Summary: Cleft lip and palate transmembrane protein 1 (CLPTM1)
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This is the Wikipedia entry entitled "Cleft lip and palate transmembrane protein 1". More...
Cleft lip and palate transmembrane protein 1 Edit Wikipedia article
| Cleft lip and palate associated transmembrane protein 1 | |||||||||||
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| Identifiers | |||||||||||
| Symbols | CLPTM1; ; | ||||||||||
| External IDs | OMIM: 604783 MGI: 1927155 HomoloGene: 37464 GeneCards: CLPTM1 Gene | ||||||||||
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| RNA expression pattern | |||||||||||
| More reference expression data | |||||||||||
| Orthologs | |||||||||||
| Species | Human | Mouse | |||||||||
| Entrez | 1209 | 56457 | |||||||||
| Ensembl | ENSG00000104853 | ENSMUSG00000002981 | |||||||||
| UniProt | O96005 | Q8VBZ3 | |||||||||
| RefSeq (mRNA) | NM_001199468.1 | NM_019649.2 | |||||||||
| RefSeq (protein) | NP_001285.1 | NP_062623.2 | |||||||||
| Location (UCSC) | Chr 19: 45.46 45.5 Mb |
Chr 7: 20.22 20.25 Mb |
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| PubMed search | [1] | [2] | |||||||||
| Identifiers | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Symbol | CLPTM1 | ||||||||
| Pfam | PF05602 | ||||||||
| InterPro | IPR008429 | ||||||||
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Cleft lip and palate transmembrane protein 1 is a protein that in humans is encoded by the CLPTM1 gene.[1][2] It belongs to a family of several eukaryotic cleft lip and palate transmembrane protein 1 sequences.
Cleft lip with or without cleft palate is a common birth defect that is genetically complex. The nonsyndromic forms have been studied genetically using linkage and candidate-gene association studies with only partial success in defining the loci responsible for orofacial clefting. CLPTM1 encodes a transmembrane protein and has strong homology to two Caenorhabditis elegans genes, suggesting that CLPTM1 may belong to a new gene family.[3] This family also contains the Homo sapiens cisplatin resistance related protein CRR9p which is associated with CDDP-induced apoptosis.[4]
[edit] References
- ^ Yoshiura K, Machida J, Daack-Hirsch S, Patil SR, Ashworth LK, Hecht JT, Murray JC (Jan 1999). "Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate". Genomics 54 (2): 23140. doi:10.1006/geno.1998.5577. PMID 9828125.
- ^ "Entrez Gene: CLPTM1 cleft lip and palate associated transmembrane protein 1". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1209.
- ^ Murray JC, Yoshiura K, Machida J, Daack-hirsch S, Patil SR, Ashworth LK, Hecht JT (1998). "Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate". Genomics 54 (2): 231240. doi:10.1006/geno.1998.5577. PMID 9828125.
- ^ Yamamoto K, Okamoto A, Isonishi S, Ochiai K, Ohtake Y (2001). "A novel gene, CRR9, which was up-regulated in CDDP-resistant ovarian tumor cell line, was associated with apoptosis". Biochem. Biophys. Res. Commun. 280 (4): 11481154. doi:10.1006/bbrc.2001.4250. PMID 11162647.
[edit] Further reading
- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 1714. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Takeuchi T, Kuro-o M, Miyazawa H, et al. (1997). "Transgenic expression of a novel thymic epithelial cell antigen stimulates aberrant development of thymocytes.". J. Immunol. 159 (2): 72633. PMID 9218588.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 14956. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 21217. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=528928.
- Rossi MR, Hawthorn L, Platt J, et al. (2005). "Identification of inactivating mutations in the JAK1, SYNJ2, and CLPTM1 genes in prostate cancer cells using inhibition of nonsense-mediated decay and microarray analysis.". Cancer Genet. Cytogenet. 161 (2): 97103. doi:10.1016/j.cancergencyto.2005.02.006. PMID 16102578.
