NEXMIF Chromosome X
Neurite extension and migration factor
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What This Gene Does
An inversion on the X chromosome which disrupts this gene and a G-protein coupled purinergic receptor gene located in the pseudoautosomal region of the X chromosome has been linked to X linked cognitive disability.[provided by RefSeq, Mar 2009]
Associated Conditions (11)
X-linked intellectual disability
Cantagrel type
NEXMIF-related disorder
Inborn genetic diseases
Thyroid cancer
nonmedullary
1
Intellectual disability
Neurodevelopmental disorder
Seizure
Continuous spike and waves during slow sleep
Key Variants
RS1022775047
Conflicting classifications of pathogenicity
Health Risk
RS1029069870
Conflicting classifications of pathogenicity
Health Risk
RS1159680987
Conflicting classifications of pathogenicity
Health Risk
RS1227333624
Conflicting classifications of pathogenicity
Health Risk
RS1256402686
Conflicting classifications of pathogenicity
X-linked intellectual disability, Cantagrel type, X-linked intellectual disability
Health Risk
RS1270039330
Conflicting classifications of pathogenicity
Health Risk
RS1281329703
Conflicting classifications of pathogenicity
X-linked intellectual disability, Cantagrel type, X-linked intellectual disability
Health Risk
RS1297277744
Conflicting classifications of pathogenicity
Health Risk
RS1305966854
Conflicting classifications of pathogenicity
Health Risk
RS1320278331
Conflicting classifications of pathogenicity
Health Risk
RS138632224
Conflicting classifications of pathogenicity
Health Risk
RS1388842555
Conflicting classifications of pathogenicity
Health Risk
All Variants (240)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1569335265 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS1569335485 | Health Risk | Pathogenic | — |
| RS1569335666 | Health Risk | Pathogenic | — |
| RS1569335738 | Health Risk | Pathogenic | Thyroid cancer, nonmedullary, 1 |
| RS1569335877 | Health Risk | Pathogenic | — |
| RS1569335893 | Health Risk | Pathogenic | — |
| RS1569336024 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS1602210960 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS1602211044 | Health Risk | Pathogenic | — |
| RS1602211123 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS1602211753 | Health Risk | Pathogenic | — |
| RS1602211981 | Health Risk | Pathogenic | — |
| RS1602212618 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS1602212778 | Health Risk | Pathogenic | — |
| RS2080098372 | Health Risk | Pathogenic | Inborn genetic diseases, Inborn genetic diseases |
| RS2080101130 | Health Risk | Pathogenic | — |
| RS2080101717 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080102486 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080102842 | Health Risk | Pathogenic | Seizure, Seizure |
| RS2080103357 | Health Risk | Pathogenic | — |
| RS2080104332 | Health Risk | Pathogenic | — |
| RS2080104580 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080104883 | Health Risk | Pathogenic | — |
| RS2080105463 | Health Risk | Pathogenic | Intellectual disability, Intellectual disability |
| RS2080105696 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080107446 | Health Risk | Pathogenic | — |
| RS2080109121 | Health Risk | Pathogenic | — |
| RS2080110445 | Health Risk | Pathogenic | — |
| RS2080111520 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080112467 | Health Risk | Pathogenic | — |
| RS2080112480 | Health Risk | Pathogenic | — |
| RS2080112579 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080113065 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080113099 | Health Risk | Pathogenic | Intellectual disability, Intellectual disability |
| RS2080113609 | Health Risk | Pathogenic | — |
| RS2080114203 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080114608 | Health Risk | Pathogenic | — |
| RS2080115006 | Health Risk | Pathogenic | Inborn genetic diseases, Inborn genetic diseases |
| RS2080115875 | Health Risk | Pathogenic | — |
| RS2080115999 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2080116341 | Health Risk | Pathogenic | — |
| RS2080116669 | Health Risk | Pathogenic | — |
| RS2080117063 | Health Risk | Pathogenic | — |
| RS2080117124 | Health Risk | Pathogenic | — |
| RS2080117161 | Health Risk | Pathogenic | — |
| RS2080117225 | Health Risk | Pathogenic | — |
| RS2080118279 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |
| RS2147439176 | Health Risk | Pathogenic | — |
| RS2147439257 | Health Risk | Pathogenic | — |
| RS2147439375 | Health Risk | Pathogenic | X-linked intellectual disability, Cantagrel type, X-linked intellectual disability |