Human Gene CRH (ENST00000276571.5_7) from GENCODE V47lift37
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Sequence and Links to Tools and Databases
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Comments and Description Text from UniProtKB
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ID: CRF_HUMAN
DESCRIPTION: RecName: Full=Corticoliberin; AltName: Full=Corticotropin-releasing factor; Short=CRF; AltName: Full=Corticotropin-releasing hormone; Flags: Precursor;
FUNCTION: This hormone from hypothalamus regulates the release of corticotropin from pituitary gland. SUBUNIT: Interacts (via C-terminus) with CRFR1 (via N-terminal extracellular domain). INTERACTION: P34998:CRHR1; NbExp=2; IntAct=EBI-3870390, EBI-3870393; SUBCELLULAR LOCATION: Secreted. SIMILARITY: Belongs to the sauvagine/corticotropin-releasing factor/urotensin I family. WEB RESOURCE: Name=Wikipedia; Note=Corticotropin-releasing hormone entry; URL="http://en.wikipedia.org/wiki/Corticotropin-releasing_hormone";
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Primer design for this transcript
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MalaCards Disease Associations
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MalaCards Gene Search: CRH
Diseases sorted by gene-association score: crh-related related nocturnal frontal lobe epilepsy, autosomal dominant* (100), autosomal dominant nocturnal frontal lobe epilepsy* (74), post-traumatic stress disorder (33), postpartum depression (28), adrenal carcinoma (28), acth deficiency (26), cushing's syndrome (25), melancholia (23), hypothalamic disease (23), adrenal gland hyperfunction (21), endogenous depression (20), chronic fatigue syndrome (16), hypoadrenalism (16), mood disorder (15), adrenal cortex disease (14), adrenal gland disease (14), panic disorder (12), nelson syndrome (11), anorexia nervosa (11), atypical depressive disorder (11), pituitary adenoma, acth-secreting (11), irritable bowel syndrome (11), pituitary carcinoma (10), adrenal adenoma (10), pituitary-dependent cushing's disease (10), hypoglycemia (10), addison's disease (10), pituitary adenoma (9), sheehan syndrome (8), major depressive disorder and accelerated response to antidepressant drug treatment (8), adrenal cortical hypofunction (8), hypopituitarism (8), gonadal disease (8), olivopontocerebellar atrophy (8), burns (7), fasting hypoglycemia (7), persistent fetal circulation syndrome (7), pituitary gland disease (7), diabetes insipidus (7), drug dependence (7), anxiety disorder (6), allergic urticaria (6), amenorrhea (6), gangliocytoma (6), mental depression (5), ectopic cushing syndrome (5), benign familial neonatal epilepsy (5), endocrine organ benign neoplasm (5), withdrawal disorder (4), premenstrual tension (4), binswanger's disease (4), epilepsy, nocturnal frontal lobe, 1 (4), pulmonary immaturity (4), avoidant personality disorder (4), west syndrome (4), metaphyseal chondrodysplasia, murk jansen type (4), alzheimer disease (3), pheochromocytoma (2), gastrointestinal system disease (2), obesity (1), disease of mental health (1), organ system benign neoplasm (1), urinary system disease (1) * = Manually curated disease association
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Comparative Toxicogenomics Database (CTD)
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Common Gene Haplotype Alleles
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RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
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Microarray Expression Data
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mRNA Secondary Structure of 3' and 5' UTRs
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The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
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Protein Domain and Structure Information
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InterPro Domains: Graphical view of domain structure IPR018446 - Corticotropin-releasing_fac_CS
IPR000187 - Corticotropin-releasing_factor
IPR003620 - Urocortin_CRF
Pfam Domains: PF00473 - Corticotropin-releasing factor family
Protein Data Bank (PDB) 3-D Structure
ModBase Predicted Comparative 3D Structure on P06850
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.
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Orthologous Genes in Other Species
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Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
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Gene Ontology (GO) Annotations with Structured Vocabulary
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Descriptions from all associated GenBank mRNAs
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KJ896643 - Synthetic construct Homo sapiens clone ccsbBroadEn_06037 CRH gene, encodes complete protein. AK075431 - Homo sapiens cDNA PSEC0122 fis, clone PLACE1003337, highly similar to CORTICOLIBERIN PRECURSOR. LF206082 - JP 2014500723-A/13585: Polycomb-Associated Non-Coding RNAs. JD377206 - Sequence 358230 from Patent EP1572962. BC011031 - Homo sapiens corticotropin releasing hormone, mRNA (cDNA clone MGC:13636 IMAGE:4280754), complete cds. JD219200 - Sequence 200224 from Patent EP1572962. JD038032 - Sequence 19056 from Patent EP1572962. LF351191 - JP 2014500723-A/158694: Polycomb-Associated Non-Coding RNAs. JD445453 - Sequence 426477 from Patent EP1572962. JD434315 - Sequence 415339 from Patent EP1572962. JD491368 - Sequence 472392 from Patent EP1572962. BC002599 - Homo sapiens corticotropin releasing hormone, mRNA (cDNA clone MGC:1770 IMAGE:3160933), complete cds. JD409994 - Sequence 391018 from Patent EP1572962. BT007453 - Homo sapiens corticotropin releasing hormone mRNA, complete cds. AB590736 - Synthetic construct DNA, clone: pFN21AE1683, Homo sapiens CRH gene for corticotropin releasing hormone, without stop codon, in Flexi system. KU177994 - Homo sapiens corticotropin releasing hormone isoform 1 (CRH) mRNA, partial cds. KU177995 - Homo sapiens corticotropin releasing hormone isoform 2 (CRH) mRNA, complete cds, alternatively spliced. JD318651 - Sequence 299675 from Patent EP1572962. LF351192 - JP 2014500723-A/158695: Polycomb-Associated Non-Coding RNAs. JD339575 - Sequence 320599 from Patent EP1572962. JD214238 - Sequence 195262 from Patent EP1572962. JD330197 - Sequence 311221 from Patent EP1572962. MA586768 - JP 2018138019-A/158694: Polycomb-Associated Non-Coding RNAs. MA586769 - JP 2018138019-A/158695: Polycomb-Associated Non-Coding RNAs. MA441659 - JP 2018138019-A/13585: Polycomb-Associated Non-Coding RNAs.
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Biochemical and Signaling Pathways
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Other Names for This Gene
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Alternate Gene Symbols: B3KQS4, CRF_HUMAN, ENST00000276571.1, ENST00000276571.2, ENST00000276571.3, ENST00000276571.4, NM_000756, P06850, uc317jku.1, uc317jku.2 UCSC ID: ENST00000276571.5_7 RefSeq Accession: NM_000756.4
Protein: P06850
(aka CRF_HUMAN)
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GeneReviews for This Gene
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GeneReviews article(s) related to gene CRH: adnfle (Autosomal Dominant Sleep-Related Hypermotor (Hyperkinetic) Epilepsy)
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Gene Model Information
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for a detailed description of the fields of the table above.
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Methods, Credits, and Use Restrictions
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for details on how this gene model was made and data restrictions if any.
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