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2024-04-19 11:23:56, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001002257 4872 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens lysocardiolipin acyltransferase 1 (LCLAT1), transcript
variant 2, mRNA.
ACCESSION NM_001002257
VERSION NM_001002257.1 GI:50659058
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 4872)
AUTHORS Zhao,Y., Chen,Y.Q., Li,S., Konrad,R.J. and Cao,G.
TITLE The microsomal cardiolipin remodeling enzyme acyl-CoA
lysocardiolipin acyltransferase is an acyltransferase of multiple
anionic lysophospholipids
JOURNAL J. Lipid Res. 50 (5), 945-956 (2009)
PUBMED 19075029
REMARK GeneRIF: Data show that ALCAT1 possesses acyltransferase activities
toward lysophosphatidylinositol and lysophosphatidylglycerol, and
identify critical amino acids that are potentially involved in
lysophospholipid substrate binding.
REFERENCE 2 (bases 1 to 4872)
AUTHORS Wang,C., Faloon,P.W., Tan,Z., Lv,Y., Zhang,P., Ge,Y., Deng,H. and
Xiong,J.W.
TITLE Mouse lysocardiolipin acyltransferase controls the development of
hematopoietic and endothelial lineages during in vitro embryonic
stem-cell differentiation
JOURNAL Blood 110 (10), 3601-3609 (2007)
PUBMED 17675553
REFERENCE 3 (bases 1 to 4872)
AUTHORS Agarwal,A.K., Barnes,R.I. and Garg,A.
TITLE Functional characterization of human 1-acylglycerol-3-phosphate
acyltransferase isoform 8: cloning, tissue distribution, gene
structure, and enzymatic activity
JOURNAL Arch. Biochem. Biophys. 449 (1-2), 64-76 (2006)
PUBMED 16620771
REFERENCE 4 (bases 1 to 4872)
AUTHORS Cao,J., Liu,Y., Lockwood,J., Burn,P. and Shi,Y.
TITLE A novel cardiolipin-remodeling pathway revealed by a gene encoding
an endoplasmic reticulum-associated acyl-CoA:lysocardiolipin
acyltransferase (ALCAT1) in mouse
JOURNAL J. Biol. Chem. 279 (30), 31727-31734 (2004)
PUBMED 15152008
REFERENCE 5 (bases 1 to 4872)
AUTHORS Clark,H.F., Gurney,A.L., Abaya,E., Baker,K., Baldwin,D., Brush,J.,
Chen,J., Chow,B., Chui,C., Crowley,C., Currell,B., Deuel,B.,
Dowd,P., Eaton,D., Foster,J., Grimaldi,C., Gu,Q., Hass,P.E.,
Heldens,S., Huang,A., Kim,H.S., Klimowski,L., Jin,Y., Johnson,S.,
Lee,J., Lewis,L., Liao,D., Mark,M., Robbie,E., Sanchez,C.,
Schoenfeld,J., Seshagiri,S., Simmons,L., Singh,J., Smith,V.,
Stinson,J., Vagts,A., Vandlen,R., Watanabe,C., Wieand,D., Woods,K.,
Xie,M.H., Yansura,D., Yi,S., Yu,G., Yuan,J., Zhang,M., Zhang,Z.,
Goddard,A., Wood,W.I., Godowski,P. and Gray,A.
TITLE The secreted protein discovery initiative (SPDI), a large-scale
effort to identify novel human secreted and transmembrane proteins:
a bioinformatics assessment
JOURNAL Genome Res. 13 (10), 2265-2270 (2003)
PUBMED 12975309
REMARK Erratum:[Genome Res. 2003 Dec;13(12):2759]
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BX647953.1, AY358702.1, AK023269.1, AA455668.1, BF513499.1,
BF439401.1, CF264801.1, BU674604.1 and BX537607.1.
Transcript Variant: This variant (2) lacks an exon in the 5' region
and uses a downstream AUG start codon, as compared to variant 1. It
encodes isoform 2 which has a shorter N-terminus, as compared to
isoform 1.
##Evidence-Data-START##
Transcript exon combination :: BX647953.1, BC146817.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025083, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-189 BX647953.1 1-189
190-1521 AY358702.1 395-1726
1522-2548 BX647953.1 1523-2549
2549-2739 AK023269.1 308-498
2740-3007 AA455668.1 202-469
3008-3034 BX647953.1 3008-3034
3035-3048 BF513499.1 503-516
3049-3079 BF439401.1 1-31 c
3080-3483 BX647953.1 3079-3482
3484-3758 CF264801.1 320-594
3759-4090 BX647953.1 3771-4102
4091-4113 BU674604.1 581-603
4114-4872 BX537607.1 769-1527
FEATURES Location/Qualifiers
source 1..4872
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2p23.1"
gene 1..4872
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/note="lysocardiolipin acyltransferase 1"
/db_xref="GeneID:253558"
/db_xref="HGNC:26756"
/db_xref="MIM:614241"
misc_feature 44..46
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/note="upstream in-frame stop codon"
variation 79
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="c"
/db_xref="dbSNP:13404307"
CDS 119..1249
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/EC_number="2.3.1.51"
/note="isoform 2 is encoded by transcript variant 2;
acyl-CoA:lysocardiolipin acyltransferase 1;
1-acylglycerol-3-phosphate O-acyltransferase 8; 1-AGP
acyltransferase 8; 1-AGPAT 8"
/codon_start=1
/product="lysocardiolipin acyltransferase 1 isoform 2"
/protein_id="NP_001002257.1"
/db_xref="GI:50659059"
/db_xref="CCDS:CCDS42670.1"
/db_xref="GeneID:253558"
/db_xref="HGNC:26756"
/db_xref="MIM:614241"
/translation="
MVSWKGIYFILTLFWGSFFGSIFMLSPFLPLMFVNPSWYRWINNRLVATWLTLPVALLETMFGVKVIITGDAFVPGERSVIIMNHRTRMDWMFLWNCLMRYSYLRLEKICLKASLKGVPGFGWAMQAAAYIFIHRKWKDDKSHFEDMIDYFCDIHEPLQLLIFPEGTDLTENSKSRSNAFAEKNGLQKYEYVLHPRTTGFTFVVDRLREGKNLDAVHDITVAYPHNIPQSEKHLLQGDFPREIHFHVHRYPIDTLPTSKEDLQLWCHKRWEEKEERLRSFYQGEKNFYFTGQSVIPPCKSELRVLVVKLLSILYWTLFSPAMCLLIYLYSLVKWYFIITIVIFVLQERIFGGLEIIELACYRLLHKQPHLNSKKNE
"
misc_feature 281..862
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/note="Lysophospholipid Acyltransferases (LPLATs) of
Glycerophospholipid Biosynthesis: LCLAT1-like; Region:
LPLAT_LCLAT1-like; cd07990"
/db_xref="CDD:153252"
misc_feature order(371..373,380..382,386..388,449..460,614..622)
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/note="putative acyl-acceptor binding pocket; other site"
/db_xref="CDD:153252"
variation 124
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:112246701"
variation 127
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:201524840"
variation 153
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:140002108"
variation 212
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:373839237"
variation 217
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:151267372"
variation 241
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:200647800"
variation 249
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:116243478"
variation 251
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:375650694"
variation 253
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:150526082"
variation 261
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:183623684"
variation 289
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:367870291"
variation 290
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:370802715"
variation 292
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:146998079"
variation 354
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:375069411"
variation 365
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:368711551"
variation 395
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:78733491"
variation 402
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:143388876"
variation 467
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:375529358"
variation 560
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:367665468"
variation 598
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:147135903"
variation 625
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:138684089"
variation 647
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:200092138"
variation 677
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:141543989"
variation 710
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:376432207"
variation 711
