Details for: CRYGC
Associated with
Other Information
Genular Protein ID: 2849810845
Symbol: CRGC_HUMAN
Name: Gamma-crystallin C
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 4065573
Title: Two human gamma-crystallin genes are linked and riddled with Alu-repeats.
PubMed ID: 4065573
PubMed ID: 4033658
Title: Structural and evolutionary relationships among five members of the human gamma-crystallin gene family.
PubMed ID: 4033658
PubMed ID: 2777080
Title: Nucleotide sequence of the rat gamma-crystallin gene region and comparison with an orthologous human region.
PubMed ID: 2777080
PubMed ID: 15815621
Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
PubMed ID: 15815621
DOI: 10.1038/nature03466
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 8999933
Title: Sequence analysis of betaA3, betaB3, and betaA4 crystallins completes the identification of the major proteins in young human lens.
PubMed ID: 8999933
PubMed ID: 12876325
Title: Methylation and carbamylation of human gamma-crystallins.
PubMed ID: 12876325
DOI: 10.1110/ps.0305403
PubMed ID: 22876111
Title: A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree.
PubMed ID: 22876111
PubMed ID: 12507494
Title: Homology models of human gamma-crystallins: structural study of the extensive charge network in gamma-crystallins.
PubMed ID: 12507494
PubMed ID: 10521291
Title: The gamma-crystallins and human cataracts: a puzzle made clearer.
PubMed ID: 10521291
DOI: 10.1086/302619
PubMed ID: 10914683
Title: A 5-base insertion in the gammaC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract.
PubMed ID: 10914683
PubMed ID: 12011157
Title: Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts.
PubMed ID: 12011157
DOI: 10.1136/jmg.39.5.352
PubMed ID: 12601044
Title: Alteration of protein-protein interactions of congenital cataract crystallin mutants.
PubMed ID: 12601044
DOI: 10.1167/iovs.02-0950
PubMed ID: 18587492
Title: Crystallin gene mutations in Indian families with inherited pediatric cataract.
PubMed ID: 18587492
PubMed ID: 21423869
Title: Mutation screening and genotype phenotype correlation of alpha-crystallin, gamma-crystallin and GJA8 gene in congenital cataract.
PubMed ID: 21423869
PubMed ID: 22052681
Title: A novel mutation impairing the tertiary structure and stability of gammaC-crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens.
PubMed ID: 22052681
DOI: 10.1002/humu.21648
PubMed ID: 29386872
Title: Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities.
PubMed ID: 29386872
PubMed ID: 29914532
Title: Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract.
PubMed ID: 29914532
PubMed ID: 33243271
Title: The genetic landscape of crystallins in congenital cataract.
PubMed ID: 33243271
Sequence Information:
- Length: 174
- Mass: 20879
- Checksum: B01DC167171A7668
- Sequence:
MGKITFYEDR AFQGRSYETT TDCPNLQPYF SRCNSIRVES GCWMLYERPN YQGQQYLLRR GEYPDYQQWM GLSDSIRSCC LIPQTVSHRL RLYEREDHKG LMMELSEDCP SIQDRFHLSE IRSLHVLEGC WVLYELPNYR GRQYLLRPQE YRRCQDWGAM DAKAGSLRRV VDLY
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.