Details for: FHL1

Gene ID: 2273

Symbol: FHL1

Ensembl ID: ENSG00000022267

Description: four and a half LIM domains 1

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: 319.0069
    Cell Significance Index: -49.6200
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 159.3182
    Cell Significance Index: -40.4100
  • Cell Name: smooth muscle fiber of ileum (CL1000278)
    Fold Change: 91.6076
    Cell Significance Index: -43.2500
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 84.1339
    Cell Significance Index: -34.1800
  • Cell Name: peripheral blood mononuclear cell (CL2000001)
    Fold Change: 77.1406
    Cell Significance Index: -39.6800
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 40.3015
    Cell Significance Index: -49.6900
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 35.8631
    Cell Significance Index: -34.2400
  • Cell Name: CD8-alpha-beta-positive, alpha-beta intraepithelial T cell (CL0000796)
    Fold Change: 16.3652
    Cell Significance Index: -43.8400
  • Cell Name: type II muscle cell (CL0002212)
    Fold Change: 14.7727
    Cell Significance Index: 238.3600
  • Cell Name: type I muscle cell (CL0002211)
    Fold Change: 14.6295
    Cell Significance Index: 356.9500
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 12.5011
    Cell Significance Index: -49.3300
  • Cell Name: pulmonary interstitial fibroblast (CL0002241)
    Fold Change: 10.0303
    Cell Significance Index: 62.0600
  • Cell Name: CD8-positive, alpha-beta regulatory T cell (CL0000795)
    Fold Change: 7.9474
    Cell Significance Index: -24.4100
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: 5.0695
    Cell Significance Index: 130.3100
  • Cell Name: enteric smooth muscle cell (CL0002504)
    Fold Change: 4.9753
    Cell Significance Index: 26.1800
  • Cell Name: adipocyte of breast (CL0002617)
    Fold Change: 4.8617
    Cell Significance Index: 61.2200
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 3.1299
    Cell Significance Index: 240.1800
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: 1.9209
    Cell Significance Index: 28.3600
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 1.8988
    Cell Significance Index: 380.9000
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: 1.6603
    Cell Significance Index: 87.1700
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: 1.6002
    Cell Significance Index: 45.8700
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: 1.5863
    Cell Significance Index: 30.9600
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 1.2829
    Cell Significance Index: 164.4600
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 1.2730
    Cell Significance Index: 85.6000
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.8539
    Cell Significance Index: 117.2700
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.8501
    Cell Significance Index: 304.9200
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: 0.7776
    Cell Significance Index: 50.1700
  • Cell Name: vascular lymphangioblast (CL0005022)
    Fold Change: 0.6881
    Cell Significance Index: 12.1600
  • Cell Name: leptomeningeal cell (CL0000708)
    Fold Change: 0.6297
    Cell Significance Index: 13.4600
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: 0.5394
    Cell Significance Index: 11.2900
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: 0.5288
    Cell Significance Index: 32.5100
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: 0.2996
    Cell Significance Index: 135.9600
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: 0.2932
    Cell Significance Index: 4.2100
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.2559
    Cell Significance Index: 113.1300
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: 0.2315
    Cell Significance Index: 16.3700
  • Cell Name: microcirculation associated smooth muscle cell (CL0008035)
    Fold Change: 0.2250
    Cell Significance Index: 1.8900
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.1400
    Cell Significance Index: 263.6000
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: 0.1377
    Cell Significance Index: 3.9300
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.0789
    Cell Significance Index: 3.4900
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.0384
    Cell Significance Index: 24.4100
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0348
    Cell Significance Index: 47.3300
  • Cell Name: subcutaneous adipocyte (CL0002521)
    Fold Change: 0.0138
    Cell Significance Index: 0.0600
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0079
    Cell Significance Index: 12.1000
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.0023
    Cell Significance Index: 2.1200
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: -0.0088
    Cell Significance Index: -0.2100
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0137
    Cell Significance Index: -8.5800
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: -0.0148
    Cell Significance Index: -0.5600
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: -0.0154
    Cell Significance Index: -28.3200
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0194
    Cell Significance Index: -14.3500
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.0356
    Cell Significance Index: -2.0000
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: -0.0380
    Cell Significance Index: -1.3200
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: -0.0428
    Cell Significance Index: -7.7100
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0476
    Cell Significance Index: -26.8400
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0496
    Cell Significance Index: -36.4000
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0600
    Cell Significance Index: -45.4200
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.0651
    Cell Significance Index: -1.0900
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: -0.0783
    Cell Significance Index: -42.7500
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: -0.0876
    Cell Significance Index: -16.6700
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: -0.0907
    Cell Significance Index: -14.7500
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.1071
    Cell Significance Index: -22.5500
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: -0.1208
    Cell Significance Index: -2.0700
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.1291
    Cell Significance Index: -37.1500
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.1542
    Cell Significance Index: -26.3300
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.1591
    Cell Significance Index: -23.1200
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.1622
    Cell Significance Index: -8.4500
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.1646
    Cell Significance Index: -17.1400
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.1830
    Cell Significance Index: -6.4300
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: -0.1849
    Cell Significance Index: -20.1100
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: -0.1890
    Cell Significance Index: -23.2400
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: -0.1953
    Cell Significance Index: -19.3200
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.2055
    Cell Significance Index: -20.9900
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: -0.2162
    Cell Significance Index: -42.9100
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: -0.2923
    Cell Significance Index: -6.4000
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: -0.3003
    Cell Significance Index: -18.0300
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.3149
    Cell Significance Index: -40.6800
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: -0.3221
    Cell Significance Index: -9.2800
  • Cell Name: pancreatic endocrine cell (CL0008024)
    Fold Change: -0.3290
    Cell Significance Index: -37.5500
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.3487
    Cell Significance Index: -39.9500
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.3492
    Cell Significance Index: -40.7000
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.3536
    Cell Significance Index: -41.7000
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: -0.3654
    Cell Significance Index: -25.2700
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.3939
    Cell Significance Index: -17.8600
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -0.4030
    Cell Significance Index: -25.4000
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.4117
    Cell Significance Index: -25.2400
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.4310
    Cell Significance Index: -8.9400
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.4694
    Cell Significance Index: -37.1800
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.5312
    Cell Significance Index: -39.5900
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.5595
    Cell Significance Index: -17.9200
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.5600
    Cell Significance Index: -26.3200
  • Cell Name: keratocyte (CL0002363)
    Fold Change: -0.5733
    Cell Significance Index: -9.1000
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.6113
    Cell Significance Index: -7.5800
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.6571
    Cell Significance Index: -14.2400
  • Cell Name: fallopian tube secretory epithelial cell (CL4030006)
    Fold Change: -0.6690
    Cell Significance Index: -10.3500
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.6999
    Cell Significance Index: -19.5600
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: -0.7483
    Cell Significance Index: -18.7100
  • Cell Name: granulosa cell (CL0000501)
    Fold Change: -0.7876
    Cell Significance Index: -20.7100
  • Cell Name: regular ventricular cardiac myocyte (CL0002131)
    Fold Change: -0.7900
    Cell Significance Index: -10.1300
  • Cell Name: CD4-positive, alpha-beta memory T cell, CD45RO-positive (CL0001204)
    Fold Change: -0.8216
    Cell Significance Index: -24.1300
  • Cell Name: skeletal muscle myoblast (CL0000515)
    Fold Change: -0.8499
    Cell Significance Index: -9.2400
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.8570
    Cell Significance Index: -44.5200

