GenomeNet

Database: UniProt
Entry: CO8A2_HUMAN
LinkDB: CO8A2_HUMAN
Original site: CO8A2_HUMAN 
ID   CO8A2_HUMAN             Reviewed;         703 AA.
AC   P25067; Q5JV31; Q8TEJ5;
DT   01-MAY-1992, integrated into UniProtKB/Swiss-Prot.
DT   15-MAR-2004, sequence version 2.
DT   27-MAR-2024, entry version 206.
DE   RecName: Full=Collagen alpha-2(VIII) chain;
DE   AltName: Full=Endothelial collagen;
DE   Flags: Precursor;
GN   Name=COL8A2;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Spleen;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=16710414; DOI=10.1038/nature04727;
RA   Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A.,
RA   Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C.,
RA   Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K.,
RA   Atkinson A., Cooper R., Jones C., Hall R.E., Andrews T.D., Lloyd C.,
RA   Ainscough R., Almeida J.P., Ambrose K.D., Anderson F., Andrew R.W.,
RA   Ashwell R.I.S., Aubin K., Babbage A.K., Bagguley C.L., Bailey J.,
RA   Beasley H., Bethel G., Bird C.P., Bray-Allen S., Brown J.Y., Brown A.J.,
RA   Buckley D., Burton J., Bye J., Carder C., Chapman J.C., Clark S.Y.,
RA   Clarke G., Clee C., Cobley V., Collier R.E., Corby N., Coville G.J.,
RA   Davies J., Deadman R., Dunn M., Earthrowl M., Ellington A.G., Errington H.,
RA   Frankish A., Frankland J., French L., Garner P., Garnett J., Gay L.,
RA   Ghori M.R.J., Gibson R., Gilby L.M., Gillett W., Glithero R.J.,
RA   Grafham D.V., Griffiths C., Griffiths-Jones S., Grocock R., Hammond S.,
RA   Harrison E.S.I., Hart E., Haugen E., Heath P.D., Holmes S., Holt K.,
RA   Howden P.J., Hunt A.R., Hunt S.E., Hunter G., Isherwood J., James R.,
RA   Johnson C., Johnson D., Joy A., Kay M., Kershaw J.K., Kibukawa M.,
RA   Kimberley A.M., King A., Knights A.J., Lad H., Laird G., Lawlor S.,
RA   Leongamornlert D.A., Lloyd D.M., Loveland J., Lovell J., Lush M.J.,
RA   Lyne R., Martin S., Mashreghi-Mohammadi M., Matthews L., Matthews N.S.W.,
RA   McLaren S., Milne S., Mistry S., Moore M.J.F., Nickerson T., O'Dell C.N.,
RA   Oliver K., Palmeiri A., Palmer S.A., Parker A., Patel D., Pearce A.V.,
RA   Peck A.I., Pelan S., Phelps K., Phillimore B.J., Plumb R., Rajan J.,
RA   Raymond C., Rouse G., Saenphimmachak C., Sehra H.K., Sheridan E.,
RA   Shownkeen R., Sims S., Skuce C.D., Smith M., Steward C., Subramanian S.,
RA   Sycamore N., Tracey A., Tromans A., Van Helmond Z., Wall M., Wallis J.M.,
RA   White S., Whitehead S.L., Wilkinson J.E., Willey D.L., Williams H.,
RA   Wilming L., Wray P.W., Wu Z., Coulson A., Vaudin M., Sulston J.E.,
RA   Durbin R.M., Hubbard T., Wooster R., Dunham I., Carter N.P., McVean G.,
RA   Ross M.T., Harrow J., Olson M.V., Beck S., Rogers J., Bentley D.R.;
RT   "The DNA sequence and biological annotation of human chromosome 1.";
RL   Nature 441:315-321(2006).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RA   Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M.,
RA   Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J.,
RA   Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S.,
RA   Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H.,
RA   Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K.,
RA   Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D.,
RA   Hunkapiller M.W., Myers E.W., Venter J.C.;
RL   Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases.
RN   [4]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 66-703.
RX   PubMed=2019595; DOI=10.1016/s0021-9258(20)89508-8;
RA   Muragaki Y., Jacenko O., Apte S., Mattei M.-G., Ninomiya Y., Olsen B.R.;
RT   "The alpha 2(VIII) collagen gene. A novel member of the short chain
RT   collagen family located on the human chromosome 1.";
RL   J. Biol. Chem. 266:7721-7727(1991).
RN   [5]
RP   PROTEOLYTIC PROCESSING.
RX   PubMed=1515454; DOI=10.1016/0925-4439(92)90103-t;
RA   Kittelberger R., Neale T.J., Francky K.T., Greenhill N.S., Gibson G.J.;
RT   "Cleavage of type VIII collagen by human neutrophil elastase.";
RL   Biochim. Biophys. Acta 1139:295-299(1992).
RN   [6]
RP   TISSUE SPECIFICITY.
RX   PubMed=10686422; DOI=10.1016/s0945-053x(99)00053-0;
RA   Greenhill N.S., Ruger B.M., Hasan Q., Davis P.F.;
RT   "The alpha1(VIII) and alpha2(VIII) collagen chains form two distinct
RT   homotrimeric proteins in vivo.";
RL   Matrix Biol. 19:19-28(2000).
RN   [7]
RP   SUBUNIT.
RX   PubMed=14990571; DOI=10.1074/jbc.m305805200;
RA   Stephan S., Sherratt M.J., Hodson N., Shuttleworth C.A., Kielty C.M.;
RT   "Expression and supramolecular assembly of recombinant alpha1(viii) and
RT   alpha2(viii) collagen homotrimers.";
RL   J. Biol. Chem. 279:21469-21477(2004).
RN   [8]
RP   TISSUE SPECIFICITY, AND INDUCTION.
RX   PubMed=17888087; DOI=10.1111/j.1365-2362.2007.01864.x;
RA   Gerth J., Cohen C.D., Hopfer U., Lindenmeyer M.T., Sommer M., Grone H.J.,
RA   Wolf G.;
RT   "Collagen type VIII expression in human diabetic nephropathy.";
RL   Eur. J. Clin. Invest. 37:767-773(2007).
RN   [9]
RP   VARIANTS FECD1 GLN-304; ARG-357; HIS-434; LYS-455 AND LEU-575, VARIANT
RP   PPCD2 LYS-455, AND VARIANTS ARG-3; GLN-155 AND ILE-645.
RX   PubMed=11689488; DOI=10.1093/hmg/10.21.2415;
RA   Biswas S., Munier F.L., Yardley J., Hart-Holden N., Perveen R., Cousin P.,
RA   Sutphin J.E., Noble B., Batterbury M., Kielty C., Hackett A., Bonshek R.,
RA   Ridgway A., McLeod D., Sheffield V.C., Stone E.M., Schorderet D.F.,
RA   Black G.C.M.;
RT   "Missense mutations in COL8A2, the gene encoding the alpha-2 chain of type
RT   VIII collagen, cause two forms of corneal endothelial dystrophy.";
RL   Hum. Mol. Genet. 10:2415-2423(2001).
RN   [10]
RP   VARIANTS GLN-155 AND MET-502.
RX   PubMed=15175909; DOI=10.1007/s10384-003-0063-6;
RA   Kobayashi A., Fujiki K., Murakami A., Kato T., Chen L.-Z., Onoe H.,
RA   Nakayasu K., Sakurai M., Takahashi M., Sugiyama K., Kanai A.;
RT   "Analysis of COL8A2 gene mutation in Japanese patients with Fuchs'
RT   endothelial dystrophy and posterior polymorphous dystrophy.";
RL   Jpn. J. Ophthalmol. 48:195-198(2004).
CC   -!- FUNCTION: Macromolecular component of the subendothelium. Major
CC       component of the Descemet's membrane (basement membrane) of corneal
CC       endothelial cells. Also a component of the endothelia of blood vessels.
CC       Necessary for migration and proliferation of vascular smooth muscle
CC       cells and thus, has a potential role in the maintenance of vessel wall
CC       integrity and structure, in particular in atherogenesis (By
CC       similarity). {ECO:0000250}.
CC   -!- SUBUNIT: Homotrimers, or heterotrimers in association with alpha
CC       2(VIII) type collagens. Four homotrimers can form a tetrahedron
CC       stabilized by central interacting C-terminal NC1 trimers.
CC       {ECO:0000269|PubMed:14990571}.
CC   -!- SUBCELLULAR LOCATION: Secreted, extracellular space, extracellular
CC       matrix, basement membrane.
CC   -!- TISSUE SPECIFICITY: Expressed primarily in the subendothelium of large
CC       blood vessels. Also expressed in arterioles and venules in muscle,
CC       heart, kidney, spleen, umbilical cord, liver and lung and is also found
CC       in connective tissue layers around hair follicles, around nerve bundles
CC       in muscle, in the dura of the optic nerve, in cornea and sclera, and in
CC       the perichondrium of cartilaginous tissues. In the kidney, expressed in
CC       mesangial cells, glomerular endothelial cells, and tubular epithelial
CC       cells. Also expressed in mast cells, and in astrocytes during the
CC       repair process. Expressed in Descemet's membrane.
CC       {ECO:0000269|PubMed:10686422, ECO:0000269|PubMed:17888087}.
CC   -!- INDUCTION: Some up-regulation in diabetic nephropathy.
CC       {ECO:0000269|PubMed:17888087}.
CC   -!- PTM: Proteolytically cleaved by neutrophil elastase, in vitro.
CC       {ECO:0000269|PubMed:1515454}.
CC   -!- PTM: Prolines at the third position of the tripeptide repeating unit
CC       (G-X-Y) are hydroxylated in some or all of the chains.
CC   -!- DISEASE: Corneal dystrophy, Fuchs endothelial, 1 (FECD1) [MIM:136800]:
CC       A corneal disease caused by loss of endothelium of the central cornea.
CC       It is characterized by focal wart-like guttata that arise from Descemet
CC       membrane and develop in the central cornea, epithelial blisters,
CC       reduced vision and pain. Descemet membrane is thickened by abnormal
CC       collagenous deposition. {ECO:0000269|PubMed:11689488}. Note=The disease
CC       is caused by variants affecting the gene represented in this entry.
CC   -!- DISEASE: Corneal dystrophy, posterior polymorphous, 2 (PPCD2)
CC       [MIM:609140]: A rare mild subtype of posterior corneal dystrophy
CC       characterized by alterations of Descemet membrane presenting as
CC       vesicles, opacities or band-like lesions on slit-lamp examination and
CC       specular microscopy. Affected patient typically are asymptomatic.
CC       {ECO:0000269|PubMed:11689488}. Note=The disease is caused by variants
CC       affecting the gene represented in this entry.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=BAB84955.1; Type=Erroneous initiation; Evidence={ECO:0000305};
CC   ---------------------------------------------------------------------------
CC   Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms
CC   Distributed under the Creative Commons Attribution (CC BY 4.0) License
CC   ---------------------------------------------------------------------------
DR   EMBL; AK074129; BAB84955.1; ALT_INIT; mRNA.
DR   EMBL; AL138787; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; CH471059; EAX07388.1; -; Genomic_DNA.
DR   EMBL; M60832; AAA62822.1; -; Genomic_DNA.
DR   CCDS; CCDS403.1; -.
DR   PIR; A57131; A57131.
DR   RefSeq; NP_001281276.1; NM_001294347.1.
DR   RefSeq; NP_005193.1; NM_005202.3.
DR   AlphaFoldDB; P25067; -.
DR   SMR; P25067; -.
DR   BioGRID; 107693; 46.
DR   ComplexPortal; CPX-1745; Collagen type VIII trimer variant 1.
DR   ComplexPortal; CPX-1747; Collagen type VIII trimer variant 3.
DR   STRING; 9606.ENSP00000380901; -.
DR   iPTMnet; P25067; -.
DR   PhosphoSitePlus; P25067; -.
DR   BioMuta; COL8A2; -.
DR   DMDM; 45644957; -.
DR   jPOST; P25067; -.
DR   MassIVE; P25067; -.
DR   PaxDb; 9606-ENSP00000380901; -.
DR   PeptideAtlas; P25067; -.
DR   ProteomicsDB; 54250; -.
DR   Antibodypedia; 56213; 180 antibodies from 24 providers.
DR   DNASU; 1296; -.
DR   Ensembl; ENST00000303143.9; ENSP00000305913.4; ENSG00000171812.13.
DR   Ensembl; ENST00000397799.2; ENSP00000380901.1; ENSG00000171812.13.
DR   GeneID; 1296; -.
DR   KEGG; hsa:1296; -.
DR   MANE-Select; ENST00000397799.2; ENSP00000380901.1; NM_005202.4; NP_005193.1.
DR   UCSC; uc001bzv.4; human.
DR   AGR; HGNC:2216; -.
DR   CTD; 1296; -.
DR   DisGeNET; 1296; -.
DR   GeneCards; COL8A2; -.
DR   HGNC; HGNC:2216; COL8A2.
DR   HPA; ENSG00000171812; Low tissue specificity.
DR   MalaCards; COL8A2; -.
DR   MIM; 120252; gene.
DR   MIM; 136800; phenotype.
DR   MIM; 609140; phenotype.
DR   neXtProt; NX_P25067; -.
DR   OpenTargets; ENSG00000171812; -.
DR   Orphanet; 98974; Fuchs endothelial corneal dystrophy.
DR   Orphanet; 98973; Posterior polymorphous corneal dystrophy.
