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TM140_HUMAN
ID   TM140_HUMAN             Reviewed;         185 AA.
AC   Q9NV12; A4D1P9; Q8WUC3;
DT   06-FEB-2007, integrated into UniProtKB/Swiss-Prot.
DT   18-MAY-2010, sequence version 2.
DT   03-AUG-2022, entry version 131.
DE   RecName: Full=Transmembrane protein 140;
GN   Name=TMEM140;
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], AND VARIANT LEU-29.
RC   TISSUE=Placenta;
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=12853948; DOI=10.1038/nature01782;
RA   Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H.,
RA   Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R., Wylie K.,
RA   Sekhon M., Becker M.C., O'Laughlin M.D., Schaller M.E., Fewell G.A.,
RA   Delehaunty K.D., Miner T.L., Nash W.E., Cordes M., Du H., Sun H.,
RA   Edwards J., Bradshaw-Cordum H., Ali J., Andrews S., Isak A., Vanbrunt A.,
RA   Nguyen C., Du F., Lamar B., Courtney L., Kalicki J., Ozersky P.,
RA   Bielicki L., Scott K., Holmes A., Harkins R., Harris A., Strong C.M.,
RA   Hou S., Tomlinson C., Dauphin-Kohlberg S., Kozlowicz-Reilly A., Leonard S.,
RA   Rohlfing T., Rock S.M., Tin-Wollam A.-M., Abbott A., Minx P., Maupin R.,
RA   Strowmatt C., Latreille P., Miller N., Johnson D., Murray J.,
RA   Woessner J.P., Wendl M.C., Yang S.-P., Schultz B.R., Wallis J.W.,
RA   Spieth J., Bieri T.A., Nelson J.O., Berkowicz N., Wohldmann P.E.,
RA   Cook L.L., Hickenbotham M.T., Eldred J., Williams D., Bedell J.A.,
RA   Mardis E.R., Clifton S.W., Chissoe S.L., Marra M.A., Raymond C., Haugen E.,
RA   Gillett W., Zhou Y., James R., Phelps K., Iadanoto S., Bubb K., Simms E.,
RA   Levy R., Clendenning J., Kaul R., Kent W.J., Furey T.S., Baertsch R.A.,
RA   Brent M.R., Keibler E., Flicek P., Bork P., Suyama M., Bailey J.A.,
RA   Portnoy M.E., Torrents D., Chinwalla A.T., Gish W.R., Eddy S.R.,
RA   McPherson J.D., Olson M.V., Eichler E.E., Green E.D., Waterston R.H.,
RA   Wilson R.K.;
RT   "The DNA sequence of human chromosome 7.";
RL   Nature 424:157-164(2003).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], AND VARIANT LEU-29.
RX   PubMed=12690205; DOI=10.1126/science.1083423;
RA   Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K.,
RA   Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R.,
RA   Zhang J., Hudek A.K., Li M., Haddad M., Duggan G.E., Fernandez B.A.,
RA   Kanematsu E., Gentles S., Christopoulos C.C., Choufani S., Kwasnicka D.,
RA   Zheng X.H., Lai Z., Nusskern D.R., Zhang Q., Gu Z., Lu F., Zeesman S.,
RA   Nowaczyk M.J., Teshima I., Chitayat D., Shuman C., Weksberg R.,
RA   Zackai E.H., Grebe T.A., Cox S.R., Kirkpatrick S.J., Rahman N.,
RA   Friedman J.M., Heng H.H.Q., Pelicci P.G., Lo-Coco F., Belloni E.,
RA   Shaffer L.G., Pober B., Morton C.C., Gusella J.F., Bruns G.A.P., Korf B.R.,
RA   Quade B.J., Ligon A.H., Ferguson H., Higgins A.W., Leach N.T.,
RA   Herrick S.R., Lemyre E., Farra C.G., Kim H.-G., Summers A.M., Gripp K.W.,
RA   Roberts W., Szatmari P., Winsor E.J.T., Grzeschik K.-H., Teebi A.,
RA   Minassian B.A., Kere J., Armengol L., Pujana M.A., Estivill X.,
RA   Wilson M.D., Koop B.F., Tosi S., Moore G.E., Boright A.P., Zlotorynski E.,
RA   Kerem B., Kroisel P.M., Petek E., Oscier D.G., Mould S.J., Doehner H.,
RA   Doehner K., Rommens J.M., Vincent J.B., Venter J.C., Li P.W., Mural R.J.,
RA   Adams M.D., Tsui L.-C.;
RT   "Human chromosome 7: DNA sequence and biology.";
RL   Science 300:767-772(2003).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], AND VARIANTS GLN-7; GLU-11 AND
RP   LEU-29.
RC   TISSUE=Brain;
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
RN   [5]
RP   VARIANT [LARGE SCALE ANALYSIS] GLU-112.
RX   PubMed=16959974; DOI=10.1126/science.1133427;
RA   Sjoeblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D.,
RA   Mandelker D., Leary R.J., Ptak J., Silliman N., Szabo S., Buckhaults P.,
RA   Farrell C., Meeh P., Markowitz S.D., Willis J., Dawson D., Willson J.K.V.,
RA   Gazdar A.F., Hartigan J., Wu L., Liu C., Parmigiani G., Park B.H.,
RA   Bachman K.E., Papadopoulos N., Vogelstein B., Kinzler K.W.,
RA   Velculescu V.E.;
RT   "The consensus coding sequences of human breast and colorectal cancers.";
RL   Science 314:268-274(2006).
CC   -!- INTERACTION:
CC       Q9NV12; Q96BI3: APH1A; NbExp=3; IntAct=EBI-2844246, EBI-2606935;
CC       Q9NV12; Q13520: AQP6; NbExp=3; IntAct=EBI-2844246, EBI-13059134;
CC       Q9NV12; P07307-3: ASGR2; NbExp=3; IntAct=EBI-2844246, EBI-12808270;
CC       Q9NV12; P20273-5: CD22; NbExp=3; IntAct=EBI-2844246, EBI-13320645;
CC       Q9NV12; P19397: CD53; NbExp=3; IntAct=EBI-2844246, EBI-6657396;
CC       Q9NV12; P11912: CD79A; NbExp=3; IntAct=EBI-2844246, EBI-7797864;
CC       Q9NV12; Q99675: CGRRF1; NbExp=3; IntAct=EBI-2844246, EBI-2130213;
CC       Q9NV12; O00501: CLDN5; NbExp=3; IntAct=EBI-2844246, EBI-18400628;
CC       Q9NV12; O95471: CLDN7; NbExp=3; IntAct=EBI-2844246, EBI-740744;
CC       Q9NV12; Q6ZS10: CLEC17A; NbExp=3; IntAct=EBI-2844246, EBI-11977093;
CC       Q9NV12; P58418: CLRN1; NbExp=3; IntAct=EBI-2844246, EBI-17274839;
CC       Q9NV12; Q15125: EBP; NbExp=3; IntAct=EBI-2844246, EBI-3915253;
CC       Q9NV12; Q5JX71: FAM209A; NbExp=3; IntAct=EBI-2844246, EBI-18304435;
CC       Q9NV12; Q96KR6: FAM210B; NbExp=3; IntAct=EBI-2844246, EBI-18938272;
CC       Q9NV12; Q8TBE3: FNDC9; NbExp=3; IntAct=EBI-2844246, EBI-12142257;
CC       Q9NV12; Q8NBJ4: GOLM1; NbExp=3; IntAct=EBI-2844246, EBI-712073;
CC       Q9NV12; Q8TDT2: GPR152; NbExp=3; IntAct=EBI-2844246, EBI-13345167;
CC       Q9NV12; O15529: GPR42; NbExp=3; IntAct=EBI-2844246, EBI-18076404;
CC       Q9NV12; Q9UM44: HHLA2; NbExp=3; IntAct=EBI-2844246, EBI-2867874;
CC       Q9NV12; Q7Z5P4: HSD17B13; NbExp=3; IntAct=EBI-2844246, EBI-18053395;
CC       Q9NV12; P38484: IFNGR2; NbExp=3; IntAct=EBI-2844246, EBI-3905457;
CC       Q9NV12; Q15842: KCNJ8; NbExp=3; IntAct=EBI-2844246, EBI-17440235;
CC       Q9NV12; P60410: KRTAP10-8; NbExp=3; IntAct=EBI-2844246, EBI-10171774;
