CT83 - cancer/testis antigen 83 Gene

Homo sapiens

Also known as KKLC1; CXorf61; KK-LC-1

Gene ID: 203413 | Gene type: protein coding

About CT83

Cytogenetic location: Xq23 Genomic coordinates (GRCh38): X:116,461,686-116,462,976 (from NCBI)

This gene has 1 transcript (splice variant) and 64 orthologues. Restricted expression toward testis (RPKM 15.4).

Located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

mRNA	Protein	Name
NM_001017978.4	NP_001017978.1	kita-kyushu lung cancer antigen 1

KKLCAg1

Protein Preferred Names

Protein Names

kita-kyushu lung cancer antigen 1

Cat. No.	Product Name	Accession	Purity
HY-P71562	CT83 Protein, Human (His, B2M)	Q5H943 (1M-113T)	≥95%

Diseases

Alias

Lung Cancer

Lung Carcinoma	Non-Small Cell Lung Carcinoma
Lung Cancer, Susceptibility To	Lung Cancer, Protection Against
Adenocarcinoma Of Lung, Somatic	Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
Nonsmall Cell Lung Cancer	Lung Neoplasm
Carcinoma Of Lung	Lung Non-Small Cell Carcinoma
Non-Small Cell Lung Cancer	Nsclc
Lung Neoplasms	Malignant Neoplasm Of Lung
Alveolar Cell Carcinoma	Nonsmall Cell Lung Cancer, Somatic
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In	Nonsmall Cell Lung Cancer, Susceptibility To
Lung Cancer, Somatic	Lung Cancer, Resistance To
Cancer Of Lung	Cancer Of Bronchus
Cancer Of The Lung	Lung Malignancies
Lung Malignant Tumors	Malignant Lung Tumor
Malignant Tumor Of Lung	Pulmonary Cancer
Pulmonary Carcinoma	Pulmonary Neoplasms
Respiratory Carcinoma	LNCR
Adenocarcinoma Of Lung	Neoplasm Of Lung
Cancer Lung	Carcinoma Non-Small Cell Lung
Carcinoma, Non-Small-Cell Lung	Lung Cancers
Lung Carcinomas	Cancer, Lung
Cancer, Lung, Non-Small Cell	Primary Malignant Neoplasm Of Lung
Bronchioloalveolar Adenocarcinoma

Martin-Probst Syndrome

Deafness-Intellectual Disability, Martin-Probst Type Syndrome	Martin-Probst Deafness-Mental Retardation Syndrome
Mental Retardation, X-Linked, Syndromic, Martin-Probst Type	MRXSMP
Deafness-Intellectual Disability Syndrome, Martin-Probst Type	Hearing Loss-Intellectual Disability Syndrome, Martin-Probst Type
X-Linked Deafness-Intellectual Disability Syndrome Syndrome	X-Linked Hearing Loss-Intellectual Disability Syndrome Syndrome

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