OMIM Entry Search - RNF144A-AS1

Search: 'RNF144A-AS1'

Results: 37 entries.

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# 607277. ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1
Cytogenetic location: 14q22.1
Matching terms: as1
► Phenotype-Gene Relationships ► Links

Phenotype-Gene Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key	Gene/Locus	Gene/Locus MIM number
14q22.1	{Asthma, susceptibility to, 1}	607277		3	PTGDR	604687

Links
Testing GTR	Protein UniProt	Clinical Resources Clinical Trials Genetic Alliance GTR	Animal Models MGI Mouse Phenotype NCBI HomoloGene

* 107741. APOLIPOPROTEIN E; APOE
Cytogenetic location: 19q13.32, Genomic coordinates (GRCh38): 19:44,905,748-44,909,394
Matching terms: as1
► Gene-Phenotype Relationships ► ICD+ ► Links

Gene-Phenotype Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key
19q13.32	Alzheimer disease-2	104310	AD	3
	Hyperlipoproteinemia, type III	617347		3
	Lipoprotein glomerulopathy	611771		3
	Sea-blue histiocyte disease	269600	AR	3
	{?Macular degeneration, age-related}	603075	AD	3
	{Coronary artery disease, severe, susceptibility to}	617347		3

Links
Testing Gene Tests GTR	Genome Ensembl NCBI Map Viewer UCSC Genome Browser	DNA Ensembl NCBI RefSeq UCSC Genome Browser	Protein HPRD Human Protein Atlas UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG NCBI Gene UCSC	Clinical Resources Gene Tests Genetics Home Reference GTR	Variation 1000 Genome ClinVar ExAC GWAS Catalog GWAS Central HGMD HGVS NHLBI EVS PharmGKB	Animal Models IMPC KOMP MGI Mouse Gene MGI Mouse Phenotype NCBI HomoloGene OMIA ZFin	Cell Lines Coriell	Cellular Pathways KEGG Reactome

ICD+
SNOMEDCT: 412642004, 398796005

# 600807. ASTHMA, SUSCEPTIBILITY TO
ASTHMA, PROTECTION AGAINST, INCLUDED
Cytogenetic locations: 2q22.1, 4q13.3, 5q31.1, 5q32, 5q32, 6p22.1, 6p21.33, 6p12.3, 10q11.21, 13q14.2, 17q12
Matching terms: as1
► Phenotype-Gene Relationships ► ICD+ ► Links

Phenotype-Gene Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key	Gene/Locus	Gene/Locus MIM number
2q22.1	{Asthma, susceptibility to}	600807	AD	3	HNMT	605238
4q13.3	{Asthma, protection against}	600807	AD	3	MUC7	158375
5q31.1	{Asthma, susceptibility to}	600807	AD	3	IL13	147683
5q32	{Asthma, susceptibility to}	600807	AD	3	SCGB3A2	606531
5q32	{Asthma, nocturnal, susceptibility to}	600807	AD	3	ADRB2	109690
6p22.1	{Asthma, susceptibility to}	600807	AD	2	HLA-G	142871
6p21.33	{Asthma, susceptibility to}	600807	AD	3	TNF	191160
6p12.3	{Asthma, susceptibility to}	600807	AD	3	PLA2G7	601690
10q11.21	{Asthma, diminished response to antileukotriene treatment in}	600807	AD	3	ALOX5	152390
13q14.2	{Asthma}	600807	AD	3	PHF11	607796
17q12	{Asthma, susceptibility to}	600807	AD	3	CCL11	601156

Links
Testing GTR	Protein UniProt	Clinical Resources Clinical Trials Genetics Home Reference GTR	Animal Models MGI Mouse Phenotype NCBI HomoloGene Wormbase Disease Ontology

ICD+
DO: 2841

# 613792. CHROMOSOME 3pter-p25 DELETION SYNDROME
Cytogenetic location: 3pter-p25, Genomic coordinates (GRCh38): 3:0-16,300,000
Matching terms: as1
► Gene-Phenotype Relationships ► ICD+ ► Links

Gene-Phenotype Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key
3pter-p25	3p- syndrome	613792	AD	4

Links
Testing GTR EuroGentest	Clinical Resources Clinical Trials EuroGentest Genetics Home Reference GTR OrphaNet POSSUM	Animal Models NCBI HomoloGene

ICD+
SNOMEDCT: 449819002 ORPHA: 1620 DO: 0060417

% 109650. BEHCET SYNDROME
Matching terms: as1
► ICD+ ► Links

Links
Testing EuroGentest	Clinical Resources Clinical Trials EuroGentest Genetics Home Reference GARD OrphaNet	Cell Lines Coriell

ICD+
SNOMEDCT: 310701003 ICD10CM: M35.2 ICD9CM: 136.1 ORPHA: 117 DO: 13241

* 613149. CDKN2B ANTISENSE RNA; CDKN2BAS
Cytogenetic location: 9p21.3, Genomic coordinates (GRCh38): 9:21,994,790-22,121,096
Matching terms: as1
► Links

Links
Testing GTR	Genome Ensembl NCBI Map Viewer UCSC Genome Browser	DNA Ensembl NCBI RefSeq UCSC Genome Browser	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG NCBI Gene UCSC	Clinical Resources GTR	Variation 1000 Genome ClinVar ExAC GWAS Catalog GWAS Central HGVS NHLBI EVS PharmGKB	Animal Models KOMP NCBI HomoloGene

* 615406. GNG12 ANTISENSE RNA 1, NONCODING; GNG12AS1
Cytogenetic location: 1p31.3, Genomic coordinates (GRCh38): 1:67,832,287-68,202,986
Matching terms: as1
► Links

Links
Genome Ensembl NCBI Map Viewer UCSC Genome Browser	DNA Ensembl NCBI RefSeq UCSC Genome Browser	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG NCBI Gene UCSC	Variation 1000 Genome ClinVar ExAC GWAS Catalog GWAS Central HGVS NHLBI EVS PharmGKB	Animal Models KOMP NCBI HomoloGene

* 616915. ZEB1 ANTISENSE RNA 1, NONCODING; ZEB1AS1
Cytogenetic location: 10p11.22, Genomic coordinates (GRCh38): 10:31,316,527-31,319,094
Matching terms: as1
► Links

Links
Genome NCBI Map Viewer UCSC Genome Browser	DNA NCBI RefSeq UCSC Genome Browser	Gene Info BioGPS GeneCards Gene Ontology KEGG NCBI Gene	Variation ClinVar GWAS Central HGVS NHLBI EVS	Animal Models KOMP NCBI HomoloGene

* 617269. SOCS2 ANTISENSE RNA 1, NONCODING; SOCS2AS1
Cytogenetic location: 12q22, Genomic coordinates (GRCh38): 12:93,565,627-93,571,397
Matching terms: as1
► Links

Links
Genome Ensembl NCBI Map Viewer UCSC Genome Browser	DNA Ensembl NCBI RefSeq UCSC Genome Browser	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG NCBI Gene UCSC	Variation 1000 Genome ClinVar ExAC GWAS Central HGVS NHLBI EVS PharmGKB	Animal Models KOMP NCBI HomoloGene

10:

# 137760. GLAUCOMA, PRIMARY OPEN ANGLE; POAG
GLAUCOMA 1, OPEN ANGLE, E, INCLUDED
Cytogenetic location: 10p13
Matching terms: as1
► Phenotype-Gene Relationships ► ICD+ ► Links

Phenotype-Gene Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key	Gene/Locus	Gene/Locus MIM number
10p13	Glaucoma 1, open angle, E	137760	AD	3	OPTN	602432

Links
Testing GTR	Protein UniProt	Clinical Resources Clinical Trials Genetic Alliance Genetics Home Reference GTR	Animal Models MGI Mouse Phenotype NCBI HomoloGene OMIA	Cell Lines Coriell

ICD+
SNOMEDCT: 77075001 ICD10CM: H40.11 ICD9CM: 365.11 DO: 1070

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Search: RNF144A-AS1

Results: 37 entries.

# 607277. ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1
Cytogenetic location: 14q22.1
Matching terms: as1
Phenotype-Gene Relationships

* 107741. APOLIPOPROTEIN E; APOE
Cytogenetic location: 19q13.32, Genomic coordinates (GRCh38): 19:44,905,748-44,909,394
Matching terms: as1
Gene-Phenotype Relationships ICD+

# 613792. CHROMOSOME 3pter-p25 DELETION SYNDROME
Cytogenetic location: 3pter-p25, Genomic coordinates (GRCh38): 3:0-16,300,000
Matching terms: as1
Gene-Phenotype Relationships ICD+

% 109650. BEHCET SYNDROME
Matching terms: as1
ICD+

* 613149. CDKN2B ANTISENSE RNA; CDKN2BAS
Cytogenetic location: 9p21.3, Genomic coordinates (GRCh38): 9:21,994,790-22,121,096
Matching terms: as1

* 615406. GNG12 ANTISENSE RNA 1, NONCODING; GNG12AS1
Cytogenetic location: 1p31.3, Genomic coordinates (GRCh38): 1:67,832,287-68,202,986
Matching terms: as1

* 616915. ZEB1 ANTISENSE RNA 1, NONCODING; ZEB1AS1
Cytogenetic location: 10p11.22, Genomic coordinates (GRCh38): 10:31,316,527-31,319,094
Matching terms: as1

* 617269. SOCS2 ANTISENSE RNA 1, NONCODING; SOCS2AS1
Cytogenetic location: 12q22, Genomic coordinates (GRCh38): 12:93,565,627-93,571,397
Matching terms: as1

10:

# 137760. GLAUCOMA, PRIMARY OPEN ANGLE; POAG
GLAUCOMA 1, OPEN ANGLE, E, INCLUDED
Cytogenetic location: 10p13
Matching terms: as1
Phenotype-Gene Relationships ICD+