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GeneBe

HTR5A-AS1

HTR5A antisense RNA 1, the group of Antisense RNAs

Basic information

Previous symbols: [ "HTR5AOS" ]

Links

ENSG00000220575NCBI:100128264HGNC:48956GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the HTR5A-AS1 gene.

  • Inborn genetic diseases (8 variants)
  • not provided (3 variants)
  • Malignant tumor of prostate (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the HTR5A-AS1 gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type Pathogenic Likely pathogenic VUS Likely benign Benign Sum
synonymous
0
missense
0
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
9
clinvar
3
clinvar
12
Total 0 0 9 0 3

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
HTR5A-AS1protein_codingprotein_codingENST00000543018 34491
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
0.00009130.352124917041249210.0000160
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense0.3028694.20.9120.00000613953
Missense in Polyphen13.00280.3330322
Synonymous0.6943742.80.8650.00000311310
Loss of Function-0.026165.931.013.46e-756

LoF frequencies by population

EthnicitySum of pLOFs p
African & African-American0.00002900.0000290
Ashkenazi Jewish0.000.00
East Asian0.000.00
Finnish0.000.00
European (Non-Finnish)0.00002660.0000264
Middle Eastern0.000.00
South Asian0.000.00
Other0.000.00

dbNSFP

Source: dbNSFP

Haploinsufficiency Scores

pHI
hipred
N
hipred_score
0.296
ghis
0.551

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium