NUDC (nuclear distribution C, dynein complex regulator) - Rat Genome Database

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Gene: NUDC (nuclear distribution C, dynein complex regulator) Homo sapiens
Analyze
Symbol: NUDC
Name: nuclear distribution C, dynein complex regulator
RGD ID: 731477
HGNC Page HGNC:8045
Description: Enables cadherin binding activity. Involved in mitotic metaphase chromosome alignment and mitotic spindle organization. Located in cytosol; midbody; and mitotic spindle.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: HNUDC; MNUDC; NPD011; nuclear distribution C homolog; nuclear distribution gene C homolog; nuclear distribution gene c homolog (aspergillus); nuclear distribution protein C homolog; nuclear migration protein nudC
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: NUDCP1   NUDCP2  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38126,900,161 - 26,946,871 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl126,900,238 - 26,946,871 (+)EnsemblGRCh38hg38GRCh38
GRCh37127,248,234 - 27,273,362 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36127,120,811 - 27,145,474 (+)NCBINCBI36Build 36hg18NCBI36
Build 34126,932,365 - 26,957,029NCBI
Celera125,645,312 - 25,669,980 (+)NCBICelera
Cytogenetic Map1p36.11NCBI
HuRef125,501,783 - 25,526,939 (+)NCBIHuRef
CHM1_1127,361,578 - 27,386,708 (+)NCBICHM1_1
T2T-CHM13v2.0126,738,224 - 26,784,927 (+)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
cytoplasm  (IBA,IDA,IEA)
cytoskeleton  (IEA)
cytosol  (IDA,TAS)
membrane  (IEA)
microtubule  (IEA)
midbody  (IDA,IEA)
mitotic spindle  (IDA)
nucleoplasm  (TAS)
nucleus  (IEA)
spindle  (IEA,TAS)

Molecular Function

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

Human Phenotype
Obesity  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Reactome: A Knowledgebase of Biological Processes Reactome
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9601647   PMID:10210332   PMID:10453739   PMID:11076863   PMID:11230166   PMID:11256614   PMID:11734602   PMID:12477932   PMID:12679384   PMID:12852857   PMID:12885786   PMID:14676831  
PMID:14744259   PMID:15342556   PMID:15489334   PMID:15489336   PMID:16088917   PMID:16381901   PMID:16710414   PMID:16860740   PMID:17081983   PMID:17353931   PMID:17658515   PMID:18029348  
PMID:18288130   PMID:19135240   PMID:19560457   PMID:19615732   PMID:19875381   PMID:20360068   PMID:20467437   PMID:20529857   PMID:20562859   PMID:20675372   PMID:21044950   PMID:21081666  
PMID:21473139   PMID:21873635   PMID:21907836   PMID:22159412   PMID:22190034   PMID:22623428   PMID:22658674   PMID:22863883   PMID:22939629   PMID:22990118   PMID:23364796   PMID:24069238  
PMID:24255178   PMID:24366813   PMID:24711643   PMID:24927568   PMID:24981860   PMID:25036637   PMID:25147182   PMID:25324306   PMID:25332235   PMID:25468996   PMID:25789526   PMID:25900982  
PMID:25921289   PMID:26269332   PMID:26344197   PMID:26496610   PMID:26499835   PMID:26638075   PMID:26752685   PMID:26777405   PMID:26816005   PMID:26831064   PMID:27035759   PMID:27074040  
PMID:27173435   PMID:27634302   PMID:27637333   PMID:27684187   PMID:27705803   PMID:27880917   PMID:27959429   PMID:28302793   PMID:28330616   PMID:28443643   PMID:28514442   PMID:28515276  
PMID:28524877   PMID:28581483   PMID:28675297   PMID:28712289   PMID:28718761   PMID:29117863   PMID:29128334   PMID:29229926   PMID:29395067   PMID:29478914   PMID:29507755   PMID:29911972  
PMID:30033366   PMID:30110629   PMID:30224337   PMID:30463901   PMID:30833792   PMID:30884312   PMID:30948266   PMID:31046837   PMID:31091453   PMID:31519766   PMID:31594818   PMID:31732153  
PMID:31871319   PMID:31980649   PMID:32129710   PMID:32457219   PMID:32552912   PMID:32640226   PMID:32687490   PMID:32694731   PMID:32707033   PMID:32807901   PMID:32814053   PMID:32877691  
PMID:32929329   PMID:32963011   PMID:32994395   PMID:33239621   PMID:33374456   PMID:33397691   PMID:33417871   PMID:33916271   PMID:33957083   PMID:33961781   PMID:34060350   PMID:34079125  
PMID:34189442   PMID:34265304   PMID:34349018   PMID:34373451   PMID:34645483   PMID:34709727   PMID:34728620   PMID:34795231   PMID:35063084   PMID:35063133   PMID:35140242   PMID:35235311  
PMID:35256949   PMID:35271311   PMID:35439318   PMID:35446349   PMID:35546148   PMID:35562734   PMID:35563538   PMID:35777956   PMID:35831314   PMID:35906200   PMID:35944360   PMID:35973513  
PMID:35987950   PMID:36114006   PMID:36215168   PMID:36517590   PMID:36526897   PMID:36543142   PMID:36604567   PMID:36674791   PMID:36774506   PMID:36964488   PMID:37039823   PMID:37071682  
PMID:37108203   PMID:37167062   PMID:37223481   PMID:37232246   PMID:37314216   PMID:37317656   PMID:37689310   PMID:37774976   PMID:37827155   PMID:38113892   PMID:38223760   PMID:38280479  
PMID:38334954   PMID:39231216  


Genomics

Comparative Map Data
NUDC
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38126,900,161 - 26,946,871 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl126,900,238 - 26,946,871 (+)EnsemblGRCh38hg38GRCh38
GRCh37127,248,234 - 27,273,362 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36127,120,811 - 27,145,474 (+)NCBINCBI36Build 36hg18NCBI36
Build 34126,932,365 - 26,957,029NCBI
Celera125,645,312 - 25,669,980 (+)NCBICelera
Cytogenetic Map1p36.11NCBI
HuRef125,501,783 - 25,526,939 (+)NCBIHuRef
CHM1_1127,361,578 - 27,386,708 (+)NCBICHM1_1
T2T-CHM13v2.0126,738,224 - 26,784,927 (+)NCBIT2T-CHM13v2.0
Nudc
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394133,259,853 - 133,273,338 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4133,259,853 - 133,273,307 (-)EnsemblGRCm39 Ensembl
GRCm384133,532,542 - 133,546,027 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4133,532,542 - 133,545,996 (-)EnsemblGRCm38mm10GRCm38
MGSCv374133,088,457 - 133,101,942 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364132,804,620 - 132,825,130 (-)NCBIMGSCv36mm8
Celera4131,701,670 - 131,715,113 (-)NCBICelera
Cytogenetic Map4D2.3NCBI
cM Map466.25NCBI
Nudc
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85151,041,878 - 151,055,260 (-)NCBIGRCr8
mRatBN7.25145,758,006 - 145,771,390 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5145,758,002 - 145,771,425 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5148,460,055 - 148,473,468 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05150,229,658 - 150,243,070 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05150,216,214 - 150,229,627 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05151,754,723 - 151,768,104 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5151,754,716 - 151,768,123 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05155,443,982 - 155,457,375 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.45151,535,900 - 151,550,041 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.15151,545,941 - 151,560,080 (+)NCBI
Celera5144,178,324 - 144,191,960 (-)NCBICelera
Cytogenetic Map5q36NCBI
Nudc
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554526,261,286 - 6,278,393 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554526,261,500 - 6,278,393 (+)NCBIChiLan1.0ChiLan1.0
NUDC
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21199,925,277 - 199,950,916 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11199,029,420 - 199,055,006 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0126,184,232 - 26,207,412 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1127,239,780 - 27,263,952 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl127,239,574 - 27,267,360 (+)Ensemblpanpan1.1panPan2
NUDC
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1273,207,945 - 73,222,027 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl273,208,146 - 73,222,020 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha269,785,990 - 69,800,075 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0273,771,708 - 73,785,789 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl273,771,713 - 73,785,782 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1270,596,734 - 70,610,791 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0271,602,099 - 71,616,194 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0272,605,104 - 72,619,184 (-)NCBIUU_Cfam_GSD_1.0
Nudc
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505845,503,199 - 45,516,577 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647411,327,942 - 11,343,672 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647411,327,986 - 11,341,357 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NUDC
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl684,238,430 - 84,252,046 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1684,238,695 - 84,252,046 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2677,808,882 - 77,822,246 (+)NCBISscrofa10.2Sscrofa10.2susScr3
NUDC
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.120105,817,738 - 105,842,188 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl20105,817,213 - 105,842,180 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603310,590,371 - 10,615,395 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nudc
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476410,908,956 - 10,925,547 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476410,889,020 - 10,925,547 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NUDC
98 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_021969.3(NR0B2):c.160C>T (p.Arg54Cys) single nucleotide variant NR0B2-related disorder [RCV003419905]|not provided [RCV000523542] Chr1:26913781 [GRCh38]
Chr1:27240272 [GRCh37]
Chr1:1p36.11		 uncertain significance
GRCh38/hg38 1p36.11-35.3(chr1:26807012-27685191)x1 copy number loss See cases [RCV000053799] Chr1:26807012..27685191 [GRCh38]
Chr1:27133503..28011702 [GRCh37]
Chr1:27006090..27884289 [NCBI36]
Chr1:1p36.11-35.3		 pathogenic
GRCh38/hg38 1p36.11-35.3(chr1:26854636-27645829)x1 copy number loss See cases [RCV000137657] Chr1:26854636..27645829 [GRCh38]
Chr1:27181127..27972340 [GRCh37]
Chr1:27053714..27844927 [NCBI36]
Chr1:1p36.11-35.3		 uncertain significance
GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3 copy number gain See cases [RCV000138891] Chr1:24381206..41401517 [GRCh38]
Chr1:24707696..41886350 [GRCh37]
Chr1:24580283..41658937 [NCBI36]
Chr1:1p36.11-34.2		 pathogenic
NM_021969.3(NR0B2):c.100C>T (p.Arg34Ter) single nucleotide variant Obesity, mild, early-onset [RCV000005759] Chr1:26913841 [GRCh38]
Chr1:27240332 [GRCh37]
Chr1:1p36.11		 pathogenic
NM_021969.3(NR0B2):c.583G>T (p.Ala195Ser) single nucleotide variant Obesity, mild, early-onset [RCV000005760]|not specified [RCV002247254] Chr1:26912036 [GRCh38]
Chr1:27238527 [GRCh37]
Chr1:1p36.11		 pathogenic|uncertain significance
NM_021969.2(NR0B2):c.369G>A (p.Leu123=) single nucleotide variant Malignant melanoma [RCV000064696] Chr1:26913572 [GRCh38]
Chr1:27240063 [GRCh37]
Chr1:27112650 [NCBI36]
Chr1:1p36.11		 not provided
NM_021969.2(NR0B2):c.195G>A (p.Lys65=) single nucleotide variant Malignant melanoma [RCV000064697] Chr1:26913746 [GRCh38]
Chr1:27240237 [GRCh37]
Chr1:27112824 [NCBI36]
Chr1:1p36.11		 not provided
NM_021969.3(NR0B2):c.532G>A (p.Asp178Asn) single nucleotide variant NR0B2-related disorder [RCV003977518]|not specified [RCV000192799] Chr1:26913409 [GRCh38]
Chr1:27239900 [GRCh37]
Chr1:1p36.11		 likely benign|uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12		 likely benign
NM_021969.3(NR0B2):c.122G>A (p.Cys41Tyr) single nucleotide variant NR0B2-related disorder [RCV004745370]|not specified [RCV000412948] Chr1:26913819 [GRCh38]
Chr1:27240310 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.512G>C (p.Gly171Ala) single nucleotide variant not provided [RCV002067111]|not specified [RCV000730964] Chr1:26913429 [GRCh38]
Chr1:27239920 [GRCh37]
Chr1:1p36.11		 benign
GRCh37/hg19 1p36.11(chr1:27119557-27547784)x3 copy number gain See cases [RCV000448699] Chr1:27119557..27547784 [GRCh37]
Chr1:1p36.11		 uncertain significance
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_006600.4(NUDC):c.244C>T (p.Arg82Trp) single nucleotide variant not specified [RCV004300072] Chr1:26941541 [GRCh38]
Chr1:27268032 [GRCh37]
Chr1:1p36.11		 uncertain significance
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_021969.3(NR0B2):c.157_166del (p.His53fs) deletion APC-mutation negative familial colorectal cancer [RCV000859985]|Inherited obesity [RCV003133593]|NR0B2-related disorder [RCV003965583]|not provided [RCV002535765]|not specified [RCV002249486] Chr1:26913775..26913784 [GRCh38]
Chr1:27240266..27240275 [GRCh37]
Chr1:1p36.11		 likely pathogenic|benign|uncertain significance
NM_021969.3(NR0B2):c.13C>G (p.Gln5Glu) single nucleotide variant not provided [RCV000883581] Chr1:26913928 [GRCh38]
Chr1:27240419 [GRCh37]
Chr1:1p36.11		 benign
NM_021969.3(NR0B2):c.227del (p.Phe76fs) deletion APC-mutation negative familial colorectal cancer [RCV000859986]|Obesity [RCV002249487] Chr1:26913714 [GRCh38]
Chr1:27240205 [GRCh37]
Chr1:1p36.11		 pathogenic|likely pathogenic
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1		 uncertain significance
NM_021969.3(NR0B2):c.293_301delinsAC (p.Leu98fs) indel APC-mutation negative familial colorectal cancer [RCV000859984]|Obesity [RCV002468047] Chr1:26913640..26913648 [GRCh38]
Chr1:27240131..27240139 [GRCh37]
Chr1:1p36.11		 likely pathogenic
NM_021969.3(NR0B2):c.473G>A (p.Ser158Asn) single nucleotide variant Obesity [RCV002468099]|not provided [RCV000963748]|not specified [RCV001819054] Chr1:26913468 [GRCh38]
Chr1:27239959 [GRCh37]
Chr1:1p36.11		 benign|uncertain significance
NM_021969.3(NR0B2):c.450A>G (p.Gln150=) single nucleotide variant NR0B2-related disorder [RCV003942897]|not provided [RCV000930066] Chr1:26913491 [GRCh38]
Chr1:27239982 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.528C>A (p.Asn176Lys) single nucleotide variant Obesity [RCV002468454] Chr1:26913413 [GRCh38]
Chr1:27239904 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.531del (p.Asp178fs) deletion Obesity [RCV001336561] Chr1:26913410 [GRCh38]
Chr1:27239901 [GRCh37]
Chr1:1p36.11		 pathogenic
NM_021969.3(NR0B2):c.339G>A (p.Pro113=) single nucleotide variant NR0B2-related disorder [RCV003923325]|not provided [RCV002542001]|not specified [RCV001817500] Chr1:26913602 [GRCh38]
Chr1:27240093 [GRCh37]
Chr1:1p36.11		 benign|likely benign
GRCh37/hg19 1p36.11(chr1:27119557-27547784) copy number gain not specified [RCV002053011] Chr1:27119557..27547784 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.712C>T (p.Arg238Cys) single nucleotide variant Inherited obesity [RCV004762193]|NR0B2-related disorder [RCV003892880]|Obesity [RCV001823855]|not specified [RCV004041005] Chr1:26911907 [GRCh38]
Chr1:27238398 [GRCh37]
Chr1:1p36.11		 uncertain significance
NC_000001.10:g.(?_27117307)_(27480825_?)dup duplication not provided [RCV001918992] Chr1:27117307..27480825 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.138C>T (p.Pro46=) single nucleotide variant NR0B2-related disorder [RCV003933396]|not provided [RCV002103275] Chr1:26913803 [GRCh38]
Chr1:27240294 [GRCh37]
Chr1:1p36.11		 likely benign
NC_000001.10:g.(?_25870190)_(27278871_?)dup duplication Retinitis pigmentosa 59 [RCV003122734] Chr1:25870190..27278871 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.278G>A (p.Gly93Asp) single nucleotide variant not provided [RCV002262221] Chr1:26913663 [GRCh38]
Chr1:27240154 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.253_254dup (p.Arg86fs) duplication Inherited obesity [RCV003131082] Chr1:26913686..26913687 [GRCh38]
Chr1:27240177..27240178 [GRCh37]
Chr1:1p36.11		 likely pathogenic
NM_022078.3(GPATCH3):c.62C>A (p.Pro21His) single nucleotide variant not specified [RCV004206525] Chr1:26900381 [GRCh38]
Chr1:27226872 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.776C>T (p.Ser259Phe) single nucleotide variant not specified [RCV004139881] Chr1:26945424 [GRCh38]
Chr1:27271915 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.224C>T (p.Ser75Phe) single nucleotide variant not specified [RCV004214271] Chr1:26913717 [GRCh38]
Chr1:27240208 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.242G>A (p.Arg81Gln) single nucleotide variant not specified [RCV004178507] Chr1:26941539 [GRCh38]
Chr1:27268030 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.310G>C (p.Ala104Pro) single nucleotide variant not specified [RCV004085303] Chr1:26913631 [GRCh38]
Chr1:27240122 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.82C>G (p.Leu28Val) single nucleotide variant not specified [RCV004186302] Chr1:26924089 [GRCh38]
Chr1:27250580 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_022078.3(GPATCH3):c.104A>G (p.Gln35Arg) single nucleotide variant not specified [RCV004078745] Chr1:26900339 [GRCh38]
Chr1:27226830 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.754del (p.Asp252fs) deletion not provided [RCV003022457] Chr1:26911865 [GRCh38]
Chr1:27238356 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_022078.3(GPATCH3):c.205A>G (p.Thr69Ala) single nucleotide variant not specified [RCV004146443] Chr1:26900238 [GRCh38]
Chr1:27226729 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.281A>C (p.Glu94Ala) single nucleotide variant not specified [RCV004185545] Chr1:26941578 [GRCh38]
Chr1:27268069 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.751G>A (p.Gly251Arg) single nucleotide variant not specified [RCV004156839] Chr1:26911868 [GRCh38]
Chr1:27238359 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.521T>C (p.Leu174Pro) single nucleotide variant not specified [RCV004143408] Chr1:26913420 [GRCh38]
Chr1:27239911 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_022078.3(GPATCH3):c.177G>T (p.Gln59His) single nucleotide variant not specified [RCV004085833] Chr1:26900266 [GRCh38]
Chr1:27226757 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_022078.3(GPATCH3):c.25G>C (p.Glu9Gln) single nucleotide variant not specified [RCV004171148] Chr1:26900418 [GRCh38]
Chr1:27226909 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.254G>A (p.Arg85Gln) single nucleotide variant NR0B2-related disorder [RCV003410248]|not specified [RCV004233024] Chr1:26913687 [GRCh38]
Chr1:27240178 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.659C>T (p.Thr220Met) single nucleotide variant not provided [RCV002607579] Chr1:26911960 [GRCh38]
Chr1:27238451 [GRCh37]
Chr1:1p36.11		 benign
NM_021969.3(NR0B2):c.250C>G (p.Gln84Glu) single nucleotide variant not provided [RCV002586166] Chr1:26913691 [GRCh38]
Chr1:27240182 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.71T>C (p.Leu24Pro) single nucleotide variant not specified [RCV004322882] Chr1:26913870 [GRCh38]
Chr1:27240361 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.637C>T (p.Arg213Cys) single nucleotide variant Inherited obesity [RCV003228577]|NR0B2-related disorder [RCV004747276] Chr1:26911982 [GRCh38]
Chr1:27238473 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.497A>G (p.Tyr166Cys) single nucleotide variant Inherited obesity [RCV003228685] Chr1:26913444 [GRCh38]
Chr1:27239935 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.502G>T (p.Asp168Tyr) single nucleotide variant not specified [RCV004268502] Chr1:26942732 [GRCh38]
Chr1:27269223 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.265G>T (p.Ala89Ser) single nucleotide variant not specified [RCV004284796] Chr1:26941562 [GRCh38]
Chr1:27268053 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.211A>G (p.Arg71Gly) single nucleotide variant Inherited obesity [RCV003336046]|NR0B2-related disorder [RCV003936747]|not specified [RCV004334149] Chr1:26913730 [GRCh38]
Chr1:27240221 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.563G>T (p.Cys188Phe) single nucleotide variant not specified [RCV004343721] Chr1:26942887 [GRCh38]
Chr1:27269378 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.557C>T (p.Pro186Leu) single nucleotide variant not specified [RCV004343720] Chr1:26942881 [GRCh38]
Chr1:27269372 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_022078.3(GPATCH3):c.79G>T (p.Ala27Ser) single nucleotide variant not specified [RCV004365934] Chr1:26900364 [GRCh38]
Chr1:27226855 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.647C>T (p.Ala216Val) single nucleotide variant not specified [RCV004360286] Chr1:26942971 [GRCh38]
Chr1:27269462 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.469G>A (p.Gly157Arg) single nucleotide variant not specified [RCV004365762] Chr1:26942699 [GRCh38]
Chr1:27269190 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.625G>A (p.Ala209Thr) single nucleotide variant NR0B2-related disorder [RCV003393149] Chr1:26911994 [GRCh38]
Chr1:27238485 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.530C>A (p.Pro177His) single nucleotide variant not specified [RCV004361247] Chr1:26913411 [GRCh38]
