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2025-05-09 18:28:04, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002857 3722 bp mRNA linear PRI 29-APR-2013
DEFINITION Homo sapiens peroxisomal biogenesis factor 19 (PEX19), transcript
variant 1, mRNA.
ACCESSION NM_002857 XM_378188
VERSION NM_002857.3 GI:197085593
KEYWORDS RefSeq.
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 3722)
AUTHORS Yagita,Y., Hiromasa,T. and Fujiki,Y.
TITLE Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and
TRC40-independent class I pathway
JOURNAL J. Cell Biol. 200 (5), 651-666 (2013)
PUBMED 23460677
REMARK GeneRIF: PEX19 formed a complex with the peroxisomal tail anchored
protein PEX26 in the cytosol and translocated it directly to
peroxisomes by a TRC40-independent class I pathway.
REFERENCE 2 (bases 1 to 3722)
AUTHORS Schmidt,F., Dietrich,D., Eylenstein,R., Groemping,Y., Stehle,T. and
Dodt,G.
TITLE The role of conserved PEX3 regions in PEX19-binding and peroxisome
biogenesis
JOURNAL Traffic 13 (9), 1244-1260 (2012)
PUBMED 22624858
REMARK GeneRIF: PEX3-PEX19 interaction is crucial for de novo formation of
peroxisomes in peroxisome-deficient cells.
REFERENCE 3 (bases 1 to 3722)
AUTHORS Sato,Y., Shibata,H., Nakatsu,T., Nakano,H., Kashiwayama,Y.,
Imanaka,T. and Kato,H.
TITLE Structural basis for docking of peroxisomal membrane protein
carrier Pex19p onto its receptor Pex3p
JOURNAL EMBO J. 29 (24), 4083-4093 (2010)
PUBMED 21102411
REMARK GeneRIF: The Pex19p peptide contains a characteristic motif,
consisting of the leucine triad (Leu18, Leu21, Leu22), and Phe29,
which are critical for the Pex3p binding and peroxisome biogenesis.
REFERENCE 4 (bases 1 to 3722)
AUTHORS Mohamed,S., El-Meleagy,E., Nasr,A., Ebberink,M.S., Wanders,R.J. and
Waterham,H.R.
TITLE A mutation in PEX19 causes a severe clinical phenotype in a patient
with peroxisomal biogenesis disorder
JOURNAL Am. J. Med. Genet. A 152A (9), 2318-2321 (2010)
PUBMED 20683989
REFERENCE 5 (bases 1 to 3722)
AUTHORS Mayerhofer,P.U., Kattenfeld,T., Roscher,A.A. and Muntau,A.C.
TITLE Two splice variants of human PEX19 exhibit distinct functions in
peroxisomal assembly
JOURNAL Biochem. Biophys. Res. Commun. 291 (5), 1180-1186 (2002)
PUBMED 11883941
REMARK GeneRIF: a considerable functional diversity of the proteins
encoded by two PEX19 splice variants and thereby provide first
experimental evidence for specific biological functions of the
different predicted domains of the PEX19 protein.
GeneRIF: ALDRP interacts with PEX19 splice variants PEX19-delta-E2
and PEX19-delta-E8.
GeneRIF: MP70 interacts with PEX19 splice variants PEX19-delta-E2
and PEX19p-delta-E8.
REFERENCE 6 (bases 1 to 3722)
AUTHORS Sacksteder,K.A., Jones,J.M., South,S.T., Li,X., Liu,Y. and
Gould,S.J.
TITLE PEX19 binds multiple peroxisomal membrane proteins, is
predominantly cytoplasmic, and is required for peroxisome membrane
synthesis
JOURNAL J. Cell Biol. 148 (5), 931-944 (2000)
PUBMED 10704444
REFERENCE 7 (bases 1 to 3722)
AUTHORS Matsuzono,Y., Kinoshita,N., Tamura,S., Shimozawa,N., Hamasaki,M.,
Ghaedi,K., Wanders,R.J., Suzuki,Y., Kondo,N. and Fujiki,Y.
TITLE Human PEX19: cDNA cloning by functional complementation, mutation
analysis in a patient with Zellweger syndrome, and potential role
in peroxisomal membrane assembly
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 96 (5), 2116-2121 (1999)
PUBMED 10051604
REFERENCE 8 (bases 1 to 3722)
AUTHORS Gotte,K., Girzalsky,W., Linkert,M., Baumgart,E., Kammerer,S.,
Kunau,W.H. and Erdmann,R.
TITLE Pex19p, a farnesylated protein essential for peroxisome biogenesis
JOURNAL Mol. Cell. Biol. 18 (1), 616-628 (1998)
PUBMED 9418908
REFERENCE 9 (bases 1 to 3722)
AUTHORS Kammerer,S., Arnold,N., Gutensohn,W., Mewes,H.W., Kunau,W.H.,
Hofler,G., Roscher,A.A. and Braun,A.
