LOCUS AAK69692.1 491 aa PRT HUM 02-JUL-2001 DEFINITION Homo sapiens C9orf12 protein. ACCESSION AF351202-1 PROTEIN_ID AAK69692.1 SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 2911) AUTHORS Hulme,D.J., Dawkins,J.L. and Nicholson,G.A. TITLE Characterization of a novel gene, C9orf12, and exclusion as the gene causing Hereditary Sensory Neuropathy Type I by mutation analysis JOURNAL Unpublished REFERENCE 2 (bases 1 to 2911) AUTHORS Hulme,D.J., Dawkins,J.L. and Nicholson,G.A. TITLE Direct Submission JOURNAL Submitted (21-FEB-2001) Department of Neurobiology, ANZAC Research Institute, University of Sydney, Concord Hospital, Concord, NSW 2139, Australia FEATURES Qualifiers source /db_xref="H-InvDB:HIT000078220" /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="9" /map="9q22.1-q22.3" /tissue_type="spinal cord" protein /note="contains no predicted transmembrane regions; similar to protein encoded by GenBank Accession Number AK023225" BEGIN 1 MEEGKMDENE WGYHGEGNKS LVVAHAQRCV VLRFLKFPPN RKKTSEEIFQ HLQNIVDFGK 61 NVMKEFLGEN YVHYGEVVQL PLEFVKQLCL KIQSERPESR CDKDLDTLSG YAMCLPNLTR 121 LQTYRFAEHR PILCVEIKPK CGFIPFSSDV THEMKHKVCR YCMHQHLKVA TGKWKQISKY 181 CPLDLYSGNK QRMHFALKSL LQEAQNNLKI FKNGELIYGC KDARSPVADW SELAHHLKPF 241 FFPSNGLASG PHCTRAVIRE LVHVITRVLL SGSDKGRAGT LSPGLGPQGP RVCEASPFSR 301 SLRCQGKNTP ERSGLPKGCL LYKTLQVQML DLLDIEGLYP LYNRVERYLE EFPEERKTLQ 361 IDGPYDEAFY QKLLDLSTED DGTVAFALTK VQQYRVAMTA KDCSIMIALS PCLQDASSDQ 421 RPVVPSSRSR FAFSVSVLDL DLKPYESIPH QYKLDGKIVN YYSKTVRAKD NAVMSTRFKE 481 SEDCTLVLHK V //