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:** The FHL1 gene is characterized by its unique four and a half LIM domains, which are involved in protein-protein interactions and the regulation of cellular processes. These domains are also known to be involved in the regulation of transcription factors and other signaling molecules. FHL1 is highly expressed in various cell types, including muscle cells, smooth muscle cells, and fibroblasts, and is involved in regulating cell growth, differentiation, and survival. The gene is also implicated in the regulation of ion channels and transporters, including potassium channels and transporters. **Pathways and Functions:** FHL1 is involved in several cellular pathways, including: 1. **Negative regulation of cell growth**: FHL1 acts as a tumor suppressor by regulating cell growth and proliferation. 2. **Cell differentiation**: FHL1 regulates cell differentiation by interacting with transcription factors and other signaling molecules. 3. **Molecular_function**: FHL1 regulates the activity of molecular functions, including ion channels and transporters. 4. **Regulation of membrane depolarization**: FHL1 regulates membrane depolarization by interacting with ion channels and transporters. 5. **Regulation of potassium ion transport**: FHL1 regulates potassium ion transport by interacting with potassium channels and transporters. **Clinical Significance:** Dysregulation of FHL1 has been implicated in various diseases, including: 1. **Cancer**: Abnormal expression of FHL1 has been associated with cancer, including breast cancer, lung cancer, and colon cancer. 2. **Cardiovascular disorders**: FHL1 is involved in the regulation of ion channels and transporters, and dysregulation of FHL1 has been implicated in cardiovascular disorders, including hypertension and cardiac arrhythmias. 3. **Muscle disorders**: FHL1 is highly expressed in muscle cells, and dysregulation of FHL1 has been implicated in muscle disorders, including muscular dystrophy and myasthenia gravis. In conclusion, the FHL1 gene is a critical regulator of cellular functions and tissue development, and its dysregulation has been implicated in various diseases. Further research is needed to fully understand the role of FHL1 in human health and disease.

Genular Protein ID: 3901787642

Symbol: FHL1_HUMAN

Name: Four and a half LIM domains protein 1

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 8753811

Title: Slim defines a novel family of LIM-proteins expressed in skeletal muscle.

PubMed ID: 8753811

DOI: 10.1006/bbrc.1996.1222

PubMed ID: 9714789

Title: Chromosomal mapping, tissue distribution and cDNA sequence of four-and-a-half LIM domain protein 1 (FHL1).

PubMed ID: 9714789

DOI: 10.1016/s0378-1119(98)00302-3

PubMed ID: 10352231

Title: Genomic structure, tissue expression and chromosomal location of the LIM-only gene, SLIM1.

PubMed ID: 10352231

DOI: 10.1016/s0378-1119(99)00125-0

PubMed ID: 10524257

Title: Characterization of a brain-specific nuclear LIM domain protein (FHL1B) which is an alternatively spliced variant of FHL1.

PubMed ID: 10524257

DOI: 10.1016/s0378-1119(99)00251-6

PubMed ID: 10480922

Title: Characterization of two isoforms of the skeletal muscle LIM protein 1, SLIM1. Localization of SLIM1 at focal adhesions and the isoform slimmer in the nucleus of myoblasts and cytoplasm of myotubes suggests distinct roles in the cytoskeleton and in nuclear-cytoplasmic communication.

PubMed ID: 10480922

DOI: 10.1074/jbc.274.38.27083

PubMed ID: 11400158

Title: Characterization of tissue-specific LIM domain protein (FHL1C) which is an alternatively spliced isoform of a human LIM-only protein (FHL1).

PubMed ID: 11400158

DOI: 10.1002/jcb.1110

PubMed ID: 14702039

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

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15772651

Title: The DNA sequence of the human X chromosome.

PubMed ID: 15772651

DOI: 10.1038/nature03440

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: 7626119

Title: The developmental regulation of a novel muscle LIM-protein.

PubMed ID: 7626119

DOI: 10.1006/bbrc.1995.2045

PubMed ID: 12665801

Title: Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides.

PubMed ID: 12665801

DOI: 10.1038/nbt810

PubMed ID: 19608861

Title: Lysine acetylation targets protein complexes and co-regulates major cellular functions.

PubMed ID: 19608861

DOI: 10.1126/science.1175371

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 25218447

Title: Uncovering global SUMOylation signaling networks in a site-specific manner.

PubMed ID: 25218447

DOI: 10.1038/nsmb.2890

PubMed ID: 26933038

Title: Exome sequencing identified a splice site mutation in FHL1 that causes Uruguay Syndrome, an X-linked disorder with skeletal muscle hypertrophy and premature cardiac death.

PubMed ID: 26933038

DOI: 10.1161/circgenetics.115.001193

PubMed ID: 18179888

Title: An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1.

PubMed ID: 18179888

DOI: 10.1016/j.ajhg.2007.09.004

PubMed ID: 18179901

Title: X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.

PubMed ID: 18179901

DOI: 10.1016/j.ajhg.2007.09.013

PubMed ID: 18274675

Title: Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.

PubMed ID: 18274675

DOI: 10.1172/jci34450

PubMed ID: 19716112

Title: Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy.

PubMed ID: 19716112

DOI: 10.1016/j.ajhg.2009.07.015

PubMed ID: 19181672

Title: Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.

PubMed ID: 19181672

DOI: 10.1093/brain/awn325

PubMed ID: 31554973

Title: FHL1 is a major host factor for chikungunya virus infection.

PubMed ID: 31554973

DOI: 10.1038/s41586-019-1578-4

PubMed ID: 33055253

Title: Structural and Functional Characterization of Host FHL1 Protein Interaction with Hypervariable Domain of Chikungunya Virus nsP3 Protein.

PubMed ID: 33055253

DOI: 10.1128/jvi.01672-20

PubMed ID: 19171836

Title: Novel FHL1 mutations in fatal and benign reducing body myopathy.

PubMed ID: 19171836

DOI: 10.1212/01.wnl.0000341311.84347.a0

PubMed ID: 19687455

Title: Consequences of mutations within the C terminus of the FHL1 gene.

PubMed ID: 19687455

DOI: 10.1212/wnl.0b013e3181b2a4b3

PubMed ID: 20186852

Title: Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation.

PubMed ID: 20186852

DOI: 10.1002/ana.21839

PubMed ID: 23169582

Title: Novel FHL1 mutation in a family with reducing body myopathy.

PubMed ID: 23169582

DOI: 10.1002/mus.23500

PubMed ID: 27234031

Title: Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population.

PubMed ID: 27234031

DOI: 10.1111/cge.12810

Sequence Information:

  • Length: 323
  • Mass: 36263
  • Checksum: 50FD17F7B2606823
  • Sequence:
  • MAEKFDCHYC RDPLQGKKYV QKDGHHCCLK CFDKFCANTC VECRKPIGAD SKEVHYKNRF 
    WHDTCFRCAK CLHPLANETF VAKDNKILCN KCTTREDSPK CKGCFKAIVA GDQNVEYKGT 
    VWHKDCFTCS NCKQVIGTGS FFPKGEDFYC VTCHETKFAK HCVKCNKAIT SGGITYQDQP 
    WHADCFVCVT CSKKLAGQRF TAVEDQYYCV DCYKNFVAKK CAGCKNPITG KRTVSRVSHP 
    VSKARKPPVC HGKRLPLTLF PSANLRGRHP GGERTCPSWV VVLYRKNRSL AAPRGPGLVK 
    APVWWPMKDN PGTTTASTAK NAP

Genular Protein ID: 1941463317

Symbol: Q5JXI2_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

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: 15772651

Title: The DNA sequence of the human X chromosome.

PubMed ID: 15772651

DOI: 10.1038/nature03440

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 25218447

Title: Uncovering global SUMOylation signaling networks in a site-specific manner.

PubMed ID: 25218447

Sequence Information:

  • Length: 210
  • Mass: 23701
  • Checksum: 2C54446BBABB394B
  • Sequence:
  • MASHRHSGPS SYKVGTMAEK FDCHYCRDPL QGKKYVQKDG HHCCLKCFDK FCANTCVECR 
    KPIGADSKEV HYKNRFWHDT CFRCAKCLHP LANETFVAKD NKILCNKCTT REDSPKCKGC 
    FKAIVAGDQN VEYKGTVWHK DCFTCSNCKQ VIGTGSFFPK GEDFYCVTCH ETKFAKHCVK 
    CNKGLVKAPV WWPMKDNPGT TTASTAKNAP

Genular Protein ID: 3728444563

Symbol: B7Z9A1_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 319
  • Mass: 36203
  • Checksum: DDE5223FAC920CBD
  • Sequence:
  • MCEFLRHLGS CFQPYPAFAE YILSATHPAW GPSSYKVGTM AEKFDCHYCR DPLQGKKYVQ 
    KDGHHCCLKC FDKFCANTCV ECRKPIGADS KEVHYKNRFW HDTCFRCAKC LHPSANETFV 
    AKDNKILCNK CTTREDSPKC KGCFKATVAG DQNVEYKGTV WHKDCFTCSN CKQVIGTGSF 
    FPKGEDFYCV TCHETKFAKH CVKCNKAITS GGITYQDQPW HADCFVCVTC SKKLAGQRFT 
    AVEDQYYCVD CYKNFVAKKC AGCKNPITGF GKGSSVVAYE GQSWHDYCFH CKKCSVNLAN 
    KRFVFHQEQV YCPDCAKKL

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.