YY1AP1 (YY1 associated protein 1) - 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 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
Advanced Search (OLGA)
Gene: YY1AP1 (YY1 associated protein 1) Homo sapiens
Analyze
Symbol: YY1AP1
Name: YY1 associated protein 1
RGD ID: 1605369
HGNC Page HGNC:30935
Description: Predicted to enable transcription coregulator activity. Involved in cell differentiation; cell population proliferation; and regulation of cell cycle. Located in Ino80 complex; fibrillar center; and nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ10875; FLJ13914; GRNG; HCCA1; HCCA2; hepatocellular carcinoma susceptibility protein; hepatocellular carcinoma-associated protein 2; YAP; YY1-associated protein 1; YY1AP
RGD Orthologs
Bonobo
Green Monkey
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
GRCh381155,659,442 - 155,688,996 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1155,659,446 - 155,689,334 (-)EnsemblGRCh38hg38GRCh38
GRCh371155,629,233 - 155,658,787 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361153,895,857 - 153,925,415 (-)NCBINCBI36Build 36hg18NCBI36
Celera1128,702,315 - 128,731,875 (-)NCBICelera
Cytogenetic Map1q22NCBI
HuRef1126,991,183 - 127,020,680 (-)NCBIHuRef
CHM1_11157,024,680 - 157,054,269 (-)NCBICHM1_1
T2T-CHM13v2.01154,798,015 - 154,827,559 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Biological Process

Cellular Component
cytoplasm  (IEA)
fibrillar center  (IDA)
Ino80 complex  (IDA)
nucleolus  (IDA,IEA)
nucleoplasm  (IDA,IEA)
nucleus  (IBA,IDA,IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:11076863   PMID:11230166   PMID:11710830   PMID:11856496   PMID:12118372   PMID:12477932   PMID:14702039   PMID:14744866   PMID:15302935   PMID:15489334   PMID:15489336  
PMID:16189514   PMID:16381901   PMID:16710414   PMID:16713569   PMID:17541814   PMID:17986458   PMID:18029348   PMID:20936779   PMID:21653829   PMID:21873635   PMID:21900206   PMID:21988832  
PMID:23184937   PMID:23769673   PMID:25597408   PMID:26186194   PMID:27939641   PMID:28332498   PMID:28514442   PMID:29117863   PMID:29330849   PMID:30415952   PMID:30556293   PMID:31270375  
PMID:31481532   PMID:31989743   PMID:32296183   PMID:32814053   PMID:32971831   PMID:33155207   PMID:33961781   PMID:33971976   PMID:34808502   PMID:35016035   PMID:35121738   PMID:35140242  
PMID:35914814   PMID:36724073   PMID:38580884   PMID:38777146  


Genomics

Comparative Map Data
YY1AP1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381155,659,442 - 155,688,996 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1155,659,446 - 155,689,334 (-)EnsemblGRCh38hg38GRCh38
GRCh371155,629,233 - 155,658,787 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361153,895,857 - 153,925,415 (-)NCBINCBI36Build 36hg18NCBI36
Celera1128,702,315 - 128,731,875 (-)NCBICelera
Cytogenetic Map1q22NCBI
HuRef1126,991,183 - 127,020,680 (-)NCBIHuRef
CHM1_11157,024,680 - 157,054,269 (-)NCBICHM1_1
T2T-CHM13v2.01154,798,015 - 154,827,559 (-)NCBIT2T-CHM13v2.0
YY1AP1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2194,163,866 - 94,192,895 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1193,895,241 - 93,924,242 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01130,995,949 - 131,024,985 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11134,594,916 - 134,623,590 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1134,594,908 - 134,623,588 (-)Ensemblpanpan1.1panPan2
YY1AP1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Vero_WHO_p1.0NW_0236660387,481,222 - 7,511,931 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in YY1AP1
106 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q22(chr1:155182457-155787428)x3 copy number gain See cases [RCV000051164] Chr1:155182457..155787428 [GRCh38]
Chr1:155154933..155757219 [GRCh37]
Chr1:153421557..154023843 [NCBI36]
Chr1:1q22		 uncertain significance
NM_001198899.1(YY1AP1):c.2199G>A (p.Glu733=) single nucleotide variant Malignant melanoma [RCV000059917] Chr1:155659678 [GRCh38]
Chr1:155629469 [GRCh37]
Chr1:153896093 [NCBI36]
Chr1:1q22		 not provided
NM_139119.3(YY1AP1):c.-151-20_-151-18del microsatellite Grange syndrome [RCV001333874] Chr1:155688219..155688221 [GRCh38]
Chr1:155658010..155658012 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2		 pathogenic
GRCh37/hg19 1q22(chr1:155412745-155755215)x3 copy number gain See cases [RCV000240095] Chr1:155412745..155755215 [GRCh37]
Chr1:1q22		 uncertain significance
Single allele inversion Pediatric metastatic thyroid tumour [RCV000585807] Chr1:154130985..156843877 [GRCh37]
Chr1:1q21.3-23.1		 likely pathogenic
GRCh37/hg19 1q21.3-23.1(chr1:153751465-156660462)x3 copy number gain not provided [RCV000585385] Chr1:153751465..156660462 [GRCh37]
Chr1:1q21.3-23.1		 likely pathogenic
NM_139119.3(YY1AP1):c.1303del (p.Gln435fs) deletion not provided [RCV003221534] Chr1:155660607 [GRCh38]
Chr1:155630398 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1489_1492del (p.Glu498fs) microsatellite Grange syndrome [RCV000417116] Chr1:155660418..155660421 [GRCh38]
Chr1:155630209..155630212 [GRCh37]
Chr1:1q22		 pathogenic
NM_139119.3(YY1AP1):c.1976T>A (p.Leu659Ter) single nucleotide variant Grange syndrome [RCV000417119] Chr1:155659934 [GRCh38]
Chr1:155629725 [GRCh37]
Chr1:1q22		 pathogenic
NM_139119.3(YY1AP1):c.250C>T (p.Gln84Ter) single nucleotide variant Grange syndrome [RCV000417120]|YY1AP1-related disorder [RCV003409584] Chr1:155676622 [GRCh38]
Chr1:155646413 [GRCh37]
Chr1:1q22		 pathogenic|likely pathogenic
NM_139119.3(YY1AP1):c.1987G>T (p.Glu663Ter) single nucleotide variant Grange syndrome [RCV000417123] Chr1:155659923 [GRCh38]
Chr1:155629714 [GRCh37]
Chr1:1q22		 pathogenic
NM_139119.3(YY1AP1):c.310C>T (p.Gln104Ter) single nucleotide variant Grange syndrome [RCV000417115] Chr1:155676562 [GRCh38]
Chr1:155646353 [GRCh37]
Chr1:1q22		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
NM_139119.3(YY1AP1):c.-151-61C>T single nucleotide variant Inborn genetic diseases [RCV003281599] Chr1:155688262 [GRCh38]
Chr1:155658053 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh38/hg38 1q22(chr1:155648847-155715659)x3 copy number gain See cases [RCV000135203] Chr1:155648847..155715659 [GRCh38]
Chr1:155618638..155685450 [GRCh37]
Chr1:153885262..153952074 [NCBI36]
Chr1:1q22		 likely benign
GRCh38/hg38 1q21.3-23.1(chr1:154566501-157624084)x3 copy number gain See cases [RCV000139902] Chr1:154566501..157624084 [GRCh38]
Chr1:154538977..157593874 [GRCh37]
Chr1:152805601..155860498 [NCBI36]
Chr1:1q21.3-23.1		 pathogenic
NM_139119.3(YY1AP1):c.893C>A (p.Thr298Asn) single nucleotide variant Inborn genetic diseases [RCV003286462] Chr1:155661410 [GRCh38]
Chr1:155631201 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.2101A>G (p.Thr701Ala) single nucleotide variant Inborn genetic diseases [RCV003281054] Chr1:155659809 [GRCh38]
Chr1:155629600 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.173C>T (p.Ala58Val) single nucleotide variant Inborn genetic diseases [RCV003243870] Chr1:155676699 [GRCh38]
Chr1:155646490 [GRCh37]
Chr1:1q22		 likely benign
GRCh37/hg19 1q22-23.1(chr1:155636337-158024499)x1 copy number loss not provided [RCV000684658] Chr1:155636337..158024499 [GRCh37]
Chr1:1q22-23.1		 pathogenic
NM_139119.3(YY1AP1):c.583+23T>G single nucleotide variant Grange syndrome [RCV000714955] Chr1:155672537 [GRCh38]
Chr1:155642328 [GRCh37]
Chr1:1q22		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
NM_139119.3(YY1AP1):c.-151-23C>T single nucleotide variant YY1AP1-related disorder [RCV003957998]|not provided [RCV000893576] Chr1:155688224 [GRCh38]
Chr1:155658015 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1719G>A (p.Met573Ile) single nucleotide variant not provided [RCV000961305] Chr1:155660191 [GRCh38]
Chr1:155629982 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.1949A>G (p.Asn650Ser) single nucleotide variant Inborn genetic diseases [RCV003268326] Chr1:155659961 [GRCh38]
Chr1:155629752 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.412-1G>A single nucleotide variant Grange syndrome [RCV000714980] Chr1:155672732 [GRCh38]
Chr1:155642523 [GRCh37]
Chr1:1q22		 pathogenic
GRCh37/hg19 1q22(chr1:155398816-155757026)x3 copy number gain not provided [RCV000684657] Chr1:155398816..155757026 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.702G>A (p.Lys234=) single nucleotide variant not provided [RCV000921082] Chr1:155670346 [GRCh38]
Chr1:155640137 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1158G>A (p.Lys386=) single nucleotide variant not provided [RCV000972367] Chr1:155660752 [GRCh38]
Chr1:155630543 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.1773C>T (p.Ala591=) single nucleotide variant YY1AP1-related disorder [RCV003910372]|not provided [RCV000880492] Chr1:155660137 [GRCh38]
Chr1:155629928 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.-151-84A>G single nucleotide variant not provided [RCV000965567] Chr1:155688285 [GRCh38]
Chr1:155658076 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1405C>G (p.Leu469Val) single nucleotide variant not provided [RCV000963773] Chr1:155660505 [GRCh38]
Chr1:155630296 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.2250T>C (p.Leu750=) single nucleotide variant YY1AP1-related disorder [RCV004751796]|not provided [RCV000900175] Chr1:155659660 [GRCh38]
Chr1:155629451 [GRCh37]
Chr1:1q22		 benign|likely benign
NM_139119.3(YY1AP1):c.1202A>G (p.Lys401Arg) single nucleotide variant Inborn genetic diseases [RCV002539310]|YY1AP1-related disorder [RCV003955850]|not provided [RCV000882542] Chr1:155660708 [GRCh38]
Chr1:155630499 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1269C>T (p.Leu423=) single nucleotide variant not provided [RCV000918335] Chr1:155660641 [GRCh38]
Chr1:155630432 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.-151-126C>T single nucleotide variant not provided [RCV000916074] Chr1:155688327 [GRCh38]
Chr1:155658118 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1461C>T (p.Pro487=) single nucleotide variant not provided [RCV000899805] Chr1:155660449 [GRCh38]
Chr1:155630240 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.-151-68T>C single nucleotide variant Inborn genetic diseases [RCV003353099]|YY1AP1-related disorder [RCV003897967]|not provided [RCV000974162] Chr1:155688269 [GRCh38]
Chr1:155658060 [GRCh37]
Chr1:1q22		 benign|likely benign
NM_139119.3(YY1AP1):c.-60T>C single nucleotide variant not provided [RCV000964162] Chr1:155688110 [GRCh38]
Chr1:155657901 [GRCh37]
Chr1:1q22		 benign|likely benign
NM_139119.3(YY1AP1):c.324+7C>T single nucleotide variant not provided [RCV000892430] Chr1:155676541 [GRCh38]
Chr1:155646332 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1737G>A (p.Ala579=) single nucleotide variant not provided [RCV000892605] Chr1:155660173 [GRCh38]
Chr1:155629964 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.975C>T (p.His325=) single nucleotide variant YY1AP1-related disorder [RCV003968156]|not provided [RCV000893546] Chr1:155661328 [GRCh38]
Chr1:155631119 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.-95G>A single nucleotide variant not provided [RCV000952813] Chr1:155688145 [GRCh38]
Chr1:155657936 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.1149A>G (p.Leu383=) single nucleotide variant YY1AP1-related disorder [RCV003978254]|not provided [RCV000953649] Chr1:155660761 [GRCh38]
Chr1:155630552 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.-30C>T single nucleotide variant not provided [RCV000894004] Chr1:155688080 [GRCh38]
Chr1:155657871 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.1304A>G (p.Gln435Arg) single nucleotide variant not provided [RCV000961306] Chr1:155660606 [GRCh38]
Chr1:155630397 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.1456A>G (p.Met486Val) single nucleotide variant not provided [RCV000962928] Chr1:155660454 [GRCh38]
Chr1:155630245 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.-49T>C single nucleotide variant not provided [RCV000955790] Chr1:155688099 [GRCh38]
Chr1:155657890 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.-151-128_-151-120del microsatellite YY1AP1-related disorder [RCV003932990]|not provided [RCV000911773] Chr1:155688321..155688329 [GRCh38]
Chr1:155658112..155658120 [GRCh37]
Chr1:1q22		 benign
GRCh37/hg19 1q22(chr1:155430631-155638366)x3 copy number gain not provided [RCV002472433] Chr1:155430631..155638366 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q22(chr1:155482007-155638366)x3 copy number gain not provided [RCV001258476] Chr1:155482007..155638366 [GRCh37]
Chr1:1q22		 uncertain significance
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44		 uncertain significance
NM_139119.3(YY1AP1):c.667G>T (p.Val223Leu) single nucleotide variant Inborn genetic diseases [RCV004686020] Chr1:155670381 [GRCh38]
Chr1:155640172 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1192C>T (p.Arg398Cys) single nucleotide variant Grange syndrome [RCV001333872] Chr1:155660718 [GRCh38]
Chr1:155630509 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1951dup (p.Ala651fs) duplication Grange syndrome [RCV001333873] Chr1:155659958..155659959 [GRCh38]
Chr1:155629749..155629750 [GRCh37]
Chr1:1q22		 pathogenic
NM_001198903.1:c.998_1293del deletion Intellectual disability [RCV001526595]   pathogenic
NM_139119.3(YY1AP1):c.-151-100dup duplication not provided [RCV001390772] Chr1:155688300..155688301 [GRCh38]
Chr1:155658091..155658092 [GRCh37]
Chr1:1q22		 pathogenic
NM_139119.3(YY1AP1):c.743del (p.Gly248fs) deletion Grange syndrome [RCV001420675] Chr1:155668763 [GRCh38]
Chr1:155638554 [GRCh37]
Chr1:1q22		 likely pathogenic
NM_139119.3(YY1AP1):c.207del (p.Lys69fs) deletion Grange syndrome [RCV002226948] Chr1:155676665 [GRCh38]
Chr1:155646456 [GRCh37]
Chr1:1q22		 likely pathogenic
NM_139119.3(YY1AP1):c.567A>T (p.Lys189Asn) single nucleotide variant not provided [RCV001756823] Chr1:155672576 [GRCh38]
Chr1:155642367 [GRCh37]
Chr1:1q22		 uncertain significance
NC_000001.10:g.(?_155581953)_(156851434_?)del deletion Charcot-Marie-Tooth disease type 2 [RCV001983077] Chr1:155581953..156851434 [GRCh37]
Chr1:1q22-23.1		 pathogenic
GRCh37/hg19 1q22(chr1:155616264-156059947) copy number loss not specified [RCV002053625] Chr1:155616264..156059947 [GRCh37]
Chr1:1q22		 uncertain significance
NC_000001.10:g.(?_154141761)_(156851434_?)dup duplication Charcot-Marie-Tooth disease type 2 [RCV001990060] Chr1:154141761..156851434 [GRCh37]
Chr1:1q21.3-23.1		 uncertain significance
NC_000001.10:g.(?_149895434)_(156851434_?)dup duplication Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency [RCV001958273]|Congenital neutropenia-myelofibrosis-nephromegaly syndrome [RCV001958271]|Kostmann syndrome [RCV003120769]|MHC class II deficiency [RCV001992607] Chr1:149895434..156851434 [GRCh37]
Chr1:1q21.2-23.1		 uncertain significance
NC_000001.10:g.(?_155581953)_(155880552_?)del deletion Noonan syndrome 8 [RCV003109581]|not provided [RCV003116546] Chr1:155581953..155880552 [GRCh37]
Chr1:1q22		 pathogenic|uncertain significance|no classifications from unflagged records
NM_139119.3(YY1AP1):c.773T>G (p.Leu258Arg) single nucleotide variant Inborn genetic diseases [RCV003242695] Chr1:155668733 [GRCh38]
Chr1:155638524 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.47A>G (p.Asn16Ser) single nucleotide variant Inborn genetic diseases [RCV003281505] Chr1:155679487 [GRCh38]
Chr1:155649278 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1484C>T (p.Pro495Leu) single nucleotide variant Grange syndrome [RCV003148178] Chr1:155660426 [GRCh38]
Chr1:155630217 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q22(chr1:155489474-156196407)x3 copy number gain not provided [RCV002473771] Chr1:155489474..156196407 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-27C>T single nucleotide variant not provided [RCV002306392] Chr1:155688077 [GRCh38]