DR   PharmGKB; PA26732; -.
DR   VEuPathDB; HostDB:ENSG00000171812; -.
DR   eggNOG; ENOG502QRST; Eukaryota.
DR   GeneTree; ENSGT00940000154317; -.
DR   InParanoid; P25067; -.
DR   OMA; IPHMKYM; -.
DR   OrthoDB; 4272636at2759; -.
DR   PhylomeDB; P25067; -.
DR   TreeFam; TF334029; -.
DR   PathwayCommons; P25067; -.
DR   Reactome; R-HSA-1442490; Collagen degradation.
DR   Reactome; R-HSA-1650814; Collagen biosynthesis and modifying enzymes.
DR   Reactome; R-HSA-2022090; Assembly of collagen fibrils and other multimeric structures.
DR   Reactome; R-HSA-216083; Integrin cell surface interactions.
DR   Reactome; R-HSA-8948216; Collagen chain trimerization.
DR   BioGRID-ORCS; 1296; 19 hits in 1141 CRISPR screens.
DR   ChiTaRS; COL8A2; human.
DR   GeneWiki; COL8A2; -.
DR   GenomeRNAi; 1296; -.
DR   Pharos; P25067; Tbio.
DR   PRO; PR:P25067; -.
DR   Proteomes; UP000005640; Chromosome 1.
DR   RNAct; P25067; Protein.
DR   Bgee; ENSG00000171812; Expressed in periodontal ligament and 163 other cell types or tissues.
DR   ExpressionAtlas; P25067; baseline and differential.
DR   Genevisible; P25067; HS.
DR   GO; GO:0005604; C:basement membrane; IBA:GO_Central.
DR   GO; GO:0005581; C:collagen trimer; IEA:UniProtKB-KW.
DR   GO; GO:0062023; C:collagen-containing extracellular matrix; HDA:BHF-UCL.
DR   GO; GO:0005788; C:endoplasmic reticulum lumen; TAS:Reactome.
DR   GO; GO:0031012; C:extracellular matrix; NAS:UniProtKB.
DR   GO; GO:0005576; C:extracellular region; TAS:Reactome.
DR   GO; GO:0005615; C:extracellular space; IBA:GO_Central.
DR   GO; GO:0005201; F:extracellular matrix structural constituent; NAS:UniProtKB.
DR   GO; GO:0030020; F:extracellular matrix structural constituent conferring tensile strength; IBA:GO_Central.
DR   GO; GO:0030674; F:protein-macromolecule adaptor activity; NAS:UniProtKB.
DR   GO; GO:0001525; P:angiogenesis; IEA:UniProtKB-KW.
DR   GO; GO:0048593; P:camera-type eye morphogenesis; IEA:Ensembl.
DR   GO; GO:0098609; P:cell-cell adhesion; NAS:UniProtKB.
DR   GO; GO:0001935; P:endothelial cell proliferation; IEA:Ensembl.
DR   GO; GO:0030198; P:extracellular matrix organization; IBA:GO_Central.
DR   Gene3D; 2.60.120.40; -; 1.
DR   InterPro; IPR001073; C1q_dom.
DR   InterPro; IPR008160; Collagen.
DR   InterPro; IPR008983; Tumour_necrosis_fac-like_dom.
DR   PANTHER; PTHR24023; COLLAGEN ALPHA; 1.
DR   PANTHER; PTHR24023:SF855; COLLAGEN ALPHA-2(VIII) CHAIN; 1.
DR   Pfam; PF00386; C1q; 1.
DR   Pfam; PF01391; Collagen; 3.
DR   PRINTS; PR00007; COMPLEMNTC1Q.
DR   SMART; SM00110; C1Q; 1.
DR   SUPFAM; SSF49842; TNF-like; 1.
DR   PROSITE; PS50871; C1Q; 1.
PE   1: Evidence at protein level;
KW   Angiogenesis; Basement membrane; Cell adhesion; Collagen;
KW   Corneal dystrophy; Disease variant; Extracellular matrix; Hydroxylation;
KW   Reference proteome; Repeat; Secreted; Signal.
FT   SIGNAL          1..28
FT                   /evidence="ECO:0000255"
FT   CHAIN           29..703
FT                   /note="Collagen alpha-2(VIII) chain"
FT                   /id="PRO_0000005835"
FT   DOMAIN          570..703
FT                   /note="C1q"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00368"
FT   REGION          29..76
FT                   /note="Nonhelical region (NC2)"
FT   REGION          70..544
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          77..536
FT                   /note="Triple-helical region"
FT   REGION          537..703
FT                   /note="Nonhelical region (NC1)"
FT   COMPBIAS        74..100
FT                   /note="Pro residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        220..234
FT                   /note="Pro residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        505..533
FT                   /note="Pro residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VARIANT         3
FT                   /note="G -> R (in dbSNP:rs115156902)"
FT                   /evidence="ECO:0000269|PubMed:11689488"
FT                   /id="VAR_017893"
FT   VARIANT         155
FT                   /note="R -> Q (in dbSNP:rs75864656)"
FT                   /evidence="ECO:0000269|PubMed:11689488,
FT                   ECO:0000269|PubMed:15175909"
FT                   /id="VAR_017894"
FT   VARIANT         304
FT                   /note="R -> Q (in FECD1; dbSNP:rs369487110)"
FT                   /evidence="ECO:0000269|PubMed:11689488"
FT                   /id="VAR_017895"
FT   VARIANT         357
FT                   /note="G -> R (in FECD1; uncertain significance;
FT                   dbSNP:rs199786966)"
FT                   /evidence="ECO:0000269|PubMed:11689488"
FT                   /id="VAR_017896"
FT   VARIANT         434
FT                   /note="R -> H (in FECD1; dbSNP:rs201235688)"
FT                   /evidence="ECO:0000269|PubMed:11689488"
FT                   /id="VAR_017897"
FT   VARIANT         455
FT                   /note="Q -> K (in FECD1 and PPCD2; dbSNP:rs80358191)"
FT                   /evidence="ECO:0000269|PubMed:11689488"
FT                   /id="VAR_017898"
FT   VARIANT         502
FT                   /note="T -> M (in dbSNP:rs117860804)"
FT                   /evidence="ECO:0000269|PubMed:15175909"
FT                   /id="VAR_021387"
FT   VARIANT         575
FT                   /note="P -> L (in FECD1; uncertain significance;
FT                   dbSNP:rs145553904)"
FT                   /evidence="ECO:0000269|PubMed:11689488"
FT                   /id="VAR_017899"
FT   VARIANT         645
FT                   /note="T -> I (in dbSNP:rs200767854)"
FT                   /evidence="ECO:0000269|PubMed:11689488"
FT                   /id="VAR_017900"
FT   CONFLICT        88
FT                   /note="R -> W (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        102
FT                   /note="M -> H (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        133
FT                   /note="K -> N (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        347
FT                   /note="E -> D (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        377..378
FT                   /note="PK -> LR (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        506
FT                   /note="T -> R (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        523
FT                   /note="P -> L (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        529..531
FT                   /note="Missing (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        585
FT                   /note="F -> L (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        677
FT                   /note="M -> I (in Ref. 4; AAA62822)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   703 AA;  67244 MW;  84BD7CBDBDECD466 CRC64;
     MLGTLTPLSS LLLLLLVLVL GCGPRASSGG GAGGAAGYAP VKYIQPMQKG PVGPPFREGK
     GQYLEMPLPL LPMDLKGEPG PPGKPGPRGP PGPPGFPGKP GMGKPGLHGQ PGPAGPPGFS
     RMGKAGPPGL PGKVGPPGQP GLRGEPGIRG DQGLRGPPGP PGLPGPSGIT IPGKPGAQGV
     PGPPGFQGEP GPQGEPGPPG DRGLKGDNGV GQPGLPGAPG QGGAPGPPGL PGPAGLGKPG
     LDGLPGAPGD KGESGPPGVP GPRGEPGAVG PKGPPGVDGV GVPGAAGLPG PQGPSGAKGE
     PGTRGPPGLI GPTGYGMPGL PGPKGDRGPA GVPGLLGDRG EPGEDGEPGE QGPQGLGGPP
     GLPGSAGLPG RRGPPGPKGE AGPGGPPGVP GIRGDQGPSG LAGKPGVPGE RGLPGAHGPP
     GPTGPKGEPG FTGRPGGPGV AGALGQKGDL GLPGQPGLRG PSGIPGLQGP AGPIGPQGLP
     GLKGEPGLPG PPGEGRAGEP GTAGPTGPPG VPGSPGITGP PGPPGPPGPP GAPGAFDETG
     IAGLHLPNGG VEGAVLGKGG KPQFGLGELS AHATPAFTAV LTSPFPASGM PVKFDRTLYN
     GHSGYNPATG IFTCPVGGVY YFAYHVHVKG TNVWVALYKN NVPATYTYDE YKKGYLDQAS
     GGAVLQLRPN DQVWVQMPSD QANGLYSTEY IHSSFSGFLL CPT
//
DBGET integrated database retrieval system