
REN95064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716250,867 - 251,093UniSTSGRCh37
Build 3616190,868 - 191,094RGDNCBI36
Celera16449,756 - 449,982RGD
Cytogenetic Map16p13.3UniSTS
HuRef16168,432 - 168,658UniSTS
REN95065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716251,063 - 251,320UniSTSGRCh37
Build 3616191,064 - 191,321RGDNCBI36
Celera16449,952 - 450,210RGD
Cytogenetic Map16p13.3UniSTS
HuRef16168,628 - 168,885UniSTS
REN95066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716251,191 - 251,421UniSTSGRCh37
Build 3616191,192 - 191,422RGDNCBI36
Celera16450,081 - 450,311RGD
Cytogenetic Map16p13.3UniSTS
HuRef16168,757 - 168,986UniSTS
REN95067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716251,402 - 251,648UniSTSGRCh37
Build 3616191,403 - 191,649RGDNCBI36
Celera16450,292 - 450,538RGD
Cytogenetic Map16p13.3UniSTS
HuRef16168,967 - 169,213UniSTS
REN95068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716252,048 - 252,296UniSTSGRCh37
Build 3616192,049 - 192,297RGDNCBI36
Celera16450,938 - 451,186RGD
Cytogenetic Map16p13.3UniSTS
HuRef16169,612 - 169,859UniSTS
REN95069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716252,266 - 252,523UniSTSGRCh37
Build 3616192,267 - 192,524RGDNCBI36
Celera16451,156 - 451,413RGD
Cytogenetic Map16p13.3UniSTS
HuRef16169,829 - 170,086UniSTS
REN95070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716252,505 - 252,761UniSTSGRCh37
Build 3616192,506 - 192,762RGDNCBI36
Celera16451,395 - 451,651RGD
Cytogenetic Map16p13.3UniSTS
HuRef16170,068 - 170,324UniSTS
REN95071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716252,738 - 252,991UniSTSGRCh37
Build 3616192,739 - 192,992RGDNCBI36
Celera16451,628 - 451,881RGD
Cytogenetic Map16p13.3UniSTS
HuRef16170,301 - 170,554UniSTS
REN95072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716252,814 - 253,080UniSTSGRCh37
Build 3616192,815 - 193,081RGDNCBI36
Celera16451,704 - 451,970RGD
Cytogenetic Map16p13.3UniSTS
HuRef16170,377 - 170,643UniSTS
REN95073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716253,260 - 253,486UniSTSGRCh37
Build 3616193,261 - 193,487RGDNCBI36
Celera16452,150 - 452,376RGD
Cytogenetic Map16p13.3UniSTS
HuRef16170,823 - 171,049UniSTS
REN95074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716253,385 - 253,638UniSTSGRCh37
Build 3616193,386 - 193,639RGDNCBI36
Celera16452,275 - 452,528RGD
Cytogenetic Map16p13.3UniSTS
HuRef16170,948 - 171,201UniSTS
REN95075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716253,820 - 254,064UniSTSGRCh37
Build 3616193,821 - 194,065RGDNCBI36
Celera16452,710 - 452,954RGD
Cytogenetic Map16p13.3UniSTS
HuRef16171,383 - 171,627UniSTS
REN95076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716254,068 - 254,320UniSTSGRCh37
Build 3616194,069 - 194,321RGDNCBI36
Celera16452,958 - 453,210RGD
Cytogenetic Map16p13.3UniSTS
HuRef16171,631 - 171,883UniSTS
REN95077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716254,268 - 254,523UniSTSGRCh37
Build 3616194,269 - 194,524RGDNCBI36
Celera16453,158 - 453,413RGD
Cytogenetic Map16p13.3UniSTS
HuRef16171,831 - 172,086UniSTS
REN95078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716254,502 - 254,732UniSTSGRCh37
Build 3616194,503 - 194,733RGDNCBI36
Celera16453,392 - 453,622RGD
Cytogenetic Map16p13.3UniSTS
HuRef16172,065 - 172,295UniSTS
REN95079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716254,730 - 254,988UniSTSGRCh37
Build 3616194,731 - 194,989RGDNCBI36
Celera16453,620 - 453,878RGD
Cytogenetic Map16p13.3UniSTS
HuRef16172,293 - 172,551UniSTS
REN95080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716254,956 - 255,192UniSTSGRCh37
Build 3616194,957 - 195,193RGDNCBI36
Celera16453,846 - 454,082RGD
Cytogenetic Map16p13.3UniSTS
HuRef16172,519 - 172,755UniSTS
REN95081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716255,088 - 255,325UniSTSGRCh37
Build 3616195,089 - 195,326RGDNCBI36
Celera16453,978 - 454,215RGD
Cytogenetic Map16p13.3UniSTS
HuRef16172,651 - 172,888UniSTS
REN95082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716255,284 - 255,535UniSTSGRCh37
Build 3616195,285 - 195,536RGDNCBI36
Celera16454,174 - 454,425RGD
Cytogenetic Map16p13.3UniSTS
HuRef16172,847 - 173,098UniSTS
REN95083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716255,331 - 255,582UniSTSGRCh37
Build 3616195,332 - 195,583RGDNCBI36
Celera16454,221 - 454,472RGD
Cytogenetic Map16p13.3UniSTS
HuRef16172,894 - 173,145UniSTS
REN95084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716255,878 - 256,111UniSTSGRCh37
Build 3616195,879 - 196,112RGDNCBI36
Celera16454,768 - 455,001RGD
Cytogenetic Map16p13.3UniSTS
HuRef16173,441 - 173,674UniSTS
REN95085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716256,089 - 256,344UniSTSGRCh37
Build 3616196,090 - 196,345RGDNCBI36
Celera16454,979 - 455,234RGD
Cytogenetic Map16p13.3UniSTS
HuRef16173,652 - 173,907UniSTS
REN95086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716256,333 - 256,582UniSTSGRCh37
Build 3616196,334 - 196,583RGDNCBI36
Celera16455,223 - 455,472RGD
Cytogenetic Map16p13.3UniSTS
HuRef16173,896 - 174,145UniSTS
REN95087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716256,520 - 256,778UniSTSGRCh37
Build 3616196,521 - 196,779RGDNCBI36
Celera16455,410 - 455,668RGD
Cytogenetic Map16p13.3UniSTS
HuRef16174,083 - 174,341UniSTS
REN95088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716256,730 - 256,970UniSTSGRCh37
Build 3616196,731 - 196,971RGDNCBI36
Celera16455,620 - 455,860RGD
Cytogenetic Map16p13.3UniSTS
HuRef16174,293 - 174,534UniSTS
REN95089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716257,267 - 257,512UniSTSGRCh37
