C11orf91

gene
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Summary

C11orf91 (chromosome 11 open reading frame 91, HGNC:34444) is a protein-coding gene on chromosome 11p13, encoding Uncharacterized protein C11orf91 (Q3C1V1).

At a glance

  • Clinical variants (ClinVar): 5 total
  • MANE Select transcript: NM_001166692

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:34444
Approved symbolC11orf91
Namechromosome 11 open reading frame 91
Location11p13
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000205177
Ensembl biotypeprotein_coding
Entrez100131378

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000379011, ENST00000531145

RefSeq mRNA: 1 — MANE Select: NM_001166692 NM_001166692

CCDS: CCDS53615

Canonical transcript exons

ENST00000379011 — 2 exons

ExonStartEnd
ENSE000021567133370024533700826
ENSE000036193913369826133698514

Expression profiles

Bgee: expression breadth ubiquitous, 125 present calls, max score 85.63.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0871 / max 8.5706, expressed in 24 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1192030.077619
1192040.00944

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047385.63silver quality
lower esophagus mucosaUBERON:003583477.49gold quality
left testisUBERON:000453374.39gold quality
esophagus mucosaUBERON:000246973.77gold quality
testisUBERON:000047373.69gold quality
right testisUBERON:000453473.61gold quality
upper lobe of left lungUBERON:000895270.85gold quality
olfactory segment of nasal mucosaUBERON:000538669.05gold quality
metanephros cortexUBERON:001053369.01gold quality
right lungUBERON:000216768.89gold quality
mucosa of stomachUBERON:000119967.68gold quality
minor salivary glandUBERON:000183066.74gold quality
omental fat padUBERON:001041465.23gold quality
esophagusUBERON:000104364.50gold quality
gastrocnemiusUBERON:000138864.31gold quality
saliva-secreting glandUBERON:000104463.73gold quality
adipose tissueUBERON:000101363.20gold quality
body of stomachUBERON:000116163.15gold quality
heart left ventricleUBERON:000208462.72gold quality
thoracic mammary glandUBERON:000520062.11gold quality
subcutaneous adipose tissueUBERON:000219061.77gold quality
vaginaUBERON:000099661.51gold quality
left uterine tubeUBERON:000130361.51gold quality
muscle of legUBERON:000138361.35gold quality
apex of heartUBERON:000209860.62gold quality
lungUBERON:000204859.45gold quality
skin of legUBERON:000151159.19gold quality
right coronary arteryUBERON:000162559.13gold quality
skin of abdomenUBERON:000141659.12gold quality
stomachUBERON:000094559.08gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.45

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

23 targeting C11orf91, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-6758-5P100.0066.211470
HSA-MIR-6856-5P100.0065.471298
HSA-MIR-12118100.0065.881270
HSA-MIR-6891-5P99.9866.531372
HSA-MIR-3173-3P99.9866.491217
HSA-MIR-589-3P99.9169.622088
HSA-MIR-430699.7270.503630
HSA-MIR-549A-3P99.5468.17825
HSA-MIR-203A-3P99.4970.562806
HSA-MIR-29799.4069.581418
HSA-MIR-5580-5P99.3866.961139
HSA-MIR-133A-5P99.2869.13941
HSA-MIR-642A-3P99.2367.671258
HSA-MIR-642B-3P99.2367.671258
HSA-MIR-6797-3P99.1766.94668
HSA-MIR-607698.6165.69637
HSA-MIR-4536-5P98.4764.39657
HSA-MIR-477398.3567.301710
HSA-MIR-5585-5P97.9568.801024
HSA-MIR-430597.9468.63533
HSA-MIR-130297.9267.27844
HSA-MIR-429897.2666.59765
HSA-MIR-59196.2968.16611

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusA930018P22RikENSMUSG00000032671
rattus_norvegicusC3h11orf91ENSRNOG00000010963

Protein

Protein identifiers

Uncharacterized protein C11orf91Q3C1V1 (reviewed: Q3C1V1)

All UniProt accessions (2): Q3C1V1, H0YDE1

Isoforms (2)

UniProt IDNamesCanonical?
Q3C1V1-11yes
Q3C1V1-22

RefSeq proteins (1): NP_001160164* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR040027C11orf91-likeFamily

Pfam: PF17669

UniProt features (7 total): sequence conflict 3, chain 1, region of interest 1, compositionally biased region 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q3C1V1-F166.120.15

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 30 (showing top): MARTENS_TRETINOIN_RESPONSE_DN, GSE14415_INDUCED_TREG_VS_FOXP3_KO_INDUCED_TREG_IL2_CULTURE_DN, HHEX_TARGET_GENES, RBM34_TARGET_GENES, UBN1_TARGET_GENES, MIR203A_3P, MIR4773, MIR133A_5P, MIR6758_5P, MIR6856_5P, BLANCO_MELO_COVID19_SARS_COV_2_INFECTION_A594_ACE2_EXPRESSING_CELLS_UP, BLANCO_MELO_COVID19_SARS_COV_2_INFECTION_A594_ACE2_EXPRESSING_CELLS_RUXOLITINIB_UP, GSE15324_ELF4_KO_VS_WT_NAIVE_CD8_TCELL_UP, GSE17721_CTRL_VS_CPG_0.5H_BMDC_DN, GSE17721_LPS_VS_POLYIC_24H_BMDC_DN

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

116 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
C11orf91FBXO3Q9UK99604
C11orf91TCP11L1Q9NUJ3507
C11orf91OR13C5Q8NGS8507
C11orf91CCDC73Q6ZRK6447
C11orf91KIAA1549LQ6ZVL6446
C11orf91IFTAPQ86VG3434
C11orf91DEPDC7Q96QD5418
C11orf91QSER1Q2KHR3415
C11orf91COMMD9Q9P000400
C11orf91ABTB2Q8N961399
C11orf91ARL14EPQ8N8R7397
C11orf91IMMP1LQ96LU5395
C11orf91SEC31BQ9NQW1380
C11orf91DNAJC24Q6P3W2370
C11orf91DCDC1P59894368

IntAct

0 interactions, top by confidence:

BioGRID (1): C11orf91 (Synthetic Lethality)

ESM2 similar proteins: A0A1B0GTI1, A7X8B3, A7X8B5, A7X8B7, A7X8B9, A7X8C2, A7X8C4, A7X8C7, A7X8C9, A7X8D2, A7X8D4, A7XW16, A7XW20, A7XW25, A8WFF7, O15054, O43151, O55087, P03186, P03234, P03333, P06186, P06401, P0C674, P0C675, P17473, P28925, P46695, Q00175, Q3C1V1, Q3KSP9, Q5NCY0, Q63449, Q66619, Q66HC8, Q6S6U0, Q6VUC0, Q7YR42, Q80WJ1, Q86UU5

Diamond homologs: A8WFF7, Q3C1V1, Q9D1Z2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance4
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

387 predictions. Top by Δscore:

VariantEffectΔscore
11:33698510:TGTGT:Tacceptor_gain1.0000
11:33700244:CAGCT:Cdonor_gain1.0000
11:33700614:T:TAdonor_gain1.0000
11:33698511:GTGT:Gacceptor_gain0.9900
11:33698512:TGT:Tacceptor_gain0.9900
11:33698513:GT:Gacceptor_gain0.9900
11:33698514:TCT:Tacceptor_loss0.9900
11:33698515:C:CAacceptor_loss0.9900
11:33698515:C:CCacceptor_gain0.9900
11:33700243:A:ACdonor_gain0.9900
11:33700244:C:CCdonor_gain0.9900
11:33700244:CAG:Cdonor_gain0.9900
11:33700265:T:TAdonor_gain0.9900
11:33700266:C:Adonor_gain0.9900
11:33700611:T:TAdonor_gain0.9900
11:33698518:C:CTacceptor_gain0.9800
11:33700593:T:TAdonor_gain0.9800
11:33700297:AAT:Adonor_gain0.9700
11:33698519:A:Tacceptor_gain0.9600
11:33700243:ACAG:Adonor_gain0.9600
11:33700244:CAGC:Cdonor_gain0.9600
11:33700246:G:Cdonor_gain0.9600
11:33700615:C:Adonor_gain0.9600
11:33700241:GCA:Gdonor_loss0.9400
11:33700242:CACAG:Cdonor_loss0.9400
11:33700243:A:AGdonor_loss0.9400
11:33700244:CA:Cdonor_gain0.9400
11:33700287:C:CAdonor_gain0.9400
11:33700589:G:Adonor_gain0.9400
11:33700134:C:CTdonor_gain0.9300

AlphaMissense

1209 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:33700294:C:AK149N0.994
11:33700294:C:GK149N0.994
11:33700283:A:GL153S0.993
11:33700617:A:GW42R0.993
11:33700617:A:TW42R0.993
11:33700615:C:AW42C0.991
11:33700615:C:GW42C0.991
11:33700672:G:CF23L0.991
11:33700672:G:TF23L0.991
11:33700674:A:GF23L0.991
11:33700417:G:CF108L0.987
11:33700417:G:TF108L0.987
11:33700419:A:GF108L0.987
11:33700673:A:GF23S0.986
11:33700289:A:GL151P0.985
11:33700304:A:GI146T0.982
11:33700258:G:CF161L0.981
11:33700258:G:TF161L0.981
11:33700260:A:GF161L0.981
11:33700301:C:GR147P0.980
11:33700673:A:CF23C0.980
11:33700310:A:GL144P0.978
11:33698492:T:AK173N0.975
11:33698492:T:GK173N0.975
11:33700304:A:CI146S0.973
11:33700603:G:CF46L0.973
11:33700603:G:TF46L0.973
11:33700605:A:GF46L0.973
11:33700616:C:GW42S0.973
11:33700274:A:GI156T0.971

dbSNP variants (sampled 300 via entrez): RS1000323866 (11:33699489 T>C), RS1000340633 (11:33703574 G>A), RS1000660125 (11:33697998 C>A), RS1000793588 (11:33705069 T>C), RS1000904572 (11:33699411 A>C,G), RS1000917536 (11:33703873 G>A,C,T), RS1001305860 (11:33704072 C>G,T), RS1002135019 (11:33704538 A>G), RS1002206682 (11:33698777 T>C), RS1002358554 (11:33704695 G>A), RS1002404576 (11:33699014 T>C), RS1002696609 (11:33698711 C>G,T), RS1002798975 (11:33708185 T>A,C), RS1002899056 (11:33701837 C>G,T), RS1003031182 (11:33707543 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

10 total (human), top 10 by PubMed support.

ChemicalActions (top 5)PubMed papers
aristolochic acid Iincreases expression1
propionaldehydeincreases expression1
abrineincreases expression1
jinfukangaffects cotreatment, decreases expression1
Resveratroldecreases expression1
Allergensdecreases expression1
Benzo(a)pyreneincreases methylation1
Cisplatindecreases expression, affects cotreatment1
Smokeincreases expression1
Tobacco Smoke Pollutionaffects expression1

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.