Mus musculus mRNA for type II cytokeratin, complete cds

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.
Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...

Development of Woolly Hair and Hairlessness in a CRISPR-Engineered Mutant Mouse Model with KRT71 Mutations. [Cells. 2023]
Development of Woolly Hair and Hairlessness in a CRISPR-Engineered Mutant Mouse Model with KRT71 Mutations.
Zhang T, Yao H, Wang H, Sui T. Cells. 2023 Jul 5; 12(13). Epub 2023 Jul 5.
BraInMap Elucidates the Macromolecular Connectivity Landscape of Mammalian Brain. [Cell Syst. 2020]
BraInMap Elucidates the Macromolecular Connectivity Landscape of Mammalian Brain.
Pourhaghighi R, Ash PEA, Phanse S, Goebels F, Hu LZM, Chen S, Zhang Y, Wierbowski SD, Boudeau S, Moutaoufik MT, et al. Cell Syst. 2020 Apr 22; 10(4):333-350.e14.
Sox13 is a novel early marker for hair follicle development. [Biochem Biophys Res Commun. 2019]
Sox13 is a novel early marker for hair follicle development.
Noto M, Noguchi N, Ishimura A, Kiyonari H, Abe T, Suzuki T, Hasunuma N, Taira M, Manabe M, Osada SI. Biochem Biophys Res Commun. 2019 Feb 19; 509(4):862-868. Epub 2019 Jan 11.

Mus musculus mRNA for type II cytokeratin, complete cds
Mus musculus mRNA for type II cytokeratin, complete cds
gi|6092074|dbj|AB033744.1|

Nucleotide
Familial congenital nasolacrimal duct obstruction
Familial congenital nasolacrimal duct obstruction

MedGen
C1835612[conceptid] (1)
MedGen
LOC127890617 [Homo sapiens]
LOC127890617 [Homo sapiens]
Gene ID:127890617

Gene
LOC129993286 [Homo sapiens]
LOC129993286 [Homo sapiens]
Gene ID:129993286

Gene

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide