TARID - TCF21 antisense RNA inducing promoter demethylation Gene

Homo sapiens

Also known as EYA4-AS1

Gene ID: 100507308 | Gene type: ncRNA

About TARID

Cytogenetic location: 6q23.2 Genomic coordinates (GRCh38): 6:133,502,252-133,889,006 (from NCBI)

This gene has 12 transcripts (splice variants). Broad expression in placenta (RPKM 2.4), ovary (RPKM 2.4) and 16 other tissues.

Diseases

Alias

Deafness, Autosomal Dominant 10

DFNA10	Autosomal Dominant Nonsyndromic Deafness 10
Autosomal Dominant Deafness 10	Deafness, Autosomal Dominant, 10
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 10	Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 10
Deafness, Autosomal Dominant, Type 10

Cardiomyopathy, Dilated, 1j

CMD1J	Dilated Cardiomyopathy 1j
Neurosensory Deafness With Dilated Cardiomyopathy	Neurosensory Hearing Loss With Dilated Cardiomyopathy
Sensorineural Deafness With Dilated Cardiomyopathy	Sensorineural Hearing Loss With Dilated Cardiomyopathy
Cardiomyopathy, Dilated, With Sensorineural Hearing Loss, Autosomal Dominant	Autosomal Dominant Dilated Cardiomyopathy With Sensorineural Hearing Loss
Cardiomyopathy, Dilated 1j	Cardiomyopathy Dilated With Sensorineural Hearing Loss Autosomal Dominant
Cardiomyopathy, Dilated, Type 1j

Kidney Clear Cell Sarcoma

Clear Cell Sarcoma Of Kidney	Childhood Kidney Clear Cell Sarcoma
Renal Clear Cell Sarcoma	Ccsk
Clear Cell Sarcoma Of The Kidney

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