TITLE Genomic organization and molecular characterization of a gene
encoding HsPXF, a human peroxisomal farnesylated protein
JOURNAL Genomics 45 (1), 200-210 (1997)
PUBMED 9339377
REFERENCE 10 (bases 1 to 3722)
AUTHORS Braun,A., Kammerer,S., Weissenhorn,W., Weiss,E.H. and Cleve,H.
TITLE Sequence of a putative human housekeeping gene (HK33) localized on
chromosome 1
JOURNAL Gene 146 (2), 291-295 (1994)
PUBMED 8076834
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DC400252.1, X75535.1,
AL513282.10 and BC064979.1.
This sequence is a reference standard in the RefSeqGene project.
On Aug 19, 2008 this sequence version replaced gi:46358408.
Summary: This gene is necessary for early peroxisomal biogenesis.
It acts both as a cytosolic chaperone and as an import receptor for
peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins
that are essential for the assembly of functional peroxisomes. The
peroxisome biogenesis disorders (PBDs) are a group of genetically
heterogeneous autosomal recessive, lethal diseases characterized by
multiple defects in peroxisome function. These disorders have at
least 14 complementation groups, with more than one phenotype being
observed for some complementation groups. Although the clinical
features of PBD patients vary, cells from all PBD patients exhibit
a defect in the import of one or more classes of peroxisomal matrix
proteins into the organelle. Defects in this gene are a cause of
Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder
complementation group 14 (PBD-CG14), which is also known as
PBD-CGJ. Alternative splicing results in multiple transcript
variants. [provided by RefSeq, Aug 2010].
Transcript Variant: This variant (1, also known as PxFall or
PEX19all) represents the longest transcript and encodes the longer
isoform (a).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: X75535.1, BC000496.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-17 DC400252.1 1-17
18-3082 X75535.1 1-3065
3083-3565 AL513282.10 12658-13140 c
3566-3666 X75535.1 3549-3649
3667-3722 BC064979.1 553-608
FEATURES Location/Qualifiers
source 1..3722
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1q23.2"
gene 1..3722
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/note="peroxisomal biogenesis factor 19"
/db_xref="GeneID:5824"
/db_xref="HGNC:9713"
/db_xref="HPRD:02610"
/db_xref="MIM:600279"
exon 1..97
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
variation 14
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2301297"
CDS 28..927
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/note="isoform a is encoded by transcript variant 1;
peroxisomal farnesylated protein; housekeeping gene, 33kD;
peroxin-19; 33 kDa housekeeping protein"
/codon_start=1
/product="peroxisomal biogenesis factor 19 isoform a"
/protein_id="NP_002848.1"
/db_xref="GI:4506339"
/db_xref="CCDS:CCDS1201.1"
/db_xref="GeneID:5824"
/db_xref="HGNC:9713"
/db_xref="HPRD:02610"
/db_xref="MIM:600279"
/translation="
MAAAEEGCSVGAEADRELEELLESALDDFDKAKPSPAPPSTTTAPDASGPQKRSPGDTAKDALFASQEKFFQELFDSELASQATAEFEKAMKELAEEEPHLVEQFQKLSEAAGRVGSDMTSQQEFTSCLKETLSGLAKNATDLQNSSMSEEELTKAMEGLGMDEGDGEGNILPIMQSIMQNLLSKDVLYPSLKEITEKYPEWLQSHRESLPPEQFEKYQEQHSVMCKICEQFEAETPTDSETTQKARFEMVLDLMQQLQDLGHPPKELAGEMPPGLNFDLDALNLSGPPGASGEQCLIM
"
misc_feature 28..300
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P40855.1);
Region: Necessary for PEX19 function on peroxisome
biogenesis"
misc_feature 28..195
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P40855.1);
Region: Docking to the peroxisome membrane and binding to
PEX3"
misc_feature 130..132
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/experiment="experimental evidence, no additional details
recorded"
/note="farnesylation site; modified site"
misc_feature 190..924
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/note="Pex19 protein family; Region: Pex19; pfam04614"
/db_xref="CDD:191045"
misc_feature 913..915
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/experiment="experimental evidence, no additional details
recorded"
/note="prenylation site; modified site"
/citation=[8]
exon 98..207
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
variation 176
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11550117"
exon 208..373
