CDC25C cell division cycle 25C [Homo sapiens (human)] - Gene

Summary

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Official Symbol: CDC25Cprovided by HGNC
Official Full Name: cell division cycle 25Cprovided by HGNC
Primary source: HGNC:1727
See related: Ensembl:ENSG00000158402; HPRD:01146; MIM:157680; Vega:OTTHUMG00000129203
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: CDC25; PPP1R60
Summary: This gene is highly conserved during evolution and it plays a key role in the regulation of cell division. The encoded protein is a tyrosine phosphatase and belongs to the Cdc25 phosphatase family. It directs dephosphorylation of cyclin B-bound CDC2 and triggers entry into mitosis. It is also thought to suppress p53-induced growth arrest. Multiple alternatively spliced transcript variants of this gene have been described, however, the full-length nature of many of them is not known. [provided by RefSeq, Jul 2008]

Genomic context

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Location :: 5q31

Sequence :: Chromosome: 5; NC_000005.9 (137620959..137667516, complement)

See CDC25C in Epigenomics, MapViewer

Chromosome 5 - NC_000005.9 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence

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Bibliography

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GeneRIFs: Gene References Into Functions What's a GeneRIF?

dose-dependent Cdc25c phosphatase acts as an early G2-phase checkpoint, thus indicating mechanistic importance in the low-dose hyper-radiosensitivity and induced radioresistance transition
Title: Cell division cycle 25 homolog c effects on low-dose hyper-radiosensitivity and induced radioresistance at elevated dosage in A549 cells.
Dysfunctional telomeres promote ATM/ATR-dependent degradation of CDC25C phosphatase to block mitotic entry, thereby preventing telomere dysfunction-driven genomic instability.
Title: ATM/ATR checkpoint activation downregulates CDC25C to prevent mitotic entry with uncapped telomeres.
data suggest that the maintenance of CDC25 activity does not fully rely on the thioredoxin reductase system in breast cancer cells, even in the presence of a major oxidative stress
Title: Protection of CDC25 phosphatases against oxidative stress in breast cancer cells: evaluation of the implication of the thioredoxin system.
cloning and functional analysis of Cdc25C
Title: [Prokaryotic expression and purification of human GST-Cdc25C fusion protein and preliminary detection of its function].
MMEQ induced G2/M arrest through the promotion of cdc25c in TSGH8301 cells.
Title: A novel synthetic 2-(3-methoxyphenyl)-6,7-methylenedioxoquinolin-4-one arrests the G2/M phase arrest via Cdc25c and induces apoptosis through caspase- and mitochondria-dependent pathways in TSGH8301 human bladder cancer cells.
Inhibition of CK2 activity by three different inhibitors led to a down-regulation of the level of cdc25C.
Title: Down-regulation of CK2 activity results in a decrease in the level of cdc25C phosphatase in different prostate cancer cell lines.
Cdc14B-dependent modulation of Cdc25 phosphatase and Cdk1/cyclin B activity is linked to correct chromosome segregation and bipolar spindle formation, processes that are required for proper progression through mitosis and maintenance of genomic stability.
Title: Human Cdc14B promotes progression through mitosis by dephosphorylating Cdc25 and regulating Cdk1/cyclin B activity.
Two additional sites other than Ser216 in the widely studied cell division cycle (Cdc) protein 25C, whose function depends on 14-3-3 binding, were identified.
Title: A robust protocol to map binding sites of the 14-3-3 interactome: Cdc25C requires phosphorylation of both S216 and S263 to bind 14-3-3.
The results show for the first time that in human mitosis, distinct phospho-isoforms of cdc25C exist with different localizations and interacting partners.
Title: Distinct pools of cdc25C are phosphorylated on specific TP sites and differentially localized in human mitotic cells.
ATM and Chk1/2 mediated phosphorylation of cdc25c plays a major role in cell cycle arrest induced by pectenotoxin2.
Title: Pectenotoxin-2 induces G2/M phase cell cycle arrest in human breast cancer cells via ATM and Chk1/2-mediated phosphorylation of cdc25C.

