- snr-2 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable snRNP binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in cytoplasm. Predicted to be part of spliceosomal complex and spliceosomal snRNP complex. Expressed in gonad. Human ortholog(s) of this gene implicated in several diseases, including Prader-Willi syndrome; cerebrocostomandibular syndrome; and mixed connective tissue disease. Is an ortholog of human SNRPN (small nuclear ribonucleoprotein polypeptide N) and SNURF (SNRPN upstream open reading frame).
- Ipw [Search on AGR]
Homo sapiens This gene is non-protein coding, is expressed exclusively from the paternal allele, and may play a role in the imprinting process. Mutations in this gene are associated with Prader-Willi syndrome. [provided by RefSeq, May 2010]
- SNORD109A [Search on AGR]
Homo sapiens This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]
- Snord64 [Search on AGR]
Homo sapiens This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]
- PWARSN [Search on AGR]
Homo sapiens This gene encodes a novel transcript, and is located in the Prader-Willi syndrome critical region on chromosome 15. This gene is expressed exclusively from the paternal allele. [provided by RefSeq, Mar 2017]
- SNORD109B [Search on AGR]
Homo sapiens This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]
- Ndn [Search on AGR]
Homo sapiens This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons. [provided by RefSeq, Jul 2008]
- Nipa2 [Search on AGR]
Homo sapiens This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]
- Snrpn [Search on AGR]
Rattus norvegicus Predicted to enable snRNP binding activity. Involved in response to hormone. Part of U1 snRNP and U2 snRNP. Human ortholog(s) of this gene implicated in Prader-Willi syndrome. Orthologous to human SNRPN (small nuclear ribonucleoprotein polypeptide N); INTERACTS WITH 2,4-dinitrotoluene; 6-propyl-2-thiouracil; alachlor.
- Snurf [Search on AGR]
Homo sapiens This gene is located within the Prader-Willi Syndrome critical region on chromosome 15. Transcripts produced from this gene initiate at an imprinting center and are paternally-imprinted. These transcripts may be bicistronic and also encode SNRPN (small nuclear ribonucleoprotein polypeptide N) from a downstream open reading frame. The small protein represented by this gene is encoded by an evolutionarily-conserved upstream open reading frame and is localized to the nucleus. Extensive alternative splicing and promoter usage occurs in this region and the full-length nature of some of these transcripts has not been determined. Alterations in the imprinting center are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]