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