Details for: PGAP2

Gene ID: 27315

Symbol: PGAP2

Ensembl ID: ENSG00000148985

Description: post-GPI attachment to proteins 2

Associated with

Cells (max top 100)

(Cell Significance Index and respective Thresholds are uniquely calculated using our advanced thresholding algorithms to reveal cell-specific gene markers)

  • Cell Name: polychromatophilic erythroblast (CL0000550)
    Fold Change: 104.5998
    Cell Significance Index: -16.2700
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 56.9500
    Cell Significance Index: -14.4500
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 36.4794
    Cell Significance Index: -14.8200
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 15.5958
    Cell Significance Index: -14.8900
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 13.9908
    Cell Significance Index: -17.2500
  • Cell Name: CD8-alpha-beta-positive, alpha-beta intraepithelial T cell (CL0000796)
    Fold Change: 5.9186
    Cell Significance Index: -15.8600
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 4.4716
    Cell Significance Index: -17.6500
  • Cell Name: epidermal Langerhans cell (CL0002457)
    Fold Change: 3.2852
    Cell Significance Index: -7.1900
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: 1.4014
    Cell Significance Index: 19.1200
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 1.3295
    Cell Significance Index: 216.2400
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 1.0282
    Cell Significance Index: 53.4100
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 0.9436
    Cell Significance Index: 109.9700
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 0.8083
    Cell Significance Index: 22.5900
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.6809
    Cell Significance Index: 135.1200
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.6359
    Cell Significance Index: 127.5700
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: 0.6206
    Cell Significance Index: 16.5700
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.5622
    Cell Significance Index: 201.6600
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: 0.5222
    Cell Significance Index: 36.9400
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.5193
    Cell Significance Index: 229.5900
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.5166
    Cell Significance Index: 14.8900
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.5160
    Cell Significance Index: 35.6900
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.5110
    Cell Significance Index: 11.0700
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.4405
    Cell Significance Index: 33.8100
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.4340
    Cell Significance Index: 19.6700
  • Cell Name: leptomeningeal cell (CL0000708)
    Fold Change: 0.3808
    Cell Significance Index: 8.1400
  • Cell Name: epidermal cell (CL0000362)
    Fold Change: 0.3726
    Cell Significance Index: 0.8400
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: 0.3704
    Cell Significance Index: 17.2700
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: 0.3573
    Cell Significance Index: 9.5800
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.3412
    Cell Significance Index: 64.9400
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: 0.3249
    Cell Significance Index: 47.2300
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.2924
    Cell Significance Index: 12.9400
  • Cell Name: paneth cell of colon (CL0009009)
    Fold Change: 0.2866
    Cell Significance Index: 4.3000
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.2493
    Cell Significance Index: 9.4400
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.2434
    Cell Significance Index: 219.7900
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.2426
    Cell Significance Index: 132.4900
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: 0.2329
    Cell Significance Index: 6.3400
  • Cell Name: lactocyte (CL0002325)
    Fold Change: 0.2199
    Cell Significance Index: 28.4100
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.2100
    Cell Significance Index: 20.7700
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.2038
    Cell Significance Index: 36.7500
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: 0.1601
    Cell Significance Index: 3.4100
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.1592
    Cell Significance Index: 3.9800
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: 0.1538
    Cell Significance Index: 11.4600
  • Cell Name: umbrella cell of urothelium (CL4030056)
    Fold Change: 0.1499
    Cell Significance Index: 1.3800
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: 0.1385
    Cell Significance Index: 16.3400
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.1384
    Cell Significance Index: 8.7200
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: 0.1342
    Cell Significance Index: 8.6600
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: 0.1266
    Cell Significance Index: 2.6500
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.1257
    Cell Significance Index: 15.4500
  • Cell Name: corneal epithelial cell (CL0000575)
    Fold Change: 0.1250
    Cell Significance Index: 1.7800
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: 0.1071
    Cell Significance Index: 6.5800
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.0855
    Cell Significance Index: 11.7400
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: 0.0731
    Cell Significance Index: 12.4900
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: 0.0726
    Cell Significance Index: 1.5900
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: 0.0627
    Cell Significance Index: 2.1800
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: 0.0461
    Cell Significance Index: 1.6200
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0427
    Cell Significance Index: 80.3200
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: 0.0424
    Cell Significance Index: 2.3800
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0223
    Cell Significance Index: 34.3900
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0200
    Cell Significance Index: 36.9200
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.0152
    Cell Significance Index: 9.6800
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 0.0117
    Cell Significance Index: 1.5000
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0042
    Cell Significance Index: 5.7500
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0106
    Cell Significance Index: -8.0400
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0119
    Cell Significance Index: -5.3800
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0136
    Cell Significance Index: -9.9800
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.0169
    Cell Significance Index: -0.7900
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: -0.0186
    Cell Significance Index: -1.2500
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0188
    Cell Significance Index: -13.9600
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0262
    Cell Significance Index: -14.8000
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.0284
    Cell Significance Index: -0.8100
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0296
    Cell Significance Index: -18.5100
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0335
    Cell Significance Index: -3.4200
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.0513
    Cell Significance Index: -14.7700
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.0586
    Cell Significance Index: -0.9800
  • Cell Name: granulosa cell (CL0000501)
    Fold Change: -0.0605
    Cell Significance Index: -1.5900
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.0707
    Cell Significance Index: -8.1000
  • Cell Name: pro-T cell (CL0000827)
    Fold Change: -0.0771
    Cell Significance Index: -1.9700
  • Cell Name: CD4-positive, alpha-beta memory T cell, CD45RO-positive (CL0001204)
    Fold Change: -0.0793
    Cell Significance Index: -2.3300
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0854
    Cell Significance Index: -17.9900
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: -0.0880
    Cell Significance Index: -2.1100
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.0927
    Cell Significance Index: -2.9700
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.0937
    Cell Significance Index: -4.8800
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.0979
    Cell Significance Index: -5.1400
  • Cell Name: peg cell (CL4033014)
    Fold Change: -0.1069
    Cell Significance Index: -2.4700
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: -0.1114
    Cell Significance Index: -1.6500
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.1449
    Cell Significance Index: -15.0900
  • Cell Name: cone retinal bipolar cell (CL0000752)
    Fold Change: -0.1492
    Cell Significance Index: -1.1500
  • Cell Name: retinal rod cell (CL0000604)
    Fold Change: -0.1552
    Cell Significance Index: -1.8500
  • Cell Name: neutrophil progenitor cell (CL0000834)
    Fold Change: -0.1559
    Cell Significance Index: -4.1700
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: -0.1657
    Cell Significance Index: -2.8400
  • Cell Name: intestinal epithelial cell (CL0002563)
    Fold Change: -0.1922
    Cell Significance Index: -1.9900
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.1939
    Cell Significance Index: -15.3600
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.2017
    Cell Significance Index: -4.2800
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.2135
    Cell Significance Index: -13.0900
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: -0.2248
    Cell Significance Index: -3.2200
  • Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
    Fold Change: -0.2310
    Cell Significance Index: -4.9900
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -0.2446
    Cell Significance Index: -4.9100
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.2644
    Cell Significance Index: -8.4200
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.2665
    Cell Significance Index: -3.3100
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.2700
    Cell Significance Index: -6.9400

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this specific cell.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Other Information

**Key Characteristics:** PGAP2 is a gene with a unique expression profile, with notable expression in cells involved in immune responses, cardiovascular health, and development. Its involvement in the biosynthetic process of GPI anchors, a crucial component of cell surface proteins, suggests a pivotal role in regulating cell-cell interactions and signaling pathways. Furthermore, the presence of PGAP2 in various cell types highlights its potential as a key regulator of cellular processes, including proliferation, differentiation, and survival. **Pathways and Functions:** PGAP2's involvement in the GPI anchor biosynthetic process highlights its role in regulating cell surface protein expression and function. The gene's expression in cells involved in immune responses, such as B-2 B cells and cardiac endothelial cells, suggests its involvement in modulating immune cell function and promoting tissue homeostasis. Additionally, PGAP2's expression in placental villous trophoblasts underscores its potential role in fetal development and maternal-fetal interactions. The gene's association with protein binding and membrane trafficking pathways further supports its involvement in regulating cellular processes. PGAP2's interaction with various proteins, including FGF receptor-activating protein 1, suggests its role as a scaffold or adapter protein, facilitating the assembly and regulation of protein complexes involved in signaling and membrane dynamics. **Clinical Significance:** PGAP2's involvement in various cellular processes and its expression in diverse cell types render it a potential candidate for therapeutic intervention in various diseases. For instance, alterations in PGAP2 expression have been linked to cardiovascular diseases, immune disorders, and cancer. Furthermore, PGAP2's role in fetal development and maternal-fetal interactions makes it an attractive target for research into pregnancy-related complications and gestational disorders. In conclusion, PGAP2 is a gene with far-reaching implications in cellular processes, from GPI anchor biosynthesis to protein binding and membrane trafficking. Its diverse expression patterns and multifaceted functions underscore its importance in maintaining tissue homeostasis and cellular function. As research into PGAP2 continues, it is likely that this gene will emerge as a key player in the development of novel therapeutic strategies for various diseases.

Genular Protein ID: 933021803

Symbol: PGAP2_HUMAN

Name: FGF receptor-activating protein 1

UniProtKB Accession Codes:

Q9UHJ9 E9PJG5 H7BXL9 Q6UC77 Q96G66 Q9UF01 Q9Y4N1

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 4 CTD 1 ChiTaRS 1 DMDM 1 DNASU 1 DisGeNET 1 EMBL 16 Ensembl 5 ExpressionAtlas 1 GO 4 GeneCards 1 GeneTree 1 GenomeRNAi 1 HGNC 1 HPA 1 InParanoid 1 IntAct 1 InterPro 2 KEGG 1 MANE-Select 1 MIM 3 MINT 1 MalaCards 1 MassIVE 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 Orphanet 1 OrthoDB 1 PANTHER 2 PIR 1 PRO 1 PathwayCommons 1 PeptideAtlas 1 Pfam 1 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 Proteomes 1 ProteomicsDB 5 RNAct 1 RefSeq 20 STRING 1 SignaLink 1 SwissPalm 1 TCDB 1 TreeFam 1 UCSC 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 neXtProt 1

Citations:

PubMed ID: 10585768

Title: Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer.

PubMed ID: 10585768

DOI: 10.1006/geno.1999.5980

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

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: 17974005

Title: The full-ORF clone resource of the German cDNA consortium.

PubMed ID: 17974005

DOI: 10.1186/1471-2164-8-399

PubMed ID: 29374258

Title: Identification of a Golgi GPI-N-acetylgalactosamine transferase with tandem transmembrane regions in the catalytic domain.

PubMed ID: 29374258

DOI: 10.1038/s41467-017-02799-0

PubMed ID: 23561846

Title: Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.

PubMed ID: 23561846

DOI: 10.1016/j.ajhg.2013.03.008

PubMed ID: 23561847

Title: PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome.

PubMed ID: 23561847

DOI: 10.1016/j.ajhg.2013.03.011

PubMed ID: 37198333

Title: De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues.

PubMed ID: 37198333

DOI: 10.1007/s00439-023-02569-7

Sequence Information:

  • Length: 254
  • Mass: 29400
  • Checksum: 2FB502D505DCCF64
  • Sequence:
    • MYQVPLPLDR DGTLVRLRFT MVALVTVCCP LVAFLFCILW SLLFHFKETT ATHCGVPNYL 
PSVSSAIGGE VPQRYVWRFC IGLHSAPRFL VAFAYWNHYL SCTSPCSCYR PLCRLNFGLN 
VVENLALLVL TYVSSSEDFT IHENAFIVFI ASSLGHMLLT CILWRLTKKH TVSQEDRKSY 
SWKQRLFIIN FISFFSALAV YFRHNMYCEA GVYTIFAILE YTVVLTNMAF HMTAWWDFGN 
KELLITSQPE EKRF

Genular Protein ID: 2744906080

Symbol: A8MYS5_HUMAN

Name: N/A

UniProtKB Accession Codes:

A8MYS5

Database IDs:

ARBA 9 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CTD 1 ChiTaRS 1 DNASU 1 DisGeNET 1 EMBL 1 Ensembl 2 ExpressionAtlas 1 GO 3 GeneTree 1 HGNC 1 InterPro 2 MassIVE 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PeptideAtlas 2 Pfam 1 Proteomes 2 ProteomicsDB 2 RefSeq 1 SAM 1 SMR 1 UCSC 1 VEuPathDB 1

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

Sequence Information:

  • Length: 311
  • Mass: 35519
  • Checksum: B72E56757D62B8CD
  • Sequence:
    • MARLGSTGGV SGRVVTQHRD SAPFLGAPRL GLRELGPIRG TAPEWHGRWN AAERSDKMYQ 
VPLPLDRDGT LVRLRFTMVA LVTVCCPLVA FLFCILWSLL FHFKETTATH CGVPNYLPSV 
SSAIGGEVPQ RYVWRFCIGL HSAPRFLVAF AYWNHYLSCT SPCSCYRPLC RLNFGLNVVE 
NLALLVLTYV SSSEDFTIHE NAFIVFIASS LGHMLLTCIL WRLTKKHTVS QEDRKSYSWK 
QRLFIINFIS FFSALAVYFR HNMYCEAGVY TIFAILEYTV VLTNMAFHMT AWWDFGNKEL 
LITSQPEEKR F

Genular Protein ID: 3566875055

Symbol: A0A0S2Z568_HUMAN

Name: N/A

UniProtKB Accession Codes:

A0A0S2Z568

Database IDs:

ARBA 9 AlphaFoldDB 1 BioGRID-ORCS 1 CTD 1 ChiTaRS 1 DNASU 1 DisGeNET 1 EMBL 2 GO 3 InterPro 2 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 Pfam 1 RefSeq 4 SAM 1

Citations:

PubMed ID: 26871637

Title: Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.

PubMed ID: 26871637

DOI: 10.1016/j.cell.2016.01.029

Sequence Information:

  • Length: 250
  • Mass: 28957
  • Checksum: 6B8A396B2A362942
  • Sequence:
    • MYQVPLPLDR DGTLVRLRFT MVALVTVCCP LVAFLFCILW SLLFHFKETT ATHCGVPNYL 
PSVSSAIGGE VPQRYVWRFC IGLHSAPRFL VAFAYWNHYL SCTSPCSCYR PLCRLNFGLN 
VVENLALLVL TYVSSSEDFT IHENAFIVFI ASSLGHMLLT CILWRLTKKH TDRKSYSWKQ 
RLFIINFISF FSALAVYFRH NMYCEAGVYT IFAILEYTVV LTNMAFHMTA WWDFGNKELL 
ITSQPEEKRF

Genular Protein ID: 2321566542

Symbol: A0A0A0MS75_HUMAN

Name: N/A

UniProtKB Accession Codes:

A0A0A0MS75

Database IDs:

ARBA 9 Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CTD 1 ChiTaRS 1 DNASU 1 DisGeNET 1 EMBL 3 Ensembl 2 GO 3 GeneTree 1 HGNC 1 HOGENOM 1 InterPro 2 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PaxDb 1 PeptideAtlas 1 Pfam 1 Proteomes 2 ProteomicsDB 1 RefSeq 2 SAM 2 UCSC 1 VEuPathDB 1

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 11181995

Title: The sequence of the human genome.

PubMed ID: 11181995

DOI: 10.1126/science.1058040

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

Sequence Information:

  • Length: 272
  • Mass: 30912
  • Checksum: BD1649B6EED64192
  • Sequence:
    • MGPWYGSASP WWPWSRSAVH LSPSSSASSG PCSSTSRRQR PHTVGTEASI GVPGIKMDGG 
DAQEHGHFLR LPQVPNYLPS VSSAIGGEVP QRYVWRFCIG LHSAPRFLVA FAYWNHYLSC 
TSPCSCYRPL CRLNFGLNVV ENLALLVLTY VSSSEDFTIH ENAFIVFIAS SLGHMLLTCI 
LWRLTKKHTV SQEDRKSYSW KQRLFIINFI SFFSALAVYF RHNMYCEAGV YTIFAILEYT 
VVLTNMAFHM TAWWDFGNKE LLITSQPEEK RF

Genular Protein ID: 1173726401

Symbol: B7Z2X5_HUMAN

Name: N/A

UniProtKB Accession Codes:

B7Z2X5

Database IDs:

Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CTD 1 ChiTaRS 1 DNASU 1 DisGeNET 1 EMBL 3 Ensembl 2 GeneTree 1 HGNC 1 HOGENOM 1 NCBI Taxonomy 1 OrthoDB 1 Proteomes 2 RefSeq 6 UCSC 1 VEuPathDB 1

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

Sequence Information:

  • Length: 211
  • Mass: 23092
  • Checksum: 2B22AF9419198B2C
  • Sequence:
    • MVEMHKNMVI SLDYPRQVPV CGGDGEGATM LLHKSQDSWG MRIQHFGPRT WKERSFGRGA 
QLPALGELSH RRGGAPALRV AFLHRPALGA SLLGGLRLLE PLPQLHLPVF LLSPALPPQL 
RPQCRGEPRV ASAHLCLLLR GLHHPRKCFH CVHCLIPRAH APHLHSLAVD QEAHSKSGGS 
QVLQLETAAL HHQLHLLLLG AGCLLSAQHV L

Genular Protein ID: 2444761710

Symbol: H0YDQ4_HUMAN

Name: N/A

UniProtKB Accession Codes:

H0YDQ4

Database IDs:

ARBA 9 Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CTD 1 ChiTaRS 1 DNASU 1 DisGeNET 1 EMBL 3 Ensembl 2 GO 3 GeneTree 1 HGNC 1 InterPro 2 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PeptideAtlas 1 Pfam 1 Proteomes 2 ProteomicsDB 1 RefSeq 1 SAM 1 UCSC 1 VEuPathDB 1

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 11181995

Title: The sequence of the human genome.

PubMed ID: 11181995

DOI: 10.1126/science.1058040

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

Sequence Information:

  • Length: 234
  • Mass: 26006
  • Checksum: FBBBCA835202E329
  • Sequence:
    • MYQVPLPLDR DGTLVRLRFT MVALVTVCCP LVAFLFCILW SLLFHFKETT ATHCGVPNYL 
PSVSSAIGGE VPQRYVWRFC IGLHSAPRFL VAFAYWNHYL SCTSPCSCYR PLCRLNFGLN 
VVENLALLVL TYVSSSEDFT IHENAFIVFI ASSLGHMLLT CILWRLTKKH TVSQEVRSIP 
SGGSKAAQKK IKDICPQDSG NGSQVLQLET AALHHQLHLL LLGAGCLLSA QHVL

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.