NBL1 (NBL1, DAN family BMP antagonist) - Rat Genome Database

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Gene: NBL1 (NBL1, DAN family BMP antagonist) Homo sapiens
Analyze
Symbol: NBL1
Name: NBL1, DAN family BMP antagonist
RGD ID: 736912
HGNC Page HGNC:7650
Description: Enables identical protein binding activity. Involved in sequestering of BMP from receptor via BMP binding activity. Located in extracellular space.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: D1S1733E; DAN; DAN domain family member 1; DAND1; differential screening-selected gene aberrant in neuroblastoma; MGC8972; NB; neuroblastoma 1, DAN family BMP antagonist; neuroblastoma candidate region, suppression of tumorigenicity 1; neuroblastoma suppressor of tumorigenicity 1; neuroblastoma, suppression of tumorigenicity 1; NO3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38119,643,229 - 19,658,452 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl119,596,979 - 19,658,456 (+)EnsemblGRCh38hg38GRCh38
GRCh37119,969,723 - 19,984,945 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36119,842,313 - 19,857,532 (+)NCBINCBI36Build 36hg18NCBI36
Build 34119,715,031 - 19,730,251NCBI
Celera118,296,492 - 18,311,717 (+)NCBICelera
Cytogenetic Map1p36.13NCBI
HuRef118,215,821 - 18,231,031 (+)NCBIHuRef
CHM1_1120,078,997 - 20,094,228 (+)NCBICHM1_1
T2T-CHM13v2.0119,466,606 - 19,481,830 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
14-Deoxy-11,12-didehydroandrographolide  (EXP)
17beta-estradiol  (ISO)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-methylcholine  (EXP)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
5-fluorouracil  (EXP)
6-propyl-2-thiouracil  (ISO)
acrylamide  (EXP,ISO)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (EXP)
amitrole  (ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
Aroclor 1254  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
atrazine  (EXP)
benzo[a]pyrene  (EXP,ISO)
bisphenol A  (ISO)
bisphenol F  (ISO)
cadmium dichloride  (ISO)
calcitriol  (EXP)
carbamazepine  (EXP)
carbon nanotube  (ISO)
carmustine  (EXP)
choline  (ISO)
chromium(6+)  (EXP)
cisplatin  (EXP,ISO)
cobalt dichloride  (EXP)
dexamethasone  (ISO)
diazinon  (EXP)
dibutyl phthalate  (ISO)
dimethylarsinic acid  (ISO)
diuron  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
entinostat  (EXP)
folic acid  (ISO)
furan  (ISO)
gentamycin  (ISO)
glycine betaine  (ISO)
L-methionine  (ISO)
lead(0)  (EXP)
methimazole  (ISO)
methotrexate  (EXP)
methylmercury chloride  (EXP)
N-methyl-N'-nitro-N-nitrosoguanidine  (EXP)
nitrofen  (ISO)
O-methyleugenol  (EXP)
paracetamol  (EXP,ISO)
perfluorohexanesulfonic acid  (ISO)
raloxifene  (ISO)
SB 431542  (EXP)
silver atom  (ISO)
silver(0)  (ISO)
sodium arsenite  (ISO)
sulfadimethoxine  (ISO)
temozolomide  (EXP)
testosterone  (EXP,ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7633401   PMID:7777541   PMID:8084583   PMID:8385338   PMID:8609050   PMID:9303440   PMID:9324305   PMID:9516839   PMID:9831647   PMID:10208746   PMID:10390159   PMID:11134349  
PMID:11594460   PMID:12150978   PMID:12477932   PMID:15489334   PMID:15528323   PMID:16344560   PMID:19995712   PMID:21743959   PMID:21873635   PMID:22948749   PMID:23063586   PMID:24810382  
PMID:24852370   PMID:25416956   PMID:25561725   PMID:26760575   PMID:27524626   PMID:32296183   PMID:35748872   PMID:35947673   PMID:37436574  


Genomics

Comparative Map Data
NBL1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38119,643,229 - 19,658,452 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl119,596,979 - 19,658,456 (+)EnsemblGRCh38hg38GRCh38
GRCh37119,969,723 - 19,984,945 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36119,842,313 - 19,857,532 (+)NCBINCBI36Build 36hg18NCBI36
Build 34119,715,031 - 19,730,251NCBI
Celera118,296,492 - 18,311,717 (+)NCBICelera
Cytogenetic Map1p36.13NCBI
HuRef118,215,821 - 18,231,031 (+)NCBIHuRef
CHM1_1120,078,997 - 20,094,228 (+)NCBICHM1_1
T2T-CHM13v2.0119,466,606 - 19,481,830 (+)NCBIT2T-CHM13v2.0
Nbl1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394138,809,602 - 138,820,437 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4138,809,595 - 138,820,304 (-)EnsemblGRCm39 Ensembl
GRCm384139,082,291 - 139,093,126 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4139,082,284 - 139,092,993 (-)EnsemblGRCm38mm10GRCm38
MGSCv374138,638,207 - 138,648,885 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364138,354,368 - 138,364,941 (-)NCBIMGSCv36mm8
Celera4140,868,231 - 140,871,576 (-)NCBICelera
Cytogenetic Map4D3NCBI
cM Map470.57NCBI
Nbl1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85156,601,986 - 156,613,182 (-)NCBIGRCr8
mRatBN7.25151,318,752 - 151,329,948 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5151,318,754 - 151,338,719 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5154,015,980 - 154,027,177 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05155,790,290 - 155,801,487 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05155,772,293 - 155,783,465 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05157,524,569 - 157,535,701 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5157,524,513 - 157,535,664 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05161,263,765 - 161,274,897 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera5149,703,598 - 149,714,771 (-)NCBICelera
Cytogenetic Map5q36NCBI
Nbl1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955452308,573 - 319,989 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955452316,867 - 319,883 (+)NCBIChiLan1.0ChiLan1.0
NBL1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21207,460,724 - 207,474,909 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11206,577,562 - 206,591,747 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0118,599,121 - 18,613,305 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1119,652,853 - 19,656,431 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl119,641,279 - 19,656,431 (+)Ensemblpanpan1.1panPan2
NBL1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1279,040,206 - 79,102,792 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl279,041,105 - 79,102,820 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha275,554,895 - 75,582,497 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0279,607,161 - 79,634,902 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl279,608,223 - 79,610,312 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1276,425,235 - 76,452,808 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0277,434,195 - 77,461,836 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0278,503,885 - 78,531,526 (-)NCBIUU_Cfam_GSD_1.0
Nbl1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505839,996,034 - 40,018,509 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364745,840,240 - 5,859,749 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364745,820,798 - 5,843,291 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NBL1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl678,059,392 - 78,071,604 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1678,046,084 - 78,071,609 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2672,138,765 - 72,142,022 (+)NCBISscrofa10.2Sscrofa10.2susScr3
NBL1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.120112,893,928 - 112,908,041 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl20112,893,633 - 112,897,355 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660333,253,483 - 3,267,595 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nbl1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247644,764,903 - 4,775,707 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247644,771,334 - 4,774,462 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NBL1
4 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p36.21-36.12(chr1:15385267-20980349)x1 copy number loss See cases [RCV000051146] Chr1:15385267..20980349 [GRCh38]
Chr1:15711763..21306842 [GRCh37]
Chr1:15584350..21179429 [NCBI36]
Chr1:1p36.21-36.12		 pathogenic
GRCh38/hg38 1p36.21-36.12(chr1:13110797-20670207)x3 copy number gain See cases [RCV000051797] Chr1:13110797..20670207 [GRCh38]
Chr1:13178269..20996700 [GRCh37]
Chr1:13100856..20869287 [NCBI36]
Chr1:1p36.21-36.12		 pathogenic
GRCh38/hg38 1p36.22-36.12(chr1:10556797-22557907)x1 copy number loss See cases [RCV000053760] Chr1:10556797..22557907 [GRCh38]
Chr1:10616854..22884400 [GRCh37]
Chr1:10539441..22756987 [NCBI36]
Chr1:1p36.22-36.12		 pathogenic
GRCh38/hg38 1p36.13-36.12(chr1:18347821-22512894)x1 copy number loss See cases [RCV000053789] Chr1:18347821..22512894 [GRCh38]
Chr1:18674315..22839387 [GRCh37]
Chr1:18546902..22711974 [NCBI36]
Chr1:1p36.13-36.12		 pathogenic
GRCh38/hg38 1p36.13(chr1:19093306-20063342)x1 copy number loss See cases [RCV000053793] Chr1:19093306..20063342 [GRCh38]
Chr1:19419800..20389835 [GRCh37]
Chr1:19292387..20262422 [NCBI36]
Chr1:1p36.13		 pathogenic
GRCh38/hg38 1p36.21-36.13(chr1:15681812-19662339)x1 copy number loss See cases [RCV000138070] Chr1:15681812..19662339 [GRCh38]
Chr1:16008307..19988832 [GRCh37]
Chr1:15880894..19861419 [NCBI36]
Chr1:1p36.21-36.13		 pathogenic
GRCh38/hg38 1p36.13-36.12(chr1:19548795-20935131)x1 copy number loss See cases [RCV000138079] Chr1:19548795..20935131 [GRCh38]
Chr1:19875289..21261624 [GRCh37]
Chr1:19747876..21134211 [NCBI36]
Chr1:1p36.13-36.12		 likely pathogenic|uncertain significance
GRCh38/hg38 1p36.13(chr1:19169253-19797307)x3 copy number gain See cases [RCV000141322] Chr1:19169253..19797307 [GRCh38]
Chr1:19495747..20123800 [GRCh37]
Chr1:19368334..19996387 [NCBI36]
Chr1:1p36.13		 likely benign
GRCh37/hg19 1p36.13-36.12(chr1:19809419-20418333)x3 copy number gain See cases [RCV000239783] Chr1:19809419..20418333 [GRCh37]
Chr1:1p36.13-36.12		 uncertain significance
Single allele complex Breast ductal adenocarcinoma [RCV000207058] Chr1:909238..24706269 [GRCh37]
Chr1:1p36.33-36.11		 uncertain significance
chr1:17555508-24706269 complex variant complex Breast ductal adenocarcinoma [RCV000207266] Chr1:17555508..24706269 [GRCh37]
Chr1:1p36.13-36.11		 uncertain significance
GRCh37/hg19 1p36.32-36.12(chr1:2749920-22564787)x1 copy number loss See cases [RCV000446470] Chr1:2749920..22564787 [GRCh37]
Chr1:1p36.32-36.12		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 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
NC_000001.10:g.(?_19199339)_(22987879_?)dup duplication Autosomal recessive early-onset Parkinson disease 6 [RCV003113320]|Congenital disorder of glycosylation type Ir [RCV003113321]|Hyperprolinemia type 2 [RCV003107740] Chr1:19199339..22987879 [GRCh37]
Chr1:1p36.13-36.12		 uncertain significance
GRCh37/hg19 1p36.13-36.12(chr1:16785250-23491592)x1 copy number loss 1p36.1 deletion syndrome [RCV001614471] Chr1:16785250..23491592 [GRCh37]
Chr1:1p36.13-36.12		 pathogenic
GRCh37/hg19 1p36.13(chr1:19809464-20123500)x3 copy number gain not provided [RCV001259566] Chr1:19809464..20123500 [GRCh37]
Chr1:1p36.13		 uncertain significance
GRCh37/hg19 1p36.13-36.12(chr1:17284906-21778495)x1 copy number loss not provided [RCV001259567] Chr1:17284906..21778495 [GRCh37]
Chr1:1p36.13-36.12		 pathogenic
GRCh37/hg19 1p36.21-36.12(chr1:16041431-21295864)x1 copy number loss not provided [RCV001259568] Chr1:16041431..21295864 [GRCh37]
Chr1:1p36.21-36.12		 pathogenic
GRCh37/hg19 1p36.13(chr1:16773001-20221073)x1 copy number loss not provided [RCV001829114] Chr1:16773001..20221073 [GRCh37]
Chr1:1p36.13		 pathogenic
NC_000001.10:g.(?_19199339)_(24690861_?)dup duplication Deficiency of hydroxymethylglutaryl-CoA lyase [RCV003122155] Chr1:19199339..24690861 [GRCh37]
Chr1:1p36.13-36.11		 uncertain significance
NM_182744.4(NBL1):c.55C>T (p.Pro19Ser) single nucleotide variant Inborn genetic diseases [RCV002986325] Chr1:19643366 [GRCh38]
Chr1:19969860 [GRCh37]
Chr1:1p36.13		 uncertain significance
NC_000001.10:g.4481271_20530242del deletion Chromosome 1p36 deletion syndrome [RCV003159574] Chr1:4481271..20530242 [GRCh37]
Chr1:1p36.32-36.12		 pathogenic
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
GRCh37/hg19 1p36.13-36.12(chr1:17291707-23016395)x4 copy number gain not provided [RCV003485339] Chr1:17291707..23016395 [GRCh37]
Chr1:1p36.13-36.12		 likely pathogenic
GRCh37/hg19 1p36.13(chr1:18127009-20315260)x3 copy number gain not provided [RCV003484009] Chr1:18127009..20315260 [GRCh37]
Chr1:1p36.13		 uncertain significance
