Evidence Details for ITIH3


Gene Symbol: | ITIH3 ( H3P ) |
---|---|
Gene Full Name: | inter-alpha (globulin) inhibitor H3 |
Band: | 3p21.1 |
Quick Links | Entrez ID:3699; OMIM: 146650; Uniprot ID:ITIH3_HUMAN; ENSEMBL ID: ENSG00000162267; HGNC ID: 6168 |
Relate to Another Database: | SFARIGene; denovo-db |


>ITIH3|3699|nucleotide
ATGGCATTTGCATGGTGGCCCTGTCTCATCTTGGCTCTGCTCTCCAGCTTGGCAGCCTCTGGCTTCCCGAGAAGCCCCTTTCGGCTGCTTGGGAAACGGAGCCTC
CCGGAAGGGGTGGCCAATGGCATCGAGGTCTACAGTACCAAAATCAACTCCAAGGTGACCTCCCGTTTTGCTCACAATGTTGTCACCATGAGAGCCGTCAACCGT
GCAGACACGGCCAAGGAGGTTTCCTTTGATGTGGAGCTGCCCAAGACGGCCTTCATCACCAACTTCACCTTGACCATCGACGGTGTTACCTACCCTGGGAATGTC
AAGGAGAAGGAAGTTGCCAAGAAGCAGTATGAAAAGGCTGTGTCCCAGGGCAAGACGGCCGGCTTGGTCAAGGCCTCTGGGAGGAAGTTGGAGAAGTTCACAGTC
TCGGTCAACGTGGCTGCAGGCAGCAAAGTCACCTTCGAGCTAACCTACGAGGAGCTGCTGAAGAGGCACAAGGGCAAGTACGAGATGTACCTCAAGGTCCAGCCT
AAGCAACTGGTCAAACACTTTGAGATCGAGGTAGACATCTTCGAGCCTCAGGGAATCAGCATGCTGGATGCTGAGGCCTCTTTCATCACCAACGACCTCCTGGGA
AGCGCCCTCACCAAGTCCTTCTCAGGGAAAAAGGGCCATGTGTCCTTCAAGCCCAGCTTAGACCAACAGCGTTCATGCCCAACCTGTACAGACTCCCTCCTCAAT
GGAGATTTCACTATCACCTATGACGTGAACAGAGAATCTCCTGGCAACGTGCAGATAGTCAATGGCTACTTCGTGCACTTCTTTGCACCTCAAGGCCTTCCAGTG
GTGCCTAAGAACGTGGCCTTTGTGATTGACATCAGCGGCTCCATGGCTGGTCGGAAATTAGAGCAGACAAAGGAGGCCCTTCTCAGAATCCTGGAAGATATGCAA
GAGGAAGACTATCTGAATTTCATCCTGTTCAGTGGAGATGTGTCCACATGGAAAGAGCACTTAGTCCAGGCCACGCCCGAGAACCTCCAGGAGGCCAGGACGTTT
GTGAAGAGCATGGAGGATAAAGGAATGACCAACATCAATGACGGGCTGCTGAGGGGCATCAGTATGCTGAACAAGGCCCGAGAGGAGCACAGAATCCCAGAGAGG
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ATGGCATTTGCATGGTGGCCCTGTCTCATCTTGGCTCTGCTCTCCAGCTTGGCAGCCTCTGGCTTCCCGAGAAGCCCCTTTCGGCTGCTTGGGAAACGGAGCCTC
CCGGAAGGGGTGGCCAATGGCATCGAGGTCTACAGTACCAAAATCAACTCCAAGGTGACCTCCCGTTTTGCTCACAATGTTGTCACCATGAGAGCCGTCAACCGT
GCAGACACGGCCAAGGAGGTTTCCTTTGATGTGGAGCTGCCCAAGACGGCCTTCATCACCAACTTCACCTTGACCATCGACGGTGTTACCTACCCTGGGAATGTC
AAGGAGAAGGAAGTTGCCAAGAAGCAGTATGAAAAGGCTGTGTCCCAGGGCAAGACGGCCGGCTTGGTCAAGGCCTCTGGGAGGAAGTTGGAGAAGTTCACAGTC
TCGGTCAACGTGGCTGCAGGCAGCAAAGTCACCTTCGAGCTAACCTACGAGGAGCTGCTGAAGAGGCACAAGGGCAAGTACGAGATGTACCTCAAGGTCCAGCCT
