Genome editing - OMIM - NCBI

Genome editing - OMIM - NCBI





From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

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• Search OMIM for "Genome editing" 

1.

*607109 - APOLIPOPROTEIN B mRNA-EDITING ENZYME, CATALYTIC POLYPEPTIDE-LIKE 3A; APOBEC3A

Cytogenetic locations: 22q13.1

OMIM:

 

607109

Gene summaries Genetic tests Medical literature

Select item 6109762.

*610976 - APOLIPOPROTEIN B mRNA EDITING ENZYME, CATALYTIC POLYPEPTIDE-LIKE 3H; APOBEC3H

Cytogenetic locations: 22q13.1

OMIM:

 

610976

Gene summaries Genetic tests Medical literature

Select item 6077503.

*607750 - APOLIPOPROTEIN B mRNA-EDITING ENZYME, CATALYTIC POLYPEPTIDE-LIKE 3C; APOBEC3C

Cytogenetic locations: 22q13.1

OMIM:

 

607750

Gene summaries Genetic tests Medical literature

Select item 6001304.

*600130 - APOLIPOPROTEIN B mRNA-EDITING ENZYME, CATALYTIC POLYPEPTIDE 1; APOBEC1

Cytogenetic locations: 12p13.31

OMIM:

 

600130

Gene summaries Genetic tests Medical literature

Select item 6071105.

*607110 - APOLIPOPROTEIN B mRNA-EDITING ENZYME, CATALYTIC POLYPEPTIDE-LIKE 3B; APOBEC3B

Cytogenetic locations: 22q13.1

OMIM:

 

607110

Gene summaries Genetic tests Medical literature

Select item 6071136.

*607113 - APOLIPOPROTEIN B mRNA-EDITING ENZYME, CATALYTIC POLYPEPTIDE-LIKE 3G; APOBEC3G

Cytogenetic locations: 22q13.1

OMIM:

 

607113

Gene summaries Genetic tests Medical literature

Select item 6010657.

*601065 - ALANYL-tRNA SYNTHETASE; AARS

Cytogenetic locations: 16q22.1

OMIM:

 

601065

Gene summaries Genetic tests Medical literature

Select item 6132128.

*613212 - ALANYL-tRNA SYNTHETASE DOMAIN-CONTAINING 1; AARSD1

Cytogenetic locations: 17q21.31

OMIM:

 

613212

Gene summaries Genetic tests Medical literature

Select item 6131139.

*613113 - NEUROFIBROMIN 1; NF1

Cytogenetic locations: 17q11.2

OMIM:

 

613113

Gene summaries Genetic tests Medical literature

Select item 60675010.

*606750 - Z-DNA BINDING PROTEIN 1; ZBP1

Cytogenetic locations: 20q13.31

OMIM:

 

606750

Gene summaries Genetic tests Medical literature

Select item 60525711.

*605257 - ACTIVATION-INDUCED CYTIDINE DEAMINASE; AICDA

Cytogenetic locations: 12p13.31

OMIM:

 

605257

Gene summaries Genetic tests Medical literature

Select item 16417712.

*164177 - POU DOMAIN, CLASS 5, TRANSCRIPTION FACTOR 1; POU5F1

POU5F1/EWS FUSION GENE, INCLUDED

Cytogenetic locations: 6p21.33

OMIM:

 

164177

Gene summaries Genetic tests Medical literature

Select item 10540013.

#105400 - AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1

AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE, INCLUDED

Cytogenetic locations: 1pter-p36.13, 22q12.2, 1pter-p36.13, 21q22.11

OMIM:

 

105400

Gene summaries Genetic tests Medical literature

Select item 30690014.

#306900 - HEMOPHILIA B; HEMB

HEMOPHILIA B(M), INCLUDED

Cytogenetic locations: Xq27.1

OMIM:

 

306900

Gene summaries Genetic tests Medical literature

Select item 30037715.

*300377 - DYSTROPHIN; DMD

APO-DYSTROPHIN 1, INCLUDED

Cytogenetic locations: Xp21.2-p21.1

OMIM:

 

300377

Gene summaries Genetic tests Medical literature

Select item 51606016.

+516060 - ATP SYNTHASE 6; MTATP6

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1, INCLUDED; MC5DM1, INCLUDED

OMIM:

 

516060

Gene summaries Genetic tests Medical literature

Select item 18883017.

*188830 - PROTEIN KINASE, cAMP-DEPENDENT, REGULATORY, TYPE I, ALPHA; PRKAR1A

PRKAR1A/RARA FUSION GENE, INCLUDED

Cytogenetic locations: 17q24.2

OMIM:

 

188830

Gene summaries Genetic tests Medical literature

Select item 61711918.

#617119 - BARDET-BIEDL SYNDROME 20; BBS20

Cytogenetic locations: 9p21.2

OMIM:

 

617119

Gene summaries Genetic tests Medical literature

Select item 60173619.

*601736 - SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY D, MEMBER 2; SMARCD2

Cytogenetic locations: 17q23.3

OMIM:

 

601736

Gene summaries Genetic tests Medical literature

Select item 60250020.

*602500 - GOLGI AUTOANTIGEN, GOLGIN SUBFAMILY B, 1; GOLGB1

Cytogenetic locations: 3q13.33

OMIM:

 

602500

Gene summaries Genetic tests Medical literature