HMX3 - H6 family homeobox 3-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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340784 HMX3

基因描述

Type	Description
Definition	H6 family homeobox 3

研究结论

Date	Results	Publications
2020-12-12 13:29:00	Aberrant expression of NKL homeobox genes HMX2 and HMX3 interferes with cell differentiation in acute myeloid leukemia.	33048949
2013-03-23 10:34:00	One sequence alteration, heterozygous c.114C->T (conservative change without alteration of amino acid) in exon 1 of HMX3, was detected in 2 of 15 patients with superior semicircular dehiscence syndrome.	22779713
2010-01-21 00:00:00	propose that hemizygous deletions of HMX2 and HMX3 are responsible for inner ear malformations, vestibular dysfunction, and congenital sensorineural hearing loss	19253379

名称对应

Type	IDs
Synonymous	NKX-5.1, NKX5.1, Nkx5-1
Gene	UniProtKB-ID: HMX3_HUMAN UniprotKB: A6NHT5 UniParc: UPI000047C635 EMBL: CH471066, AC012391 Ensembl: ENSG00000188620 KO: hsa:340784
Nucleutide sequences	EMBL-CDS: EAW49289.1 Ensembl_TRS: ENST00000357878
Protein sequencees	Ensembl_PRO: ENSP00000350549 RefSeq: NP_001099044.1
Others	UniRef100: UniRef100_A6NHT5 UniRef90: UniRef90_A6NHT5 UniRef50: UniRef50_P42581 UniGene: Hs.531194 CCDS: CCDS41575.1

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mRNA

Protein

UniprotKB

Description

Refseq

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Pubmed编号	文献信息	发表日期	相关基因
33048949	Aberrant expression of NKL homeobox genes HMX2 and HMX3 interferes with cell differentiation in acute myeloid leukemia. PLoS One Stefan Nagel , Claudia Pommerenke , Corinna Meyer , Roderick A F MacLeod , Hans G Drexler	2020-01-01	-
31091453	PLEKHA4/kramer Attenuates Dishevelled Ubiquitination to Modulate Wnt and Planar Cell Polarity Signaling. Cell Rep Adnan Shami Shah , Alex G Batrouni , Dongsung Kim , Amith Punyala , Wendy Cao , Chun Han , Michael L Goldberg , Marcus B Smolka , Jeremy M Baskin	2019-05-14	-
29478914	Genome-wide CRISPR-Cas9 Screen Identifies Leukemia-Specific Dependence on a Pre-mRNA Metabolic Pathway Regulated by DCPS. Cancer Cell Takuji Yamauchi , Takeshi Masuda , Matthew C Canver , Michael Seiler , Yuichiro Semba , Mohammad Shboul , Mohammed Al-Raqad , Manami Maeda , Vivien A C Schoonenberg , Mitchel A Cole , Claudio Macias-Trevino , Yuichi Ishikawa , Qiuming Yao , Michitaka Nakano , Fumio Arai , Stuart H Orkin , Bruno Reversade , Silvia Buonamici , Luca Pinello , Koichi Akashi , Daniel E Bauer , Takahiro Maeda	2018-03-12	-
24024966	Genome-wide association study of chronic periodontitis in a general German population. J. Clin. Periodontol. Alexander Teumer , Birte Holtfreter , Uwe VÃ¶lker , Astrid Petersmann , Matthias Nauck , Reiner Biffar , Henry VÃ¶lzke , Heyo K Kroemer , Peter Meisel , Georg Homuth , Thomas Kocher	2013-11-01	PDCD6IP, ST20-MTHFS, CDH13, LOC101927025, LOC101927661, LOC101928114, LOC101928134, LOC102724761, MTHFS, CHD1, PTPRT, GPN1, C1orf87, WDR36, NRSN1, PSMA8, ZNF524, CCDC13, NKAIN2, FAM47A, ZNF579, PARP15, DEFA1, C10orf91, ADAMTS15, ABCA1, EPHA3, ETS2, NLGN1, DKK1, KDM4B, NPAP1, FRG1, ERC2, DAOA, LINC00907, SUMF1, NKAIN3, GRIK1, LRP12, HLA-DOA, FOXA1, BIRC5, C12orf74, HMX3, IGF2R, IGL, KCNJ16, FAM180A, LBP, ST20, LOC400867, NPM1P2, FAM135B, PIK3C3, LRP1B, ETAA1, RBFOX1, PGPEP1, ETNK2, NMUR2, RGMA, ERGIC1, PTEN, SEMA6A, RIT2, ROBO2, RYR3, BCORL1, SCN2A, BLK, SETMAR, CSMD1, MFSD1, SMURF2, PRB2, SNRPN, SNTB1, SS18, TGIF1, TIMP2, ROCK1P1, VPREB1, ZNF385D, THSD4, CAMK4, LINC00208, RAB6C, FAM126A, FIZ1, WDR73, ITGA8, ACTN1, ACTN2, MBD2, HS6ST2, IQSEC1
22779713	Mutation analysis of Netrin 1 and HMX3 genes in patients with superior semicircular canal dehiscence syndrome. Acta Otolaryngol. Nikola Roknic , Alexander Huber , Stefan C A Hegemann , Rudolf HÃ¤usler , Nicolas GÃ¼rtler	2012-10-01	HMX3, NTN1
21873635	Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas	2011-09-01	-
19615732	Defining the human deubiquitinating enzyme interaction landscape. Cell Mathew E Sowa , Eric J Bennett , Steven P Gygi , J Wade Harper	2009-07-23	-
19274049	A census of human transcription factors: function, expression and evolution. Nat Rev Genet Juan M Vaquerizas , Sarah K Kummerfeld , Sarah A Teichmann , Nicholas M Luscombe	2009-04-01	-
19253379	Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function. Am J Med Genet A Nathaniel D Miller , Melonie A Nance , Elizabeth S Wohler , Julie E Hoover-Fong , Emily Lisi , George H Thomas , Jonathan Pevsner	2009-02-15	-
15164054	The DNA sequence and comparative analysis of human chromosome 10. Nature P Deloukas , M E Earthrowl , D V Grafham , M Rubenfield , L French , C A Steward , S K Sims , M C Jones , S Searle , C Scott , K Howe , S E Hunt , T D Andrews , J G R Gilbert , D Swarbreck , J L Ashurst , A Taylor , J Battles , C P Bird , R Ainscough , J P Almeida , R I S Ashwell , K D Ambrose , A K Babbage , C L Bagguley , J Bailey , R Banerjee , K Bates , H Beasley , S Bray-Allen , A J Brown , J Y Brown , D C Burford , W Burrill , J Burton , P Cahill , D Camire , N P Carter , J C Chapman , S Y Clark , G Clarke , C M Clee , S Clegg , N Corby , A Coulson , P Dhami , I Dutta , M Dunn , L Faulkner , A Frankish , J A Frankland , P Garner , J Garnett , S Gribble , C Griffiths , R Grocock , E Gustafson , S Hammond , J L Harley , E Hart , P D Heath , T P Ho , B Hopkins , J Horne , P J Howden , E Huckle , C Hynds , C Johnson , D Johnson , A Kana , M Kay , A M Kimberley , J K Kershaw , M Kokkinaki , G K Laird , S Lawlor , H M Lee , D A Leongamornlert , G Laird , C Lloyd , D M Lloyd , J Loveland , J Lovell , S McLaren , K E McLay , A McMurray , M Mashreghi-Mohammadi , L Matthews , S Milne , T Nickerson , M Nguyen , E Overton-Larty , S A Palmer , A V Pearce , A I Peck , S Pelan , B Phillimore , K Porter , C M Rice , A Rogosin , M T Ross , T Sarafidou , H K Sehra , R Shownkeen , C D Skuce , M Smith , L Standring , N Sycamore , J Tester , A Thorpe , W Torcasso , A Tracey , A Tromans , J Tsolas , M Wall , J Walsh , H Wang , K Weinstock , A P West , D L Willey , S L Whitehead , L Wilming , P W Wray , L Young , Y Chen , R C Lovering , N K Moschonas , R Siebert , K Fechtel , D Bentley , R Durbin , T Hubbard , L Doucette-Stamm , S Beck , D R Smith , J Rogers	2004-05-27	TLX1NB, ABI1, C10orf131, ZNF503-AS2, LOC100132418, FAM25BP, FAM25G, FRAT1, TIMM23, MTRNR2L7, HSPD1P17, MTRNR2L5, ERVK-16, TIMM23B, PPIF, ACTR1A, OPTN, ADARB2, NEBL, PITRM1, RPP30, RPP38, DPYSL4, TACC2, ERLIN1, LBX1, NRG3, YME1L1, ZMYND11, PRDX3, VAX1, C10orf10, AKR1C4, HOGA1, CHUK, SORCS1, C10orf71, ZNF511, C10orf90, BTBD16, ZNF488, ZFYVE27, COMTD1, FRA10AC1, ANKRD22, PDZD8, AGAP4, BORCS7, LYZL2, GSTO2, SFR1, CALHM3, CLRN3, ANAPC16, SFXN4, COL17A1, KLF6, MAP3K8, TRUB1, DYDC1, HECTD2, FGFBP3, CACUL1, ADRA2A, CTSLP8, CYP2C19, CYP2C18, CYP17A1, USP54, NKX2-3, SLC35G1, CFAP58, AKR1C1, C10orf91, PWWP2B, DMBT1, DNA2, TRDMT1, ECHS1, EGR2, ANTXRL, PAGE2, ERCC6, PLAC9, ZCCHC24, ENKUR, STOX1, C10orf35, CCNY, TBATA, OTUD1, ZNF438, MARCH8, C10orf25, ZNF485, REEP3, UCMA, C10orf111, FAM171A1

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