Submit: New GeneRIF Correction See all (53)

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

HIV-1 protein interactions

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Protein	Gene	Interaction	Pubs
Envelope surface glycoprotein gp120	env	HIV-1 gp120 decreases adult neural progenitor cell proliferation via the p38 MAPK-MAPKAPK2-Cdc25C signaling pathway	PubMed
Tat, p14	tat	The DNA repair gene DNA-PKcs and cell cycle-related genes Cdc20, Cdc25C, KIF2C and CTS1 are downregulated in HIV-1 Tat-expressing human rhabdomyosarcoma cells	PubMed
Vpr, p15	vpr	Kinase Srk1 is required for the Vpr-mediated nuclear export of Cdc25	PubMed
	vpr	HIV-1 Vpr induces subcellular relocalization of Cdc25 from nuclear to cytoplasm and Vpr-induced nuclear exclusion of Cdc25 depends on the serine/threonine phosphorylation of Cdc25 and the presence of Rad24/14-3-3 protein	PubMed
	vpr	Vpr-induced cell cycle G2/M arrest reveals a dramatic increase in the amount of Cdk1, Cdc25C, and CyclinB1 bound to 14-3-3 theta	PubMed
	vpr	HIV-1 Vpr forms a triple complex with 14-3-3 eta and Cdc25C and thereby promotes cell cycle arrest at the G(2)/M phase by facilitating association of 14-3-3 and Cdc25C	PubMed
	vpr	Binding of Cdc25c to HIV-1 Vpr is required for Vpr-mediated G2 arrest in HeLa cells	PubMed
	vpr	A minimal domain between amino acids 334 and 379 of Cdc25c, upstream of its catalytic site, is sufficient to bind HIV-1 Vpr; mutation at residue E352 of Cdc25c greatly reduces binding of Vpr to Cdc25c	PubMed
	vpr	Rupture of HIV-1 Vpr-induced nuclear envelope herniations produces transient loss of the subcellular compartmentalization of Wee1, Cdc25C, cyclin B1, and presumably other soluble cellular components, resulting in their release into the cytoplasm	PubMed
	vpr	The human Vpr interacting protein (hVIP/MOV34) is a likely cellular cofactor for HIV-1 Vpr inactivation of the cdc2-cyclin B kinase complex through Cdc25c and induction of cell cycle arrest	PubMed
	vpr	Inactivation of the cdc2-cyclin B kinase complex through Cdc25c and arrest in the G2 phase of the cell cycle has been mapped to the C-terminus of HIV-1 Vpr, including amino acids 73, 80 and 84-96	PubMed
	vpr	HIV-1 Vpr inactivates the cdc2-cyclin B kinase complex by inactivating cdc25C, the phosphatase that dephosphorylates and activates cdc2	PubMed

Go to the HIV-1, Human Protein Interaction Database

Interactions

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Products	Interactant	Other Gene	Source	Pubs	Description
AY497474.1	NP_612482.2	SP1	BIND	PubMed	Sp1 interacts with the cdc25c promoter.
AY497474.1	NP_000537.2	TP53	BIND	PubMed	p53 interacts with the cdc25c promoter.
P30307	Q8TDC3	BRSK1	HPRD	PubMed
P30307	Q8IWQ3	BRSK2	HPRD	PubMed
P30307	P20248	CCNA2	HPRD	PubMed
P30307	P14635	CCNB1	HPRD	PubMed
P30307	P06493	CDK1	HPRD	PubMed
P30307	O14757	CHEK1	HPRD	PubMed
P30307	O96017	CHEK2	HPRD	PubMed
P30307	P01112	HRAS	HPRD	PubMed
P30307	P06239	LCK	HPRD	PubMed
P30307	Q9Y250	LZTS1	HPRD	PubMed
P30307	Q16539	MAPK14	HPRD	PubMed
P30307	P27448	MARK3	HPRD	PubMed
P30307	P46934	NEDD4	HPRD	PubMed
P30307	P12004	PCNA	HPRD	PubMed
P30307	Q13526	PIN1	HPRD	PubMed
P30307	Q16512	PKN1	HPRD	PubMed
P30307	P53350	PLK1	HPRD	PubMed
P30307	Q9H4B4	PLK3	HPRD	PubMed
P30307	P04637	TP53	HPRD	PubMed
P30307	P31946	YWHAB	HPRD	PubMed
P30307	Q04917	YWHAH	HPRD	PubMed
P30307	P27348	YWHAQ	HPRD	PubMed
P30307	P63104	YWHAZ	HPRD	PubMed
BioGRID:107430	BioGRID:119591	ANAPC11	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:118937	ANAPC2	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:114491	BRSK2	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:107332	CCNB1	BioGRID	PubMed	Reconstituted Complex
BioGRID:107430	BioGRID:107434	CDH1	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:107420	CDK1	BioGRID	PubMed	Reconstituted Complex
BioGRID:107430	BioGRID:107452	CDK2	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:107471	CDS1	BioGRID	PubMed	Biochemical Activity
	NP_001265.1	CHEK1	BIND	PubMed	CHEK1 (Chk1) phosphorylates an unspecified isoform of CDC25C.
BioGRID:107430	BioGRID:107536	CHEK1	BioGRID	PubMed	Biochemical Activity; Reconstituted Complex
BioGRID:107430	BioGRID:116369	CHEK2	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:198624	Cdk1	BioGRID	PubMed	Affinity Capture-MS
BioGRID:107430	BioGRID:111580	MAPK1	BioGRID	PubMed	Affinity Capture-Western; Reconstituted Complex
BioGRID:107430	BioGRID:107819	MAPK14	BioGRID	PubMed	Biochemical Activity; Reconstituted Complex
BioGRID:107430	BioGRID:111581	MAPK3	BioGRID	PubMed	Affinity Capture-Western; Reconstituted Complex
BioGRID:107430	BioGRID:111587	MAPK9	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:110310	MARK3	BioGRID	PubMed	Affinity Capture-Western; Biochemical Activity; Reconstituted Complex
BioGRID:107430	BioGRID:110811	NEDD4	BioGRID	PubMed	Affinity Capture-Western; Protein-peptide
BioGRID:107430	BioGRID:111142	PCNA	BioGRID	PubMed	Affinity Capture-Western; Reconstituted Complex; Two-hybrid
BioGRID:107430	BioGRID:111317	PIN1	BioGRID	PubMed	Affinity Capture-Western; Far Western; Protein-peptide
	NP_005021.2	PLK1	BIND	PubMed	Plk1 phosphorylates an unspecified isoform of CDC25C. This interaction was modeled on a demonstrated phosphorylation of CDC25C from an unspecified species by human Plk1.
BioGRID:107430	BioGRID:111362	PLK1	BioGRID	PubMed	Affinity Capture-Western; Biochemical Activity
BioGRID:107430	BioGRID:107663	PLK3	BioGRID	PubMed	Affinity Capture-Western; Biochemical Activity; Reconstituted Complex
BioGRID:107430	BioGRID:112592	SRC	BioGRID	PubMed	Biochemical Activity
BioGRID:107430	BioGRID:113164	UBC	BioGRID	PubMed	Affinity Capture-MS; Affinity Capture-Western; Reconstituted Complex
BioGRID:107430	BioGRID:132019	USP17L2	BioGRID	PubMed	Affinity Capture-Western
BioGRID:107430	BioGRID:113361	YWHAB	BioGRID	PubMed	Affinity Capture-Western; Two-hybrid
BioGRID:107430	BioGRID:113363	YWHAE	BioGRID	PubMed	Affinity Capture-Western
BioGRID:107430	BioGRID:113365	YWHAH	BioGRID	PubMed	Affinity Capture-Western
BioGRID:107430	BioGRID:116168	YWHAQ	BioGRID	PubMed	Affinity Capture-Western
BioGRID:107430	BioGRID:113366	YWHAZ	BioGRID	PubMed	Affinity Capture-Western

Pathways from BioSystems

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Activation of ATR in response to replication stress, organism-specific biosystem (from REACTOME)
Activation of ATR in response to replication stress, organism-specific biosystemGenotoxic stress caused by DNA damage or stalled replication forks can lead to genomic instability. To guard against such instability, genotoxically-stressed cells activate checkpoint factors that ha...
Cell Cycle, organism-specific biosystem (from REACTOME)
Cell Cycle, organism-specific biosystem
Cell Cycle
Cell Cycle Checkpoints, organism-specific biosystem (from REACTOME)
Cell Cycle Checkpoints, organism-specific biosystemA hallmark of the human cell cycle in normal somatic cells is its precision. This remarkable fidelity is achieved by a number of signal transduction pathways, known as checkpoints, which monitor cell...
Cell Cycle, Mitotic, organism-specific biosystem (from REACTOME)
Cell Cycle, Mitotic, organism-specific biosystemThe replication of the genome and the subsequent segregation of chromosomes into daughter cells are controlled by a series of events collectively known as the cell cycle. DNA replication is carried o...
Cell cycle, organism-specific biosystem (from WikiPathways)
Cell cycle, organism-specific biosystemThe cell cycle is the series of events that takes place in a cell leading to its division and duplication (replication). Regulation of the cell cycle involves processes crucial to the survival of a c...
Cell cycle, organism-specific biosystem (from KEGG)
Cell cycle, organism-specific biosystemMitotic cell cycle progression is accomplished through a reproducible sequence of events, DNA replication (S phase) and mitosis (M phase) separated temporally by gaps known as G1 and G2 phases. Cycli...
Cell cycle, conserved biosystem (from KEGG)
Cell cycle, conserved biosystemMitotic cell cycle progression is accomplished through a reproducible sequence of events, DNA replication (S phase) and mitosis (M phase) separated temporally by gaps known as G1 and G2 phases. Cycli...
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex, organism-specific biosystem (from REACTOME)
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex, organism-specific biosystemDNA damage induced activation of the checkpoint kinases Chk1/Chk2(Cds1) results in the conversion and/or maintenance of CyclinB:Cdc2 complex in its Tyrosine 15 phosphorylated (inactive) state. Cdc2...
Cyclin A/B1 associated events during G2/M transition, organism-specific biosystem (from REACTOME)
Cyclin A/B1 associated events during G2/M transition, organism-specific biosystemCell cycle progression is regulated by cyclin-dependent protein kinases at both the G1/S and the G2/M transitions by cyclin-dependent protein kinases. The G2/M transition is regulated through the pho...
Cyclin B2 mediated events, organism-specific biosystem (from REACTOME)
Cyclin B2 mediated events, organism-specific biosystemThe two B-type cyclins localize to different regions within the cell and and are thought to have specific roles as CDK1-activating subunits (see Bellanger et al., 2007). Cyclin B1 is primarily cytop...
DNA damage response, organism-specific biosystem (from WikiPathways)
DNA damage response, organism-specific biosystemThis is the first pathway out of two pathways which deals with DNA damage response. It has two central gene products (ATM and ATR) which are connected to the sources of DNA damage (in blue). The two ...
G2/M Checkpoints, organism-specific biosystem (from REACTOME)
G2/M Checkpoints, organism-specific biosystemG2/M checkpoints include the checks for damaged DNA, unreplicated DNA, and checks that ensure that the genome is replicated once and only once per cell cycle. If cells pass these checkpoints, they f...
G2/M DNA damage checkpoint, organism-specific biosystem (from REACTOME)
G2/M DNA damage checkpoint, organism-specific biosystemThroughout the cell cycle, the genome is constantly monitored for damage, resulting either from errors of replication, by-products of metabolism or through extrinsic sources such as ultra-violet or i...
G2/M Transition, organism-specific biosystem (from REACTOME)
G2/M Transition, organism-specific biosystemCyclin A can also form complexes with Cdc2 (Cdk1). Together with three B-type cyclins, Cdc2 (Cdk1) regulates the transition from G2 into mitosis. These complexes are activated by dephosphorylation of...
Integrated Pancreatic Cancer Pathway, organism-specific biosystem (from WikiPathways)
Integrated Pancreatic Cancer Pathway, organism-specific biosystemAn integrated pathway model which displays the protein-protein interactions (PPIs) among the relevant proteins for pancreatic cancer. This pathway is a collection of different mechanistic protein pat...
Mitotic G2-G2/M phases, organism-specific biosystem (from REACTOME)
Mitotic G2-G2/M phases, organism-specific biosystem
Mitotic G2-G2/M phases
Monoamine Transport, organism-specific biosystem (from WikiPathways)
Monoamine Transport, organism-specific biosystem
Monoamine Transport
Oocyte meiosis, organism-specific biosystem (from KEGG)
Oocyte meiosis, organism-specific biosystemDuring meiosis, a single round of DNA replication is followed by two rounds of chromosome segregation, called meiosis I and meiosis II. At meiosis I, homologous chromosomes recombine and then segrega...
Oocyte meiosis, conserved biosystem (from KEGG)
Oocyte meiosis, conserved biosystemDuring meiosis, a single round of DNA replication is followed by two rounds of chromosome segregation, called meiosis I and meiosis II. At meiosis I, homologous chromosomes recombine and then segrega...
PLK1 signaling events, organism-specific biosystem (from Pathway Interaction Database)
PLK1 signaling events, organism-specific biosystem
PLK1 signaling events
PLK3 signaling events, organism-specific biosystem (from Pathway Interaction Database)
PLK3 signaling events, organism-specific biosystem
PLK3 signaling events
Polo-like kinase mediated events, organism-specific biosystem (from REACTOME)
Polo-like kinase mediated events, organism-specific biosystemAt mitotic entry, Plk1 phosphorylates and activates Cdc25C phosphatase, whereas it phosphorylates and down-regulates Wee1A. Plk1 also phosphorylates and inhibits Myt1 activity. Cyclin B1-bound Cdc2...
Progesterone-mediated oocyte maturation, organism-specific biosystem (from KEGG)
Progesterone-mediated oocyte maturation, organism-specific biosystemXenopus oocytes are naturally arrested at G2 of meiosis I. Exposure to either insulin/IGF-1 or the steroid hormone progesterone breaks this arrest and induces resumption of the two meiotic division c...
Progesterone-mediated oocyte maturation, conserved biosystem (from KEGG)
Progesterone-mediated oocyte maturation, conserved biosystemXenopus oocytes are naturally arrested at G2 of meiosis I. Exposure to either insulin/IGF-1 or the steroid hormone progesterone breaks this arrest and induces resumption of the two meiotic division c...
Wnt Signaling Pathway NetPath, organism-specific biosystem (from WikiPathways)
Wnt Signaling Pathway NetPath, organism-specific biosystemWnt family of proteins are a large family of cysteine-rich secreted glycoproteins that regulate cell-cell interactions. They bind to members of the Frizzled family of 7 transmembrane receptors. Bindi...

General gene information

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Markers

STS-T96364 (e-PCR)
- UniSTS:3197

RH69126 (e-PCR)
- UniSTS:47532

Homology

Homologs of the CDC25C gene: The CDC25C gene is conserved in chimpanzee, Rhesus monkey, dog, cow, mouse, and rat.
Map Viewer (Mouse, Rat)
OrthoDB: The Hierarchical Catalog of Eukaryotic Orthologs

Gene Ontology Provided by GOA

Function	Evidence Code	Pubs
WW domain binding	IPI Inferred from Physical Interaction more info	PubMed
protein binding	IPI Inferred from Physical Interaction more info	PubMed
protein kinase binding	IPI Inferred from Physical Interaction more info	PubMed
protein tyrosine phosphatase activity	NAS Non-traceable Author Statement more info	PubMed

Process	Evidence Code	Pubs
DNA replication	TAS Traceable Author Statement more info
G2/M transition of mitotic cell cycle	IGI Inferred from Genetic Interaction more info	PubMed
G2/M transition of mitotic cell cycle	TAS Traceable Author Statement more info
M phase of mitotic cell cycle	IEA Inferred from Electronic Annotation more info
cell cycle checkpoint	TAS Traceable Author Statement more info
cell division	IEA Inferred from Electronic Annotation more info
cell proliferation	TAS Traceable Author Statement more info	PubMed
mitosis	IEA Inferred from Electronic Annotation more info
mitotic cell cycle	TAS Traceable Author Statement more info
peptidyl-tyrosine dephosphorylation	NAS Non-traceable Author Statement more info	PubMed
regulation of cell cycle	TAS Traceable Author Statement more info
regulation of cyclin-dependent protein serine/threonine kinase activity	TAS Traceable Author Statement more info	PubMed
regulation of mitosis	TAS Traceable Author Statement more info	PubMed
virus-host interaction	IEA Inferred from Electronic Annotation more info

Component	Evidence Code	Pubs
cytosol	TAS Traceable Author Statement more info
nucleoplasm	TAS Traceable Author Statement more info
nucleus	IDA Inferred from Direct Assay more info	PubMed

General protein information

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Preferred Names: M-phase inducer phosphatase 3

Names: M-phase inducer phosphatase 3; mitosis inducer CDC25; phosphotyrosine phosphatase; dual specificity phosphatase CDC25C; protein phosphatase 1, regulatory subunit 60

NP_001781.2

EC 3.1.3.48

NP_073720.1

EC 3.1.3.48

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

NM_001790.3 → NP_001781.2 M-phase inducer phosphatase 3 isoform a

Status: REVIEWED

Description

Transcript Variant: This variant (1) encodes the longer isoform (a).

Source sequence(s)

AC104116, DB040755, M34065

Consensus CDS

CCDS4202.1

UniProtKB/Swiss-Prot

P30307

Related

ENSP00000321656, OTTHUMP00000159489, ENST00000323760, OTTHUMT00000251280

Conserved Domains (2) summary

cd01530
Location:302 – 421
Blast Score: 453

Cdc25; Cdc25 phosphatases are members of the Rhodanese Homology Domain superfamily. They activate the cell division kinases throughout the cell cycle progression. Cdc25 phosphatases dephosphorylate phosphotyrosine and phosphothreonine residues, in order to ...

pfam06617
Location:93 – 272
Blast Score: 439

M-inducer_phosp; M-phase inducer phosphatase
NM_022809.2 → NP_073720.1 M-phase inducer phosphatase 3 isoform b

Status: REVIEWED

Description

Transcript Variant: This variant (2) lacks two regions in the coding region as compared to variant 1, and encodes an isoform (b) which is 73 aa shorter than isoform a.

Source sequence(s)

AC104116, AJ304504, AU098899

Consensus CDS

CCDS4203.1

UniProtKB/Swiss-Prot

P30307

Related

ENSP00000345205, ENST00000348983

Conserved Domains (2) summary

cd01530
Location:229 – 348
Blast Score: 446

Cdc25; Cdc25 phosphatases are members of the Rhodanese Homology Domain superfamily. They activate the cell division kinases throughout the cell cycle progression. Cdc25 phosphatases dephosphorylate phosphotyrosine and phosphothreonine residues, in order to ...

pfam06617
Location:78 – 199
Blast Score: 315

M-inducer_phosp; M-phase inducer phosphatase

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 104

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh37.p10 Primary Assembly

Genomic

NC_000005.9 Reference GRCh37.p10 Primary Assembly

Range

137620959..137667516, complement

Download

GenBank, FASTA, Sequence Viewer (Graphics)

Alternate HuRef

Genomic

AC_000137.1 Alternate HuRef

Range

132811846..132858438, complement

Download

GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.0

Genomic

NC_018916.1 Alternate CHM1_1.0

Range

137897118..137943759, complement

Download

GenBank, FASTA, Sequence Viewer (Graphics)

Nucleotide		Protein
Heading	Accession and Version	Protein
genomic	ABBA01068681.1 (20855..26271)	None
genomic	ABBA01068682.1	None
genomic	ABBA01068683.1	None
genomic	ABBA01068684.1	None
genomic	ABBA01068685.1	None
genomic	ABBA01068686.1	None
genomic	ABBA01068687.1	None
genomic	AC104116.3 (13600..60158)	None
genomic	AMYH01015641.1 (164957..202161)	None
genomic	AMYH01015642.1	None
genomic	AY497474.1	AAR32098.1
genomic	CH471062.2	EAW62145.1
		EAW62146.1
		EAW62147.1
		EAW62148.1
		EAW62149.1
		EAW62150.1
genomic	Z29077.1	None
mRNA	AF086323.1	None
mRNA	AF277723.1	AAG41885.1
mRNA	AF277724.1	AAG41886.1
mRNA	AF277725.1	AAG41887.1
mRNA	AF277726.1	AAG41888.1
mRNA	AF312681.1	AAL26835.1
mRNA	AJ304504.1	CAC19192.1
mRNA	AK097710.1	None
mRNA	AK301828.1	BAG63273.1
mRNA	AU098899.1	None
mRNA	BC019089.2	AAH19089.1
mRNA	DB040755.1	None
mRNA	M34065.1	AAA35666.1
other-genetic	EU832624.1	ACE87715.1
other-genetic	EU832697.1	ACE87029.1