GRCh37/hg19 1p36.21-36.12(chr1:16194137-20561434)x1 copy number loss not specified [RCV003986551] Chr1:16194137..20561434 [GRCh37]
Chr1:1p36.21-36.12		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4577
Count of miRNA genes:852
Interacting mature miRNAs:1045
Transcripts:ENST00000289749, ENST00000375136, ENST00000425400, ENST00000427894, ENST00000428975, ENST00000439278, ENST00000439664, ENST00000451758, ENST00000548815
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
D1S1764E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37119,984,307 - 19,984,407UniSTSGRCh37
Build 36119,856,894 - 19,856,994RGDNCBI36
Celera118,311,079 - 18,311,179RGD
Cytogenetic Map1p36.13UniSTS
HuRef118,230,389 - 18,230,489UniSTS
D1S1733E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37119,983,389 - 19,983,497UniSTSGRCh37
Build 36119,855,976 - 19,856,084RGDNCBI36
Celera118,310,158 - 18,310,266RGD
Cytogenetic Map1p36.13UniSTS
HuRef118,229,468 - 18,229,576UniSTS
RH68284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37119,984,625 - 19,984,770UniSTSGRCh37
Build 36119,857,212 - 19,857,357RGDNCBI36
Celera118,311,397 - 18,311,542RGD
Cytogenetic Map1p36.13UniSTS
HuRef118,230,707 - 18,230,852UniSTS
GeneMap99-GB4 RH Map185.21UniSTS
RH68234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37119,984,612 - 19,984,770UniSTSGRCh37
Build 36119,857,199 - 19,857,357RGDNCBI36
Celera118,311,384 - 18,311,542RGD
Cytogenetic Map1p36.13UniSTS
HuRef118,230,694 - 18,230,852UniSTS
GeneMap99-GB4 RH Map172.75UniSTS
NCBI RH Map1110.0UniSTS
NBL1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37119,981,633 - 19,981,845UniSTSGRCh37
Celera118,308,402 - 18,308,614UniSTS
HuRef118,227,711 - 18,227,923UniSTS


Expression


Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001204084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278164 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278165 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_182744 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AK292101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300872 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL031727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL703187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY049783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM988954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ671197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT019423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D28124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D89013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA384331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA921297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA924824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA929341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB016315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB253522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB482000 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY084536 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000289749   ⟹   ENSP00000289749
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,643,232 - 19,657,129 (+)Ensembl
RefSeq Acc Id: ENST00000375136   ⟹   ENSP00000364278
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,644,311 - 19,658,452 (+)Ensembl
RefSeq Acc Id: ENST00000425400   ⟹   ENSP00000400250
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,645,372 - 19,656,933 (+)Ensembl
RefSeq Acc Id: ENST00000427894   ⟹   ENSP00000394079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,647,610 - 19,657,076 (+)Ensembl
RefSeq Acc Id: ENST00000428975   ⟹   ENSP00000412419
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,640,554 - 19,656,934 (+)Ensembl
RefSeq Acc Id: ENST00000439278   ⟹   ENSP00000391858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,645,766 - 19,655,436 (+)Ensembl
RefSeq Acc Id: ENST00000439664   ⟹   ENSP00000399333
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,643,714 - 19,656,911 (+)Ensembl
RefSeq Acc Id: ENST00000451758   ⟹   ENSP00000390607
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,643,409 - 19,656,969 (+)Ensembl
RefSeq Acc Id: ENST00000548815   ⟹   ENSP00000449007
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,647,610 - 19,658,456 (+)Ensembl
RefSeq Acc Id: ENST00000602662   ⟹   ENSP00000473411
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,596,979 - 19,658,056 (+)Ensembl
RefSeq Acc Id: ENST00000615215   ⟹   ENSP00000478223
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,645,766 - 19,658,456 (+)Ensembl
RefSeq Acc Id: ENST00000618761   ⟹   ENSP00000483061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,645,372 - 19,658,456 (+)Ensembl
RefSeq Acc Id: ENST00000621723   ⟹   ENSP00000478885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,643,714 - 19,658,456 (+)Ensembl
RefSeq Acc Id: ENST00000622566   ⟹   ENSP00000480391
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl119,643,409 - 19,658,456 (+)Ensembl
RefSeq Acc Id: NM_001204084   ⟹   NP_001191013
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,643,714 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)ENTREZGENE
HuRef118,215,821 - 18,231,031 (+)ENTREZGENE
CHM1_1120,079,482 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,467,091 - 19,481,830 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204085   ⟹   NP_001191014
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,645,372 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)ENTREZGENE
HuRef118,215,821 - 18,231,031 (+)ENTREZGENE
CHM1_1120,081,140 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,468,749 - 19,481,830 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001204086   ⟹   NP_001191015
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,645,766 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)ENTREZGENE
HuRef118,215,821 - 18,231,031 (+)ENTREZGENE
CHM1_1120,081,534 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,469,143 - 19,481,830 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278164   ⟹   NP_001265093
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,643,229 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)NCBI
HuRef118,215,821 - 18,231,031 (+)NCBI
CHM1_1120,078,997 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,466,606 - 19,481,830 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278165   ⟹   NP_001265094
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,643,409 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)NCBI
HuRef118,215,821 - 18,231,031 (+)NCBI
CHM1_1120,079,177 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,466,786 - 19,481,830 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278166   ⟹   NP_001265095
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,647,610 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)NCBI
HuRef118,215,821 - 18,231,031 (+)NCBI
CHM1_1120,083,378 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,470,987 - 19,481,830 (+)NCBI
Sequence:
RefSeq Acc Id: NM_005380   ⟹   NP_005371
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,644,311 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)ENTREZGENE
Build 36119,843,395 - 19,857,532 (+)NCBI Archive
HuRef118,215,821 - 18,231,031 (+)ENTREZGENE
CHM1_1120,079,941 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,467,688 - 19,481,830 (+)NCBI
Sequence:
RefSeq Acc Id: NM_182744   ⟹   NP_877421
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,643,229 - 19,658,452 (+)NCBI
GRCh37119,969,723 - 19,984,949 (+)ENTREZGENE
Build 36119,842,313 - 19,857,532 (+)NCBI Archive
HuRef118,215,821 - 18,231,031 (+)ENTREZGENE
CHM1_1120,078,997 - 20,094,228 (+)NCBI
T2T-CHM13v2.0119,466,606 - 19,481,830 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001191013 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191014 (Get FASTA)   NCBI Sequence Viewer  
  NP_001191015 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265093 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265094 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265095 (Get FASTA)   NCBI Sequence Viewer  
  NP_005371 (Get FASTA)   NCBI Sequence Viewer  
  NP_877421 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH12037 (Get FASTA)   NCBI Sequence Viewer  
  AAL15440 (Get FASTA)   NCBI Sequence Viewer  
  AAV38230 (Get FASTA)   NCBI Sequence Viewer  
  BAA05671 (Get FASTA)   NCBI Sequence Viewer  
  BAA92265 (Get FASTA)   NCBI Sequence Viewer  
  BAF84790 (Get FASTA)   NCBI Sequence Viewer  
  BAG36074 (Get FASTA)   NCBI Sequence Viewer  
  BAG62517 (Get FASTA)   NCBI Sequence Viewer  
  EAW94894 (Get FASTA)   NCBI Sequence Viewer  
  EAW94895 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000289749
  ENSP00000289749.2
  ENSP00000364278
  ENSP00000364278.4
  ENSP00000390607.1
  ENSP00000391858.1
  ENSP00000394079.1
  ENSP00000399333.1
  ENSP00000400250.1
  ENSP00000412419.1
  ENSP00000449007
  ENSP00000449007.2
  ENSP00000473411.1
  ENSP00000478223
  ENSP00000478223.1
  ENSP00000478885
  ENSP00000478885.1
  ENSP00000480391
  ENSP00000480391.1
  ENSP00000483061
  ENSP00000483061.1
GenBank Protein P41271 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_877421   ⟸   NM_182744
- Peptide Label: isoform 1
- UniProtKB: P41271 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001191013   ⟸   NM_001204084
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5U0N4 (UniProtKB/Swiss-Prot),   Q5TGZ2 (UniProtKB/Swiss-Prot),   A3KFI7 (UniProtKB/Swiss-Prot),   Q96L68 (UniProtKB/Swiss-Prot),   P41271 (UniProtKB/Swiss-Prot),   E5RFZ1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191014   ⟸   NM_001204085
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5U0N4 (UniProtKB/Swiss-Prot),   Q5TGZ2 (UniProtKB/Swiss-Prot),   A3KFI7 (UniProtKB/Swiss-Prot),   Q96L68 (UniProtKB/Swiss-Prot),   P41271 (UniProtKB/Swiss-Prot),   E5RFZ1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191015   ⟸   NM_001204086
- Peptide Label: isoform 3
- UniProtKB: A0A087WTY6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_005371   ⟸   NM_005380
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5U0N4 (UniProtKB/Swiss-Prot),   Q5TGZ2 (UniProtKB/Swiss-Prot),   A3KFI7 (UniProtKB/Swiss-Prot),   Q96L68 (UniProtKB/Swiss-Prot),   P41271 (UniProtKB/Swiss-Prot),   E5RFZ1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265093   ⟸   NM_001278164
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5U0N4 (UniProtKB/Swiss-Prot),   Q5TGZ2 (UniProtKB/Swiss-Prot),   A3KFI7 (UniProtKB/Swiss-Prot),   Q96L68 (UniProtKB/Swiss-Prot),   P41271 (UniProtKB/Swiss-Prot),   E5RFZ1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265094   ⟸   NM_001278165
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5U0N4 (UniProtKB/Swiss-Prot),   Q5TGZ2 (UniProtKB/Swiss-Prot),   A3KFI7 (UniProtKB/Swiss-Prot),   Q96L68 (UniProtKB/Swiss-Prot),   P41271 (UniProtKB/Swiss-Prot),   E5RFZ1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265095   ⟸   NM_001278166
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5U0N4 (UniProtKB/Swiss-Prot),   Q5TGZ2 (UniProtKB/Swiss-Prot),   A3KFI7 (UniProtKB/Swiss-Prot),   Q96L68 (UniProtKB/Swiss-Prot),   P41271 (UniProtKB/Swiss-Prot),   E5RFZ1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000391858   ⟸   ENST00000439278
RefSeq Acc Id: ENSP00000400250   ⟸   ENST00000425400
RefSeq Acc Id: ENSP00000364278   ⟸   ENST00000375136
RefSeq Acc Id: ENSP00000473411   ⟸   ENST00000602662
RefSeq Acc Id: ENSP00000483061   ⟸   ENST00000618761
RefSeq Acc Id: ENSP00000412419   ⟸   ENST00000428975
RefSeq Acc Id: ENSP00000289749   ⟸   ENST00000289749
RefSeq Acc Id: ENSP00000480391   ⟸   ENST00000622566
RefSeq Acc Id: ENSP00000478223   ⟸   ENST00000615215
RefSeq Acc Id: ENSP00000390607   ⟸   ENST00000451758
RefSeq Acc Id: ENSP00000399333   ⟸   ENST00000439664
RefSeq Acc Id: ENSP00000478885   ⟸   ENST00000621723
RefSeq Acc Id: ENSP00000449007   ⟸   ENST00000548815
RefSeq Acc Id: ENSP00000394079   ⟸   ENST00000427894
Protein Domains
CTCK   DAN

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P41271-F1-model_v2 AlphaFold P41271 1-181 view protein structure

Promoters
RGD ID:6854340
Promoter ID:EPDNEW_H333
Type:initiation region
Name:NBL1_3
Description:neuroblastoma 1, DAN family BMP antagonist
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H334  EPDNEW_H335  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,643,714 - 19,643,774EPDNEW
RGD ID:6854338
Promoter ID:EPDNEW_H334
Type:initiation region
Name:NBL1_2
Description:neuroblastoma 1, DAN family BMP antagonist
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H333  EPDNEW_H335  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,644,205 - 19,644,265EPDNEW
RGD ID:6854342
Promoter ID:EPDNEW_H335
Type:initiation region
Name:NBL1_1
Description:neuroblastoma 1, DAN family BMP antagonist
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H334  EPDNEW_H333  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38119,644,313 - 19,644,373EPDNEW
RGD ID:6786101
Promoter ID:HG_KWN:1100
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000313740
Position:
Human AssemblyChrPosition (strand)Source
Build 36119,839,411 - 19,839,911 (+)MPROMDB
RGD ID:6786099
Promoter ID:HG_KWN:1101
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Lymphoblastoid
Transcripts:NM_182744,   OTTHUMT00000007681,   OTTHUMT00000313739,   UC009VPM.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36119,843,141 - 19,843,641 (+)MPROMDB
RGD ID:6786102
Promoter ID:HG_KWN:1102
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000313742,   OTTHUMT00000313743
Position:
Human AssemblyChrPosition (strand)Source
Build 36119,843,911 - 19,845,112 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7650 AgrOrtholog
COSMIC NBL1 COSMIC
Ensembl Genes ENSG00000158747 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000289749 ENTREZGENE
  ENST00000289749.6 UniProtKB/Swiss-Prot
  ENST00000375136 ENTREZGENE
  ENST00000375136.8 UniProtKB/Swiss-Prot
  ENST00000425400.5 UniProtKB/TrEMBL
  ENST00000427894.5 UniProtKB/TrEMBL
  ENST00000428975.5 UniProtKB/TrEMBL
  ENST00000439278.5 UniProtKB/TrEMBL
  ENST00000439664.5 UniProtKB/TrEMBL
  ENST00000451758.5 UniProtKB/TrEMBL
  ENST00000548815 ENTREZGENE
  ENST00000548815.2 UniProtKB/Swiss-Prot
  ENST00000602662.1 UniProtKB/Swiss-Prot
  ENST00000615215 ENTREZGENE
  ENST00000615215.4 UniProtKB/TrEMBL
  ENST00000618761 ENTREZGENE
  ENST00000618761.4 UniProtKB/Swiss-Prot
  ENST00000621723 ENTREZGENE
  ENST00000621723.4 UniProtKB/Swiss-Prot
  ENST00000622566 ENTREZGENE
  ENST00000622566.4 UniProtKB/Swiss-Prot
Gene3D-CATH 2.10.90.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000158747 GTEx
HGNC ID HGNC:7650 ENTREZGENE
Human Proteome Map NBL1 Human Proteome Map
InterPro Cys_knot_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cystine-knot_cytokine UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DAN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Neuroblast_suppress_tumour_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:100532736 UniProtKB/Swiss-Prot
  hsa:4681 UniProtKB/Swiss-Prot
NCBI Gene 4681 ENTREZGENE
OMIM 600613 OMIM
PANTHER GREMLIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NEUROBLASTOMA SUPPRESSOR OF TUMORIGENICITY 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DAN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31456 PharmGKB
PIRSF DAN_sub UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SM00041 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WTY6 ENTREZGENE, UniProtKB/TrEMBL
  A3KFI1_HUMAN UniProtKB/TrEMBL
  A3KFI2_HUMAN UniProtKB/TrEMBL
  A3KFI3_HUMAN UniProtKB/TrEMBL
  A3KFI4_HUMAN UniProtKB/TrEMBL
  A3KFI5_HUMAN UniProtKB/TrEMBL
  A3KFI7 ENTREZGENE
  E5RFZ1 ENTREZGENE, UniProtKB/TrEMBL
  NBL1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q5TGZ2 ENTREZGENE
  Q5U0N4 ENTREZGENE
  Q96L68 ENTREZGENE
UniProt Secondary A3KFI7 UniProtKB/Swiss-Prot
  E5RFC8 UniProtKB/TrEMBL
  E5RFY3 UniProtKB/TrEMBL
  E5RFZ2 UniProtKB/TrEMBL
  E5RG89 UniProtKB/TrEMBL
  Q5TGZ2 UniProtKB/Swiss-Prot
  Q5U0N4 UniProtKB/Swiss-Prot
  Q96L68 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-05-15 NBL1  NBL1, DAN family BMP antagonist    neuroblastoma 1, DAN family BMP antagonist  Symbol and/or name change 5135510 APPROVED
2013-03-06 NBL1  neuroblastoma 1, DAN family BMP antagonist    neuroblastoma, suppression of tumorigenicity 1  Symbol and/or name change 5135510 APPROVED