NVL (nuclear VCP like) - Rat Genome Database

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Gene: NVL (nuclear VCP like) Homo sapiens
Analyze
Symbol: NVL
Name: nuclear VCP like
RGD ID: 1322636
HGNC Page HGNC:8070
Description: Enables ATP binding activity and preribosome binding activity. Involved in rRNA processing; regulation of protein localization to nucleolus; and ribosomal large subunit biogenesis. Located in nuclear exosome (RNase complex); nucleolus; and nucleoplasm. Part of telomerase holoenzyme complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: nuclear valosin-containing protein-like; nuclear VCP-like; nuclear VCP-like protein; NVL2; NVLp
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381224,227,345 - 224,330,172 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1224,227,334 - 224,330,189 (-)EnsemblGRCh38hg38GRCh38
GRCh371224,415,047 - 224,517,874 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361222,481,659 - 222,584,495 (-)NCBINCBI36Build 36hg18NCBI36
Build 341220,721,771 - 220,824,607NCBI
Celera1197,605,972 - 197,708,808 (-)NCBICelera
Cytogenetic Map1q42.11NCBI
HuRef1194,934,993 - 195,038,171 (-)NCBIHuRef
CHM1_11225,687,528 - 225,790,385 (-)NCBICHM1_1
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:9286697   PMID:10737800   PMID:12429849   PMID:12477932   PMID:12927788   PMID:15342556   PMID:15469983   PMID:15489334   PMID:16169070   PMID:16782053   PMID:18029348  
PMID:19851296   PMID:19946888   PMID:20198315   PMID:21042317   PMID:21145461   PMID:21474449   PMID:21516116   PMID:21873635   PMID:21900206   PMID:22226966   PMID:22586326   PMID:22658674  
PMID:25277244   PMID:25544563   PMID:25665578   PMID:25693804   PMID:25891250   PMID:26166824   PMID:26186194   PMID:26456651   PMID:26496610   PMID:26638075   PMID:26949251   PMID:27503909  
PMID:28077445   PMID:28186131   PMID:28416111   PMID:28514442   PMID:28927264   PMID:29107693   PMID:29395067   PMID:29499938   PMID:29509190   PMID:29568061   PMID:29844126   PMID:30415952  
PMID:30554943   PMID:30585729   PMID:30631154   PMID:31059266   PMID:31091453   PMID:31358741   PMID:31586073   PMID:31665637   PMID:32296183   PMID:32416067   PMID:32780723   PMID:32807901  
PMID:32814769   PMID:33060197   PMID:33422691   PMID:33729478   PMID:33957083   PMID:33961781   PMID:34079125   PMID:34133714   PMID:34244565   PMID:34373451   PMID:34578187   PMID:34672954  
PMID:35013218   PMID:35013556   PMID:35182466   PMID:35271311   PMID:35439318   PMID:35850772   PMID:36089195   PMID:36215168   PMID:36373674   PMID:36912080   PMID:37827155   PMID:37866880  


Genomics

Comparative Map Data
NVL
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381224,227,345 - 224,330,172 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1224,227,334 - 224,330,189 (-)EnsemblGRCh38hg38GRCh38
GRCh371224,415,047 - 224,517,874 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361222,481,659 - 222,584,495 (-)NCBINCBI36Build 36hg18NCBI36
Build 341220,721,771 - 220,824,607NCBI
Celera1197,605,972 - 197,708,808 (-)NCBICelera
Cytogenetic Map1q42.11NCBI
HuRef1194,934,993 - 195,038,171 (-)NCBIHuRef
CHM1_11225,687,528 - 225,790,385 (-)NCBICHM1_1
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBIT2T-CHM13v2.0
Nvl
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391180,914,703 - 180,974,557 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1180,914,703 - 180,971,769 (-)EnsemblGRCm39 Ensembl
GRCm381181,087,138 - 181,144,214 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1181,087,138 - 181,144,204 (-)EnsemblGRCm38mm10GRCm38
MGSCv371183,023,554 - 183,074,288 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361182,930,098 - 182,980,832 (-)NCBIMGSCv36mm8
Celera1188,160,290 - 188,211,164 (-)NCBICelera
Cytogenetic Map1H4NCBI
cM Map184.53NCBI
Nvl
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81395,385,389 - 95,438,490 (-)NCBIGRCr8
mRatBN7.21392,851,023 - 92,906,749 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1392,853,650 - 92,906,049 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1395,358,969 - 95,411,370 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01396,758,872 - 96,811,272 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01393,934,464 - 93,986,919 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01399,410,026 - 99,468,783 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1399,410,026 - 99,468,778 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.013104,407,045 - 104,465,204 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41396,862,759 - 96,917,215 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11397,051,898 - 97,105,918 (-)NCBI
Celera1392,394,917 - 92,447,334 (-)NCBICelera
Cytogenetic Map13q26NCBI
Nvl
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555201,011,621 - 1,062,286 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555201,010,966 - 1,069,176 (+)NCBIChiLan1.0ChiLan1.0
NVL
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2125,198,255 - 25,300,948 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1125,149,198 - 25,251,886 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01199,695,388 - 199,798,080 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11204,704,095 - 204,807,027 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1204,704,371 - 204,806,959 (-)Ensemblpanpan1.1panPan2
NVL
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1740,041,692 - 40,131,984 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl740,041,394 - 40,131,823 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha739,523,642 - 39,614,138 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0739,876,221 - 39,966,969 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl739,876,247 - 39,966,968 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1739,717,305 - 39,807,555 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0739,724,584 - 39,815,053 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0739,993,455 - 40,083,964 (+)NCBIUU_Cfam_GSD_1.0
Nvl
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934453,365,252 - 53,472,551 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365261,272,389 - 1,382,048 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365261,274,760 - 1,381,997 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NVL
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1012,588,135 - 12,670,625 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11012,564,891 - 12,670,641 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
NVL
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1255,455,812 - 5,555,666 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl255,455,646 - 5,556,770 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660555,633,241 - 5,737,550 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nvl
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248355,913,699 - 5,970,503 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248355,896,014 - 5,977,581 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NVL
23 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q41-42.12(chr1:223882252-224902629)x1 copy number loss See cases [RCV000050819] Chr1:223882252..224902629 [GRCh38]
Chr1:224069954..225090331 [GRCh37]
Chr1:222136577..223156954 [NCBI36]
Chr1:1q41-42.12		 uncertain significance
GRCh38/hg38 1q32.3-44(chr1:214023812-248918469)x3 copy number gain See cases [RCV000050981] Chr1:214023812..248918469 [GRCh38]
Chr1:214197155..249212668 [GRCh37]
Chr1:212263778..247179291 [NCBI36]
Chr1:1q32.3-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223347693-248918469)x3 copy number gain See cases [RCV000050581] Chr1:223347693..248918469 [GRCh38]
Chr1:223521035..249212668 [GRCh37]
Chr1:221587658..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:221902539-248918469)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051875]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051875]|See cases [RCV000051875] Chr1:221902539..248918469 [GRCh38]
Chr1:222075881..249212668 [GRCh37]
Chr1:220142504..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223828500-248891309)x3 copy number gain See cases [RCV000051878] Chr1:223828500..248891309 [GRCh38]
Chr1:224016202..249185508 [GRCh37]
Chr1:222082825..247152131 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3 copy number gain See cases [RCV000051857] Chr1:187143981..224299417 [GRCh38]
Chr1:187113113..224487119 [GRCh37]
Chr1:185379736..222553742 [NCBI36]
Chr1:1q31.1-42.11		 pathogenic
GRCh38/hg38 1q41-44(chr1:223887780-248891309)x3 copy number gain See cases [RCV000051880] Chr1:223887780..248891309 [GRCh38]
Chr1:224075482..249185508 [GRCh37]
Chr1:222142105..247152131 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q42.11-44(chr1:224096488-248918469)x3 copy number gain See cases [RCV000051882] Chr1:224096488..248918469 [GRCh38]
Chr1:224284190..249212668 [GRCh37]
Chr1:222350813..247179291 [NCBI36]
Chr1:1q42.11-44		 pathogenic
GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3 copy number gain See cases [RCV000051861] Chr1:209646207..248931113 [GRCh38]
Chr1:209819552..249225312 [GRCh37]
Chr1:207886175..247191935 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh38/hg38 1q42.11-42.13(chr1:224096288-227859548)x1 copy number loss See cases [RCV000052311] Chr1:224096288..227859548 [GRCh38]
Chr1:224283990..228047249 [GRCh37]
Chr1:222350613..226113872 [NCBI36]
Chr1:1q42.11-42.13		 pathogenic
GRCh38/hg38 1q41-42.13(chr1:221519280-228862141)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053955]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053955]|See cases [RCV000053955] Chr1:221519280..228862141 [GRCh38]
Chr1:221692622..228997888 [GRCh37]
Chr1:219759245..227064511 [NCBI36]
Chr1:1q41-42.13		 pathogenic
NM_002533.3(NVL):c.2025C>T (p.Pro675=) single nucleotide variant Malignant melanoma [RCV000060096] Chr1:224275396 [GRCh38]
Chr1:224463098 [GRCh37]
Chr1:222529721 [NCBI36]
Chr1:1q42.11		 not provided
NM_002533.3(NVL):c.395C>T (p.Pro132Leu) single nucleotide variant Malignant melanoma [RCV000060097] Chr1:224308211 [GRCh38]
Chr1:224495913 [GRCh37]
Chr1:222562536 [NCBI36]
Chr1:1q42.11		 not provided
GRCh38/hg38 1q41-42.12(chr1:223749425-224604271)x1 copy number loss See cases [RCV000135362] Chr1:223749425..224604271 [GRCh38]
Chr1:223937127..224791973 [GRCh37]
Chr1:222003750..222858596 [NCBI36]
Chr1:1q41-42.12		 uncertain significance
GRCh38/hg38 1q32.2-44(chr1:209963625-248918469)x3 copy number gain See cases [RCV000134979] Chr1:209963625..248918469 [GRCh38]
Chr1:210136970..249212668 [GRCh37]
Chr1:208203593..247179291 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223815147-248918469)x3 copy number gain See cases [RCV000135839] Chr1:223815147..248918469 [GRCh38]
Chr1:224002849..249212668 [GRCh37]
Chr1:222069472..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q41-42.13(chr1:223347693-228556332)x1 copy number loss See cases [RCV000136636] Chr1:223347693..228556332 [GRCh38]
Chr1:223521035..228744033 [GRCh37]
Chr1:221587658..226810656 [NCBI36]
Chr1:1q41-42.13		 pathogenic
GRCh38/hg38 1q42.11-44(chr1:224022862-248918469)x3 copy number gain See cases [RCV000137769] Chr1:224022862..248918469 [GRCh38]
Chr1:224210564..249212668 [GRCh37]
Chr1:222277187..247179291 [NCBI36]
Chr1:1q42.11-44		 pathogenic
GRCh38/hg38 1q32.1-42.12(chr1:204764914-225408698)x3 copy number gain See cases [RCV000142054] Chr1:204764914..225408698 [GRCh38]
Chr1:204734042..225596400 [GRCh37]
Chr1:203000665..223663023 [NCBI36]
Chr1:1q32.1-42.12		 pathogenic
GRCh38/hg38 1q32.2-44(chr1:207346642-248930485)x3 copy number gain See cases [RCV000143727] Chr1:207346642..248930485 [GRCh38]
Chr1:207519987..249224684 [GRCh37]
Chr1:205586610..247191307 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh37/hg19 1q31.3-42.13(chr1:197811907-228997888)x3 copy number gain See cases [RCV000240137] Chr1:197811907..228997888 [GRCh37]
Chr1:1q31.3-42.13		 pathogenic
GRCh37/hg19 1q42.11-42.12(chr1:224340881-225147932) copy number loss not provided [RCV000767548] Chr1:224340881..225147932 [GRCh37]
Chr1:1q42.11-42.12		 pathogenic
GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3 copy number gain See cases [RCV000449172] Chr1:195483439..249213000 [GRCh37]
Chr1:1q31.3-44		 pathogenic
GRCh37/hg19 1q41-44(chr1:214697099-249224684)x3 copy number gain See cases [RCV000449210] Chr1:214697099..249224684 [GRCh37]
Chr1:1q41-44		 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 1q42.11-44(chr1:224105294-249224684)x3 copy number gain See cases [RCV000510981] Chr1:224105294..249224684 [GRCh37]
Chr1:1q42.11-44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q41-44(chr1:218252551-249224684)x3 copy number gain not provided [RCV000684700] Chr1:218252551..249224684 [GRCh37]
Chr1:1q41-44		 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
GRCh37/hg19 1q41-42.2(chr1:223653722-234591807)x1 copy number loss not provided [RCV001005180] Chr1:223653722..234591807 [GRCh37]
Chr1:1q41-42.2		 pathogenic
GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3 copy number gain not provided [RCV000845852] Chr1:182388773..249111240 [GRCh37]
Chr1:1q25.3-44		 pathogenic
GRCh37/hg19 1q41-42.13(chr1:222641389-228137574)x1 copy number loss not provided [RCV001005178] Chr1:222641389..228137574 [GRCh37]
Chr1:1q41-42.13		 pathogenic
GRCh37/hg19 1q41-43(chr1:219916966-239004378)x3 copy number gain not provided [RCV001005175] Chr1:219916966..239004378 [GRCh37]
Chr1:1q41-43		 pathogenic
GRCh37/hg19 1q42.11-42.12(chr1:224486843-225283297)x3 copy number gain not provided [RCV000845738] Chr1:224486843..225283297 [GRCh37]
Chr1:1q42.11-42.12		 uncertain significance
GRCh38/hg38 1q42.11-42.12(chr1:224304638-224434886)x1 copy number loss Skraban-Deardorff syndrome [RCV003327628] Chr1:224304638..224434886 [GRCh38]
Chr1:1q42.11-42.12		 pathogenic
GRCh37/hg19 1q32.1-44(chr1:204045948-249218992)x3 copy number gain See cases [RCV001007407] Chr1:204045948..249218992 [GRCh37]
Chr1:1q32.1-44		 pathogenic
GRCh37/hg19 1q32.2-44(chr1:210152794-249218992)x3 copy number gain See cases [RCV001194578] Chr1:210152794..249218992 [GRCh37]
Chr1:1q32.2-44		 pathogenic
GRCh37/hg19 1q41-42.12(chr1:222605125-224696628)x1 copy number loss not provided [RCV001259110] Chr1:222605125..224696628 [GRCh37]
Chr1:1q41-42.12		 pathogenic
GRCh37/hg19 1q42.11-42.12(chr1:224442473-224794913)x1 copy number loss not provided [RCV001259111] Chr1:224442473..224794913 [GRCh37]
Chr1:1q42.11-42.12		 pathogenic
GRCh37/hg19 1q41-42.12(chr1:223552998-224761890) copy number loss Global developmental delay [RCV001291986] Chr1:223552998..224761890 [GRCh37]
Chr1:1q41-42.12		 pathogenic
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44		 uncertain significance
GRCh37/hg19 1q41-42.13(chr1:221303919-227461343) copy number gain not specified [RCV002052845] Chr1:221303919..227461343 [GRCh37]
Chr1:1q41-42.13		 pathogenic
GRCh37/hg19 1q42.11-42.12(chr1:224432682-225142704) copy number loss Chromosome 1q41-q42 deletion syndrome [RCV002280724] Chr1:224432682..225142704 [GRCh37]
Chr1:1q42.11-42.12		 pathogenic
GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3 copy number gain See cases [RCV002287837] Chr1:197867914..249224684 [GRCh37]
Chr1:1q31.3-44		 pathogenic
GRCh37/hg19 1q41-42.12(chr1:221325488-225804228)x1 copy number loss not provided [RCV002474859] Chr1:221325488..225804228 [GRCh37]
Chr1:1q41-42.12		 uncertain significance
GRCh38/hg38 1q32.2-42.13(chr1:228006998-228061271)x2 copy number loss Orofacial cleft 2 [RCV002481175] Chr1:228006998..228061271 [GRCh38]
Chr1:1q32.2-42.13		 association
NM_002533.4(NVL):c.380A>G (p.Tyr127Cys) single nucleotide variant not specified [RCV004227680] Chr1:224308226 [GRCh38]
Chr1:224495928 [GRCh37]
Chr1:1q42.11		 uncertain significance
GRCh37/hg19 1q41-44(chr1:223972939-249224684)x3 copy number gain not provided [RCV002475745] Chr1:223972939..249224684 [GRCh37]
Chr1:1q41-44		 pathogenic
NM_002533.4(NVL):c.1207C>T (p.Arg403Trp) single nucleotide variant not specified [RCV004186591] Chr1:224294385 [GRCh38]
