Xq25-q26.1 - OMIM - NCBI

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The following terms were not found in OMIM: q26.1, Xq25-q26.1.

Select item 3009791.

#300979 - CHROMOSOME Xq25 DUPLICATION SYNDROME

CHROMOSOME Xq25 TRIPLICATION SYNDROME, INCLUDED

Cytogenetic locations: 23637084

OMIM:: 300979

Gene summaries Genetic tests Medical literature

Select item 3007792.

%300779 - CORNEAL DYSTROPHY, ENDOTHELIAL, X-LINKED; XECD

Cytogenetic locations: 308380

OMIM:: 300779

Gene summaries Genetic tests Medical literature

Select item 3007033.

%300703 - SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5

Cytogenetic locations: 18241076

OMIM:: 300703

Gene summaries Genetic tests Medical literature

Select item 3004364.

%300436 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 46; XLID46

Cytogenetic locations: 19783701

OMIM:: 300436

Gene summaries Genetic tests Medical literature

Select item 3011245.

*301124 - TESTIS-EXPRESSED GENE 13D; TEX13D

OMIM:: 301124

Gene summaries Genetic tests Medical literature

Select item 3011236.

*301123 - TESTIS-EXPRESSED GENE 13C; TEX13C

OMIM:: 301123

Gene summaries Genetic tests Medical literature

Select item 3138507.

%313850 - THORACOABDOMINAL SYNDROME; THAS

MIDLINE DEFECTS, X-LINKED, INCLUDED

Cytogenetic locations: Xq13.1

OMIM:: 313850

Gene summaries Genetic tests Medical literature

Select item 3001798.

%300179 - X INACTIVATION, FAMILIAL SKEWED, 2; SXI2

Cytogenetic locations: 21412246

OMIM:: 300179

Gene summaries Genetic tests Medical literature

Select item 3011279.

#301127 - ARTHROGRYPOSIS MULTIPLEX CONGENITA 7, X-LINKED; AMC7

OMIM:: 301127

Gene summaries Genetic tests Medical literature

Select item 30001210.

*300012 - SWI/SNF-RELATED, MATRIX-ASSOCIATED, ACTIN-DEPENDENT REGULATOR OF CHROMATIN, SUBFAMILY A, MEMBER 1; SMARCA1

Cytogenetic locations: SVA

OMIM:: 300012

Gene summaries Genetic tests Medical literature

Select item 30104311.

#301043 - HOLOPROSENCEPHALY 13, X-LINKED; HPE13

Cytogenetic locations: 300061

OMIM:: 301043

Gene summaries Genetic tests Medical literature

Select item 30058812.

*300588 - TENEURIN TRANSMEMBRANE PROTEIN 1; TENM1

Cytogenetic locations: Xq13.1

OMIM:: 300588

Gene summaries Genetic tests Medical literature

Select item 31207013.

*312070 - UBIQUITIN-LIKE 4A; UBL4A

Cytogenetic locations: Xq25

OMIM:: 312070

Gene summaries Genetic tests Medical literature

Select item 30048714.

*300487 - ACTIN-RELATED PROTEIN T1; ACTRT1

Cytogenetic locations: Xq13.1

OMIM:: 300487

Gene summaries Genetic tests Medical literature

Select item 30069915.

#300699 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WU TYPE; MRXSW

Cytogenetic locations: 17989220

OMIM:: 300699

Gene summaries Genetic tests Medical literature

Select item 30110816.

#301108 - CATARACTS, HEARING IMPAIRMENT, NEPHROTIC SYNDROME, AND ENTEROCOLITIS 1; CHINE1

Cytogenetic locations: Xq25

OMIM:: 301108

Gene summaries Genetic tests Medical literature

Select item 30591517.

*305915 - GLUTAMATE RECEPTOR, IONOTROPIC, AMPA 3; GRIA3

Cytogenetic locations: 11144349

OMIM:: 305915

Gene summaries Genetic tests Medical literature

Select item 30102218.

#301022 - MULLEGAMA-KLEIN-MARTINEZ SYNDROME; MKMS

Cytogenetic locations: 300061

OMIM:: 301022

Gene summaries Genetic tests Medical literature

Select item 30095719.

#300957 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, KUMAR TYPE; MRXSK

Cytogenetic locations: 32116545

OMIM:: 300957

Gene summaries Genetic tests Medical literature

Select item 30824020.

#308240 - LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1

Cytogenetic locations: 2Mb

OMIM:: 308240

Gene summaries Genetic tests Medical literature

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Xq25-q26.1 (69)
OMIM
Novel human gene from chromosome 20, similar to S68401: cattle glucose induced g...
Novel human gene from chromosome 20, similar to S68401: cattle glucose induced gene
gi|6012998|emb|AL121740.1|

Nucleotide

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