Symbol Name ID |
Tubb5
tubulin, beta 5 class I MGI:107812 |
Age | E8 | E10 | E10.5 | E12 | E12.5 | E13.5 | E14 | E14.5 | E15 | E15.5 | E16 | E16.5 | E17.5 | E18 | E18.5 | P |
In situ RNA (section) | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | ||||||||
In situ RNA (whole mount) | 2 | 2 | ||||||||||||||
Northern blot | 1 | 1 | 1 | 1 | 1 | |||||||||||
Western blot | 1 | |||||||||||||||
RT-PCR | 3 | 2 | 1 | 2 | 1 | 2 | 1 | 2 | 3 | 3 | 6 | |||||
cDNA clones | 2 | 1 | 1 |
Tubb5 tubulin, beta 5 class I (Synonyms: B130022C14Rik) | |
Results | Reference |
5* | J:93300 Blackshaw S, Harpavat S, Trimarchi J, Cai L, Huang H, Kuo WP, Weber G, Lee K, Fraioli RE, Cho SH, Yung R, Asch E, Ohno-Machado L, Wong WH, Cepko CL, Genomic analysis of mouse retinal development. PLoS Biol. 2004 Oct;2(9):E247 |
9* | J:196330 Breuss M, Heng JI, Poirier K, Tian G, Jaglin XH, Qu Z, Braun A, Gstrein T, Ngo L, Haas M, Bahi-Buisson N, Moutard ML, Passemard S, Verloes A, Gressens P, Xie Y, Robson KJ, Rani DS, Thangaraj K, Clausen T, Chelly J, Cowan NJ, Keays DA, Mutations in the beta-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities. Cell Rep. 2012 Dec 27;2(6):1554-62 |
1* | J:148410 Combes AN, Lesieur E, Harley VR, Sinclair AH, Little MH, Wilhelm D, Koopman P, Three-dimensional visualization of testis cord morphogenesis, a novel tubulogenic mechanism in development. Dev Dyn. 2009 May;238(5):1033-41 |
2* | J:81851 Fowles LF, Bennetts JS, Berkman JL, Williams E, Koopman P, Teasdale RD, Wicking C, Genomic screen for genes involved in mammalian craniofacial development. Genesis. 2003 Feb;35(2):73-87 |
3* | J:46439 Freeman TC, Dixon AK, Campbell EA, Tait TM, Richardson PJ, Rice KM, Maslen GL, Metcalfe AD, Streuli CH, Bentley DR, Expression Mapping of Mouse Genes. MGI Direct Data Submission. 1998; |
1* | J:171409 GUDMAP Consortium, GUDMAP: the GenitoUrinary Development Molecular Anatomy Project. www.gudmap.org. 2004; |
4* | J:74177 Hembree MJ, Prasadan K, Manna P, Preuett B, Spilde T, Bhatia A, Kobayashi H, Buckingham B, Snyder CL, Gittes GK, Semiquantitative polymerase chain reaction in RNase-producing tissues: Analysis of the developing pancreas. J Pediatr Surg. 2001 Nov;36(11):1629-32 |
1 | J:270401 Latremoliere A, Cheng L, DeLisle M, Wu C, Chew S, Hutchinson EB, Sheridan A, Alexandre C, Latremoliere F, Sheu SH, Golidy S, Omura T, Huebner EA, Fan Y, Whitman MC, Nguyen E, Hermawan C, Pierpaoli C, Tischfield MA, Woolf CJ, Engle EC, Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration. Cell Rep. 2018 Aug 14;24(7):1865-1879.e9 |
7* | J:19085 Lewis SA, Lee MG, Cowan NJ, Five mouse tubulin isotypes and their regulated expression during development. J Cell Biol. 1985 Sep;101(3):852-61 |
6 | J:330439 Liu H, He L, Cheng Q, Luo W, Zhao T, Yang D, Validation of superior reference genes in mouse submandibular glands under developmental and functional regeneration states. Int J Mol Med. 2022 Nov;50(5) |
1 | J:78343 Loebel DA, O'Rourke MP, Steiner KA, Banyer J, Tam PP, Isolation of differentially expressed genes from wild-type and Twist mutant mouse limb buds. Genesis. 2002 Jul;33(3):103-13 |
1* | J:138696 Sato A, Sekine Y, Saruta C, Nishibe H, Morita N, Sato Y, Sadakata T, Shinoda Y, Kojima T, Furuichi T, Cerebellar development transcriptome database (CDT-DB): profiling of spatio-temporal gene expression during the postnatal development of mouse cerebellum. Neural Netw. 2008 Oct;21(8):1056-69 |
2 | J:295090 Stoupa A, Adam F, Kariyawasam D, Strassel C, Gawade S, Szinnai G, Kauskot A, Lasne D, Janke C, Natarajan K, Schmitt A, Bole-Feysot C, Nitschke P, Leger J, Jabot-Hanin F, Tores F, Michel A, Munnich A, Besmond C, Scharfmann R, Lanza F, Borgel D, Polak M, Carre A, TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology. EMBO Mol Med. 2018 Dec;10(12) |
4* | J:87314 Tateossian H, Powles N, Dickinson R, Ficker M, Maconochie M, Determination of downstream targets of FGF signalling using gene trap and cDNA subtractive approaches. Exp Cell Res. 2004 Jan 1;292(1):101-14 |
1 | J:344223 Zhang W, Zhang R, Wu L, Zhu C, Zhang C, Xu C, Zhao S, Liu X, Guo T, Lu Y, Gao Z, Yu X, Li L, Chen ZJ, Qin Y, Jiao X, NLRP14 deficiency causes female infertility with oocyte maturation defects and early embryonic arrest by impairing cytoplasmic UHRF1 abundance. Cell Rep. 2023 Dec 26;42(12):113531 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/10/2024 MGI 6.24 |
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