Build 3616197,268 - 197,513RGDNCBI36
Celera16456,157 - 456,402RGD
Cytogenetic Map16p13.3UniSTS
HuRef16174,831 - 175,076UniSTS
REN95090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716257,489 - 257,714UniSTSGRCh37
Build 3616197,490 - 197,715RGDNCBI36
Celera16456,379 - 456,604RGD
Cytogenetic Map16p13.3UniSTS
HuRef16175,053 - 175,278UniSTS
REN95091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716258,039 - 258,264UniSTSGRCh37
Build 3616198,040 - 198,265RGDNCBI36
Celera16456,929 - 457,154RGD
Cytogenetic Map16p13.3UniSTS
HuRef16175,603 - 175,828UniSTS
REN95092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716258,247 - 258,498UniSTSGRCh37
Build 3616198,248 - 198,499RGDNCBI36
Celera16457,137 - 457,388RGD
Cytogenetic Map16p13.3UniSTS
HuRef16175,811 - 176,062UniSTS
REN95093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716258,483 - 258,724UniSTSGRCh37
Build 3616198,484 - 198,725RGDNCBI36
Celera16457,373 - 457,614RGD
Cytogenetic Map16p13.3UniSTS
HuRef16176,047 - 176,288UniSTS
REN95094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716258,672 - 258,897UniSTSGRCh37
Build 3616198,673 - 198,898RGDNCBI36
Celera16457,562 - 457,787RGD
Cytogenetic Map16p13.3UniSTS
HuRef16176,236 - 176,461UniSTS
REN95095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716258,874 - 259,144UniSTSGRCh37
Build 3616198,875 - 199,145RGDNCBI36
Celera16457,764 - 458,034RGD
Cytogenetic Map16p13.3UniSTS
HuRef16176,438 - 176,708UniSTS
REN95096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716259,287 - 259,526UniSTSGRCh37
Build 3616199,288 - 199,527RGDNCBI36
Celera16458,177 - 458,417RGD
Cytogenetic Map16p13.3UniSTS
HuRef16176,851 - 177,090UniSTS
REN95097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716259,524 - 259,781UniSTSGRCh37
Build 3616199,525 - 199,782RGDNCBI36
Celera16458,415 - 458,672RGD
Cytogenetic Map16p13.3UniSTS
HuRef16177,088 - 177,345UniSTS
REN95098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716259,758 - 259,984UniSTSGRCh37
Build 3616199,759 - 199,985RGDNCBI36
Celera16458,649 - 458,875RGD
Cytogenetic Map16p13.3UniSTS
HuRef16177,322 - 177,548UniSTS
REN95099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716260,295 - 260,520UniSTSGRCh37
Build 3616200,296 - 200,521RGDNCBI36
Celera16459,186 - 459,411RGD
Cytogenetic Map16p13.3UniSTS
HuRef16177,859 - 178,084UniSTS
REN95100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716260,501 - 260,747UniSTSGRCh37
Build 3616200,502 - 200,748RGDNCBI36
Celera16459,392 - 459,638RGD
Cytogenetic Map16p13.3UniSTS
HuRef16178,065 - 178,311UniSTS
REN95101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716260,537 - 260,775UniSTSGRCh37
Build 3616200,538 - 200,776RGDNCBI36
Celera16459,428 - 459,666RGD
Cytogenetic Map16p13.3UniSTS
HuRef16178,101 - 178,339UniSTS
REN95102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716260,986 - 261,229UniSTSGRCh37
Build 3616200,987 - 201,230RGDNCBI36
Celera16459,877 - 460,120RGD
Cytogenetic Map16p13.3UniSTS
HuRef16178,550 - 178,793UniSTS
REN95103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716261,206 - 261,470UniSTSGRCh37
Build 3616201,207 - 201,471RGDNCBI36
Celera16460,097 - 460,361RGD
Cytogenetic Map16p13.3UniSTS
HuRef16178,770 - 179,034UniSTS
REN95104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716261,449 - 261,702UniSTSGRCh37
Build 3616201,450 - 201,703RGDNCBI36
Celera16460,340 - 460,593RGD
Cytogenetic Map16p13.3UniSTS
HuRef16179,013 - 179,266UniSTS
REN95105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716261,678 - 261,934UniSTSGRCh37
Build 3616201,679 - 201,935RGDNCBI36
Celera16460,569 - 460,825RGD
Cytogenetic Map16p13.3UniSTS
HuRef16179,242 - 179,498UniSTS
REN95106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716261,770 - 262,004UniSTSGRCh37
Build 3616201,771 - 202,005RGDNCBI36
Celera16460,661 - 460,895RGD
Cytogenetic Map16p13.3UniSTS
HuRef16179,334 - 179,568UniSTS
REN95107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716262,295 - 262,531UniSTSGRCh37
Build 3616202,296 - 202,532RGDNCBI36
Celera16461,186 - 461,422RGD
Cytogenetic Map16p13.3UniSTS
HuRef16179,859 - 180,095UniSTS
REN95108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716262,522 - 262,758UniSTSGRCh37
Build 3616202,523 - 202,759RGDNCBI36
Celera16461,413 - 461,649RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,086 - 180,322UniSTS
REN95109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716262,752 - 262,976UniSTSGRCh37
Build 3616202,753 - 202,977RGDNCBI36
Celera16461,643 - 461,867RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,316 - 180,540UniSTS
REN95110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716262,935 - 263,190UniSTSGRCh37
Build 3616202,936 - 203,191RGDNCBI36
Celera16461,826 - 462,081RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,499 - 180,754UniSTS
REN95111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716263,167 - 263,397UniSTSGRCh37
Build 3616203,168 - 203,398RGDNCBI36
Celera16462,058 - 462,288RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,731 - 180,961UniSTS
REN95112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716263,361 - 263,611UniSTSGRCh37
Build 3616203,362 - 203,612RGDNCBI36
Celera16462,252 - 462,502RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,925 - 181,175UniSTS
REN95113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716263,417 - 263,651UniSTSGRCh37
Build 3616203,418 - 203,652RGDNCBI36
Celera16462,308 - 462,542RGD
Cytogenetic Map16p13.3UniSTS
HuRef16180,981 - 181,215UniSTS
REN95114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716263,694 - 263,929UniSTSGRCh37
Build 3616203,695 - 203,930RGDNCBI36
Celera16462,585 - 462,820RGD
Cytogenetic Map16p13.3UniSTS
HuRef16181,258 - 181,493UniSTS
REN95115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716264,054 - 264,301UniSTSGRCh37
Build 3616204,055 - 204,302RGDNCBI36
Celera16462,945 - 463,192RGD
Cytogenetic Map16p13.3UniSTS
HuRef16181,618 - 181,865UniSTS
REN95116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716264,275 - 264,502UniSTSGRCh37
Build 3616204,276 - 204,503RGDNCBI36
Celera16463,166 - 463,393RGD
Cytogenetic Map16p13.3UniSTS
HuRef16181,839 - 182,066UniSTS
REN95117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716264,472 - 264,734UniSTSGRCh37
Build 3616204,473 - 204,735RGDNCBI36
Celera16463,363 - 463,625RGD
Cytogenetic Map16p13.3UniSTS
HuRef16182,036 - 182,298UniSTS
REN95118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716264,711 - 264,972UniSTSGRCh37
Build 3616204,712 - 204,973RGDNCBI36
Celera16463,602 - 463,863RGD
Cytogenetic Map16p13.3UniSTS
HuRef16182,275 - 182,536UniSTS
REN95119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716264,952 - 265,212UniSTSGRCh37
Build 3616204,953 - 205,213RGDNCBI36
Celera16463,843 - 464,103RGD
Cytogenetic Map16p13.3UniSTS
HuRef16182,516 - 182,776UniSTS
REN95120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716265,189 - 265,452UniSTSGRCh37
Build 3616205,190 - 205,453RGDNCBI36
Celera16464,080 - 464,343RGD
Cytogenetic Map16p13.3UniSTS
HuRef16182,753 - 183,016UniSTS
REN95121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716265,722 - 265,973UniSTSGRCh37
Build 3616205,723 - 205,974RGDNCBI36
Celera16464,613 - 464,864RGD
Cytogenetic Map16p13.3UniSTS
HuRef16183,286 - 183,537UniSTS
REN95122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716266,315 - 266,581UniSTSGRCh37
Build 3616206,316 - 206,582RGDNCBI36
Celera16465,206 - 465,472RGD
Cytogenetic Map16p13.3UniSTS
HuRef16183,879 - 184,144UniSTS
REN95123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716266,562 - 266,825UniSTSGRCh37
Build 3616206,563 - 206,826RGDNCBI36
Celera16465,453 - 465,716RGD
Cytogenetic Map16p13.3UniSTS
HuRef16184,125 - 184,388UniSTS
REN95124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716266,814 - 267,071UniSTSGRCh37
Build 3616206,815 - 207,072RGDNCBI36
Celera16465,705 - 465,962RGD
Cytogenetic Map16p13.3UniSTS
HuRef16184,377 - 184,634UniSTS
REN95125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716267,052 - 267,315UniSTSGRCh37
Build 3616207,053 - 207,316RGDNCBI36
Celera16465,943 - 466,206RGD
Cytogenetic Map16p13.3UniSTS
HuRef16184,615 - 184,878UniSTS
REN95126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716267,192 - 267,416UniSTSGRCh37
Build 3616207,193 - 207,417RGDNCBI36
Celera16466,083 - 466,307RGD
Cytogenetic Map16p13.3UniSTS
HuRef16184,755 - 184,979UniSTS
REN95127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716267,336 - 267,589UniSTSGRCh37
Build 3616207,337 - 207,590RGDNCBI36
Celera16466,227 - 466,480RGD
Cytogenetic Map16p13.3UniSTS
HuRef16184,899 - 185,152UniSTS
REN95128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716267,740 - 267,964UniSTSGRCh37
Build 3616207,741 - 207,965RGDNCBI36
Celera16466,631 - 466,855RGD
Cytogenetic Map16p13.3UniSTS
HuRef16185,302 - 185,526UniSTS
REN95129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716267,940 - 268,192UniSTSGRCh37
Build 3616207,941 - 208,193RGDNCBI36
Celera16466,831 - 467,083RGD
Cytogenetic Map16p13.3UniSTS
HuRef16185,502 - 185,755UniSTS
REN95130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716268,166 - 268,394UniSTSGRCh37
Build 3616208,167 - 208,395RGDNCBI36
Celera16467,057 - 467,285RGD
Cytogenetic Map16p13.3UniSTS
HuRef16185,729 - 185,957UniSTS
REN95131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716268,368 - 268,615UniSTSGRCh37
Build 3616208,369 - 208,616RGDNCBI36
Celera16467,259 - 467,506RGD
Cytogenetic Map16p13.3UniSTS
HuRef16185,931 - 186,178UniSTS
REN95132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716268,588 - 268,819UniSTSGRCh37
Build 3616208,589 - 208,820RGDNCBI36
Celera16467,479 - 467,710RGD
Cytogenetic Map16p13.3UniSTS
HuRef16186,151 - 186,382UniSTS
REN95133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716268,795 - 269,044UniSTSGRCh37
Build 3616208,796 - 209,045RGDNCBI36
Celera16467,686 - 467,934RGD
Cytogenetic Map16p13.3UniSTS
HuRef16186,358 - 186,605UniSTS
REN95134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716268,827 - 269,053UniSTSGRCh37
Build 3616208,828 - 209,054RGDNCBI36
Celera16467,718 - 467,943RGD
Cytogenetic Map16p13.3UniSTS
HuRef16186,390 - 186,614UniSTS
REN95135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716269,931 - 270,160UniSTSGRCh37
Build 3616209,932 - 210,161RGDNCBI36
Celera16468,821 - 469,050RGD
Cytogenetic Map16p13.3UniSTS
HuRef16187,492 - 187,721UniSTS
REN95136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716270,152 - 270,376UniSTSGRCh37
Build 3616210,153 - 210,377RGDNCBI36
Celera16469,042 - 469,266RGD
Cytogenetic Map16p13.3UniSTS
HuRef16187,713 - 187,937UniSTS
REN95137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716270,374 - 270,623UniSTSGRCh37
Build 3616210,375 - 210,624RGDNCBI36
Celera16469,264 - 469,513RGD
Cytogenetic Map16p13.3UniSTS
HuRef16187,935 - 188,184UniSTS
REN95138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716270,610 - 270,874UniSTSGRCh37
Build 3616210,611 - 210,875RGDNCBI36
Celera16469,500 - 469,764RGD
Cytogenetic Map16p13.3UniSTS
HuRef16188,171 - 188,435UniSTS
REN95139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716270,770 - 271,037UniSTSGRCh37
Build 3616210,771 - 211,038RGDNCBI36
Celera16469,660 - 469,927RGD
Cytogenetic Map16p13.3UniSTS
HuRef16188,331 - 188,598UniSTS
