Details for: GRIN2A
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: smooth muscle fiber of ileum (CL1000278)
Fold Change: 129.0131
Cell Significance Index: -60.9100 - Cell Name: hippocampal granule cell (CL0001033)
Fold Change: 6.5139
Cell Significance Index: 438.0000 - Cell Name: hippocampal pyramidal neuron (CL1001571)
Fold Change: 5.9090
Cell Significance Index: 168.6300 - Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
Fold Change: 5.1261
Cell Significance Index: 1838.6300 - Cell Name: epidermal Langerhans cell (CL0002457)
Fold Change: 4.2059
Cell Significance Index: -9.2100 - Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
Fold Change: 3.5140
Cell Significance Index: 704.9000 - Cell Name: L6 intratelencephalic projecting glutamatergic neuron of the primary motor cortex (CL4023050)
Fold Change: 3.3734
Cell Significance Index: 45.0000 - Cell Name: indirect pathway medium spiny neuron (CL4023029)
Fold Change: 2.6661
Cell Significance Index: 117.9300 - Cell Name: hippocampal interneuron (CL1001569)
Fold Change: 2.4590
Cell Significance Index: 31.8900 - Cell Name: GABAergic amacrine cell (CL4030027)
Fold Change: 2.4324
Cell Significance Index: 30.1700 - Cell Name: direct pathway medium spiny neuron (CL4023026)
Fold Change: 2.2008
Cell Significance Index: 83.3400 - Cell Name: forebrain neuroblast (CL1000042)
Fold Change: 2.0765
Cell Significance Index: 127.6300 - Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
Fold Change: 1.8746
Cell Significance Index: 1190.5500 - Cell Name: pyramidal neuron (CL0000598)
Fold Change: 1.5150
Cell Significance Index: 11.6200 - Cell Name: GABAergic interneuron (CL0011005)
Fold Change: 1.4567
Cell Significance Index: 1007.4900 - Cell Name: cerebral cortex neuron (CL0010012)
Fold Change: 1.4325
Cell Significance Index: 13.6300 - Cell Name: corneal epithelial cell (CL0000575)
Fold Change: 1.4036
Cell Significance Index: 19.9800 - Cell Name: cortical interneuron (CL0008031)
Fold Change: 1.0328
Cell Significance Index: 24.7700 - Cell Name: cerebellar granule cell (CL0001031)
Fold Change: 0.7790
Cell Significance Index: 13.3500 - Cell Name: pigmented epithelial cell (CL0000529)
Fold Change: 0.6825
Cell Significance Index: 1285.0400 - Cell Name: enteroendocrine cell of colon (CL0009042)
Fold Change: 0.6664
Cell Significance Index: 126.8200 - Cell Name: tuft cell of colon (CL0009041)
Fold Change: 0.3972
Cell Significance Index: 358.6300 - Cell Name: anterior lens cell (CL0002223)
Fold Change: 0.3394
Cell Significance Index: 625.9100 - Cell Name: L6 corticothalamic-projecting glutamatergic cortical neuron (CL4023042)
Fold Change: 0.2493
Cell Significance Index: 2.7500 - Cell Name: ciliary muscle cell (CL1000443)
Fold Change: 0.2226
Cell Significance Index: 101.0100 - Cell Name: colon goblet cell (CL0009039)
Fold Change: 0.1972
Cell Significance Index: 19.5100 - Cell Name: lens epithelial cell (CL0002224)
Fold Change: 0.0535
Cell Significance Index: 82.3300 - Cell Name: epithelial cell of small intestine (CL0002254)
Fold Change: -0.0116
Cell Significance Index: -1.8900 - Cell Name: secondary lens fiber (CL0002225)
Fold Change: -0.0136
Cell Significance Index: -18.5500 - Cell Name: small intestine goblet cell (CL1000495)
Fold Change: -0.0421
Cell Significance Index: -1.4800 - Cell Name: skeletal muscle fiber (CL0008002)
Fold Change: -0.0619
Cell Significance Index: -1.5900 - Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
Fold Change: -0.0773
Cell Significance Index: -1.6400 - Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
Fold Change: -0.0788
Cell Significance Index: -57.7900 - Cell Name: pancreatic A cell (CL0000171)
Fold Change: -0.0806
Cell Significance Index: -59.7300 - Cell Name: cell in vitro (CL0001034)
Fold Change: -0.0976
Cell Significance Index: -53.3200 - Cell Name: type B pancreatic cell (CL0000169)
Fold Change: -0.1021
Cell Significance Index: -57.5700 - Cell Name: hair follicular keratinocyte (CL2000092)
Fold Change: -0.1040
Cell Significance Index: -45.9800 - Cell Name: sst GABAergic cortical interneuron (CL4023017)
Fold Change: -0.1062
Cell Significance Index: -2.1000 - Cell Name: pancreatic PP cell (CL0002275)
Fold Change: -0.1065
Cell Significance Index: -66.5300 - Cell Name: OFF midget ganglion cell (CL4033047)
Fold Change: -0.1091
Cell Significance Index: -1.3600 - Cell Name: intestinal tuft cell (CL0019032)
Fold Change: -0.1169
Cell Significance Index: -7.1700 - Cell Name: pigmented ciliary epithelial cell (CL0002303)
Fold Change: -0.1185
Cell Significance Index: -17.2200 - Cell Name: enterocyte of epithelium of small intestine (CL1000334)
Fold Change: -0.1378
Cell Significance Index: -3.9700 - Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
Fold Change: -0.1494
Cell Significance Index: -2.1400 - Cell Name: VIP GABAergic cortical interneuron (CL4023016)
Fold Change: -0.1611
Cell Significance Index: -3.2400 - Cell Name: glutamatergic neuron (CL0000679)
Fold Change: -0.1634
Cell Significance Index: -1.7800 - Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
Fold Change: -0.1725
Cell Significance Index: -4.8200 - Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
Fold Change: -0.1735
Cell Significance Index: -18.0700 - Cell Name: dopaminergic neuron (CL0000700)
Fold Change: -0.1791
Cell Significance Index: -51.5300 - Cell Name: neoplastic cell (CL0001063)
Fold Change: -0.2116
Cell Significance Index: -42.0000 - Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
Fold Change: -0.2175
Cell Significance Index: -4.7000 - Cell Name: intestinal crypt stem cell of colon (CL0009043)
Fold Change: -0.2194
Cell Significance Index: -23.8600 - Cell Name: intermediate cell of urothelium (CL4030055)
Fold Change: -0.2465
Cell Significance Index: -44.4300 - Cell Name: enteroendocrine cell of small intestine (CL0009006)
Fold Change: -0.2550
Cell Significance Index: -6.3800 - Cell Name: pancreatic D cell (CL0000173)
Fold Change: -0.3019
Cell Significance Index: -63.5900 - Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
Fold Change: -0.3124
Cell Significance Index: -9.9500 - Cell Name: enterocyte of epithelium of large intestine (CL0002071)
Fold Change: -0.3228
Cell Significance Index: -14.6300 - Cell Name: eukaryotic cell (CL0000255)
Fold Change: -0.3319
Cell Significance Index: -14.4300 - Cell Name: pancreatic acinar cell (CL0002064)
Fold Change: -0.3420
Cell Significance Index: -58.3900 - Cell Name: cardiac muscle myoblast (CL0000513)
Fold Change: -0.3522
Cell Significance Index: -27.0300 - Cell Name: basal cell of urothelium (CL1000486)
Fold Change: -0.3758
Cell Significance Index: -46.2100 - Cell Name: stromal cell of ovary (CL0002132)
Fold Change: -0.4292
Cell Significance Index: -58.9400 - Cell Name: epithelial cell of stomach (CL0002178)
Fold Change: -0.4456
Cell Significance Index: -51.9300 - Cell Name: lactocyte (CL0002325)
Fold Change: -0.4506
Cell Significance Index: -58.2100 - Cell Name: ON midget ganglion cell (CL4033046)
Fold Change: -0.4659
Cell Significance Index: -5.8800 - Cell Name: odontoblast (CL0000060)
Fold Change: -0.4698
Cell Significance Index: -60.2300 - Cell Name: pancreatic ductal cell (CL0002079)
Fold Change: -0.5192
