C1QTNF1 C1q and TNF related 1

Information
Symbol
C1QTNF1
Type
protein-coding
Description
C1q and TNF related 1
Entrez Gene ID
114897
Genome
hg19
Position
chr17:77,020,253-77,045,869
Genome
hg38
Position
chr17:79,024,171-79,049,787
MIM
610365 OMIM
HGNC
HGNC:14324 HGNC
Ensembl
ENSG00000173918 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
48
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CTRP1
SYNONYM GIP
SYNONYM ZSIG37
MIM 610365 OMIM
HGNC HGNC:14324 HGNC
Ensembl ENSG00000173918 Ensembl
AllianceGenome HGNC:14324
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000354124.7 hg38 chr17 79,022,934 79,049,787 26,854
ENST00000578229.5 hg38 chr17 79,022,814 79,048,247 25,434
ENST00000583904.5 hg38 chr17 79,041,726 79,048,247 6,522
ENST00000580454.5 hg38 chr17 79,022,971 79,048,247 25,277
ENST00000581774.5 hg38 chr17 79,034,185 79,048,247 14,063
ENST00000311661.4 hg38 chr17 79,024,261 79,049,787 25,527
ENST00000339142.6 hg38 chr17 79,024,171 79,049,787 25,617
ENST00000579760.6 hg38 chr17 79,024,169 79,049,788 25,620
ENST00000580474.1 hg38 chr17 79,043,593 79,048,466 4,874
ENST00000392445.6 hg38 chr17 79,025,663 79,049,788 24,126
ENST00000578229.5 hg19 chr17 77,018,896 77,044,329 25,434
ENST00000354124.7 hg19 chr17 77,019,016 77,045,869 26,854
ENST00000580454.5 hg19 chr17 77,019,053 77,044,329 25,277
ENST00000579760.6 hg19 chr17 77,020,251 77,045,870 25,620
ENST00000339142.6 hg19 chr17 77,020,253 77,045,869 25,617
ENST00000311661.4 hg19 chr17 77,020,343 77,045,869 25,527
ENST00000392445.6 hg19 chr17 77,021,745 77,045,870 24,126
ENST00000581774.5 hg19 chr17 77,030,267 77,044,329 14,063
ENST00000583904.5 hg19 chr17 77,037,808 77,044,329 6,522
ENST00000580474.1 hg19 chr17 77,039,675 77,044,548 4,874
Genome browser