Chr1:27239902 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.434C>T (p.Ala145Val) single nucleotide variant NR0B2-related disorder [RCV003946501]|not provided [RCV003730546]|not specified [RCV004340488] Chr1:26913507 [GRCh38]
Chr1:27239998 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.749T>C (p.Leu250Pro) single nucleotide variant Inherited obesity [RCV003448637]|NR0B2-related disorder [RCV003939045]|not provided [RCV003553943] Chr1:26911870 [GRCh38]
Chr1:27238361 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.101G>C (p.Arg34Pro) single nucleotide variant NR0B2-related disorder [RCV003420689] Chr1:26913840 [GRCh38]
Chr1:27240331 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.91G>A (p.Ala31Thr) single nucleotide variant NR0B2-related disorder [RCV003408432] Chr1:26913850 [GRCh38]
Chr1:27240341 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.203C>T (p.Ala68Val) single nucleotide variant NR0B2-related disorder [RCV003427860]|not specified [RCV004654210] Chr1:26913738 [GRCh38]
Chr1:27240229 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.352C>G (p.Leu118Val) single nucleotide variant NR0B2-related disorder [RCV003402995] Chr1:26913589 [GRCh38]
Chr1:27240080 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.50G>A (p.Arg17His) single nucleotide variant NR0B2-related disorder [RCV003399992] Chr1:26913891 [GRCh38]
Chr1:27240382 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.100C>G (p.Arg34Gly) single nucleotide variant NR0B2-related disorder [RCV003420894] Chr1:26913841 [GRCh38]
Chr1:27240332 [GRCh37]
Chr1:1p36.11		 uncertain significance
GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3 copy number gain Trisomy 12p [RCV003447845] Chr1:99125..34026935 [GRCh38]
Chr1:1p36.33-35.1		 pathogenic
NM_021969.3(NR0B2):c.734A>G (p.Asp245Gly) single nucleotide variant NR0B2-related disorder [RCV003412028]|not specified [RCV004362786] Chr1:26911885 [GRCh38]
Chr1:27238376 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.718A>G (p.Ile240Val) single nucleotide variant NR0B2-related disorder [RCV003427911] Chr1:26911901 [GRCh38]
Chr1:27238392 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.739G>A (p.Ala247Thr) single nucleotide variant NR0B2-related disorder [RCV003412211] Chr1:26911880 [GRCh38]
Chr1:27238371 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.769A>G (p.Arg257Gly) single nucleotide variant NR0B2-related disorder [RCV003420933] Chr1:26911850 [GRCh38]
Chr1:27238341 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.647G>A (p.Arg216His) single nucleotide variant NR0B2-related disorder [RCV003397736] Chr1:26911972 [GRCh38]
Chr1:27238463 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.638G>A (p.Arg213His) single nucleotide variant NR0B2-related disorder [RCV003414523] Chr1:26911981 [GRCh38]
Chr1:27238472 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.257G>A (p.Arg86Gln) single nucleotide variant NR0B2-related disorder [RCV003416802] Chr1:26913684 [GRCh38]
Chr1:27240175 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.256C>T (p.Arg86Trp) single nucleotide variant NR0B2-related disorder [RCV003417070] Chr1:26913685 [GRCh38]
Chr1:27240176 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.338C>T (p.Pro113Leu) single nucleotide variant NR0B2-related disorder [RCV003418884] Chr1:26913603 [GRCh38]
Chr1:27240094 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.113G>A (p.Arg38His) single nucleotide variant NR0B2-related disorder [RCV003410846] Chr1:26913828 [GRCh38]
Chr1:27240319 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.265C>T (p.Gln89Ter) single nucleotide variant NR0B2-related disorder [RCV003418812] Chr1:26913676 [GRCh38]
Chr1:27240167 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.55G>A (p.Ala19Thr) single nucleotide variant NR0B2-related disorder [RCV003966485]|not provided [RCV003546158] Chr1:26913886 [GRCh38]
Chr1:27240377 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.134G>A (p.Arg45Gln) single nucleotide variant NR0B2-related disorder [RCV003939202]|not provided [RCV003739272] Chr1:26913807 [GRCh38]
Chr1:27240298 [GRCh37]
Chr1:1p36.11		 likely benign|uncertain significance
NM_021969.3(NR0B2):c.553G>A (p.Ala185Thr) single nucleotide variant NR0B2-related disorder [RCV004747316]|not provided [RCV003573251] Chr1:26912066 [GRCh38]
Chr1:27238557 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.343C>T (p.Pro115Ser) single nucleotide variant NR0B2-related disorder [RCV003981113]|not provided [RCV003737539] Chr1:26913598 [GRCh38]
Chr1:27240089 [GRCh37]
Chr1:1p36.11		 likely benign|uncertain significance
NM_021969.3(NR0B2):c.121T>C (p.Cys41Arg) single nucleotide variant not provided [RCV003869796] Chr1:26913820 [GRCh38]
Chr1:27240311 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.672C>T (p.Leu224=) single nucleotide variant NR0B2-related disorder [RCV004747344]|not provided [RCV003721810] Chr1:26911947 [GRCh38]
Chr1:27238438 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.389G>C (p.Gly130Ala) single nucleotide variant not provided [RCV003679314] Chr1:26913552 [GRCh38]
Chr1:27240043 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.54C>T (p.Pro18=) single nucleotide variant NR0B2-related disorder [RCV003906934] Chr1:26913887 [GRCh38]
Chr1:27240378 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.170G>A (p.Arg57Gln) single nucleotide variant NR0B2-related disorder [RCV003912071] Chr1:26913771 [GRCh38]
Chr1:27240262 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.632A>G (p.Gln211Arg) single nucleotide variant NR0B2-related disorder [RCV003982053] Chr1:26911987 [GRCh38]
Chr1:27238478 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.129G>A (p.Gln43=) single nucleotide variant NR0B2-related disorder [RCV003894404] Chr1:26913812 [GRCh38]
Chr1:27240303 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.328G>C (p.Ala110Pro) single nucleotide variant not specified [RCV004491201] Chr1:26913613 [GRCh38]
Chr1:27240104 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.55G>T (p.Ala19Ser) single nucleotide variant not specified [RCV004491202] Chr1:26913886 [GRCh38]
Chr1:27240377 [GRCh37]
Chr1:1p36.11		 uncertain significance
NC_000001.11:g.26900659A>G single nucleotide variant GPATCH3-related disorder [RCV003959285] Chr1:26900659 [GRCh38]
Chr1:27227150 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.415C>T (p.Pro139Ser) single nucleotide variant NR0B2-related disorder [RCV003976766] Chr1:26913526 [GRCh38]
Chr1:27240017 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.303C>T (p.Ala101=) single nucleotide variant NR0B2-related disorder [RCV003901866] Chr1:26913638 [GRCh38]
Chr1:27240129 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.101G>A (p.Arg34Gln) single nucleotide variant NR0B2-related disorder [RCV003967386] Chr1:26913840 [GRCh38]
Chr1:27240331 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.144G>A (p.Gln48=) single nucleotide variant NR0B2-related disorder [RCV003971937] Chr1:26913797 [GRCh38]
Chr1:27240288 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.618G>A (p.Trp206Ter) single nucleotide variant NR0B2-related disorder [RCV003966954] Chr1:26912001 [GRCh38]
Chr1:27238492 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.426C>T (p.Ser142=) single nucleotide variant NR0B2-related disorder [RCV003934377] Chr1:26913515 [GRCh38]
Chr1:27240006 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.66C>T (p.Tyr22=) single nucleotide variant NR0B2-related disorder [RCV003914055] Chr1:26913875 [GRCh38]
Chr1:27240366 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.139G>A (p.Val47Ile) single nucleotide variant NR0B2-related disorder [RCV003893612] Chr1:26913802 [GRCh38]
Chr1:27240293 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.606C>T (p.Ile202=) single nucleotide variant NUDC-related condition [RCV004759078] Chr1:26942930 [GRCh38]
Chr1:27269421 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.435G>A (p.Ala145=) single nucleotide variant NR0B2-related disorder [RCV003909425] Chr1:26913506 [GRCh38]
Chr1:27239997 [GRCh37]
Chr1:1p36.11		 likely benign
NM_006600.4(NUDC):c.209G>A (p.Arg70Gln) single nucleotide variant not specified [RCV004496126] Chr1:26941506 [GRCh38]
Chr1:27267997 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.895A>G (p.Met299Val) single nucleotide variant not specified [RCV004496130] Chr1:26945637 [GRCh38]
Chr1:27272128 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.962C>T (p.Pro321Leu) single nucleotide variant not specified [RCV004496131] Chr1:26946147 [GRCh38]
Chr1:27272638 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.299C>T (p.Ser100Leu) single nucleotide variant not specified [RCV004496127] Chr1:26941596 [GRCh38]
Chr1:27268087 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.767G>A (p.Arg256His) single nucleotide variant not specified [RCV004496128] Chr1:26945415 [GRCh38]
Chr1:27271906 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.884G>A (p.Arg295Gln) single nucleotide variant not specified [RCV004496129] Chr1:26945626 [GRCh38]
Chr1:27272117 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.622C>T (p.Arg208Trp) single nucleotide variant not specified [RCV004652614] Chr1:26942946 [GRCh38]
Chr1:27269437 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.238G>A (p.Glu80Lys) single nucleotide variant not specified [RCV004652615] Chr1:26941535 [GRCh38]
Chr1:27268026 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.746A>G (p.Asn249Ser) single nucleotide variant not specified [RCV004652616] Chr1:26945394 [GRCh38]
Chr1:27271885 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.254C>T (p.Ala85Val) single nucleotide variant not specified [RCV004638823] Chr1:26941551 [GRCh38]
Chr1:27268042 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_022078.3(GPATCH3):c.106T>C (p.Phe36Leu) single nucleotide variant not specified [RCV004632219] Chr1:26900337 [GRCh38]
Chr1:27226828 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.449A>C (p.Glu150Ala) single nucleotide variant not specified [RCV004638824] Chr1:26942679 [GRCh38]
Chr1:27269170 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.562A>T (p.Ile188Phe) single nucleotide variant not specified [RCV004638654] Chr1:26912057 [GRCh38]
Chr1:27238548 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_006600.4(NUDC):c.403G>A (p.Gly135Ser) single nucleotide variant not specified [RCV004638822] Chr1:26941792 [GRCh38]
Chr1:27268283 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.599G>A (p.Cys200Tyr) single nucleotide variant NR0B2-related disorder [RCV004746613] Chr1:26912020 [GRCh38]
Chr1:27238511 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.629C>T (p.Ala210Val) single nucleotide variant NR0B2-related disorder [RCV004746930] Chr1:26911990 [GRCh38]
Chr1:27238481 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.376C>G (p.Pro126Ala) single nucleotide variant NR0B2-related disorder [RCV004747972] Chr1:26913565 [GRCh38]
Chr1:27240056 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.290T>C (p.Leu97Pro) single nucleotide variant NR0B2-related disorder [RCV004746896] Chr1:26913651 [GRCh38]
Chr1:27240142 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.646C>T (p.Arg216Cys) single nucleotide variant NR0B2-related disorder [RCV004746969] Chr1:26911973 [GRCh38]
Chr1:27238464 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.476T>C (p.Leu159Pro) single nucleotide variant NR0B2-related disorder [RCV004747600] Chr1:26913465 [GRCh38]
Chr1:27239956 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.153A>C (p.Ala51=) single nucleotide variant NR0B2-related disorder [RCV004726606] Chr1:26913788 [GRCh38]
Chr1:27240279 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.27C>T (p.Cys9=) single nucleotide variant NR0B2-related disorder [RCV004745746] Chr1:26913914 [GRCh38]
Chr1:27240405 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.221C>T (p.Pro74Leu) single nucleotide variant NR0B2-related disorder [RCV004745866] Chr1:26913720 [GRCh38]
Chr1:27240211 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.730G>C (p.Val244Leu) single nucleotide variant NR0B2-related disorder [RCV004745950] Chr1:26911889 [GRCh38]
Chr1:27238380 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.596T>C (p.Leu199Pro) single nucleotide variant Inherited obesity [RCV004764676] Chr1:26912023 [GRCh38]
Chr1:27238514 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.451T>C (p.Cys151Arg) single nucleotide variant NR0B2-related disorder [RCV004745744] Chr1:26913490 [GRCh38]
Chr1:27239981 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.317C>T (p.Thr106Ile) single nucleotide variant NR0B2-related disorder [RCV004746682] Chr1:26913624 [GRCh38]
Chr1:27240115 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.253C>T (p.Arg85Trp) single nucleotide variant NR0B2-related disorder [RCV004747762] Chr1:26913688 [GRCh38]
Chr1:27240179 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.70C>T (p.Leu24Phe) single nucleotide variant NR0B2-related disorder [RCV004728252] Chr1:26913871 [GRCh38]
Chr1:27240362 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.692T>C (p.Leu231Pro) single nucleotide variant NR0B2-related disorder [RCV004729911] Chr1:26911927 [GRCh38]
Chr1:27238418 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.561C>T (p.His187=) single nucleotide variant NR0B2-related disorder [RCV004745731] Chr1:26912058 [GRCh38]
Chr1:27238549 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.716C>T (p.Pro239Leu) single nucleotide variant NR0B2-related disorder [RCV004745883] Chr1:26911903 [GRCh38]
Chr1:27238394 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.461A>C (p.Glu154Ala) single nucleotide variant NR0B2-related disorder [RCV004746717] Chr1:26913480 [GRCh38]
Chr1:27239971 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.2T>C (p.Met1Thr) single nucleotide variant NR0B2-related disorder [RCV004728164] Chr1:26913939 [GRCh38]