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:201968892"
variation 728
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:369988749"
variation 735
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:139333259"
variation 773
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:140036224"
variation 784
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:143567069"
variation 817
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="c"
/db_xref="dbSNP:76277684"
variation 838..839
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="c"
/db_xref="dbSNP:34921674"
variation 856
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:12467646"
variation 857
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:370170585"
variation 872
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:12471868"
variation 885
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:372382354"
variation 887
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:200690380"
variation 925
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:141993926"
variation 929
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:150085223"
variation 937
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:200693287"
variation 947
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:142697372"
variation 950
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:374373733"
STS 973..1509
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/standard_name="UNQ1849__5010"
/db_xref="UniSTS:463335"
variation 978
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:371408205"
variation 988
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:138425181"
variation 989
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:201388736"
variation 996
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:202201453"
variation 997
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:190394850"
variation 998
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:144671570"
variation 1037
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:376154500"
variation 1041
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:368413889"
variation 1043
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:114923117"
variation 1057
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:371735450"
variation 1091
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:375762424"
variation 1177
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:6732314"
variation 1203
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:183125454"
variation 1224
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:139228736"
variation 1233
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:376342311"
variation 1281
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:369803873"
variation 1339
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:188210387"
variation 1415
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="t"
/db_xref="dbSNP:10189926"
variation 1424
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="t"
/db_xref="dbSNP:6719587"
variation 1472
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:10200589"
variation 1498
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="t"
/db_xref="dbSNP:190951529"
variation 1521
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:182852917"
variation 1648
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:72863050"
variation 1666
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="t"
/db_xref="dbSNP:201100961"
variation 1714..1717
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tcct"
/db_xref="dbSNP:368777763"
variation 1770
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:6723023"
variation 1783
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:369981251"
variation 1799
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="c"
/db_xref="dbSNP:79397953"
variation 1872
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:73922675"
variation 1925
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:186627062"
variation 1999
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:80257598"
variation 2077
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:17395619"
variation 2090
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:2609945"
variation 2142
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:369614361"
variation 2172
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:192561099"
variation 2318..2320
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="taa"