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
variation 281
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:11550119"
variation 338
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="a"
/replace="t"
/db_xref="dbSNP:11550118"
exon 374..459
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
exon 460..621
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
exon 622..798
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
STS 718..835
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/standard_name="PMC26746P1"
/db_xref="UniSTS:272349"
variation 790..791
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace=""
/replace="a"
/db_xref="dbSNP:62641227"
exon 799..843
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
exon 844..3669
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/inference="alignment:Splign:1.39.8"
variation 1825
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="a"
/replace="g"
/db_xref="dbSNP:8989"
variation 1878
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:3198504"
polyA_signal 1978..1983
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
variation 1988
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057962"
polyA_site 1995
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
polyA_site 1998
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
variation 2398
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2301299"
variation 2474
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057973"
STS 2815..3099
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/standard_name="WI-19186"
/db_xref="UniSTS:13417"
variation 3083
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="c"
/replace="g"
/db_xref="dbSNP:10594"
variation 3280
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/replace="g"
/replace="t"
/db_xref="dbSNP:9853"
STS 3395..3476
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/standard_name="RH67926"
/db_xref="UniSTS:49669"
STS 3486..3628
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
/standard_name="RH70904"
/db_xref="UniSTS:38573"
polyA_signal 3586..3591
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
polyA_site 3604
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
polyA_site 3611
/gene="PEX19"
/gene_synonym="D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF;
PXMP1"
ORIGIN
ctcctacggcaagtcggaggtagcaagatggccgccgctgaggaaggctgtagtgtcggggccgaagcggacagggaattggaggagcttctggaaagtgctcttgatgatttcgataaagccaaaccctccccagcacccccttctaccaccacggcccctgatgcttcggggccccagaagagatcgccaggagacactgccaaagatgccctcttcgcttcccaagagaagtttttccaggaactattcgacagtgaactggcttcccaagccactgcggagttcgagaaggcaatgaaggagttggctgaggaagaaccccacctggtggagcagttccaaaagctctcagaggctgcagggagagtgggcagtgatatgacctcccaacaagaattcacttcttgcctaaaggaaacactaagtggattagccaaaaatgccactgaccttcagaactccagcatgtcggaagaagagctgaccaaggccatggaggggctaggcatggacgaaggggatggggaagggaacatcctccccatcatgcagagtattatgcagaacctactctccaaggatgtgctgtacccatcactgaaggagatcacagaaaagtatccagaatggttgcagagtcatcgggaatctctacctccagagcagtttgaaaaatatcaggagcagcacagcgtcatgtgcaaaatatgtgagcagtttgaggcagagacccccacagacagtgaaaccactcaaaaggctcgttttgagatggtgctggatcttatgcagcagctacaagatttaggccatcctccaaaagagctggctggagagatgcctcctggcctcaactttgacctggatgccctcaatctttcgggcccaccaggtgccagtggtgaacagtgtctgatcatgtgaaacacaacacgttttcctctctgagtcccagctatggggaacatctggagtcagcagaaccattgggacctgaggcaggagtgtcacctgcgggagaagtctgcccgctgccctctgtcatcccattcaagattgtgccataccagctgaggtttttcctctgtctctctaggaatagggtctgtttcacaggccatttctgtgaaccctactccattgtggtttctgccactatcaaagttccagctacctgcaaggtgaaggaaggcatcccttttggggcatgcactttctttcctttctcaaaataatgttatatgtggccacactgatgttcacctttacgtccagggtctttgtgccttgtctctactccctctcttggatctggggaggaggggcagagacctgggactctgtatttctatagttctcctggcagagcctttgagaatggggagaaacagcctgggctggggctacaggtctgtcactatgctctcttgccttcagacagaccattctgaattctctaaagggaaagggcttttgcatctaatcacaatagagttgaaagagaggccttaggattctcctctctctaggtgctgagccctcacctccctgttccaggctgagaactcaaatggttaccctgcttcttcctacaatgctgtgtgatatgggtgaacccagcccctgaccttcctctatcccctgcccatcctcccttttacctcctctcttttttaaacacctgtttatcccaacctttttgagctcaagctgtgataaagaagggcccatcctatttcccctcatctagtccatttacgattctcactgactccccgtcttcctggcagacacaaataaacccagtgtcaggtctaggaaattaatggctattcttccccagatacattctggcttatttgagatacatgattctcttagaatcctgtcccttggttcaggaaagtagcttggaaaaggagtaggggtatagcttgggtcccttttcctgcaaggccccatggggcagaatataataaatattctgagtgaggagtgtggtctttttctgatcttcctcagcttccgtaagttgcagagtgaggtatattaggagactagttctacacaatattgtaatgctgggttccatcaacacccaccttccacaactcagtctgcacctcagttggcaaaggagactggatggccatctttcctcatgttcccttgagtatttcaatgtagaaagcccttcaagtggtattatattttaaccttttacattattgttattaatgttagtaatatattgttatgttttctaaattatttttctttaagctgacgtggctttttttctgtggctcccagtgggtctacggaccttggctgacatatgttggtaggtactctggtcagctcagctggctgtcctggttcactcagaagataagtctctccaaagcaaattcacatgcattatgagtcgctttgagcttctgacatgtcacttgccccgaggttaaaacttttcaccccttgaagaccttacatgttttatggtattggtgaggaaggaaatgttctcaaggtctcaggctatttgggaaattccaactcctataccttaccagagcatggaagagcccagatctgaatgtaaaacgtctctgttctgccagagatggaaaaaatacaggtatacttgtgatatagtcatggggcttcagtgtcactattttctccttaaagctccagccaaaaactggacaaggatagagaggaggagggaagaacaaaagagcccttctctatgaaccttgtgccttctgtcctaccagttttcttttacagattctcacttctgctagcctagccagggcttactccaggaatctaaatagatgccctagtccactttatctttgttcccaaggcactcatttttattttgattttgattgaatgtgagcaggttgacctcaggtcacactttgttccaaaaacttttggaattattccaggacttgtggtggagttatggtactctagggcagtctttctcaaactatgtatggtaaaggaccaggttttttgttttccagtccttcacttatcaatatgcattcctattgcccatgacaggtatggagttcacactgtgtgctgccgacccggcaagtttgacagcacccaaactggccagactgttctgtaggttaagtccattgatcatgtacttggatatcacagcaacattgaaatgctaaaaagtttttaaacactctcaatttctaattcaccatgtcacagactggtgaaaaaaaaaaaaaggtgttcactgaccagcacaagtctgcagatcatctttgagtagcactgttttggggccctcggtctctctgaagaccctagcagaactgatacctacctgtatctcttgttctctcctatttgagtttcacttccagagaacttgttcttcagcaagaatgtgtcactagtaaggacatctctagcatttctctagccttccttttctgctgctcaaaaataatcgttacaaagcttaggtttaagctgtatatgaaatatttatgcgactctcaaactttaaaggagttgctcctttgttccaaaattaaatgtgttagataaatttgtgattgtatgggtggcttcatgaattaagaattgaattaatacagactttttgataattggaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:5824 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:5824 -> Molecular function: GO:0036105 [peroxisome membrane class-1 targeting sequence binding] evidence: IDA
GeneID:5824 -> Molecular function: GO:0047485 [protein N-terminus binding] evidence: IPI
GeneID:5824 -> Molecular function: GO:0051117 [ATPase binding] evidence: IPI
GeneID:5824 -> Biological process: GO:0006625 [protein targeting to peroxisome] evidence: IDA
GeneID:5824 -> Biological process: GO:0006625 [protein targeting to peroxisome] evidence: IMP
GeneID:5824 -> Biological process: GO:0007031 [peroxisome organization] evidence: IMP
GeneID:5824 -> Biological process: GO:0007031 [peroxisome organization] evidence: NAS
GeneID:5824 -> Biological process: GO:0016557 [peroxisome membrane biogenesis] evidence: IDA
GeneID:5824 -> Biological process: GO:0016559 [peroxisome fission] evidence: IMP
GeneID:5824 -> Biological process: GO:0045046 [protein import into peroxisome membrane] evidence: IDA
GeneID:5824 -> Biological process: GO:0050821 [protein stabilization] evidence: IDA
GeneID:5824 -> Biological process: GO:0055085 [transmembrane transport] evidence: TAS
GeneID:5824 -> Biological process: GO:0061077 [chaperone-mediated protein folding] evidence: IDA
GeneID:5824 -> Biological process: GO:0072321 [chaperone-mediated protein transport] evidence: IDA
GeneID:5824 -> Biological process: GO:0072663 [establishment of protein localization to peroxisome] evidence: IMP
GeneID:5824 -> Biological process: GO:1900131 [negative regulation of lipid binding] evidence: IDA
GeneID:5824 -> Cellular component: GO:0005634 [nucleus] evidence: IMP
GeneID:5824 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:5824 -> Cellular component: GO:0005737 [cytoplasm] evidence: IMP
GeneID:5824 -> Cellular component: GO:0005737 [cytoplasm] evidence: ISS
GeneID:5824 -> Cellular component: GO:0005777 [peroxisome] evidence: IDA
GeneID:5824 -> Cellular component: GO:0005777 [peroxisome] evidence: ISS
GeneID:5824 -> Cellular component: GO:0005778 [peroxisomal membrane] evidence: IDA
GeneID:5824 -> Cellular component: GO:0005829 [cytosol] evidence: IDA
GeneID:5824 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:5824 -> Cellular component: GO:0016021 [integral to membrane] evidence: IDA
GeneID:5824 -> Cellular component: GO:0031526 [brush border membrane] evidence: ISS
GeneID:5824 -> Cellular component: GO:0043234 [protein complex] evidence: IDA
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DBCLS
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