Cell Significance Index: -59.4800 - Cell Name: microfold cell of epithelium of small intestine (CL1000353)
Fold Change: -0.5299
Cell Significance Index: -36.6500 - Cell Name: tonsil germinal center B cell (CL2000006)
Fold Change: -0.5310
Cell Significance Index: -62.6200 - Cell Name: abnormal cell (CL0001061)
Fold Change: -0.5653
Cell Significance Index: -57.7500 - Cell Name: neural cell (CL0002319)
Fold Change: -0.5914
Cell Significance Index: -6.9000 - Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
Fold Change: -0.5981
Cell Significance Index: -14.9200 - Cell Name: eye photoreceptor cell (CL0000287)
Fold Change: -0.6275
Cell Significance Index: -39.5500 - Cell Name: GABAergic neuron (CL0000617)
Fold Change: -0.6411
Cell Significance Index: -8.0900 - Cell Name: L6b glutamatergic cortical neuron (CL4023038)
Fold Change: -0.6417
Cell Significance Index: -21.0100 - Cell Name: melanocyte of skin (CL1000458)
Fold Change: -0.6528
Cell Significance Index: -9.1500 - Cell Name: gut absorptive cell (CL0000677)
Fold Change: -0.7109
Cell Significance Index: -42.6800 - Cell Name: glycinergic neuron (CL1001509)
Fold Change: -0.7660
Cell Significance Index: -40.2200 - Cell Name: inhibitory interneuron (CL0000498)
Fold Change: -0.7810
Cell Significance Index: -9.3400 - Cell Name: neuron (CL0000540)
Fold Change: -0.7907
Cell Significance Index: -7.5000 - Cell Name: sebum secreting cell (CL0000317)
Fold Change: -0.8017
Cell Significance Index: -56.7000 - Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
Fold Change: -0.8040
Cell Significance Index: -59.9200 - Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
Fold Change: -0.8541
Cell Significance Index: -29.9200 - Cell Name: retinal progenitor cell (CL0002672)
Fold Change: -0.9438
Cell Significance Index: -52.9600 - Cell Name: lung endothelial cell (CL1001567)
Fold Change: -0.9619
Cell Significance Index: -50.1100 - Cell Name: L2/3 intratelencephalic projecting glutamatergic neuron (CL4030059)
Fold Change: -0.9886
Cell Significance Index: -13.1800 - Cell Name: paneth cell of epithelium of small intestine (CL1000343)
Fold Change: -1.0829
Cell Significance Index: -23.4600 - Cell Name: bladder urothelial cell (CL1001428)
Fold Change: -1.1889
Cell Significance Index: -61.7600 - Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
Fold Change: -1.2139
Cell Significance Index: -57.0500 - Cell Name: acinar cell of salivary gland (CL0002623)
Fold Change: -1.3027
Cell Significance Index: -60.7400 - Cell Name: leptomeningeal cell (CL0000708)
Fold Change: -1.3703
Cell Significance Index: -29.2900 - Cell Name: myeloid dendritic cell (CL0000782)
Fold Change: -1.3962
Cell Significance Index: -10.9500 - Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
Fold Change: -1.3974
Cell Significance Index: -48.5600 - Cell Name: skeletal muscle fibroblast (CL0011027)
Fold Change: -1.5084
Cell Significance Index: -10.2200 - Cell Name: chandelier pvalb GABAergic cortical interneuron (CL4023036)
Fold Change: -1.5193
Cell Significance Index: -31.7100 - Cell Name: stratified epithelial cell (CL0000079)
Fold Change: -1.5666
Cell Significance Index: -57.5100 - Cell Name: kidney epithelial cell (CL0002518)
Fold Change: -1.5831
Cell Significance Index: -46.6300 - Cell Name: endothelial cell of venule (CL1000414)
Fold Change: -1.6100
Cell Significance Index: -18.2900 - Cell Name: caudal ganglionic eminence derived cortical interneuron (CL4023064)
Fold Change: -1.6138
Cell Significance Index: -32.1800 - Cell Name: transit amplifying cell of colon (CL0009011)
Fold Change: -1.6526
Cell Significance Index: -52.9300
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.
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.
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
Genular Protein ID: 2967465034
Symbol: NMDE1_HUMAN
Name: Glutamate [NMDA] receptor subunit epsilon-1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 8061049
Title: Human N-methyl-D-aspartate receptor modulatory subunit hNR2A: cloning and sequencing of the cDNA and primary structure of the protein.
PubMed ID: 8061049
PubMed ID: 8768735
Title: Cloning and functional characterization of human heteromeric N-methyl-D-aspartate receptors.
PubMed ID: 8768735
PubMed ID: 15616553
Title: The sequence and analysis of duplication-rich human chromosome 16.
PubMed ID: 15616553
DOI: 10.1038/nature03187
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: 26919761
Title: Discovery of GluN2A-Selective NMDA Receptor Positive Allosteric Modulators (PAMs): Tuning Deactivation Kinetics via Structure-Based Design.
PubMed ID: 26919761
PubMed ID: 26875626
Title: Positive Allosteric Modulators of GluN2A-Containing NMDARs with Distinct Modes of Action and Impacts on Circuit Function.
PubMed ID: 26875626
PubMed ID: 28105280
Title: GluN2A-Selective Pyridopyrimidinone Series of NMDAR Positive Allosteric Modulators with an Improved in Vivo Profile.
PubMed ID: 28105280
PubMed ID: 20890276
Title: Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
PubMed ID: 20890276
DOI: 10.1038/ng.677
PubMed ID: 21499247
Title: Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
PubMed ID: 21499247
DOI: 10.1038/ng.810
PubMed ID: 22833210
Title: Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia.
PubMed ID: 22833210
DOI: 10.1038/tp.2011.52
PubMed ID: 23033978
Title: Diagnostic exome sequencing in persons with severe intellectual disability.
PubMed ID: 23033978
PubMed ID: 23933820
Title: GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
PubMed ID: 23933820
DOI: 10.1038/ng.2726
PubMed ID: 23933819
Title: Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
PubMed ID: 23933819
DOI: 10.1038/ng.2728
PubMed ID: 23933818
Title: GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
PubMed ID: 23933818
DOI: 10.1038/ng.2727
PubMed ID: 24455489
Title: Evidence that GRIN2A mutations in melanoma correlate with decreased survival.
PubMed ID: 24455489
PubMed ID: 24903190
Title: Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.
PubMed ID: 24903190
DOI: 10.1111/epi.12663
PubMed ID: 24504326
Title: Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.
PubMed ID: 24504326
DOI: 10.1038/ncomms4251
PubMed ID: 26637798
Title: Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
PubMed ID: 26637798
PubMed ID: 27839871
Title: Mechanistic insight into NMDA receptor dysregulation by rare variants in the GluN2A and GluN2B agonist binding domains.
PubMed ID: 27839871
PubMed ID: 27288002
Title: Altered zinc sensitivity of NMDA receptors harboring clinically-relevant mutations.
PubMed ID: 27288002
PubMed ID: 27864847
Title: Diagnostic targeted resequencing in 349 patients with drug-resistant pediatric epilepsies identifies causative mutations in 30 different genes.
PubMed ID: 27864847
DOI: 10.1002/humu.23149
PubMed ID: 28126851
Title: Functional evaluation of a de novo GRIN2A mutation identified in a patient with profound global developmental delay and refractory epilepsy.
PubMed ID: 28126851
PubMed ID: 28182669
Title: A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia.
