EMC1

protein-coding gene in the species Homo sapiens

EMC1 is …
instance of (P31):
geneQ7187

sublass of (P279):
protein-coding geneQ20747295

External links are
P594Ensembl gene IDENSG00000127463
P704Ensembl transcript IDENST00000375199
ENST00000375208
ENST00000461353
ENST00000462505
ENST00000467423
ENST00000475079
ENST00000477853
ENST00000480380
ENST00000486238
ENST00000486405
ENST00000488681
ENST00000494770
ENST00000685099
ENST00000685594
ENST00000688219
ENST00000688332
ENST00000688538
ENST00000688667
ENST00000688918
ENST00000689748
ENST00000690451
ENST00000690732
ENST00000690823
ENST00000691945
ENST00000692207
ENST00000692400
ENST00000693007
P351Entrez Gene ID23065
P2888exact matchhttp://identifiers.org/ncbigene/23065
P353HGNC gene symbolEMC1
P354HGNC ID28957
P593HomoloGene ID9002
P492OMIM ID616846
616846
P639RefSeq RNA IDNM_001271427
NM_001271428
NM_001271429
NM_001375820
NM_001375821
NM_015047
P2892UMLS CUIC3541711

P1057chromosomehuman chromosome 1Q430258
P4196cytogenetic location1p36.13
P688encodesER membrane protein complex subunit 1Q21204276
P5572expressed insmooth muscle tissueQ208453
islet of LangerhansQ728309
gastrocnemius muscleQ943203
sural nerveQ6135922
ventricular zoneQ28455175
right ovaryQ66502831
muscle of thighQ66514508
cartilage tissueQ66526729
stromal cell of endometriumQ66592424
epithelium of colonQ66714209
P703found in taxonHomo sapiensQ15978631
P645genomic end19578046
19251552
P644genomic start19542158
19215660
P684orthologEmc1Q18297891
Emc1Q24361914
emc-1Q29671317
EMC1Q29709930
emc1Q29771927
P2548strand orientationreverse strandQ22809711

Reverse relations

regulates (molecular biology) (P128)
Q27595285hsa-miR-106a-5p
Q27594907hsa-miR-106b-5p
Q27593173hsa-miR-125b-5p
Q27592789hsa-miR-1273g-3p
Q27594174hsa-miR-1285-3p
Q27592867hsa-miR-1295b-3p
Q27594390hsa-miR-130b-5p
Q27593323hsa-miR-17-5p
Q27593105hsa-miR-192-5p
Q27593625hsa-miR-193b-3p
Q27593208hsa-miR-196a-3p
Q27593329hsa-miR-20a-5p
Q27595281hsa-miR-20b-5p
Q27592906hsa-miR-215-5p
Q27594162hsa-miR-216b-3p
Q27595118hsa-miR-23b-3p
Q27594627hsa-miR-302a-3p
Q27594631hsa-miR-302b-3p
Q27594629hsa-miR-302c-3p
Q27594625hsa-miR-302d-3p
Q27593047hsa-miR-302e
Q27593914hsa-miR-3187-5p
Q27593426hsa-miR-323a-5p
Q27594111hsa-miR-372-3p
Q27594114hsa-miR-373-3p
Q27592718hsa-miR-4252
Q27593510hsa-miR-4537
Q27593502hsa-miR-4710
Q27593719hsa-miR-4731-5p
Q27593896hsa-miR-4743-3p
Q27594170hsa-miR-4778-5p
Q27594459hsa-miR-4792
Q27594481hsa-miR-4793-3p
Q27594576hsa-miR-4797-5p
Q27595321hsa-miR-507
Q27595322hsa-miR-508-5p
Q27593793hsa-miR-5089-5p
Q27594042hsa-miR-512-3p
Q27594546hsa-miR-5186
Q27593685hsa-miR-5189-5p
Q27594081hsa-miR-519d-3p
Q27594057hsa-miR-520a-3p
Q27594070hsa-miR-520b
Q27594074hsa-miR-520c-3p
Q27594085hsa-miR-520d-3p
Q27594045hsa-miR-520e
Q27594059hsa-miR-526b-3p
Q27592863hsa-miR-557
Q27593371hsa-miR-5586-3p
Q27593942hsa-miR-5589-5p
Q27593116hsa-miR-612
Q27593259hsa-miR-619-5p
Q27593637hsa-miR-6506-5p
Q27594224hsa-miR-6512-3p
Q27595048hsa-miR-661
Q27594756hsa-miR-6720-5p
Q27594130hsa-miR-6807-5p
Q27595062hsa-miR-6849-3p
Q27593121hsa-miR-6860
Q27594212hsa-miR-6888-3p
Q27593312hsa-miR-759
Q27595274hsa-miR-766-3p
Q27593357hsa-miR-7703
Q27593374hsa-miR-7855-5p
Q27594500hsa-miR-8064
Q27595079hsa-miR-876-3p
Q27592847hsa-miR-9-5p
Q27594905hsa-miR-93-5p
Q27595059hsa-miR-939-3p

ortholog (P684)
Q29709930EMC1
Q18297891Emc1
Q24361914Emc1
Q29671317emc-1
Q29771927emc1

Q55785026cerebellar atrophy, visual impairment, and psychomotor retardation;genetic associationP2293
Q21204276ER membrane protein complex subunit 1encoded byP702