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Gene Expression Literature Summary
Symbol
Name
ID
Dct
dopachrome tautomerase
MGI:102563

124 matching records from 124 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.
Age E9.5 E10 E10.5 E11 E11.5 E12 E12.5 E13 E13.5 E14 E14.5 E15 E15.5 E16 E16.5 E17.5 E18 E18.5 E19.5 E20 E P
Immunohistochemistry (section) 1 2 4 3 5 1 4 5 1 4 8 5 3 1 4 2 1 16
In situ RNA (section) 4 2 8 2 16 5 14 1 9 2 14 1 5 1 6 1 2 9 1 14
Immunohistochemistry (whole mount) 1 1 1 1 1 1 2
In situ RNA (whole mount) 3 1 10 3 18 2 12 6 1 1
In situ reporter (knock in) 1
Western blot 4
RT-PCR 1 1 1 2 3 1 1 1 10
cDNA clones 1 1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available
Dct  dopachrome tautomerase   (Synonyms: TRP-2, TRP2, tyrosinase-related protein-2, Tyrp-2, Tyrp2)
Results  Reference
1J:157307 Adameyko I, Lallemend F, Aquino JB, Pereira JA, Topilko P, Muller T, Fritz N, Beljajeva A, Mochii M, Liste I, Usoskin D, Suter U, Birchmeier C, Ernfors P, Schwann cell precursors from nerve innervation are a cellular origin of melanocytes in skin. Cell. 2009 Oct 16;139(2):366-79
2J:178973 Adameyko I, Lallemend F, Furlan A, Zinin N, Aranda S, Kitambi SS, Blanchart A, Favaro R, Nicolis S, Lubke M, Muller T, Birchmeier C, Suter U, Zaitoun I, Takahashi Y, Ernfors P, Sox2 and Mitf cross-regulatory interactions consolidate progenitor and melanocyte lineages in the cranial neural crest. Development. 2012 Jan;139(2):397-410
1J:173609 Agarwal P, Verzi MP, Nguyen T, Hu J, Ehlers ML, McCulley DJ, Xu SM, Dodou E, Anderson JP, Wei ML, Black BL, The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10. Development. 2011 Jun;138(12):2555-65
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1*J:272120 Bachg AC, Horsthemke M, Skryabin BV, Klasen T, Nagelmann N, Faber C, Woodham E, Machesky LM, Bachg S, Stange R, Jeong HW, Adams RH, Bahler M, Hanley PJ, Phenotypic analysis of Myo10 knockout (Myo10(tm2/tm2)) mice lacking full-length (motorized) but not brain-specific headless myosin X. Sci Rep. 2019 Jan 24;9(1):597
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2*J:78163 Baxter LL, Pavan WJ, The oculocutaneous albinism type IV gene Matp is a new marker of pigment cell precursors during mouse embryonic development. Mech Dev. 2002 Aug;116(1-2):209-12
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11J:355488 Erjavec E, Angee C, Hadjadj D, Passet B, David P, Kostic C, Dode E, Zanlonghi X, Cagnard N, Nedelec B, Crippa SV, Bole-Feysot C, Zarhrate M, Creuzet S, Castille J, Vilotte JL, Calvas P, Plaisancie J, Chassaing N, Kaplan J, Rozet JM, Taie LF, Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia. Am J Hum Genet. 2024 Oct 3;111(10):2265-2282
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14*J:31646 Steel KP, Davidson DR, Jackson IJ, TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor. Development. 1992 Aug;115(4):1111-9
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