Chr1:155657868 [GRCh37]
Chr1:1q22		 likely pathogenic
NM_139119.3(YY1AP1):c.1939G>A (p.Asp647Asn) single nucleotide variant Inborn genetic diseases [RCV002861176] Chr1:155659971 [GRCh38]
Chr1:155629762 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.986T>C (p.Phe329Ser) single nucleotide variant Inborn genetic diseases [RCV002748873] Chr1:155661317 [GRCh38]
Chr1:155631108 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-122C>T single nucleotide variant Inborn genetic diseases [RCV002687072] Chr1:155688323 [GRCh38]
Chr1:155658114 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.2095C>T (p.Arg699Cys) single nucleotide variant Inborn genetic diseases [RCV002864287] Chr1:155659815 [GRCh38]
Chr1:155629606 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.976C>T (p.Arg326Trp) single nucleotide variant Inborn genetic diseases [RCV002683577] Chr1:155661327 [GRCh38]
Chr1:155631118 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-152+213A>G single nucleotide variant Inborn genetic diseases [RCV002774519] Chr1:155688446 [GRCh38]
Chr1:155658237 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.2179T>A (p.Ser727Thr) single nucleotide variant Inborn genetic diseases [RCV002733915] Chr1:155659731 [GRCh38]
Chr1:155629522 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-141C>T single nucleotide variant Inborn genetic diseases [RCV002945119] Chr1:155688191 [GRCh38]
Chr1:155657982 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1426A>C (p.Ser476Arg) single nucleotide variant Inborn genetic diseases [RCV002844894] Chr1:155660484 [GRCh38]
Chr1:155630275 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.38G>T (p.Gly13Val) single nucleotide variant Inborn genetic diseases [RCV002924803] Chr1:155679496 [GRCh38]
Chr1:155649287 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-58C>T single nucleotide variant Inborn genetic diseases [RCV002980931] Chr1:155688259 [GRCh38]
Chr1:155658050 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1909A>G (p.Met637Val) single nucleotide variant Inborn genetic diseases [RCV002759371] Chr1:155660001 [GRCh38]
Chr1:155629792 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.260A>C (p.Glu87Ala) single nucleotide variant Inborn genetic diseases [RCV002950753] Chr1:155676612 [GRCh38]
Chr1:155646403 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.225G>C (p.Gln75His) single nucleotide variant Inborn genetic diseases [RCV002981911] Chr1:155676647 [GRCh38]
Chr1:155646438 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.872T>C (p.Ile291Thr) single nucleotide variant Inborn genetic diseases [RCV002713180] Chr1:155668634 [GRCh38]
Chr1:155638425 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1460C>G (p.Pro487Arg) single nucleotide variant Inborn genetic diseases [RCV002763131] Chr1:155660450 [GRCh38]
Chr1:155630241 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.575A>G (p.Lys192Arg) single nucleotide variant Inborn genetic diseases [RCV002850465] Chr1:155672568 [GRCh38]
Chr1:155642359 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-43T>A single nucleotide variant not provided [RCV002966241] Chr1:155688244 [GRCh38]
Chr1:155658035 [GRCh37]
Chr1:1q22		 pathogenic
NM_139119.3(YY1AP1):c.1136G>A (p.Arg379Gln) single nucleotide variant Inborn genetic diseases [RCV002935434] Chr1:155660774 [GRCh38]
Chr1:155630565 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-90C>T single nucleotide variant Inborn genetic diseases [RCV003008804] Chr1:155688140 [GRCh38]
Chr1:155657931 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-185G>A single nucleotide variant Inborn genetic diseases [RCV002896105]|not provided [RCV004691525] Chr1:155688386 [GRCh38]
Chr1:155658177 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-206G>A single nucleotide variant Inborn genetic diseases [RCV003214276] Chr1:155688407 [GRCh38]
Chr1:155658198 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.596C>A (p.Pro199His) single nucleotide variant Inborn genetic diseases [RCV003220365] Chr1:155670452 [GRCh38]
Chr1:155640243 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1823T>C (p.Leu608Pro) single nucleotide variant Inborn genetic diseases [RCV003203146] Chr1:155660087 [GRCh38]
Chr1:155629878 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-20C>T single nucleotide variant Inborn genetic diseases [RCV003309060] Chr1:155688221 [GRCh38]
Chr1:155658012 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1643T>C (p.Ile548Thr) single nucleotide variant Inborn genetic diseases [RCV003262448] Chr1:155660267 [GRCh38]
Chr1:155630058 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.2095C>A (p.Arg699Ser) single nucleotide variant Inborn genetic diseases [RCV003309946] Chr1:155659815 [GRCh38]
Chr1:155629606 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q12-23.1(chr1:142535935-157648813)x3 copy number gain Chromosome 1q21.1 duplication syndrome [RCV003329522] Chr1:142535935..157648813 [GRCh37]
Chr1:1q12-23.1		 pathogenic
NM_139119.3(YY1AP1):c.1061A>G (p.Asn354Ser) single nucleotide variant Inborn genetic diseases [RCV003369479] Chr1:155660849 [GRCh38]
Chr1:155630640 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.442A>G (p.Ile148Val) single nucleotide variant Inborn genetic diseases [RCV003385276] Chr1:155672701 [GRCh38]
Chr1:155642492 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.729T>G (p.Asn243Lys) single nucleotide variant Inborn genetic diseases [RCV003347646] Chr1:155668777 [GRCh38]
Chr1:155638568 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q22(chr1:155587741-155728855)x1 copy number loss not provided [RCV003483405] Chr1:155587741..155728855 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1755C>T (p.Pro585=) single nucleotide variant not provided [RCV003456667] Chr1:155660155 [GRCh38]
Chr1:155629946 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.384G>A (p.Pro128=) single nucleotide variant not provided [RCV003566429] Chr1:155675037 [GRCh38]
Chr1:155644828 [GRCh37]
Chr1:1q22		 likely benign
GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3 copy number gain not specified [RCV003986717] Chr1:144368497..158992086 [GRCh37]
Chr1:1q21.1-23.1		 pathogenic
GRCh37/hg19 1q21.3-23.1(chr1:154302443-156868186)x1 copy number loss not specified [RCV003986928] Chr1:154302443..156868186 [GRCh37]
Chr1:1q21.3-23.1		 pathogenic
GRCh37/hg19 1q21.1-23.1(chr1:146577511-157155587)x3 copy number gain not specified [RCV003987261] Chr1:146577511..157155587 [GRCh37]
Chr1:1q21.1-23.1		 pathogenic
NM_139119.3(YY1AP1):c.-151-186A>G single nucleotide variant YY1AP1-related disorder [RCV003969632] Chr1:155688387 [GRCh38]
Chr1:155658178 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.2073A>G (p.Gly691=) single nucleotide variant YY1AP1-related disorder [RCV003966935] Chr1:155659837 [GRCh38]
Chr1:155629628 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.-145T>A single nucleotide variant YY1AP1-related disorder [RCV003961919] Chr1:155688195 [GRCh38]
Chr1:155657986 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1483_1484dup (p.Ser497fs) duplication Grange syndrome [RCV003990953] Chr1:155660425..155660426 [GRCh38]
Chr1:155630216..155630217 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.405A>G (p.Ile135Met) single nucleotide variant not provided [RCV004555107] Chr1:155675016 [GRCh38]
Chr1:155644807 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.457C>G (p.Gln153Glu) single nucleotide variant Inborn genetic diseases [RCV004478569] Chr1:155672686 [GRCh38]
Chr1:155642477 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q22(chr1:155381014-155746362)x3 copy number gain not provided [RCV000845969] Chr1:155381014..155746362 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q22(chr1:155536092-155657052)x1 copy number loss not provided [RCV000848133] Chr1:155536092..155657052 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.2053G>A (p.Asp685Asn) single nucleotide variant Inborn genetic diseases [RCV003251428] Chr1:155659857 [GRCh38]
Chr1:155629648 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q22(chr1:155426829-155644583)x3 copy number gain not provided [RCV001258475] Chr1:155426829..155644583 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-59C>T single nucleotide variant Inborn genetic diseases [RCV004686018] Chr1:155688109 [GRCh38]
Chr1:155657900 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.374A>G (p.Asn125Ser) single nucleotide variant Inborn genetic diseases [RCV004686019] Chr1:155675047 [GRCh38]
Chr1:155644838 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.403A>G (p.Ile135Val) single nucleotide variant not provided [RCV001763659] Chr1:155675018 [GRCh38]
Chr1:155644809 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.2087G>A (p.Ser696Asn) single nucleotide variant Inborn genetic diseases [RCV003196843] Chr1:155659823 [GRCh38]
Chr1:155629614 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1762A>G (p.Ile588Val) single nucleotide variant Inborn genetic diseases [RCV003359660] Chr1:155660148 [GRCh38]
Chr1:155629939 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.822A>C (p.Gln274His) single nucleotide variant Inborn genetic diseases [RCV003359974] Chr1:155668684 [GRCh38]
Chr1:155638475 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.433C>G (p.Gln145Glu) single nucleotide variant Inborn genetic diseases [RCV003367427] Chr1:155672710 [GRCh38]
Chr1:155642501 [GRCh37]
Chr1:1q22		 uncertain significance
GRCh37/hg19 1q22(chr1:155426830-155708996)x3 copy number gain not provided [RCV003484042] Chr1:155426830..155708996 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-21+1G>T single nucleotide variant Grange syndrome [RCV003990551] Chr1:155688070 [GRCh38]
Chr1:155657861 [GRCh37]
Chr1:1q22		 likely pathogenic
NM_139119.3(YY1AP1):c.-151-161G>C single nucleotide variant Inborn genetic diseases [RCV004478551] Chr1:155688362 [GRCh38]
Chr1:155658153 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.818G>A (p.Arg273His) single nucleotide variant Inborn genetic diseases [RCV004478552] Chr1:155668688 [GRCh38]
Chr1:155638479 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1028G>A (p.Arg343Gln) single nucleotide variant Inborn genetic diseases [RCV004478553] Chr1:155660882 [GRCh38]
Chr1:155630673 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.1135C>T (p.Arg379Trp) single nucleotide variant Inborn genetic diseases [RCV004478554] Chr1:155660775 [GRCh38]
Chr1:155630566 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-91C>A single nucleotide variant Inborn genetic diseases [RCV004478555] Chr1:155688292 [GRCh38]
Chr1:155658083 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1339G>A (p.Val447Met) single nucleotide variant Inborn genetic diseases [RCV004478556] Chr1:155660571 [GRCh38]
Chr1:155630362 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.-151-89A>G single nucleotide variant Inborn genetic diseases [RCV004478557] Chr1:155688290 [GRCh38]
Chr1:155658081 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1349T>C (p.Ile450Thr) single nucleotide variant Inborn genetic diseases [RCV004478558] Chr1:155660561 [GRCh38]
Chr1:155630352 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1417G>A (p.Gly473Arg) single nucleotide variant Inborn genetic diseases [RCV004478559] Chr1:155660493 [GRCh38]
Chr1:155630284 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1528A>G (p.Lys510Glu) single nucleotide variant Inborn genetic diseases [RCV004478560] Chr1:155660382 [GRCh38]
Chr1:155630173 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1582C>T (p.Arg528Trp) single nucleotide variant Inborn genetic diseases [RCV004478561] Chr1:155660328 [GRCh38]
Chr1:155630119 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1708G>A (p.Gly570Ser) single nucleotide variant Inborn genetic diseases [RCV004478562] Chr1:155660202 [GRCh38]
Chr1:155629993 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1733A>G (p.Asn578Ser) single nucleotide variant Inborn genetic diseases [RCV004478563] Chr1:155660177 [GRCh38]
Chr1:155629968 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.-151-38C>T single nucleotide variant Inborn genetic diseases [RCV004478564] Chr1:155688239 [GRCh38]
Chr1:155658030 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139121.3(YY1AP1):c.-420T>A single nucleotide variant not specified [RCV004018138] Chr1:155688975 [GRCh38]
Chr1:155658766 [GRCh37]
Chr1:1q22		 benign
NM_139119.3(YY1AP1):c.-151-34A>G single nucleotide variant Inborn genetic diseases [RCV004478565] Chr1:155688235 [GRCh38]
Chr1:155658026 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.2179T>C (p.Ser727Pro) single nucleotide variant Inborn genetic diseases [RCV004478566] Chr1:155659731 [GRCh38]
Chr1:155629522 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.58G>C (p.Asp20His) single nucleotide variant Inborn genetic diseases [RCV004478567] Chr1:155679476 [GRCh38]
Chr1:155649267 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.310C>G (p.Gln104Glu) single nucleotide variant Inborn genetic diseases [RCV004478568] Chr1:155676562 [GRCh38]
Chr1:155646353 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1217A>G (p.Gln406Arg) single nucleotide variant Inborn genetic diseases [RCV004686017] Chr1:155660693 [GRCh38]
Chr1:155630484 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.923G>C (p.Cys308Ser) single nucleotide variant Grange syndrome [RCV004595122] Chr1:155661380 [GRCh38]
Chr1:155631171 [GRCh37]
Chr1:1q22		 uncertain significance
NM_139119.3(YY1AP1):c.1453G>A (p.Ala485Thr) single nucleotide variant YY1AP1-related disorder [RCV004752241] Chr1:155660457 [GRCh38]
Chr1:155630248 [GRCh37]
Chr1:1q22		 likely benign
NM_139119.3(YY1AP1):c.977G>A (p.Arg326Gln) single nucleotide variant Inborn genetic diseases [RCV004686016] Chr1:155661326 [GRCh38]
Chr1:155631117 [GRCh37]
Chr1:1q22		 uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR375hsa-miR-375Mirtarbaseexternal_infoLuciferase reporter assay//Western blotFunctional MTI20226166

Predicted Target Of
Summary Value
Count of predictions:7424
Count of miRNA genes:1119
Interacting mature miRNAs:1362
Transcripts:ENST00000295566, ENST00000311573, ENST00000347088, ENST00000354691, ENST00000355499, ENST00000359205, ENST00000361140, ENST00000361831, ENST00000368330, ENST00000368339, ENST00000368340, ENST00000404643, ENST00000405763, ENST00000407221, ENST00000436865, ENST00000438245, ENST00000442834, ENST00000443231, ENST00000454523, ENST00000466366, ENST00000476027, ENST00000476093, ENST00000477470, ENST00000488784, ENST00000493625, ENST00000496324, ENST00000535662
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1357381BW57_HBody weight QTL 57 (human)10.0001Body weightfat free mass after exercise training1140630236166630236Human
407340068GWAS989044_Hserum urea measurement QTL GWAS989044 (human)2e-10serum urea measurementserum urea level (CMO:0003877)1155670324155670325Human
406997338GWAS646314_Hbody height QTL GWAS646314 (human)3e-11body height (VT:0001253)body height (CMO:0000106)1155670324155670325Human
407069771GWAS718747_Htestosterone measurement QTL GWAS718747 (human)1e-08testosterone measurementserum testosterone level (CMO:0000568)1155670324155670325Human
406996284GWAS645260_Htestosterone measurement QTL GWAS645260 (human)2e-08testosterone measurementserum testosterone level (CMO:0000568)1155670324155670325Human
407326473GWAS975449_Hserum gamma-glutamyl transferase measurement QTL GWAS975449 (human)3e-12serum gamma-glutamyl transferase measurementserum gamma-glutamyltransferase activity level (CMO:0002241)1155670324155670325Human

Markers in Region
RH104507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371155,629,294 - 155,629,447UniSTSGRCh37