REN95140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716271,355 - 271,610UniSTSGRCh37
Build 3616211,356 - 211,611RGDNCBI36
Celera16470,238 - 470,493RGD
Cytogenetic Map16p13.3UniSTS
HuRef16188,904 - 189,159UniSTS
REN95141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716271,587 - 271,813UniSTSGRCh37
Build 3616211,588 - 211,814RGDNCBI36
Celera16470,470 - 470,696RGD
Cytogenetic Map16p13.3UniSTS
HuRef16189,136 - 189,362UniSTS
REN95142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716271,800 - 272,053UniSTSGRCh37
Build 3616211,801 - 212,054RGDNCBI36
Celera16470,683 - 470,936RGD
Cytogenetic Map16p13.3UniSTS
HuRef16189,349 - 189,602UniSTS
REN95143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716272,030 - 272,273UniSTSGRCh37
Build 3616212,031 - 212,274RGDNCBI36
Celera16470,913 - 471,156RGD
Cytogenetic Map16p13.3UniSTS
HuRef16189,579 - 189,822UniSTS
REN95144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716272,170 - 272,405UniSTSGRCh37
Build 3616212,171 - 212,406RGDNCBI36
Celera16471,053 - 471,288RGD
Cytogenetic Map16p13.3UniSTS
HuRef16189,719 - 189,955UniSTS
REN95145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716272,372 - 272,636UniSTSGRCh37
Build 3616212,373 - 212,637RGDNCBI36
Celera16471,255 - 471,519RGD
Cytogenetic Map16p13.3UniSTS
HuRef16189,922 - 190,186UniSTS
REN95146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716273,038 - 273,286UniSTSGRCh37
Build 3616213,039 - 213,287RGDNCBI36
Celera16471,921 - 472,169RGD
Cytogenetic Map16p13.3UniSTS
HuRef16190,588 - 190,836UniSTS
REN95147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716273,265 - 273,515UniSTSGRCh37
Build 3616213,266 - 213,516RGDNCBI36
Celera16472,148 - 472,398RGD
Cytogenetic Map16p13.3UniSTS
HuRef16190,815 - 191,065UniSTS
REN95148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716273,414 - 273,667UniSTSGRCh37
Build 3616213,415 - 213,668RGDNCBI36
Celera16472,297 - 472,550RGD
Cytogenetic Map16p13.3UniSTS
HuRef16190,964 - 191,217UniSTS
REN95149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716273,923 - 274,152UniSTSGRCh37
Build 3616213,924 - 214,153RGDNCBI36
Celera16472,806 - 473,035RGD
Cytogenetic Map16p13.3UniSTS
HuRef16191,471 - 191,700UniSTS
REN95150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716274,132 - 274,400UniSTSGRCh37
Build 3616214,133 - 214,401RGDNCBI36
Celera16473,015 - 473,283RGD
Cytogenetic Map16p13.3UniSTS
HuRef16191,680 - 191,948UniSTS
REN95151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716274,773 - 275,009UniSTSGRCh37
Build 3616214,774 - 215,010RGDNCBI36
Celera16473,656 - 473,892RGD
Cytogenetic Map16p13.3UniSTS
HuRef16192,321 - 192,557UniSTS
REN95152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716274,947 - 275,206UniSTSGRCh37
Build 3616214,948 - 215,207RGDNCBI36
Celera16473,830 - 474,089RGD
Cytogenetic Map16p13.3UniSTS
HuRef16192,495 - 192,754UniSTS
REN95153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716275,468 - 275,702UniSTSGRCh37
Build 3616215,469 - 215,703RGDNCBI36
Celera16474,351 - 474,585RGD
Cytogenetic Map16p13.3UniSTS
REN95154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716275,670 - 275,919UniSTSGRCh37
Build 3616215,671 - 215,920RGDNCBI36
Celera16474,553 - 474,802RGD
Cytogenetic Map16p13.3UniSTS
HuRef16193,209 - 193,458UniSTS
REN95155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716275,896 - 276,148UniSTSGRCh37
Build 3616215,897 - 216,149RGDNCBI36
Celera16474,779 - 475,031RGD
Cytogenetic Map16p13.3UniSTS
HuRef16193,435 - 193,686UniSTS
REN95156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716276,115 - 276,344UniSTSGRCh37
Build 3616216,116 - 216,345RGDNCBI36
Celera16474,998 - 475,227RGD
Cytogenetic Map16p13.3UniSTS
HuRef16193,653 - 193,882UniSTS
REN95157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716276,326 - 276,576UniSTSGRCh37
Build 3616216,327 - 216,577RGDNCBI36
Celera16475,209 - 475,459RGD
Cytogenetic Map16p13.3UniSTS
HuRef16193,864 - 194,114UniSTS
REN95158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716276,548 - 276,774UniSTSGRCh37
Build 3616216,549 - 216,775RGDNCBI36
Celera16475,431 - 475,657RGD
Cytogenetic Map16p13.3UniSTS
HuRef16194,086 - 194,312UniSTS
REN95159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716276,690 - 276,933UniSTSGRCh37
Build 3616216,691 - 216,934RGDNCBI36
Celera16475,573 - 475,816RGD
Cytogenetic Map16p13.3UniSTS
HuRef16194,228 - 194,471UniSTS
REN95160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716276,910 - 277,134UniSTSGRCh37
Build 3616216,911 - 217,135RGDNCBI36
Celera16475,793 - 476,017RGD
Cytogenetic Map16p13.3UniSTS
HuRef16194,448 - 194,672UniSTS
REN95161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,090 - 277,348UniSTSGRCh37
Build 3616217,091 - 217,349RGDNCBI36
Celera16475,973 - 476,231RGD
Cytogenetic Map16p13.3UniSTS
HuRef16194,628 - 194,886UniSTS
REN95162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,332 - 277,581UniSTSGRCh37
Build 3616217,333 - 217,582RGDNCBI36
Celera16476,215 - 476,464RGD
Cytogenetic Map16p13.3UniSTS
HuRef16194,870 - 195,119UniSTS
REN95163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,578 - 277,804UniSTSGRCh37
Build 3616217,579 - 217,805RGDNCBI36
Celera16476,461 - 476,687RGD
Cytogenetic Map16p13.3UniSTS
HuRef16195,116 - 195,342UniSTS
REN95164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,776 - 278,023UniSTSGRCh37
Build 3616217,777 - 218,024RGDNCBI36
Celera16476,659 - 476,906RGD
Cytogenetic Map16p13.3UniSTS
HuRef16195,314 - 195,561UniSTS
REN95165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716278,000 - 278,224UniSTSGRCh37
Build 3616218,001 - 218,225RGDNCBI36
Celera16476,883 - 477,107RGD
Cytogenetic Map16p13.3UniSTS
HuRef16195,538 - 195,762UniSTS
REN95166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716278,199 - 278,433UniSTSGRCh37
Build 3616218,200 - 218,434RGDNCBI36
Celera16477,082 - 477,316RGD
Cytogenetic Map16p13.3UniSTS
HuRef16195,737 - 195,971UniSTS
REN95167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716278,422 - 278,673UniSTSGRCh37
Build 3616218,423 - 218,674RGDNCBI36
Celera16477,305 - 477,556RGD
Cytogenetic Map16p13.3UniSTS
HuRef16195,960 - 196,211UniSTS
REN95168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716278,664 - 278,896UniSTSGRCh37
Build 3616218,665 - 218,897RGDNCBI36
Celera16477,547 - 477,779RGD
Cytogenetic Map16p13.3UniSTS
HuRef16196,202 - 196,434UniSTS
REN95169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716278,873 - 279,123UniSTSGRCh37
Build 3616218,874 - 219,124RGDNCBI36
Celera16477,756 - 478,006RGD
Cytogenetic Map16p13.3UniSTS
HuRef16196,411 - 196,661UniSTS
REN95170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716279,059 - 279,286UniSTSGRCh37
Build 3616219,060 - 219,287RGDNCBI36
Celera16477,942 - 478,169RGD
Cytogenetic Map16p13.3UniSTS
HuRef16196,597 - 196,824UniSTS
REN95171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716279,259 - 279,520UniSTSGRCh37
Build 3616219,260 - 219,521RGDNCBI36
Celera16478,142 - 478,403RGD
Cytogenetic Map16p13.3UniSTS
HuRef16196,797 - 197,058UniSTS
REN95172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716279,510 - 279,746UniSTSGRCh37
Build 3616219,511 - 219,747RGDNCBI36
Celera16478,393 - 478,629RGD
Cytogenetic Map16p13.3UniSTS
HuRef16197,048 - 197,284UniSTS
REN95173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716279,707 - 279,952UniSTSGRCh37
Build 3616219,708 - 219,953RGDNCBI36
Celera16478,590 - 478,835RGD
Cytogenetic Map16p13.3UniSTS
HuRef16197,245 - 197,490UniSTS
REN95174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716279,947 - 280,171UniSTSGRCh37
Build 3616219,948 - 220,172RGDNCBI36
Celera16478,830 - 479,054RGD
Cytogenetic Map16p13.3UniSTS
HuRef16197,485 - 197,709UniSTS
REN95175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716279,972 - 280,235UniSTSGRCh37
Build 3616219,973 - 220,236RGDNCBI36
Celera16478,855 - 479,118RGD
Cytogenetic Map16p13.3UniSTS
HuRef16197,510 - 197,773UniSTS
REN95176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716280,335 - 280,601UniSTSGRCh37
Build 3616220,336 - 220,602RGDNCBI36
Celera16479,218 - 479,484RGD
Cytogenetic Map16p13.3UniSTS
HuRef16197,873 - 198,139UniSTS
REN95177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716280,577 - 280,842UniSTSGRCh37
Build 3616220,578 - 220,843RGDNCBI36
Celera16479,460 - 479,725RGD
Cytogenetic Map16p13.3UniSTS
HuRef16198,115 - 198,380UniSTS
REN95178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716280,821 - 281,050UniSTSGRCh37
Build 3616220,822 - 221,051RGDNCBI36
Celera16479,704 - 479,933RGD
Cytogenetic Map16p13.3UniSTS
HuRef16198,359 - 198,588UniSTS
REN95179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716280,927 - 281,165UniSTSGRCh37
Build 3616220,928 - 221,166RGDNCBI36
Celera16479,810 - 480,048RGD
Cytogenetic Map16p13.3UniSTS
HuRef16198,465 - 198,703UniSTS
REN95180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716281,143 - 281,407UniSTSGRCh37
Build 3616221,144 - 221,408RGDNCBI36
Celera16480,026 - 480,290RGD
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map16p13.3UniSTS
HuRef16198,681 - 198,945UniSTS
stSG608935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716238,752 - 239,932UniSTSGRCh37
Build 3616178,753 - 179,933RGDNCBI36
Celera16437,642 - 438,822RGD
HuRef16156,318 - 157,498UniSTS
stSG608936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716239,913 - 241,314UniSTSGRCh37
Build 3616179,914 - 181,315RGDNCBI36
Celera16438,803 - 440,204RGD
HuRef16157,479 - 158,880UniSTS
stSG608937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716241,314 - 242,473UniSTSGRCh37
Build 3616181,315 - 182,474RGDNCBI36
Celera16440,204 - 441,363RGD
HuRef16158,880 - 160,039UniSTS
stSG608938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716241,929 - 242,966UniSTSGRCh37
Build 3616181,930 - 182,967RGDNCBI36
Celera16440,819 - 441,856RGD
HuRef16159,495 - 160,532UniSTS
stSG608939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716243,052 - 244,500UniSTSGRCh37
Build 3616183,053 - 184,501RGDNCBI36
Celera16441,942 - 443,390RGD
HuRef16160,618 - 162,067UniSTS
stSG608940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716244,571 - 245,840UniSTSGRCh37
Build 3616184,572 - 185,841RGDNCBI36
Celera16443,461 - 444,730RGD
HuRef16162,138 - 163,407UniSTS
stSG608941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716247,626 - 248,642UniSTSGRCh37
Build 3616187,627 - 188,643RGDNCBI36
Celera16446,516 - 447,531RGD
HuRef16165,193 - 166,208UniSTS
stSG608942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716248,423 - 249,426UniSTSGRCh37
Build 3616188,424 - 189,427RGDNCBI36
Celera16447,312 - 448,315RGD
HuRef16165,989 - 166,992UniSTS
stSG608943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716255,935 - 256,205UniSTSGRCh37
Build 3616195,936 - 196,206RGDNCBI36
Celera16454,825 - 455,095RGD
HuRef16173,498 - 173,768UniSTS
stSG608945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716257,598 - 258,673UniSTSGRCh37
Build 3616197,599 - 198,674RGDNCBI36
Celera16456,488 - 457,563RGD
HuRef16175,162 - 176,237UniSTS
stSG608946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716258,654 - 259,949UniSTSGRCh37
Build 3616198,655 - 199,950RGDNCBI36
Celera16457,544 - 458,840RGD
HuRef16176,218 - 177,513UniSTS
stSG608947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716259,947 - 261,295UniSTSGRCh37
Build 3616199,948 - 201,296RGDNCBI36
Celera16458,838 - 460,186RGD
HuRef16177,511 - 178,859UniSTS
stSG608948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716261,276 - 261,527UniSTSGRCh37
Build 3616201,277 - 201,528RGDNCBI36
Celera16460,167 - 460,418RGD
HuRef16178,840 - 179,091UniSTS
stSG608949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716261,546 - 262,692UniSTSGRCh37
Build 3616201,547 - 202,693RGDNCBI36
Celera16460,437 - 461,583RGD
HuRef16179,110 - 180,256UniSTS
stSG608950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716262,325 - 263,347UniSTSGRCh37
Build 3616202,326 - 203,348RGDNCBI36
Celera16461,216 - 462,238RGD
HuRef16179,889 - 180,911UniSTS
stSG608952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716265,835 - 266,757UniSTSGRCh37
Build 3616205,836 - 206,758RGDNCBI36
Celera16464,726 - 465,648RGD
HuRef16183,399 - 184,320UniSTS
stSG608954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716270,279 - 271,393UniSTSGRCh37
Build 3616210,280 - 211,394RGDNCBI36
Celera16469,169 - 470,276RGD
stSG608955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716271,016 - 272,305UniSTSGRCh37
Build 3616211,017 - 212,306RGDNCBI36
Celera16469,906 - 471,188RGD
HuRef16188,577 - 189,854UniSTS
stSG608956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716272,288 - 273,563UniSTSGRCh37
Build 3616212,289 - 213,564RGDNCBI36
Celera16471,171 - 472,446RGD
HuRef16189,837 - 191,113UniSTS
stSG608957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716273,544 - 275,009UniSTSGRCh37
Build 3616213,545 - 215,010RGDNCBI36
Celera16472,427 - 473,892RGD
HuRef16191,094 - 192,557UniSTS
stSG608960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,592 - 278,819UniSTSGRCh37
Build 3616217,593 - 218,820RGDNCBI36
Celera16476,475 - 477,702RGD
HuRef16195,130 - 196,357UniSTS
stSG608962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716280,041 - 281,166UniSTSGRCh37
Build 3616220,042 - 221,167RGDNCBI36
Celera16478,924 - 480,049RGD
Cytogenetic Map16p13.3UniSTS
HuRef16197,579 - 198,704UniSTS
LUC7L__7341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716238,894 - 239,631UniSTSGRCh37
Build 3616178,895 - 179,632RGDNCBI36
Celera16437,784 - 438,521RGD
HuRef16156,460 - 157,197UniSTS
SHGC-60792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3716277,751 - 277,876UniSTSGRCh37
Build 3616217,752 - 217,877RGDNCBI36
Celera16476,634 - 476,759RGD
Cytogenetic Map16p13.3UniSTS
HuRef16195,289 - 195,414UniSTS
GeneMap99-GB4 RH Map1625.71UniSTS
Whitehead-RH Map160.0UniSTS
GDB:434012  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map10p11.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map14q31UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS
D11S3159  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16p13.3UniSTS


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 2410 2395 1640 545 1567 386 4034 1705 3642 320 1428 1565 174 1 1204 2482 5 2
Low 27 596 85 78 384 78 323 492 92 99 32 48 1 306 1
Below cutoff 2 1 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001320226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_201412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522561 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434359 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313457 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AE006462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ404326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX875997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY005111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB105153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ431198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF212273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY095072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z69706 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z69890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z84716 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000293872   ⟹   ENSP00000293872
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,990 - 229,449 (-)Ensembl
RefSeq Acc Id: ENST00000337351   ⟹   ENSP00000337507
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,969 - 229,463 (-)Ensembl
RefSeq Acc Id: ENST00000397780   ⟹   ENSP00000380882
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16189,896 - 227,686 (-)Ensembl
RefSeq Acc Id: ENST00000397783   ⟹   ENSP00000380885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,971 - 229,463 (-)Ensembl
RefSeq Acc Id: ENST00000418978   ⟹   ENSP00000393551
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16190,122 - 229,374 (-)Ensembl
RefSeq Acc Id: ENST00000419516   ⟹   ENSP00000414860
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16189,896 - 229,434 (-)Ensembl
RefSeq Acc Id: ENST00000426094   ⟹   ENSP00000390953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,969 - 229,439 (-)Ensembl
RefSeq Acc Id: ENST00000428363   ⟹   ENSP00000409977
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16220,649 - 228,722 (-)Ensembl
RefSeq Acc Id: ENST00000429378   ⟹   ENSP00000413033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,990 - 206,087 (-)Ensembl
RefSeq Acc Id: ENST00000430864   ⟹   ENSP00000406695
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16190,541 - 229,422 (-)Ensembl
RefSeq Acc Id: ENST00000442701   ⟹   ENSP00000407781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16189,115 - 190,549 (-)Ensembl
RefSeq Acc Id: ENST00000443357   ⟹   ENSP00000414508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16206,004 - 227,656 (-)Ensembl
RefSeq Acc Id: ENST00000464711
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16189,098 - 209,773 (-)Ensembl
RefSeq Acc Id: ENST00000467552
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16228,124 - 228,990 (-)Ensembl
RefSeq Acc Id: ENST00000468732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,990 - 190,595 (-)Ensembl
RefSeq Acc Id: ENST00000469109
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16220,171 - 227,614 (-)Ensembl
RefSeq Acc Id: ENST00000490762
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,990 - 229,451 (-)Ensembl
RefSeq Acc Id: ENST00000494366
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16208,633 - 229,142 (-)Ensembl
RefSeq Acc Id: ENST00000494545
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16228,229 - 229,340 (-)Ensembl
RefSeq Acc Id: ENST00000495349
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16190,001 - 208,508 (-)Ensembl
RefSeq Acc Id: ENST00000629543   ⟹   ENSP00000485761
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl16188,975 - 229,450 (-)Ensembl
RefSeq Acc Id: NM_001320226   ⟹   NP_001307155
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816188,990 - 229,449 (-)NCBI
CHM1_116238,910 - 279,410 (-)NCBI
T2T-CHM13v2.016182,837 - 223,275 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001330420   ⟹   NP_001317349
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816188,990 - 229,449 (-)NCBI
T2T-CHM13v2.016182,837 - 223,275 (-)NCBI
Sequence:
RefSeq Acc Id: NM_018032   ⟹   NP_060502
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816188,990 - 229,449 (-)NCBI
GRCh3716238,970 - 279,449 (-)NCBI
Build 3616178,971 - 219,450 (-)NCBI Archive
Celera16437,860 - 478,332 (-)RGD
HuRef16156,536 - 196,987 (-)ENTREZGENE
CHM1_116238,910 - 279,410 (-)NCBI
T2T-CHM13v2.016182,837 - 223,275 (-)NCBI
Sequence:
RefSeq Acc Id: NM_201412   ⟹   NP_958815
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816188,990 - 229,449 (-)NCBI
GRCh3716238,970 - 279,449 (-)NCBI
Build 3616178,975 - 219,450 (-)NCBI Archive
Celera16437,860 - 478,332 (-)RGD
HuRef16156,536 - 196,987 (-)ENTREZGENE
CHM1_116238,910 - 279,410 (-)NCBI
T2T-CHM13v2.016182,837 - 223,275 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005255427   ⟹   XP_005255484
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816188,990 - 229,449 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011522561   ⟹   XP_011520863
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816188,990 - 229,449 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017023438   ⟹   XP_016878927
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816188,990 - 220,746 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047434359   ⟹   XP_047290315
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816189,931 - 229,449 (-)NCBI
RefSeq Acc Id: XM_054313455   ⟹   XP_054169430
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.016182,837 - 223,275 (-)NCBI
RefSeq Acc Id: XM_054313456   ⟹   XP_054169431
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.016182,837 - 223,275 (-)NCBI
RefSeq Acc Id: XM_054313457   ⟹   XP_054169432
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.016182,837 - 214,584 (-)NCBI
RefSeq Acc Id: XM_054313458   ⟹   XP_054169433
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.016183,778 - 223,275 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001307155 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317349 (Get FASTA)   NCBI Sequence Viewer  
  NP_060502 (Get FASTA)   NCBI Sequence Viewer  
  NP_958815 (Get FASTA)   NCBI Sequence Viewer  
  XP_005255484 (Get FASTA)   NCBI Sequence Viewer  
  XP_011520863 (Get FASTA)   NCBI Sequence Viewer  
  XP_016878927 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290315 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169430 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169431 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169432 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169433 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAG22846 (Get FASTA)   NCBI Sequence Viewer  
  AAH03194 (Get FASTA)   NCBI Sequence Viewer  
  AAH65198 (Get FASTA)   NCBI Sequence Viewer  
  AAK61218 (Get FASTA)   NCBI Sequence Viewer  
  ABD95913 (Get FASTA)   NCBI Sequence Viewer  
  BAA91500 (Get FASTA)   NCBI Sequence Viewer  
  BAD96804 (Get FASTA)   NCBI Sequence Viewer  
  CAB93981 (Get FASTA)   NCBI Sequence Viewer  
  CAB93982 (Get FASTA)   NCBI Sequence Viewer  
  CAE89085 (Get FASTA)   NCBI Sequence Viewer  
  CAM26669 (Get FASTA)   NCBI Sequence Viewer  
  CAM26670 (Get FASTA)   NCBI Sequence Viewer  
  CAM26671 (Get FASTA)   NCBI Sequence Viewer  
  CAM26672 (Get FASTA)   NCBI Sequence Viewer  
  CAX15222 (Get FASTA)   NCBI Sequence Viewer  
  CAX15223 (Get FASTA)   NCBI Sequence Viewer  
  CAX15224 (Get FASTA)   NCBI Sequence Viewer  
  EAW85850 (Get FASTA)   NCBI Sequence Viewer  
  EAW85851 (Get FASTA)   NCBI Sequence Viewer  
  EAW85852 (Get FASTA)   NCBI Sequence Viewer  
  EAW85853 (Get FASTA)   NCBI Sequence Viewer  
  EAW85854 (Get FASTA)   NCBI Sequence Viewer  
  EAW85855 (Get FASTA)   NCBI Sequence Viewer  
  EAW85856 (Get FASTA)   NCBI Sequence Viewer  
  EAW85857 (Get FASTA)   NCBI Sequence Viewer  
  EAW85858 (Get FASTA)   NCBI Sequence Viewer  
  EAW85859 (Get FASTA)   NCBI Sequence Viewer  
  EAW85860 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000293872
  ENSP00000293872.8
  ENSP00000337507
  ENSP00000337507.4
  ENSP00000380882
  ENSP00000380882.1
  ENSP00000380885
  ENSP00000380885.1
  ENSP00000390953.1
  ENSP00000393551.1
