Crystallin, gamma D

CRYGD
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1H4A, 1HK0, 2G98, 2KFB, 2KLJ, 4GR7, 4JGF
Identifiers
Aliases	CRYGD, CACA, CCA3, CCP, CRYG4, CTRCT4, PCC, cry-g-D, crystallin gamma D
External IDs	MGI: 88524 HomoloGene: 36213 GeneCards: CRYGD
Gene ontology Molecular function • protein binding • structural constituent of eye lens Cellular component • cytoplasm • nucleus Biological process • cellular response to reactive oxygen species • lens development in camera-type eye • lens fiber cell differentiation • response to stimulus • visual perception Sources:Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	1421	12967
Ensembl	ENSG00000118231	ENSMUSG00000067299
UniProt	P07320	P04342
RefSeq (mRNA)	NM_006891	NM_007776
RefSeq (protein)	NP_008822.2	NP_031802.2
Location (UCSC)	Chr 2: 208.12 – 208.12 Mb	Chr 1: 65.06 – 65.06 Mb
PubMed search	[1]	[2]
Wikidata

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Gamma-crystallin D is a protein that in humans is encoded by the CRYGD gene.^[3]

Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Gamma-crystallins are a homogeneous group of highly symmetrical, monomeric proteins typically lacking connecting peptides and terminal extensions. They are differentially regulated after early development. Four gamma-crystallin genes (gamma-A through gamma-D) and three pseudogenes (gamma-E, gamma-F, gamma-G) are tandemly organized in a genomic segment as a gene cluster. Whether due to aging or mutations in specific genes, gamma-crystallins have been involved in cataract formation.^[3]

References

1. "Human PubMed Reference:".
2. "Mouse PubMed Reference:".
3. "Entrez Gene: CRYGD crystallin, gamma D".

Further reading

• Graw J (1998). "The crystallins: genes, proteins and diseases". Biol. Chem. 378 (11): 1331–48. doi:10.1515/bchm.1997.378.11.1299. PMID 9426193.
• Slingsby C, Clout NJ (2000). "Structure of the crystallins". Eye (London, England). 13 ( Pt 3b): 395–402. doi:10.1038/eye.1999.113. PMID 10627816.
• Brakenhoff RH, Aarts HJ, Reek FH, et al. (1991). "Human gamma-crystallin genes. A gene family on its way to extinction". J. Mol. Biol. 216 (3): 519–32. doi:10.1016/0022-2836(90)90380-5. PMID 2258929.
• Shiloh Y, Donlon T, Bruns G, et al. (1986). "Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36". Hum. Genet. 73 (1): 17–9. doi:10.1007/BF00292656. PMID 3011643.
• Lubsen NH, Renwick JH, Tsui LC, et al. (1987). "A locus for a human hereditary cataract is closely linked to the gamma-crystallin gene family". Proc. Natl. Acad. Sci. U.S.A. 84 (2): 489–92. doi:10.1073/pnas.84.2.489. PMC 304234. PMID 3025877.
• Meakin SO, Du RP, Tsui LC, Breitman ML (1987). "Gamma-crystallins of the human eye lens: expression analysis of five members of the gene family". Mol. Cell. Biol. 7 (8): 2671–9. PMC 367883. PMID 3670288.
• Meakin SO, Breitman ML, Tsui LC (1985). "Structural and evolutionary relationships among five members of the human gamma-crystallin gene family". Mol. Cell. Biol. 5 (6): 1408–14. PMC 366871. PMID 4033658.
• Rogaev EI, Rogaeva EA, Korovaitseva GI, et al. (1997). "Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35". Hum. Mol. Genet. 5 (5): 699–703. doi:10.1093/hmg/5.5.699. PMID 8733140.
• Andley UP, Mathur S, Griest TA, Petrash JM (1997). "Cloning, expression, and chaperone-like activity of human alphaA-crystallin". J. Biol. Chem. 271 (50): 31973–80. doi:10.1074/jbc.271.50.31973. PMID 8943244.
• Lampi KJ, Ma Z, Shih M, et al. (1997). "Sequence analysis of betaA3, betaB3, and betaA4 crystallins completes the identification of the major proteins in young human lens". J. Biol. Chem. 272 (4): 2268–75. doi:10.1074/jbc.272.4.2268. PMID 8999933.
• Stephan DA, Gillanders E, Vanderveen D, et al. (1999). "Progressive juvenile-onset punctate cataracts caused by mutation of the γD-crystallin gene". Proc. Natl. Acad. Sci. U.S.A. 96 (3): 1008–12. doi:10.1073/pnas.96.3.1008. PMC 15341. PMID 9927684.
• Héon E, Priston M, Schorderet DF, et al. (1999). "The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer". Am. J. Hum. Genet. 65 (5): 1261–7. doi:10.1086/302619. PMC 1288278. PMID 10521291.
• Pande A, Pande J, Asherie N, et al. (2000). "Molecular basis of a progressive juvenile-onset hereditary cataract". Proc. Natl. Acad. Sci. U.S.A. 97 (5): 1993–8. doi:10.1073/pnas.040554397. PMC 15742. PMID 10688888.
• Kmoch S, Brynda J, Asfaw B, et al. (2000). "Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography". Hum. Mol. Genet. 9 (12): 1779–86. doi:10.1093/hmg/9.12.1779. PMID 10915766.
• Pande A, Pande J, Asherie N, et al. (2001). "Crystal cataracts: Human genetic cataract caused by protein crystallization". Proc. Natl. Acad. Sci. U.S.A. 98 (11): 6116–20. doi:10.1073/pnas.101124798. PMC 33431. PMID 11371638.
• Santhiya ST, Shyam Manohar M, Rawlley D, et al. (2002). "Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts". J. Med. Genet. 39 (5): 352–8. doi:10.1136/jmg.39.5.352. PMC 1735119. PMID 12011157.
• MacCoss MJ, McDonald WH, Saraf A, et al. (2002). "Shotgun identification of protein modifications from protein complexes and lens tissue". Proc. Natl. Acad. Sci. U.S.A. 99 (12): 7900–5. doi:10.1073/pnas.122231399. PMC 122992. PMID 12060738.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.