Details for: OCRL
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: 120.8652
Cell Significance Index: -18.8000 - Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
Fold Change: 73.7256
Cell Significance Index: -18.7000 - Cell Name: smooth muscle fiber of ileum (CL1000278)
Fold Change: 40.7839
Cell Significance Index: -19.2600 - Cell Name: ciliated cell of the bronchus (CL0002332)
Fold Change: 17.1669
Cell Significance Index: -16.3900 - Cell Name: orthochromatic erythroblast (CL0000552)
Fold Change: 15.3371
Cell Significance Index: -18.9100 - Cell Name: epidermal Langerhans cell (CL0002457)
Fold Change: 5.4464
Cell Significance Index: -11.9200 - Cell Name: stromal cell of bone marrow (CL0010001)
Fold Change: 4.8175
Cell Significance Index: -19.0100 - Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
Fold Change: 0.9314
Cell Significance Index: 186.8300 - Cell Name: intestinal crypt stem cell of colon (CL0009043)
Fold Change: 0.8581
Cell Significance Index: 93.3400 - Cell Name: gut absorptive cell (CL0000677)
Fold Change: 0.8207
Cell Significance Index: 49.2700 - Cell Name: epithelial cell of small intestine (CL0002254)
Fold Change: 0.7648
Cell Significance Index: 124.4000 - Cell Name: epithelial cell of stomach (CL0002178)
Fold Change: 0.7319
Cell Significance Index: 85.3000 - Cell Name: conjunctival epithelial cell (CL1000432)
Fold Change: 0.7058
Cell Significance Index: 9.6300 - Cell Name: hippocampal pyramidal neuron (CL1001571)
Fold Change: 0.6397
Cell Significance Index: 18.2600 - Cell Name: tuft cell of colon (CL0009041)
Fold Change: 0.5622
Cell Significance Index: 507.6100 - Cell Name: neoplastic cell (CL0001063)
Fold Change: 0.5614
Cell Significance Index: 111.4100 - Cell Name: paneth cell of epithelium of small intestine (CL1000343)
Fold Change: 0.5567
Cell Significance Index: 12.0600 - Cell Name: bladder urothelial cell (CL1001428)
Fold Change: 0.5223
Cell Significance Index: 27.1300 - Cell Name: hippocampal granule cell (CL0001033)
Fold Change: 0.5095
Cell Significance Index: 34.2600 - Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
Fold Change: 0.4486
Cell Significance Index: 160.9000 - Cell Name: microfold cell of epithelium of small intestine (CL1000353)
Fold Change: 0.4337
Cell Significance Index: 29.9900 - Cell Name: enterocyte of epithelium of small intestine (CL1000334)
Fold Change: 0.4146
Cell Significance Index: 11.9500 - Cell Name: intermediate cell of urothelium (CL4030055)
Fold Change: 0.3955
Cell Significance Index: 71.2900 - Cell Name: enterocyte of epithelium of large intestine (CL0002071)
Fold Change: 0.3909
Cell Significance Index: 17.7200 - Cell Name: cardiac muscle myoblast (CL0000513)
Fold Change: 0.3529
Cell Significance Index: 27.0800 - Cell Name: enteroendocrine cell of colon (CL0009042)
Fold Change: 0.1994
Cell Significance Index: 37.9500 - Cell Name: colon goblet cell (CL0009039)
Fold Change: 0.1928
Cell Significance Index: 19.0700 - Cell Name: GABAergic interneuron (CL0011005)
Fold Change: 0.1782
Cell Significance Index: 123.2700 - Cell Name: enteroendocrine cell of small intestine (CL0009006)
Fold Change: 0.1748
Cell Significance Index: 4.3700 - Cell Name: indirect pathway medium spiny neuron (CL4023029)
Fold Change: 0.1664
Cell Significance Index: 7.3600 - Cell Name: direct pathway medium spiny neuron (CL4023026)
Fold Change: 0.1640
Cell Significance Index: 6.2100 - Cell Name: cortical cell of adrenal gland (CL0002097)
Fold Change: 0.1317
Cell Significance Index: 3.5300 - Cell Name: basal cell of urothelium (CL1000486)
Fold Change: 0.1010
Cell Significance Index: 12.4300 - Cell Name: ciliary muscle cell (CL1000443)
Fold Change: 0.0949
Cell Significance Index: 43.0800 - Cell Name: acinar cell of salivary gland (CL0002623)
Fold Change: 0.0832
Cell Significance Index: 3.8800 - Cell Name: cell in vitro (CL0001034)
Fold Change: 0.0753
Cell Significance Index: 41.1100 - Cell Name: pigmented epithelial cell (CL0000529)
Fold Change: 0.0673
Cell Significance Index: 126.7600 - Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
Fold Change: 0.0637
Cell Significance Index: 40.4800 - Cell Name: pancreatic acinar cell (CL0002064)
Fold Change: 0.0622
Cell Significance Index: 10.6200 - Cell Name: stromal cell of ovary (CL0002132)
Fold Change: 0.0572
Cell Significance Index: 7.8500 - Cell Name: Sertoli cell (CL0000216)
Fold Change: 0.0478
Cell Significance Index: 0.6700 - Cell Name: hair follicular keratinocyte (CL2000092)
Fold Change: 0.0456
Cell Significance Index: 20.1500 - Cell Name: skeletal muscle fiber (CL0008002)
Fold Change: 0.0377
Cell Significance Index: 0.9700 - Cell Name: small intestine goblet cell (CL1000495)
Fold Change: 0.0268
Cell Significance Index: 0.9400 - Cell Name: lens epithelial cell (CL0002224)
Fold Change: 0.0203
Cell Significance Index: 31.1800 - Cell Name: anterior lens cell (CL0002223)
Fold Change: 0.0154
Cell Significance Index: 28.3600 - Cell Name: secondary lens fiber (CL0002225)
Fold Change: 0.0119
Cell Significance Index: 16.1600 - Cell Name: pigmented ciliary epithelial cell (CL0002303)
Fold Change: 0.0106
Cell Significance Index: 1.5400 - Cell Name: forebrain neuroblast (CL1000042)
Fold Change: 0.0106
Cell Significance Index: 0.6500 - Cell Name: placental villous trophoblast (CL2000060)
Fold Change: -0.0071
Cell Significance Index: -0.1900 - Cell Name: pancreatic A cell (CL0000171)
Fold Change: -0.0073
Cell Significance Index: -5.4000 - Cell Name: transit amplifying cell of small intestine (CL0009012)
Fold Change: -0.0121
Cell Significance Index: -0.2500 - Cell Name: pancreatic PP cell (CL0002275)
Fold Change: -0.0123
Cell Significance Index: -7.6900 - Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
Fold Change: -0.0171
Cell Significance Index: -12.5400 - Cell Name: pulmonary alveolar epithelial cell (CL0000322)
Fold Change: -0.0182
Cell Significance Index: -13.8100 - Cell Name: retinal progenitor cell (CL0002672)
Fold Change: -0.0191
Cell Significance Index: -1.0700 - Cell Name: pancreatic ductal cell (CL0002079)
Fold Change: -0.0212
Cell Significance Index: -2.4300 - Cell Name: type B pancreatic cell (CL0000169)
Fold Change: -0.0224
Cell Significance Index: -12.6600 - Cell Name: pancreatic endocrine cell (CL0008024)
Fold Change: -0.0266
Cell Significance Index: -3.0400 - Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
Fold Change: -0.0362
Cell Significance Index: -0.7700 - Cell Name: odontoblast (CL0000060)
Fold Change: -0.0367
Cell Significance Index: -4.7100 - Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
Fold Change: -0.0383
Cell Significance Index: -1.0700 - Cell Name: pancreatic D cell (CL0000173)
Fold Change: -0.0492
Cell Significance Index: -10.3700 - Cell Name: dopaminergic neuron (CL0000700)
Fold Change: -0.0552
Cell Significance Index: -15.8900 - Cell Name: eye photoreceptor cell (CL0000287)
Fold Change: -0.0687
Cell Significance Index: -4.3300 - Cell Name: abnormal cell (CL0001061)
Fold Change: -0.0690
Cell Significance Index: -7.0500 - Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
Fold Change: -0.0694
Cell Significance Index: -7.2300 - Cell Name: granulosa cell (CL0000501)
Fold Change: -0.1012
Cell Significance Index: -2.6600 - Cell Name: lactocyte (CL0002325)
Fold Change: -0.1090
Cell Significance Index: -14.0800 - Cell Name: sebum secreting cell (CL0000317)
Fold Change: -0.1325
Cell Significance Index: -9.3700 - Cell Name: cerebellar granule cell (CL0001031)
Fold Change: -0.1406
Cell Significance Index: -2.4100 - Cell Name: tonsil germinal center B cell (CL2000006)
Fold Change: -0.1421
Cell Significance Index: -16.7600 - Cell Name: transit amplifying cell of colon (CL0009011)
Fold Change: -0.1530
Cell Significance Index: -4.9000 - Cell Name: preadipocyte (CL0002334)
Fold Change: -0.1552
Cell Significance Index: -3.0300 - Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
Fold Change: -0.1669
Cell Significance Index: -12.4400 - Cell Name: centrilobular region hepatocyte (CL0019029)
Fold Change: -0.1722
Cell Significance Index: -2.9000 - Cell Name: glycinergic neuron (CL1001509)
Fold Change: -0.1819
Cell Significance Index: -9.5500 - Cell Name: Purkinje cell (CL0000121)
Fold Change: -0.1859
Cell Significance Index: -4.0700 - Cell Name: basal cell of prostate epithelium (CL0002341)
Fold Change: -0.1927
Cell Significance Index: -5.2500 - Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
Fold Change: -0.1949
Cell Significance Index: -9.1600 - Cell Name: lung endothelial cell (CL1001567)
Fold Change: -0.2000
Cell Significance Index: -10.4200 - Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
Fold Change: -0.2154
Cell Significance Index: -17.0600 - Cell Name: intestinal tuft cell (CL0019032)
Fold Change: -0.2161
Cell Significance Index: -13.2500 - Cell Name: early pro-B cell (CL0002046)
Fold Change: -0.2227
Cell Significance Index: -14.3700 - Cell Name: cortical interneuron (CL0008031)
Fold Change: -0.2406
Cell Significance Index: -5.7700 - Cell Name: leptomeningeal cell (CL0000708)
Fold Change: -0.2552
Cell Significance Index: -5.4600 - Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
Fold Change: -0.2756
Cell Significance Index: -5.8500 - Cell Name: periportal region hepatocyte (CL0019026)
Fold Change: -0.3022
Cell Significance Index: -4.4600 - Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
Fold Change: -0.3256
Cell Significance Index: -10.3700 - Cell Name: keratocyte (CL0002363)
Fold Change: -0.3259
Cell Significance Index: -5.1700 - Cell Name: fibro/adipogenic progenitor cell (CL0009099)
Fold Change: -0.3300
Cell Significance Index: -16.6800 - Cell Name: L6b glutamatergic cortical neuron (CL4023038)
Fold Change: -0.3311
Cell Significance Index: -10.8400 - Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
Fold Change: -0.3448
Cell Significance Index: -11.9800 - Cell Name: cardiac muscle cell (CL0000746)
Fold Change: -0.3448
Cell Significance Index: -5.0900 - Cell Name: paneth cell of colon (CL0009009)
Fold Change: -0.3584
Cell Significance Index: -5.3700 - Cell Name: cardiac endothelial cell (CL0010008)
Fold Change: -0.3598
Cell Significance Index: -5.1800 - Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
Fold Change: -0.3707
Cell Significance Index: -8.0100 - Cell Name: sst GABAergic cortical interneuron (CL4023017)
Fold Change: -0.3864
Cell Significance Index: -7.6400 - Cell Name: fibroblast of mammary gland (CL0002555)
Fold Change: -0.3900
Cell Significance Index: -11.1800 - Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
Fold Change: -0.4111
Cell Significance Index: -14.4000
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: 161556438
Symbol: OCRL_HUMAN
Name: Inositol polyphosphate 5-phosphatase OCRL-1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 1321346
Title: The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.
PubMed ID: 1321346
DOI: 10.1038/358239a0
PubMed ID: 9048911
Title: Physical mapping and genomic structure of the Lowe syndrome gene OCRL1.
PubMed ID: 9048911
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
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: 8504307
Title: Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of Lowe.
PubMed ID: 8504307
DOI: 10.1093/hmg/2.4.461
PubMed ID: 7761412
Title: The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase.
PubMed ID: 7761412
PubMed ID: 9430698
Title: Cell lines from kidney proximal tubules of a patient with Lowe syndrome lack OCRL inositol polyphosphate 5-phosphatase and accumulate phosphatidylinositol 4,5-bisphosphate.
PubMed ID: 9430698
PubMed ID: 10764818
Title: The isolation and characterization of a cDNA encoding phospholipid-specific inositol polyphosphate 5-phosphatase.
PubMed ID: 10764818
PubMed ID: 15474001
Title: Type II phosphoinositide 5-phosphatases have unique sensitivities towards fatty acid composition and head group phosphorylation.
PubMed ID: 15474001
PubMed ID: 20133602
Title: Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1.
PubMed ID: 20133602
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 21971085
Title: OCRL controls trafficking through early endosomes via PtdIns4,5P(2)-dependent regulation of endosomal actin.
PubMed ID: 21971085
PubMed ID: 21233288
Title: The PH domain proteins IPIP27A and B link OCRL1 to receptor recycling in the endocytic pathway.
PubMed ID: 21233288
PubMed ID: 22543976
Title: OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome.
PubMed ID: 22543976
DOI: 10.1093/hmg/dds163
PubMed ID: 22228094
Title: The Lowe syndrome protein OCRL1 is involved in primary cilia assembly.
PubMed ID: 22228094
DOI: 10.1093/hmg/ddr615
PubMed ID: 22072788
Title: Recruitment of OCRL and Inpp5B to phagosomes by Rab5 and APPL1 depletes phosphoinositides and attenuates Akt signaling.
PubMed ID: 22072788
PubMed ID: 22381590
Title: Inositol 5-phosphatases: insights from the Lowe syndrome protein OCRL.
PubMed ID: 22381590
PubMed ID: 25869668
Title: Sac2/INPP5F is an inositol 4-phosphatase that functions in the endocytic pathway.
PubMed ID: 25869668
PubMed ID: 19536138
Title: A PH domain within OCRL bridges clathrin-mediated membrane trafficking to phosphoinositide metabolism.
PubMed ID: 19536138
PubMed ID: 21378754
Title: A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1.
PubMed ID: 21378754
PubMed ID: 17765681
Title: A role of the Lowe syndrome protein OCRL in early steps of the endocytic pathway.
PubMed ID: 17765681
PubMed ID: 21666675
Title: Recognition of the F&H motif by the Lowe syndrome protein OCRL.
PubMed ID: 21666675
DOI: 10.1038/nsmb.2071
PubMed ID: 9199559
Title: Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome.
PubMed ID: 9199559
DOI: 10.1086/515471
PubMed ID: 9682219
Title: Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients.
PubMed ID: 9682219
PubMed ID: 9632163
Title: Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypes.
PubMed ID: 9632163
DOI: 10.1002/(sici)1096-8628(19980605)77:5<348::aid-ajmg2>3.3.co;2-h
PubMed ID: 9788721
Title: Identification of two novel mutations in the OCRL1 gene in Japanese families with Lowe syndrome.
PubMed ID: 9788721
PubMed ID: 10923037
Title: OCRL1 mutation analysis in French Lowe syndrome patients: implications for molecular diagnosis strategy and genetic counseling.
PubMed ID: 10923037
DOI: 10.1002/1098-1004(200008)16:2<157::aid-humu8>3.0.co;2-9
PubMed ID: 10767176
Title: Carrier assessment in families with Lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination.
PubMed ID: 10767176
PubMed ID: 15627218
PubMed ID: 17384968
Title: OCRL1 mutations in patients with Dent disease phenotype in Japan.
PubMed ID: 17384968
PubMed ID: 19168822
Title: Magnetic resonance imaging, magnetic resonance spectroscopy, and facial dysmorphism in a case of Lowe syndrome with novel OCRL1 gene mutation.
PubMed ID: 19168822
PubMed ID: 21031565
Title: From Lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes.
PubMed ID: 21031565
DOI: 10.1002/humu.21391
Sequence Information:
- Length: 901
- Mass: 104205
- Checksum: 476BFCCC3655C1FE
- Sequence:
MEPPLPVGAQ PLATVEGMEM KGPLREPCAL TLAQRNGQYE LIIQLHEKEQ HVQDIIPINS HFRCVQEAEE TLLIDIASNS GCKIRVQGDW IRERRFEIPD EEHCLKFLSA VLAAQKAQSQ LLVPEQKDSS SWYQKLDTKD KPSVFSGLLG FEDNFSSMNL DKKINSQNQP TGIHREPPPP PFSVNKMLPR EKEASNKEQP KVTNTMRKLF VPNTQSGQRE GLIKHILAKR EKEYVNIQTF RFFVGTWNVN GQSPDSGLEP WLNCDPNPPD IYCIGFQELD LSTEAFFYFE SVKEQEWSMA VERGLHSKAK YKKVQLVRLV GMMLLIFARK DQCRYIRDIA TETVGTGIMG KMGNKGGVAV RFVFHNTTFC IVNSHLAAHV EDFERRNQDY KDICARMSFV VPNQTLPQLN IMKHEVVIWL GDLNYRLCMP DANEVKSLIN KKDLQRLLKF DQLNIQRTQK KAFVDFNEGE IKFIPTYKYD SKTDRWDSSG KCRVPAWCDR ILWRGTNVNQ LNYRSHMELK TSDHKPVSAL FHIGVKVVDE RRYRKVFEDS VRIMDRMEND FLPSLELSRR EFVFENVKFR QLQKEKFQIS NNGQVPCHFS FIPKLNDSQY CKPWLRAEPF EGYLEPNETV DISLDVYVSK DSVTILNSGE DKIEDILVLH LDRGKDYFLT ISGNYLPSCF GTSLEALCRM KRPIREVPVT KLIDLEEDSF LEKEKSLLQM VPLDEGASER PLQVPKEIWL LVDHLFKYAC HQEDLFQTPG MQEELQQIID CLDTSIPETI PGSNHSVAEA LLIFLEALPE PVICYELYQR CLDSAYDPRI CRQVISQLPR CHRNVFRYLM AFLRELLKFS EYNSVNANMI ATLFTSLLLR PPPNLMARQT PSDRQRAIQF LLGFLLGSEE D
Genular Protein ID: 1011353205
Symbol: A0A2X0TVZ9_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 893
- Mass: 103227
- Checksum: E61E59C6AD0AC650
- Sequence:
MEPPLPVGAQ PLATVEGMEM KGPLREPCAL TLAQRNGQYE LIIQLHEKEQ HVQDIIPINS HFRCVQEAEE TLLIDIASNS GCKIRVQGDW IRERRFEIPD EEHCLKFLSA VLAAQKAQSQ LLVPEQKDSS SWYQKLDTKD KPSVFSGLLG FEDNFSSMNL DKKINSQNQP TGIHREPPPP PFSVNKMLPR EKEASNKEQP KVTNTMRKLF VPNTQSGQRE GLIKHILAKR EKEYVNIQTF RFFVGTWNVN GQSPDSGLEP WLNCDPNPPD IYCIGFQELD LSTEAFFYFE SVKEQEWSMA VERGLHSKAK YKKVQLVRLV GMMLLIFARK DQCRYIRDIA TETVGTGIMG KMGNKGGVAV RFVFHNTTFC IVNSHLAAHV EDFERRNQDY KDICARMSFV VPNQTLPQLN IMKHEVVIWL GDLNYRLCMP DANEVKSLIN KKDLQRLLKF DQLNIQRTQK KAFVDFNEGE IKFIPTYKYD SKTDRWDSSG KCRVPAWCDR ILWRGTNVNQ LNYRSHMELK TSDHKPVSAL FHIGVKVVDE RRYRKVFEDS VRIMDRMEND FLPSLELSRR EFVFENVKFR QLQKEKFQIS NNGQVPCHFS FIPKLNDSQY CKPWLRAEPF EGYLEPNETV DISLDVYVSK DSVTILNSGE DKIEDILVLH LDRGKDYFLT ISGNYLPSCF GTSLEALCRM KRPIREVPVT KLIDLEKSLL QMVPLDEGAS ERPLQVPKEI WLLVDHLFKY ACHQEDLFQT PGMQEELQQI IDCLDTSIPE TIPGSNHSVA EALLIFLEAL PEPVICYELY QRCLDSAYDP RICRQVISQL PRCHRNVFRY LMAFLRELLK FSEYNSVNAN MIATLFTSLL LRPPPNLMAR QTPSDRQRAI QFLLGFLLGS EED
Genular Protein ID: 652428974
Symbol: Q504W7_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: 893
- Mass: 103181
- Checksum: 1EF7E1812E182B79
- Sequence:
MEPPLPVGAQ PLATVEGMEM KGPLREPCAL TLAQRNGQYE LIIQLHEKEQ HVQDIIPINS HFRCVQEAEE TLLIDIASNS GCKIRVQGDW IRERRFEIPD EEHCLKFLSA VLAAQKAQSQ LLVPEQKDSS SWYQKLDTKD KPSVFSGLLG FEDNFSSMNL DKKINSQNQP TGIHREPPPP PFSVNKMLPR EKEASNKEQP KVTNTMRKLF VPNTQSGQRE GLIKHILAKR EKEYVNIQTF RFFVGTWNVN GQSPDSGLEP WLNCDPNPPD IYCIGFQELD LSTEAFFYFE SVKEQEWSMA VERGLHSKAK YKKVQLVRLV GMMLLIFARK DQCRYIRDIA TETVGTGIMG KMGNKGGVAV RFVFHNTTFC IVNSHLAAHV EDFERRNQDY KDICARMSFV VPNQTLPQLN IMKHEVVIWL GDLNYRLGMP DANEVKSLIN KKDLQRLLKF DQLNIQRTQK KAFVDFNEGE IKFIPTYKYD SKTDRWDSSG KCRVPAWCDR ILWRGTNVNQ LNYRSHMELK TSDHKPVSAL FHIGVKVVDE RRYRKVFEDS VRIMDRMEND FLPSLELSRR EFVFENVKFR QLQKEKFQIS NNGQVPCHFS FIPKLNDSQY CKPWLRAEPF EGYLEPNETV DISLDVYVSK DSVTILNSGE DKIEDILVLH LDRGKDYFLT ISGNYLPSCF GTSLEALCRM KRPIREVPVT KLIDLEKSLL QMVPLDEGAS ERPLQVPKEI WLLVDHLFKY ACHQEDLFQT PGMQEELQQI IDCLDTSIPE TIPGSNHSVA EALLIFLEAL PEPVICYELY QRCLDSAYDP RICRQVISQL PRCHRNVFRY LMAFLRELLK FSEYNSVNAN MIATLFTSLL LRPPPNLMAR QTPSDRQRAI QFLLGFLLGS EED
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.