WDYHV1

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; OMA:NTAQ1 - orthologs
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 58,004,773 bp [2] End 58,022,061 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in ganglionic eminence secondary oocyte lateral nuclear group of thalamus gonad islet of Langerhans pons left ventricle gastrocnemius muscle C1 segment ventricular zone Top expressed in bone marrow thymus granulocyte pancreas spleen adrenal gland epiblast islet of Langerhans genital tubercle ileum More reference expression data BioGPS More reference expression data
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 – 58.02 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

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

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. Bibcode:2002PNAS...9916899M. 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. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID   16189514. S2CID   4427026.
• 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. S2CID   13709685.

External links

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