Evidence Details for CHGB
Basic Information Top
| Gene Symbol: | CHGB ( SCG1 ) |
|---|---|
| Gene Full Name: | chromogranin B (secretogranin 1) |
| Band: | 20p12.3 |
| Quick Links | Entrez ID:1114; OMIM: 118920; Uniprot ID:SCG1_HUMAN; ENSEMBL ID: ENSG00000089199; HGNC ID: 1930 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>CHGB|1114|nucleotide
ATGCAGCCAACGCTGCTTCTCAGCCTCCTGGGAGCCGTGGGGCTGGCGGCTGTCAATTCCATGCCAGTGGATAACAGGAACCACAATGAAGGAATGGTGACTCGC
TGCATCATTGAGGTCCTCTCAAATGCCTTGTCGAAGTCCAGCGCTCCACCCATCACCCCTGAGTGCCGCCAAGTCCTGAAGACGAGTAGAAAAGACGTCAAAGAC
AAAGAGACAACTGAAAATGAAAACACAAAGTTTGAAGTAAGATTGTTAAGAGACCCAGCTGATGCCTCGGAAGCCCACGAGTCCTCCAGCAGGGGAGAGGCAGGA
GCCCCAGGGGAGGAGGACATCCAAGGCCCAACAAAGGCAGACACAGAGAAATGGGCAGAGGGAGGCGGGCACAGCCGAGAGCGAGCGGATGAGCCCCAGTGGAGC
CTCTATCCCTCCGACAGCCAAGTCTCTGAAGAAGTGAAGACACGCCATTCTGAGAAGAGCCAGAGAGAGGATGAGGAGGAGGAGGAGGGAGAGAACTATCAAAAA
GGGGAGCGAGGGGAAGATAGCAGTGAAGAGAAACACCTTGAAGAGCCAGGAGAGACACAAAACGCTTTTCTCAATGAAAGAAAGCAGGCTTCAGCTATAAAAAAA
GAGGAGTTAGTGGCCAGATCGGAAACACATGCTGCCGGGCATTCTCAGGAGAAGACACATAGCCGAGAGAAGAGTAGCCAGGAGAGTGGAGAGGAGACAGGGAGC
CAGGAGAATCACCCCCAGGAGTCTAAAGGCCAACCCCGAAGCCAGGAAGAATCTGAGGAAGGTGAGGAAGATGCCACCTCTGAGGTGGACAAACGACGCACGAGG
CCCAGACACCACCACGGGAGGAGCAGGCCCGACAGGTCCTCTCAAGGAGGGAGTCTTCCCTCTGAGGAAAAGGGACACCCCCAGGAGGAATCTGAGGAGTCAAAC
GTCAGCATGGCCAGTTTAGGGGAAAAGAGGGACCACCATTCAACCCACTACAGGGCTTCAGAGGAAGAACCTGAATATGGAGAAGAAATAAAGGGTTATCCAGGC
GTCCAGGCCCCTGAGGACCTGGAGTGGGAGCGCTATAGGGGCAGAGGAAGTGAAGAATACAGGGCTCCAAGACCTCAGAGTGAGGAGAGTTGGGATGAGGAGGAC
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ATGCAGCCAACGCTGCTTCTCAGCCTCCTGGGAGCCGTGGGGCTGGCGGCTGTCAATTCCATGCCAGTGGATAACAGGAACCACAATGAAGGAATGGTGACTCGC
TGCATCATTGAGGTCCTCTCAAATGCCTTGTCGAAGTCCAGCGCTCCACCCATCACCCCTGAGTGCCGCCAAGTCCTGAAGACGAGTAGAAAAGACGTCAAAGAC
AAAGAGACAACTGAAAATGAAAACACAAAGTTTGAAGTAAGATTGTTAAGAGACCCAGCTGATGCCTCGGAAGCCCACGAGTCCTCCAGCAGGGGAGAGGCAGGA
GCCCCAGGGGAGGAGGACATCCAAGGCCCAACAAAGGCAGACACAGAGAAATGGGCAGAGGGAGGCGGGCACAGCCGAGAGCGAGCGGATGAGCCCCAGTGGAGC
CTCTATCCCTCCGACAGCCAAGTCTCTGAAGAAGTGAAGACACGCCATTCTGAGAAGAGCCAGAGAGAGGATGAGGAGGAGGAGGAGGGAGAGAACTATCAAAAA
