Obesity Due To Sim1 Deficiency

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Obesity Due To Sim1 Deficiency

SIM1

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Obesity Due To Sim1 Deficiency

Global developmental delay
Short stature
Muscular hypotonia
Cognitive impairment
Feeding difficulties
Obesity
Autistic behavior
Attention deficit hyperactivity disorder
Hypotension
Memory impairment

And another 7 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Obesity Due To Sim1 Deficiency Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Monogenic Obesity Sequencing Panel. By Genetic Services Laboratory University of Chicago (United States). SDCCAG8, SIM1, UCP3, ARL6, TRIM32, AFF4, PHF6, SETD2, BBS7, TTC8, IFT74, VPS13B, CUL4B, PRMT7, BBS10, BBS12, WDPCP, CEP290, KIDINS220, BBS9 , (...) View the complete list with 18 more genes Panel complete gene list SDCCAG8, SIM1, UCP3, ARL6, TRIM32, AFF4, PHF6, SETD2, BBS7, TTC8, IFT74, VPS13B, CUL4B, PRMT7, BBS10, BBS12, WDPCP, CEP290, KIDINS220, BBS9, IFT172, DYRK1B, ALMS1, GNAS, LEP, LEPR, MAGEL2, MC4R, MKKS, MKS1, NR0B2, NTRK2, PCSK1, POMC, BBS1, BBS2, BBS4, BBS5 Specificity 3 % Genes 100 %
Monogenic Obesity Deletion/Duplication Panel. By Genetic Services Laboratory University of Chicago (United States). SDCCAG8, SIM1, UCP3, ARL6, TRIM32, AFF4, PHF6, SETD2, BBS7, TTC8, IFT74, VPS13B, CUL4B, PRMT7, BBS10, BBS12, WDPCP, CEP290, KIDINS220, BBS9 , (...) View the complete list with 18 more genes Panel complete gene list SDCCAG8, SIM1, UCP3, ARL6, TRIM32, AFF4, PHF6, SETD2, BBS7, TTC8, IFT74, VPS13B, CUL4B, PRMT7, BBS10, BBS12, WDPCP, CEP290, KIDINS220, BBS9, IFT172, DYRK1B, ALMS1, GNAS, LEP, LEPR, MAGEL2, MC4R, MKKS, MKS1, NR0B2, NTRK2, PCSK1, POMC, BBS1, BBS2, BBS4, BBS5 Specificity 3 % Genes 100 %
SIM1. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). SIM1 Specificity 100 % Genes 100 %
Obesity (sequence analysis of SIM1 gene). By CGC Genetics (Portugal). SIM1 Specificity 100 % Genes 100 %
Non-Syndromic Monogenic Obesity Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SIM1, UCP3, KSR2, SH2B1, LEP, LEPR, MC4R, NR0B2, NTRK2, PCSK1, POMC Specificity 10 % Genes 100 %
Monogenic Obesity via SIM1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SIM1 Specificity 100 % Genes 100 %
Comprehensive Monogenic Obesity Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). BDNF, SDCCAG8, SIM1, TUB, UCP3, KDM6A, ARL6, RAB23, TRIM32, PHF6, KSR2, IFT27, BBS7, TTC8, MRAP2, IFT74, VPS13B, CPE, CUL4B, BBS10 , (...) View the complete list with 31 more genes Panel complete gene list BDNF, SDCCAG8, SIM1, TUB, UCP3, KDM6A, ARL6, RAB23, TRIM32, PHF6, KSR2, IFT27, BBS7, TTC8, MRAP2, IFT74, VPS13B, CPE, CUL4B, BBS10, BBS12, C8orf37, WDPCP, BBIP1, TMEM67, CEP290, BBS9, SH2B1, DYRK1B, ALMS1, GNAS, MCHR1, LEP, LEPR, LZTFL1, MAGEL2, MC3R, MC4R, MKKS, MKS1, KMT2D, NR0B2, NTRK2, PCSK1, POMC, PPARG, BBS1, BBS2, BBS4, BBS5, RAI1 Specificity 2 % Genes 100 %
Obesity, severe, susceptibility to,. By Praxis fuer Humangenetik Wien (Austria). SIM1 Specificity 100 % Genes 100 %

You can get up to 9 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

ORPHANET Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1 DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM LEUKODYSTROPHY, HYPOMYELINATING, 12; HLD12 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D COHEN-GIBSON SYNDROME; COGIS DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23