Chr1:27240430 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.441G>A (p.Gln147=) single nucleotide variant NR0B2-related disorder [RCV004746027] Chr1:26913500 [GRCh38]
Chr1:27239991 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.155C>G (p.Pro52Arg) single nucleotide variant NR0B2-related disorder [RCV004747520] Chr1:26913786 [GRCh38]
Chr1:27240277 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.392G>A (p.Gly131Asp) single nucleotide variant NR0B2-related disorder [RCV004745680] Chr1:26913549 [GRCh38]
Chr1:27240040 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.41del (p.Ala14fs) deletion NR0B2-related disorder [RCV004745641] Chr1:26913900 [GRCh38]
Chr1:27240391 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.-8C>A single nucleotide variant NR0B2-related disorder [RCV004745752] Chr1:26913948 [GRCh38]
Chr1:27240439 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.620G>A (p.Cys207Tyr) single nucleotide variant NR0B2-related disorder [RCV004745804] Chr1:26911999 [GRCh38]
Chr1:27238490 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.-5T>C single nucleotide variant NR0B2-related disorder [RCV004745857] Chr1:26913945 [GRCh38]
Chr1:27240436 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.531C>T (p.Pro177=) single nucleotide variant NR0B2-related disorder [RCV004746034] Chr1:26913410 [GRCh38]
Chr1:27239901 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.85C>T (p.Leu29Phe) single nucleotide variant NR0B2-related disorder [RCV004746615] Chr1:26913856 [GRCh38]
Chr1:27240347 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.533-4A>G single nucleotide variant NR0B2-related disorder [RCV004746665] Chr1:26912090 [GRCh38]
Chr1:27238581 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.564T>C (p.Ile188=) single nucleotide variant NR0B2-related disorder [RCV004746870] Chr1:26912055 [GRCh38]
Chr1:27238546 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.468C>T (p.Phe156=) single nucleotide variant NR0B2-related disorder [RCV004746872] Chr1:26913473 [GRCh38]
Chr1:27239964 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.186T>C (p.Val62=) single nucleotide variant NR0B2-related disorder [RCV004746927] Chr1:26913755 [GRCh38]
Chr1:27240246 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.405G>A (p.Leu135=) single nucleotide variant NR0B2-related disorder [RCV004746883] Chr1:26913536 [GRCh38]
Chr1:27240027 [GRCh37]
Chr1:1p36.11		 likely benign
NM_021969.3(NR0B2):c.172dup (p.Glu58fs) duplication NR0B2-related disorder [RCV004747569] Chr1:26913768..26913769 [GRCh38]
Chr1:27240259..27240260 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.86T>C (p.Leu29Pro) single nucleotide variant NR0B2-related disorder [RCV004747662] Chr1:26913855 [GRCh38]
Chr1:27240346 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.123T>G (p.Cys41Trp) single nucleotide variant NR0B2-related disorder [RCV004747887] Chr1:26913818 [GRCh38]
Chr1:27240309 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.134G>C (p.Arg45Pro) single nucleotide variant NR0B2-related disorder [RCV004747985] Chr1:26913807 [GRCh38]
Chr1:27240298 [GRCh37]
Chr1:1p36.11		 uncertain significance
NM_021969.3(NR0B2):c.594G>A (p.Val198=) single nucleotide variant NR0B2-related disorder [RCV004730104] Chr1:26912025 [GRCh38]
Chr1:27238516 [GRCh37]
Chr1:1p36.11		 likely benign
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR483hsa-miR-483-3pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248

Predicted Target Of
Summary Value
Count of predictions:1486
Count of miRNA genes:673
Interacting mature miRNAs:770
Transcripts:ENST00000321265, ENST00000435827, ENST00000452707, ENST00000484772
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407210949GWAS859925_Hlipoprotein A measurement QTL GWAS859925 (human)8e-12triglycerides:total lipids ratio, low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)12693605426936055Human
407307846GWAS956822_Hglycoprotein measurement QTL GWAS956822 (human)4e-09glycoprotein measurement12693605426936055Human
406954240GWAS603216_Hplatelet crit QTL GWAS603216 (human)2e-12fatty acid measurementplateletcrit (CMO:0001349)12693605426936055Human
407125191GWAS774167_Hsexual dimorphism measurement QTL GWAS774167 (human)3e-19sexual dimorphism measurement12690287826902879Human
407312899GWAS961875_Hvery low density lipoprotein cholesterol measurement, cholesterol:total lipids ratio QTL GWAS961875 (human)3e-14very low density lipoprotein cholesterol measurement, cholesterol:total lipids ratioblood very low density lipoprotein cholesterol level (CMO:0000648)12693605426936055Human
407038663GWAS687639_Htotal lipids in chylomicrons and extremely large VLDL measurement QTL GWAS687639 (human)5e-11total lipids in chylomicrons and extremely large VLDL measurement 12693429226934293Human
407412430GWAS1061406_Hhigh density lipoprotein cholesterol measurement QTL GWAS1061406 (human)9e-09high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)12691377426913775Human
407041412GWAS690388_Htriglycerides in LDL measurement QTL GWAS690388 (human)6e-10triglycerides in LDL measurement 12693429226934293Human
407042053GWAS691029_Htriglycerides in chylomicrons and extremely large VLDL measurement QTL GWAS691029 (human)2e-10triglycerides in chylomicrons and extremely large VLDL measurement 12693429226934293Human
407317967GWAS966943_Hvery low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio QTL GWAS966943 (human)3e-09very low density lipoprotein cholesterol measurement, phospholipids:total lipids ratioblood very low density lipoprotein cholesterol level (CMO:0000648)12693605426936055Human
407316876GWAS965852_Hcholesterol:total lipids ratio, low density lipoprotein cholesterol measurement QTL GWAS965852 (human)2e-08cholesterol:total lipids ratio, low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)12693605426936055Human
407190731GWAS839707_Htriglycerides:total lipids ratio, low density lipoprotein cholesterol measurement QTL GWAS839707 (human)6e-11triglycerides:total lipids ratio, low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)12693605426936055Human
1576329MYI9_HMyocardial infarction susceptibility QTL 9 (human)12Myocardial infarction susceptibilityearly-onset1758550333585503Human
407253463GWAS902439_Htriglycerides:total lipids ratio, low density lipoprotein cholesterol measurement QTL GWAS902439 (human)3e-10triglycerides:total lipids ratio, low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)12693605426936055Human
407412891GWAS1061867_Hprotein-glutamine gamma-glutamyltransferase e measurement QTL GWAS1061867 (human)1e-08protein-glutamine gamma-glutamyltransferase e measurement12691377426913775Human
407270165GWAS919141_Htriglycerides:total lipids ratio, intermediate density lipoprotein measurement QTL GWAS919141 (human)4e-13triglycerides:total lipids ratio, intermediate density lipoprotein measurementblood intermediate density lipoprotein cholesterol level (CMO:0001562)12693605426936055Human
