CRYBG3
Very large A-kinase anchor protein
Also known as: CRBG3_HUMAN, DKFZp667G2110
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q68DQ2
- Gene
- CRYBG3
- Ensembl
- ENSG00000080200
- Chromosome
- 3
- Canonical length
- 2970 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Primary cilium
OverviewNCBI Gene
Enables protein kinase A binding activity. Predicted to be involved in lens development in camera-type eye and visual perception. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
2970 residues, UniProt reviewed canonical sequence.
>Q68DQ2|CRYBG3
1 MSSGRRRGSA PWHSFSRFFA PRSPSRDKEE EEEERPGTSP PPAPGRSAAS VENEPMSTSQ
61 KKENVLSSEA VKIRQSEDKR NHAEKPVTLP VQEDPKKAYD LSSSTSDTKI GESDRQPKES
121 FFQFLGNLFN ISGKSSLGEA KQSSFKDDQD KTEKDLQNPS DHHEDGIKRE REIFSGSLRT
181 QTHPTEEQDS NSSELSDAFS LDTTQDSDQE TTNLLKQIDG KPEKPSVTYA TYRGPRHIGK
241 YLKQQTGLAT VNTLDRENES SDSSTNRHID PGSEIEAGVL PLLLSASTDS SMKGNLLEGP
301 LEDSDCSKTS FNKENSLTNN PELQNIASSN NLLNKNAWGS IERNRSSPSS VTNSSYDGES
361 DSQHHLSCEP VSQTNRNLVC SALLTGSNHR KVPCSPDFQR VTTTENTIKE NSTVMSNRTL
421 VQREELVEPQ GPAISDFSCS KSDGSDTTEQ ESTNLPSPNK SIRHEHLQLP ESECSDKQTI
481 DSSSKQAATH TNIIALQRHA VTDTEFVNEG KRLSAQDSQK NVAVREIRRE TESASAGESI
541 ASSHVKAPED KIESLPKDTD QYFETKAKKL DFRSHDKIPH IRMNKKDLAS LNYISESAVV
601 ASLGNENAPE LKFELNRSHI SETPLDSESP QQAEVSPDAK TSLSLDCKKL NFSISPPTFV
661 SGVGMLSKLD IPDLMNEGSP VPIETGNVNI VGISYQPRKC KEENVKNHVE AAGRKSPPPS
721 FCLEYTSAIF EFKEVLSNSE KCQVLPGSEA SGPHLTGLEL LSFDSGNLSK DCSSILSQDP
781 NRVELVSSNT KANMSIIEKS DSLSLEAKTA NIVSKAEIDG QNNVLVESHS GRGKTISLSK
841 VSLSKVEPRN ISQDKMSSFP LKITHVPEKP ILSELTFLEV EQGKRFQSIN HNEIGEKCSD
901 AGLKENCQAE LSPAASKYED KPEPEVDALG SPPALLKSNI SWILPPIHDE KISRQMAQNC
961 EAHTCVFHQS LDICGTKKIS GHSEMAELSL TNISPKFQET GSMKVNSPFL DSDSSLEKNS
1021 SASEDSSFLK VPSVLKLEKK SSSYRKKENI HFLNGGIDSV SSSSSYPEEV SMIVNSHKPQ
1081 NNLDSIQVTK DLTHEGTSVT NLLYPTTSYL EFETSVSIGT EVTPFQEHFG IYTGKISIDF
1141 PTAAQFDNLV EAETGAVAGP AASVNSSGQQ CSEASAEHIE ARRRAHDQLL DLKSSLLKKA
1201 DTLIGEIFNS VREELKFKHT VSTCQEHIAI EGIMNLGTLK EDISEKNPSE VTLTEIQQTE
1261 GLEEQGMENM SEVKEKPCVS PTVGEKNLLV DPNSMNVSCL LEDKARELVN EIIYVAQEKL
1321 RNDTFEDTED TWDSELQANT SKILNSDSVK PHDVVREFLV SEQPVNQSTQ ISENKVLNEF
1381 FSLSNLASGT ESIKGGEIVL YQKSLFSGNG SGLSDSINLQ ESDTVLLAED MSHKRLDDRV
1441 KTHLFRSEDC NETMEIENVD NNKTETEDRR TLVLNFKWPP LVNDDIHAPG TSKSSLSDSL
1501 VCISEKNLPG HSKNTPLAMS DVGKVHKKDN EINIGKIELI PSMLETGKTN KKDAELNILK
1561 YEAVPPMIEM GRIHKMDAEL NVTKTEPKAN VFKMGEVYQM DAESCIEKTE GSAVILGMEK
1621 AYKMKDTEGD IGKIEVIPMM PEVKNIHQKD AEGDIVKTEM TPVTVDMENI YQTHAEGDIG
1681 KTGTIALSEV ENIHQKGGEG ISEKAEVIPV TLAMENTYQK DAEGDIGKAE VMPVRLEMEN
1741 TYPKDTERDG GKTEVMPLAL EVVNTYQKNA KGFTGNTEGS VLKMEATYRK TAEEVIKNTE
1801 IVPCVLKVKE AHETAPAPLE MEKACKRDVK ETIGATVSTP SVIEMEKISP EDRGENIGKH
1861 KVLPAVVDIE KIHGTGLELT TKQGEAMLPA FESKTPQEYA EGSVEETKEE PTEIKEGLIA
1921 HENRLPTYFR GYESPTLSKD YEGYPAPAMP DFQPGDTTVR LDKRMSLTAI YDKRRETDYS
1981 DKGYNLAFVS QDEQENSSFT ILYEEPLQEE DKYASAEARQ TQSVLFHDTS ADSMPVLACE
2041 RSESRTDLVH HFEKGTKLGE TFDSDSSEMF LSVEAKRYKI YPLALSPIYE DDSSQEDILS
2101 SEVSPGHHGP RKSRDSENQS SSVLSLLQSV SERLKMNFDE DDREAADEEE EEEEAAVLHK
2161 GDLRAGSGER VTFQLPDPSI TFYPDDQESV GISKNSYVMP NEPTTSNLQV GLWPEKTSFL
2221 QKSDLTSKLH SSLKSAYHQY LQTSQSHSSE KGARFGGIFQ EPVSKYFRVQ DSPGRLSPFI
2281 ENVDKQTLRC NPRPGKMVIY DLHESTYKQE VYCNIPDATS WSFPNGVLIK VVRGCWILYE
2341 KPHFRGQKCV LEEGEKVLNR DWILQNRRHP QRNFILGSLK RVLKDCSIPE IELFPQSDPA
2401 CCPVYIQRAV PNLEELNISK SVSFTVKSGV WLAYPDINFK GQATVLEEDH GLFEISTAEM
2461 KSLHPLQMGG LKVEMPMNLK VIIYEKPHFH GQAKEFSEHI DSVPNFLKNN GDFHRIGSIR
2521 VIGGVWVAYE KEHFKGQQFL LEEGDFEDSN ACGALSSPIL SFRYLQANFI ESSVTLFESD
2581 LESGKFIDIT NQEISDLEEI GFGSKTRSIH VKSGVWVAYQ QKFFCGEQYI LEKGKYKCFF
2641 DWGGSNNIIM SIRPIQLEPL GINEPPHLLK AFSKPGFQGE CIDFTEETSD LTSLMPCSFK
2701 VLRGCWLLYY QEDMFVNHCV LEEGLYADLT SCGCPASKVK SLKPIDYVFE EPSISLFALE
2761 HCEGRELHLE EAVNSVLNKD LHFYTQSVWV KSGLWIAYEG SNFLGRQILL RPNEIPNWTA
2821 FSRWKTIGSL RPMKQPAVYI RIKNRAQGEY LTVTGSLADT RATSVCISPY SGKNTQIWYY
2881 CRGLFKSKAS DTCLDVIGGR DTPGAKVALW TEHGQFRQKW RLNKNGTISS YLSDQLVLDV
2941 KGGNYCDKTH VIVNQPLEGE ETQKWDIEILLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CRYBG3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 25 nTPM
- testis: 13 nTPM
- skin: 12 nTPM
- placenta: 10 nTPM
- adipose tissue: 9.9 nTPM
- tongue: 9.2 nTPM
Single-cell type
- retinal bipolar cells: 269 nCPM
- renal collecting duct intercalated cells: 263 nCPM
- late spermatids: 182 nCPM
- late primary spermatocytes: 180 nCPM
- ocular epithelial cells: 177 nCPM
- adipocytes: 175 nCPM
Immune cell
- plasmacytoid DC: 3.6 nTPM
- basophil: 1.5 nTPM
- classical monocyte: 1.4 nTPM
- myeloid DC: 1.4 nTPM
- non-classical monocyte: 1 nTPM
- intermediate monocyte: 0.9 nTPM
Brain region
- white matter: 40 nTPM
- medulla oblongata: 39 nTPM
- basal ganglia: 31 nTPM
- spinal cord: 30 nTPM
- pons: 28 nTPM
- hypothalamus: 28 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.49
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.47
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CRYBG3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CRYBG3 as an antibody target. Whether an autoantibody or antibody against CRYBG3 could matter depends on whether native CRYBG3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CRYBG3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CRYBG3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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