RGD Annotation Report for female-restricted syndromic X-linked intellectual disability 99Rat Genome Database

GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from OMIM Disease Annotation Pipeline
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:150520374 (Homo sapiens)
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X
Curation Notes: ClinVar Annotator: match by term: Intellectual disability, X-linked 99, syndromic, female-restricted
Original References(s): PMID:25741868 PMID:34008892

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred from experiment (EXP)
The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X
Curation Notes: CTD Direct Evidence: marker/mechanism

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens) & RGD:126740813\|RGD:127243999\|RGD:12849446\|RGD:13508640\|RGD:13704220\|RGD:13704891\|RGD:14395661\|RGD:150435263\|RGD:151348661\|RGD:151661333\|RGD:151662110\|RGD:151755841\|RGD:151755929\|RGD:152088446\|RGD:153345707\|RGD:155265477\|RGD:155267190\|RGD:155642756\|RGD:155994461\|RGD:243050128\|RGD:329846528\|RGD:329846530\|RGD:329846623\|RGD:34888553\|RGD:38598279\|RGD:401875554\|RGD:401901798\|RGD:401944401\|RGD:404999964 (Homo sapiens)
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X
Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED \| ClinVar Annotator: match by term: Intellectual disability, X-linked 99, syndromic, female-restricted \| ClinVar Annotator: match by term: USP9X-related condition
Original References(s): PMID:25741868

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens) & RGD:11633692\|RGD:13508886\|RGD:150546815\|RGD:151662395\|RGD:155644383\|RGD:401733179\|RGD:401857196\|RGD:401905509\|RGD:401931279\|RGD:40886365\|RGD:40886438 (Homo sapiens)
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X
Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED \| ClinVar Annotator: match by term: Intellectual disability, X-linked 99, syndromic, female-restricted

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens) & RGD:13527703\|RGD:14349855\|RGD:150446864\|RGD:150517486\|RGD:150534703\|RGD:15123474\|RGD:15143392\|RGD:15156009\|RGD:15177840\|RGD:152064187\|RGD:156362952\|RGD:156414988\|RGD:401926766\|RGD:405115245\|RGD:405150608 (Homo sapiens)
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X
Curation Notes: ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED \| ClinVar Annotator: match by term: Intellectual disability, X-linked 99, syndromic, female-restricted \| ClinVar Annotator: match by term: USP9X-related condition
Original References(s): PMID:25741868 PMID:28492532

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:12894581 (Homo sapiens)
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X
Curation Notes: ClinVar Annotator: match by term: USP9X-related condition
Original References(s): PMID:25741868 PMID:28492532 PMID:31443933

An association has been curated linking USP9X and female-restricted syndromic X-linked intellectual disability 99 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred by association of genotype and phenotype with RGD:11050421\|RGD:11050423\|RGD:11050424\|RGD:11050426\|RGD:11050427 (Homo sapiens) & RGD:11050421\|RGD:11050423\|RGD:11050424\|RGD:11050426\|RGD:11050427 (Homo sapiens) & RGD:11050421\|RGD:11050423\|RGD:11050424\|RGD:11050426\|RGD:11050427 (Homo sapiens) & RGD:11050421\|RGD:11050423\|RGD:11050424\|RGD:11050426\|RGD:11050427 (Homo sapiens) & RGD:11050421\|RGD:11050423\|RGD:11050424\|RGD:11050426\|RGD:11050427 (Homo sapiens)
1 RGD objects have been annotated to female-restricted syndromic X-linked intellectual disability 99 (DOID:0112025)
4 papers in RGD have been used to annotate USP9X
Curation Notes: ClinVar Annotator: match by term: Intellectual disability, X-linked 99, syndromic, female-restricted
Original References(s): PMID:26833328

Go Back to source page

Continue to Ontology report

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message

GENE - TERM ANNOTATION REPORT

8 Annotations Found.