407343315GWAS992291_Htriglyceride measurement, high density lipoprotein cholesterol measurement QTL GWAS992291 (human)4e-10triglyceride measurement, high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)12693605426936055Human
407269468GWAS918444_Hcholesterol:total lipids ratio, intermediate density lipoprotein measurement QTL GWAS918444 (human)6e-13cholesterol:total lipids ratio, intermediate density lipoprotein measurementblood intermediate density lipoprotein cholesterol level (CMO:0001562)12693605426936055Human
407100440GWAS749416_Hcholesterol to total lipids in medium HDL percentage QTL GWAS749416 (human)5e-13cholesterol to total lipids in medium HDL percentage 12693429226934293Human
1576325MYI1_HMyocardial infarction susceptibility QTL 1 (human)11.681e-12Myocardial infarction susceptibilityearly-onset1758550333585503Human
407256920GWAS905896_Hfatty acid measurement QTL GWAS905896 (human)2e-09low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratioblood low density lipoprotein cholesterol level (CMO:0000053)12693605426936055Human
407040541GWAS689517_Hconcentration of chylomicrons and extremely large VLDL particles measurement QTL GWAS689517 (human)3e-11phospholipids in VLDL measurement 12693429226934293Human
407133606GWAS782582_Htriglyceride:HDL cholesterol ratio QTL GWAS782582 (human)0.000005triglyceride:HDL cholesterol ratio12691551826915519Human
407117542GWAS766518_Htriglycerides in IDL measurement QTL GWAS766518 (human)8e-10triglycerides in IDL measurementblood lipoprotein triglyceride level (CMO:0002685)12693429226934293Human
407138150GWAS787126_Hsexual dimorphism measurement QTL GWAS787126 (human)3e-12sexual dimorphism measurement12693605426936055Human
407332835GWAS981811_Hvery low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio QTL GWAS981811 (human)7e-16very low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratioblood very low density lipoprotein cholesterol level (CMO:0000648)12693605426936055Human
407117603GWAS766579_Hsexual dimorphism measurement QTL GWAS766579 (human)3e-08sex hormone-binding globulin measurement12693605426936055Human
407308000GWAS956976_Hchylomicron measurement, very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio QTL GWAS956976 (human)4e-08chylomicron measurement, very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratioblood very low density lipoprotein cholesterol level (CMO:0000648)12693605426936055Human
407084778GWAS733754_Hfree cholesterol to total lipids in medium LDL percentage QTL GWAS733754 (human)7e-10free cholesterol to total lipids in medium LDL percentage 12693429226934293Human
407309997GWAS958973_Htriglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement QTL GWAS958973 (human)4e-12triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurementblood very low density lipoprotein cholesterol level (CMO:0000648)12693605426936055Human
407188974GWAS837950_Hlow density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio QTL GWAS837950 (human)8e-13low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratioblood low density lipoprotein cholesterol level (CMO:0000053)12693605426936055Human
407119528GWAS768504_Hsystolic blood pressure QTL GWAS768504 (human)6e-12systolic blood pressuresystolic blood pressure (CMO:0000004)12693605426936055Human
1643380BW316_HBody weight QTL 316 (human)2.620.0002Body weightBMI1758550333585503Human
407098222GWAS747198_Hcholesteryl esters to total lipids in very small VLDL percentage QTL GWAS747198 (human)1e-10triglyceride measurement, intermediate density lipoprotein measurementblood intermediate density lipoprotein cholesterol level (CMO:0001562)12693605426936055Human
407237931GWAS886907_Hplatelet count QTL GWAS886907 (human)1e-13platelet quantity (VT:0003179)platelet count (CMO:0000029)12693605426936055Human
407040877GWAS689853_Htotal lipids in small VLDL QTL GWAS689853 (human)7e-11total lipids in small VLDL12693429226934293Human
407110955GWAS759931_Hapolipoprotein B to apolipoprotein A1 ratio QTL GWAS759931 (human)4e-12apolipoprotein B to apolipoprotein A1 ratio 12693429226934293Human
407127157GWAS776133_Htriglyceride:HDL cholesterol ratio QTL GWAS776133 (human)6e-10triglyceride:HDL cholesterol ratio12691551826915519Human
407041843GWAS690819_Hvery low density lipoprotein cholesterol measurement QTL GWAS690819 (human)9e-12very low density lipoprotein cholesterol measurementblood very low density lipoprotein cholesterol level (CMO:0000648)12693429226934293Human
407310965GWAS959941_HC-reactive protein measurement QTL GWAS959941 (human)1e-08C-reactive protein measurementblood C-reactive protein level (CMO:0003160)12693469826934699Human
407029878GWAS678854_Hfree cholesterol in VLDL measurement QTL GWAS678854 (human)3e-10blood lipid amount (VT:0003949)blood very low density lipoprotein cholesterol level (CMO:0000648)12693429226934293Human
407013687GWAS662663_Htestosterone measurement QTL GWAS662663 (human)1e-12testosterone measurementserum testosterone level (CMO:0000568)12693605426936055Human
407033396GWAS682372_Htriglycerides in very small VLDL measurement QTL GWAS682372 (human)1e-11triglycerides in very small VLDL measurementblood very low density lipoprotein triglyceride level (CMO:0002688)12693429226934293Human
407036600GWAS685576_Hcholesteryl ester measurement QTL GWAS685576 (human)1e-10blood lipid amount (VT:0003949)12693429226934293Human
407099199GWAS748175_Hcholesteryl esters to total lipids in medium HDL percentage QTL GWAS748175 (human)4e-13triglycerides to total lipids in medium HDL percentage 12693429226934293Human
407050558GWAS699534_Hsexual dimorphism measurement QTL GWAS699534 (human)3e-09sexual dimorphism measurement12693465826934659Human

Markers in Region
RH69664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372153,247,025 - 153,247,184UniSTSGRCh37
GRCh37127,272,105 - 27,272,707UniSTSGRCh37
Build 362152,955,271 - 152,955,430RGDNCBI36
Celera125,669,198 - 25,669,800UniSTS
Celera2146,861,504 - 146,861,663RGD
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map2q23.3UniSTS
HuRef2145,133,034 - 145,133,193UniSTS
HuRef125,525,679 - 25,526,284UniSTS
GeneMap99-GB4 RH Map2556.53UniSTS
SHGC-33625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37127,255,595 - 27,255,721UniSTSGRCh37
Build 36127,128,182 - 27,128,308RGDNCBI36
Celera125,652,691 - 25,652,817RGD
Cytogenetic Map1p35-p34UniSTS
HuRef125,509,311 - 25,509,437UniSTS
GeneMap99-GB4 RH Map194.37UniSTS
Whitehead-RH Map197.3UniSTS
D11S2560  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map8q21.13UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map8q11.21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map20q11.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6p24UniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map9q31.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map14q32.32UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map5q11UniSTS
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 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_006600 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011540530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017000096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333923 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054333924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB019408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF086922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF100760 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF125465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF130736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF241788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL356390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC002399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC021139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP348144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000321265   ⟹   ENSP00000319664
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl126,921,743 - 26,946,871 (+)Ensembl
Ensembl Acc Id: ENST00000435827   ⟹   ENSP00000404020
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl126,900,238 - 26,942,776 (+)Ensembl
Ensembl Acc Id: ENST00000452707   ⟹   ENSP00000400981
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl126,922,142 - 26,942,776 (+)Ensembl
Ensembl Acc Id: ENST00000484772
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl126,945,135 - 26,946,184 (+)Ensembl
RefSeq Acc Id: NM_006600   ⟹   NP_006591
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38126,921,743 - 26,946,871 (+)NCBI
GRCh37127,248,187 - 27,273,362 (+)NCBI
Build 36127,120,811 - 27,145,474 (+)NCBI Archive
HuRef125,501,783 - 25,526,939 (+)NCBI
CHM1_1127,361,578 - 27,386,708 (+)NCBI
T2T-CHM13v2.0126,759,801 - 26,784,927 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024452486   ⟹   XP_024308254
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38126,900,511 - 26,946,871 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047439143   ⟹   XP_047295099
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38126,900,161 - 26,946,871 (+)NCBI
RefSeq Acc Id: XM_047439200   ⟹   XP_047295156
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38126,900,553 - 26,946,871 (+)NCBI
RefSeq Acc Id: XM_047439206   ⟹   XP_047295162
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38126,900,188 - 26,946,871 (+)NCBI
RefSeq Acc Id: XM_054333921   ⟹   XP_054189896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0126,738,224 - 26,784,927 (+)NCBI
RefSeq Acc Id: XM_054333922   ⟹   XP_054189897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0126,738,574 - 26,784,927 (+)NCBI
RefSeq Acc Id: XM_054333923   ⟹   XP_054189898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0126,738,616 - 26,784,927 (+)NCBI
RefSeq Acc Id: XM_054333924   ⟹   XP_054189899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0126,738,251 - 26,784,927 (+)NCBI
RefSeq Acc Id: NP_006591   ⟸   NM_006600
- UniProtKB: Q9H0N2 (UniProtKB/Swiss-Prot),   Q5QP35 (UniProtKB/Swiss-Prot),   Q5QP31 (UniProtKB/Swiss-Prot),   Q9Y2B6 (UniProtKB/Swiss-Prot),   Q9Y266 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_024308254   ⟸   XM_024452486
- Peptide Label: isoform X1
- Sequence:
Ensembl Acc Id: ENSP00000400981   ⟸   ENST00000452707
Ensembl Acc Id: ENSP00000319664   ⟸   ENST00000321265
Ensembl Acc Id: ENSP00000404020   ⟸   ENST00000435827
RefSeq Acc Id: XP_047295099   ⟸   XM_047439143
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047295162   ⟸   XM_047439206
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047295156   ⟸   XM_047439200
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054189896   ⟸   XM_054333921
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054189899   ⟸   XM_054333924
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054189897   ⟸   XM_054333922
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054189898   ⟸   XM_054333923
- Peptide Label: isoform X1
Protein Domains
CS   Nuclear migration protein nudC

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y266-F1-model_v2 AlphaFold Q9Y266 1-331 view protein structure

Promoters
RGD ID:6854660
Promoter ID:EPDNEW_H495
Type:initiation region
Name:NUDC_1
Description:nuclear distribution C, dynein complex regulator
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
GRCh38126,921,756 - 26,921,816EPDNEW
RGD ID:6786162
Promoter ID:HG_KWN:1540
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:OTTHUMT00000012172,   OTTHUMT00000012173,   UC001BNH.1,   UC009VSQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36127,120,664 - 27,121,164 (+)MPROMDB
RGD ID:6852750
Promoter ID:EP74188
Type:initiation region
Name:HS_NUDC
Description:Nuclear distribution gene C homolog (A. nidulans).
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 36127,120,836 - 27,120,896EPD

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8045 AgrOrtholog
COSMIC NUDC COSMIC
Ensembl Genes ENSG00000090273 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000321265 ENTREZGENE
  ENST00000321265.10 UniProtKB/Swiss-Prot
  ENST00000435827.6 UniProtKB/TrEMBL
  ENST00000452707.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.790 UniProtKB/Swiss-Prot
GTEx ENSG00000090273 GTEx
HGNC ID HGNC:8045 ENTREZGENE
Human Proteome Map NUDC Human Proteome Map
InterPro CS_dom UniProtKB/Swiss-Prot
  HSP20-like_chaperone UniProtKB/Swiss-Prot
  NuDC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NudC_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NudC_N_dom UniProtKB/Swiss-Prot
KEGG Report hsa:10726 UniProtKB/Swiss-Prot
NCBI Gene 10726 ENTREZGENE
OMIM 610325 OMIM
PANTHER NUCLEAR MIGRATION PROTEIN NUDC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR12356 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam NuDC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nudc_N UniProtKB/Swiss-Prot
  PF04969 UniProtKB/Swiss-Prot
PharmGKB PA31827 PharmGKB
PROSITE PROKAR_LIPOPROTEIN UniProtKB/TrEMBL
  PS51203 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF49764 UniProtKB/Swiss-Prot
UniProt A0A0A0MSS4_HUMAN UniProtKB/TrEMBL
  A0A0A0MSU9_HUMAN UniProtKB/TrEMBL
  NUDC_HUMAN UniProtKB/Swiss-Prot
  Q5QP31 ENTREZGENE
  Q5QP35 ENTREZGENE
  Q9H0N2 ENTREZGENE
  Q9Y266 ENTREZGENE
  Q9Y2B6 ENTREZGENE
UniProt Secondary Q5QP31 UniProtKB/Swiss-Prot
  Q5QP35 UniProtKB/Swiss-Prot
  Q9H0N2 UniProtKB/Swiss-Prot
  Q9Y2B6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-21 NUDC  nuclear distribution C, dynein complex regulator  NUDC  nudC nuclear distribution protein  Symbol and/or name change 5135510 APPROVED
2013-08-13 NUDC  nudC nuclear distribution protein  NUDC  nuclear distribution C homolog (A. nidulans)  Symbol and/or name change 5135510 APPROVED
2012-03-01 NUDC  nuclear distribution C homolog (A. nidulans)  NUDC  nuclear distribution gene C homolog (A. nidulans)  Symbol and/or name change 5135510 APPROVED