AAGCAACTGGTCAAACACTTTGAGATCGAGGTAGACATCTTCGAGCCTCAGGGAATCAGCATGCTGGATGCTGAGGCCTCTTTCATCACCAACGACCTCCTGGGA
AGCGCCCTCACCAAGTCCTTCTCAGGGAAAAAGGGCCATGTGTCCTTCAAGCCCAGCTTAGACCAACAGCGTTCATGCCCAACCTGTACAGACTCCCTCCTCAAT
GGAGATTTCACTATCACCTATGACGTGAACAGAGAATCTCCTGGCAACGTGCAGATAGTCAATGGCTACTTCGTGCACTTCTTTGCACCTCAAGGCCTTCCAGTG
GTGCCTAAGAACGTGGCCTTTGTGATTGACATCAGCGGCTCCATGGCTGGTCGGAAATTAGAGCAGACAAAGGAGGCCCTTCTCAGAATCCTGGAAGATATGCAA
GAGGAAGACTATCTGAATTTCATCCTGTTCAGTGGAGATGTGTCCACATGGAAAGAGCACTTAGTCCAGGCCACGCCCGAGAACCTCCAGGAGGCCAGGACGTTT
GTGAAGAGCATGGAGGATAAAGGAATGACCAACATCAATGACGGGCTGCTGAGGGGCATCAGTATGCTGAACAAGGCCCGAGAGGAGCACAGAATCCCAGAGAGG
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>ITIH3|3699|protein
MAFAWWPCLILALLSSLAASGFPRSPFRLLGKRSLPEGVANGIEVYSTKINSKVTSRFAHNVVTMRAVNRADTAKEVSFDVELPKTAFITNFTLTIDGVTYPGNV
KEKEVAKKQYEKAVSQGKTAGLVKASGRKLEKFTVSVNVAAGSKVTFELTYEELLKRHKGKYEMYLKVQPKQLVKHFEIEVDIFEPQGISMLDAEASFITNDLLG
SALTKSFSGKKGHVSFKPSLDQQRSCPTCTDSLLNGDFTITYDVNRESPGNVQIVNGYFVHFFAPQGLPVVPKNVAFVIDISGSMAGRKLEQTKEALLRILEDMQ
EEDYLNFILFSGDVSTWKEHLVQATPENLQEARTFVKSMEDKGMTNINDGLLRGISMLNKAREEHRIPERSTSIVIMLTDGDANVGESRPEKIQENVRNAIGGKF
PLYNLGFGNNLNYNFLENMALENHGFARRIYEDSDADLQLQGFYEEVANPLLTGVEMEYPENAILDLTQNTYQHFYDGSEIVVAGRLVDEDMNSFKADVKGHGAT
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MAFAWWPCLILALLSSLAASGFPRSPFRLLGKRSLPEGVANGIEVYSTKINSKVTSRFAHNVVTMRAVNRADTAKEVSFDVELPKTAFITNFTLTIDGVTYPGNV
KEKEVAKKQYEKAVSQGKTAGLVKASGRKLEKFTVSVNVAAGSKVTFELTYEELLKRHKGKYEMYLKVQPKQLVKHFEIEVDIFEPQGISMLDAEASFITNDLLG
SALTKSFSGKKGHVSFKPSLDQQRSCPTCTDSLLNGDFTITYDVNRESPGNVQIVNGYFVHFFAPQGLPVVPKNVAFVIDISGSMAGRKLEQTKEALLRILEDMQ
EEDYLNFILFSGDVSTWKEHLVQATPENLQEARTFVKSMEDKGMTNINDGLLRGISMLNKAREEHRIPERSTSIVIMLTDGDANVGESRPEKIQENVRNAIGGKF
PLYNLGFGNNLNYNFLENMALENHGFARRIYEDSDADLQLQGFYEEVANPLLTGVEMEYPENAILDLTQNTYQHFYDGSEIVVAGRLVDEDMNSFKADVKGHGAT
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | (0) |














Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |






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