/db_xref="dbSNP:200452584"
variation 2343..2346
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tttt"
/db_xref="dbSNP:139847393"
variation 2461..2463
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tct"
/db_xref="dbSNP:3841597"
variation 2480
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:62139653"
variation 2492
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:78799722"
variation 2500
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:184789792"
variation 2518
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="t"
/db_xref="dbSNP:67960987"
variation 2520..2521
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="ttttc"
/db_xref="dbSNP:199959171"
variation 2521..2522
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tttctttttc"
/db_xref="dbSNP:370555402"
variation 2522..2526
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="ttttc"
/db_xref="dbSNP:372750488"
variation 2524..2525
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="ctttt"
/db_xref="dbSNP:200086642"
variation 2525
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:77842936"
variation 2526
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="c"
/db_xref="dbSNP:201114653"
variation 2526
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:76739247"
variation 2527
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:77152743"
variation 2531
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:200385257"
variation 2532
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:2028963"
variation 2534..2535
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="ttc"
/db_xref="dbSNP:72469834"
variation 2535..2538
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tttc"
/db_xref="dbSNP:370805047"
variation 2536
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:200771819"
variation 2538..2539
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="t"
/db_xref="dbSNP:11400317"
variation 2538
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:3030198"
variation 2538
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="ctttt"
/db_xref="dbSNP:367705592"
variation 2551
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:11889783"
variation 2553
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:1060737"
STS 2566..2657
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/standard_name="SHGC-60157"
/db_xref="UniSTS:50434"
variation 2610
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:60820628"
variation 2655
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:111440336"
variation 2677
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:11558821"
variation 2740
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:3816591"
variation 2744
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:1447193"
variation 2812
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:1060734"
variation 2848
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:115646016"
variation 2939
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:3816593"
variation 2997
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:72798187"
variation 3019..3020
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="t"
/db_xref="dbSNP:199519917"
variation 3022..3025
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tttc"
/db_xref="dbSNP:200870191"
variation 3030
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:201539534"
variation 3031..3032
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tt"
/db_xref="dbSNP:201407023"
variation 3031
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:71877849"
variation 3035
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:2121601"
variation 3036
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:200720157"
variation 3037
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:2028962"
variation 3048..3049
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="t"
/replace="tt"
/db_xref="dbSNP:35741069"
variation 3048
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="t"
/db_xref="dbSNP:13021261"
variation 3048
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="t"
/db_xref="dbSNP:374306937"
variation 3049
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="t"
/db_xref="dbSNP:60198740"
variation 3050
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="t"
/db_xref="dbSNP:74261472"
variation 3170
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:370880037"
variation 3179
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:56818448"
variation 3225