PubMed ID: 28182669
PubMed ID: 28095420
Title: Molecular mechanism of disease-associated mutations in the pre-M1 helix of NMDA receptors and potential rescue pharmacology.
PubMed ID: 28095420
PubMed ID: 28242877
Title: Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency - molecular profiling and functional rescue.
PubMed ID: 28242877
PubMed ID: 29644724
Title: A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder.
PubMed ID: 29644724
DOI: 10.1002/mds.27315
PubMed ID: 30544257
Title: GRIN2A-related disorders: genotype and functional consequence predict phenotype.
PubMed ID: 30544257
DOI: 10.1093/brain/awy304
PubMed ID: 36117210
Title: Complex functional phenotypes of NMDA receptor disease variants.
PubMed ID: 36117210
PubMed ID: 35396579
Title: Rare coding variants in ten genes confer substantial risk for schizophrenia.
PubMed ID: 35396579
PubMed ID: 38538865
Title: De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor.
PubMed ID: 38538865
PubMed ID: 38307912
Title: Differential functional consequences of GRIN2A mutations associated with schizophrenia and neurodevelopmental disorders.
PubMed ID: 38307912
Sequence Information:
- Length: 1464
- Mass: 165283
- Checksum: AF5EDD599EC0B1E3
- Sequence:
MGRVGYWTLL VLPALLVWRG PAPSAAAEKG PPALNIAVML GHSHDVTERE LRTLWGPEQA AGLPLDVNVV ALLMNRTDPK SLITHVCDLM SGARIHGLVF GDDTDQEAVA QMLDFISSHT FVPILGIHGG ASMIMADKDP TSTFFQFGAS IQQQATVMLK IMQDYDWHVF SLVTTIFPGY REFISFVKTT VDNSFVGWDM QNVITLDTSF EDAKTQVQLK KIHSSVILLY CSKDEAVLIL SEARSLGLTG YDFFWIVPSL VSGNTELIPK EFPSGLISVS YDDWDYSLEA RVRDGIGILT TAASSMLEKF SYIPEAKASC YGQMERPEVP MHTLHPFMVN VTWDGKDLSF TEEGYQVHPR LVVIVLNKDR EWEKVGKWEN HTLSLRHAVW PRYKSFSDCE PDDNHLSIVT LEEAPFVIVE DIDPLTETCV RNTVPCRKFV KINNSTNEGM NVKKCCKGFC IDILKKLSRT VKFTYDLYLV TNGKHGKKVN NVWNGMIGEV VYQRAVMAVG SLTINEERSE VVDFSVPFVE TGISVMVSRS NGTVSPSAFL EPFSASVWVM MFVMLLIVSA IAVFVFEYFS PVGYNRNLAK GKAPHGPSFT IGKAIWLLWG LVFNNSVPVQ NPKGTTSKIM VSVWAFFAVI FLASYTANLA AFMIQEEFVD QVTGLSDKKF QRPHDYSPPF RFGTVPNGST ERNIRNNYPY MHQYMTKFNQ KGVEDALVSL KTGKLDAFIY DAAVLNYKAG RDEGCKLVTI GSGYIFATTG YGIALQKGSP WKRQIDLALL