SPDYE9
gene geneOn this page
Summary
SPDYE9 (speedy/RINGO cell cycle regulator family member E9, HGNC:45034) is a protein-coding gene on chromosome 7q11.23, encoding Speedy protein E9 (A0A494C191).
Enables acetylcholine receptor regulator activity.
Source: NCBI Gene 643909 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001382554
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:45034 |
| Approved symbol | SPDYE9 |
| Name | speedy/RINGO cell cycle regulator family member E9 |
| Location | 7q11.23 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000262461 |
| Ensembl biotype | protein_coding |
| Entrez | 643909 |
Gene structure
Transcript identifiers
Ensembl transcripts: 2 — 1 protein_coding_CDS_not_defined, 1 protein_coding
ENST00000571071, ENST00000575125
RefSeq mRNA: 2 — MANE Select: NM_001382554
NM_001382554, NM_001422015
CCDS: CCDS94116
Canonical transcript exons
ENST00000575125 — 8 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002642934 | 73075972 | 73077453 |
| ENSE00002669599 | 73085917 | 73086038 |
| ENSE00003488592 | 73082888 | 73083106 |
| ENSE00003603507 | 73081796 | 73081854 |
| ENSE00003637163 | 73084109 | 73084691 |
| ENSE00003843422 | 73078534 | 73078777 |
| ENSE00003847105 | 73080483 | 73080568 |
| ENSE00003849681 | 73078307 | 73078411 |
Expression profiles
Bgee: expression breadth ubiquitous, 125 present calls, max score 64.79.
Top tissues by expression
130 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| bone marrow cell | CL:0002092 | 64.79 | silver quality |
| colonic epithelium | UBERON:0000397 | 61.24 | silver quality |
| stromal cell of endometrium | CL:0002255 | 60.91 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 59.60 | gold quality |
| ventricular zone | UBERON:0003053 | 59.38 | gold quality |
| testis | UBERON:0000473 | 59.07 | gold quality |
| right testis | UBERON:0004534 | 58.98 | gold quality |
| muscle tissue | UBERON:0002385 | 58.84 | gold quality |
| left testis | UBERON:0004533 | 58.46 | gold quality |
| ganglionic eminence | UBERON:0004023 | 56.72 | gold quality |
| monocyte | CL:0000576 | 56.20 | gold quality |
| cortical plate | UBERON:0005343 | 56.14 | gold quality |
| leukocyte | CL:0000738 | 56.07 | gold quality |
| granulocyte | CL:0000094 | 56.01 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 55.10 | silver quality |
| superior frontal gyrus | UBERON:0002661 | 53.87 | gold quality |
| liver | UBERON:0002107 | 52.19 | silver quality |
| prefrontal cortex | UBERON:0000451 | 52.09 | gold quality |
| primary visual cortex | UBERON:0002436 | 51.38 | gold quality |
| adrenal tissue | UBERON:0018303 | 50.28 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 48.73 | gold quality |
| mucosa of stomach | UBERON:0001199 | 48.53 | gold quality |
| kidney | UBERON:0002113 | 48.50 | gold quality |
| placenta | UBERON:0001987 | 48.47 | gold quality |
| blood | UBERON:0000178 | 48.31 | gold quality |
| endometrium | UBERON:0001295 | 48.21 | gold quality |
| cortex of kidney | UBERON:0001225 | 48.17 | gold quality |
| lymph node | UBERON:0000029 | 47.87 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 47.83 | gold quality |
| frontal cortex | UBERON:0001870 | 47.57 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.32 |
Regulation
Is transcription factor: no
Cross-species orthologs
3 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Spdye4b | ENSMUSG00000029586 |
| mus_musculus | Spdye4a | ENSMUSG00000039296 |
| rattus_norvegicus | Spdye4 | ENSRNOG00000058563 |
Paralogs (18): SPDYE1 (ENSG00000136206), SPDYE5 (ENSG00000170092), SPDYE2B (ENSG00000173678), SPDYE4 (ENSG00000183318), SPDYE12 (ENSG00000184616), SPDYE16 (ENSG00000185040), SPDYE17 (ENSG00000186645), SPDYE2 (ENSG00000205238), SPDYE18 (ENSG00000205482), SPDYE3 (ENSG00000214300), SPDYE21 (ENSG00000230358), SPDYE6 (ENSG00000260097), SPDYE8 (ENSG00000273520), SPDYE10 (ENSG00000274570), SPDYE11 (ENSG00000275976), SPDYE15 (ENSG00000286014), SPDYE13 (ENSG00000286038), SPDYE14 (ENSG00000286137)
Protein
Protein identifiers
Speedy protein E9 — A0A494C191 (reviewed: A0A494C191)
All UniProt accessions (1): A0A494C191
UniProt curated annotations — full annotation on UniProt →
Similarity. Belongs to the Speedy/Ringo family.
RefSeq proteins (2): NP_001369483, NP_001408944 (=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR020984 | Speedy | Family |
| IPR057742 | Speedy_E | Family |
Pfam: PF11357
UniProt features (3 total): chain 1, region of interest 1, compositionally biased region 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A0A494C191-F1 | 70.95 | 0.43 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 1 (showing top):
chr7q11
GO Biological Process (1): positive regulation of cyclin-dependent protein serine/threonine kinase activity (GO:0045737)
GO Molecular Function (1): protein kinase binding (GO:0019901)
GO Cellular Component (0):
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| regulation of cyclin-dependent protein serine/threonine kinase activity | 1 |
| cyclin-dependent protein serine/threonine kinase activity | 1 |
| positive regulation of cell cycle | 1 |
| positive regulation of protein serine/threonine kinase activity | 1 |
| positive regulation of cyclin-dependent protein kinase activity | 1 |
| kinase binding | 1 |
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A0A0J9YY54, A0A494C086, A0A494C0Z2, A0A494C191, A6NHP3, A6NIY4, A6NJR5, A6NNV3, B4DH59, F6SZT2, P0C6Y7, P0CI01, P0DKJ7, P0DKJ8, P0DTA3, P0DUD1, P0DUD2, P0DUD3, P0DUD4, P0DUX0, P0DUX1, P0DV79, P79386, Q08AG5, Q13342, Q16666, Q3BBV2, Q495Y8, Q587J8, Q5JRC9, Q5QGU6, Q5RD14, Q5RKG3, Q63HK3, Q6ITT4, Q7TQI8, Q86T75, Q8IWY8, Q8N660, Q8NFV5
Diamond homologs: A0A494C086, A0A494C0Z2, A0A494C191, A6NHP3, A6NIY4, A6NJR5, A6NKU9, A6NLX3, A6NNV3, P0CI01, P0DTA3, P0DUD1, P0DUD2, P0DUD3, P0DUD4, P0DUX0, P0DUX1, P0DV79, Q495Y7, Q495Y8, Q5IBH6, Q5IBH7, Q5MJ68, Q5MJ70, Q8NFV5, Q8R496, Q9PU13, Q9YGL1
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
1742 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 7:73082901:G:C | F112L | 0.966 |
| 7:73082901:G:T | F112L | 0.966 |
| 7:73082903:A:G | F112L | 0.966 |
| 7:73080539:G:C | F146L | 0.943 |
| 7:73080539:G:T | F146L | 0.943 |
| 7:73080541:A:G | F146L | 0.943 |
| 7:73078735:T:A | K179N | 0.930 |
| 7:73078735:T:G | K179N | 0.930 |
| 7:73081821:T:G | D128A | 0.907 |
| 7:73078379:C:A | W257C | 0.897 |
| 7:73078379:C:G | W257C | 0.897 |
| 7:73081821:T:A | D128V | 0.895 |
| 7:73080491:G:C | F162L | 0.885 |
| 7:73080491:G:T | F162L | 0.885 |
| 7:73080493:A:G | F162L | 0.885 |
| 7:73080494:G:C | F161L | 0.884 |
| 7:73080494:G:T | F161L | 0.884 |
| 7:73080496:A:G | F161L | 0.884 |
| 7:73078736:T:A | K179I | 0.882 |
| 7:73078717:G:C | F185L | 0.872 |
| 7:73078717:G:T | F185L | 0.872 |
| 7:73078719:A:G | F185L | 0.872 |
| 7:73080554:C:A | M141I | 0.868 |
| 7:73080554:C:G | M141I | 0.868 |
| 7:73080554:C:T | M141I | 0.868 |
| 7:73081822:C:G | D128H | 0.866 |
| 7:73081820:G:C | D128E | 0.865 |
| 7:73081820:G:T | D128E | 0.865 |
| 7:73080510:T:G | Y156S | 0.861 |
| 7:73078381:A:G | W257R | 0.859 |
dbSNP variants (sampled 300 via entrez): RS10241464 (7:73086377 A>G), RS1157161344 (7:73087477 C>T), RS1157208724 (7:73083737 T>C), RS1158102460 (7:73086178 T>C), RS1158169052 (7:73080478 C>T), RS1160655146 (7:73084062 C>G), RS1162269857 (7:73086397 A>G), RS1162522284 (7:73083289 C>T), RS1165844180 (7:73085733 TAGTC>T), RS1166250624 (7:73086449 CCTGT>C), RS1166570013 (7:73083424 A>C), RS1167373719 (7:73085781 G>A,T), RS1168041690 (7:73083653 A>C), RS1169721310 (7:73087162 A>C,G,T), RS1170534113 (7:73083445 G>C,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)
CTD chemical–gene interactions
2 total (human), top 2 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| lead acetate | affects cotreatment, increases expression | 1 |
| zinc protoporphyrin | affects cotreatment, increases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.