Build 361153,895,918 - 153,896,071RGDNCBI36
Celera1128,702,376 - 128,702,529RGD
Cytogenetic Map1q22UniSTS
HuRef1126,991,244 - 126,991,397UniSTS
GeneMap99-GB4 RH Map1552.19UniSTS
D1S2539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371155,638,131 - 155,638,330UniSTSGRCh37
Build 361153,904,755 - 153,904,954RGDNCBI36
Celera1128,711,216 - 128,711,415RGD
Cytogenetic Map1q22UniSTS
HuRef1127,000,081 - 127,000,280UniSTS
YAP_v447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371155,629,253 - 155,629,924UniSTSGRCh37
Build 361153,895,877 - 153,896,548RGDNCBI36
Celera1128,702,335 - 128,703,006RGD
HuRef1126,991,203 - 126,991,874UniSTS
D1S1799E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371155,629,407 - 155,629,494UniSTSGRCh37
Build 361153,896,031 - 153,896,118RGDNCBI36
Celera1128,702,489 - 128,702,576RGD
Cytogenetic Map1q22UniSTS
HuRef1126,991,357 - 126,991,444UniSTS
GeneMap99-GB4 RH Map1553.86UniSTS
NCBI RH Map11217.3UniSTS
RH15932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371155,629,310 - 155,629,436UniSTSGRCh37
Build 361153,895,934 - 153,896,060RGDNCBI36
Celera1128,702,392 - 128,702,518RGD
Cytogenetic Map1q22UniSTS
HuRef1126,991,260 - 126,991,386UniSTS
GeneMap99-GB4 RH Map1553.86UniSTS
NCBI RH Map11217.3UniSTS
RH12294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371155,630,757 - 155,630,865UniSTSGRCh37
Build 361153,897,381 - 153,897,489RGDNCBI36
Celera1128,703,839 - 128,703,947RGD
Cytogenetic Map1q22UniSTS
HuRef1126,992,707 - 126,992,815UniSTS
GeneMap99-GB4 RH Map1553.86UniSTS
NCBI RH Map11217.3UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2438 2788 2253 4974 1726 2351 6 624 1951 465 2270 7305 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001198899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_139118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_139119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_139121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF203474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF206328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF466401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023976 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303944 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315049 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY604179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001655 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008766 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009358 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC025272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC044887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG325066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX088689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC300265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC346197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC388975 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC399389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC406177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OP794508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000295566   ⟹   ENSP00000295566
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,689,000 (-)Ensembl
Ensembl Acc Id: ENST00000311573   ⟹   ENSP00000311138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,294 (-)Ensembl
Ensembl Acc Id: ENST00000347088   ⟹   ENSP00000316079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,698 (-)Ensembl
Ensembl Acc Id: ENST00000354691   ⟹   ENSP00000346722
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,686 (-)Ensembl
Ensembl Acc Id: ENST00000355499   ⟹   ENSP00000347686
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,454 - 155,688,774 (-)Ensembl
Ensembl Acc Id: ENST00000359205   ⟹   ENSP00000352134
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,774 (-)Ensembl
Ensembl Acc Id: ENST00000361140   ⟹   ENSP00000354716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,748 (-)Ensembl
Ensembl Acc Id: ENST00000361831   ⟹   ENSP00000355298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,705 (-)Ensembl
Ensembl Acc Id: ENST00000368330   ⟹   ENSP00000357314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,689,000 (-)Ensembl
Ensembl Acc Id: ENST00000368339   ⟹   ENSP00000357323
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,455 - 155,688,660 (-)Ensembl
Ensembl Acc Id: ENST00000368340   ⟹   ENSP00000357324
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,670 (-)Ensembl
Ensembl Acc Id: ENST00000404643   ⟹   ENSP00000385390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,757 (-)Ensembl
Ensembl Acc Id: ENST00000405763   ⟹   ENSP00000384583
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,660,717 - 155,688,475 (-)Ensembl
Ensembl Acc Id: ENST00000407221   ⟹   ENSP00000385791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,774 (-)Ensembl
Ensembl Acc Id: ENST00000436865   ⟹   ENSP00000390116
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,688,973 (-)Ensembl
Ensembl Acc Id: ENST00000442834
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,446 - 155,671,091 (-)Ensembl
Ensembl Acc Id: ENST00000443231   ⟹   ENSP00000409203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,454 - 155,688,669 (-)Ensembl
Ensembl Acc Id: ENST00000454523   ⟹   ENSP00000413240
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,467 - 155,688,660 (-)Ensembl
Ensembl Acc Id: ENST00000466366
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,454 - 155,688,693 (-)Ensembl
Ensembl Acc Id: ENST00000476027
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,718 (-)Ensembl
Ensembl Acc Id: ENST00000476093
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,670,324 - 155,688,975 (-)Ensembl
Ensembl Acc Id: ENST00000477470
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,496 - 155,688,687 (-)Ensembl
Ensembl Acc Id: ENST00000488784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,709 (-)Ensembl
Ensembl Acc Id: ENST00000493625
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,660,831 - 155,680,427 (-)Ensembl
Ensembl Acc Id: ENST00000496324
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,672,362 - 155,680,456 (-)Ensembl
Ensembl Acc Id: ENST00000714536   ⟹   ENSP00000519777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,469 - 155,688,698 (-)Ensembl
Ensembl Acc Id: ENST00000714537   ⟹   ENSP00000519778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,477 - 155,688,676 (-)Ensembl
Ensembl Acc Id: ENST00000714538   ⟹   ENSP00000519779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,477 - 155,688,692 (-)Ensembl
Ensembl Acc Id: ENST00000714539   ⟹   ENSP00000519781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,492 - 155,688,652 (-)Ensembl
Ensembl Acc Id: ENST00000714548   ⟹   ENSP00000519793
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,461 - 155,688,715 (-)Ensembl
Ensembl Acc Id: ENST00000714549   ⟹   ENSP00000519794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,469 - 155,688,721 (-)Ensembl
Ensembl Acc Id: ENST00000714550   ⟹   ENSP00000519795
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,987 (-)Ensembl
Ensembl Acc Id: ENST00000714551   ⟹   ENSP00000519796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,671,737 - 155,688,717 (-)Ensembl
Ensembl Acc Id: ENST00000714552   ⟹   ENSP00000519797
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,671,739 - 155,688,708 (-)Ensembl
Ensembl Acc Id: ENST00000714707   ⟹   ENSP00000519936
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,454 - 155,688,712 (-)Ensembl
Ensembl Acc Id: ENST00000714708   ⟹   ENSP00000519937
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,469 - 155,688,695 (-)Ensembl
Ensembl Acc Id: ENST00000714709   ⟹   ENSP00000519938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,471 - 155,688,670 (-)Ensembl
Ensembl Acc Id: ENST00000714710   ⟹   ENSP00000519939
