WDYHV1

Protein N-terminal glutamine amidohydrolase is an enzyme that in humans is encoded by the WDYHV1 gene.[5][6]

NTAQ1
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 3C9Q, 4W79
Identifiers
Aliases	NTAQ1, C8orf32, WDYHV motif containing 1, N-terminal glutamine amidase 1, WDYHV1
External IDs	MGI: 1924023 HomoloGene: 9968 GeneCards: NTAQ1
Gene location (Human) Chr. Chromosome 8 (human)[1] Band 8q24.13 Start 123,416,726 bp[1] End 123,470,028 bp[1]
Gene location (Mouse) Chr. Chromosome 15 (mouse)[2] Band 15 D1|15 Start 58,141,377 bp[2] End 58,158,665 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides • GO:0001948 protein binding • hydrolase activity • protein-N-terminal glutamine amidohydrolase activity • protein-N-terminal asparagine amidohydrolase activity Cellular component • cytoplasm • cytosol • cell nucleus Biological process • cellular protein modification process Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	55093	76773
Ensembl	ENSG00000156795	ENSMUSG00000022359
UniProt	Q96HA8	Q80WB5
RefSeq (mRNA)	NM_001283024 NM_001283027 NM_018024	NM_029734 NM_001326599 NM_001326602
RefSeq (protein)	NP_001269953 NP_001269956 NP_060494	NP_001313528 NP_001313531 NP_084010
Location (UCSC)	Chr 8: 123.42 – 123.47 Mb	Chr 15: 58.14 – 58.16 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000156795 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000022359 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, Jordan H, Moore T, Max SI, Wang J, Hsieh F, Diatchenko L, Marusina K, Farmer AA, Rubin GM, Hong L, Stapleton M, Soares MB, Bonaldo MF, Casavant TL, Scheetz TE, Brownstein MJ, Usdin TB, Toshiyuki S, Carninci P, Prange C, Raha SS, Loquellano NA, Peters GJ, Abramson RD, Mullahy SJ, Bosak SA, McEwan PJ, McKernan KJ, Malek JA, Gunaratne PH, Richards S, Worley KC, Hale S, Garcia AM, Gay LJ, Hulyk SW, Villalon DK, Muzny DM, Sodergren EJ, Lu X, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madan A, Young AC, Shevchenko Y, Bouffard GG, Blakesley RW, Touchman JW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Krzywinski MI, Skalska U, Smailus DE, Schnerch A, Schein JE, Jones SJ, Marra MA (Dec 2002). "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): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
6. "Entrez Gene: C8orf32 chromosome 8 open reading frame 32".

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): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
• 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): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
• Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569.

External links

• Human WDYHV1 genome location and WDYHV1 gene details page in the UCSC Genome Browser.