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:140893427"
variation 3292
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:144803491"
variation 3325
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:187606708"
variation 3388
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:192091067"
variation 3521
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:201834336"
variation 3618..3621
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="taac"
/db_xref="dbSNP:151314094"
variation 3755
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:114925184"
variation 3761
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:184936423"
variation 3806
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:146159299"
variation 3985
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:372481344"
variation 4091
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:148341125"
variation 4116..4119
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="cttc"
/db_xref="dbSNP:200602730"
variation 4119..4122
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="cctt"
/db_xref="dbSNP:370608674"
variation 4171
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="c"
/db_xref="dbSNP:4021840"
variation 4200
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:189831441"
variation 4271..4272
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="tt"
/db_xref="dbSNP:377475639"
variation 4495
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:150073890"
variation 4496
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="c"
/db_xref="dbSNP:144868945"
variation 4537
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:149035876"
variation 4546
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:4952168"
variation 4572
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="g"
/replace="t"
/db_xref="dbSNP:181100623"
variation 4600
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:143061809"
STS 4625..4827
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/standard_name="WIAF-2200"
/db_xref="UniSTS:53948"
variation 4658
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="t"
/db_xref="dbSNP:138605079"
variation 4717
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace=""
/replace="t"
/db_xref="dbSNP:35863705"
variation 4756
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286"
variation 4782
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="c"
/db_xref="dbSNP:11558822"
variation 4800
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:184514649"
variation 4805
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
/replace="a"
/replace="g"
/db_xref="dbSNP:57797549"
polyA_signal 4843..4848
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
polyA_site 4855
/gene="LCLAT1"
/gene_synonym="1AGPAT8; AGPAT8; ALCAT1; HSRG1849; LYCAT;
UNQ1849"
ORIGIN
ggcgttacgggatgaattaacggcgggttccgcacggaggttgtgacccctacggagccccagcttgcccacgcaccccactcggcgtcgcgcggcgtgccctgcttgtcacagaatcatggtgtcatggaaagggatttactttatactgactctgttttggggaagcttttttggaagcattttcatgctgagtccctttttacctttgatgtttgtaaacccatcttggtatcgctggatcaacaaccgccttgtggcaacatggctcaccctacctgtggcattattggagaccatgtttggtgtaaaagtgattataactggggatgcatttgttcctggagaaagaagtgtcattatcatgaaccatcggacaagaatggactggatgttcctgtggaattgcctgatgcgatatagctacctcagattggagaaaatttgcctcaaagcgagtctcaaaggtgttcctggatttggttgggccatgcaggctgctgcctatatcttcattcataggaaatggaaggatgacaagagccatttcgaagacatgattgattacttttgtgatattcacgaaccacttcaactcctcatattcccagaagggactgatctcacagaaaacagcaagtctcgaagtaatgcatttgctgaaaaaaatggacttcagaaatatgaatatgttttacatccaagaactacaggctttacttttgtggtagaccgtctaagagaaggtaagaaccttgatgctgtccatgatatcactgtggcgtatcctcacaacattcctcaatcagagaagcacctcctccaaggagactttcccagggaaatccactttcacgtccaccggtatccaatagacaccctccccacatccaaggaggaccttcaactctggtgccacaaacggtgggaagagaaagaagagaggctgcgttccttctatcaaggggagaagaatttttattttaccggacagagtgtcattccaccttgcaagtctgaactcagggtccttgtggtcaaattgctctctatactgtattggaccctgttcagccctgcaatgtgcctactcatatatttgtacagtcttgttaagtggtattttataatcaccattgtaatctttgtgctgcaagagagaatatttggtggactggagatcatagaacttgcatgttaccgacttttacacaaacagccacatttaaattcaaagaaaaatgagtaagattataaggtttgccatgtgaaaacctagagcatattttggaaatgttctaaacctttctaagctcagatgcatttttgcatgactatgtcgaatatttcttactgccatcattatttgttaaagatattttgcacttaattttgtgggaaaaatattgctacaattttttttaatctctgaatgtaatttcgatactgtgtacatagcagggagtgatcggggtgaaataacttgggccagaatattattaaacaatcatcaggcttttagcgacaaggaacacacacatttttcttaaaggcccaatcctaacagactccccgtaccagaggcagatctggaactcgtcaacaacagcccggatcacatgctgttactggactgcccaggtcacctcattgaggtgagcgctgtccctccaggtactcaggcaggtggtgcccaggctccctcccttggcgtccttcttcctgcgccaaacccatctcatccttaagatcagaaaatggaaccccctttgtcgtgaaaccgatcaagcattttgacaggaagcccttcattattcataacattgtatgctgaccaagacgtcagaagaccacctgtgcccttttctctcgtggaagataaaacctggactcagggagcaaccacaggctctccactttgaaactttagtttgaattttaaaagataggaagtaatacagtttaagttcctttctcacactcagtattgcatgcttagtgctggttttcttacaacattttggcaggtgtagctttttctgttaaaaatggtatacatgaagtcacatacttttttaaaggaacactcggaacattctgtcattccagtcagaaactgtcttttgaaatatttctttacaacctaccaaaaaaggaaggttgttttttctacatgtgcttgggtatctaacatctaccattaaaacaacaaatggcttgcagacagggcagtaatggtttatcctaaattactcaaccccttgtagccttgacaaattttaccttaaaaccaaaatgaaacacaaaaattaatccttaataatgatagcaagtgatctttctttttagttttagccttcctttttcaatagtaatatttaaacccacttttgaccaattgtttgcccaaatattcttgtcatttggagtcagtggaaaatccagcacaccaagcaccagtcttcttctgaggcaaaagaaaagtgttgtcattttcactctgttggagctgcacacttttttttctttttttttttctttttttttttgtcgtgtaagaaggatgctggtcagagctgcagaaaatatgaggcaattaaaagtctttagctgttagcaaacctgttagttttacttctgcattgaaccagcctcagaagctacttactgctttatgtactctttgggcattaatgccttctctgtaattatatctcgtttttgcttgacagtgacctacccaataattgcatcgtgcattgccatgaaaggtaaacacattgtgaactgaacttaccaagcagattctgtgagaaagcactggttgaggctgaacactgttgacacatcatttttattggaagagtattaactggtgcctcttctgaaacacaccaacccatattcctctgctcccccaaagctgtttctgatcctgctgggagcaactaactagttattatgcacatctgctccagacccagctctttaacttcatggttttacagcttgttttttctttttcttttctttttttttttttttttttaaaaaagcacctttttttgttgtttccccttaataaaagaggtttctaatttatgtttctctaagatttcctttggttgtatttagaaacacaaatagttttataatcaggattgcatttgtgctgggtaaaagaggagagctgtgctttctaccccaaagttgttggtaatggagccggtctgcccttcctacaaactcaagaggctcattgttcaaggtgtaacaacatttaattgcatgtcctctaacgctttgaaacctttagagggaagatcctcattttttacaattttgttccttttcatcatagaaaacatgtttaagataaaatacaaactttacctaccccaaattcataaagtacatttagtgctgtatagcactaaaacttagagatacagacactgtacttactttttaagaattagagacagtaactccaaaaataattgtccttttttctttctttctttttttacaataaggctcttgaaaattgtcattacttgtgttttcctatacattcatctgtgtgaaagcctttttcttctttgatttaaaaaaattaactatacagttaatggtttagaacttagaactacttagaattaatgctaaagtgtcaggaagaaattaatttagcttcaataattgtgactggcctcaggaattctcccttccacacctgcccacctcacctcactgcaccgcaccgcaccagagccagagcagctgcttgtctgcagcaggacacagttcctacatacgtttcagttctttcatggtaagctcaatggactttgaattgtttacagtgctgtatgtccaattgttaaatgtaccattctgaacgatgttaaagcaagtgtggtttatttatggcatgaaccatgtaacttgaaatatgaacttacaaggaggggcactcattaggtaacaagttcttacaccaaacttccttgatgaaataagccaaaataatcctaaaattcattagaagaacttgataaaagactcaaataaatgttagaaagagcccgtaattttaggactcctataaaattcttccttgtttgttaatgctattaaaactcagattcaagggaaataccagcttccacttgagtcactttgaaatagttaattcaacagcaccatgttagaaatatattggcagccaagactctgaactctgcagaaacatttgtttcacccagacttcaaactctagccctgactatgatgcccctgtgtgcatttacaataaagactccaacggagggagcctgttggtgttaaattgtttacatttctttatacaaataatgtgctttcagtgccttagttacagctccctttctgtttcttgttccaaggattctgtagtatgtagtgtgtttcttaggtaaagtctctttttgctactgaaagggaaatggtctctaaacactggtcactgtagcaggtaaacactactctaacgtggagaaatgagcttcatgctgaggtagtggttgccttagagctgttatttatgctgtagaaaacgaaaatggttttgctacctgataagcttcagattagatatagccctaaagttatcctgtacctgcattaaattttcattttagaagagaatcttggttttggtaattcatttttttttaagatcattatgtgcaaaacaccaagttttaaaaataactcacagaatggccttagttttcaatgtctgatggtatatttgtgagttgtgttatctgtaatatacatcccagaataaaggagtgaattaaatagtttaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:253558 -> Molecular function: GO:0003841 [1-acylglycerol-3-phosphate O-acyltransferase activity] evidence: IEA
GeneID:253558 -> Biological process: GO:0006644 [phospholipid metabolic process] evidence: TAS
GeneID:253558 -> Biological process: GO:0006654 [phosphatidic acid biosynthetic process] evidence: TAS
GeneID:253558 -> Biological process: GO:0007275 [multicellular organismal development] evidence: IEA
GeneID:253558 -> Biological process: GO:0016024 [CDP-diacylglycerol biosynthetic process] evidence: IEA
GeneID:253558 -> Biological process: GO:0019432 [triglyceride biosynthetic process] evidence: TAS
GeneID:253558 -> Biological process: GO:0035965 [cardiolipin acyl-chain remodeling] evidence: TAS
GeneID:253558 -> Biological process: GO:0044255 [cellular lipid metabolic process] evidence: TAS
GeneID:253558 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS
GeneID:253558 -> Biological process: GO:0046474 [glycerophospholipid biosynthetic process] evidence: TAS
GeneID:253558 -> Cellular component: GO:0005789 [endoplasmic reticulum membrane] evidence: TAS
GeneID:253558 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_001002257 -> EC 2.3.1.51
by
@meso_cacase at
DBCLS
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