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,476 - 155,688,710 (-)Ensembl
Ensembl Acc Id: ENST00000714711   ⟹   ENSP00000519940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,697 (-)Ensembl
Ensembl Acc Id: ENST00000714712   ⟹   ENSP00000519941
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,722 (-)Ensembl
Ensembl Acc Id: ENST00000714713   ⟹   ENSP00000519942
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,575 - 155,688,698 (-)Ensembl
Ensembl Acc Id: ENST00000714714   ⟹   ENSP00000519943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,660,689 - 155,688,670 (-)Ensembl
Ensembl Acc Id: ENST00000714786   ⟹   ENSP00000519994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,469 - 155,688,668 (-)Ensembl
Ensembl Acc Id: ENST00000714787   ⟹   ENSP00000519995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,491 - 155,688,656 (-)Ensembl
Ensembl Acc Id: ENST00000714788   ⟹   ENSP00000519996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,494 - 155,688,670 (-)Ensembl
Ensembl Acc Id: ENST00000714789   ⟹   ENSP00000519997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,499 - 155,688,670 (-)Ensembl
Ensembl Acc Id: ENST00000714790   ⟹   ENSP00000519998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,503 - 155,688,710 (-)Ensembl
Ensembl Acc Id: ENST00000714791   ⟹   ENSP00000519999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,589 - 155,688,668 (-)Ensembl
Ensembl Acc Id: ENST00000714830   ⟹   ENSP00000520031
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,469 - 155,688,703 (-)Ensembl
Ensembl Acc Id: ENST00000714831   ⟹   ENSP00000520032
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,620 (-)Ensembl
Ensembl Acc Id: ENST00000714832   ⟹   ENSP00000520033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,496 - 155,688,700 (-)Ensembl
Ensembl Acc Id: ENST00000714833   ⟹   ENSP00000520034
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,671,737 - 155,688,703 (-)Ensembl
Ensembl Acc Id: ENST00000715137   ⟹   ENSP00000520338
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,469 - 155,688,703 (-)Ensembl
Ensembl Acc Id: ENST00000715138   ⟹   ENSP00000520339
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,474 - 155,688,985 (-)Ensembl
Ensembl Acc Id: ENST00000715139   ⟹   ENSP00000520340
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,480 - 155,688,699 (-)Ensembl
Ensembl Acc Id: ENST00000715140   ⟹   ENSP00000520341
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,685 (-)Ensembl
Ensembl Acc Id: ENST00000715141   ⟹   ENSP00000520342
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,703 (-)Ensembl
Ensembl Acc Id: ENST00000715142   ⟹   ENSP00000520343
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,482 - 155,688,774 (-)Ensembl
Ensembl Acc Id: ENST00000715143   ⟹   ENSP00000520344
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,498 - 155,688,709 (-)Ensembl
Ensembl Acc Id: ENST00000715144   ⟹   ENSP00000520345
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,501 - 155,688,670 (-)Ensembl
Ensembl Acc Id: ENST00000715145   ⟹   ENSP00000520346
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,501 - 155,688,699 (-)Ensembl
Ensembl Acc Id: ENST00000715146   ⟹   ENSP00000520347
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,501 - 155,689,334 (-)Ensembl
Ensembl Acc Id: ENST00000715147   ⟹   ENSP00000520348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,505 - 155,688,718 (-)Ensembl
Ensembl Acc Id: ENST00000715169   ⟹   ENSP00000520365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,448 - 155,688,755 (-)Ensembl
Ensembl Acc Id: ENST00000715170   ⟹   ENSP00000520366
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,454 - 155,688,754 (-)Ensembl
Ensembl Acc Id: ENST00000715171   ⟹   ENSP00000520367
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,456 - 155,688,670 (-)Ensembl
Ensembl Acc Id: ENST00000715172   ⟹   ENSP00000520368
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,456 - 155,688,713 (-)Ensembl
Ensembl Acc Id: ENST00000715173   ⟹   ENSP00000520369
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1155,659,493 - 155,688,755 (-)Ensembl
RefSeq Acc Id: NM_001198899   ⟹   NP_001185828
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,679,829 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,045,055 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,818,394 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198900   ⟹   NP_001185829
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,774 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,014 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,337 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198901   ⟹   NP_001185830
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,996 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,265 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,559 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198902   ⟹   NP_001185831
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,774 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,053,961 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,337 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198903   ⟹   NP_001185832
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,442 - 155,688,656 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,053,893 (-)NCBI
T2T-CHM13v2.01154,798,015 - 154,827,219 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198904   ⟹   NP_001185833
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,442 - 155,688,656 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,053,893 (-)NCBI
T2T-CHM13v2.01154,798,015 - 154,827,219 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198905   ⟹   NP_001185834
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,774 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,014 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,337 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198906   ⟹   NP_001185835
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,996 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,269 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,559 (-)NCBI
Sequence:
RefSeq Acc Id: NM_018253   ⟹   NP_060723
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,774 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,014 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,337 (-)NCBI
Sequence:
RefSeq Acc Id: NM_139118   ⟹   NP_620829
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,996 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)NCBI
Build 361153,895,870 - 153,925,415 (-)NCBI Archive
Celera1128,702,315 - 128,731,875 (-)RGD
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,269 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,559 (-)NCBI
Sequence:
RefSeq Acc Id: NM_139119   ⟹   NP_620830
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,774 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
GRCh371155,629,233 - 155,658,823 (-)NCBI
Build 361153,895,857 - 153,925,189 (-)NCBI Archive
Celera1128,702,315 - 128,731,875 (-)RGD
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,011 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,337 (-)NCBI
Sequence:
RefSeq Acc Id: NM_139121   ⟹   NP_620832
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,659,454 - 155,688,996 (-)NCBI
GRCh371155,629,233 - 155,658,823 (-)ENTREZGENE
HuRef1126,991,183 - 127,020,680 (-)ENTREZGENE
CHM1_11157,024,680 - 157,054,210 (-)NCBI
T2T-CHM13v2.01154,798,027 - 154,827,559 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001185828 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185829 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185830 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185831 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185832 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185833 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185834 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185835 (Get FASTA)   NCBI Sequence Viewer  
