Evidence Details for HLX
Basic Information Top
| Gene Symbol: | HLX ( HB24,HLX1 ) |
|---|---|
| Gene Full Name: | H2.0-like homeobox |
| Band: | 1q41 |
| Quick Links | Entrez ID:3142; OMIM: 142995; Uniprot ID:HLX_HUMAN; ENSEMBL ID: ENSG00000136630; HGNC ID: 4978 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>HLX|3142|nucleotide
ATGTTCGCAGCCGGGCTGGCTCCCTTCTACGCCTCCAACTTCAGCCTCTGGTCGGCCGCTTACTGCTCCTCGGCCGGCCCAGGCGGCTGCTCCTTCCCCTTGGAC
CCCGCCGCCGTCAAAAAGCCCTCCTTCTGCATCGCAGACATTCTGCACGCCGGCGTGGGGGATCTGGGGGCGGCCCCGGAGGGCCTGGCAGGGGCCTCGGCCGCC
GCCCTCACCGCGCACTTGGGCTCGGTTCACCCGCACGCCTCTTTCCAAGCGGCGGCCAGATCCCCGCTTCGACCCACCCCAGTGGTGGCGCCCTCCGAAGTCCCG
GCTGGCTTCCCGCAGCGGCTGTCTCCGCTCTCAGCCGCCTACCACCACCATCACCCGCAACAACAACAGCAGCAGCAACAGCCGCAGCAGCAACAGCCTCCGCCT
CCGCCCCGGGCTGGCGCCCTGCAGCCCCCGGCCTCGGGGACGCGAGTGGTTCCGAACCCCCACCACAGTGGCTCTGCCCCGGCCCCCTCCAGCAAAGACCTCAAA
TTTGGAATTGACCGCATTTTATCTGCAGAATTTGACCCAAAAGTCAAAGAAGGCAACACGCTGAGAGATCTCACTTCCCTGCTAACCGGTGGGCGGCCCGCCGGG
GTGCACCTCTCAGGCCTGCAGCCCTCGGCCGGCCAGTTCTTCGCATCTCTAGATCCCATTAACGAGGCTTCTGCAATCCTGAGTCCCTTAAACTCGAACCCAAGA
AATTCAGTTCAGCATCAGTTCCAAGACACGTTTCCAGGTCCCTATGCTGTGCTCACGAAGGACACCATGCCGCAGACGTACAAAAGGAAGCGTTCATGGTCGCGC
GCTGTGTTCTCCAACCTGCAGAGGAAAGGCCTGGAGAAAAGGTTTGAGATTCAGAAGTACGTGACCAAGCCGGACCGAAAGCAGCTGGCGGCGATGCTGGGCCTC
ACGGACGCACAGGTGAAGGTGTGGTTCCAGAACCGGCGGATGAAGTGGCGGCACTCCAAGGAGGCCCAGGCCCAAAAGGACAAGGACAAGGAGGCTGGCGAGAAG
CCATCAGGTGGAGCCCCGGCTGCGGATGGCGAGCAGGACGAGAGGAGCCCCAGCCGTTCTGAAGGCGAGGCTGAGAGCGAGAGCAGCGACTCCGAGTCCCTGGAC
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ATGTTCGCAGCCGGGCTGGCTCCCTTCTACGCCTCCAACTTCAGCCTCTGGTCGGCCGCTTACTGCTCCTCGGCCGGCCCAGGCGGCTGCTCCTTCCCCTTGGAC
CCCGCCGCCGTCAAAAAGCCCTCCTTCTGCATCGCAGACATTCTGCACGCCGGCGTGGGGGATCTGGGGGCGGCCCCGGAGGGCCTGGCAGGGGCCTCGGCCGCC
GCCCTCACCGCGCACTTGGGCTCGGTTCACCCGCACGCCTCTTTCCAAGCGGCGGCCAGATCCCCGCTTCGACCCACCCCAGTGGTGGCGCCCTCCGAAGTCCCG
GCTGGCTTCCCGCAGCGGCTGTCTCCGCTCTCAGCCGCCTACCACCACCATCACCCGCAACAACAACAGCAGCAGCAACAGCCGCAGCAGCAACAGCCTCCGCCT
CCGCCCCGGGCTGGCGCCCTGCAGCCCCCGGCCTCGGGGACGCGAGTGGTTCCGAACCCCCACCACAGTGGCTCTGCCCCGGCCCCCTCCAGCAAAGACCTCAAA
TTTGGAATTGACCGCATTTTATCTGCAGAATTTGACCCAAAAGTCAAAGAAGGCAACACGCTGAGAGATCTCACTTCCCTGCTAACCGGTGGGCGGCCCGCCGGG
GTGCACCTCTCAGGCCTGCAGCCCTCGGCCGGCCAGTTCTTCGCATCTCTAGATCCCATTAACGAGGCTTCTGCAATCCTGAGTCCCTTAAACTCGAACCCAAGA
AATTCAGTTCAGCATCAGTTCCAAGACACGTTTCCAGGTCCCTATGCTGTGCTCACGAAGGACACCATGCCGCAGACGTACAAAAGGAAGCGTTCATGGTCGCGC
GCTGTGTTCTCCAACCTGCAGAGGAAAGGCCTGGAGAAAAGGTTTGAGATTCAGAAGTACGTGACCAAGCCGGACCGAAAGCAGCTGGCGGCGATGCTGGGCCTC
ACGGACGCACAGGTGAAGGTGTGGTTCCAGAACCGGCGGATGAAGTGGCGGCACTCCAAGGAGGCCCAGGCCCAAAAGGACAAGGACAAGGAGGCTGGCGAGAAG
CCATCAGGTGGAGCCCCGGCTGCGGATGGCGAGCAGGACGAGAGGAGCCCCAGCCGTTCTGAAGGCGAGGCTGAGAGCGAGAGCAGCGACTCCGAGTCCCTGGAC
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>HLX|3142|protein
MFAAGLAPFYASNFSLWSAAYCSSAGPGGCSFPLDPAAVKKPSFCIADILHAGVGDLGAAPEGLAGASAAALTAHLGSVHPHASFQAAARSPLRPTPVVAPSEVP
AGFPQRLSPLSAAYHHHHPQQQQQQQQPQQQQPPPPPRAGALQPPASGTRVVPNPHHSGSAPAPSSKDLKFGIDRILSAEFDPKVKEGNTLRDLTSLLTGGRPAG
VHLSGLQPSAGQFFASLDPINEASAILSPLNSNPRNSVQHQFQDTFPGPYAVLTKDTMPQTYKRKRSWSRAVFSNLQRKGLEKRFEIQKYVTKPDRKQLAAMLGL
TDAQVKVWFQNRRMKWRHSKEAQAQKDKDKEAGEKPSGGAPAADGEQDERSPSRSEGEAESESSDSESLDMAPSDTERTEGSERSLHQTTVIKAPVTGALITASS
AGSGGSSGGGGNSFSFSSASSLSSSSTSAGCASSLGGGGASELLPATQPTASSAPKSPEPAQGALGCL
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MFAAGLAPFYASNFSLWSAAYCSSAGPGGCSFPLDPAAVKKPSFCIADILHAGVGDLGAAPEGLAGASAAALTAHLGSVHPHASFQAAARSPLRPTPVVAPSEVP
AGFPQRLSPLSAAYHHHHPQQQQQQQQPQQQQPPPPPRAGALQPPASGTRVVPNPHHSGSAPAPSSKDLKFGIDRILSAEFDPKVKEGNTLRDLTSLLTGGRPAG
VHLSGLQPSAGQFFASLDPINEASAILSPLNSNPRNSVQHQFQDTFPGPYAVLTKDTMPQTYKRKRSWSRAVFSNLQRKGLEKRFEIQKYVTKPDRKQLAAMLGL
TDAQVKVWFQNRRMKWRHSKEAQAQKDKDKEAGEKPSGGAPAADGEQDERSPSRSEGEAESESSDSESLDMAPSDTERTEGSERSLHQTTVIKAPVTGALITASS
AGSGGSSGGGGNSFSFSSASSLSSSSTSAGCASSLGGGGASELLPATQPTASSAPKSPEPAQGALGCL
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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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top

