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ABCC9 information


ABCC9
Identifiers
AliasesABCC9, ABC37, ATFB12, CANTU, CMD1O, SUR2, ATP binding cassette subfamily C member 9, IDMYS
External IDsOMIM: 601439; MGI: 1352630; HomoloGene: 56521; GeneCards: ABCC9; OMA:ABCC9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005691
NM_020297
NM_020298
NM_001377273
NM_001377274

RefSeq (protein)

NP_005682
NP_064693
NP_001364202
NP_001364203

NP_001038185
NP_001297072
NP_035641
NP_066378
NP_066379

Location (UCSC)Chr 12: 21.8 – 21.94 MbChr 6: 142.53 – 142.65 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

ATP-binding cassette, sub-family C member 9 (ABCC9) also known as sulfonylurea receptor 2 (SUR2) is an ATP-binding cassette transporter that in humans is encoded by the ABCC9 gene.[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000069431 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030249 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Aguilar-Bryan L, Clement JP, Gonzalez G, Kunjilwar K, Babenko A, Bryan J (January 1998). "Toward understanding the assembly and structure of KATP channels". Physiological Reviews. 78 (1): 227–245. doi:10.1152/physrev.1998.78.1.227. PMID 9457174. S2CID 11851627.
  6. ^ Bienengraeber M, Olson TM, Selivanov VA, Kathmann EC, O'Cochlain F, Gao F, et al. (April 2004). "ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating". Nature Genetics. 36 (4): 382–387. doi:10.1038/ng1329. PMC 1995438. PMID 15034580.

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ABCC9

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member 9 (ABCC9) also known as sulfonylurea receptor 2 (SUR2) is an ATP-binding cassette transporter that in humans is encoded by the ABCC9 gene. The...

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Dilated cardiomyopathy

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SGCD 5q33 CMD1M 607482 CSRP3 11p15.1 CMD1N 607487 TCAP 17q12 CMD1O 608569 ABCC9 12p12.1 CMD1P 609909 PLN 6q22.1 CMD1Q 609915 7q22.3-q31.1 CMD1R ACTC 15q14...

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Sulfonylurea receptor

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gene, and SUR2A and SUR2B, which are splice variants arising from a single ABCC9 gene. The primary function of the sulfonylurea receptor is to sense intracellular...

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List of distinct cell types in the adult human body

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cell Epididymal basal cell Endothelial cells Circulatory system, capillary ABCC9, KCNJ8, RGS5 Planum semilunar epithelial cell of vestibular system of ear...

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Brugada syndrome

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sarcoplasmic reticulum – influences trafficking of NaV1.5. BrS13 601439 ABCC9 SUR2A, the adenosine triphosphate (ATP)-binding cassette transporter of...

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Sleep

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clock has its own set of genes. Genes which may influence sleep include ABCC9, DEC2, Dopamine receptor D2 and variants near PAX 8 and VRK2. While the...

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Benign early repolarization

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with ER and ATP sensitive potassium current channel mutations are KCNJ8, ABCC9 Others associated with transient outward potassium current - KCNE5, DPP10...

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Atrial fibrillation

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the genes of K+ channels, including mutations in KCNE1-5, KCNH2, KCNJ5 or ABCC9 among others. Six variations in genes of Na+ channels that include SCN1-4B...

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ABCC8

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Düfer M, Drews G, Krippeit-Drews P, et al. (February 2007). "ABCC8 and ABCC9: ABC transporters that regulate K+ channels". Pflügers Archiv. 453 (5):...

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Transmembrane domain of ABC transporters

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ABCC10; ABCC11; ABCC12; ABCC13; ABCC2; ABCC3; ABCC4; ABCC5; ABCC6; ABCC8; ABCC9; CFTR; TAP1; TAP2; TAPL; Kerr ID (2002). "Structure and association of ATP-binding...

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List of OMIM disorder codes

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Cardiomyopathy, dilated, 1N; 607487; TCAP Cardiomyopathy, dilated, 1O; 608569; ABCC9 Cardiomyopathy, dilated, 1P; 609909; PLN Cardiomyopathy, dilated, 1R; 613424;...

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