GCSAM germinal center associated signaling and motility
Information
- Symbol
- GCSAM
- Type
- protein-coding
- Description
- germinal center associated signaling and motility
- Entrez Gene ID
- 257144
- Genome
- hg19
- Position
- chr3:111,841,943-111,852,101
- Genome
- hg38
- Position
- chr3:112,123,096-112,133,254
- MIM
- 607792 OMIM
- HGNC
- HGNC:20253 HGNC
- Ensembl
- ENSG00000174500 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
18 |
![]() |
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 |
Type | ID |
---|---|
SYNONYM | GCAT2 |
SYNONYM | GCET2 |
SYNONYM | HGAL |
MIM | 607792 OMIM |
HGNC | HGNC:20253 HGNC |
Ensembl | ENSG00000174500 Ensembl |
AllianceGenome | HGNC:20253 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000484193.5 | hg38 | chr3 | 112,123,096 | 112,133,254 | 10,159 |
ENST00000460387.6 | hg38 | chr3 | 112,123,455 | 112,133,251 | 9,797 |
ENST00000308910.9 | hg38 | chr3 | 112,120,839 | 112,133,248 | 12,410 |
ENST00000488580.6 | hg38 | chr3 | 112,123,455 | 112,133,225 | 9,771 |
ENST00000487901.2 | hg38 | chr3 | 112,123,455 | 112,133,270 | 9,816 |
ENST00000308910.9 | hg19 | chr3 | 111,839,686 | 111,852,095 | 12,410 |
ENST00000484193.5 | hg19 | chr3 | 111,841,943 | 111,852,101 | 10,159 |
ENST00000488580.6 | hg19 | chr3 | 111,842,302 | 111,852,072 | 9,771 |
ENST00000460387.6 | hg19 | chr3 | 111,842,302 | 111,852,098 | 9,797 |
ENST00000487901.2 | hg19 | chr3 | 111,842,302 | 111,852,117 | 9,816 |
Genome browser