MID1

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protein-coding gene in the species Homo sapiens

External resources

Freebase ಐಡಿ	/m/02kfnlz
Ensembl transcript ID	ENST00000616003^[೧] ENST00000317552^[೧] ENST00000380779^[೧] ENST00000380780^[೧] ENST00000380782^[೧] ENST00000380785^[೧] ENST00000380787^[೧] ENST00000413894^[೧] ENST00000453318^[೧] ENST00000479925^[೧] ENST00000610939^[೧] ENST00000674917^[೧] ENST00000675358^[೧] ENST00000675073^[೧] ENST00000693721^[೧] ENST00000689773^[೧] ENST00000690004^[೧] ENST00000691943^[೧] ENST00000689180^[೧] ENST00000691913^[೧] ENST00000686012^[೧] ENST00000687008^[೧] ENST00000689988^[೧]
Entrez Gene ID	4281^[೨]
HGNC ID	7095^[೨]
Ensembl gene ID	ENSG00000101871^[೧]
UMLS CUI	C1417167^[೩]
OMIM ID	300552^[೪]
HGNC gene symbol	MID1^[೨]
RefSeq RNA ID	NM_000381^[೨] NM_001098624^[೨] NM_001193277^[೨] NM_001193278^[೨] NM_001193279^[೨] NM_001193280^[೨] NM_001193281^[೨] NM_033289^[೨] NM_033290^[೨] NM_033291^[೨] NM_001347733^[೨]

ಉದಾಹರಣೆಗೆ

ವಂಶವಾಹಿ^[೧]

ಉಪವರ್ಗ

protein-coding gene^[೫]

found in taxon

Homo sapiens^[೧]

encodes

Midline 1^[೬]

gene inversion association with

Opitz-GBBB syndrome^[೭]^[೮]

determination method or standard: case study

chromosome

human X chromosome^[೧]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand^[೧]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

10445310^[೧]

genomic assembly: genome assembly GRCh38

chromosome: human X chromosome

10413350^[೧]

genomic assembly: Genome assembly GRCh37

chromosome: human X chromosome

genomic end

10833654^[೧]

genomic assembly: genome assembly GRCh38

chromosome: human X chromosome

10851773^[೧]

genomic assembly: Genome assembly GRCh37

chromosome: human X chromosome

cytogenetic location

Xp22.2^[೨]

HomoloGene ID

7837^[೨]

Gene Atlas image

increased expression in

ಆಲ್ ಝೈಮರ್ ನ ಕಾಯಿಲೆ^[೯]^[೮]

determination method or standard: IEP

prostate cancer^[೧೦]^[೮]

determination method or standard: IEP

ortholog

Mid1^[೧೧]^[೧೨]

found in taxon: house mouse

Mid1^[೧೧]^[೧೨]

found in taxon: brown rat

mid1^[೧೧]

found in taxon: Danio rerio

expressed in

mucosa of paranasal sinus^[೧೩]

series ordinal: 1

ventricular zone^[೧೩]

series ordinal: 2

pancreatic ductal cell^[೧೩]

series ordinal: 3

hair follicle^[೧೩]

series ordinal: 4

bronchial epithelial cell^[೧೩]

series ordinal: 5

seminal vesicula^[೧೩]

series ordinal: 6

right ventricle^[೧೩]

series ordinal: 7

Epithelium of choroid plexus^[೧೩]

series ordinal: 8

ganglionic eminence^[೧೩]

series ordinal: 9

mucosa of urinary bladder^[೧೩]

series ordinal: 10

exact match

http://identifiers.org/ncbigene/4281^[೧೪]

Reference

↑ ^೧.೦೦ ^೧.೦೧ ^೧.೦೨ ^೧.೦೩ ^೧.೦೪ ^೧.೦೫ ^೧.೦೬ ^೧.೦೭ ^೧.೦೮ ^೧.೦೯ ^೧.೧೦ ^೧.೧೧ ^೧.೧೨ ^೧.೧೩ ^೧.೧೪ ^೧.೧೫ ^೧.೧೬ ^೧.೧೭ ^೧.೧೮ ^೧.೧೯ ^೧.೨೦ ^೧.೨೧ ^೧.೨೨ ^೧.೨೩ ^೧.೨೪ ^೧.೨೫ ^೧.೨೬ ^೧.೨೭ ^೧.೨೮ ^೧.೨೯ ^೧.೩೦ ^೧.೩೧ ensembl Release 106, ENSG00000101871
↑ ^೨.೦೦ ^೨.೦೧ ^೨.೦೨ ^೨.೦೩ ^೨.೦೪ ^೨.೦೫ ^೨.೦೬ ^೨.೦೭ ^೨.೦೮ ^೨.೦೯ ^೨.೧೦ ^೨.೧೧ ^೨.೧೨ ^೨.೧೩ ^೨.೧೪ ^೨.೧೫ NCBI Gene, ೧೫ ಮೇ 2022, 4281
↑ UMLS 2023, ೧೫ ಜೂನ್ 2023, inferred by common HGNC mappings on source and on Wikidata
↑ Online Mendelian Inheritance in Man, ೧೯ ಆಗಸ್ಟ್ 2019
↑ Ensembl Release 87, ENSG00000101871
↑ UniProt, ೬ ಜುಲೈ 2017, O15344
↑ Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22, case study
↑ ^೮.೦ ^೮.೧ ^೮.೨ The MID1 gene product in physiology and disease, review article
↑ Resveratrol induces dephosphorylation of Tau by interfering with the MID1-PP2A complex
↑ A hormone-dependent feedback-loop controls androgen receptor levels by limiting MID1, a novel translation enhancer and promoter of oncogenic signaling
↑ ^೧೧.೦ ^೧೧.೧ ^೧೧.೨ HomoloGene build68, 7837
↑ ^೧೨.೦ ^೧೨.೧ Orthologous MAtrix, https://omabrowser.org/oma/vps/O15344/
↑ ^{೧೩.೦೦} ^{೧೩.೦೧} ^{೧೩.೦೨} ^{೧೩.೦೩} ^{೧೩.೦೪} ^{೧೩.೦೫} ^{೧೩.೦೬} ^{೧೩.೦೭} ^{೧೩.೦೮} ^{೧೩.೦೯} Bgee, ೭ ಜೂನ್ 2024, https://www.bgee.org/gene/ENSG00000101871
↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

[r6973ba7a-1] ೧.೦೦ ^೧.೦೧ ^೧.೦೨ ^೧.೦೩ ^೧.೦೪ ^೧.೦೫ ^೧.೦೬ ^೧.೦೭ ^೧.೦೮ ^೧.೦೯ ^೧.೧೦ ^೧.೧೧ ^೧.೧೨ ^೧.೧೩ ^೧.೧೪ ^೧.೧೫ ^೧.೧೬ ^೧.೧೭ ^೧.೧೮ ^೧.೧೯ ^೧.೨೦ ^೧.೨೧ ^೧.೨೨ ^೧.೨೩ ^೧.೨೪ ^೧.೨೫ ^೧.೨೬ ^೧.೨೭ ^೧.೨೮ ^೧.೨೯ ^೧.೩೦ ^೧.೩೧ ensembl Release 106, ENSG00000101871

[r01d2998f-2] ೨.೦೦ ^೨.೦೧ ^೨.೦೨ ^೨.೦೩ ^೨.೦೪ ^೨.೦೫ ^೨.೦೬ ^೨.೦೭ ^೨.೦೮ ^೨.೦೯ ^೨.೧೦ ^೨.೧೧ ^೨.೧೨ ^೨.೧೩ ^೨.೧೪ ^೨.೧೫ NCBI Gene, ೧೫ ಮೇ 2022, 4281

[reb0a93a5-3] UMLS 2023, ೧೫ ಜೂನ್ 2023, inferred by common HGNC mappings on source and on Wikidata

[r8fdf1270-4] Online Mendelian Inheritance in Man, ೧೯ ಆಗಸ್ಟ್ 2019

[r82d40651-5] Ensembl Release 87, ENSG00000101871

[r3ed468d8-6] UniProt, ೬ ಜುಲೈ 2017, O15344

[r33e7f58d-7] Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22, case study

[rd503d6ae-8] ೮.೦ ^೮.೧ ^೮.೨ The MID1 gene product in physiology and disease, review article

[r44e99549-9] Resveratrol induces dephosphorylation of Tau by interfering with the MID1-PP2A complex

[rb4e1e531-10] A hormone-dependent feedback-loop controls androgen receptor levels by limiting MID1, a novel translation enhancer and promoter of oncogenic signaling

[r043d36d7-11] ೧೧.೦ ^೧೧.೧ ^೧೧.೨ HomoloGene build68, 7837

[r9138f598-12] ೧೨.೦ ^೧೨.೧ Orthologous MAtrix, https://omabrowser.org/oma/vps/O15344/

[r64b9ecbc-13] {೧೩.೦೦} ^{೧೩.೦೧} ^{೧೩.೦೨} ^{೧೩.೦೩} ^{೧೩.೦೪} ^{೧೩.೦೫} ^{೧೩.೦೬} ^{೧೩.೦೭} ^{೧೩.೦೮} ^{೧೩.೦೯} Bgee, ೭ ಜೂನ್ 2024, https://www.bgee.org/gene/ENSG00000101871

[r99e80de4-14] Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

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