chr2:101436601:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr2:101,436,601-101,613,291
hg38 chr2:100,820,139-100,996,829 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.003 Colorectal Neoplasms NA LHGDN Detail
0.002 Mental Depression NA GAD Detail
<0.001 glioblastoma NA BeFree Detail
<0.001 Creutzfeldt-Jakob disease NA BeFree Detail
<0.001 chronic lymphocytic leukemia Lack of association of the NPAS2 gene Ala394Thr polymorphism (rs2305160:G>A) wit... BeFree 25227809 Detail
<0.001 lymphoma NA BeFree Detail
0.005 Lymphoma, Non-Hodgkin NA GAD,LHGDN Detail
0.002 Prostatic Neoplasms NA GAD Detail
<0.001 restless legs syndrome We investigated whether CLOCK and NPAS2 gene polymorphisms are associated with R... BeFree 24824748 Detail
<0.001 schizoaffective disorder NA BeFree Detail
0.003 schizophrenia Association between restless legs syndrome and CLOCK and NPAS2 gene polymorphism... BeFree,GAD 24824748 Detail
0.004 seasonal affective disorder NA BeFree,LHGDN Detail
0.002 breast carcinoma However, when accounting for potential effect modification, rs23051560 (Ala394Th... BeFree 22473669 Detail
0.009 Malignant neoplasm of breast However, when accounting for potential effect modification, rs23051560 (Ala394Th... BeFree 22473669 Detail
0.005 Malignant neoplasm of prostate NA BeFree,GAD Detail
0.002 Metabolic syndrome X NA GAD Detail
<0.001 Carcinogenesis NA BeFree Detail
<0.001 prostate carcinoma NA BeFree Detail
0.002 breast carcinoma NA BeFree Detail
0.002 Sleep Disorders NA GAD Detail
<0.001 bipolar I disorder NA BeFree Detail
<0.001 winter depression NA BeFree Detail
0.002 breast carcinoma In women with three consecutive night shifts, a reduced risk of breast cancer wa... BeFree 23822714 Detail
0.009 Malignant neoplasm of breast In women with three consecutive night shifts, a reduced risk of breast cancer wa... BeFree 23822714 Detail
0.003 Mammary Neoplasms NA LHGDN Detail
<0.001 Glioblastoma multiforme NA BeFree Detail
<0.001 Azoospermia, Nonobstructive Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family w... BeFree 25956372 Detail
0.123 autistic disorder NA BeFree,CTD_human,GAD Detail
0.005 bipolar disorder NA GAD Detail
0.009 Malignant neoplasm of breast NA BeFree,GAD Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Lack of association of the NPAS2 gene Ala394Thr polymorphism (rs2305160:G>A) with risk of chronic ly... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We investigated whether CLOCK and NPAS2 gene polymorphisms are associated with RLS in schizophrenic ... DisGeNET Detail
NA DisGeNET Detail
Association between restless legs syndrome and CLOCK and NPAS2 gene polymorphisms in schizophrenia. DisGeNET Detail
NA DisGeNET Detail
However, when accounting for potential effect modification, rs23051560 (Ala394Thr) in the largest ci... DisGeNET Detail
However, when accounting for potential effect modification, rs23051560 (Ala394Thr) in the largest ci... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
In women with three consecutive night shifts, a reduced risk of breast cancer was associated with ca... DisGeNET Detail
In women with three consecutive night shifts, a reduced risk of breast cancer was associated with ca... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive a... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs131113549 dbSNP
Genome
hg19
Position
chr2:101,436,601-101,613,291
Variant Type
snv
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