GGGGAGCGAGGGGAAGATAGCAGTGAAGAGAAACACCTTGAAGAGCCAGGAGAGACACAAAACGCTTTTCTCAATGAAAGAAAGCAGGCTTCAGCTATAAAAAAA
GAGGAGTTAGTGGCCAGATCGGAAACACATGCTGCCGGGCATTCTCAGGAGAAGACACATAGCCGAGAGAAGAGTAGCCAGGAGAGTGGAGAGGAGACAGGGAGC
CAGGAGAATCACCCCCAGGAGTCTAAAGGCCAACCCCGAAGCCAGGAAGAATCTGAGGAAGGTGAGGAAGATGCCACCTCTGAGGTGGACAAACGACGCACGAGG
CCCAGACACCACCACGGGAGGAGCAGGCCCGACAGGTCCTCTCAAGGAGGGAGTCTTCCCTCTGAGGAAAAGGGACACCCCCAGGAGGAATCTGAGGAGTCAAAC
GTCAGCATGGCCAGTTTAGGGGAAAAGAGGGACCACCATTCAACCCACTACAGGGCTTCAGAGGAAGAACCTGAATATGGAGAAGAAATAAAGGGTTATCCAGGC
GTCCAGGCCCCTGAGGACCTGGAGTGGGAGCGCTATAGGGGCAGAGGAAGTGAAGAATACAGGGCTCCAAGACCTCAGAGTGAGGAGAGTTGGGATGAGGAGGAC
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>CHGB|1114|protein
MQPTLLLSLLGAVGLAAVNSMPVDNRNHNEGMVTRCIIEVLSNALSKSSAPPITPECRQVLKTSRKDVKDKETTENENTKFEVRLLRDPADASEAHESSSRGEAG
APGEEDIQGPTKADTEKWAEGGGHSRERADEPQWSLYPSDSQVSEEVKTRHSEKSQREDEEEEEGENYQKGERGEDSSEEKHLEEPGETQNAFLNERKQASAIKK
EELVARSETHAAGHSQEKTHSREKSSQESGEETGSQENHPQESKGQPRSQEESEEGEEDATSEVDKRRTRPRHHHGRSRPDRSSQGGSLPSEEKGHPQEESEESN
VSMASLGEKRDHHSTHYRASEEEPEYGEEIKGYPGVQAPEDLEWERYRGRGSEEYRAPRPQSEESWDEEDKRNYPSLELDKMAHGYGEESEEERGLEPGKGRHHR
GRGGEPRAYFMSDTREEKRFLGEGHHRVQENQMDKARRHPQGAWKELDRNYLNYGEEGAPGKWQQQGDLQDTKENREEARFQDKQYSSHHTAEKRKRLGELFNPY
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MQPTLLLSLLGAVGLAAVNSMPVDNRNHNEGMVTRCIIEVLSNALSKSSAPPITPECRQVLKTSRKDVKDKETTENENTKFEVRLLRDPADASEAHESSSRGEAG
APGEEDIQGPTKADTEKWAEGGGHSRERADEPQWSLYPSDSQVSEEVKTRHSEKSQREDEEEEEGENYQKGERGEDSSEEKHLEEPGETQNAFLNERKQASAIKK
EELVARSETHAAGHSQEKTHSREKSSQESGEETGSQENHPQESKGQPRSQEESEEGEEDATSEVDKRRTRPRHHHGRSRPDRSSQGGSLPSEEKGHPQEESEESN
VSMASLGEKRDHHSTHYRASEEEPEYGEEIKGYPGVQAPEDLEWERYRGRGSEEYRAPRPQSEESWDEEDKRNYPSLELDKMAHGYGEESEEERGLEPGKGRHHR
GRGGEPRAYFMSDTREEKRFLGEGHHRVQENQMDKARRHPQGAWKELDRNYLNYGEEGAPGKWQQQGDLQDTKENREEARFQDKQYSSHHTAEKRKRLGELFNPY
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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) | 0 (0) | 0 (0) | 0 (0) | 2 (2) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 3 (3) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top

