Trait
Small retruded chin
Clinical name: Microretrognathia
A form of developmental hypoplasia of the mandible in which the mandible is mislocalised posteriorly.
Summary
- Also called
- Retromicrognathia
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Small retruded chin, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test80 genes linked to Small retruded chin
Changes in these genes cause rare conditions in which Small retruded chin 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 |
|---|---|---|
| ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunit | Always | In 1 condition |
| AMOTL1angiomotin like 1 | Always | In 1 condition |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Always | In 1 condition |
| BANF1barrier to autointegration nuclear assembly factor 1 | Always | In 1 condition |
| C2CD3C2 domain containing 3 centriole elongation regulator | Always | In 2 conditions |
| CANT1calcium activated nucleotidase 1 | Always | In 1 condition |
| CEP55centrosomal protein 55 | Always | In 1 condition |
| CHST14carbohydrate sulfotransferase 14 | Always | In 2 conditions |
| COL2A1collagen type II alpha 1 chain | Always | In 1 condition |
| CREB3L1cAMP responsive element binding protein 3 like 1 | Always | In 1 condition |
| DHCR77-dehydrocholesterol reductase | Always | In 1 condition |
| DONSONDNA replication fork stabilization factor DONSON | Always | In 1 condition |
| EIF4A3eukaryotic translation initiation factor 4A3 | Always | In 2 conditions |
| ESAMendothelial cell adhesion molecule | Always | In 1 condition |
| GMNNgeminin DNA replication inhibitor | Always | In 1 condition |
| HIVEP2HIVEP zinc finger 2 | Always | In 1 condition |
| IFT140intraflagellar transport 140 | Always | In 1 condition |
| MED16mediator complex subunit 16 | Always | In 1 condition |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Always | In 1 condition |
| PAX1paired box 1 | Always | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Always | In 1 condition |
| SEC24DSEC24 homolog D, COPII component | Always | In 1 condition |
| TRIP4thyroid hormone receptor interactor 4 | Always | In 1 condition |
| CTNND2catenin delta 2 | Very often (80–99%) | In 1 condition |
| INTS1integrator complex subunit 1 | Very often (80–99%) | In 1 condition |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Very often (80–99%) | In 1 condition |
| SEMA5Asemaphorin 5A | Very often (80–99%) | In 1 condition |
| SF3B4splicing factor 3b subunit 4 | Very often (80–99%) | In 1 condition |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Often (30–79%) | In 1 condition |
| DSEdermatan sulfate epimerase | Often (30–79%) | In 1 condition |
| FBXL3F-box and leucine rich repeat protein 3 | Often (30–79%) | In 1 condition |
| KAT6Alysine acetyltransferase 6A | Often (30–79%) | In 2 conditions |
| KATNB1katanin regulatory subunit B1 | Often (30–79%) | In 1 condition |
| KCNK9potassium two pore domain channel subfamily K member 9 | Often (30–79%) | In 1 condition |
| LMNAlamin A/C | Often (30–79%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Often (30–79%) | In 2 conditions |
| NDE1nudE neurodevelopment protein 1 | Often (30–79%) | In 1 condition |
| NFIXnuclear factor I X | Often (30–79%) | In 1 condition |
| POLR1DRNA polymerase I and III subunit D | Often (30–79%) | In 1 condition |
| PUF60poly(U) binding splicing factor 60 | Often (30–79%) | In 2 conditions |
Show 40 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| RBSNrabenosyn, RAB effector | Often (30–79%) | In 1 condition |
| RELNreelin | Often (30–79%) | In 1 condition |
| RPL10ribosomal protein L10 | Often (30–79%) | In 2 conditions |
| TAF1TATA-box binding protein associated factor 1 | Often (30–79%) | In 1 condition |
| TASP1taspase 1 | Often (30–79%) | In 1 condition |
| TUBA1Atubulin alpha 1a | Often (30–79%) | In 1 condition |
| WDR11WD repeat domain 11 | Often (30–79%) | In 1 condition |
| YARS1tyrosyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Sometimes (5–29%) | In 1 condition |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Sometimes (5–29%) | In 1 condition |
| CHST3carbohydrate sulfotransferase 3 | Sometimes (5–29%) | In 1 condition |
| GAD1glutamate decarboxylase 1 | Sometimes (5–29%) | In 1 condition |
| GLDNgliomedin | Sometimes (5–29%) | In 1 condition |
| GLI3GLI family zinc finger 3 | Sometimes (5–29%) | In 1 condition |
| IPO8importin 8 | Sometimes (5–29%) | In 1 condition |
| KIF7kinesin family member 7 | Sometimes (5–29%) | In 1 condition |
| KPTNkaptin, actin binding protein | Sometimes (5–29%) | In 1 condition |
| MYH7myosin heavy chain 7 | Sometimes (5–29%) | In 1 condition |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Sometimes (5–29%) | In 1 condition |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Sometimes (5–29%) | In 1 condition |
| PRDM13PR/SET domain 13 | Sometimes (5–29%) | In 1 condition |
| PRORPprotein only RNase P catalytic subunit | Sometimes (5–29%) | In 1 condition |
| RSPO2R-spondin 2 | Sometimes (5–29%) | In 1 condition |
| RTTNrotatin | Sometimes (5–29%) | In 1 condition |
| SELENONselenoprotein N | Sometimes (5–29%) | In 1 condition |
| TELO2telomere maintenance 2 | Sometimes (5–29%) | In 1 condition |
| TTNtitin | Sometimes (5–29%) | In 1 condition |
| TXNDC15thioredoxin domain containing 15 | Sometimes (5–29%) | In 1 condition |
| CTCFCCCTC-binding factor | Rarely (1–4%) | In 1 condition |
| CEP120centrosomal protein 120 | Not recorded | In 1 condition |
| CRIPTCXXC repeat containing interactor of PDZ3 domain | Not recorded | In 1 condition |
| EBPEBP cholestenol delta-isomerase | Not recorded | In 1 condition |
| OCLNoccludin | Not recorded | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Not recorded | In 1 condition |
| ORC6origin recognition complex subunit 6 | Not recorded | In 1 condition |
| SIN3ASIN3 transcription regulator family member A | Not recorded | In 1 condition |
| SLC10A7solute carrier family 10 member 7 | Not recorded | In 1 condition |
| SLC35A3solute carrier family 35 member A3 | Not recorded | In 1 condition |
| TMEM70transmembrane protein 70 | Not recorded | In 1 condition |
| ZC4H2zinc finger C4H2-type containing | 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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks