Trait
Loss of peripheral vision
Clinical name: Peripheral visual field loss
Loss of peripheral vision with retention of central vision, resulting in a constricted circular tunnel-like field of vision.
Summary
- Also called
- Tunnel vision, Kalnienk vision
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Loss of peripheral vision, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test127 genes linked to Loss of peripheral vision
Changes in these genes cause rare conditions in which Loss of peripheral vision 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 |
|---|---|---|
| ARL6ARF like GTPase 6 | Always | In 2 conditions |
| BBS1Bardet-Biedl syndrome 1 | Always | In 2 conditions |
| BBS2Bardet-Biedl syndrome 2 | Always | In 2 conditions |
| CCDC28Bcoiled-coil domain containing 28B | Always | In 1 condition |
| CNGA1cyclic nucleotide gated channel subunit alpha 1 | Always | In 2 conditions |
| CNGB1cyclic nucleotide gated channel subunit beta 1 | Always | In 2 conditions |
| IFT140intraflagellar transport 140 | Always | In 2 conditions |
| PDE6Aphosphodiesterase 6A | Always | In 2 conditions |
| PRPF6pre-mRNA processing factor 6 | Always | In 2 conditions |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Always | In 1 condition |
| SLC6A6solute carrier family 6 member 6 | Always | In 1 condition |
| TMEM216transmembrane protein 216 | Always | In 2 conditions |
| UBAP1Lubiquitin associated protein 1 like | Always | In 1 condition |
| ZNF513zinc finger protein 513 | Always | In 2 conditions |
| ABCA4ATP binding cassette subfamily A member 4 | Often (30–79%) | In 2 conditions |
| ADGRV1adhesion G protein-coupled receptor V1 | Often (30–79%) | In 1 condition |
| AGBL5AGBL carboxypeptidase 5 | Often (30–79%) | In 2 conditions |
| AHI1Abelson helper integration site 1 | Often (30–79%) | In 1 condition |
| AHRaryl hydrocarbon receptor | Often (30–79%) | In 1 condition |
| ALMS1ALMS1 centrosome and basal body associated protein | Often (30–79%) | In 1 condition |
| ARHGEF18Rho/Rac guanine nucleotide exchange factor 18 | Often (30–79%) | In 1 condition |
| ARL2BPARF like GTPase 2 binding protein | Often (30–79%) | In 1 condition |
| ARL3ARF like GTPase 3 | Often (30–79%) | In 1 condition |
| BEST1bestrophin 1 | Often (30–79%) | In 1 condition |
| CA4carbonic anhydrase 4 | Often (30–79%) | In 1 condition |
| CABP4calcium binding protein 4 | Often (30–79%) | In 1 condition |
| CC2D2Acoiled-coil and C2 domain containing 2A | Often (30–79%) | In 1 condition |
| CDH23cadherin related 23 | Often (30–79%) | In 1 condition |
| CDHR1cadherin related family member 1 | Often (30–79%) | In 1 condition |
| CERKLCERK like autophagy regulator | Often (30–79%) | In 1 condition |
| CFAP20cilia and flagella associated protein 20 | Often (30–79%) | In 1 condition |
| CFAP418cilia and flagella associated protein 418 | Often (30–79%) | In 1 condition |
| CHMCHM Rab escort protein | Often (30–79%) | In 1 condition |
| CLRN1clarin 1 | Often (30–79%) | In 1 condition |
| COQ8Bcoenzyme Q8B | Often (30–79%) | In 1 condition |
| CRB1crumbs cell polarity complex component 1 | Often (30–79%) | In 1 condition |
| CRXcone-rod homeobox | Often (30–79%) | In 2 conditions |
| CYP1B1cytochrome P450 family 1 subfamily B member 1 | Often (30–79%) | In 1 condition |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Often (30–79%) | In 1 condition |
| DHX38DEAH-box helicase 38 | Often (30–79%) | In 1 condition |
Show 87 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Often (30–79%) | In 1 condition |
| ESPNespin | Often (30–79%) | In 1 condition |
| EYSEGF-like photoreceptor maintenance factor | Often (30–79%) | In 1 condition |
| FAM161AFAM161 centrosomal protein A | Often (30–79%) | In 1 condition |
| FSCN2fascin actin-bundling protein 2, retinal | Often (30–79%) | In 1 condition |
| FSD1Lfibronectin type III and SPRY domain containing 1 like | Often (30–79%) | In 1 condition |
| GUCA1Bguanylate cyclase activator 1B | Often (30–79%) | In 1 condition |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Often (30–79%) | In 1 condition |
| HKDC1hexokinase domain containing 1 | Often (30–79%) | In 1 condition |
| IDH3Aisocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha | Often (30–79%) | In 1 condition |
| IDH3Bisocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta | Often (30–79%) | In 1 condition |
| IFT172intraflagellar transport 172 | Often (30–79%) | In 1 condition |
| IFT43intraflagellar transport 43 | Often (30–79%) | In 1 condition |
| IFT88intraflagellar transport 88 | Often (30–79%) | In 1 condition |
| IMPDH1inosine monophosphate dehydrogenase 1 | Often (30–79%) | In 1 condition |
| IMPG1interphotoreceptor matrix proteoglycan 1 | Often (30–79%) | In 1 condition |
| IMPG2interphotoreceptor matrix proteoglycan 2 | Often (30–79%) | In 1 condition |
| KCNJ13potassium inwardly rectifying channel subfamily J member 13 | Often (30–79%) | In 1 condition |
