Evidence Details for CMTM3
Basic Information Top
Gene Symbol: | CMTM3 ( BNAS2,CKLFSF3,FLJ31762,MGC51956 ) |
---|---|
Gene Full Name: | CKLF-like MARVEL transmembrane domain containing 3 |
Band: | 16q22.1 |
Quick Links | Entrez ID:123920; OMIM: 607886; Uniprot ID:CKLF3_HUMAN; ENSEMBL ID: ENSG00000140931; HGNC ID: 19174 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>CMTM3|123920|nucleotide
ATGTGGCCCCCAGACCCCGACCCCGACCCGGACCCCGAGCCTGCCGGCGGCTCCCGTCCCGGCCCCGCGGTCCCCGGGCTCCGCGCCCTGCTGCCGGCGCGGGCT
TTCCTCTGCTCTCTCAAAGGCCGCCTCCTGCTGGCCGAGTCGGGTCTCTCATTCATCACTTTTATCTGCTATGTGGCGTCCTCAGCATCTGCCTTCCTCACAGCG
CCTCTGCTGGAGTTCCTGCTGGCCTTGTACTTCCTCTTTGCTGATGCCATGCAGCTGAATGACAAGTGGCAGGGCTTGTGCTGGCCCATGATGGACTTCCTGCGC
TGTGTCACCGCGGCCCTCATCTACTTTGCTATCTCCATCACGGCCATCGCCAAGTACTCGGATGGGGCTTCCAAAGCCGCTGGGGTGTTTGGCTTCTTTGCTACC
ATCGTGTTTGCAACTGATTTCTACCTGATCTTTAACGACGTGGCCAAATTCCTCAAACAAGGGGACTCTGCAGATGAGACCACAGCCCACAAGACAGAAGAAGAG
AATTCCGACTCGGACTCTGACTGA
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ATGTGGCCCCCAGACCCCGACCCCGACCCGGACCCCGAGCCTGCCGGCGGCTCCCGTCCCGGCCCCGCGGTCCCCGGGCTCCGCGCCCTGCTGCCGGCGCGGGCT
TTCCTCTGCTCTCTCAAAGGCCGCCTCCTGCTGGCCGAGTCGGGTCTCTCATTCATCACTTTTATCTGCTATGTGGCGTCCTCAGCATCTGCCTTCCTCACAGCG
CCTCTGCTGGAGTTCCTGCTGGCCTTGTACTTCCTCTTTGCTGATGCCATGCAGCTGAATGACAAGTGGCAGGGCTTGTGCTGGCCCATGATGGACTTCCTGCGC
TGTGTCACCGCGGCCCTCATCTACTTTGCTATCTCCATCACGGCCATCGCCAAGTACTCGGATGGGGCTTCCAAAGCCGCTGGGGTGTTTGGCTTCTTTGCTACC
ATCGTGTTTGCAACTGATTTCTACCTGATCTTTAACGACGTGGCCAAATTCCTCAAACAAGGGGACTCTGCAGATGAGACCACAGCCCACAAGACAGAAGAAGAG
AATTCCGACTCGGACTCTGACTGA
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>CMTM3|123920|protein
MWPPDPDPDPDPEPAGGSRPGPAVPGLRALLPARAFLCSLKGRLLLAESGLSFITFICYVASSASAFLTAPLLEFLLALYFLFADAMQLNDKWQGLCWPMMDFLR
CVTAALIYFAISITAIAKYSDGASKAAGVFGFFATIVFATDFYLIFNDVAKFLKQGDSADETTAHKTEEENSDSDSD
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MWPPDPDPDPDPEPAGGSRPGPAVPGLRALLPARAFLCSLKGRLLLAESGLSFITFICYVASSASAFLTAPLLEFLLALYFLFADAMQLNDKWQGLCWPMMDFLR
CVTAALIYFAISITAIAKYSDGASKAAGVFGFFATIVFATDFYLIFNDVAKFLKQGDSADETTAHKTEEENSDSDSD
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Evidence summary Top
Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
---|---|---|---|---|---|---|---|---|---|---|---|
Score (No. of Studies) | No | 0 (0) | 1 (2) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 3 (3) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Wassink, 2001 | USA | Chromosomal analysis of G-band | autism | - | - | - | - | 278 | - | 278 | ||
Pinto, 2010 | - | SNP microarray, qPCR | ASD | - | - | - | - | 996 | 1287 | 2283 |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 1
Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Ghahramani Seno, 2010_1 | Unknown | lymphoblastoid cell-line | 20 (35.00%) | - | AD | 22 (13.64%) |
-1.23 | Down | 0.154 | |||
|
Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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