Evidence Details for FAM181B
Basic Information Top
| Gene Symbol: | FAM181B ( MGC33846 ) |
|---|---|
| Gene Full Name: | family with sequence similarity 181, member B |
| Band: | 11q14.1 |
| Quick Links | Entrez ID:220382; OMIM: NA; Uniprot ID:F181B_HUMAN; ENSEMBL ID: ENSG00000182103; HGNC ID: 28512 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>FAM181B|220382|nucleotide
ATGGCGGTGCAGGCGGCGCTCCTCAGCACGCACCCTTTCGTGCCCTTCGGCTTCGGGGGCTCCCCGGACGGGCTAGGGGGCGCCTTCGGAGCCCTGGACAAGGGC
TGCTGTTTCGAGGACGATGAGACCGGGGCTCCGGCGGGTGCGCTGCTGTCGGGAGCCGAAGGAGGGGACGTGCGCGAGGCCACCCGCGATCTACTCAGCTTCATT
GACTCGGCGTCCAGCAACATCAAGCTGGCGCTGGACAAGCCGGGCAAGTCGAAGCGGAAGGTGAACCACCGCAAGTACCTGCAGAAGCAGATCAAGCGCTGCAGC
GGCCTCATGGGCGCCGCGCCCCCCGGCCCGCCCTCCCCGAGCGCCGCCGACACGCCAGCCAAACGGCCGCTGGCCGCCCCTAGCGCCCCGACAGTCGCGGCCCCG
GCCCACGGCAAGGCTGCCCCCCGGCGGGAGGCGTCGCAGGCCGCCGCGGCCGCCAGCTTGCAAAGCCGAAGTCTGGCCGCGCTCTTCGACTCGCTGCGCCACGTC
CCCGGGGGTGCCGAGCCGGCGGGGGGTGAGGTGGCTGCGCCGGCGGCCGGGCTAGGAGGTGCGGGCACTGGGGGCGCGGGAGGGGACGTGGCAGGCCCCGCGGGG
GCCACGGCGATCCCAGGGGCCAGGAAGGTCCCGCTGCGGGCACGCAATCTGCCTCCGTCCTTCTTCACGGAGCCGTCCCGGGCAGGCGGCGGCGGGTGTGGCCCG
TCGGGGCCGGACGTGAGCTTGGGCGACCTGGAGAAGGGCGCGGAGGCCGTGGAGTTCTTTGAGCTGCTGGGGCCCGACTACGGCGCCGGCACGGAGGCGGCAGTC
TTGCTTGCCGCCGAGCCTCTCGACGTGTTCCCCGCCGGAGCCTCCGTACTGCGGGGACCCCCGGAGCTGGAGCCCGGCCTCTTTGAGCCGCCGCCGGCAGTGGTG
GGAAACCTACTGTACCCCGAGCCCTGGAGCGTCCCGGGCTGCTCCCCGACCAAAAAGAGCCCCCTGACTGCCCCCCGCGGCGGCTTGACCTTGAACGAGCCCTTG
AGCCCCCTGTACCCCGCCGCTGCGGATTCTCCCGGCGGGGAGGACGGGCGGGGCCATTTGGCCTCTTTCGCCCCCTTCTTTCCAGACTGCGCCCTGCCCCCGCCG
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ATGGCGGTGCAGGCGGCGCTCCTCAGCACGCACCCTTTCGTGCCCTTCGGCTTCGGGGGCTCCCCGGACGGGCTAGGGGGCGCCTTCGGAGCCCTGGACAAGGGC
TGCTGTTTCGAGGACGATGAGACCGGGGCTCCGGCGGGTGCGCTGCTGTCGGGAGCCGAAGGAGGGGACGTGCGCGAGGCCACCCGCGATCTACTCAGCTTCATT
GACTCGGCGTCCAGCAACATCAAGCTGGCGCTGGACAAGCCGGGCAAGTCGAAGCGGAAGGTGAACCACCGCAAGTACCTGCAGAAGCAGATCAAGCGCTGCAGC
GGCCTCATGGGCGCCGCGCCCCCCGGCCCGCCCTCCCCGAGCGCCGCCGACACGCCAGCCAAACGGCCGCTGGCCGCCCCTAGCGCCCCGACAGTCGCGGCCCCG
