17q23.2 - OMIM - NCBI

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Select item 6202721.

*620272 - TRANSMEMBRANE PROTEIN 235; TMEM235

Cytogenetic locations: 17q23.2

OMIM:: 620272

Gene summaries Genetic tests Medical literature

Select item 6092742.

*609274 - NASCENT POLYPEPTIDE-ASSOCIATED COMPLEX, ALPHA POLYPEPTIDE, 2; NACA2

Cytogenetic locations: 616934

OMIM:: 609274

Gene summaries Genetic tests Medical literature

Select item 6129673.

%612967 - BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 15; BMIQ15

Cytogenetic locations: 19576566

OMIM:: 612967

Gene summaries Genetic tests Medical literature

Select item 6189024.

*618902 - METHYLTRANSFERASE 2A, METHYLCYTIDINE; METTL2A

Cytogenetic locations: 28655767

OMIM:: 618902

Gene summaries Genetic tests Medical literature

Select item 6113465.

*611346 - INTEGRATOR COMPLEX SUBUNIT 2; INTS2

Cytogenetic locations: 10574462

OMIM:: 611346

Gene summaries Genetic tests Medical literature

Select item 6195676.

*619567 - EF-HAND CALCIUM-BINDING DOMAIN-CONTAINING PROTEIN 3; EFCAB3

Cytogenetic locations: 30275530

OMIM:: 619567

Gene summaries Genetic tests Medical literature

Select item 6133377.

*613337 - MEMBRANE-ASSOCIATED RING-CH FINGER PROTEIN 10; MARCHF10

Cytogenetic locations: 17604280

OMIM:: 613337

Gene summaries Genetic tests Medical literature

Select item 6053248.

*605324 - AMYLOID BETA PRECURSOR PROTEIN-BINDING PROTEIN 2; APPBP2

Cytogenetic locations: 607759

OMIM:: 605324

Gene summaries Genetic tests Medical literature

Select item 6090549.

#609054 - FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ

Cytogenetic locations: -

OMIM:: 609054

Gene summaries Genetic tests Medical literature

Select item 61745010.

#617450 - JANSEN-DE VRIES SYNDROME; JDVS

Cytogenetic locations: 28343630

OMIM:: 617450

Gene summaries Genetic tests Medical literature

Select item 61822311.

#618223 - VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD

Cytogenetic locations: 29726930

OMIM:: 618223

Gene summaries Genetic tests Medical literature

Select item 61226412.

*612264 - MANNOSE RECEPTOR, C-TYPE, 2; MRC2

Cytogenetic locations: 12972549

OMIM:: 612264

Gene summaries Genetic tests Medical literature

Select item 60085213.

#600852 - RETINITIS PIGMENTOSA 17; RP17

Cytogenetic locations: 15563508

OMIM:: 600852

Gene summaries Genetic tests Medical literature

Select item 61964114.

#619641 - HENGEL-MAROOFIAN-SCHOLS SYNDROME; HEMARS

Cytogenetic locations: 607759

OMIM:: 619641

Gene summaries Genetic tests Medical literature

Select item 61800915.

#618009 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 61; MRD61

Cytogenetic locations: 29740699

OMIM:: 618009

Gene summaries Genetic tests Medical literature

Select item 61890616.

#618906 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS

Cytogenetic locations: 31616000

OMIM:: 618906

Gene summaries Genetic tests Medical literature

Select item 60380817.

*603808 - MEDIATOR COMPLEX SUBUNIT 13; MED13

Cytogenetic locations: 29740699

OMIM:: 603808

Gene summaries Genetic tests Medical literature

Select item 61805018.

#618050 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 57; MRD57

Cytogenetic locations: 17q21.31

OMIM:: 618050

Gene summaries Genetic tests Medical literature

Select item 60747019.

*607470 - BCAS3 MICROTUBULE-ASSOCIATED CELL MIGRATION FACTOR; BCAS3

Cytogenetic locations: 34022130

OMIM:: 607470

Gene summaries Genetic tests Medical literature

Select item 60136020.

#601360 - AMELIA, POSTERIOR, WITH PELVIC AND PULMONARY HYPOPLASIA SYNDROME; PAPPAS

Cytogenetic locations: 31965066

OMIM:: 601360

Gene summaries Genetic tests Medical literature

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