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Trait
Low blood sugar in newborn
Clinical name: Neonatal hypoglycemia
Summary
- Body system
- Laboratory abnormality
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/neonatal-hypoglycemia.json"
page <- fromJSON(url)
page$trait$nameLow blood sugar in newbornHP:0001998
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Get my Genome Test55 genes linked to Low blood sugar in newborn
Changes in these genes cause rare conditions in which Low blood sugar in newborn is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| NSD1nuclear receptor binding SET domain protein 1 | Always | In 2 conditions |
| OTX2orthodenticle homeobox 2 | Always | In 1 condition |
| SLC25A20solute carrier family 25 member 20 | Always | In 1 condition |
| TBX19T-box transcription factor 19 | Always | In 1 condition |
| YARS1tyrosyl-tRNA synthetase 1 | Always | In 1 condition |
| AKT2AKT serine/threonine kinase 2 | Very often (80–99%) | In 2 conditions |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Very often (80–99%) | In 2 conditions |
| HADHhydroxyacyl-CoA dehydrogenase | Very often (80–99%) | In 1 condition |
| HNF1AHNF1 homeobox A | Very often (80–99%) | In 2 conditions |
| HNF4Ahepatocyte nuclear factor 4 alpha | Very often (80–99%) | In 2 conditions |
| MSL3MSL complex subunit 3 | Very often (80–99%) | In 1 condition |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Often (30–79%) | In 1 condition |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Often (30–79%) | In 1 condition |
| KDM6Alysine demethylase 6A | Often (30–79%) | In 1 condition |
| MADDMAP kinase activating death domain | Often (30–79%) | In 1 condition |
| NOS3nitric oxide synthase 3 | Often (30–79%) | In 1 condition |
| SERAC1serine active site containing 1 | Often (30–79%) | In 1 condition |
| ZRSR2zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | Often (30–79%) | In 1 condition |
| ABCC8ATP binding cassette subfamily C member 8 | Sometimes (5–29%) | In 1 condition |
| APPL1adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 | Sometimes (5–29%) | In 1 condition |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| CELcarboxyl ester lipase | Sometimes (5–29%) | In 1 condition |
| CICcapicua transcriptional repressor | Sometimes (5–29%) | In 1 condition |
| CLPBClpB family mitochondrial disaggregase | Sometimes (5–29%) | In 2 conditions |
| DBHdopamine beta-hydroxylase | Sometimes (5–29%) | In 1 condition |
| DNAJC19DnaJ heat shock protein family (Hsp40) member C19 | Sometimes (5–29%) | In 1 condition |
| DOT1LDOT1 like histone lysine methyltransferase | Sometimes (5–29%) | In 1 condition |
| EBPEBP cholestenol delta-isomerase | Sometimes (5–29%) | In 1 condition |
| FBP1fructose-bisphosphatase 1 | Sometimes (5–29%) | In 1 condition |
| GCKglucokinase | Sometimes (5–29%) | In 1 condition |
| GFM2GTP dependent ribosome recycling factor mitochondrial 2 | Sometimes (5–29%) | In 1 condition |
| H19H19 imprinted maternally expressed transcript | Sometimes (5–29%) | In 1 condition |
| HERC1HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 | Sometimes (5–29%) | In 1 condition |
| HTRA2HtrA serine peptidase 2 | Sometimes (5–29%) | In 1 condition |
| IGF2insulin like growth factor 2 | Sometimes (5–29%) | In 2 conditions |
| INSinsulin | Sometimes (5–29%) | In 1 condition |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Sometimes (5–29%) | In 2 conditions |
| KLF11KLF transcription factor 11 | Sometimes (5–29%) | In 1 condition |
| MYT1Lmyelin transcription factor 1 like | Sometimes (5–29%) | In 1 condition |
| NEUROD1neuronal differentiation 1 | Sometimes (5–29%) | In 1 condition |
Show 15 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| PAX4paired box 4 | Sometimes (5–29%) | In 1 condition |
| PCK1phosphoenolpyruvate carboxykinase 1 | Sometimes (5–29%) | In 1 condition |
| PCK2phosphoenolpyruvate carboxykinase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| PDX1pancreatic and duodenal homeobox 1 | Sometimes (5–29%) | In 1 condition |
| PET100PET100 cytochrome c oxidase chaperone | Sometimes (5–29%) | In 1 condition |
| POLR1ARNA polymerase I subunit A | Sometimes (5–29%) | In 1 condition |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| APC2APC regulator of Wnt signaling pathway 2 | Rarely (1–4%) | In 1 condition |
| MTORmechanistic target of rapamycin kinase | Rarely (1–4%) | In 1 condition |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Not recorded | In 1 condition |
| GYS2glycogen synthase 2 | Not recorded | In 1 condition |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Not recorded | In 1 condition |
| KCNQ1OT1KCNQ1 opposite strand/antisense transcript 1 | Not recorded | In 1 condition |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Not recorded | In 1 condition |
| PROP1PROP paired-like homeobox 1 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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