3q27.3 - OMIM

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Select item 6113341.

*611334 - SMALL NUCLEOLAR RNA, H/ACA BOX, 81; SNORA81

Cytogenetic locations: 16361266

OMIM:: 611334

Gene summaries Genetic tests Medical literature

Select item 6093502.

*609350 - RECEPTOR-TRANSPORTING PROTEIN 4; RTP4

Cytogenetic locations: 15550249

OMIM:: 609350

Gene summaries Genetic tests Medical literature

Select item 6075473.

*607547 - RIBOSOMAL PROTEIN L39-LIKE; RPL39L

Cytogenetic locations: Kelch-like

OMIM:: 607547

Gene summaries Genetic tests Medical literature

Select item 1806474.

*180647 - SMALL NUCLEOLAR RNA, H/ACA BOX, 63; SNORA63

Cytogenetic locations: 609010

OMIM:: 180647

Gene summaries Genetic tests Medical literature

Select item 6091385.

*609138 - RECEPTOR-TRANSPORTING PROTEIN 2; RTP2

Cytogenetic locations: 15550249

OMIM:: 609138

Gene summaries Genetic tests Medical literature

Select item 6091376.

*609137 - RECEPTOR-TRANSPORTING PROTEIN 1; RTP1

Cytogenetic locations: 615333

OMIM:: 609137

Gene summaries Genetic tests Medical literature

Select item 6198487.

*619848 - TBCC DOMAIN-CONTAINING PROTEIN 1; TBCCD1

Cytogenetic locations: 600819

OMIM:: 619848

Gene summaries Genetic tests Medical literature

Select item 6059548.

*605954 - FETUIN B; FETUB

Cytogenetic locations: 10947975

OMIM:: 605954

Gene summaries Genetic tests Medical literature

Select item 6007009.

*600700 - LIM DOMAIN-CONTAINING PREFERRED TRANSLOCATION PARTNER IN LIPOMA; LPP

LPP/MLL FUSION GENE, INCLUDED

Cytogenetic locations: 607858

OMIM:: 600700

Gene summaries Genetic tests Medical literature

Select item 10257710.

*102577 - REPLICATION FACTOR C, SUBUNIT 4; RFC4

Cytogenetic locations: 10783165

OMIM:: 102577

Gene summaries Genetic tests Medical literature

Select item 61936311.

#619363 - ANGIOEDEMA, HEREDITARY, 6; HAE6

Cytogenetic locations: 33114181

OMIM:: 619363

Gene summaries Genetic tests Medical literature

Select item 20365012.

#203650 - ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 1; APMR1

Cytogenetic locations: 17451405

OMIM:: 203650

Gene summaries Genetic tests Medical literature

Select item 11610013.

#116100 - CATARACT 20, MULTIPLE TYPES; CTRCT20

Cytogenetic locations: 600819

OMIM:: 116100

Gene summaries Genetic tests Medical literature

Select item 12373014.

*123730 - CRYSTALLIN, GAMMA-S; CRYGS

Cytogenetic locations: 600819

OMIM:: 123730

Gene summaries Genetic tests Medical literature

Select item 10967515.

*109675 - ST6 BETA-GALACTOSAMIDE ALPHA-2,6-SIALYLTRANSFERASE 1; ST6GAL1

Cytogenetic locations: 12878221

OMIM:: 109675

Gene summaries Genetic tests Medical literature

Select item 61806116.

#618061 - POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD6

Cytogenetic locations: Fxr1

OMIM:: 618061

Gene summaries Genetic tests Medical literature

Select item 22896017.

#228960 - HIGH MOLECULAR WEIGHT KININOGEN DEFICIENCY

KININOGEN DEFICIENCY, TOTAL, INCLUDED

Cytogenetic locations: 12127805

OMIM:: 228960

Gene summaries Genetic tests Medical literature

Select item 18245018.

*182450 - SOMATOSTATIN; SST

SOMATOSTATIN 28, INCLUDED

Cytogenetic locations: Yeats2

OMIM:: 182450

Gene summaries Genetic tests Medical literature

Select item 61311619.

#613116 - THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY; THPH11

THROMBOPHILIA DUE TO ELEVATED HISTIDINE-RICH GLYCOPROTEIN, INCLUDED

Cytogenetic locations: 18815595

OMIM:: 613116

Gene summaries Genetic tests Medical literature

Select item 62045520.

#620455 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND SPEECH DELAY, WITH OR WITHOUT SEIZURES; NEDHSS

Cytogenetic locations: 36528028

OMIM:: 620455

Gene summaries Genetic tests Medical literature

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