  ENSP00000406695.1
  ENSP00000407781.1
  ENSP00000409977.1
  ENSP00000413033.1
  ENSP00000414508.1
  ENSP00000414860.1
  ENSP00000485761.1
GenBank Protein Q9NQ29 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_060502   ⟸   NM_018032
- Peptide Label: isoform a
- UniProtKB: Q1W6G4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_958815   ⟸   NM_201412
- Peptide Label: isoform b
- UniProtKB: Q96S32 (UniProtKB/Swiss-Prot),   B8ZZ13 (UniProtKB/Swiss-Prot),   Q9NPH4 (UniProtKB/Swiss-Prot),   Q9NQ29 (UniProtKB/Swiss-Prot),   Q53G47 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005255484   ⟸   XM_005255427
- Peptide Label: isoform X2
- UniProtKB: Q53G47 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011520863   ⟸   XM_011522561
- Peptide Label: isoform X1
- UniProtKB: Q53G47 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001307155   ⟸   NM_001320226
- Peptide Label: isoform a
- UniProtKB: Q1W6G4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016878927   ⟸   XM_017023438
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: NP_001317349   ⟸   NM_001330420
- Peptide Label: isoform c
- UniProtKB: A8MYV2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000293872   ⟸   ENST00000293872
RefSeq Acc Id: ENSP00000390953   ⟸   ENST00000426094
RefSeq Acc Id: ENSP00000409977   ⟸   ENST00000428363
RefSeq Acc Id: ENSP00000413033   ⟸   ENST00000429378
RefSeq Acc Id: ENSP00000337507   ⟸   ENST00000337351
RefSeq Acc Id: ENSP00000407781   ⟸   ENST00000442701
RefSeq Acc Id: ENSP00000414508   ⟸   ENST00000443357
RefSeq Acc Id: ENSP00000393551   ⟸   ENST00000418978
RefSeq Acc Id: ENSP00000414860   ⟸   ENST00000419516
RefSeq Acc Id: ENSP00000485761   ⟸   ENST00000629543
RefSeq Acc Id: ENSP00000406695   ⟸   ENST00000430864
RefSeq Acc Id: ENSP00000380885   ⟸   ENST00000397783
RefSeq Acc Id: ENSP00000380882   ⟸   ENST00000397780
RefSeq Acc Id: XP_047290315   ⟸   XM_047434359
- Peptide Label: isoform X4
- UniProtKB: A8MYV2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054169430   ⟸   XM_054313455
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054169431   ⟸   XM_054313456
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054169432   ⟸   XM_054313457
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054169433   ⟸   XM_054313458
- Peptide Label: isoform X4
- UniProtKB: A8MYV2 (UniProtKB/TrEMBL)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NQ29-F1-model_v2 AlphaFold Q9NQ29 1-371 view protein structure

Promoters
RGD ID:6793258
Promoter ID:HG_KWN:22579
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000134253,   OTTHUMT00000134254
Position:
Human AssemblyChrPosition (strand)Source
Build 3616180,956 - 181,456 (-)MPROMDB
RGD ID:6793271
Promoter ID:HG_KWN:22582
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000397780,   ENST00000397783,   OTTHUMT00000134237,   OTTHUMT00000134239,   OTTHUMT00000134240,   OTTHUMT00000134242,   OTTHUMT00000134245,   OTTHUMT00000134246,   OTTHUMT00000134248,   OTTHUMT00000134249,   OTTHUMT00000134251,   OTTHUMT00000321073,   OTTHUMT00000321074,   UC002CGD.1,   UC010BQQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 3616219,086 - 219,586 (-)MPROMDB
RGD ID:6852428
Promoter ID:EP74023
Type:initiation region
Name:HS_LUC7L
Description:LUC7-like (S. cerevisiae).
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 3616219,433 - 219,493EPD
RGD ID:7230737
Promoter ID:EPDNEW_H21114
Type:initiation region
Name:LUC7L_1
Description:LUC7 like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3816229,416 - 229,476EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6723 AgrOrtholog
COSMIC LUC7L COSMIC
Ensembl Genes ENSG00000007392 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000293872 ENTREZGENE
  ENST00000293872.13 UniProtKB/Swiss-Prot
  ENST00000337351 ENTREZGENE
  ENST00000337351.8 UniProtKB/Swiss-Prot
  ENST00000397780 ENTREZGENE
  ENST00000397780.5 UniProtKB/TrEMBL
  ENST00000397783 ENTREZGENE
  ENST00000397783.5 UniProtKB/Swiss-Prot
  ENST00000418978.5 UniProtKB/TrEMBL
  ENST00000419516.5 UniProtKB/TrEMBL
  ENST00000426094.5 UniProtKB/TrEMBL
  ENST00000428363.1 UniProtKB/TrEMBL
  ENST00000429378.5 UniProtKB/TrEMBL
  ENST00000430864.5 UniProtKB/TrEMBL
  ENST00000442701.1 UniProtKB/TrEMBL
  ENST00000443357.5 UniProtKB/TrEMBL
  ENST00000490762 ENTREZGENE
  ENST00000629543.2 UniProtKB/TrEMBL
GTEx ENSG00000007392 GTEx
HGNC ID HGNC:6723 ENTREZGENE
Human Proteome Map LUC7L Human Proteome Map
InterPro Luc7-rel UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55692 UniProtKB/Swiss-Prot
NCBI Gene 55692 ENTREZGENE
OMIM 607782 OMIM
PANTHER PTHR12375 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RNA-BINDING PROTEIN LUC7-LIKE 1-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam LUC7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30485 PharmGKB
UniProt A8MYV2 ENTREZGENE, UniProtKB/TrEMBL
  B8ZZ08_HUMAN UniProtKB/TrEMBL
  B8ZZ09_HUMAN UniProtKB/TrEMBL
  B8ZZ10_HUMAN UniProtKB/TrEMBL
  B8ZZ12_HUMAN UniProtKB/TrEMBL
  B8ZZ13 ENTREZGENE
  F2Z322_HUMAN UniProtKB/TrEMBL
  F8WBC1_HUMAN UniProtKB/TrEMBL
  H7C2U4_HUMAN UniProtKB/TrEMBL
  LUC7L_HUMAN UniProtKB/Swiss-Prot
  Q1W6G4 ENTREZGENE, UniProtKB/TrEMBL
  Q53G47 ENTREZGENE, UniProtKB/TrEMBL
  Q96S32 ENTREZGENE
  Q9NPH4 ENTREZGENE
  Q9NQ29 ENTREZGENE
UniProt Secondary B8ZZ13 UniProtKB/Swiss-Prot
  Q96S32 UniProtKB/Swiss-Prot
  Q9NPH4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-28 LUC7L  LUC7 like  LUC7L  LUC7-like  Symbol and/or name change 5135510 APPROVED
2015-06-30 LUC7L  LUC7-like  LUC7L  LUC7-like (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED