Details for: PKNOX1

Gene ID: 5316

Gene Type:  Protein-coding  - A gene that serves as a template for producing a messenger RNA (mRNA) molecule, which is then translated into a functional protein.

Symbol: PKNOX1

Ensembl ID: ENSG00000160199

Description: PBX/knotted 1 homeobox 1

Selected Context(s):  Overall

Cell Significance Landscape

Contexts:

Associated with

Significant Cells

Cell Significance Index (CSI) scores for the chosen context(s)

  • progenitor cell CL0011026
    CSI 10.02
    rCSI 21.31%
    PRS 73.79
  • mesothelial cell CL0000077
    CSI 6.89
    rCSI 26.96%
    PRS 58.01
  • near-projecting glutamatergic cortical neuron CL4023012
    CSI 6.41
    rCSI 24.23%
    PRS 61.82
  • L6b glutamatergic cortical neuron CL4023038
    CSI 5.14
    rCSI 16.07%
    PRS 62.96
  • differentiation-committed oligodendrocyte precursor CL4023059
    CSI 5.13
    rCSI 9.32%
    PRS 70.85
  • stromal cell CL0000499
    CSI 5.07
    rCSI 14.27%
    PRS 74.43
  • epithelial cell of proximal tubule CL0002306
    CSI 4.24
    rCSI 10.36%
    PRS 71.77
  • lung ciliated cell CL1000271
    CSI 4.22
    rCSI 4.88%
    PRS 71.59
  • corticothalamic-projecting glutamatergic cortical neuron CL4023013
    CSI 3.7
    rCSI 21.79%
    PRS 62.05
  • L2/3-6 intratelencephalic projecting glutamatergic neuron CL4023040
    CSI 3.69
    rCSI 8.97%
    PRS 59.37
  • medium spiny neuron CL1001474
    CSI 3.42
    rCSI 29.51%
    PRS 67.61
  • cardiac endothelial cell CL0010008
    CSI 3.4
    rCSI 13.72%
    PRS 78.97
  • chandelier pvalb GABAergic cortical interneuron CL4023036
    CSI 3.39
    rCSI 10.61%
    PRS 65.36
  • respiratory suprabasal cell CL4033048
    CSI 3.15
    rCSI 4.04%
    PRS 82.68
  • alveolar type 1 fibroblast cell CL4028004
    CSI 3.15
    rCSI 3.45%
    PRS 81.36
  • melanocyte CL0000148
    CSI 3.02
    rCSI 2.23%
    PRS 72.88
  • choroid plexus epithelial cell CL0000706
    CSI 3
    rCSI 4.92%
    PRS 68.85
  • BEST4+ enteroycte CL4030026
    CSI 2.99
    rCSI 3.72%
    PRS 80.41
  • ciliated epithelial cell CL0000067
    CSI 2.99
    rCSI 2.63%
    PRS 68.5
  • mesodermal cell CL0000222
    CSI 2.93
    rCSI 3.52%
    PRS 77.03
  • cerebral cortex endothelial cell CL1001602
    CSI 2.93
    rCSI 5.07%
    PRS 70.9
  • cerebellar granule cell CL0001031
    CSI 2.93
    rCSI 4.3%
    PRS 72.35
  • plasmacytoid dendritic cell, human CL0001058
    CSI 2.92
    rCSI 2.04%
    PRS 82.6
  • precursor B cell CL0000817
    CSI 2.8
    rCSI 2.45%
    PRS 86.48
  • Mueller cell CL0000636
    CSI 2.68
    rCSI 6.12%
    PRS 70.86
  • neural crest cell CL0011012
    CSI 2.68
    rCSI 2.12%
    PRS 67.99
  • pancreatic A cell CL0000171
    CSI 2.67
    rCSI 2.8%
    PRS 82.68
  • neuroblast (sensu Vertebrata) CL0000031
    CSI 2.6
    rCSI 3.33%
    PRS 75.4
  • cerebral cortex GABAergic interneuron CL0010011
    CSI 2.56
    rCSI 7.56%
    PRS 80.3
  • type B pancreatic cell CL0000169
    CSI 2.55
    rCSI 5.65%
    PRS 78.65
  • sst GABAergic cortical interneuron CL4023017
    CSI 2.5
    rCSI 3.22%
    PRS 62.44
  • L5 extratelencephalic projecting glutamatergic cortical neuron CL4023041
    CSI 2.49
    rCSI 8.95%
    PRS 59.23
  • Kupffer cell CL0000091
    CSI 2.47
    rCSI 5.64%
    PRS 80.04
  • enteric smooth muscle cell CL0002504
    CSI 2.46
    rCSI 3.51%
    PRS 80.24
  • fibroblast of lung CL0002553
    CSI 2.45
    rCSI 2.28%
    PRS 80.11
  • VIP GABAergic cortical interneuron CL4023016
    CSI 2.44
    rCSI 2.92%
    PRS 61.43
  • pvalb GABAergic cortical interneuron CL4023018
    CSI 2.41
    rCSI 2.99%
    PRS 59.23
  • vascular leptomeningeal cell CL4023051
    CSI 2.41
    rCSI 4.22%
    PRS 73.02
  • perivascular cell CL4033054
    CSI 2.4
    rCSI 3.28%
    PRS 83.71
  • kidney interstitial alternatively activated macrophage CL1000695
    CSI 2.36
    rCSI 6.16%
    PRS 80.39
  • interneuron CL0000099
    CSI 2.33
    rCSI 4.67%
    PRS 69.48
  • pancreatic D cell CL0000173
    CSI 2.32
    rCSI 2.29%
    PRS 81.93
  • basal cell CL0000646
    CSI 2.31
    rCSI 3.09%
    PRS 78.12
  • stem cell CL0000034
    CSI 2.3
    rCSI 2.22%
    PRS 72.52
  • placental villous trophoblast CL2000060
    CSI 2.25
    rCSI 3.48%
    PRS 78.41
  • central memory CD8-positive, alpha-beta T cell CL0000907
    CSI 2.21
    rCSI 1.49%
    PRS 91.16
  • neuroblast (sensu Nematoda and Protostomia) CL0000338
    CSI 2.08
    rCSI 2.4%
    PRS 71.5
  • retinal blood vessel endothelial cell CL0002585
    CSI 2.06
    rCSI 3.29%
    PRS 83.06
  • chondrocyte CL0000138
    CSI 1.96
    rCSI 3.12%
    PRS 72.32
  • retina horizontal cell CL0000745
    CSI 1.95
    rCSI 2.98%
    PRS 76.27
  • early lymphoid progenitor CL0000936
    CSI 1.95
    rCSI 1.71%
    PRS 84.24
  • ependymal cell CL0000065
    CSI 1.93
    rCSI 3.92%
    PRS 57.9
  • fibroblast of cardiac tissue CL0002548
    CSI 1.9
    rCSI 9.1%
    PRS 79.34
  • bronchus fibroblast of lung CL2000093
    CSI 1.89
    rCSI 1.54%
    PRS 78.77
  • inhibitory interneuron CL0000498
    CSI 1.87
    rCSI 4.33%
    PRS 67.43
  • renal beta-intercalated cell CL0002201
    CSI 1.87
    rCSI 4.47%
    PRS 79.58
  • direct pathway medium spiny neuron CL4023026
    CSI 1.86
    rCSI 44.56%
    PRS 59.68
  • fallopian tube secretory epithelial cell CL4030006
    CSI 1.86
    rCSI 1.79%
    PRS 78.65
  • group 3 innate lymphoid cell CL0001071
    CSI 1.85
    rCSI 1.39%
    PRS 84.95
  • indirect pathway medium spiny neuron CL4023029
    CSI 1.79
    rCSI 43.15%
    PRS 60.25
  • granulocyte CL0000094
    CSI 1.78
    rCSI 2.72%
    PRS 86.48
  • Bergmann glial cell CL0000644
    CSI 1.77
    rCSI 2.42%
    PRS 71.16
  • vascular associated smooth muscle cell CL0000359
    CSI 1.74
    rCSI 5.64%
    PRS 77.5
  • CD14-low, CD16-positive monocyte CL0002396
    CSI 1.71
    rCSI 1.31%
    PRS 82.09
  • GABAergic neuron CL0000617
    CSI 1.7
    rCSI 5.71%
    PRS 63.41
  • extravillous trophoblast CL0008036
    CSI 1.67
    rCSI 2.07%
    PRS 77.18
  • retinal pigment epithelial cell CL0002586
    CSI 1.63
    rCSI 3.23%
    PRS 75.13
  • kidney loop of Henle thin ascending limb epithelial cell CL1001107
    CSI 1.62
    rCSI 4.19%
    PRS 74.72
  • retinal cone cell CL0000573
    CSI 1.58
    rCSI 2.55%
    PRS 69.35
  • sncg GABAergic cortical interneuron CL4023015
    CSI 1.52
    rCSI 2.45%
    PRS 63.01
  • lung secretory cell CL1000272
    CSI 1.51
    rCSI 3.73%
    PRS 78.94
  • kidney loop of Henle thin descending limb epithelial cell CL1001111
    CSI 1.5
    rCSI 2.12%
    PRS 76
  • intestinal crypt stem cell of small intestine CL0009017
    CSI 1.48
    rCSI 4%
    PRS 84.24
  • T-helper 1 cell CL0000545
    CSI 1.45
    rCSI 2.62%
    PRS 93.69
  • astrocyte of the cerebral cortex CL0002605
    CSI 1.4
    rCSI 3.13%
    PRS 62.11
  • caudal ganglionic eminence derived cortical interneuron CL4023064
    CSI 1.34
    rCSI 2.37%
    PRS 60.65
  • peripheral nervous system neuron CL2000032
    CSI 1.32
    rCSI 1.81%
    PRS 70.95
  • amacrine cell CL0000561
    CSI 1.3
    rCSI 3.77%
    PRS 68.87
  • parietal epithelial cell CL1000452
    CSI 1.3
    rCSI 3.47%
    PRS 71.07
  • glutamatergic neuron CL0000679
    CSI 1.18
    rCSI 2.42%
    PRS 67.06
  • L2/3 intratelencephalic projecting glutamatergic neuron CL4030059
    CSI 1.17
    rCSI 2.55%
    PRS 67.21
  • retinal bipolar neuron CL0000748
    CSI 1.17
    rCSI 2.19%
    PRS 67.73
  • retinal ganglion cell CL0000740
    CSI 1.14
    rCSI 2.52%
    PRS 65.16
  • L4 intratelencephalic projecting glutamatergic neuron CL4030063
    CSI 1.1
    rCSI 2.63%
    PRS 66.46
  • renal interstitial pericyte CL1001318
    CSI 1.08
    rCSI 2.98%
    PRS 74.4
  • alveolar adventitial fibroblast CL4028006
    CSI 1.01
    rCSI 1.59%
    PRS 81
  • neural progenitor cell CL0011020
    CSI 0.98
    rCSI 4.29%
    PRS 67.86
  • kidney connecting tubule epithelial cell CL1000768
    CSI 0.96
    rCSI 2.43%
    PRS 69.7
  • L5/6 near-projecting glutamatergic neuron CL4030067
    CSI 0.92
    rCSI 3.03%
    PRS 65.74
  • central nervous system neuron CL2000029
    CSI 0.88
    rCSI 6.46%
    PRS 66.79
  • paneth cell of epithelium of small intestine CL1000343
    CSI 0.84
    rCSI 2.35%
    PRS 86.46
  • lamp5 GABAergic cortical interneuron CL4023011
    CSI 0.81
    rCSI 1.35%
    PRS 61.32
  • stromal cell of ovary CL0002132
    CSI 0.69
    rCSI 1.88%
    PRS 86.24
  • blood vessel smooth muscle cell CL0019018
    CSI 0.65
    rCSI 5.25%
    PRS 73.44
  • dopaminergic neuron CL0000700
    CSI 0.62
    rCSI 3.48%
    PRS 65.45
  • podocyte CL0000653
    CSI 0.61
    rCSI 2.71%
    PRS 79.88
  • ON parasol ganglion cell CL4033052
    CSI 0.4
    rCSI 5.72%
    PRS 70.45

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.
Network Configuration

Explore relationships of the current gene. Select an Interaction Source: 'ONTOLOGY' for shared pathways (GO/Reactome) or 'STRING' for protein-protein interactions. Further refine by selecting context genes and comparing Cell Significance Index (CSI) scores between baseline and target cell types and their specific contexts.

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Comma-separated if multiple.

Legend:
  • Query Gene
  • Node Color (Target Cell CSI, relative to current network):
    • Very High
    • High
    • Medium
    • Low
    • Very Low
    • CSI N/A
  • Node Size: Proportional to Target Cell CSI magnitude
  • STRING PPI Edge
  • Shared Pathway Edge (ONTOLOGY)

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Other Information

This section provides additional information about the gene, including a description generated by an AI language model and details about associated proteins.

## Summary [PKNOX1](/details-gene/5316) (PBX/knotted 1 homeobox 1) is a protein-coding gene located on chromosome 21q22.3 that encodes a homeodomain-containing transcription factor. As a member of the TALE (three-amino-acid loop extension) class of homeodomain proteins, it functions as a critical regulator of gene expression, often by forming complexes with other transcription factors such as PBX proteins [Link](https://pubmed.ncbi.nlm.nih.gov/9479508/). Its primary molecular functions involve sequence-specific DNA binding ([GO:1990837](https://www.ebi.ac.uk/QuickGO/term/GO:1990837)) and positive regulation of transcription ([GO:0045944](https://www.ebi.ac.uk/QuickGO/term/GO:0045944)). **Overall**, expression data reveals that [PKNOX1](/details-gene/5316) has the highest significance in undifferentiated '[progenitor cell](/details-cell/CL0011026)s' (CSI: 10.02), as well as in diverse specialized cell types including '[mesothelial cell](/details-cell/CL0000077)s', and various classes of '[near-projecting glutamatergic cortical neuron](/details-cell/CL4023012)s'. This expression pattern, combined with its established role in activating HOX genes during development, underscores its importance in cellular differentiation and lineage specification across multiple tissues. Clinical associations are noted under OMIM entry `[602100](https://omim.org/entry/602100)`. ## Cellular Roles and Expression Landscape The expression profile of [PKNOX1](/details-gene/5316) suggests a fundamental role in establishing and maintaining cellular identity across diverse lineages. Its most significant expression is observed in '[progenitor cell](/details-cell/CL0011026)s', which is consistent with its function as a developmental transcription factor. Beyond this, it shows high significance in various differentiated cell types, indicating a continued role in cell state maintenance. Functionally, these cells can be grouped into several categories: * **Development and Tissue Structure:** High significance in '[progenitor cell](/details-cell/CL0011026)s', '[mesothelial cell](/details-cell/CL0000077)s', '[stromal cell](/details-cell/CL0000499)s', and '[alveolar type 1 fibroblast cell](/details-cell/CL4028004)s' points to a role in development, tissue scaffolding, and organ maintenance. * **Neuronal Identity:** [PKNOX1](/details-gene/5316) appears to be a key marker for specific neuronal subtypes, particularly glutamatergic neurons in the cortex, including '[near-projecting glutamatergic cortical neuron](/details-cell/CL4023012)s', '[L6b glutamatergic cortical neuron](/details-cell/CL4023038)s', and '[corticothalamic-projecting glutamatergic cortical neuron](/details-cell/CL4023013)s'. Its presence in '[medium spiny neuron](/details-cell/CL1001474)s' and '[chandelier pvalb GABAergic cortical interneuron](/details-cell/CL4023036)s' further supports a broad, but specific, role in neuronal function and subtype specification. * **Epithelial and Endothelial Function:** Significant expression in '[epithelial cell of proximal tubule](/details-cell/CL0002306)s', '[lung ciliated cell](/details-cell/CL1000271)s', and '[cardiac endothelial cell](/details-cell/CL0010008)s' suggests its involvement in the function of specialized barrier and transport tissues. **Overall**, the broad yet specific expression pattern highlights [PKNOX1](/details-gene/5316) as a key transcriptional regulator involved in both the initial commitment of progenitor cells and the subsequent maintenance of terminally differentiated cell states, particularly within the nervous system and in structural tissues. ## Pathways and Molecular Function [PKNOX1](/details-gene/5316) is a nuclear ([GO:0005634](https://www.ebi.ac.uk/QuickGO/term/GO:0005634)) and cytoplasmic ([GO:0005737](https://www.ebi.ac.uk/QuickGO/term/GO:0005737)) protein that functions primarily as a DNA-binding transcription factor ([GO:0003700](https://www.ebi.ac.uk/QuickGO/term/GO:0003700)). It binds to chromatin ([GO:0003682](https://www.ebi.ac.uk/QuickGO/term/GO:0003682)) and specifically recognizes cis-regulatory regions to regulate RNA polymerase II-driven transcription ([GO:0000978](https://www.ebi.ac.uk/QuickGO/term/GO:0000978)). Its involvement in high-level developmental processes is well-annotated. The Reactome pathway database highlights its role in '[Developmental Biology](/details-pathway/R-HSA-1266738)' and more specifically in the '[Activation of HOX genes during differentiation](/details-pathway/R-HSA-5619507)'. This function is consistent with its high expression in '[progenitor cell](/details-cell/CL0011026)s', where precise control of developmental gene programs is critical for lineage determination. Gene Ontology annotations also point to roles in more specific differentiation programs, including '[T cell differentiation](/details-cell/GO:0030217)', '[erythrocyte differentiation](/details-cell/GO:0030218)', '[angiogenesis](/details-cell/GO:0001525)', and '[camera-type eye development](/details-cell/GO:0043010)'. Although these cell types are not among the top-ranked in the **Overall** context, these annotations suggest that the function of [PKNOX1](/details-gene/5316) is highly context-dependent, playing specialized roles during the development of multiple organ systems. ## Research Directions The available data highlights [PKNOX1](/details-gene/5316) as a key transcriptional regulator in development and cell identity. Future research should focus on elucidating its specific downstream targets and regulatory networks in different cellular contexts. **Testable Hypotheses:** 1. Given its high expression in multiple glutamatergic neuron subtypes and its role as a transcription factor, [PKNOX1](/details-gene/5316) is essential for the specification and maintenance of cortical glutamatergic neuron identity by directly regulating the expression of genes involved in synaptic function and neurotransmission. 2. Based on its high significance in '[progenitor cell](/details-cell/CL0011026)s' and its known function in regulating HOX genes, dysregulation of [PKNOX1](/details-gene/5316) expression contributes to developmental defects or oncogenesis by disrupting the normal differentiation trajectories of stem and progenitor cell populations. **Proposed Key Experiment:** To test the first hypothesis regarding the role of [PKNOX1](/details-gene/5316) in neuronal identity, a multi-modal approach could be used. CRISPR-Cas9-mediated knockout of [PKNOX1](/details-gene/5316) could be performed in human induced pluripotent stem cells (iPSCs), which would then be subjected to directed differentiation protocols to generate cortical neurons. Single-cell RNA sequencing (scRNA-seq) and ATAC-seq on both knockout and wild-type organoids or cultures would reveal changes in cell type composition and chromatin accessibility. Concurrently, CUT&RUN sequencing for PKNOX1 in wild-type cortical neurons would identify its direct genomic binding sites, allowing for the correlation of target gene occupancy with the expression changes observed upon its deletion. **Therapeutic Potential:** As a nuclear transcription factor, [PKNOX1](/details-gene/5316) represents a challenging therapeutic target for direct inhibition or activation with small molecules. However, its crucial role in defining cellular identity suggests that modulating its activity could be beneficial in contexts of developmental disease or cancer. Given its location on chromosome 21, its dosage may be relevant to pathologies associated with aneuploidy. Rather than targeting [PKNOX1](/details-gene/5316) itself, a more viable strategy may be to identify and target its critical downstream effectors, which could be more druggable enzymes or cell-surface proteins. Understanding its protein-protein interactions, particularly with PBX family members, may also reveal interfaces that could be targeted to modulate its transcriptional activity in a disease-specific manner.

Genular Protein ID: 1203806922

Symbol: PKNX1_HUMAN

Name: Homeobox protein PKNOX1

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 9143494

Title: Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3.

PubMed ID: 9143494

DOI: 10.1006/geno.1997.4632

PubMed ID: 9479508

Title: PKNOX1, a gene encoding PREP1, a new regulator of Pbx activity, maps on human chromosome 21q22.3 and murine chromosome 17B/C.

PubMed ID: 9479508

DOI: 10.1006/geno.1997.5086

PubMed ID: 15468914

Title: Molecular cloning for an alternatively splicing cDNA of human PKNOX1 gene and it's expression analysis.

PubMed ID: 15468914

PubMed ID: 10830953

Title: The DNA sequence of human chromosome 21.

PubMed ID: 10830953

DOI: 10.1038/35012518

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

PubMed ID: 31839203

Title: Gain-of-function MN1 truncation variants cause a recognizable syndrome with craniofacial and brain abnormalities.

PubMed ID: 31839203

DOI: 10.1016/j.ajhg.2019.11.011

PubMed ID: 16959974

Title: The consensus coding sequences of human breast and colorectal cancers.

PubMed ID: 16959974

DOI: 10.1126/science.1133427

Sequence Information:

  • Length: 436
  • Mass: 47607
  • Checksum: 381E901F435AC5F2
  • Sequence:
  • MMATQTLSID SYQDGQQMQV VTELKTEQDP NCSEPDAEGV SPPPVESQTP MDVDKQAIYR 
    HPLFPLLALL FEKCEQSTQG SEGTTSASFD VDIENFVRKQ EKEGKPFFCE DPETDNLMVK 
    AIQVLRIHLL ELEKVNELCK DFCSRYIACL KTKMNSETLL SGEPGSPYSP VQSQQIQSAI 
    TGTISPQGIV VPASALQQGN VAMATVAGGT VYQPVTVVTP QGQVVTQTLS PGTIRIQNSQ 
    LQLQLNQDLS ILHQDDGSSK NKRGVLPKHA TNVMRSWLFQ HIGHPYPTED EKKQIAAQTN 
    LTLLQVNNWF INARRRILQP MLDSSCSETP KTKKKTAQNR PVQRFWPDSI ASGVAQPPPS 
    ELTMSEGAVV TITTPVNMNV DSLQSLSSDG ATLAVQQVMM AGQSEDESVD STEEDAGALA 
    PAHISGLVLE NSDSLQ

Genular Protein ID: 3255815686

Symbol: E7EPN6_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 10830953

Title: The DNA sequence of human chromosome 21.

PubMed ID: 10830953

DOI: 10.1038/35012518

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

Sequence Information:

  • Length: 319
  • Mass: 34519
  • Checksum: D0D47039D1B45670
  • Sequence:
  • MVKAIQVLRI HLLELEKVNE LCKDFCSRYI ACLKTKMNSE TLLSGEPGSP YSPVQSQQIQ 
    SAITGTISPQ GIVVPASALQ QGNVAMATVA GGTVYQPVTV VTPQGQVVTQ TLSPGTIRIQ 
    NSQLQLQLNQ DLSILHQDDG SSKNKRGVLP KHATNVMRSW LFQHIGHPYP TEDEKKQIAA 
    QTNLTLLQVN NWFINARRRI LQPMLDSSCS ETPKTKKKTA QNRPVQRFWP DSIASGVAQP 
    PPSELTMSEG AVVTITTPVN MNVDSLQSLS SDGATLAVQQ VMMAGQSEDE SVDSTEEDAG 
    ALAPAHISGL VLENSDSLQ

Genular Protein ID: 1512031010

Symbol: B4DGV5_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 319
  • Mass: 34547
  • Checksum: 54463854676F3B36
  • Sequence:
  • MVKAIQVLRI HLLELEKVNE LCKDFCSRYI ACLKTKMNSE TLLSGEPGSP YSPVQSQQIQ 
    SAITGTISPQ GIVVPASALQ RGNVAMATVA GGTVYQPVTV VTPQGQVVTQ TLSPGTIRIQ 
    NSQLQLQLNQ DLSILHQDDG SSKNKRGVLP KHATNVMRSW LFQHIGHPYP TEDEKKQIAA 
    QTNLTLLQVN NWFINARRRI LQPMLDSSCS ETPKTKKKTA QNRPVQRFWP DSIASGVAQP 
    PPSELTMSEG AVVTITTPVN MNVDSLQSLS SDGATLAVQQ VMMAGQSEDE SVDSTEEDAG 
    ALAPAHISGL VLENSDSLQ

Genular Protein ID: 2663857688

Symbol: Q6PKH2_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

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

Sequence Information:

  • Length: 336
  • Mass: 37296
  • Checksum: 7CDB474D4C3A455B
  • Sequence:
  • MMATQTLSID SYQDGQQMQV VTELKTEQDP NCSEPDAEGV SPPPVESQTP MDVDKQAIYR 
    HPLFPLLALL FEKCEQSTQG SEGTTSASFD VDIENFVRKQ EKEGKPFFCE DPETDNLMVK 
    AIQVLRIHLL ELEKVNELCK DFCSRYIACL KTKMNSETLL SGEPGSPYSP VQSQQIQSAI 
    TGTISPQGIV VPASALQQGN VAMATVAGGT VYQPVTVVTP QGQVVTQTLS PGTIRIQNSQ 
    LQLQLNQDLS ILHQDDGSSK NKRGVLPKHA TNVMRSWLFQ HIGHPYPTED EKKQIAAQTN 
    LTLLQVNNWF INARRRILQP MLDSSCSETP KKKKKK