CSNK2A2IP

gene
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Summary

CSNK2A2IP (casein kinase 2 subunit alpha’ interacting protein, HGNC:53637) is a protein-coding gene on chromosome 3p11.1, encoding Casein kinase II subunit alpha’-interacting protein (A0A1B0GTH6). May play a role in chromatin regulation of male germ cells.

Predicted to be located in male germ cell nucleus.

Source: NCBI Gene 111064647 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 2 total
  • MANE Select transcript: NM_001368165

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:53637
Approved symbolCSNK2A2IP
Namecasein kinase 2 subunit alpha’ interacting protein
Location3p11.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000283434
Ensembl biotypeprotein_coding
Entrez111064647

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 5 protein_coding_CDS_not_defined, 1 protein_coding

ENST00000635844, ENST00000636323, ENST00000636504, ENST00000636795, ENST00000637986, ENST00000638109

RefSeq mRNA: 4 — MANE Select: NM_001368165 NM_001368165, NM_001368166, NM_001368167, NM_001368168

CCDS: CCDS93323

Canonical transcript exons

ENST00000637986 — 2 exons

ExonStartEnd
ENSE000037940618846508888467594
ENSE000037974978833845688338643

Expression profiles

Bgee: expression breadth broad, 56 present calls, max score 88.16.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0246 / max 23.0053, expressed in 3 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
374640.02463

Top tissues by expression

111 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047388.16gold quality
left testisUBERON:000453385.12gold quality
testisUBERON:000047384.59gold quality
right testisUBERON:000453481.44gold quality
Brodmann (1909) area 9UBERON:001354058.82gold quality
dorsolateral prefrontal cortexUBERON:000983457.50gold quality
right frontal lobeUBERON:000281054.41gold quality
primary visual cortexUBERON:000243653.67gold quality
cerebellar hemisphereUBERON:000224552.08gold quality
cerebellar cortexUBERON:000212951.51gold quality
cerebellumUBERON:000203751.27gold quality
right hemisphere of cerebellumUBERON:001489050.20gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099149.87silver quality
anterior cingulate cortexUBERON:000983549.56gold quality
cerebral cortexUBERON:000095649.36gold quality
substantia nigraUBERON:000203848.61gold quality
hypothalamusUBERON:000189847.74gold quality
colonic epitheliumUBERON:000039746.47gold quality
frontal cortexUBERON:000187046.24gold quality
brainUBERON:000095545.32gold quality
amygdalaUBERON:000187645.08gold quality
superior frontal gyrusUBERON:000266144.88gold quality
temporal lobeUBERON:000187144.86gold quality
C1 segment of cervical spinal cordUBERON:000646944.13gold quality
Ammon’s hornUBERON:000195444.04gold quality
nucleus accumbensUBERON:000188242.77gold quality
ventricular zoneUBERON:000305341.92gold quality
putamenUBERON:000187441.78gold quality
prefrontal cortexUBERON:000045140.87gold quality
sural nerveUBERON:001548839.32gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no2.93

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusCsnk2a2ipENSMUSG00000068167
rattus_norvegicusCsnka2ipENSRNOG00000068003

Protein

Protein identifiers

Casein kinase II subunit alpha’-interacting proteinA0A1B0GTH6 (reviewed: A0A1B0GTH6)

Alternative names: Casein kinase 2 alpha prime interacting protein

All UniProt accessions (1): A0A1B0GTH6

UniProt curated annotations — full annotation on UniProt →

Function. May play a role in chromatin regulation of male germ cells.

Subunit / interactions. Interacts (via C-terminus) with CSNK2A2.

Subcellular location. Nucleus.

Post-translational modifications. Phosphorylated by CK2 (casein kinase II), specifically by complexes containing catalytic subunit CSNK2A2.