Chr1:224482087 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.626A>C (p.Asp209Ala) single nucleotide variant not specified [RCV004156643] Chr1:224305156 [GRCh38]
Chr1:224492858 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.1930A>C (p.Ile644Leu) single nucleotide variant not specified [RCV004156515] Chr1:224281155 [GRCh38]
Chr1:224468857 [GRCh37]
Chr1:1q42.11		 uncertain significance
GRCh37/hg19 1q42.11-43(chr1:224230307-243181599)x3 copy number gain not provided [RCV002509019] Chr1:224230307..243181599 [GRCh37]
Chr1:1q42.11-43		 not provided
NM_002533.4(NVL):c.1627G>A (p.Glu543Lys) single nucleotide variant not specified [RCV004085264] Chr1:224287942 [GRCh38]
Chr1:224475644 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.844A>G (p.Ile282Val) single nucleotide variant not specified [RCV004102594] Chr1:224303839 [GRCh38]
Chr1:224491541 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.1283G>A (p.Arg428Gln) single nucleotide variant not specified [RCV004075155] Chr1:224294309 [GRCh38]
Chr1:224482011 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.1289T>C (p.Ile430Thr) single nucleotide variant not specified [RCV004170670] Chr1:224294303 [GRCh38]
Chr1:224482005 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.311A>G (p.Asp104Gly) single nucleotide variant not specified [RCV004257477] Chr1:224311831 [GRCh38]
Chr1:224499533 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.616G>A (p.Asp206Asn) single nucleotide variant not specified [RCV004260842] Chr1:224305166 [GRCh38]
Chr1:224492868 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.259G>T (p.Ala87Ser) single nucleotide variant not specified [RCV004251944] Chr1:224317719 [GRCh38]
Chr1:224505421 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.2410G>T (p.Ala804Ser) single nucleotide variant not specified [RCV004275228] Chr1:224233246 [GRCh38]
Chr1:224420948 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.1105A>G (p.Ile369Val) single nucleotide variant not specified [RCV004258135] Chr1:224296576 [GRCh38]
Chr1:224484278 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.434A>G (p.Glu145Gly) single nucleotide variant not specified [RCV004329727] Chr1:224308172 [GRCh38]
Chr1:224495874 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.16G>A (p.Ala6Thr) single nucleotide variant not specified [RCV004346733] Chr1:224330112 [GRCh38]
Chr1:224517814 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.2546G>A (p.Arg849His) single nucleotide variant not specified [RCV004363694] Chr1:224227651 [GRCh38]
Chr1:224415353 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.2049G>A (p.Val683=) single nucleotide variant not provided [RCV003414800] Chr1:224275372 [GRCh38]
Chr1:224463074 [GRCh37]
Chr1:1q42.11		 likely benign
NM_002533.4(NVL):c.1245G>A (p.Ser415=) single nucleotide variant not provided [RCV003414801] Chr1:224294347 [GRCh38]
Chr1:224482049 [GRCh37]
Chr1:1q42.11		 likely benign
NM_002533.4(NVL):c.1361C>T (p.Pro454Leu) single nucleotide variant not specified [RCV004488778] Chr1:224289698 [GRCh38]
Chr1:224477400 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.1612C>G (p.Gln538Glu) single nucleotide variant not specified [RCV004488781] Chr1:224287957 [GRCh38]
Chr1:224475659 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.324A>C (p.Glu108Asp) single nucleotide variant not specified [RCV004488785] Chr1:224311818 [GRCh38]
Chr1:224499520 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.515G>A (p.Gly172Glu) single nucleotide variant not specified [RCV004488786] Chr1:224308091 [GRCh38]
Chr1:224495793 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.1366G>A (p.Ala456Thr) single nucleotide variant not specified [RCV004488779] Chr1:224289693 [GRCh38]
Chr1:224477395 [GRCh37]
Chr1:1q42.11		 likely benign
Single allele complex Skraban-Deardorff syndrome [RCV003992105] Chr1:224317411..224403138 [GRCh38]
Chr1:1q42.11-42.12		 pathogenic
NM_002533.4(NVL):c.1237C>T (p.Pro413Ser) single nucleotide variant not specified [RCV004488777] Chr1:224294355 [GRCh38]
Chr1:224482057 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.2125A>T (p.Met709Leu) single nucleotide variant not specified [RCV004488782] Chr1:224268091 [GRCh38]
Chr1:224455793 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.95T>A (p.Ile32Asn) single nucleotide variant not specified [RCV004488787] Chr1:224326427 [GRCh38]
Chr1:224514129 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.1460A>G (p.Asn487Ser) single nucleotide variant not specified [RCV004488780] Chr1:224289599 [GRCh38]
Chr1:224477301 [GRCh37]
Chr1:1q42.11		 likely benign
GRCh37/hg19 1q41-42.12(chr1:216147522-226765691)x1 copy number loss not provided [RCV004442774] Chr1:216147522..226765691 [GRCh37]
Chr1:1q41-42.12		 pathogenic
NM_002533.4(NVL):c.2440A>G (p.Ser814Gly) single nucleotide variant not specified [RCV004488783] Chr1:224233216 [GRCh38]
Chr1:224420918 [GRCh37]
Chr1:1q42.11		 uncertain significance
NM_002533.4(NVL):c.2545C>T (p.Arg849Cys) single nucleotide variant not specified [RCV004488784] Chr1:224227652 [GRCh38]
Chr1:224415354 [GRCh37]
Chr1:1q42.11		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3492
Count of miRNA genes:905
Interacting mature miRNAs:1057
Transcripts:ENST00000281701, ENST00000340871, ENST00000361463, ENST00000391875, ENST00000436927, ENST00000461466, ENST00000461546, ENST00000462893, ENST00000467882, ENST00000468088, ENST00000468673, ENST00000469075, ENST00000469968, ENST00000470903, ENST00000470989, ENST00000481213, ENST00000482491, ENST00000483094, ENST00000487758, ENST00000488718, ENST00000489194, ENST00000492281, ENST00000493060, ENST00000496393, ENST00000498767
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
D1S2763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,461,673 - 224,461,825UniSTSGRCh37
Build 361222,528,296 - 222,528,448RGDNCBI36
Celera1197,652,608 - 197,652,772RGD
Cytogenetic Map1q41-q42.2UniSTS
HuRef1194,981,930 - 194,982,094UniSTS
Marshfield Genetic Map1242.34RGD
Marshfield Genetic Map1242.34UniSTS
Genethon Genetic Map1246.2UniSTS
SHGC-52483  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,415,134 - 224,415,293UniSTSGRCh37
Build 361222,481,757 - 222,481,916RGDNCBI36
Celera1197,606,070 - 197,606,229RGD
Cytogenetic Map1q41-q42.2UniSTS
HuRef1194,935,091 - 194,935,250UniSTS
TNG Radiation Hybrid Map1111685.0UniSTS
GeneMap99-G3 RH Map18717.0UniSTS
SHGC-84009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,517,213 - 224,517,515UniSTSGRCh37
Build 361222,583,836 - 222,584,138RGDNCBI36
Celera1197,708,149 - 197,708,451RGD
Cytogenetic Map1q41-q42.2UniSTS
HuRef1195,037,493 - 195,037,795UniSTS
TNG Radiation Hybrid Map1111743.0UniSTS
AFM249yg9  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,468,957 - 224,469,112UniSTSGRCh37
Build 361222,535,580 - 222,535,735RGDNCBI36
Celera1197,659,904 - 197,660,061RGD
Cytogenetic Map1q41-q42.2UniSTS
HuRef1194,989,204 - 194,989,361UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
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


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1416 1058 1064 125 1079 75 3018 573 1516 182 1223 1360 68 1 527 1830 6 1
Low 1023 1914 662 499 857 390 1339 1620 2217 237 237 253 107 677 958 1
Below cutoff 19 15 4 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_206840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011544196 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011544198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011544199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011544200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047421637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC092809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF401208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293923 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW997091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC005897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP284587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ883523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU683548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U68140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U78772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000281701   ⟹   ENSP00000281701
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,345 - 224,330,172 (-)Ensembl
RefSeq Acc Id: ENST00000340871   ⟹   ENSP00000341362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,454 - 224,330,139 (-)Ensembl
RefSeq Acc Id: ENST00000391875   ⟹   ENSP00000375747
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,334 - 224,330,170 (-)Ensembl
RefSeq Acc Id: ENST00000436927   ⟹   ENSP00000394884
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,304,736 - 224,330,128 (-)Ensembl
RefSeq Acc Id: ENST00000461466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,307,993 - 224,330,179 (-)Ensembl
RefSeq Acc Id: ENST00000461546   ⟹   ENSP00000418085
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,308,183 - 224,330,179 (-)Ensembl
RefSeq Acc Id: ENST00000462893
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,289,185 - 224,294,341 (-)Ensembl
RefSeq Acc Id: ENST00000467882   ⟹   ENSP00000419930
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,289,682 - 224,330,137 (-)Ensembl
RefSeq Acc Id: ENST00000468088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,317,694 - 224,330,172 (-)Ensembl
RefSeq Acc Id: ENST00000468673
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,312,540 - 224,330,148 (-)Ensembl
RefSeq Acc Id: ENST00000469075   ⟹   ENSP00000417826
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,369 - 224,330,138 (-)Ensembl
RefSeq Acc Id: ENST00000469968   ⟹   ENSP00000419420
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,334 - 224,330,121 (-)Ensembl
RefSeq Acc Id: ENST00000470903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,307,986 - 224,330,187 (-)Ensembl
RefSeq Acc Id: ENST00000470989   ⟹   ENSP00000419586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,305,084 - 224,330,168 (-)Ensembl
RefSeq Acc Id: ENST00000481213   ⟹   ENSP00000479235
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,334 - 224,233,289 (-)Ensembl
RefSeq Acc Id: ENST00000482491   ⟹   ENSP00000417213
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,337 - 224,330,189 (-)Ensembl
RefSeq Acc Id: ENST00000483094
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,334 - 224,236,582 (-)Ensembl
RefSeq Acc Id: ENST00000487758
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,312,727 - 224,330,132 (-)Ensembl
RefSeq Acc Id: ENST00000488718   ⟹   ENSP00000419828
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,304,735 - 224,330,138 (-)Ensembl
RefSeq Acc Id: ENST00000489194
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,334 - 224,268,133 (-)Ensembl
RefSeq Acc Id: ENST00000492281   ⟹   ENSP00000418380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,304,735 - 224,330,139 (-)Ensembl
RefSeq Acc Id: ENST00000493060
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,227,334 - 224,236,647 (-)Ensembl
RefSeq Acc Id: ENST00000496393
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,231,266 - 224,269,915 (-)Ensembl
RefSeq Acc Id: ENST00000498767
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1224,308,008 - 224,312,124 (-)Ensembl
RefSeq Acc Id: NM_001243146   ⟹   NP_001230075
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
HuRef1194,934,993 - 195,038,171 (-)NCBI
CHM1_11225,687,528 - 225,790,385 (-)NCBI
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001243147   ⟹   NP_001230076
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
GRCh371224,415,036 - 224,517,891 (-)NCBI
HuRef1194,934,993 - 195,038,171 (-)NCBI
CHM1_11225,687,528 - 225,790,385 (-)NCBI
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
Sequence:
RefSeq Acc Id: NM_002533   ⟹   NP_002524
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
GRCh371224,415,036 - 224,517,891 (-)NCBI
Build 361222,481,659 - 222,584,495 (-)NCBI Archive
Celera1197,605,972 - 197,708,808 (-)RGD
HuRef1194,934,993 - 195,038,171 (-)NCBI
CHM1_11225,687,528 - 225,790,385 (-)NCBI
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
Sequence:
RefSeq Acc Id: NM_206840   ⟹   NP_996671
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
GRCh371224,415,036 - 224,517,891 (-)NCBI
Build 361222,481,659 - 222,584,495 (-)NCBI Archive
Celera1197,605,972 - 197,708,808 (-)RGD
HuRef1194,934,993 - 195,038,171 (-)NCBI
CHM1_11225,687,528 - 225,790,385 (-)NCBI
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011544196   ⟹   XP_011542498
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001378   ⟹   XP_016856867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001379   ⟹   XP_016856868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001380   ⟹   XP_016856869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,232,648 - 224,330,172 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001383   ⟹   XP_016856872
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,330,172 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001384   ⟹   XP_016856873
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,267,004 - 224,330,172 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017001385   ⟹   XP_016856874
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,271,645 - 224,330,172 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047421613   ⟹   XP_047277569
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,227,345 - 224,317,786 (-)NCBI
RefSeq Acc Id: XM_047421618   ⟹   XP_047277574
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,267,004 - 224,330,172 (-)NCBI
RefSeq Acc Id: XM_047421621   ⟹   XP_047277577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,267,004 - 224,330,172 (-)NCBI
RefSeq Acc Id: XM_047421626   ⟹   XP_047277582
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,271,645 - 224,330,172 (-)NCBI
RefSeq Acc Id: XM_047421631   ⟹   XP_047277587
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,267,004 - 224,330,172 (-)NCBI
RefSeq Acc Id: XM_047421635   ⟹   XP_047277591
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,271,645 - 224,330,172 (-)NCBI
RefSeq Acc Id: XM_047421637   ⟹   XP_047277593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,271,645 - 224,330,172 (-)NCBI
RefSeq Acc Id: XM_054336806   ⟹   XP_054192781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336807   ⟹   XP_054192782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336808   ⟹   XP_054192783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,421,571 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336809   ⟹   XP_054192784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336810   ⟹   XP_054192785
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,416,266 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336811   ⟹   XP_054192786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,455,920 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336812   ⟹   XP_054192787
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,416,266 - 223,506,669 (-)NCBI
RefSeq Acc Id: XM_054336813   ⟹   XP_054192788
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,455,920 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336814   ⟹   XP_054192789
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,457,981 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336815   ⟹   XP_054192790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,455,920 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336816   ⟹   XP_054192791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,457,981 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336817   ⟹   XP_054192792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,455,920 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336818   ⟹   XP_054192793
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,457,981 - 223,519,053 (-)NCBI
RefSeq Acc Id: XM_054336819   ⟹   XP_054192794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01223,457,981 - 223,519,053 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001230075 (Get FASTA)   NCBI Sequence Viewer  
  NP_001230076 (Get FASTA)   NCBI Sequence Viewer  
  NP_002524 (Get FASTA)   NCBI Sequence Viewer  
  NP_996671 (Get FASTA)   NCBI Sequence Viewer  
  XP_011542498 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856867 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856868 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856869 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856872 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856873 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856874 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277569 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277574 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277577 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277582 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277587 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277591 (Get FASTA)   NCBI Sequence Viewer  
  XP_047277593 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192781 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192782 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192783 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192784 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192785 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192786 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192787 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192788 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192789 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192790 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192791 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192792 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192793 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192794 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB70457 (Get FASTA)   NCBI Sequence Viewer  
  AAB70460 (Get FASTA)   NCBI Sequence Viewer  
  AAH05897 (Get FASTA)   NCBI Sequence Viewer  
  AAH12105 (Get FASTA)   NCBI Sequence Viewer  
  AAL02167 (Get FASTA)   NCBI Sequence Viewer  
  BAG57304 (Get FASTA)   NCBI Sequence Viewer  
  BAG59590 (Get FASTA)   NCBI Sequence Viewer  
  BAG59836 (Get FASTA)   NCBI Sequence Viewer  
  BAG60510 (Get FASTA)   NCBI Sequence Viewer  
  BAG60956 (Get FASTA)   NCBI Sequence Viewer  
  EAW69714 (Get FASTA)   NCBI Sequence Viewer  
  EAW69715 (Get FASTA)   NCBI Sequence Viewer  
  EAW69716 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000281701
  ENSP00000281701.6
  ENSP00000341362
  ENSP00000341362.4
  ENSP00000375747
  ENSP00000375747.2
  ENSP00000394884.1
  ENSP00000417213.2
  ENSP00000417826
  ENSP00000417826.1
  ENSP00000418085.1
  ENSP00000418380.1
  ENSP00000419420.2
  ENSP00000419586.1
  ENSP00000419828.1
  ENSP00000419930.1
  ENSP00000479235.1
GenBank Protein O15381 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_002524   ⟸   NM_002533
- Peptide Label: isoform 1
- UniProtKB: B4DP98 (UniProtKB/Swiss-Prot),   B4DMC4 (UniProtKB/Swiss-Prot),   Q96EM7 (UniProtKB/Swiss-Prot),   O15381 (UniProtKB/Swiss-Prot),   B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_996671   ⟸   NM_206840
- Peptide Label: isoform 2
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001230075   ⟸   NM_001243146
- Peptide Label: isoform 3
- UniProtKB: O15381 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001230076   ⟸   NM_001243147
- Peptide Label: isoform 4
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011542498   ⟸   XM_011544196
- Peptide Label: isoform X4
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856872   ⟸   XM_017001383
- Peptide Label: isoform X5
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856868   ⟸   XM_017001379
- Peptide Label: isoform X2
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856867   ⟸   XM_017001378
- Peptide Label: isoform X1
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856869   ⟸   XM_017001380
- Peptide Label: isoform X3
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856873   ⟸   XM_017001384
- Peptide Label: isoform X6
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856874   ⟸   XM_017001385
- Peptide Label: isoform X9
- UniProtKB: B4DLM8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000418380   ⟸   ENST00000492281
RefSeq Acc Id: ENSP00000281701   ⟸   ENST00000281701
RefSeq Acc Id: ENSP00000419930   ⟸   ENST00000467882
RefSeq Acc Id: ENSP00000419420   ⟸   ENST00000469968
RefSeq Acc Id: ENSP00000417826   ⟸   ENST00000469075
RefSeq Acc Id: ENSP00000479235   ⟸   ENST00000481213
RefSeq Acc Id: ENSP00000417213   ⟸   ENST00000482491
RefSeq Acc Id: ENSP00000419586   ⟸   ENST00000470989
RefSeq Acc Id: ENSP00000375747   ⟸   ENST00000391875
RefSeq Acc Id: ENSP00000341362   ⟸   ENST00000340871
RefSeq Acc Id: ENSP00000419828   ⟸   ENST00000488718
RefSeq Acc Id: ENSP00000418085   ⟸   ENST00000461546
RefSeq Acc Id: ENSP00000394884   ⟸   ENST00000436927
RefSeq Acc Id: XP_047277569   ⟸   XM_047421613
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047277587   ⟸   XM_047421631
- Peptide Label: isoform X12
RefSeq Acc Id: XP_047277577   ⟸   XM_047421621
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047277574   ⟸   XM_047421618
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047277593   ⟸   XM_047421637
- Peptide Label: isoform X14
RefSeq Acc Id: XP_047277591   ⟸   XM_047421635
- Peptide Label: isoform X13
RefSeq Acc Id: XP_047277582   ⟸   XM_047421626
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054192785   ⟸   XM_054336810
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054192784   ⟸   XM_054336809
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054192782   ⟸   XM_054336807
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054192781   ⟸   XM_054336806
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054192787   ⟸   XM_054336812
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054192783   ⟸   XM_054336808
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054192792   ⟸   XM_054336817
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054192790   ⟸   XM_054336815
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054192788   ⟸   XM_054336813
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054192786   ⟸   XM_054336811
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054192794   ⟸   XM_054336819
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054192793   ⟸   XM_054336818
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054192791   ⟸   XM_054336816
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054192789   ⟸   XM_054336814
- Peptide Label: isoform X9
Protein Domains
AAA+ ATPase   NVL2 nucleolin binding

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O15381-F1-model_v2 AlphaFold O15381 1-856 view protein structure

Promoters
RGD ID:6786166
Promoter ID:HG_KWN:7522
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000091464
Position:
Human AssemblyChrPosition (strand)Source
Build 361222,522,466 - 222,522,966 (-)MPROMDB
RGD ID:6786167
Promoter ID:HG_KWN:7529
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:ENST00000340871,   ENST00000361463,   NM_206840,   OTTHUMT00000091455,   OTTHUMT00000091456,   OTTHUMT00000091457,   OTTHUMT00000091458,   OTTHUMT00000091459,   OTTHUMT00000091461
Position:
Human AssemblyChrPosition (strand)Source
Build 361222,584,331 - 222,584,832 (-)MPROMDB
RGD ID:6859090
Promoter ID:EPDNEW_H2709
Type:initiation region
Name:NVL_1
Description:nuclear VCP-like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,330,140 - 224,330,200EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8070 AgrOrtholog
COSMIC NVL COSMIC
Ensembl Genes ENSG00000143748 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000281701 ENTREZGENE
  ENST00000281701.11 UniProtKB/Swiss-Prot
  ENST00000340871 ENTREZGENE
  ENST00000340871.8 UniProtKB/Swiss-Prot
  ENST00000391875 ENTREZGENE
  ENST00000391875.6 UniProtKB/Swiss-Prot
  ENST00000436927.5 UniProtKB/TrEMBL
  ENST00000461546.2 UniProtKB/TrEMBL
  ENST00000467882.5 UniProtKB/TrEMBL
  ENST00000469075 ENTREZGENE
  ENST00000469075.5 UniProtKB/Swiss-Prot
  ENST00000469968.5 UniProtKB/Swiss-Prot
  ENST00000470989.5 UniProtKB/TrEMBL
  ENST00000481213.5 UniProtKB/TrEMBL
  ENST00000482491.5 UniProtKB/Swiss-Prot
  ENST00000488718.5 UniProtKB/TrEMBL
  ENST00000492281.5 UniProtKB/TrEMBL
Gene3D-CATH 1.10.10.2010 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.10.8.60 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000143748 GTEx
HGNC ID HGNC:8070 ENTREZGENE
Human Proteome Map NVL Human Proteome Map
InterPro AAA+_ATPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AAA_lid_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_AAA_core UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ATPase_AAA_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NLV2_N_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NVL2_nucleolin-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:4931 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 4931 ENTREZGENE
OMIM 602426 OMIM
PANTHER AAA-FAMILY ATPASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  COILED-COIL DOMAIN CONTAINING 122 UniProtKB/TrEMBL
  NUCLEAR VALOSIN-CONTAINING PROTEIN-LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PRIMATE-EXPANDED PROTEIN FAMILY UniProtKB/TrEMBL
Pfam AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AAA_lid_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nucleolin_bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31857 PharmGKB
PRINTS F138DOMAIN UniProtKB/TrEMBL
PROSITE AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP P-loop containing nucleoside triphosphate hydrolases UniProtKB/TrEMBL, UniProtKB/Swiss-Prot
UniProt A0A087WV72_HUMAN UniProtKB/TrEMBL
  A0JLP9_HUMAN UniProtKB/TrEMBL
  B4DF43_HUMAN UniProtKB/TrEMBL
  B4DLM8 ENTREZGENE, UniProtKB/TrEMBL
  B4DMC4 ENTREZGENE
  B4DP98 ENTREZGENE
  C9J6P7_HUMAN UniProtKB/TrEMBL
  C9JP83_HUMAN UniProtKB/TrEMBL
  E7EWK7_HUMAN UniProtKB/TrEMBL
  E9PGD8_HUMAN UniProtKB/TrEMBL
  E9PH71_HUMAN UniProtKB/TrEMBL
  F8WF01_HUMAN UniProtKB/TrEMBL
  NVL_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q96EM7 ENTREZGENE
  Q96PA2_HUMAN UniProtKB/TrEMBL
UniProt Secondary B4DMC4 UniProtKB/Swiss-Prot
  B4DP98 UniProtKB/Swiss-Prot
  Q96EM7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-02-19 NVL  nuclear VCP like  NVL  nuclear VCP-like  Symbol and/or name change 5135510 APPROVED