specific learning disability Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Impairment of certain skills such as reading or writing, coordination, self-control, or attention that interfere with the ability to learn. The impairment is not related to a global deficiency of intelligence. (Human Phenotype Ontology, HP_0001328)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001328
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Genes

47 genes associated with the specific learning disability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARL6 ADP-ribosylation factor-like 6
ARX aristaless related homeobox
BBS1 Bardet-Biedl syndrome 1
BBS10 Bardet-Biedl syndrome 10
BBS12 Bardet-Biedl syndrome 12
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
BBS5 Bardet-Biedl syndrome 5
BBS7 Bardet-Biedl syndrome 7
BBS9 Bardet-Biedl syndrome 9
BLM Bloom syndrome, RecQ helicase-like
C10ORF2 chromosome 10 open reading frame 2
C9ORF72 chromosome 9 open reading frame 72
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CEP290 centrosomal protein 290kDa
CHMP2B charged multivesicular body protein 2B
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
IFT27 intraflagellar transport 27
JAG1 jagged 1
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
LZTFL1 leucine zipper transcription factor-like 1
MKKS McKusick-Kaufman syndrome
MKS1 Meckel syndrome, type 1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NDN necdin, melanoma antigen (MAGE) family member
NF1 neurofibromin 1
SBDS Shwachman-Bodian-Diamond syndrome
SHH sonic hedgehog
SLC25A15 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SNRPN small nuclear ribonucleoprotein polypeptide N
SOX2 SRY (sex determining region Y)-box 2
SPG11 spastic paraplegia 11 (autosomal recessive)
SPRED1 sprouty-related, EVH1 domain containing 1
STIM1 stromal interaction molecule 1
SYN1 synapsin I
TBX1 T-box 1
TERC telomerase RNA component
TRIM32 tripartite motif containing 32
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2
TTC8 tetratricopeptide repeat domain 8
TUBB2B tubulin, beta 2B class IIb
TUBB3 tubulin, beta 3 class III
TUBB4A tubulin, beta 4A class IVa
WDPCP WD repeat containing planar cell polarity effector