RefSeq proteins (4): NP_001355094, NP_001355095, NP_001355096, NP_001355097 (=MANE)

Domains & families (InterPro)

IDNameType
IPR038954CSNKA2IPFamily

UniProt features (3 total): chain 1, region of interest 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A1B0GTH6-F144.730.01

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 2 (showing top): GSE12003_4D_VS_8D_CULTURE_BM_PROGENITOR_DN, chr3p11

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (1): nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

100 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CSNK2A2IPCYLC2Q14093547
CSNK2A2IPRIMS2Q9UQ26449
CSNK2A2IPUTP3Q9NQZ2437
CSNK2A2IPKATNB1Q9BVA0405
CSNK2A2IPDPEP3Q9H4B8398
CSNK2A2IPZPBP2Q6X784389
CSNK2A2IPCABYRO75952379
CSNK2A2IPTRIM52Q96A61378
CSNK2A2IPSPATA16Q9BXB7377
CSNK2A2IPTEX12Q9BXU0370
CSNK2A2IPTSSK2Q96PF2370
CSNK2A2IPNDRG2Q9UN36370
CSNK2A2IPTBPL1P62380310
CSNK2A2IPSPAG1Q07617310
CSNK2A2IPCROCCQ5TZA2300

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A1B0GTH6, A0A1D5RMD1, A1KXM5, A2AEY4, A6NCI8, A6QQS3, A7KBS4, C4P6S0, O94713, P0C9Z7, P53963, P53976, Q0P670, Q0VAV2, Q10668, Q196W1, Q2KHR3, Q2YDJ5, Q32MG2, Q3V0A6, Q3V3Q4, Q4V8E9, Q5JRM2, Q68FV4, Q6AXV6, Q6AYN3, Q6NS59, Q7TSG5, Q80VJ6, Q80Y39, Q80YD3, Q810T2, Q86XD8, Q8C5U4, Q8CH19, Q8IWI9, Q8K4E0, Q8NDH2, Q8NEV8, Q8NFU7

Diamond homologs: A0A1B0GTH6, Q8CH19

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

2 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

4742 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
3:88466637:T:AV427D0.981
3:88466783:T:CC476R0.979
3:88466865:T:AV503D0.978
3:88467413:T:CF686L0.978
3:88467415:T:AF686L0.978
3:88467415:T:GF686L0.978
3:88467404:T:AW683R0.976
3:88467404:T:CW683R0.976
3:88466785:C:GC476W0.974
3:88466722:A:CR455S0.973
3:88466722:A:TR455S0.973
3:88466781:T:AV475D0.972
3:88466859:T:AL501H0.968
3:88466622:T:AV422D0.966
3:88466700:T:CL448P0.964
3:88466859:T:CL501P0.962
3:88466721:G:CR455T0.961
3:88466688:T:CI444T0.960
3:88466731:G:CR458S0.960
3:88466731:G:TR458S0.960
3:88466853:C:AA499E0.960
3:88466727:T:CM457T0.959
3:88467387:T:CL677S0.959
3:88467406:G:CW683C0.959
3:88467406:G:TW683C0.959
3:88467140:T:AW595R0.958
3:88467140:T:CW595R0.958
3:88466725:G:CR456S0.957
3:88466725:G:TR456S0.957
3:88467414:T:CF686S0.957

dbSNP variants (sampled 300 via entrez): RS1000081669 (3:88371227 G>A), RS1000090434 (3:88412051 A>T), RS1000119705 (3:88357291 A>T), RS1000120158 (3:88411760 A>T), RS1000174117 (3:88357022 G>A), RS1000180002 (3:88434059 C>A,T), RS1000218521 (3:88393060 TG>T,TGG), RS1000315603 (3:88405756 C>T), RS1000360972 (3:88439650 G>A), RS1000380581 (3:88362131 T>A), RS1000477825 (3:88418194 T>C), RS1000492731 (3:88373051 C>T), RS1000570553 (3:88393410 A>G), RS1000657392 (3:88352158 G>A,C), RS1000766656 (3:88400977 TAGA>T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.