Lnc-CTSZ-5:1

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Annotated Information

Transcriptomic Nomeclature

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Function

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Regulation

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Expression

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Allelic Information and Variation

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Evolution

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Labs working on this lncRNA

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Basic Information

Transcript ID	lnc-CTSZ-5:1
Source	LNCipedia2.1
Same with	,
Classification	intergenic
Length	1158 nt
Genomic location	chr20-:57393972..57425958
Exon number	,
Exons	,
Genome context
Sequence	000001 TAGGGGGCGC CGCGTTGGAA CGCCCGAAGA GGTGCTGCTG GGGTGGTTGG AAGCCGGTGG GGGGCGGGTG TATGGCGGCT 000080 000081 AGGCCTGGAA GACCACGAGG ACCGCTAGCG CCGTGGGGTC ACTCTTCCTC ATGCCACAGG TTGCCGAGCC TCGGGGGAGA 000160 000161 GGTGGGGTCC CAGGGGCCAA CCCTTGGGTG TGTTGATGGC GGCAGGCTAA CCCAGCCAAC GGGGTGCCAC TGCCGGGCAA 000240 000241 GGTGAGGAGC AAGAAGATTT CCAGGGCTGG GAGGTAGAGG GCCAGGACCC CAAGGAGAGG GCTTACTGCG AGGAGCAGCC 000320 000321 CAGGATGGAT AAGGAGTTGA GGCCCCAGGG ATGCTGAGCC TGCACAAGTG GAAGTGACTG GCTACCAGAC TCTGAAAAAC 000400 000401 CTAAGTCCTT TAGGGAAGAC CACAAAAGCA TCCAACCACA GTCTGCGCTG CAGCCCGGCA GAACTAAGTC TTGGGCGCCG 000480 000481 CGACGCCTTT CCTACGGAAT AGGTCCTGGA AGGAAGACCA TTTAAGTCTT TCCCCCCAGG ACTGGCGAGG AGAGCACGCC 000560 000561 TTCCCTTCCG AAGGTGCGTT ACCAGATTGC TGCCGTTTTT GTGCTGGGTC ATCAGAGCAG ATTCCCCTCC AGGTTACAGA 000640 000641 TTAAACTTAA CTCTACCCGT GCTGAAAATG GCCGGAGCAC GCCGCCTCGC CTCCCCTCCC CAAGGCTGCC GGAGCCGCCG 000720 000721 GCCCCTGCCT CCTTTTCGAC GACTGATCGT CCAAGGACTG GCGCCGGATC CAACACCTTT CCCCAGCTCT GCGCGTACCG 000800 000801 CGCTCTTTGG AAACGAATTG GTCCCTGTCT GCTTCCAAGG GTCCCTGGAA CCTTCTGCAG CTGTGCCTCT CCAGAGCTCC 000880 000881 GCCTCATTAG TGCCACGTTC CTGGTTTGAA AACCATAGTA CTTCAACCTC TTCTAGATGG GAGTTAACCT TTGCCCTCTG 000960 000961 AAAGAAAGGT TTGATAAGCA AAGAGAGTTT GGTGAGCAAG ATCCTTGAGG TAAGAGCTGA TCTCTGACGT CCGCTGGGAA 001040 001041 CTGGCTGCTC TGCAGGTTTC TGTATCACAT TTTCTGCACA TGTCCATTAG AATTGGAGAT GGGGCGTATC TAGTGTTGAA 001120 001121 TAAAGGCCCG GCAGGCCCTC CCAGATGCAC CCTGTCAA

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Annotation (From lncRNAdb)

[lnc-CTSZ-5:1]

Section	Description
ID	Nespas
Characteristics	Northern blot with a probe for Nespas detects a smear and discrete band of 4.4kb and larger (Wroe (2000)). In addition to an unspliced form, five alternatively spliced forms of up to 1.4 kb in length have also been detected (Williamson (2002)). Imprinted (transcribed from the paternal allele). Transcribed from intron 2 of Nesp (Gnas), encompassing exons 2 through 1. The imprinted GNAS locus encodes the alpha-subunit of the stimulatory G protein as well as additional imprinted transcripts including the maternally expressed NESP55 and other paternally expressed transcripts (XLalphas and A/B transcripts).
Expression	Tissue-specific expression with signal in heart, in cerebral cortex, adrenal, and spleen, where Nesp is also expressed. Nesp and Nespas transcripts show expression from opposite parental alleles in most (but not all) tissues (Li (2000)), and Nespas may be abundant in some tissues where Nesp is not detected (Williamson (2002)). Furthermore, the Nesp transcripts can also remain imprinted in tissues that lack Nespas.
Function	A 4.2 kb microdeletion in humans that ablates two GNAS antisense exons is associated with pseudohypoparathyroidism type Ib. When maternally transmitted, this mutation causes loss of maternal GNAS imprints, partial gain of NESP55 methylation, and resistance to parathyroid hormone (PTH) in affected and obligate carrier individuals. Paternal transmission leads to epigenetic alterations in cis, including a partial loss of NESP55 methylation and a partial gain of A/B methylation. (Chillambhi (2010)). Nespas RNA was identified as binding to the repressive PRC2 chromatin modification complex in mouse embryonic stem cells, suggesting that like noncoding RNAs from other imprinted region, nespas could act to regulate the imprinting cluster it is transcribed from (Zhao (2010)).
Conservation	N/A
Misc	**Annotation in progress**

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