deoxyribonuclease TATDN1 isoform X1 [Homo sapiens]

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Human and bacterial TatD enzymes exhibit apurinic/apyrimidinic (AP) endonuclease activity. [Nucleic Acids Res. 2023]
Human and bacterial TatD enzymes exhibit apurinic/apyrimidinic (AP) endonuclease activity.
Dorival J, Eichman BF. Nucleic Acids Res. 2023 Apr 11; 51(6):2838-2849.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing. [Neuro Oncol. 2023]
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing.
Demirdizen E, Al-Ali R, Narayanan A, Sun X, Varga JP, Steffl B, Brom M, Krunic D, Schmidt C, Schmidt G, et al. Neuro Oncol. 2023 Jun 2; 25(6):1031-1043.
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery. [Nat Commun. 2022]
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.
Havugimana PC, Goel RK, Phanse S, Youssef A, Padhorny D, Kotelnikov S, Kozakov D, Emili A. Nat Commun. 2022 Jul 13; 13(1):4043. Epub 2022 Jul 13.

RefSeq mRNA
See reference mRNA sequence for the TATDN1 gene (XM_006716666.5).
RefSeq protein isoforms
See 35 reference sequence protein isoforms for the TATDN1 gene.

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Nucleotide
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SNP
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deoxyribonuclease TATDN1 isoform X1 [Homo sapiens]
deoxyribonuclease TATDN1 isoform X1 [Homo sapiens]
gi|578816201|ref|XP_006716729.1|

Protein
Rattus norvegicus SIL1 nucleotide exchange factor (Sil1), mRNA
Rattus norvegicus SIL1 nucleotide exchange factor (Sil1), mRNA
gi|40786442|ref|NM_199376.1|

Nucleotide
Insulin, Regular, Human
Insulin, Regular, Human
Regular insulin preparations that contain the HUMAN insulin peptide sequence.<br/>Year introduced: 2012

MeSH
Canavan Disease
Canavan Disease
A rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy appearance. Aspartoacylase...<br/>Year introduced: 1994

MeSH
Lafora Disease
Lafora Disease
A form of stimulus sensitive MYOCLONIC EPILEPSY inherited as an autosomal recessive condition. The most common presenting feature is a single seizure in the second decade of l...<br/>Year introduced: 2000

MeSH

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Protein