8q22.1 - OMIM

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Select item 6138951.

*613895 - DPY19-LIKE 4; DPY19L4

Cytogenetic locations: 16526957

OMIM:: 613895

Gene summaries Genetic tests Medical literature

Select item 6130942.

#613094 - MICROPHTHALMIA, ISOLATED 4; MCOP4

Cytogenetic locations: 601653

OMIM:: 613094

Gene summaries Genetic tests Medical literature

Select item 6163063.

*616306 - FIBRINOGEN SILENCER-BINDING PROTEIN; FSBP

Cytogenetic locations: 8q13.1

OMIM:: 616306

Gene summaries Genetic tests Medical literature

Select item 6030174.

*603017 - CADHERIN 17; CDH17

Cytogenetic locations: 617720

OMIM:: 603017

Gene summaries Genetic tests Medical literature

Select item 6159915.

#615991 - BARDET-BIEDL SYNDROME 14; BBS14

Cytogenetic locations: 1p36, 1p36

OMIM:: 615991

Gene summaries Genetic tests Medical literature

Select item 6021086.

*602108 - MATRILIN 2; MATN2

Cytogenetic locations: 11124542

OMIM:: 602108

Gene summaries Genetic tests Medical literature

Select item 6164477.

*616447 - VIR-LIKE M6A METHYLTRANSFERASE-ASSOCIATED PROTEIN; VIRMA

Cytogenetic locations: Centrosome

OMIM:: 616447

Gene summaries Genetic tests Medical literature

Select item 6137038.

#613703 - MICROPHTHALMIA/COLOBOMA 6; MCOPCB6

Cytogenetic locations: 1p36, 1p36

OMIM:: 613703

Gene summaries Genetic tests Medical literature

Select item 6187549.

*618754 - CARBOXYPEPTIDASE Q; CPQ

Cytogenetic locations: 10206990

OMIM:: 618754

Gene summaries Genetic tests Medical literature

Select item 61515810.

#615158 - MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3; MC3DN3

Cytogenetic locations: 603628

OMIM:: 615158

Gene summaries Genetic tests Medical literature

Select item 60618511.

*606185 - TUMOR PROTEIN p53-INDUCIBLE NUCLEAR PROTEIN 1; TP53INP1

Cytogenetic locations: 601993

OMIM:: 606185

Gene summaries Genetic tests Medical literature

Select item 61821912.

#618219 - POLYDACTYLY, POSTAXIAL, TYPE A9; PAPA9

OMIM:: 618219

Gene summaries Genetic tests Medical literature

Select item 61472113.

*614721 - TSPY-LIKE 5; TSPYL5

Cytogenetic locations: 11214970

OMIM:: 614721

Gene summaries Genetic tests Medical literature

Select item 61857214.

#618572 - NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY; NEDCHS

Cytogenetic locations: 28542170

OMIM:: 618572

Gene summaries Genetic tests Medical literature

Select item 15120015.

#151200 - CHROMOSOME 8q22.1 DUPLICATION SYNDROME

Cytogenetic locations: 16794698

OMIM:: 151200

Gene summaries Genetic tests Medical literature

Select item 61801316.

#618013 - DEAFNESS, AUTOSOMAL RECESSIVE 109; DFNB109

Cytogenetic locations: 29107558

OMIM:: 618013

Gene summaries Genetic tests Medical literature

Select item 61693017.

*616930 - TRANSCRIPTION TERMINATION FACTOR 3, MITOCHONDRIAL; MTERF3

Cytogenetic locations: 20430012

OMIM:: 616930

Gene summaries Genetic tests Medical literature

Select item 61520818.

*615208 - PLECKSTRIN HOMOLOGY DOMAIN-CONTAINING PROTEIN, FAMILY F, MEMBER 2; PLEKHF2

Cytogenetic locations: 22816767

OMIM:: 615208

Gene summaries Genetic tests Medical literature

Select item 61536019.

#615360 - LEBER CONGENITAL AMAUROSIS 17; LCA17

Cytogenetic locations: 601653

OMIM:: 615360

Gene summaries Genetic tests Medical literature

Select item 61135120.

*611351 - INTEGRATOR COMPLEX SUBUNIT 8; INTS8

Cytogenetic locations: 28542170

OMIM:: 611351

Gene summaries Genetic tests Medical literature

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