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Gene: AC092384.1 (novel transcript, antisense to CBFA2T3) Homo sapiens

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Symbol:

AC092384.1

Name:

novel transcript, antisense to CBFA2T3

RGD ID:

16551567

Description:

ASSOCIATED WITH Autism; autistic disorder; KBG syndrome

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

VALIDATED

Previously known as:

LOC100129697; uncharacterized LOC100129697

RGD Orthologs

Bonobo

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38.p14 Ensembl - Human Genome Assembly GRCh38 Ensembl

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	88,939,271 - 88,953,782 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	88,939,789 - 88,951,524 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	89,005,679 - 89,020,190 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	16	q24.3	NCBI
HuRef	16	74,704,050 - 74,715,097 (+)	NCBI		HuRef
CHM1_1	16	90,417,049 - 90,429,225 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	16	95,016,690 - 95,031,162 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
AC092384.1	Human	autistic disorder		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Autism	ClinVar
AC092384.1	Human	KBG syndrome		IAGP	(Homo sapiens) more ...	8554872	ClinVar Annotator: match by term: KBG syndrome	ClinVar	PMID:31690835

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
AC092384.1	Human	Autism		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Autism	ClinVar

AC092384.1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	88,939,271 - 88,953,782 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	88,939,789 - 88,951,524 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	89,005,679 - 89,020,190 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Cytogenetic Map	16	q24.3	NCBI
HuRef	16	74,704,050 - 74,715,097 (+)	NCBI		HuRef
CHM1_1	16	90,417,049 - 90,429,225 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	16	95,016,690 - 95,031,162 (+)	NCBI		T2T-CHM13v2.0

LOC117976169
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	18	98,719,607 - 98,733,604 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	104,631,770 - 104,645,737 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	16	69,660,447 - 69,672,129 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3

Variants in AC092384.1
5 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 16q24.2-24.3(chr16:87853401-90081985)x3	copy number gain	See cases [RCV000052428]	Chr16:87853401..90081985 [GRCh38] Chr16:87887007..90148393 [GRCh37] Chr16:86444508..88675894 [NCBI36] Chr16:16q24.2-24.3	pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80717291-90096662)x3	copy number gain	See cases [RCV000141128]	Chr16:80717291..90096662 [GRCh38] Chr16:80751188..90163070 [GRCh37] Chr16:79308689..88690571 [NCBI36] Chr16:16q23.2-24.3	pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:87306529-89269079)x1	copy number loss	See cases [RCV000053362]	Chr16:87306529..89269079 [GRCh38] Chr16:87340135..89335487 [GRCh37] Chr16:85897636..87862988 [NCBI36] Chr16:16q24.2-24.3	pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:87848216-90096995)x3	copy number gain	See cases [RCV000138161]	Chr16:87848216..90096995 [GRCh38] Chr16:87881822..90163403 [GRCh37] Chr16:86439323..88690904 [NCBI36] Chr16:16q24.2-24.3	likely pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:75377981-90081992)x3	copy number gain	See cases [RCV000139302]	Chr16:75377981..90081992 [GRCh38] Chr16:75411879..90148400 [GRCh37] Chr16:73969380..88675901 [NCBI36] Chr16:16q23.1-24.3	pathogenic
GRCh38/hg38 16q24.1-24.3(chr16:86950106-89335814)x1	copy number loss	See cases [RCV000143624]	Chr16:86950106..89335814 [GRCh38] Chr16:86983712..89402222 [GRCh37] Chr16:85541213..87929723 [NCBI36] Chr16:16q24.1-24.3	pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:78816291-90081985)x3	copy number gain	See cases [RCV000050840]	Chr16:78816291..90081985 [GRCh38] Chr16:78850188..90148393 [GRCh37] Chr16:77407689..88675894 [NCBI36] Chr16:16q23.1-24.3	pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70514631-90081985)x3	copy number gain	See cases [RCV000052422]	Chr16:70514631..90081985 [GRCh38] Chr16:70548534..90148393 [GRCh37] Chr16:69106035..88675894 [NCBI36] Chr16:16q22.1-24.3	pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:83478453-89932910)x3	copy number gain	See cases [RCV000137980]	Chr16:83478453..89932910 [GRCh38] Chr16:83512058..89999318 [GRCh37] Chr16:82069559..88526819 [NCBI36] Chr16:16q23.3-24.3	likely pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80067315-90057871)x3	copy number gain	See cases [RCV000142698]	Chr16:80067315..90057871 [GRCh38] Chr16:80101212..90124279 [GRCh37] Chr16:78658713..88651780 [NCBI36] Chr16:16q23.2-24.3	pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3	copy number gain	See cases [RCV000052421]	Chr16:65313395..90081985 [GRCh38] Chr16:65347298..90148393 [GRCh37] Chr16:63904799..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3	copy number gain	See cases [RCV000143425]	Chr16:52899183..90088654 [GRCh38] Chr16:52933095..90155062 [GRCh37] Chr16:51490596..88682563 [NCBI36] Chr16:16q12.2-24.3	pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:83988570-90081985)x3	copy number gain	See cases [RCV000135659]	Chr16:83988570..90081985 [GRCh38] Chr16:84022175..90148393 [GRCh37] Chr16:82579676..88675894 [NCBI36] Chr16:16q23.3-24.3	likely pathogenic
GRCh38/hg38 16q24.1-24.3(chr16:85552976-90096995)x3	copy number gain	See cases [RCV000139658]	Chr16:85552976..90096995 [GRCh38] Chr16:85586582..90163403 [GRCh37] Chr16:84144083..88690904 [NCBI36] Chr16:16q24.1-24.3	pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:76336203-90088654)x3	copy number gain	See cases [RCV000141700]	Chr16:76336203..90088654 [GRCh38] Chr16:76370100..90155062 [GRCh37] Chr16:74927601..88682563 [NCBI36] Chr16:16q23.1-24.3	pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:82173150-90081985)x3	copy number gain	See cases [RCV000052424]	Chr16:82173150..90081985 [GRCh38] Chr16:82206755..90148393 [GRCh37] Chr16:80764256..88675894 [NCBI36] Chr16:16q23.3-24.3	pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70749398-90096995)x3	copy number gain	See cases [RCV000137495]	Chr16:70749398..90096995 [GRCh38] Chr16:70783301..90163403 [GRCh37] Chr16:69340802..88690904 [NCBI36] Chr16:16q22.1-24.3	pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:88159660-89506042)x1	copy number loss	See cases [RCV000053363]	Chr16:88159660..89506042 [GRCh38] Chr16:88193266..89572450 [GRCh37] Chr16:86750767..88099951 [NCBI36] Chr16:16q24.2-24.3	pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:88640116-89530475)x1	copy number loss	See cases [RCV000053380]	Chr16:88640116..89530475 [GRCh38] Chr16:88706524..89596883 [GRCh37] Chr16:87234025..88124384 [NCBI36] Chr16:16q24.2-24.3	pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:88662702-89454555)x1	copy number loss	See cases [RCV000053381]	Chr16:88662702..89454555 [GRCh38] Chr16:88729110..89520963 [GRCh37] Chr16:87256611..88048464 [NCBI36] Chr16:16q24.2-24.3	pathogenic
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3	copy number gain	See cases [RCV000139426]	Chr16:65511483..90096995 [GRCh38] Chr16:65545386..90163403 [GRCh37] Chr16:64102887..88690904 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3	copy number gain	See cases [RCV000142578]	Chr16:64389378..90081985 [GRCh38] Chr16:64423281..90148393 [GRCh37] Chr16:62980782..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:76873569-90081985)x3	copy number gain	See cases [RCV000052423]	Chr16:76873569..90081985 [GRCh38] Chr16:76907466..90148393 [GRCh37] Chr16:75464967..88675894 [NCBI36] Chr16:16q23.1-24.3	pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80946659-90081985)x3	copy number gain	See cases [RCV000136898]	Chr16:80946659..90081985 [GRCh38] Chr16:80980556..90148393 [GRCh37] Chr16:79538057..88675894 [NCBI36] Chr16:16q23.2-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 16q24.3(chr16:88818756-89413158)x1	copy number loss	See cases [RCV000050963]	Chr16:88818756..89413158 [GRCh38] Chr16:88885164..89479566 [GRCh37] Chr16:87412665..88007067 [NCBI36] Chr16:16q24.3	pathogenic
Single allele	deletion	KBG syndrome [RCV003388955]	Chr16:88621654..89376245 [GRCh38] Chr16:16q24.2-24.3	pathogenic
Single allele	deletion	KBG syndrome [RCV003388953]	Chr16:87169884..89487487 [GRCh38] Chr16:16q24.2-24.3	pathogenic
NM_005187.6(CBFA2T3):c.151+26120G>A	single nucleotide variant	not provided [RCV003419502]	Chr16:88950537 [GRCh38] Chr16:89016945 [GRCh37] Chr16:16q24.3	likely benign
Single allele	deletion	KBG syndrome [RCV003388954]	Chr16:88197484..89331695 [GRCh38] Chr16:16q24.2-24.3	pathogenic
NR_168285.1(LOC100129697):n.977G>A	single nucleotide variant	Autism [RCV004698701]	Chr16:88940247 [GRCh38] Chr16:89006655 [GRCh37] Chr16:16q24.3	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	191
Count of miRNA genes:	165
Interacting mature miRNAs:	170
Transcripts:	ENST00000378347, ENST00000593752
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

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	renal system	reproductive system	respiratory system	sensory system
1203	2294	2676	2088	4617	1496	1925	1	417	1840	256	2023	6572	6149	14	3610	703	1524	1408	162


RefSeq Transcripts	NG_029533	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001290330	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_168285	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC092384	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK130238	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU949339	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY074528	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000378347

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	88,939,789 - 88,951,524 (+)	Ensembl

RefSeq Acc Id:

NR_168285

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	88,939,271 - 88,953,782 (+)	NCBI
T2T-CHM13v2.0	16	95,016,690 - 95,031,162 (+)	NCBI

Sequence:

show sequence

ACTCACCAGCCCTGGCTTCACAGGTGGTGACAGCACGGCCCCAGCACCACGAACCACTCATGTGAACTTCCCTTCTCCCCTGTCACTAGAGGATCCCAGCACATCCCAGGAGAGATGGAGCCTGCCGG
AAGACTGATCCTGATGCGACACTCTCTTCCCTCCCTGAGCCCCAATCTCGGGTGGAGGCCACATCTGTTCCTCCTGCTCTGGGCGCTTCTTCCTTTCTGTTTCCCTTTCAGTGTGGAAGAGTGGCCGC
TTGCCCAGCAGGACGGTCCCAAATAGCATGGCTTTTCCAGGCACGGTGCTGTCGGCCGCACAGAACAGGACCCTCCCGGCAGCTCCGGCTTGCACAGCATCCGCCTGTCTGGCCCCTGTGGAAGTATC
TGACTCCCAACGCCCAGACTGGAGCGGGGGCAAAGGACACAGCCCGACCCCAGAGGCACACAGAGCCAGCCCTCCACGGAAGAACGTGCCCAGGAACTGTGGGCTGGGCCTTCCTGCCTCCTCCCCTG
CCGCGAAAGCGATGCCAGGGGCAGGTGAGGGTCGGACGCGCTCAGGCCCAGCCCTCGCCCCTTCAGGTCTGGGGGACACAGTGGAGTCCCAGCCTCAAGAAGTTTCCCCAACCTCTCAGAAACTTGAA
GGGCAATGCCAGGTACCGAAAAACCGGCCCCCGCCCCTTATCCCCGGCCGACCCGTCCGCCGAGGTGGCTGCCCTGGGAACCTCCTGTTCCTCGTCCAGGAGAGGAAACGCACACCCGGGCCGGACGC
ACAGAAGCCGCACCCTGGCTGGGGCCACAAGCCTGACAGCTACCGACAAGCCCCCACCCACAGGAGCACGCGACGTGCTCTCTTTTCAAGGGAAAGGTTTTTCTTCCTGGGCCCTGGAATGGGCCTGA
AGTCAGCCGGCCTCAGCCCACAGGGTGAATGAGGGGTGGGCACAGCCCGGCCGCGGCCCCAGCACACACGGGCGGACGCAGGGGCGGGGGAGCGCCAGCCCCGCAGTGTGTTCGGAGCCCAGCGGCTC
TGAGTCGCCGCCACCAGCCTGGCCGCCTTCTGCTCCACGTCTGTTCACCCGTCCCCTGGACCGGCACCGCCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGGTCAGTTCACCCGTCCCCTGGAC
CGGCACCGCCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGGTCAGTTCACCCGTCCCCTGGACCGGCACCGGCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGATCTGTTCACCCCTCCC
CCGGACCGGCACCGCCACAGAGGGTCAGGAGTGTTGGCACCTGTCTTCCGGGTCAGTTCACCCGTCCCCTGGACCGGCACCGCCACAGAGGGTCAGGAGTGTTGGCACCTGTCTTCCGGATCTGTTCA
CCCGTCCCCTGGACCGGCACCGCCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGATCTGTTCACCCGTCCCCTGGACCGGCACCGCCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGATC
TGTTCACCCGTCCCCTGGACCGGCACCGCCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGATCTGTTCACCCGTCCCCTGGACCGGCACCGCCACAGAGGGTCAGAGTGTTGGCACCTGTCTTC
CGGATCTGTTCACCCCTCCCCTGGATCGGCACCGGCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGATCTGTTCACCCGTCCCCTGGACCGGCACCGCCACAGAGGGTCAGAGTGTTGGCACCT
GTCTTCCGGATCTGTTCACCCCTCGCCTGGACCGGCACCGGCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGATCTGTTCACCCCTCCCCTGGACCGGCACCGCCACAGAGGGTCAGAGTGTTG
GCACCTGTCTTCCGGATCTGTTCACCCCTCCCCTGGATCGGCACCGGCACAGAGGGTCAGAGTGTTGGCACCTGTCTTCCGGATCTGTTCACCCGTCCCCTGGACCGGCACCGGCACAGAGGGTCAGA
GTGTTGGCACCTGTCTTCCGGGTCTGTTCACCCGTCCCCTGGACTGGCACCAGCACAGAGGGTCGAGTGTTGGCACCTGTCTTCTGGGTCTCCATCCCTCCCTTTGTTTGTTGAGTGACTGCATGTTC
TCATTTCCTTATCATACAATTCTTTGAGAGGTATCATTAGCTGCGTCTTATTTTATTTTCACCTTCTTTTCTGTTACCTGTATGTTTGAATTTTCCTATAAGTATTTTTGTTTCATCTTTGCTTTTTT
AAATTAAAAAATCAGTTTTAAAATTGCACCTGCAGTACAAAATCAGGGTGGCGACCGGGTTGCTGCCATTCCCTCCCCTCGGGTCTGTGGCTTCTCAGCTCCAGCTCGGGTCACAGACCTGCTGCCAC
GGCCCCAGGGTGGGCACAGGGCTAGCAGGACAGTCATGCAGGCAGCCGCGGCCCCAGCGATTGGTCCAGGAGGAGGGCAGGTGACCACACGCGGCCAATCACAATCCTTCCCTGGGAGTTTTTGAACT
GGAACAAGAGAGGAAGGACCTCTTCTTTGATCTGCGTGGGAGGCAAGCCCAGAGTGGCCTGGACAGCCGCTGGGAAGAGAAGGTGGGCAGAGCGGCGGAGGGTGTGCTAATGGTTGGGTCTGTGGGGC
CTGAAACCGGTGCCCCTGCCCATCCTATAGTTTGGTGCTTGAGCCAGCACAGTCCCAGGTGTCCCTGACGCCTCCGAGCTGGGTTTCTGTCACTCGCAGCTGCAGCATTCTGGCACAGACCCTTGGCC
CAGGACCCCTGTGCAGAGGTGGGTTTGGGTCTCCCCGGCCCCAGCAGCCCCAGGAGCCTGTGAGATCTAAGCCGGAAGCTGCTCTGGGCACCTGAGTGCTGACAGCCCGAGTGATGGGAACAGGCTCG
CTACTATGCAGAGACAGAGAGACTAATTTTTATCAGCCAGATACCTGGCCAGGCCCCAGGGTGGACAATCTCCAAACCGCATGCATCCCGGCACTGACAAAGCCGTCTATCATTGCTGGAGCCAGGAC
ACCCGGGGAGGCTGTGCCAGGCCACGGGGTGAGGGAGCTGCCTCCCTCCAGTCCTTCTCCCGTGGGGCACTGAGACGGCTTTCAGCAAGACAAATGCCCAGGCCACAGGGTGAGGGAGCTGCCGCCCT
CCAATCCTTCTCCCGCGGGGCACCAAAATGGCTTTCAGCAGGACAAATGCCCAGGCCATGGGGTGAGGGAGTTGCCGCCCTCCAGTCCTTCTCCCACGGGGCACCGAGACGGCTTTCAGCAAGACAAA
TGCGGCCCTGCCACTCCCTGACCGAGATAAAGTCTCAGCTCCTGAGCCTGGGGTGCCTGCTGCTCGCCCCCATCGCCTCTCTGAGCTCCAGCCTCACAGGCACACACCGCTCCCCTGCCCAGAACATT
CTGCCCACAAACTCCTCTTAGCCTCAGGTCCCTGCTGAGTGGCCATTCCTGCTGGGAGGCAGGAATTCCCTGATCTACCCTTCCTGAGTCTGGGAGAGACGCCTCCCATACCCCCATGACAGCCCATC
ACAATTGTTCACGGATCTCTGTGTTCTCCCTCAACAAATACTTGGCGGACCCCCTGGAGCCACAGCTCAAGGCTTCCTTCCCCCCCACCCCCACACCCTGGGGACAGCATGTCCAGGACCCCCACGCA
GGGCCTGTGTCGAGACGGCATGTCCAGGACCCCCACGCAGGGCCTGTGTCGAGACGGCATGTCCAGGACCCCCACGCAGGGCCTGTGTCGAGACGGCATGTCCCGCCATCGGGTTTGCTGCTGAATGA
GCAGATGATCTAATGAGTGACCGTCCTCACCCACGAGAAAAAACACAACCTGGTCTCCGTCTGCCGGTTAGATCGGCCCCCAGTCCTGCTGGCCCCAGCGATGACAGAGGAGGAGGAATGAGGAGTGC
CGTGCCTGGGCTGGGCCATCGCCTCTCTCCCTCGGCTGGGTTTGTCATGCTCAGCCAGACCCGCTCCCGGTGGAGAGGCCGAGGGACCCTCATTTCTACGTTTGCATCCCTTTCTTCCAGGGCCTGCG
GGGCTGACAGGCACACAGCCAGTGGTGAAGGTTCACGGAAGAACGAAGGAAGGAGTGAGCGTGGGGAGAGCCAGCCAGGCTCCCCATGTCCACCCAGATGGTGAGCTGGCCCTGCCCTGGAGACACTG
TGTCCAGAGGCCAGCATAGCCCTCAAAACGGTTCCCACAGCTCCCAGCGGAGCCCTCAAAATGGTCCCCACAGCTGCCGCCCACTCTTGGGACCCTGAGTGTGGGGAGGCTGGGGTTGAGCAGTGGGG
ATCAGGATCTGGCAGGATCGGAATGTAGAGGCCTGGGGGCTCCCGGCTGGGGACAGTGCCAGCAGGAGTGGCCGGGACGATGACGAGGTGAGGTGTCTGCTCCCAGGCTGTGTGTGGCTTGGATGCCA
AAGCGCCTTTTGCTGTATTCGGCACCCTGAGACCCTTATGTCTGCCTATTGAAGGCACAGTTTACTCCCGGGAAAATAAACATTTGGGTTTATTTCGCTGTGACTGCA

hide sequence


Protein RefSeqs	NP_001277259	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	BAC85311	(Get FASTA)	NCBI Sequence Viewer

Database	Acc Id	Source(s)
COSMIC	AC092384.1	COSMIC
Ensembl Genes	ENSG00000205018	Ensembl
GTEx	ENSG00000205018	GTEx
Human Proteome Map	AC092384.1	Human Proteome Map
NCBI Gene	LOC100129697	ENTREZGENE
RNAcentral	URS00007DCF6E	RNACentral
	URS0001BBE657	RNACentral
UniProt	Q6ZP14_HUMAN	UniProtKB/TrEMBL

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2020-12-03	AC092384.1	novel transcript, antisense to CBFA2T3	AC092384.1	uncharacterized LOC100129697	Symbol and/or name change	19259462	PROVISIONAL
2020-06-25	AC092384.1	uncharacterized LOC100129697	LOC100129697	uncharacterized LOC100129697	Symbol and/or name change	19259462	PROVISIONAL
2020-06-18	LOC100129697	uncharacterized LOC100129697	AC092384.1	uncharacterized LOC100129697	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailable


InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailable


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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