Associated with
Other Information
Genular Protein ID: 4220186972
Symbol: PROM1_HUMAN
Name: Prominin-1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9389721
Title: A novel five-transmembrane hematopoietic stem cell antigen: isolation, characterization, and molecular cloning.
PubMed ID: 9389721
PubMed ID: 12042327
Title: AC133-2, a novel isoform of human AC133 stem cell antigen.
PubMed ID: 12042327
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15815621
Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
PubMed ID: 15815621
DOI: 10.1038/nature03466
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 9389720
Title: AC133, a novel marker for human hematopoietic stem and progenitor cells.
PubMed ID: 9389720
PubMed ID: 17874118
Title: Differential expression of prominin-1 (CD133) and prominin-2 in major cephalic exocrine glands of adult mice.
PubMed ID: 17874118
PubMed ID: 17498271
Title: Nomenclature of prominin-1 (CD133) splice variants - an update.
PubMed ID: 17498271
PubMed ID: 18096722
Title: The stem cell marker prominin-1/CD133 on membrane particles in human cerebrospinal fluid offers novel approaches for studying central nervous system disease.
PubMed ID: 18096722
PubMed ID: 19302789
Title: Release of extracellular membrane vesicles from microvilli of epithelial cells is enhanced by depleting membrane cholesterol.
PubMed ID: 19302789
PubMed ID: 20818439
Title: CD133 suppresses neuroblastoma cell differentiation via signal pathway modification.
PubMed ID: 20818439
DOI: 10.1038/onc.2010.383
PubMed ID: 10587575
Title: A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.
PubMed ID: 10587575
DOI: 10.1093/hmg/9.1.27
PubMed ID: 17605048
Title: Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
PubMed ID: 17605048
PubMed ID: 21406692
Title: System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.
PubMed ID: 21406692
PubMed ID: 24556617
Title: Post-translational regulation of CD133 by ATase1/ATase2-mediated lysine acetylation.
PubMed ID: 24556617
PubMed ID: 18654668
Title: Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.
PubMed ID: 18654668
DOI: 10.1172/jci35891
PubMed ID: 35947379
Title: Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1.
PubMed ID: 35947379
DOI: 10.1167/iovs.63.9.14
Sequence Information:
- Length: 865
- Mass: 97202
- Checksum: D21CBC05ADB2DEDF
- Sequence:
MALVLGSLLL LGLCGNSFSG GQPSSTDAPK AWNYELPATN YETQDSHKAG PIGILFELVH IFLYVVQPRD FPEDTLRKFL QKAYESKIDY DKPETVILGL KIVYYEAGII LCCVLGLLFI ILMPLVGYFF CMCRCCNKCG GEMHQRQKEN GPFLRKCFAI SLLVICIIIS IGIFYGFVAN HQVRTRIKRS RKLADSNFKD LRTLLNETPE QIKYILAQYN TTKDKAFTDL NSINSVLGGG ILDRLRPNII PVLDEIKSMA TAIKETKEAL ENMNSTLKSL HQQSTQLSSS LTSVKTSLRS SLNDPLCLVH PSSETCNSIR LSLSQLNSNP ELRQLPPVDA ELDNVNNVLR TDLDGLVQQG YQSLNDIPDR VQRQTTTVVA GIKRVLNSIG SDIDNVTQRL PIQDILSAFS VYVNNTESYI HRNLPTLEEY DSYWWLGGLV ICSLLTLIVI FYYLGLLCGV CGYDRHATPT TRGCVSNTGG VFLMVGVGLS FLFCWILMII VVLTFVFGAN VEKLICEPYT SKELFRVLDT PYLLNEDWEY YLSGKLFNKS KMKLTFEQVY SDCKKNRGTY GTLHLQNSFN ISEHLNINEH TGSISSELES LKVNLNIFLL GAAGRKNLQD FAACGIDRMN YDSYLAQTGK SPAGVNLLSF AYDLEAKANS LPPGNLRNSL KRDAQTIKTI HQQRVLPIEQ SLSTLYQSVK ILQRTGNGLL ERVTRILASL DFAQNFITNN TSSVIIEETK KYGRTIIGYF EHYLQWIEFS ISEKVASCKP VATALDTAVD VFLCSYIIDP LNLFWFGIGK ATVFLLPALI FAVKLAKYYR RMDSEDVYDD VETIPMKNME NGNNGYHKDH VYGIHNPVMT SPSQH
Genular Protein ID: 3355318844
Symbol: A0A0A0N0M1_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 856
- Mass: 96251
- Checksum: DFF0B7AFE0A02582
- Sequence:
MALVLGSLLL LGLCGNSFSG GQPSSTDAPK AWNYELPATN YETQDSHKAG PIGILFELVH IFLYVVQPRD FPEDTLRKFL QKAYESKIDY DKIVYYEAGI ILCCVLGLLF IILMPLVGYF FCMCRCCNKC GGEMHQRQKE NGPFLRKCFA ISLLVICIII SIGIFYGFVA NHQVRTRIKR SRKLADSNFK DLRTLLNETP EQIKYILAQY NTTKDKAFTD LNSINSVLGG GILDRLRPNI IPVLDEIKSM ATAIKETKEA LENMNSTLKS LHQQSTQLSS SLTSVKTSLR SSLNDPLCLV HPSSETCNSI RLSLSQLNSN PELRQLPPVD AELDNVNNVL RTDLDGLVQQ GYQSLNDIPD RVQRQTTTVV AGIKRVLNSI GSDIDNVTQR LPIQDILSAF SVYVNNTESY IHRNLPTLEE YDSYWWLGGL VICSLLTLIV IFYYLGLLCG VCGYDRHATP TTRGCVSNTG GVFLMVGVGL SFLFCWILMI IVVLTFVFGA NVEKLICEPY TSKELFRVLD TPYLLNEDWE YYLSGKLFNK SKMKLTFEQV YSDCKKNRGT YGTLHLQNSF NISEHLNINE HTGSISSELE SLKVNLNIFL LGAAGRKNLQ DFAACGIDRM NYDSYLAQTG KSPAGVNLLS FAYDLEAKAN SLPPGNLRNS LKRDAQTIKT IHQQRVLPIE QSLSTLYQSV KILQRTGNGL LERVTRILAS LDFAQNFITN NTSSVIIEET KKYGRTIIGY FEHYLQWIEF SISEKVASCK PVATALDTAV DVFLCSYIID PLNLFWFGIG KATVFLLPAL IFAVKLAKYY RRMDSEDVYD DVETIPMKNM ENGNNGYHKD HVYGIHNPVM TSPSQH
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.