Ensembl ID ENSG00000126777 Gene ID 3895 Accession 6467
Gene Symbol KTN1 Alias CG1;KNT;MU-RMS-40.19 Full Name kinectin 1
Position 14 : 55559072 - 55701526 Length 142455 bases Strand Plus strand
Status Confidence Main interacting RNAsN.A.RBP type Non-canonical_RBPs
Summary This gene encodes an integral membrane protein that is a member of the kinectin protein family. The encoded protein is primarily localized to the endoplasmic reticulum membrane. This protein binds kinesin and may be involved in intracellular organelle motility. This protein also binds translation elongation factor-delta and may be involved in the assembly of the elongation factor-1 complex. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, Aug 2012]

ENSG00000126777 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000126777 KTN1 -0.8 4.00e-30 KIRC
ENSG00000126777 KTN1 -0.7 4.19e-15 COAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000126777 KTN1 tumor 16207330
ENSG00000126777 KTN1 breast cancer 20560667
ENSG00000126777 KTN1 Tumor 25795305
ENSG00000126777 KTN1 colorectal cancer 27676367
ENSG00000126777 KTN1 tumor 30683916
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000126777 KTN1 papillary thyroid carcinoma gene_fusion 49.38% (80/162) 3 entries
ENSG00000126777 KTN1 Thyroid Gland Oncocytic Follicular Carcinoma gene_fusion 48.65% (36/74) 1 entry
ENSG00000126777 KTN1 Follicular Variant Thyroid Gland Papillary Carcinoma gene_fusion 50.0% (13/26) 1 entry
ENSG00000126777 KTN1 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma gene_fusion 20.0% (2/10) 1 entry
ENSG00000126777 KTN1 colon adenocarcinoma frameshift_variant 2.571% (19/739) 2 entries
ENSG00000126777 KTN1 colorectal adenocarcinoma frameshift_variant 2.988% (34/1138) 1 entry
ENSG00000126777 KTN1 breast ductal adenocarcinoma missense_variant 9.562% (59/617) 1 entry
ENSG00000126777 KTN1 ovarian serous adenocarcinoma missense_variant 0.2972% (2/673) 1 entry
ENSG00000126777 KTN1 cecum adenocarcinoma missense_variant 2.381% (3/126) 1 entry
ENSG00000126777 KTN1 pancreatic ductal adenocarcinoma missense_variant 3.018% (38/1259) 1 entry
ENSG00000126777 KTN1 colorectal adenocarcinoma sequence_alteration 2.988% (34/1138) 1 entry
ENSG00000126777 KTN1 clear cell renal carcinoma sequence_alteration 0.2903% (4/1378) 1 entry
ENSG00000126777 KTN1 lung adenocarcinoma sequence_alteration 1.311% (16/1220) 2 entries
ENSG00000126777 KTN1 squamous cell lung carcinoma missense_variant 1.939% (16/825) 1 entry
ENSG00000126777 KTN1 clear cell renal carcinoma missense_variant 0.2903% (4/1378) 1 entry
ENSG00000126777 KTN1 prostate carcinoma sequence_alteration 1.033% (5/484) 1 entry
ENSG00000126777 KTN1 colon adenocarcinoma sequence_alteration 2.571% (19/739) 3 entries
ENSG00000126777 KTN1 hepatocellular carcinoma stop_gained 1.885% (17/902) 1 entry
ENSG00000126777 KTN1 gastric intestinal type adenocarcinoma missense_variant 2.353% (2/85) 1 entry
ENSG00000126777 KTN1 chronic lymphocytic leukemia sequence_alteration 0.7883% (7/888) 1 entry
ENSG00000126777 KTN1 prostate adenocarcinoma missense_variant 3.37% (49/1454) 2 entries
ENSG00000126777 KTN1 papillary renal cell carcinoma missense_variant 0.8955% (3/335) 1 entry
ENSG00000126777 KTN1 gastric adenocarcinoma missense_variant 0.8961% (5/558) 1 entry
ENSG00000126777 KTN1 breast carcinoma missense_variant 0.567% (8/1411) 1 entry
ENSG00000126777 KTN1 colon adenocarcinoma missense_variant 2.571% (19/739) 3 entries
ENSG00000126777 KTN1 esophageal squamous cell carcinoma missense_variant 1.185% (8/675) 4 entries
ENSG00000126777 KTN1 nasopharyngeal squamous cell carcinoma missense_variant 1.198% (2/167) 1 entry
ENSG00000126777 KTN1 colorectal adenocarcinoma missense_variant 2.988% (34/1138) 2 entries
ENSG00000126777 KTN1 lung adenocarcinoma missense_variant 1.311% (16/1220) 4 entries
ENSG00000126777 KTN1 skin melanoma missense_variant 0.8273% (8/967) 2 entries
ENSG00000126777 KTN1 hepatocellular carcinoma missense_variant 1.885% (17/902) 1 entry
ENSG00000126777 KTN1 small cell lung carcinoma missense_variant 2.154% (7/325) 2 entries
ENSG00000126777 KTN1 small cell lung carcinoma frameshift_variant 2.154% (7/325) 2 entries
ENSG00000126777 KTN1 metaplastic breast carcinoma missense_variant 3.922% (2/51) 2 entries
ENSG00000126777 KTN1 squamous cell lung carcinoma sequence_alteration 1.939% (16/825) 2 entries
ENSG00000126777 KTN1 ovarian neoplasm missense_variant 1.724% (1/58) 1 entry
ENSG00000126777 KTN1 rectal adenocarcinoma frameshift_variant 0.8734% (2/229) 1 entry
ENSG00000126777 KTN1 ependymoma sequence_alteration 2.174% (1/46) 1 entry
ENSG00000126777 KTN1 chromophobe renal cell carcinoma missense_variant 0.8696% (1/115) 1 entry
ENSG00000126777 KTN1 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000126777 KTN1 skin melanoma sequence_alteration 0.8273% (8/967) 1 entry
ENSG00000126777 KTN1 oral squamous cell carcinoma missense_variant 0.4878% (1/205) 1 entry
ENSG00000126777 KTN1 HER2 Positive Breast Carcinoma missense_variant 2.516% (4/159) 1 entry
ENSG00000126777 KTN1 squamous cell lung carcinoma stop_gained 1.939% (16/825) 1 entry
ENSG00000126777 KTN1 gastric adenocarcinoma frameshift_variant 0.8961% (5/558) 1 entry
ENSG00000126777 KTN1 Mixed Lobular and Ductal Breast Carcinoma missense_variant 25.0% (1/4) 1 entry
ENSG00000126777 KTN1 diffuse gastric adenocarcinoma sequence_alteration 1.266% (1/79) 1 entry
ENSG00000126777 KTN1 melanoma missense_variant 1.98% (2/101) 1 entry
ENSG00000126777 KTN1 esophageal squamous cell carcinoma frameshift_variant 1.185% (8/675) 1 entry
ENSG00000126777 KTN1 osteosarcoma sequence_alteration 0.8621% (1/116) 1 entry
ENSG00000126777 KTN1 Ampulla of Vater Carcinoma missense_variant 1.176% (1/85) 1 entry
ENSG00000126777 KTN1 female breast carcinoma missense_variant 0.2558% (1/391) 1 entry
ENSG00000126777 KTN1 Gastrointestinal stromal tumor stop_gained 9.091% (1/11) 1 entry
ENSG00000126777 KTN1 melanoma frameshift_variant 1.98% (2/101) 1 entry
ENSG00000126777 KTN1 Merkel cell skin cancer sequence_alteration 6.667% (2/30) 1 entry
ENSG00000126777 KTN1 Malignant Germ Cell Tumor missense_variant 100.0% (1/1) 1 entry
ENSG00000126777 KTN1 pulmonary blastoma missense_variant 4.167% (1/24) 1 entry
ENSG00000126777 KTN1 renal carcinoma missense_variant 14.29% (1/7) 1 entry
ENSG00000126777 KTN1 lung adenocarcinoma stop_gained 1.311% (16/1220) 1 entry
ENSG00000126777 KTN1 head and neck squamous cell carcinoma stop_gained 0.1597% (1/626) 1 entry
ENSG00000126777 KTN1 bladder transitional cell carcinoma missense_variant 0.7299% (1/137) 1 entry
ENSG00000126777 KTN1 Merkel cell skin cancer missense_variant 6.667% (2/30) 1 entry
ENSG00000126777 KTN1 basal cell carcinoma frameshift_variant 1.724% (1/58) 1 entry
ENSG00000126777 KTN1 prostate carcinoma missense_variant 1.033% (5/484) 1 entry
ENSG00000126777 KTN1 colorectal adenocarcinoma stop_gained 2.988% (34/1138) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000126777 KTN1 MESO 0.0052 low
ENSG00000126777 KTN1 SARC 0.018 high
ENSG00000126777 KTN1 UCEC 0.015 high
ENSG00000126777 KTN1 LGG 0.043 high
ENSG00000126777 KTN1 LUSC 0.015 low
ENSG00000126777 KTN1 KIRP 0.025 high
ENSG00000126777 KTN1 KICH 0.0012 high
ENSG00000126777 KTN1 LUAD 0.029 high
ENSG00000126777 KTN1 PCPG 0.0027 high
ENSG00000126777 KTN1 BRCA 0.0093 high
ENSG00000126777 KTN1 UCS 0.0026 high
ENSG00000126777 KTN1 DLBC 0.039 high
ENSG00000126777 KTN1 TGCT 0.038 low
ENSG00000126777 KTN1 LAML 0.018 low
ENSG00000126777 KTN1 GBM 0.014 low
ENSG00000126777 KTN1 CESC 0.047 high
ENSG00000126777 KTN1 LIHC 0.00032 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000126777 KTN1 LGG Del 0.791398 0.039887 0.496034 0.175439
ENSG00000126777 KTN1 OV Del 0.917749 0.179694 0.528139 0.461140