CC       Q9NV12; Q16553: LY6E; NbExp=3; IntAct=EBI-2844246, EBI-18234679;
CC       Q9NV12; Q9GZY8-5: MFF; NbExp=3; IntAct=EBI-2844246, EBI-11956541;
CC       Q9NV12; O14880: MGST3; NbExp=3; IntAct=EBI-2844246, EBI-724754;
CC       Q9NV12; Q7Z6M3: MILR1; NbExp=3; IntAct=EBI-2844246, EBI-18391669;
CC       Q9NV12; Q96HJ5: MS4A3; NbExp=3; IntAct=EBI-2844246, EBI-12806656;
CC       Q9NV12; Q15800: MSMO1; NbExp=3; IntAct=EBI-2844246, EBI-949102;
CC       Q9NV12; Q13113: PDZK1IP1; NbExp=3; IntAct=EBI-2844246, EBI-716063;
CC       Q9NV12; Q96TC7: RMDN3; NbExp=3; IntAct=EBI-2844246, EBI-1056589;
CC       Q9NV12; Q9NY72: SCN3B; NbExp=3; IntAct=EBI-2844246, EBI-17247926;
CC       Q9NV12; Q3SXP7: SHISAL1; NbExp=3; IntAct=EBI-2844246, EBI-18037857;
CC       Q9NV12; Q9Y3P8: SIT1; NbExp=3; IntAct=EBI-2844246, EBI-6977215;
CC       Q9NV12; Q9NUM3: SLC39A9; NbExp=3; IntAct=EBI-2844246, EBI-2823239;
CC       Q9NV12; Q9HBV2: SPACA1; NbExp=3; IntAct=EBI-2844246, EBI-17498703;
CC       Q9NV12; P27105: STOM; NbExp=3; IntAct=EBI-2844246, EBI-1211440;
CC       Q9NV12; Q8N205: SYNE4; NbExp=3; IntAct=EBI-2844246, EBI-7131783;
CC       Q9NV12; Q8N6K0: TEX29; NbExp=3; IntAct=EBI-2844246, EBI-19027521;
CC       Q9NV12; Q6ZP80: TMEM182; NbExp=3; IntAct=EBI-2844246, EBI-10255122;
CC       Q9NV12; Q6UW68: TMEM205; NbExp=3; IntAct=EBI-2844246, EBI-6269551;
CC       Q9NV12; Q6UWW9: TMEM207; NbExp=3; IntAct=EBI-2844246, EBI-13301303;
CC       Q9NV12; Q9P0T7: TMEM9; NbExp=3; IntAct=EBI-2844246, EBI-723976;
CC       Q9NV12; Q9Y320: TMX2; NbExp=3; IntAct=EBI-2844246, EBI-6447886;
CC       Q9NV12; O95859: TSPAN12; NbExp=3; IntAct=EBI-2844246, EBI-2466403;
CC       Q9NV12; Q5TGU0: TSPO2; NbExp=3; IntAct=EBI-2844246, EBI-12195249;
CC   -!- SUBCELLULAR LOCATION: Membrane {ECO:0000305}; Multi-pass membrane
CC       protein {ECO:0000305}.
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DR   EMBL; AK001862; BAA91948.1; -; mRNA.
DR   EMBL; AC083862; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; CH236950; EAL24065.1; -; Genomic_DNA.
DR   EMBL; BC020942; AAH20942.1; -; mRNA.
DR   CCDS; CCDS5837.1; -.
DR   RefSeq; NP_060765.4; NM_018295.4.
DR   AlphaFoldDB; Q9NV12; -.
DR   BioGRID; 120569; 57.
DR   IntAct; Q9NV12; 49.
DR   MINT; Q9NV12; -.
DR   STRING; 9606.ENSP00000275767; -.
DR   GlyGen; Q9NV12; 1 site.
DR   iPTMnet; Q9NV12; -.
DR   PhosphoSitePlus; Q9NV12; -.
DR   BioMuta; TMEM140; -.
DR   DMDM; 296452934; -.
DR   PaxDb; Q9NV12; -.
DR   PeptideAtlas; Q9NV12; -.
DR   PRIDE; Q9NV12; -.
DR   Antibodypedia; 18112; 31 antibodies from 7 providers.
DR   DNASU; 55281; -.
DR   Ensembl; ENST00000275767.3; ENSP00000275767.2; ENSG00000146859.6.
DR   GeneID; 55281; -.
DR   KEGG; hsa:55281; -.
DR   MANE-Select; ENST00000275767.3; ENSP00000275767.2; NM_018295.5; NP_060765.4.
DR   UCSC; uc003vsi.4; human.
DR   CTD; 55281; -.
DR   DisGeNET; 55281; -.
DR   GeneCards; TMEM140; -.
DR   HGNC; HGNC:21870; TMEM140.
DR   HPA; ENSG00000146859; Tissue enhanced (skeletal).
DR   neXtProt; NX_Q9NV12; -.
DR   OpenTargets; ENSG00000146859; -.
DR   PharmGKB; PA144596261; -.
DR   VEuPathDB; HostDB:ENSG00000146859; -.
DR   eggNOG; ENOG502S6FP; Eukaryota.
DR   GeneTree; ENSGT00390000014089; -.
DR   HOGENOM; CLU_125527_0_0_1; -.
DR   InParanoid; Q9NV12; -.
DR   OMA; NFCLWNQ; -.
DR   OrthoDB; 1420340at2759; -.
DR   PhylomeDB; Q9NV12; -.
DR   TreeFam; TF336296; -.
DR   PathwayCommons; Q9NV12; -.
DR   SignaLink; Q9NV12; -.
DR   BioGRID-ORCS; 55281; 12 hits in 1081 CRISPR screens.
DR   ChiTaRS; TMEM140; human.
DR   GenomeRNAi; 55281; -.
DR   Pharos; Q9NV12; Tdark.
DR   PRO; PR:Q9NV12; -.
DR   Proteomes; UP000005640; Chromosome 7.
DR   RNAct; Q9NV12; protein.
DR   Bgee; ENSG00000146859; Expressed in blood and 158 other tissues.
DR   Genevisible; Q9NV12; HS.
DR   GO; GO:0016021; C:integral component of membrane; IEA:UniProtKB-KW.
DR   InterPro; IPR028038; TM140.
DR   PANTHER; PTHR16103; PTHR16103; 1.
DR   Pfam; PF14985; TM140; 1.
PE   1: Evidence at protein level;
KW   Glycoprotein; Membrane; Reference proteome; Transmembrane;
KW   Transmembrane helix.
FT   CHAIN           1..185
FT                   /note="Transmembrane protein 140"
FT                   /id="PRO_0000274357"
FT   TOPO_DOM        1..11
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        12..32
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        33..77
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        78..98
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        99..114
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        115..135
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        136..150
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        151..171
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        172..185
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        38
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   VARIANT         6
FT                   /note="P -> S (in dbSNP:rs292500)"
FT                   /id="VAR_030262"
FT   VARIANT         7
FT                   /note="R -> Q (in dbSNP:rs3800592)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_030263"
FT   VARIANT         11
FT                   /note="Q -> E (in dbSNP:rs11558290)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_030264"
FT   VARIANT         29
FT                   /note="F -> L (in dbSNP:rs292501)"
FT                   /evidence="ECO:0000269|PubMed:12690205,
FT                   ECO:0000269|PubMed:14702039, ECO:0000269|PubMed:15489334"
FT                   /id="VAR_030265"
FT   VARIANT         112
FT                   /note="A -> E (in a colorectal cancer sample; somatic
FT                   mutation; dbSNP:rs292502)"
FT                   /evidence="ECO:0000269|PubMed:16959974"
FT                   /id="VAR_035670"
SQ   SEQUENCE   185 AA;  20419 MW;  6BD0CE084FDBC53A CRC64;
     MAGPRPRWRD QLLFMSIIVL VIVVICLMFY ALLWEAGNLT DLPNLRIGFY NFCLWNEDTS
     TLQCHQFPEL EALGVPRVGL GLARLGVYGS LVLTLFAPQP LLLAQCNSDE RAWRLAVGFL
     AVSSVLLAGG LGLFLSYVWK WVRLSLPGPG FLALGSAQAL LILLLIAMAV FPLRAERAES
     KLESC
 
 
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