- Lewandrowski U, Moebius J, Walter U, Sickmann A (2006). "Elucidation of N-glycosylation sites on human platelet proteins: a glycoproteomic approach.". Mol. Cell Proteomics 5 (2): 22633. doi:10.1074/mcp.M500324-MCP200. PMID 16263699.
- Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.". DNA Res. 12 (2): 11726. doi:10.1093/dnares/12.2.117. PMID 16303743.
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This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.
Cleft lip and palate transmembrane protein 1 (CLPTM1) Provide feedback
This family consists of several eukaryotic cleft lip and palate transmembrane protein 1 sequences. Cleft lip with or without cleft palate is a common birth defect that is genetically complex. The nonsyndromic forms have been studied genetically using linkage and candidate-gene association studies with only partial success in defining the loci responsible for orofacial clefting. CLPTM1 encodes a transmembrane protein and has strong homology to two Caenorhabditis elegans genes, suggesting that CLPTM1 may belong to a new gene family [1]. This family also contains the human cisplatin resistance related protein CRR9p which is associated with CDDP-induced apoptosis [2].
Literature references
-
Yoshiura K, Machida J, Daack-Hirsch S, Patil SR, Ashworth LK, Hecht JT, Murray JC; , Genomics 1998;54:231-240.: Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate. PUBMED:9828125 EPMC:9828125
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Yamamoto K, Okamoto A, Isonishi S, Ochiai K, Ohtake Y; , Biochem Biophys Res Commun 2001;280:1148-1154.: A novel gene, CRR9, which was up-regulated in CDDP-resistant ovarian tumor cell line, was associated with apoptosis. PUBMED:11162647 EPMC:11162647
External database links
| PANDIT: | PF05602 |
| Pseudofam: | PF05602 |
| SYSTERS: | CLPTM1 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR008429
Clefts of the lip and/or palate (CL/P) are some of the most common birth defects. They may be categorised into syndromic or non-syndromic types, with syndromic defects having an underlying chromosomal or teratogenic cause. Around 70% of clefts are non-syndromic and individuals have no typical physical or developmental abnormalities; these clefts generally show polygenetic behaviour and complex inheritance [PUBMED:16122939]. Studies have identified regions on chromosomes 19 and 11 which may be involved in non-syndromic cleft lip and palates; this included a novel gene on chromosome 19, cleft lip and palate-associated transmembrane protein 1 (CLPTM1) [PUBMED:9828125]. The Poliovirus receptor-related 1 gene (PVRL1), which is located on chromosome 11, has also been shown to associate with non-syndromic cleft lip and palates [PUBMED:11559849, PUBMED:19715471].
CLPTM1 encodes a transmembrane protein and has strong homology to two Caenorhabditis elegans genes, suggesting that CLPTM1 may belong to a new gene family [PUBMED:9828125]. This family also contains the Homo sapiens cisplatin resistance related protein CRR9p which is associated with CDDP-induced apoptosis [PUBMED:11162647].
Domain organisation
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Alignments
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| Seed (26) |
Full (492) |
Representative proteomes | NCBI (471) |
Meta (12) |
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| RP15 (122) |
RP35 (178) |
RP55 (264) |
RP75 (331) |
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| PP/heatmap | 1 | |||||||
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| Seed (26) |
Full (492) |
Representative proteomes | NCBI (471) |
Meta (12) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (122) |
RP35 (178) |
RP55 (264) |
RP75 (331) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
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Curation and family details
This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.
Curation
| Seed source: | Pfam-B_8636 (release 8.0) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Moxon SJ |
| Number in seed: | 26 |
| Number in full: | 492 |
| Average length of the domain: | 368.50 aa |
| Average identity of full alignment: | 30 % |
| Average coverage of the sequence by the domain: | 71.07 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 438 | ||||||||||||
| Family (HMM) version: | 7 | ||||||||||||
| Download: | download the raw HMM for this family |
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