GCCCACGGCAAGGCTGCCCCCCGGCGGGAGGCGTCGCAGGCCGCCGCGGCCGCCAGCTTGCAAAGCCGAAGTCTGGCCGCGCTCTTCGACTCGCTGCGCCACGTC
CCCGGGGGTGCCGAGCCGGCGGGGGGTGAGGTGGCTGCGCCGGCGGCCGGGCTAGGAGGTGCGGGCACTGGGGGCGCGGGAGGGGACGTGGCAGGCCCCGCGGGG
GCCACGGCGATCCCAGGGGCCAGGAAGGTCCCGCTGCGGGCACGCAATCTGCCTCCGTCCTTCTTCACGGAGCCGTCCCGGGCAGGCGGCGGCGGGTGTGGCCCG
TCGGGGCCGGACGTGAGCTTGGGCGACCTGGAGAAGGGCGCGGAGGCCGTGGAGTTCTTTGAGCTGCTGGGGCCCGACTACGGCGCCGGCACGGAGGCGGCAGTC
TTGCTTGCCGCCGAGCCTCTCGACGTGTTCCCCGCCGGAGCCTCCGTACTGCGGGGACCCCCGGAGCTGGAGCCCGGCCTCTTTGAGCCGCCGCCGGCAGTGGTG
GGAAACCTACTGTACCCCGAGCCCTGGAGCGTCCCGGGCTGCTCCCCGACCAAAAAGAGCCCCCTGACTGCCCCCCGCGGCGGCTTGACCTTGAACGAGCCCTTG
AGCCCCCTGTACCCCGCCGCTGCGGATTCTCCCGGCGGGGAGGACGGGCGGGGCCATTTGGCCTCTTTCGCCCCCTTCTTTCCAGACTGCGCCCTGCCCCCGCCG
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>FAM181B|220382|protein
MAVQAALLSTHPFVPFGFGGSPDGLGGAFGALDKGCCFEDDETGAPAGALLSGAEGGDVREATRDLLSFIDSASSNIKLALDKPGKSKRKVNHRKYLQKQIKRCS
GLMGAAPPGPPSPSAADTPAKRPLAAPSAPTVAAPAHGKAAPRREASQAAAAASLQSRSLAALFDSLRHVPGGAEPAGGEVAAPAAGLGGAGTGGAGGDVAGPAG
ATAIPGARKVPLRARNLPPSFFTEPSRAGGGGCGPSGPDVSLGDLEKGAEAVEFFELLGPDYGAGTEAAVLLAAEPLDVFPAGASVLRGPPELEPGLFEPPPAVV
GNLLYPEPWSVPGCSPTKKSPLTAPRGGLTLNEPLSPLYPAAADSPGGEDGRGHLASFAPFFPDCALPPPPPPHQVSYDYSAGYSRTAYSSLWRSDGVWEGAPGE
EGAHRD
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MAVQAALLSTHPFVPFGFGGSPDGLGGAFGALDKGCCFEDDETGAPAGALLSGAEGGDVREATRDLLSFIDSASSNIKLALDKPGKSKRKVNHRKYLQKQIKRCS
GLMGAAPPGPPSPSAADTPAKRPLAAPSAPTVAAPAHGKAAPRREASQAAAAASLQSRSLAALFDSLRHVPGGAEPAGGEVAAPAAGLGGAGTGGAGGDVAGPAG
ATAIPGARKVPLRARNLPPSFFTEPSRAGGGGCGPSGPDVSLGDLEKGAEAVEFFELLGPDYGAGTEAAVLLAAEPLDVFPAGASVLRGPPELEPGLFEPPPAVV
GNLLYPEPWSVPGCSPTKKSPLTAPRGGLTLNEPLSPLYPAAADSPGGEDGRGHLASFAPFFPDCALPPPPPPHQVSYDYSAGYSRTAYSSLWRSDGVWEGAPGE
EGAHRD
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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) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 1 (1) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top

