Entry Search - 188000 610855

Search: '188000 610855 (Search in: MIM number)'

Results: 2 entries.

* 610855. ANKYRIN REPEAT DOMAIN-CONTAINING PROTEIN 26; ANKRD26
Cytogenetic location: 10p12.1, Genomic coordinates (GRCh38): 10:26,947,582-27,100,494
Matching terms: 610855
► Gene-Phenotype Relationships ► Links

Gene-Phenotype Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key
10p12.1	Thrombocytopenia 2	188000	AD	3

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Links
Testing GTR	Genome Ensembl NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl (MANE Select) NCBI RefSeq NCBI RefSeq (MANE Select) UCSC Genome Browser	Protein HPRD Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene UCSC	Clinical Resources ClinGen Dosage ClinGen Validity GTR	Variation ClinVar DECIPHER gnomAD GWAS Catalog GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OMIA OrthoDB	Cellular Pathways Reactome

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# 188000. THROMBOCYTOPENIA 2; THC2
Cytogenetic location: 10p12.1
Matching terms: 188000
► Phenotype-Gene Relationships ► Phenotypic Series ► ICD+ ► Links

Phenotype-Gene Relationships
Location	Phenotype	Phenotype MIM number	Inheritance	Phenotype mapping key	Gene/Locus	Gene/Locus MIM number
10p12.1	Thrombocytopenia 2	188000	AD	3	ANKRD26	610855

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Thrombocytopenia - PS313900 - 14 Entries

Location	Phenotype	Inheritance	Phenotype mapping key	Phenotype MIM number	Gene/Locus	Gene/Locus MIM number
1p36.11	Thrombocytopenia 13, syndromic	AR	3	620776	GALE	606953
3q27.1	Thrombocytopenia 9	AD	3	620478	THPO	600044
5p13.1	Thrombocytopenia 3	AR	3	273900	FYB1	602731
7p22.1	Thrombocytopenia 8, with dysmorphic features and developmental delay	AD	3	620475	ACTB	102630
7p15.3	Thrombocytopenia 4	AD	3	612004	CYCS	123970
9p13.3	Thrombocytopenia 12 with or without myopathy	AR	3	620757	GNE	603824
10p12.1	Thrombocytopenia 2	AD	3	188000	ANKRD26	610855
10q26.13	Thrombocytopenia, autosomal dominant, 7	AD	3	619130	IKZF5	606238
11p11.2	Thrombocytopenia 10	AR	3	620484	PTPRJ	600925
12p13.2	Thrombocytopenia 5	AD	3	616216	ETV6	600618
12q15	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies	AD	3	620654	RAP1B	179530
20q11.23	?Thrombocytopenia 6	AD	3	616937	SRC	190090
Xp11.23	Thrombocytopenia, X-linked, intermittent	XLR	3	313900	WAS	300392
Xp11.23	Thrombocytopenia, X-linked	XLR	3	313900	WAS	300392

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Links
Testing GTR EuroGentest Autosomal thrombocytopenia… Hereditary thrombocytopeni…	Clinical Resources Clinical Trials EuroGentest Autosomal thrombocytopenia… Hereditary thrombocytopeni… Gene Reviews Genetic Alliance GTR OrphaNet Autosomal thrombocytopenia… Hereditary thrombocytopeni…	Animal Models Alliance Genome MGI Mouse Phenotype OMIA Wormbase Disease Ontology	Cell Lines Coriell

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ICD+
ORPHA: 168629, 268322 DO: 1588

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Search: 188000 610855 (Search in: MIM number)

Results: 2 entries.

* 610855. ANKYRIN REPEAT DOMAIN-CONTAINING PROTEIN 26; ANKRD26
Cytogenetic location: 10p12.1, Genomic coordinates (GRCh38): 10:26,947,582-27,100,494
Matching terms: 610855

# 188000. THROMBOCYTOPENIA 2; THC2
Cytogenetic location: 10p12.1
Matching terms: 188000

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