  NP_060723 (Get FASTA)   NCBI Sequence Viewer  
  NP_620829 (Get FASTA)   NCBI Sequence Viewer  
  NP_620830 (Get FASTA)   NCBI Sequence Viewer  
  NP_620832 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH01655 (Get FASTA)   NCBI Sequence Viewer  
  AAH01843 (Get FASTA)   NCBI Sequence Viewer  
  AAH08766 (Get FASTA)   NCBI Sequence Viewer  
  AAH09358 (Get FASTA)   NCBI Sequence Viewer  
  AAH14906 (Get FASTA)   NCBI Sequence Viewer  
  AAH44887 (Get FASTA)   NCBI Sequence Viewer  
  AAL74055 (Get FASTA)   NCBI Sequence Viewer  
  AAL75971 (Get FASTA)   NCBI Sequence Viewer  
  AAO13249 (Get FASTA)   NCBI Sequence Viewer  
  AAT34990 (Get FASTA)   NCBI Sequence Viewer  
  BAA91871 (Get FASTA)   NCBI Sequence Viewer  
  BAB14748 (Get FASTA)   NCBI Sequence Viewer  
  BAG59954 (Get FASTA)   NCBI Sequence Viewer  
  BAG61012 (Get FASTA)   NCBI Sequence Viewer  
  BAG64166 (Get FASTA)   NCBI Sequence Viewer  
  BAG64442 (Get FASTA)   NCBI Sequence Viewer  
  BAG64872 (Get FASTA)   NCBI Sequence Viewer  
  CAH18650 (Get FASTA)   NCBI Sequence Viewer  
  EAW53052 (Get FASTA)   NCBI Sequence Viewer  
  EAW53053 (Get FASTA)   NCBI Sequence Viewer  
  EAW53054 (Get FASTA)   NCBI Sequence Viewer  
  EAW53055 (Get FASTA)   NCBI Sequence Viewer  
  EAW53056 (Get FASTA)   NCBI Sequence Viewer  
  EAW53057 (Get FASTA)   NCBI Sequence Viewer  
  EAW53058 (Get FASTA)   NCBI Sequence Viewer  
  EAW53059 (Get FASTA)   NCBI Sequence Viewer  
  EAW53060 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000295566
  ENSP00000295566.4
  ENSP00000311138.5
  ENSP00000316079
  ENSP00000316079.6
  ENSP00000346722.5
  ENSP00000347686
  ENSP00000347686.4
  ENSP00000352134
  ENSP00000352134.5
  ENSP00000354716.4
  ENSP00000355298
  ENSP00000355298.5
  ENSP00000357314
  ENSP00000357314.2
  ENSP00000357323
  ENSP00000357323.5
  ENSP00000357324
  ENSP00000357324.5
  ENSP00000384583.3
  ENSP00000385390
  ENSP00000385390.1
  ENSP00000385791.1
  ENSP00000390116.1
  ENSP00000409203.2
  ENSP00000413240.2
  ENSP00000519776.1
  ENSP00000519777.1
  ENSP00000519778.1
  ENSP00000519779.1
  ENSP00000519780.1
  ENSP00000519781.1
  ENSP00000519791.1
  ENSP00000519792.1
  ENSP00000519793.1
  ENSP00000519794.1
  ENSP00000519795.1
  ENSP00000519796.1
  ENSP00000519797.1
  ENSP00000519936.1
  ENSP00000519937.1
  ENSP00000519938.1
  ENSP00000519939.1
  ENSP00000519940.1
  ENSP00000519941.1
  ENSP00000519943.1
  ENSP00000519994.1
  ENSP00000519996.1
  ENSP00000519997.1
  ENSP00000519999.1
  ENSP00000520031.1
  ENSP00000520033.1
  ENSP00000520034.1
  ENSP00000520338.1
  ENSP00000520339.1
  ENSP00000520340.1
  ENSP00000520341.1
  ENSP00000520342.1
  ENSP00000520343.1
  ENSP00000520344.1
  ENSP00000520345.1
  ENSP00000520346.1
  ENSP00000520347.1
  ENSP00000520348.1
  ENSP00000520367.1
  ENSP00000520368.1
  ENSP00000520369.1
GenBank Protein Q9H869 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_620829   ⟸   NM_139118
- Peptide Label: isoform 2
- UniProtKB: Q9BQ64 (UniProtKB/Swiss-Prot),   Q96HB6 (UniProtKB/Swiss-Prot),   Q8TF04 (UniProtKB/Swiss-Prot),   Q8TEW5 (UniProtKB/Swiss-Prot),   Q8IXA6 (UniProtKB/Swiss-Prot),   Q7L5E2 (UniProtKB/Swiss-Prot),   Q7L4C3 (UniProtKB/Swiss-Prot),   Q5VYZ7 (UniProtKB/Swiss-Prot),   Q5VYZ4 (UniProtKB/Swiss-Prot),   Q5VYZ1 (UniProtKB/Swiss-Prot),   H7BY62 (UniProtKB/Swiss-Prot),   D3DV98 (UniProtKB/Swiss-Prot),   D3DV96 (UniProtKB/Swiss-Prot),   B4E0I0 (UniProtKB/Swiss-Prot),   B4DMP2 (UniProtKB/Swiss-Prot),   B0QZ54 (UniProtKB/Swiss-Prot),   Q9NV84 (UniProtKB/Swiss-Prot),   Q9H869 (UniProtKB/Swiss-Prot),   A0AAQ5BIA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_620830   ⟸   NM_139119
- Peptide Label: isoform 3
- UniProtKB: I6L9C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185835   ⟸   NM_001198906
- Peptide Label: isoform 9
- UniProtKB: B4DQQ0 (UniProtKB/TrEMBL),   A0AAQ5BI93 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185830   ⟸   NM_001198901
- Peptide Label: isoform 3
- UniProtKB: I6L9C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_620832   ⟸   NM_139121
- Peptide Label: isoform 5
- UniProtKB: I6L9C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185829   ⟸   NM_001198900
- Peptide Label: isoform 1
- UniProtKB: I6L9C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185834   ⟸   NM_001198905
- Peptide Label: isoform 8
- UniProtKB: A0AAQ5BI56 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_060723   ⟸   NM_018253
- Peptide Label: isoform 1
- UniProtKB: I6L9C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185831   ⟸   NM_001198902
- Peptide Label: isoform 3
- UniProtKB: I6L9C2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185833   ⟸   NM_001198904
- Peptide Label: isoform 7
- UniProtKB: A0AAQ5BIA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185832   ⟸   NM_001198903
- Peptide Label: isoform 6
- UniProtKB: A0AAQ5BIA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185828   ⟸   NM_001198899
- Peptide Label: isoform 1
- UniProtKB: I6L9C2 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000352134   ⟸   ENST00000359205
Ensembl Acc Id: ENSP00000316079   ⟸   ENST00000347088
Ensembl Acc Id: ENSP00000295566   ⟸   ENST00000295566
Ensembl Acc Id: ENSP00000354716   ⟸   ENST00000361140
Ensembl Acc Id: ENSP00000355298   ⟸   ENST00000361831
Ensembl Acc Id: ENSP00000413240   ⟸   ENST00000454523
Ensembl Acc Id: ENSP00000409203   ⟸   ENST00000443231
Ensembl Acc Id: ENSP00000311138   ⟸   ENST00000311573
Ensembl Acc Id: ENSP00000385390   ⟸   ENST00000404643
Ensembl Acc Id: ENSP00000384583   ⟸   ENST00000405763
Ensembl Acc Id: ENSP00000385791   ⟸   ENST00000407221
Ensembl Acc Id: ENSP00000346722   ⟸   ENST00000354691
Ensembl Acc Id: ENSP00000357324   ⟸   ENST00000368340
Ensembl Acc Id: ENSP00000357314   ⟸   ENST00000368330
Ensembl Acc Id: ENSP00000357323   ⟸   ENST00000368339
Ensembl Acc Id: ENSP00000347686   ⟸   ENST00000355499
Ensembl Acc Id: ENSP00000390116   ⟸   ENST00000436865
Ensembl Acc Id: ENSP00000519995   ⟸   ENST00000714787
Ensembl Acc Id: ENSP00000520344   ⟸   ENST00000715143
Ensembl Acc Id: ENSP00000519997   ⟸   ENST00000714789
Ensembl Acc Id: ENSP00000520033   ⟸   ENST00000714832
Ensembl Acc Id: ENSP00000520346   ⟸   ENST00000715145
Ensembl Acc Id: ENSP00000520366   ⟸   ENST00000715170
Ensembl Acc Id: ENSP00000520031   ⟸   ENST00000714830
Ensembl Acc Id: ENSP00000519937   ⟸   ENST00000714708
Ensembl Acc Id: ENSP00000520338   ⟸   ENST00000715137
Ensembl Acc Id: ENSP00000519781   ⟸   ENST00000714539
Ensembl Acc Id: ENSP00000520341   ⟸   ENST00000715140
Ensembl Acc Id: ENSP00000519796   ⟸   ENST00000714551
Ensembl Acc Id: ENSP00000520343   ⟸   ENST00000715142
Ensembl Acc Id: ENSP00000519998   ⟸   ENST00000714790
Ensembl Acc Id: ENSP00000519793   ⟸   ENST00000714548
Ensembl Acc Id: ENSP00000519777   ⟸   ENST00000714536
Ensembl Acc Id: ENSP00000520340   ⟸   ENST00000715139
Ensembl Acc Id: ENSP00000519779   ⟸   ENST00000714538
Ensembl Acc Id: ENSP00000520367   ⟸   ENST00000715171
Ensembl Acc Id: ENSP00000519994   ⟸   ENST00000714786
Ensembl Acc Id: ENSP00000520345   ⟸   ENST00000715144
Ensembl Acc Id: ENSP00000519941   ⟸   ENST00000714712
Ensembl Acc Id: ENSP00000519794   ⟸   ENST00000714549
Ensembl Acc Id: ENSP00000519795   ⟸   ENST00000714550
Ensembl Acc Id: ENSP00000520368   ⟸   ENST00000715172
Ensembl Acc Id: ENSP00000520339   ⟸   ENST00000715138
Ensembl Acc Id: ENSP00000520032   ⟸   ENST00000714831
Ensembl Acc Id: ENSP00000519996   ⟸   ENST00000714788
Ensembl Acc Id: ENSP00000520348   ⟸   ENST00000715147
Ensembl Acc Id: ENSP00000519938   ⟸   ENST00000714709
Ensembl Acc Id: ENSP00000519936   ⟸   ENST00000714707
Ensembl Acc Id: ENSP00000520369   ⟸   ENST00000715173
Ensembl Acc Id: ENSP00000520347   ⟸   ENST00000715146
Ensembl Acc Id: ENSP00000519999   ⟸   ENST00000714791
Ensembl Acc Id: ENSP00000519797   ⟸   ENST00000714552
Ensembl Acc Id: ENSP00000519778   ⟸   ENST00000714537
Ensembl Acc Id: ENSP00000519943   ⟸   ENST00000714714
Ensembl Acc Id: ENSP00000519942   ⟸   ENST00000714713
Ensembl Acc Id: ENSP00000519940   ⟸   ENST00000714711
Ensembl Acc Id: ENSP00000520034   ⟸   ENST00000714833
Ensembl Acc Id: ENSP00000520342   ⟸   ENST00000715141
Ensembl Acc Id: ENSP00000520365   ⟸   ENST00000715169
Ensembl Acc Id: ENSP00000519939   ⟸   ENST00000714710

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H869-F1-model_v2 AlphaFold Q9H869 1-796 view protein structure

Promoters
RGD ID:6785001
Promoter ID:HG_KWN:5419
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:ENST00000368336,   NM_139119,   OTTHUMT00000086036,   OTTHUMT00000086038,   OTTHUMT00000086039,   OTTHUMT00000086040,   OTTHUMT00000086048,   OTTHUMT00000086049,   OTTHUMT00000086052,   OTTHUMT00000086053,   UC001FLH.1,   UC001FLJ.1,   UC001FLK.1,   UC001FLL.1,   UC001FLM.1,   UC001FLN.1,   UC001FLO.1,   UC001FLP.1,   UC001FLQ.1,   UC001FLS.1,   UC001FLT.1,   UC001FLU.1,   UC009WQT.1,   UC009WQU.1,   UC009WQV.1,   UC009WQW.1,   UC009WQX.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361153,924,966 - 153,925,617 (+)MPROMDB
RGD ID:6857498
Promoter ID:EPDNEW_H1914
Type:initiation region
Name:YY1AP1_1
Description:YY1 associated protein 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1915  EPDNEW_H1917  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,688,687 - 155,688,747EPDNEW
RGD ID:6857500
Promoter ID:EPDNEW_H1915
Type:initiation region
Name:YY1AP1_2
Description:YY1 associated protein 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1914  EPDNEW_H1917  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381155,688,996 - 155,689,056EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30935 AgrOrtholog
COSMIC YY1AP1 COSMIC
Ensembl Genes ENSG00000163374 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000295566 ENTREZGENE
  ENST00000295566.8 UniProtKB/Swiss-Prot
  ENST00000311573.9 UniProtKB/Swiss-Prot
  ENST00000347088 ENTREZGENE
  ENST00000347088.9 UniProtKB/Swiss-Prot
  ENST00000354691.9 UniProtKB/TrEMBL
  ENST00000355499 ENTREZGENE
  ENST00000355499.9 UniProtKB/Swiss-Prot
  ENST00000359205 ENTREZGENE
  ENST00000359205.9 UniProtKB/Swiss-Prot
  ENST00000361140.8 UniProtKB/TrEMBL
  ENST00000361831 ENTREZGENE
  ENST00000361831.9 UniProtKB/Swiss-Prot
  ENST00000368330 ENTREZGENE
  ENST00000368330.6 UniProtKB/Swiss-Prot
  ENST00000368339 ENTREZGENE
  ENST00000368339.10 UniProtKB/Swiss-Prot
  ENST00000368340 ENTREZGENE
  ENST00000368340.10 UniProtKB/Swiss-Prot
  ENST00000404643 ENTREZGENE
  ENST00000404643.5 UniProtKB/Swiss-Prot
  ENST00000405763.7 UniProtKB/TrEMBL
  ENST00000407221.5 UniProtKB/Swiss-Prot
  ENST00000436865.5 UniProtKB/TrEMBL
  ENST00000443231.6 UniProtKB/TrEMBL
  ENST00000454523.6 UniProtKB/TrEMBL
  ENST00000466366.2 UniProtKB/TrEMBL
  ENST00000476027.6 UniProtKB/TrEMBL
  ENST00000477470.2 UniProtKB/TrEMBL
  ENST00000488784.6 UniProtKB/TrEMBL
  ENST00000714536.1 UniProtKB/TrEMBL
  ENST00000714537.1 UniProtKB/TrEMBL
  ENST00000714538.1 UniProtKB/TrEMBL
  ENST00000714539.1 UniProtKB/TrEMBL
  ENST00000714548.1 UniProtKB/TrEMBL
  ENST00000714549.1 UniProtKB/TrEMBL
  ENST00000714550.1 UniProtKB/TrEMBL
  ENST00000714551.1 UniProtKB/TrEMBL
  ENST00000714552.1 UniProtKB/TrEMBL
  ENST00000714707.1 UniProtKB/TrEMBL
  ENST00000714708.1 UniProtKB/TrEMBL
  ENST00000714709.1 UniProtKB/TrEMBL
  ENST00000714710.1 UniProtKB/TrEMBL
  ENST00000714711.1 UniProtKB/TrEMBL
  ENST00000714712.1 UniProtKB/TrEMBL
  ENST00000714714.1 UniProtKB/TrEMBL
  ENST00000714786.1 UniProtKB/TrEMBL
  ENST00000714788.1 UniProtKB/TrEMBL
  ENST00000714789.1 UniProtKB/TrEMBL
  ENST00000714791.1 UniProtKB/TrEMBL
  ENST00000714830.1 UniProtKB/TrEMBL
  ENST00000714832.1 UniProtKB/TrEMBL
  ENST00000714833.1 UniProtKB/TrEMBL
  ENST00000715137.1 UniProtKB/TrEMBL
  ENST00000715138.1 UniProtKB/TrEMBL
  ENST00000715139.1 UniProtKB/TrEMBL
  ENST00000715140.1 UniProtKB/TrEMBL
  ENST00000715141.1 UniProtKB/TrEMBL
  ENST00000715142.1 UniProtKB/TrEMBL
  ENST00000715143.1 UniProtKB/TrEMBL
  ENST00000715144.1 UniProtKB/TrEMBL
  ENST00000715145.1 UniProtKB/TrEMBL
  ENST00000715146.1 UniProtKB/TrEMBL
  ENST00000715147.1 UniProtKB/TrEMBL
  ENST00000715171.1 UniProtKB/TrEMBL
  ENST00000715172.1 UniProtKB/TrEMBL
  ENST00000715173.1 UniProtKB/TrEMBL
GTEx ENSG00000163374 GTEx
HGNC ID HGNC:30935 ENTREZGENE
Human Proteome Map YY1AP1 Human Proteome Map
InterPro YY1-Transcr_Regul UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55249 UniProtKB/Swiss-Prot
NCBI Gene 55249 ENTREZGENE
OMIM 607860 OMIM
PANTHER YY1 ASSOCIATED PROTEIN-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  YY1-ASSOCIATED PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142670546 PharmGKB
UniProt A0AAQ5BI46_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI48_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI55_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI56 ENTREZGENE, UniProtKB/TrEMBL
  A0AAQ5BI62_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI67_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI69_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI71_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI72_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI74_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI75_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI83_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI84_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI85_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI87_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI90_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI92_HUMAN UniProtKB/TrEMBL
  A0AAQ5BI93 ENTREZGENE, UniProtKB/TrEMBL
  A0AAQ5BI94_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIA0_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIA1 ENTREZGENE, UniProtKB/TrEMBL
  A0AAQ5BIA3_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIA7_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIA8_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIB0_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIB1_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIB2_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIB3_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIB5_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIB7_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIC5_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIE2_HUMAN UniProtKB/TrEMBL
  A0AAQ5BIE9_HUMAN UniProtKB/TrEMBL
  A3KFK1_HUMAN UniProtKB/TrEMBL
  A3KFK2_HUMAN UniProtKB/TrEMBL
  B0QZ54 ENTREZGENE
  B0QZ55_HUMAN UniProtKB/TrEMBL
  B4DMP2 ENTREZGENE
  B4DQQ0 ENTREZGENE, UniProtKB/TrEMBL
  B4DZQ4_HUMAN UniProtKB/TrEMBL
  B4E0I0 ENTREZGENE
  D3DV96 ENTREZGENE
  D3DV98 ENTREZGENE
  F8WD62_HUMAN UniProtKB/TrEMBL
  H7BY62 ENTREZGENE
  I6L9C2 ENTREZGENE, UniProtKB/TrEMBL
  Q5VYZ1 ENTREZGENE
  Q5VYZ4 ENTREZGENE
  Q5VYZ7 ENTREZGENE
  Q68CT8_HUMAN UniProtKB/TrEMBL
  Q7L4C3 ENTREZGENE
  Q7L5E2 ENTREZGENE
  Q8IXA6 ENTREZGENE
  Q8TEW5 ENTREZGENE
  Q8TF04 ENTREZGENE
  Q96HB6 ENTREZGENE
  Q9BQ64 ENTREZGENE
  Q9H869 ENTREZGENE
  Q9NV84 ENTREZGENE
  YYAP1_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B0QZ54 UniProtKB/Swiss-Prot
  B4DMP2 UniProtKB/Swiss-Prot
  B4E0I0 UniProtKB/Swiss-Prot
  D3DV96 UniProtKB/Swiss-Prot
  D3DV98 UniProtKB/Swiss-Prot
  H7BY62 UniProtKB/Swiss-Prot
  Q5VYZ1 UniProtKB/Swiss-Prot
  Q5VYZ4 UniProtKB/Swiss-Prot
  Q5VYZ7 UniProtKB/Swiss-Prot
  Q7L4C3 UniProtKB/Swiss-Prot
  Q7L5E2 UniProtKB/Swiss-Prot
  Q8IXA6 UniProtKB/Swiss-Prot
  Q8TEW5 UniProtKB/Swiss-Prot
  Q8TF04 UniProtKB/Swiss-Prot
  Q96HB6 UniProtKB/Swiss-Prot
  Q9BQ64 UniProtKB/Swiss-Prot
  Q9NV84 UniProtKB/Swiss-Prot