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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q76L83 |
| Protein name |
Putative Polycomb group protein ASXL2 (Additional sex combs-like protein 2) |
| Protein function |
Putative Polycomb group (PcG) protein. PcG proteins act by forming multiprotein complexes, which are required to maintain the transcriptionally repressive state of homeotic genes throughout development. PcG proteins are not required to initiate |
| PDB |
9ATN
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| Family and domains |
Pfam
| Accession |
ID |
Position in sequence |
Description |
Type |
| PF05066 |
HARE-HTH |
11 → 83 |
HB1, ASXL, restriction endonuclease HTH domain |
Family |
| PF13919 |
ASXH |
256 → 380 |
Asx homology domain |
Domain |
| PF13922 |
PHD_3 |
1373 → 1433 |
PHD domain of transcriptional enhancer, Asx |
Domain |
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| Sequence |
MREKGRRKKGRTWAEAAKTVLEKYPNTPMSHKEILQVIQREGLKEIRSGTSPLACLNAML HTNSRGEEGIFYKVPGRMGVYTLKKDVPDGVKELSEGSEESSDGQSDSQSSENSSSSSDG GSNKEGKKSRWKRKVSSSSPQSGCPSPTIPAGKVISPSQKHSKKALKQALKQQQQKKQQQ QCRPSISISSNQHLSLKTVKAASDSVPAKPATWEGKQSDGQTGSPQNSNSSFSSSVKVEN TLLGLGKKSFQRSERLHTRQMKRTKCADIDVETPDSILVNTNLRALINKHTFSVLPGDCQ QRLLLLLPEVDRQVGPDGLMKLNGSALNNEFFTSAAQGWKERLSEGEFTPEMQVRIRQEI EKEKKVEPWKEQFFESYYGQSSGLSLEDSKKLTASPSDPKVKKTPAEQPKSMPVSEASLI RIVPVVSQSECKEEALQMSSPGRKEECESQGEVQPNFSTSSEPLLSSALNTHELSSILPI KCPKDEDLLEQKPVTSAEQESEKNHLTTASNYNKSESQESLVTSPSKPKSPGVEKPIVKP TAGAGPQETNMKEPLATLVDQSPESLKRKSSLTQEEAPVSWEKRPRVTENRQHQQPFQVS PQPFLNRGDRIQVRKVPPLKIPVSRISPMPFHPSQVSPRARFPVSITSPNRTGARTLADI KAKAQLVKAQRAAAAAAAAAAAAASVGGTIPGPGPGGGQGPGEGGEGQTARGGSPGSDRV SETGKGPTLELAGTGSRGGTRELLPCGPETQPQSETKTTPSQAQPHSVSGAQLQQTPPVP PTPAVSGACTSVPSPAHIEKLDNEKLNPTRATATVASVSHPQGPSSCRQEKAPSPTGPAL ISGASPVHCAADGTVELKAGPSKNIPNPSASSKTDASVPVAVTPSPLTSLLTTATLEKLP VPQVSATTAPAGSAPPSSTLPAASSLKTPGTSLNMNGPTLRPTSSIPANNPLVTQLLQGK DVPMEQILPKPLTKVEMKTVPLTAKEERGMGALIATNTTENSTREEVNERQSHPATQQQL GKTLQSKQLPQVPRPLQLFSAKELRDSSIDTHQYHEGLSKATQDQILQTLIQRVRRQNLL SVVPPSQFNFAHSGFQLEDISTSQRFMLGFAGRRTSKPAMAGHYLLNISTYGRGSESFRR THSVNPEDRFCLSSPTEALKMGYTDCKNATGESSSSKEDDTDEESTGDEQESVTVKEEPQ VSQSAGKGDTSSGPHSRETLSTSDCLASKNVKAEIPLNEQTTLSKENYLFTRGQTFDEKT LARDLIQAAQKQMAHAVRGKAIRSSPELFSSTVLPLPADSPTHQPLLLPPLQTPKLYGSP TQIGPSYRGMINVSTSSDMDHNSAVPGSQVSSNVGDVMSFSVTVTTIPASQAMNPSSHGQ TIPVQAFSEENSIEGTPSKCYCRLKAMIMCKGCGAFCHDDCIGPSKLCVSCLVVR
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| Sequence length |
1435 |
| Interactions |
View interactions |
| Phenotype Name |
Clinical Significance |
dbSNP ID |
RCV Accession |
| Autism spectrum disorder |
Likely pathogenic |
rs1574390972 |
RCV003127412 |
| Shashi-Pena syndrome |
Pathogenic; Likely pathogenic |
rs1574390728, rs2149136105, rs2465315580, rs2465305772, rs886041065, rs886041066, rs886041067, rs886041068, rs886041069, rs886041070, rs2465315449, rs1574395471, rs1574395479 |
RCV002227946 RCV001823012 RCV002795915 RCV003140538 RCV000258822 RCV000258833 RCV000258843 RCV000258823 RCV000258835 RCV000258846 RCV004577266 RCV000825018 RCV000824972 |
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| Phenotype Name |
Clinical Significance |
dbSNP ID |
RCV Accession |
| Abnormal cerebellum morphology |
Uncertain significance |
rs2149146353 |
RCV001391292 |
| Acute myeloid leukemia |
Benign |
rs144145474 |
RCV005913250 |
| ASXL2-related disorder |
Conflicting classifications of pathogenicity; Likely benign; Benign; Uncertain significance |
rs572342520, rs376795439, rs371658847, rs200842793, rs768734738, rs758650452, rs368969988, rs200059955, rs2088015648, rs2465305255, rs2465467795, rs1237021764, rs2465314747, rs2465314149, rs371044436, rs1156706109, rs2465450582, rs1475770803, rs750562932, rs62130126, rs192716734, rs139975547, rs190136878, rs146506022, rs150279913, rs113503588, rs201808592, rs184535083, rs371375230, rs376517297, rs367997831, rs757588385, rs553046267 View all (18 more) |
RCV004743622 RCV003911129 RCV004744303 RCV003950952 RCV003963602 RCV003953889 RCV003916592 RCV003936463 RCV003399690 RCV003402475 RCV003402397 RCV003397314 RCV003394376 RCV003394393 RCV003966644 RCV003971854 RCV003931419 RCV003946999 RCV004741764 RCV003913304 RCV003926084 RCV003962858 RCV004726747 RCV003920660 RCV003910654 RCV003923097 RCV003932883 RCV003958094 RCV003977982 RCV003960449 RCV004726734 RCV003962958 RCV003972983 |
| Cholangiocarcinoma |
Benign |
rs144145474 |
RCV005913251 |
| Developmental disorder |
Uncertain significance |
rs1262911220 |
RCV003127413 |
| Intellectual disability |
Conflicting classifications of pathogenicity |
rs565110158 |
RCV005626592 |
| Malignant tumor of esophagus |
Benign |
rs142755541 |
RCV005928035 |
| Neurodevelopmental disorder |
Uncertain significance |
rs2465305443 |
RCV003389161 |
| See cases |
Conflicting classifications of pathogenicity |
rs1287433846 |
RCV002252722 |
| Severe hydrocephalus |
Uncertain significance |
rs2149146353 |
RCV001391292 |
| Vascular disorder |
Uncertain significance |
rs2465314149 |
RCV005626812 |
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| Disease Name |
Relationship Type |
References |
| Atherosclerosis |
Associate |
32945427 |
| Bainbridge Ropers syndrome |
Associate |
27693232 |
| Colorectal Neoplasms |
Associate |
32945427 |
| Developmental Disabilities |
Associate |
27693232, 37493007 |
| Diabetes Mellitus |
Associate |
32945427 |
| Esophageal Squamous Cell Carcinoma |
Associate |
32945427 |
| Growth Disorders |
Associate |
27693232 |
| Heart Diseases |
Associate |
37493007 |
| Hypertension |
Associate |
32945427 |
| Intellectual Disability |
Associate |
27693232 |
| Ischemic Stroke |
Associate |
32945427 |
| Leukemia Myeloid Acute |
Associate |
24973361, 30251205 |
| Megalencephaly |
Associate |
27693232 |
| Muscle Hypotonia |
Associate |
27693232, 37493007 |
| Myelodysplastic Syndromes |
Associate |
19388938, 22186017 |
| Myocardial Infarction |
Associate |
32945427 |
| Neoplasms |
Associate |
24121791, 24710217, 26416890, 28335073, 32945427 |
| Orofaciodigital syndrome Shashi type |
Associate |
33751773, 37493007 |
| Port Wine Stain |
Associate |
27693232, 37493007 |
| Precursor T Cell Lymphoblastic Leukemia Lymphoma |
Associate |
27470916 |
| Renal Insufficiency Chronic |
Associate |
32945427 |
| Respiratory Tract Infections |
Associate |
37493007 |
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