| KIAA1549KIAA1549 | Often (30–79%) | In 1 condition |
| KIZkizuna centrosomal protein | Often (30–79%) | In 1 condition |
| KLHL7kelch like family member 7 | Often (30–79%) | In 1 condition |
| LCA5lebercilin LCA5 | Often (30–79%) | In 1 condition |
| LRATlecithin retinol acyltransferase | Often (30–79%) | In 2 conditions |
| MAKmale germ cell associated kinase | Often (30–79%) | In 1 condition |
| MERTKMER proto-oncogene, tyrosine kinase | Often (30–79%) | In 1 condition |
| MYO7Amyosin VIIA | Often (30–79%) | In 2 conditions |
| MYOCmyocilin | Often (30–79%) | In 1 condition |
| NEK2NIMA related kinase 2 | Often (30–79%) | In 1 condition |
| NR2E3nuclear receptor subfamily 2 group E member 3 | Often (30–79%) | In 1 condition |
| NRLneural retina leucine zipper | Often (30–79%) | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Often (30–79%) | In 1 condition |
| OTX2orthodenticle homeobox 2 | Often (30–79%) | In 1 condition |
| PCAREphotoreceptor cilium actin regulator | Often (30–79%) | In 1 condition |
| PCDH15protocadherin related 15 | Often (30–79%) | In 1 condition |
| PDE6Bphosphodiesterase 6B | Often (30–79%) | In 1 condition |
| PDE6Gphosphodiesterase 6G | Often (30–79%) | In 1 condition |
| PDZD7PDZ domain containing 7 | Often (30–79%) | In 1 condition |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Often (30–79%) | In 1 condition |
| POU3F4POU class 3 homeobox 4 | Often (30–79%) | In 1 condition |
| PRCDphotoreceptor disc component | Often (30–79%) | In 1 condition |
| PROM1prominin 1 | Often (30–79%) | In 2 conditions |
| PRPF3pre-mRNA processing factor 3 | Often (30–79%) | In 1 condition |
| PRPF31pre-mRNA processing factor 31 | Often (30–79%) | In 1 condition |
| PRPF4pre-mRNA splicing tri-snRNP complex factor PRPF4 | Often (30–79%) | In 1 condition |
| PRPF8pre-mRNA processing factor 8 | Often (30–79%) | In 1 condition |
| PRPH2peripherin 2 | Often (30–79%) | In 3 conditions |
| RBP3retinol binding protein 3 | Often (30–79%) | In 1 condition |
| RDH12retinol dehydrogenase 12 | Often (30–79%) | In 1 condition |
| RDH5retinol dehydrogenase 5 | Often (30–79%) | In 1 condition |
| REEP6receptor accessory protein 6 | Often (30–79%) | In 1 condition |
| RGRretinal G protein coupled receptor | Often (30–79%) | In 1 condition |
| RHOrhodopsin | Often (30–79%) | In 2 conditions |
| RLBP1retinaldehyde binding protein 1 | Often (30–79%) | In 2 conditions |
| RNU4-2RNA, U4 small nuclear 2 | Often (30–79%) | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Often (30–79%) | In 1 condition |
| RNU6-1RNA, U6 small nuclear 1 | Often (30–79%) | In 1 condition |
| RNU6-2RNA, U6 small nuclear 2 | Often (30–79%) | In 1 condition |
| RNU6-8RNA, U6 small nuclear 8 | Often (30–79%) | In 1 condition |
| RNU6-9RNA, U6 small nuclear 9 | Often (30–79%) | In 1 condition |
| ROM1retinal outer segment membrane protein 1 | Often (30–79%) | In 1 condition |
| RP1RP1 axonemal microtubule associated | Often (30–79%) | In 1 condition |
| RP1L1RP1 like 1 | Often (30–79%) | In 1 condition |
| RP2RP2 activator of ARL3 GTPase | Often (30–79%) | In 1 condition |
| RP9RP9 pre-mRNA splicing factor | Often (30–79%) | In 1 condition |
| RPE65retinoid isomerohydrolase RPE65 | Often (30–79%) | In 3 conditions |
| RPGRretinitis pigmentosa GTPase regulator | Often (30–79%) | In 1 condition |
| SAGS-antigen visual arrestin | Often (30–79%) | In 1 condition |
| SAXO6stabilizer of axonemal microtubules 6 | Often (30–79%) | In 1 condition |
| SCAPERS-phase cyclin A associated protein in the ER | Often (30–79%) | In 1 condition |
| SEMA4Asemaphorin 4A | Often (30–79%) | In 2 conditions |
| SLC7A14solute carrier family 7 member 14 | Often (30–79%) | In 1 condition |
| SNRNP200small nuclear ribonucleoprotein U5 subunit 200 | Often (30–79%) | In 1 condition |
| SPATA7spermatogenesis associated 7 | Often (30–79%) | In 2 conditions |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Often (30–79%) | In 1 condition |
| TTC8tetratricopeptide repeat domain 8 | Often (30–79%) | In 1 condition |
| TUBTUB bipartite transcription factor | Often (30–79%) | In 1 condition |
| TULP1TUB like protein 1 | Often (30–79%) | In 1 condition |
| USH1CUSH1 protein network component harmonin | Often (30–79%) | In 1 condition |
| USH1GUSH1 protein network component sans | Often (30–79%) | In 1 condition |
| USH2Ausherin | Often (30–79%) | In 2 conditions |
| WHRNwhirlin | Often (30–79%) | In 1 condition |
| ZNF408zinc finger protein 408 | Often (30–79%) | In 1 condition |
| DLATdihydrolipoamide S-acetyltransferase | Sometimes (5–29%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sometimes (5–29%) | In 1 condition |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Rarely (1–4%) | In 1 condition |
| CWC27CWC27 spliceosome associated cyclophilin | Not recorded | In 1 condition |
| GUCY2Dguanylate cyclase 2D, retinal | 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