Human Gene CHGA (ENST00000216492.10_7) from GENCODE V47lift37
Description: chromogranin A, transcript variant 1 (from RefSeq NM_001275.4)
Gencode Transcript: ENST00000216492.10_7
Gencode Gene: ENSG00000100604.13_9
Transcript (Including UTRs)
Position: hg19 chr14:93,389,495-93,401,630 Size: 12,136 Total Exon Count: 8 Strand: +
Coding Region
Position: hg19 chr14:93,389,705-93,401,229 Size: 11,525 Coding Exon Count: 8
Data last updated at UCSC: 2024-08-22 23:36:26
Sequence and Links to Tools and Databases
Comments and Description Text from UniProtKB
ID: CMGA_HUMAN
DESCRIPTION: RecName: Full=Chromogranin-A; Short=CgA; AltName: Full=Pituitary secretory protein I; Short=SP-I; Contains: RecName: Full=Vasostatin-1; AltName: Full=Vasostatin I; Contains: RecName: Full=Vasostatin-2; AltName: Full=Vasostatin II; Contains: RecName: Full=EA-92; Contains: RecName: Full=ES-43; Contains: RecName: Full=Pancreastatin; Contains: RecName: Full=SS-18; Contains: RecName: Full=WA-8; Contains: RecName: Full=WE-14; Contains: RecName: Full=LF-19; Contains: RecName: Full=AL-11; Contains: RecName: Full=GV-19; Contains: RecName: Full=GR-44; Contains: RecName: Full=ER-37; Flags: Precursor;
FUNCTION: Pancreastatin strongly inhibits glucose induced insulin release from the pancreas.SUBUNIT: Interacts with SCG3 (By similarity).SUBCELLULAR LOCATION: Cytoplasmic vesicle, secretory vesicle lumen (By similarity). Cytoplasmic vesicle, secretory vesicle membrane (By similarity). Secreted. Note=Associated with the secretory granule membrane through direct interaction to SCG3 that in turn binds to cholesterol-enriched lipid rafts in intragranular conditions (By similarity).PTM: Sulfated on tyrosine residues and/or contains sulfated glycans.PTM: O-glycosylated with core 1 or possibly core 8 glycans.MISCELLANEOUS: Binds calcium with a low-affinity.SIMILARITY: Belongs to the chromogranin/secretogranin protein family.
Primer design for this transcript
MalaCards Disease Associations
MalaCards Gene Search: CHGA
Diseases sorted by gene-association score: neuroendocrine tumor (58), atrophic gastritis (32), acinar cell carcinoma (31), tubular adenocarcinoma (30), mixed ductal-endocrine carcinoma (24), lymphocytic colitis (22), somatostatinoma (21), glucagonoma (19), islet cell tumor (19), large cell carcinoma (18), large cell neuroendocrine carcinoma (18), vipoma (18), autoimmune atrophic gastritis (18), small cell carcinoma of the bladder (18), primary hepatic neuroendocrine carcinoma (18), carcinoid syndrome (18), small cell neuroendocrine carcinoma (17), gastrinoma (17), gastric small cell carcinoma (16), clear cell meningioma (16), liver leiomyosarcoma (15), auditory system cancer (15), merkel cell carcinoma (15), epithelioid malignant peripheral nerve sheath tumor (15), endocrine gland cancer (15), ureter small cell carcinoma (15), zollinger-ellison syndrome (15), female urethral cancer (15), urinary bladder small cell neuroendocrine carcinoma (15), ovarian large-cell neuroendocrine carcinoma (15), atypical follicular adenoma (14), paraganglioma (14), adrenal cortical carcinoma (13), small cell carcinoma (13), pulmonary large cell neuroendocrine carcinoma (13), goblet cell carcinoid (13), chordoid meningioma (13), ganglioglioma (12), pituitary carcinoma (12), sclerosing hemangioma (12), prostate adenocarcinoma (12), pulmonary sclerosing hemangioma (12), small cell cancer of the lung, somatic (12), pancreatoblastoma (11), gastritis (11), dermoid cyst (11), non-functioning pancreatic endocrine tumor (11), carcinoid tumors, intestinal (11), adult teratoma (10), pancreatic serous cystadenoma (10), gastric tubular adenocarcinoma (10), acinar cell cystadenocarcinoma (10), olfactory neuroblastoma (10), intracranial primitive neuroectodermal tumor (10), parathyroid adenoma (10), gastrointestinal neuroendocrine benign tumor (10), gastric neuroendocrine neoplasm (10), chronic myocardial ischemia (10), gallbladder small cell carcinoma (10), phaeochromocytoma (10), gastric adenocarcinoma (10), collagenous colitis (10), ureter cancer (9), binswanger's disease (9), central neurocytoma (9), subependymoma (9), medullary thyroid carcinoma, familial (9), gastrointestinal neuroendocrine tumor (8), diarrhea 4, malabsorptive, congenital (8), cellular ependymoma (8), peritoneal serous adenocarcinoma (8), sclerosing hepatic carcinoma (8), multiple endocrine neoplasia (8), ganglioneuroma (8), pulmonary blastoma (8), pheochromocytoma (8), serotonin syndrome (8), pleomorphic xanthoastrocytoma (7), cervix small cell carcinoma (7), basaloid squamous cell carcinoma (7), von hippel-lindau syndrome (7), insulinoma (7), multiple endocrine neoplasia 1 (7), cranial nerve malignant neoplasm (7), primary pigmented nodular adrenocortical disease (7), lung cancer (7), lung benign neoplasm (7), nodular ganglioneuroblastoma (7), chief cell adenoma (7), pick disease (7), hemangioma of lung (7), cystadenoma (7), signet ring cell adenocarcinoma (7), vaginal benign neoplasm (7), vaginal adenoma (7), vaginal tubulovillous adenoma (7), pancreatic acinar cell adenocarcinoma (7), irritable bowel syndrome (6), olfactory groove meningioma (6), anterior cranial fossa meningioma (6), pancreatic cystadenocarcinoma (6), hyperparathyroidism (6), endodermal sinus tumor (6), pineocytoma (6), cauda equina neoplasm (6), syndrome of inappropriate antidiuretic hormone (6), glycogen storage disease vi (6), sensory organ benign neoplasm (6), urethral benign neoplasm (6), acute thyroiditis (6), conventional angiosarcoma (6), liver sarcoma (6), horseshoe kidney (6), respiratory system benign neoplasm (5), olfactory nerve neoplasm (5), granulosa cell tumor of the ovary (5), gastric leiomyoma (5), hyperparathyroidism, familial primary (5), cecal disease (5), gastric squamous cell carcinoma (5), breast papillary carcinoma (5), pancreatic gastrinoma (5), prostate cancer (5), auditory neuropathy (5), diffuse pulmonary fibrosis (5), cecum adenocarcinoma (5), spinal canal and spinal cord meningioma (5), desmoplastic small round cell tumor (5), spinal meningioma (4), papillary ependymoma (4), tanycytic ependymoma (4), malignant skin fibrous histiocytoma (4), malignant dermis tumor (4), cowden disease (4), cerebellar liponeurocytoma (4), meninges hemangiopericytoma (3), pancreatic cancer (3), ewing sarcoma (2), male reproductive organ cancer (1), cell type benign neoplasm (1), cell type cancer (1), thyroid cancer, nonmedullary, 2 (1)
Comparative Toxicogenomics Database (CTD)
Common Gene Haplotype Alleles
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RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
Microarray Expression Data
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mRNA Secondary Structure of 3' and 5' UTRs
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.
Protein Domain and Structure Information
InterPro Domains: Graphical view of domain structure IPR001819 - Chromogranin_AB
IPR018054 - Chromogranin_CS
IPR001990 - Granin
Pfam Domains: PF01271 - Granin (chromogranin or secretogranin)
Protein Data Bank (PDB) 3-D Structure
ModBase Predicted Comparative 3D Structure on P10645
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.
Orthologous Genes in Other Species
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.
Gene Ontology (GO) Annotations with Structured Vocabulary
Descriptions from all associated GenBank mRNAs
LF209629 - JP 2014500723-A/17132: Polycomb-Associated Non-Coding RNAs.AK313757 - Homo sapiens cDNA, FLJ94358, highly similar to Homo sapiens chromogranin A (parathyroid secretory protein 1) (CHGA), mRNA.AK223381 - Homo sapiens mRNA for chromogranin A variant, clone: FCC106D09.JD255080 - Sequence 236104 from Patent EP1572962.BC006459 - Homo sapiens chromogranin A (parathyroid secretory protein 1), mRNA (cDNA clone MGC:1781 IMAGE:3503641), complete cds.BX248263 - human full-length cDNA clone CS0DN001YP04 of Adult brain of Homo sapiens (human).JD462887 - Sequence 443911 from Patent EP1572962.JD128440 - Sequence 109464 from Patent EP1572962.J03483 - Human chromogranin A mRNA, complete cds.JD455698 - Sequence 436722 from Patent EP1572962.BC001059 - Homo sapiens chromogranin A (parathyroid secretory protein 1), mRNA (cDNA clone MGC:2080 IMAGE:3509603), complete cds.J03915 - Human chromogranin A mRNA, complete cds.DQ891820 - Synthetic construct clone IMAGE:100004450; FLH180269.01X; RZPDo839A05134D chromogranin A (parathyroid secretory protein 1) (CHGA) gene, encodes complete protein.DQ895007 - Synthetic construct Homo sapiens clone IMAGE:100009467; FLH180265.01L; RZPDo839A05133D chromogranin A (parathyroid secretory protein 1) (CHGA) gene, encodes complete protein.CU674536 - Synthetic construct Homo sapiens gateway clone IMAGE:100023443 5' read CHGA mRNA.KJ896596 - Synthetic construct Homo sapiens clone ccsbBroadEn_05990 CHGA gene, encodes complete protein.KR709826 - Synthetic construct Homo sapiens clone CCSBHm_00006427 CHGA (CHGA) mRNA, encodes complete protein.KR709827 - Synthetic construct Homo sapiens clone CCSBHm_00006428 CHGA (CHGA) mRNA, encodes complete protein.BT006869 - Homo sapiens chromogranin A (parathyroid secretory protein 1) mRNA, complete cds.BC009384 - Homo sapiens chromogranin A (parathyroid secretory protein 1), mRNA (cDNA clone IMAGE:4127895), partial cds.BC012755 - Homo sapiens chromogranin A (parathyroid secretory protein 1), mRNA (cDNA clone IMAGE:3627785), partial cds.LF330250 - JP 2014500723-A/137753: Polycomb-Associated Non-Coding RNAs.BC106953 - Homo sapiens cDNA clone IMAGE:40035584, **** WARNING: chimeric clone ****.LF330251 - JP 2014500723-A/137754: Polycomb-Associated Non-Coding RNAs.JD343547 - Sequence 324571 from Patent EP1572962.JD162677 - Sequence 143701 from Patent EP1572962.JD401327 - Sequence 382351 from Patent EP1572962.JD242085 - Sequence 223109 from Patent EP1572962.JD039580 - Sequence 20604 from Patent EP1572962.JD402435 - Sequence 383459 from Patent EP1572962.JD534063 - Sequence 515087 from Patent EP1572962.JD199210 - Sequence 180234 from Patent EP1572962.MA565827 - JP 2018138019-A/137753: Polycomb-Associated Non-Coding RNAs.MA565828 - JP 2018138019-A/137754: Polycomb-Associated Non-Coding RNAs.MA445206 - JP 2018138019-A/17132: Polycomb-Associated Non-Coding RNAs.
Biochemical and Signaling Pathways
Other Names for This Gene
Alternate Gene Symbols: B2R9E9, CMGA_HUMAN, ENST00000216492.1, ENST00000216492.2, ENST00000216492.3, ENST00000216492.4, ENST00000216492.5, ENST00000216492.6, ENST00000216492.7, ENST00000216492.8, ENST00000216492.9, NM_001275, P10645, Q53FA8, Q6NR84, Q96E84, Q96GL7, Q9BQB5, uc317crh.1, uc317crh.2UCSC ID: ENST00000216492.10_7RefSeq Accession: NM_001275.4
Protein: P10645
(aka CMGA_HUMAN)
Gene Model Information
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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.