NOL4 (nucleolar protein 4) - Rat Genome Database

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Gene: NOL4 (nucleolar protein 4) Homo sapiens
Analyze
Symbol: NOL4
Name: nucleolar protein 4
RGD ID: 1321698
HGNC Page HGNC:7870
Description: Predicted to enable RNA binding activity. Predicted to be located in nucleolus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: cancer/testis antigen 125; CT125; HRIHFB2255; NOLP; nucleolar localized protein; nucleolar-localized protein
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
GRCh381833,851,100 - 34,224,913 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1833,851,100 - 34,224,952 (-)EnsemblGRCh38hg38GRCh38
GRCh371831,431,064 - 31,804,877 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361829,685,062 - 30,057,444 (-)NCBINCBI36Build 36hg18NCBI36
Build 341829,686,409 - 30,057,513NCBI
Celera1828,239,387 - 28,611,397 (-)NCBICelera
Cytogenetic Map18q12.1NCBI
HuRef1828,290,445 - 28,662,648 (-)NCBIHuRef
CHM1_11831,358,224 - 31,730,679 (-)NCBICHM1_1
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)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

Cellular Component
nucleolus  (IEA,TAS)
nucleus  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:9813152   PMID:9853615   PMID:12477932   PMID:14702039   PMID:15489334   PMID:16169070   PMID:16189514   PMID:16344560   PMID:16730941   PMID:19846067   PMID:20379614  
PMID:21900206   PMID:22747683   PMID:24337411   PMID:24722188   PMID:25416956   PMID:26186194   PMID:27229929   PMID:28514442   PMID:28700943   PMID:29666346   PMID:29987050   PMID:31753913  
PMID:32296183   PMID:33961781   PMID:34065612   PMID:34709266   PMID:35140242   PMID:36089195   PMID:36282054   PMID:36710296   PMID:38297188  


Genomics

Comparative Map Data
NOL4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381833,851,100 - 34,224,913 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1833,851,100 - 34,224,952 (-)EnsemblGRCh38hg38GRCh38
GRCh371831,431,064 - 31,804,877 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361829,685,062 - 30,057,444 (-)NCBINCBI36Build 36hg18NCBI36
Build 341829,686,409 - 30,057,513NCBI
Celera1828,239,387 - 28,611,397 (-)NCBICelera
Cytogenetic Map18q12.1NCBI
HuRef1828,290,445 - 28,662,648 (-)NCBIHuRef
CHM1_11831,358,224 - 31,730,679 (-)NCBICHM1_1
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBIT2T-CHM13v2.0
Nol4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391822,826,209 - 23,174,926 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1822,826,238 - 23,174,710 (-)EnsemblGRCm39 Ensembl
GRCm381822,693,152 - 23,042,640 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1822,693,181 - 23,041,653 (-)EnsemblGRCm38mm10GRCm38
MGSCv371822,851,656 - 23,200,154 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361822,836,416 - 23,181,666 (-)NCBIMGSCv36mm8
Celera1823,176,162 - 23,536,179 (-)NCBICelera
Cytogenetic Map18A2NCBI
cM Map1811.96NCBI
Nol4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81814,207,303 - 14,569,697 (-)NCBIGRCr8
mRatBN7.21813,932,499 - 14,294,873 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1813,932,510 - 14,296,286 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1814,118,579 - 14,480,839 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01814,906,228 - 15,268,504 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01814,175,243 - 14,543,815 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01813,658,260 - 14,016,713 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1813,658,271 - 14,016,713 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01813,441,528 - 13,801,153 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41814,312,224 - 14,718,842 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11814,340,233 - 14,744,196 (-)NCBI
Celera1813,911,298 - 14,272,965 (-)NCBICelera
Cytogenetic Map18p12NCBI
Nol4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540220,780,251 - 21,106,508 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495540220,781,485 - 21,106,508 (-)NCBIChiLan1.0ChiLan1.0
NOL4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21751,224,685 - 51,606,604 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11836,917,282 - 37,299,195 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01827,054,678 - 27,435,085 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11830,646,179 - 31,025,952 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1830,646,179 - 31,026,620 (-)Ensemblpanpan1.1panPan2
NOL4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1755,617,119 - 56,007,790 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl755,618,123 - 56,006,041 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha754,919,320 - 55,440,480 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0755,454,410 - 55,977,017 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl755,586,330 - 55,976,997 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1755,142,088 - 55,663,223 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0755,162,627 - 55,684,834 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0755,459,157 - 55,980,811 (+)NCBIUU_Cfam_GSD_1.0
Nol4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494451,340,391 - 51,651,163 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493651710,669,193 - 10,978,769 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493651710,668,250 - 10,978,766 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NOL4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6117,631,227 - 118,087,992 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16117,631,631 - 118,088,026 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.26109,982,552 - 110,275,172 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NOL4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11846,519,566 - 46,901,694 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1846,521,206 - 46,901,764 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605021,021,668 - 21,420,272 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nol4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247798,359,584 - 8,685,781 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247798,359,844 - 8,687,368 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NOL4
45 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 18q12.1-12.3(chr18:31655749-42564094)x3 copy number gain See cases [RCV000050773] Chr18:31655749..42564094 [GRCh38]
Chr18:29235712..40144059 [GRCh37]
Chr18:27489710..38398057 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
GRCh38/hg38 18q12.1-12.3(chr18:29444510-40403652)x1 copy number loss See cases [RCV000051090] Chr18:29444510..40403652 [GRCh38]
Chr18:27024475..37983616 [GRCh37]
Chr18:25278473..36237614 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000051048] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q11.1-23(chr18:20960320-80234429)x3 copy number gain See cases [RCV000052543] Chr18:20960320..80234429 [GRCh38]
Chr18:18540281..77992312 [GRCh37]
Chr18:16794279..76093303 [NCBI36]
Chr18:18q11.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:53345-80209986)x3 copy number gain See cases [RCV000052501] Chr18:53345..80209986 [GRCh38]
Chr18:53345..77967869 [GRCh37]
Chr18:43345..76068860 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q11.1-23(chr18:20989762-80209986)x3 copy number gain See cases [RCV000052549] Chr18:20989762..80209986 [GRCh38]
Chr18:18569723..77967869 [GRCh37]
Chr18:16823721..76068860 [NCBI36]
Chr18:18q11.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148763-80252290)x3 copy number gain See cases [RCV000052507] Chr18:148763..80252290 [GRCh38]
Chr18:148763..78010173 [GRCh37]
Chr18:138763..76111164 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1-22.1(chr18:29249202-65448117)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]|See cases [RCV000052563] Chr18:29249202..65448117 [GRCh38]
Chr18:26829167..63115353 [GRCh37]
Chr18:25083165..61266333 [NCBI36]
Chr18:18q12.1-22.1		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80244381)x3 copy number gain See cases [RCV000052514] Chr18:148963..80244381 [GRCh38]
Chr18:148963..78002264 [GRCh37]
Chr18:138963..76103255 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1-12.3(chr18:32111530-44070219)x1 copy number loss See cases [RCV000053829] Chr18:32111530..44070219 [GRCh38]
Chr18:29691493..41650184 [GRCh37]
Chr18:27945491..39904182 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
GRCh38/hg38 18q12.1-12.3(chr18:34047118-41394354)x1 copy number loss See cases [RCV000053830] Chr18:34047118..41394354 [GRCh38]
Chr18:31627082..38974318 [GRCh37]
Chr18:29881080..37228316 [NCBI36]
Chr18:18q12.1-12.3		 pathogenic
NM_001198546.1(NOL4):c.1651G>A (p.Gly551Arg) single nucleotide variant Malignant melanoma [RCV000071817] Chr18:33852916 [GRCh38]
Chr18:31432880 [GRCh37]
Chr18:29686878 [NCBI36]
Chr18:18q12.1		 not provided
NM_001198547.1(NOL4):c.1045T>G (p.Leu349Val) single nucleotide variant Malignant melanoma [RCV000071818] Chr18:33957487 [GRCh38]
Chr18:31537451 [GRCh37]
Chr18:29791449 [NCBI36]
Chr18:18q12.1		 not provided
NM_001198546.1(NOL4):c.1350+27468C>A single nucleotide variant Lung cancer [RCV000100774] Chr18:33915597 [GRCh38]
Chr18:31495561 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_001198546.1(NOL4):c.527-427T>C single nucleotide variant Lung cancer [RCV000100775] Chr18:34104586 [GRCh38]
Chr18:31684550 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_001198546.1(NOL4):c.265-40445A>T single nucleotide variant Lung cancer [RCV000100776] Chr18:34170465 [GRCh38]
Chr18:31750429 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_001198546.1(NOL4):c.264+12342A>G single nucleotide variant Lung cancer [RCV000100777] Chr18:34210648 [GRCh38]
Chr18:31790612 [GRCh37]
Chr18:18q12.1		 uncertain significance
GRCh38/hg38 18p11.32-q23(chr18:149089-80234391)x3 copy number gain See cases [RCV000134110] Chr18:149089..80234391 [GRCh38]
Chr18:149089..77992274 [GRCh37]
Chr18:139089..76093265 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1-23(chr18:32123105-80252149)x3 copy number gain See cases [RCV000136890] Chr18:32123105..80252149 [GRCh38]
Chr18:29703068..78010032 [GRCh37]
Chr18:27957066..76111023 [NCBI36]
Chr18:18q12.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:118760-80254946)x3 copy number gain See cases [RCV000138656] Chr18:118760..80254946 [GRCh38]
Chr18:118760..78012829 [GRCh37]
Chr18:108760..76113817 [NCBI36]
Chr18:18p11.32-q23		 pathogenic|conflicting data from submitters
GRCh38/hg38 18q12.1-12.2(chr18:33373798-37364748)x1 copy number loss See cases [RCV000138295] Chr18:33373798..37364748 [GRCh38]
Chr18:30953762..34944711 [GRCh37]
Chr18:29207760..33198709 [NCBI36]
Chr18:18q12.1-12.2		 likely pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80254936)x3 copy number gain See cases [RCV000139397] Chr18:149089..80254936 [GRCh38]
Chr18:149089..78012819 [GRCh37]
Chr18:139089..76113807 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1(chr18:32462656-34463256)x1 copy number loss See cases [RCV000141483] Chr18:32462656..34463256 [GRCh38]
Chr18:30042619..32043220 [GRCh37]
Chr18:28296617..30297218 [NCBI36]
Chr18:18q12.1		 benign
GRCh38/hg38 18q11.1-12.1(chr18:20949378-34363455)x3 copy number gain See cases [RCV000141646] Chr18:20949378..34363455 [GRCh38]
Chr18:18529339..31943419 [GRCh37]
Chr18:16783337..30197417 [NCBI36]
Chr18:18q11.1-12.1		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136227-80256240)x3 copy number gain See cases [RCV000142244] Chr18:136227..80256240 [GRCh38]
Chr18:136227..78014123 [GRCh37]
Chr18:126227..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q11.1-12.3(chr18:20941324-40360620)x3 copy number gain See cases [RCV000142226] Chr18:20941324..40360620 [GRCh38]
Chr18:18521285..37940584 [GRCh37]
Chr18:16775283..36194582 [NCBI36]
Chr18:18q11.1-12.3		 pathogenic
GRCh38/hg38 18q11.1-22.3(chr18:20962119-74691446)x3 copy number gain See cases [RCV000143057] Chr18:20962119..74691446 [GRCh38]
Chr18:18542080..72403402 [GRCh37]
Chr18:16796078..70532390 [NCBI36]
Chr18:18q11.1-22.3		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136226-80256240)x3 copy number gain See cases [RCV000143218] Chr18:136226..80256240 [GRCh38]
Chr18:136226..78014123 [GRCh37]
Chr18:126226..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000148072] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005236)x3 copy number gain See cases [RCV000240130] Chr18:163323..78005236 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q11.1-23(chr18:18548019-77954165)x3 copy number gain See cases [RCV000240476] Chr18:18548019..77954165 [GRCh37]
Chr18:18q11.1-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123)x3 copy number gain See cases [RCV000446047] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005185)x3 copy number gain See cases [RCV000445851] Chr18:163323..78005185 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q11.2-12.2(chr18:20069932-36887326)x1 copy number loss See cases [RCV000510691] Chr18:20069932..36887326 [GRCh37]
Chr18:18q11.2-12.2		 pathogenic
GRCh37/hg19 18p11.32-q21.1(chr18:136227-46171053)x3 copy number gain See cases [RCV000511857] Chr18:136227..46171053 [GRCh37]
Chr18:18p11.32-q21.1		 pathogenic
GRCh37/hg19 18q12.1-12.2(chr18:30368042-36078516)x1 copy number loss See cases [RCV000511858] Chr18:30368042..36078516 [GRCh37]
Chr18:18q12.1-12.2		 likely pathogenic
GRCh37/hg19 18q11.1-22.1(chr18:18521285-64495798)x3 copy number gain See cases [RCV000511734] Chr18:18521285..64495798 [GRCh37]
Chr18:18q11.1-22.1		 pathogenic
GRCh37/hg19 18p11.21-q23(chr18:14869204-78014123)x3 copy number gain See cases [RCV000512030] Chr18:14869204..78014123 [GRCh37]
Chr18:18p11.21-q23		 pathogenic
GRCh37/hg19 18q11.2-21.1(chr18:24835114-46917217)x3 copy number gain See cases [RCV000511124] Chr18:24835114..46917217 [GRCh37]
Chr18:18q11.2-21.1		 likely benign
GRCh37/hg19 18p11.32-q23(chr18:136227-78014123) copy number gain See cases [RCV000511189] Chr18:136227..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
NM_003787.5(NOL4):c.1199C>T (p.Thr400Ile) single nucleotide variant Inborn genetic diseases [RCV003280685] Chr18:33958276 [GRCh38]
Chr18:31538240 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.223G>T (p.Gly75Cys) single nucleotide variant Inborn genetic diseases [RCV003248289] Chr18:34223031 [GRCh38]
Chr18:31802995 [GRCh37]
Chr18:18q12.1		 uncertain significance
GRCh37/hg19 18q12.1-12.2(chr18:29711972-35866193)x1 copy number loss not provided [RCV000684043] Chr18:29711972..35866193 [GRCh37]
Chr18:18q12.1-12.2		 pathogenic
GRCh37/hg19 18q11.1-21.2(chr18:18539806-49926444)x2 copy number gain not provided [RCV000739776] Chr18:18539806..49926444 [GRCh37]
Chr18:18q11.1-21.2		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:12842-78015180)x3 copy number gain not provided [RCV000752245] Chr18:12842..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:13034-78015180)x3 copy number gain not provided [RCV000752246] Chr18:13034..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
NM_003787.5(NOL4):c.224G>T (p.Gly75Val) single nucleotide variant Inborn genetic diseases [RCV003248290] Chr18:34223030 [GRCh38]
Chr18:31802994 [GRCh37]
Chr18:18q12.1		 uncertain significance
GRCh37/hg19 18q12.1(chr18:30863773-31433693)x1 copy number loss not provided [RCV000847866] Chr18:30863773..31433693 [GRCh37]
Chr18:18q12.1		 pathogenic
GRCh37/hg19 18q11.2-21.2(chr18:20689919-49455212)x3 copy number gain not provided [RCV001006980] Chr18:20689919..49455212 [GRCh37]
Chr18:18q11.2-21.2		 pathogenic
NM_003787.5(NOL4):c.134C>T (p.Ser45Leu) single nucleotide variant Inborn genetic diseases [RCV003250184] Chr18:34223120 [GRCh38]
Chr18:31803084 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.122A>G (p.Asn41Ser) single nucleotide variant Inborn genetic diseases [RCV003293813] Chr18:34223132 [GRCh38]
Chr18:31803096 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.961A>G (p.Ile321Val) single nucleotide variant Inborn genetic diseases [RCV003253529] Chr18:34019413 [GRCh38]
Chr18:31599377 [GRCh37]
Chr18:18q12.1		 uncertain significance
GRCh37/hg19 18q11.2-12.2(chr18:22868759-34335753)x1 copy number loss not provided [RCV001006964] Chr18:22868759..34335753 [GRCh37]
Chr18:18q11.2-12.2		 pathogenic
GRCh37/hg19 18q11.2-23(chr18:23626739-78014976)x3 copy number gain not provided [RCV001537911] Chr18:23626739..78014976 [GRCh37]
Chr18:18q11.2-23		 pathogenic
GRCh37/hg19 18q11.2-12.2(chr18:23971647-33737300)x1 copy number loss See cases [RCV001263022] Chr18:23971647..33737300 [GRCh37]
Chr18:18q11.2-12.2		 pathogenic
Single allele deletion Intellectual disability [RCV001787257] Chr18:1262336..53254747 [GRCh37]
Chr18:18p11.32-q21.2		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123) copy number gain not specified [RCV002052616] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q12.1(chr18:31341181-32407667) copy number gain not specified [RCV002052630] Chr18:31341181..32407667 [GRCh37]
Chr18:18q12.1		 uncertain significance
GRCh37/hg19 18p11.32-q23(chr18:1-78077248) copy number gain Trisomy 18 [RCV002280660] Chr18:1..78077248 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
NM_003787.5(NOL4):c.952G>C (p.Glu318Gln) single nucleotide variant Inborn genetic diseases [RCV002684680] Chr18:34019422 [GRCh38]
Chr18:31599386 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.302G>A (p.Arg101Gln) single nucleotide variant Inborn genetic diseases [RCV002682172] Chr18:34129983 [GRCh38]
Chr18:31709947 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.1031G>A (p.Arg344Gln) single nucleotide variant Inborn genetic diseases [RCV002749218] Chr18:34019343 [GRCh38]
Chr18:31599307 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.1757C>T (p.Ala586Val) single nucleotide variant Inborn genetic diseases [RCV002660098] Chr18:33853002 [GRCh38]
Chr18:31432966 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.1063G>A (p.Ala355Thr) single nucleotide variant Inborn genetic diseases [RCV002767292] Chr18:33958412 [GRCh38]
Chr18:31538376 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.1010T>C (p.Ile337Thr) single nucleotide variant Inborn genetic diseases [RCV002803057] Chr18:34019364 [GRCh38]
Chr18:31599328 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.1030C>G (p.Arg344Gly) single nucleotide variant Inborn genetic diseases [RCV002984878] Chr18:34019344 [GRCh38]
Chr18:31599308 [GRCh37]
Chr18:18q12.1		 uncertain significance
NM_003787.5(NOL4):c.652A>G (p.Ile218Val) single nucleotide variant Inborn genetic diseases [RCV003345486] Chr18:34093585 [GRCh38]
Chr18:31673549 [GRCh37]
Chr18:18q12.1		 uncertain significance
GRCh37/hg19 18q12.1-12.3(chr18:26595964-38643072)x1 copy number loss not provided [RCV003483335] Chr18:26595964..38643072 [GRCh37]
Chr18:18q12.1-12.3		 pathogenic
NM_003787.5(NOL4):c.301C>T (p.Arg101Trp) single nucleotide variant not provided [RCV003413436] Chr18:34129984 [GRCh38]
Chr18:31709948 [GRCh37]
Chr18:18q12.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3760
Count of miRNA genes:1098
Interacting mature miRNAs:1365
Transcripts:ENST00000261592, ENST00000269185, ENST00000535384, ENST00000535475, ENST00000538587, ENST00000586309, ENST00000586314, ENST00000586553, ENST00000587953, ENST00000587971, ENST00000588280, ENST00000588355, ENST00000589544, ENST00000590712, ENST00000590846, ENST00000591917
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
D18S536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,588,286 - 31,588,438UniSTSGRCh37
Build 361829,842,284 - 29,842,436RGDNCBI36
Celera1828,396,612 - 28,396,764RGD
Cytogenetic Map18q12UniSTS
HuRef1828,447,678 - 28,447,822UniSTS
Marshfield Genetic Map1862.29RGD
Marshfield Genetic Map1862.29UniSTS
deCODE Assembly Map1855.88UniSTS
Whitehead-RH Map18280.7UniSTS
Whitehead-YAC Contig Map18 UniSTS
NCBI RH Map18391.8UniSTS
SHGC-79750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,663,227 - 31,663,513UniSTSGRCh37
Build 361829,917,225 - 29,917,511RGDNCBI36
Celera1828,471,550 - 28,471,836RGD
Cytogenetic Map18q12UniSTS
HuRef1828,522,595 - 28,522,881UniSTS
TNG Radiation Hybrid Map1811632.0UniSTS
SHGC-82933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,778,690 - 31,779,010UniSTSGRCh37
Build 361830,032,688 - 30,033,008RGDNCBI36
Celera1828,586,483 - 28,586,803RGD
Cytogenetic Map18q12UniSTS
HuRef1828,637,816 - 28,638,136UniSTS
TNG Radiation Hybrid Map1811594.0UniSTS
RH120891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,668,058 - 31,668,355UniSTSGRCh37
Build 361829,922,056 - 29,922,353RGDNCBI36
Celera1828,476,381 - 28,476,678RGD
Cytogenetic Map18q12UniSTS
HuRef1828,527,426 - 28,527,723UniSTS
TNG Radiation Hybrid Map1811622.0UniSTS
RH122103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,667,309 - 31,667,642UniSTSGRCh37
Build 361829,921,307 - 29,921,640RGDNCBI36
Celera1828,475,632 - 28,475,965RGD
Cytogenetic Map18q12UniSTS
HuRef1828,526,677 - 28,527,010UniSTS
TNG Radiation Hybrid Map1811625.0UniSTS
G60124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,557,845 - 31,558,063UniSTSGRCh37
Build 361829,811,843 - 29,812,061RGDNCBI36
Celera1828,366,170 - 28,366,388RGD
Cytogenetic Map18q12UniSTS
HuRef1828,417,234 - 28,417,452UniSTS
TNG Radiation Hybrid Map1811532.0UniSTS
SHGC-106862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,764,503 - 31,764,774UniSTSGRCh37
Build 361830,018,501 - 30,018,772RGDNCBI36
Celera1828,572,295 - 28,572,566RGD
Cytogenetic Map18q12UniSTS
HuRef1828,623,616 - 28,623,887UniSTS
TNG Radiation Hybrid Map1811603.0UniSTS
SHGC-68719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,456,816 - 31,457,036UniSTSGRCh37
Build 361829,710,814 - 29,711,034RGDNCBI36
Celera1828,265,139 - 28,265,359RGD
Cytogenetic Map18q12UniSTS
HuRef1828,316,201 - 28,316,421UniSTS
TNG Radiation Hybrid Map1811491.0UniSTS
IB3519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,432,533 - 31,432,687UniSTSGRCh37
Build 361829,686,531 - 29,686,685RGDNCBI36
Celera1828,240,856 - 28,241,010RGD
Cytogenetic Map18q12UniSTS
HuRef1828,291,914 - 28,292,068UniSTS
Whitehead-RH Map18280.8UniSTS
NCBI RH Map18389.8UniSTS
WI-15749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,431,081 - 31,431,210UniSTSGRCh37
Build 361829,685,079 - 29,685,208RGDNCBI36
Celera1828,239,404 - 28,239,533RGD
Cytogenetic Map18q12UniSTS
HuRef1828,290,462 - 28,290,591UniSTS
Whitehead-RH Map18280.7UniSTS
NOL4__3915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371831,432,264 - 31,432,988UniSTSGRCh37
Build 361829,686,262 - 29,686,986RGDNCBI36
Celera1828,240,587 - 28,241,311RGD
HuRef1828,291,645 - 28,292,369UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 2 135 21 5 778 4 203 62
Low 36 503 972 138 286 138 577 16 2228 120 302 694 7 470
Below cutoff 2073 1823 395 358 823 203 2897 1459 565 162 658 618 157 919 1746 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001198546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001353232 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001353233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001353234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001353235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001353236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001353237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003787 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006722563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002958188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_935261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA430033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB015339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB017800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC018972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC087397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM973283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT006763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA865522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CK822635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR456730 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA780731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC350556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC375356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456371 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000261592   ⟹   ENSP00000261592
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1833,851,100 - 34,224,913 (-)Ensembl
RefSeq Acc Id: ENST00000535384   ⟹   ENSP00000445733
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1833,852,290 - 34,048,594 (-)Ensembl
RefSeq Acc Id: ENST00000538587   ⟹   ENSP00000443472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1833,852,589 - 34,222,092 (-)Ensembl
RefSeq Acc Id: ENST00000586309   ⟹   ENSP00000464790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1834,105,125 - 34,222,289 (-)Ensembl
RefSeq Acc Id: ENST00000586314   ⟹   ENSP00000464704
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1833,852,450 - 34,222,318 (-)Ensembl
RefSeq Acc Id: ENST00000586553   ⟹   ENSP00000467015
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1833,883,365 - 34,023,639 (-)Ensembl
RefSeq Acc Id: ENST00000587953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1834,104,124 - 34,158,629 (-)Ensembl
RefSeq Acc Id: ENST00000587971
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1834,104,054 - 34,222,323 (-)Ensembl
RefSeq Acc Id: ENST00000588280
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1834,093,461 - 34,156,693 (-)Ensembl
RefSeq Acc Id: ENST00000588355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1834,223,935 - 34,224,910 (-)Ensembl
RefSeq Acc Id: ENST00000589544   ⟹   ENSP00000465450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1833,852,450 - 34,223,471 (-)Ensembl
RefSeq Acc Id: ENST00000590712   ⟹   ENSP00000467629
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1833,852,589 - 34,223,205 (-)Ensembl
RefSeq Acc Id: ENST00000590846
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1834,223,332 - 34,224,952 (-)Ensembl
RefSeq Acc Id: ENST00000591917   ⟹   ENSP00000467326
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1834,104,052 - 34,222,110 (-)Ensembl
RefSeq Acc Id: NM_001198546   ⟹   NP_001185475
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,223,551 (-)NCBI
GRCh371831,431,064 - 31,803,515 (-)ENTREZGENE
HuRef1828,290,445 - 28,662,648 (-)ENTREZGENE
CHM1_11831,358,224 - 31,730,679 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,415,403 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198547   ⟹   NP_001185476
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,222,470 (-)NCBI
GRCh371831,431,064 - 31,803,515 (-)ENTREZGENE
HuRef1828,290,445 - 28,662,648 (-)ENTREZGENE
CHM1_11831,358,224 - 31,729,598 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,414,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198548   ⟹   NP_001185477
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,223,551 (-)NCBI
GRCh371831,431,064 - 31,803,515 (-)ENTREZGENE
HuRef1828,290,445 - 28,662,648 (-)ENTREZGENE
CHM1_11831,358,224 - 31,730,679 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,415,403 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198549   ⟹   NP_001185478
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,048,612 (-)NCBI
GRCh371831,431,064 - 31,803,515 (-)ENTREZGENE
HuRef1828,290,445 - 28,662,648 (-)ENTREZGENE
CHM1_11831,358,224 - 31,555,739 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,240,465 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282527   ⟹   NP_001269456
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,222,470 (-)NCBI
HuRef1828,290,445 - 28,662,648 (-)NCBI
CHM1_11831,358,224 - 31,729,598 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,414,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001353232   ⟹   NP_001340161
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,223,551 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,415,403 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001353233   ⟹   NP_001340162
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,223,551 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,415,403 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001353234   ⟹   NP_001340163
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,222,470 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,414,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001353235   ⟹   NP_001340164
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,222,470 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,414,322 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001353236   ⟹   NP_001340165
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,048,612 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,240,465 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001353237   ⟹   NP_001340166
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,223,551 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,415,403 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384467   ⟹   NP_001371396
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384468   ⟹   NP_001371397
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384469   ⟹   NP_001371398
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384470   ⟹   NP_001371399
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384471   ⟹   NP_001371400
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384472   ⟹   NP_001371401
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384473   ⟹   NP_001371402
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: NM_003787   ⟹   NP_003778
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
GRCh371831,431,064 - 31,803,515 (-)ENTREZGENE
Build 361829,685,062 - 30,057,444 (-)NCBI Archive
Celera1828,239,387 - 28,611,397 (-)RGD
HuRef1828,290,445 - 28,662,648 (-)ENTREZGENE
CHM1_11831,358,224 - 31,730,679 (-)NCBI
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006722563   ⟹   XP_006722626
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011526237   ⟹   XP_011524539
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011526238   ⟹   XP_011524540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011526239   ⟹   XP_011524541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,121,700 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026052   ⟹   XP_016881541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,108,152 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026053   ⟹   XP_016881542
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,113,037 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026058   ⟹   XP_016881547
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,121,341 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024451279   ⟹   XP_024307047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,130,339 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047437901   ⟹   XP_047293857
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
RefSeq Acc Id: XM_047437902   ⟹   XP_047293858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,224,913 (-)NCBI
RefSeq Acc Id: XM_047437903   ⟹   XP_047293859
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381834,019,513 - 34,224,913 (-)NCBI
RefSeq Acc Id: XM_047437904   ⟹   XP_047293860
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381834,019,318 - 34,224,913 (-)NCBI
RefSeq Acc Id: XM_047437905   ⟹   XP_047293861
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,851,100 - 34,121,339 (-)NCBI
RefSeq Acc Id: XM_054319291   ⟹   XP_054175266
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
RefSeq Acc Id: XM_054319292   ⟹   XP_054175267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
RefSeq Acc Id: XM_054319293   ⟹   XP_054175268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,042,633 - 34,416,765 (-)NCBI
RefSeq Acc Id: XM_054319294   ⟹   XP_054175269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,042,633 - 34,322,182 (-)NCBI
RefSeq Acc Id: XM_054319295   ⟹   XP_054175270
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,042,633 - 34,299,999 (-)NCBI
RefSeq Acc Id: XM_054319296   ⟹   XP_054175271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,042,633 - 34,304,881 (-)NCBI
RefSeq Acc Id: XM_054319297   ⟹   XP_054175272
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,042,633 - 34,313,543 (-)NCBI
RefSeq Acc Id: XM_054319298   ⟹   XP_054175273
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,211,321 - 34,416,765 (-)NCBI
RefSeq Acc Id: XM_054319299   ⟹   XP_054175274
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,211,126 - 34,416,765 (-)NCBI
RefSeq Acc Id: XR_008485030
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01834,149,227 - 34,416,765 (-)NCBI
RefSeq Acc Id: XR_935261
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381833,957,428 - 34,224,913 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001185475 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185476 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185477 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185478 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269456 (Get FASTA)   NCBI Sequence Viewer  
  NP_001340161 (Get FASTA)   NCBI Sequence Viewer  
  NP_001340162 (Get FASTA)   NCBI Sequence Viewer  
  NP_001340163 (Get FASTA)   NCBI Sequence Viewer  
  NP_001340164 (Get FASTA)   NCBI Sequence Viewer  
  NP_001340165 (Get FASTA)   NCBI Sequence Viewer  
  NP_001340166 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371396 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371397 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371398 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371399 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371400 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371401 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371402 (Get FASTA)   NCBI Sequence Viewer  
  NP_003778 (Get FASTA)   NCBI Sequence Viewer  
  XP_006722626 (Get FASTA)   NCBI Sequence Viewer  
  XP_011524539 (Get FASTA)   NCBI Sequence Viewer  
  XP_011524540 (Get FASTA)   NCBI Sequence Viewer  
  XP_011524541 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881541 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881542 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881547 (Get FASTA)   NCBI Sequence Viewer  
  XP_024307047 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293857 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293858 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293859 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293860 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293861 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175266 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175267 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175268 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175269 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175270 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175271 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175272 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175273 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175274 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH00313 (Get FASTA)   NCBI Sequence Viewer  
  AAP35409 (Get FASTA)   NCBI Sequence Viewer  
  BAA34576 (Get FASTA)   NCBI Sequence Viewer  
  BAA34797 (Get FASTA)   NCBI Sequence Viewer  
  BAG52366 (Get FASTA)   NCBI Sequence Viewer  
  BAG59674 (Get FASTA)   NCBI Sequence Viewer  
  BAG61712 (Get FASTA)   NCBI Sequence Viewer  
  BAH12383 (Get FASTA)   NCBI Sequence Viewer  
  CAG33011 (Get FASTA)   NCBI Sequence Viewer  
  EAX01310 (Get FASTA)   NCBI Sequence Viewer  
  EAX01311 (Get FASTA)   NCBI Sequence Viewer  
  EAX01312 (Get FASTA)   NCBI Sequence Viewer  
  EAX01313 (Get FASTA)   NCBI Sequence Viewer  
  EAX01314 (Get FASTA)   NCBI Sequence Viewer  
  EAX01315 (Get FASTA)   NCBI Sequence Viewer  
  EAX01316 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000261592
  ENSP00000261592.4
  ENSP00000443472
  ENSP00000443472.1
  ENSP00000445733
  ENSP00000445733.1
  ENSP00000464704.1
  ENSP00000464790.1
  ENSP00000465450
  ENSP00000465450.1
  ENSP00000467015.1
  ENSP00000467326.1
  ENSP00000467629
  ENSP00000467629.1
GenBank Protein O94818 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_003778   ⟸   NM_003787
- Peptide Label: isoform 1
- UniProtKB: Q6IBS2 (UniProtKB/Swiss-Prot),   F5H1E3 (UniProtKB/Swiss-Prot),   B7Z3Z7 (UniProtKB/Swiss-Prot),   B4DSQ0 (UniProtKB/Swiss-Prot),   Q9BWF1 (UniProtKB/Swiss-Prot),   O94818 (UniProtKB/Swiss-Prot),   K7EQ17 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185477   ⟸   NM_001198548
- Peptide Label: isoform 4
- UniProtKB: K7EQ17 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185475   ⟸   NM_001198546
- Peptide Label: isoform 2
- UniProtKB: K7EQ17 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185476   ⟸   NM_001198547
- Peptide Label: isoform 3
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185478   ⟸   NM_001198549
- Peptide Label: isoform 5
- UniProtKB: O94818 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001269456   ⟸   NM_001282527
- Peptide Label: isoform 6
- UniProtKB: B3KRF4 (UniProtKB/TrEMBL),   B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006722626   ⟸   XM_006722563
- Peptide Label: isoform X1
- UniProtKB: Q6IBS2 (UniProtKB/Swiss-Prot),   F5H1E3 (UniProtKB/Swiss-Prot),   B7Z3Z7 (UniProtKB/Swiss-Prot),   B4DSQ0 (UniProtKB/Swiss-Prot),   Q9BWF1 (UniProtKB/Swiss-Prot),   O94818 (UniProtKB/Swiss-Prot),   K7EQ17 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011524540   ⟸   XM_011526238
- Peptide Label: isoform X2
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011524539   ⟸   XM_011526237
- Peptide Label: isoform X1
- UniProtKB: Q6IBS2 (UniProtKB/Swiss-Prot),   F5H1E3 (UniProtKB/Swiss-Prot),   B7Z3Z7 (UniProtKB/Swiss-Prot),   B4DSQ0 (UniProtKB/Swiss-Prot),   Q9BWF1 (UniProtKB/Swiss-Prot),   O94818 (UniProtKB/Swiss-Prot),   K7EQ17 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011524541   ⟸   XM_011526239
- Peptide Label: isoform X4
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881547   ⟸   XM_017026058
- Peptide Label: isoform X4
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881542   ⟸   XM_017026053
- Peptide Label: isoform X4
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881541   ⟸   XM_017026052
- Peptide Label: isoform X3
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001340161   ⟸   NM_001353232
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: NP_001340162   ⟸   NM_001353233
- Peptide Label: isoform 8
- Sequence:
RefSeq Acc Id: NP_001340166   ⟸   NM_001353237
- Peptide Label: isoform 6
- UniProtKB: B3KRF4 (UniProtKB/TrEMBL),   B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001340163   ⟸   NM_001353234
- Peptide Label: isoform 9
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001340164   ⟸   NM_001353235
- Peptide Label: isoform 10
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001340165   ⟸   NM_001353236
- Peptide Label: isoform 11
- Sequence:
RefSeq Acc Id: XP_024307047   ⟸   XM_024451279
- Peptide Label: isoform X2
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000464704   ⟸   ENST00000586314
RefSeq Acc Id: ENSP00000464790   ⟸   ENST00000586309
RefSeq Acc Id: ENSP00000467015   ⟸   ENST00000586553
RefSeq Acc Id: ENSP00000445733   ⟸   ENST00000535384
RefSeq Acc Id: ENSP00000465450   ⟸   ENST00000589544
RefSeq Acc Id: ENSP00000443472   ⟸   ENST00000538587
RefSeq Acc Id: ENSP00000261592   ⟸   ENST00000261592
RefSeq Acc Id: ENSP00000467629   ⟸   ENST00000590712
RefSeq Acc Id: ENSP00000467326   ⟸   ENST00000591917
RefSeq Acc Id: NP_001371399   ⟸   NM_001384470
- Peptide Label: isoform 16
- UniProtKB: B4DLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001371402   ⟸   NM_001384473
- Peptide Label: isoform 17
RefSeq Acc Id: NP_001371397   ⟸   NM_001384468
- Peptide Label: isoform 14
- UniProtKB: K7EQ17 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001371396   ⟸   NM_001384467
- Peptide Label: isoform 13
- UniProtKB: K7EQ17 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001371400   ⟸   NM_001384471
- Peptide Label: isoform 6
- UniProtKB: B3KRF4 (UniProtKB/TrEMBL),   B4DLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001371401   ⟸   NM_001384472
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001371398   ⟸   NM_001384469
- Peptide Label: isoform 15
- UniProtKB: K7EQ17 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293858   ⟸   XM_047437902
- Peptide Label: isoform X1
- UniProtKB: Q6IBS2 (UniProtKB/Swiss-Prot),   O94818 (UniProtKB/Swiss-Prot),   F5H1E3 (UniProtKB/Swiss-Prot),   B7Z3Z7 (UniProtKB/Swiss-Prot),   B4DSQ0 (UniProtKB/Swiss-Prot),   Q9BWF1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047293857   ⟸   XM_047437901
- Peptide Label: isoform X1
- UniProtKB: Q6IBS2 (UniProtKB/Swiss-Prot),   O94818 (UniProtKB/Swiss-Prot),   F5H1E3 (UniProtKB/Swiss-Prot),   B7Z3Z7 (UniProtKB/Swiss-Prot),   B4DSQ0 (UniProtKB/Swiss-Prot),   Q9BWF1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047293861   ⟸   XM_047437905
- Peptide Label: isoform X7
- UniProtKB: B3KRF4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293860   ⟸   XM_047437904
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047293859   ⟸   XM_047437903
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054175268   ⟸   XM_054319293
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054175267   ⟸   XM_054319292
- Peptide Label: isoform X1
- UniProtKB: Q9BWF1 (UniProtKB/Swiss-Prot),   Q6IBS2 (UniProtKB/Swiss-Prot),   O94818 (UniProtKB/Swiss-Prot),   F5H1E3 (UniProtKB/Swiss-Prot),   B7Z3Z7 (UniProtKB/Swiss-Prot),   B4DSQ0 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054175266   ⟸   XM_054319291
- Peptide Label: isoform X1
- UniProtKB: Q9BWF1 (UniProtKB/Swiss-Prot),   Q6IBS2 (UniProtKB/Swiss-Prot),   O94818 (UniProtKB/Swiss-Prot),   F5H1E3 (UniProtKB/Swiss-Prot),   B7Z3Z7 (UniProtKB/Swiss-Prot),   B4DSQ0 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054175269   ⟸   XM_054319294
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054175272   ⟸   XM_054319297
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054175271   ⟸   XM_054319296
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054175270   ⟸   XM_054319295
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054175274   ⟸   XM_054319299
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054175273   ⟸   XM_054319298
- Peptide Label: isoform X5

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O94818-F1-model_v2 AlphaFold O94818 1-638 view protein structure

Promoters
RGD ID:6811445
Promoter ID:HG_ACW:37877
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:NOL4.KAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361829,993,116 - 29,993,616 (-)MPROMDB
RGD ID:6794893
Promoter ID:HG_KWN:27863
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC002KXR.2,   UC010DMH.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361830,056,374 - 30,056,874 (-)MPROMDB
RGD ID:6794947
Promoter ID:HG_KWN:27864
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000399171,   UC002KXT.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361830,057,001 - 30,057,697 (-)MPROMDB
RGD ID:6814623
Promoter ID:HG_XEF:3693
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:NM_001107401,   NM_199024
Position:
Human AssemblyChrPosition (strand)Source
Build 361830,058,476 - 30,058,976 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7870 AgrOrtholog
COSMIC NOL4 COSMIC
Ensembl Genes ENSG00000101746 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000261592 ENTREZGENE
  ENST00000261592.10 UniProtKB/Swiss-Prot
  ENST00000535384 ENTREZGENE
  ENST00000535384.5 UniProtKB/Swiss-Prot
  ENST00000538587 ENTREZGENE
  ENST00000538587.5 UniProtKB/Swiss-Prot
  ENST00000586309.1 UniProtKB/TrEMBL
  ENST00000586314.5 UniProtKB/TrEMBL
  ENST00000586553.1 UniProtKB/TrEMBL
  ENST00000589544 ENTREZGENE
  ENST00000589544.5 UniProtKB/Swiss-Prot
  ENST00000590712 ENTREZGENE
  ENST00000590712.5 UniProtKB/TrEMBL
  ENST00000591917.5 UniProtKB/TrEMBL
GTEx ENSG00000101746 GTEx
HGNC ID HGNC:7870 ENTREZGENE
Human Proteome Map NOL4 Human Proteome Map
InterPro NOL4/NOL4L UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8715 UniProtKB/Swiss-Prot
NCBI Gene 8715 ENTREZGENE
OMIM 603577 OMIM
PANTHER PTHR12449 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR12449:SF17 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31674 PharmGKB
UniProt B3KRF4 ENTREZGENE, UniProtKB/TrEMBL
  B4DLW2 ENTREZGENE, UniProtKB/TrEMBL
  B4DSQ0 ENTREZGENE
  B7Z3Z7 ENTREZGENE
  F5H1E3 ENTREZGENE
  K7EID6_HUMAN UniProtKB/TrEMBL
  K7EIK8_HUMAN UniProtKB/TrEMBL
  K7ENM5_HUMAN UniProtKB/TrEMBL
  K7EPC5_HUMAN UniProtKB/TrEMBL
  K7EQ17 ENTREZGENE, UniProtKB/TrEMBL
  NOL4_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q6IBS2 ENTREZGENE
  Q9BWF1 ENTREZGENE
UniProt Secondary B4DSQ0 UniProtKB/Swiss-Prot
  B7Z3Z7 UniProtKB/Swiss-Prot
  F5H1E3 UniProtKB/Swiss-Prot
  Q6IBS2 UniProtKB/Swiss-Prot
  Q9BWF1 UniProtKB/Swiss-Prot