QFVGDGEMEE LETLWLTGIC HNEKNEVMSS QLDIDNMAGV FYMLAAAMAL SLITFIWEHL FYWKLRFCFT GVCSDRPGLL FSISRGIYSC IHGVHIEEKK KSPDFNLTGS QSNMLKLLRS AKNISSMSNM NSSRMDSPKR AADFIQRGSL IMDMVSDKGN LMYSDNRSFQ GKESIFGDNM NELQTFVANR QKDNLNNYVF QGQHPLTLNE SNPNTVEVAV STESKANSRP RQLWKKSVDS IRQDSLSQNP VSQRDEATAE NRTHSLKSPR YLPEEMAHSD ISETSNRATC HREPDNSKNH KTKDNFKRSV ASKYPKDCSE VERTYLKTKS SSPRDKIYTI DGEKEPGFHL DPPQFVENVT LPENVDFPDP YQDPSENFRK GDSTLPMNRN PLHNEEGLSN NDQYKLYSKH FTLKDKGSPH SETSERYRQN STHCRSCLSN MPTYSGHFTM RSPFKCDACL RMGNLYDIDE DQMLQETGNP ATGEQVYQQD WAQNNALQLQ KNKLRISRQH SYDNIVDKPR ELDLSRPSRS ISLKDRERLL EGNFYGSLFS VPSSKLSGKK SSLFPQGLED SKRSKSLLPD HTSDNPFLHS HRDDQRLVIG RCPSDPYKHS LPSQAVNDSY LRSSLRSTAS YCSRDSRGHN DVYISEHVMP YAANKNNMYS TPRVLNSCSN RRVYKKMPSI ESDV
Genular Protein ID: 2318442707
Symbol: Q59EW6_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 1491
- Mass: 168031
- Checksum: 05F8E12D0AA8A0D1
- Sequence:
GGRDARARSA PHCILDLLGL QGPSVATMGR VGYWTLLVLP ALLVWRGPAP SAAAEKGPPA LNIAVMLGHS HDVTERELRT LWGPEQAAGL PLDVNVVALL MNRTDPKSLI THVCDLMSGA RIHGLVFGDD TDQEAVAQML DFISSHTFVP ILGIHGGASM IMADKDPTST FFQFGASIQQ QATVMLKIMQ DYDWHVFSLV TTIFPGYREF ISFVKTTVDN SFVGWDMQNV ITLDTSFEDA KTQVQLKKIH SSVILLYCSK DEAVLILSEA RSLGLTGYDF FWIVPSLVSG NTELIPKEFP SGLISVSYDD WDYSLEARVR DGIGILTTAA SSMLEKFSYI PEAKASCYGQ MERPEVPMHT LHPFMVNVTW DGKDLSFTEE GYQVHPRLVV IVLNKDREWE KVGKWENHTL SLRHAVWPRY KSFSDCEPDD NHLSIVTLEE APFVIVEDID PLTETCVRNT VPCRKFVKIN NSTNEGMNVK KCCKGFCIDI LKKLSRTVKF TYDLYLVTNG KHGKKVNNVW NGMIGEVVYQ RAVMAVGSLT INEERSEVVD FSVPFVETGI SVMVSRSNGT VSPSAFLEPF SASVWVMMFV MLLIVSAIAV FVFEYFSPVG YNRNLAKGKA PHGPSFTIGK AIWLLWGLVF NNSVPVQNPK GTTSKIMVSV WAFFAVIFLA SYTANLAAFM IQEEFVDQVT GLSDKKFQRP HDYSPPFRFG TVPNGSTERN IRNNYPYMHQ YMTKFNQKGV EDALVSLKTG KLDAFIYDAA VLNYKAGRDE GCKLVTIGSG YIFATTGYGI ALQKGSPWKR QIDLALLQFV GDGEMEELET LWLTGICHNE KNEVMSSQLD IDNMAGVFYM LAAAMALSLI TFIWEHLFYW KLRFCFTGVC SDRPGLLFSI SRGIYSCIHG VHIEEKKKSP DFNLTGSQSN MLKLLRSAKN ISSMSNMNSS RMDSPKRAAD FIQRGSLIMD MVSDKGNLMY SDNRSFQGKE SIFGDNMNEL QTFVANRQKD NLNNYVFQGQ HPLTLNESNP NTVEVAVSTE SKANSRPRQL WKKSVDSIRQ DSLSQNPVSQ RDEATAENRT HSLKSPRYLP EEMAHSDFSE TSNRATCHRE PDNSKNHKTK DNFKRSVASK YPKDCSEVER TYLKTKSSSP RDKIYTIDGE KEPGFHLDPP QFVENVTLPE NVDFPDPYQD PSENFRKGDS TLPMNRNPLH NEEGLSNNDQ YKLYSKHFTL KDKGSPHSET SERYRQNSTH CRSCLSNMPT YSGHFTMRSP FKCDACLRMG NLYDIDEDQM LQETGNPATG EQVYQQDWAQ NNALQLQKNK LRISRQHSYD NIVDKPRELD LSRPSRSISL KDRERLLEGN FYGSLFSVPS SKLSGKKSSL FPQGLEDSKR SKSLLPDHTS DNPFLHSHRD DQRLVIGRCP SDPYKHSLPS QAVNDSYLRS SLRSTASYCS RDSRGHNDVY ISEHVMPYAA NKNNMYSTPR VLNSCSNRRV YKKMPSIESD V
Genular Protein ID: 2005397464
Symbol: A0A890YTL4_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 1281
- Mass: 144431
- Checksum: 7454CF24F5BE8373
- Sequence:
MGRVGYWTLL VLPALLVWRG PAPSAAAEKG PPALNIAVML GHSHDVTERE LRTLWGPEQA AGLPLDVNVV ALLMNRTDPK SLITHVCDLM SGARIHGLVF GDDTDQEAVA QMLDFISSHT FVPILGIHGG ASMIMADKDP TSTFFQFGAS IQQQATVMLK IMQDYDWHVF SLVTTIFPGY REFISFVKTT VDNSFVGWDM QNVITLDTSF EDAKTQVQLK KIHSSVILLY CSKDEAVLIL SEARSLGLTG YDFFWIVPSL VSGNTELIPK EFPSGLISVS YDDWDYSLEA RVRDGIGILT TAASSMLEKF SYIPEAKASC YGQMERPEVP MHTLHPFMVN VTWDGKDLSF TEEGYQVHPR LVVIVLNKDR EWEKVGKWEN HTLSLRHAVW PRYKSFSDCE PDDNHLSIVT LEEAPFVIVE DIDPLTETCV RNTVPCRKFV KINNSTNEGM NVKKCCKGFC IDILKKLSRT VKFTYDLYLV TNGKHGKKVN NVWNGMIGEV VYQRAVMAVG SLTINEERSE VVDFSVPFVE TGISVMVSRS NGTVSPSAFL EPFSASVWVM MFVMLLIVSA IAVFVFEYFS PVGYNRNLAK GKAPHGPSFT IGKAIWLLWG LVFNNSVPVQ NPKGTTSKIM VSVWAFFAVI FLASYTANLA AFMIQEEFVD QVTGLSDKKF QRPHDYSPPF RFGTVPNGST ERNIRNNYPY MHQYMTKFNQ KGVEDALVSL KTGKLDAFIY DAAVLNYKAG RDEGCKLVTI GSGYIFATTG YGIALQKGSP WKRQIDLALL QFVGDGEMEE LETLWLTGIC HNEKNEVMSS QLDIDNMAGV FYMLAAAMAL SLITFIWEHL FYWKLRFCFT GVCSDRPGLL FSISRGIYSC IHGVHIEEKK KSPDFNLTGS QSNMLKLLRS AKNISSMSNM NSSRMDSPKR AADFIQRGSL IMDMVSDKGN LMYSDNRSFQ GKESIFGDNM NELQTFVANR QKDNLNNYVF QGQHPLTLNE SNPNTVEVAV STESKANSRP RQLWKKSVDS IRQDSLSQNP VSQRDEATAE NRTHSLKSPR YLPEEMAHSD ISETSNRATC HREPDNSKNH KTKDNFKRSV ASKYPKDCSE VERTYLKTKS SSPRDKIYTI DGEKEPGFHL DPPQFVENVT LPENVDFPDP YQDPSENFRK GDSTLPMNRN PLHNEEGLSN NDQYKLYSKH FTLKDKGSPH SETSERYRQN STHCRSCLSN MPTYSGHFTM RSPFKCDACL RMGNLYDIDE DQMLQETGMT NAWLLGDAPR TLTNTRCHPR R
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.