1. Gene
  2. NEXMIF - neurite extension and migration factor Gene

NEXMIF - neurite extension and migration factor Gene

Homo sapiens

Also known as XPN; MRX98; KIDLIA; XLID98; KIAA2022

Gene ID: 340533 | Gene type: protein coding

About NEXMIF

Cytogenetic location: Xq13.3 Genomic coordinates (GRCh38): X:74,732,856-74,925,452 (from NCBI)

This gene has 3 transcripts (splice variants), 217 orthologues, 3 paralogues and is associated with 5 phenotypes. Biased expression in brain (RPKM 2.3), adrenal (RPKM 0.6) and 12 other tissues.

Summary

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]

NEXMIF Products(1)

mRNA Protein Name
NM_001008537.3 NP_001008537.1 neurite extension and migration factor
Protein Preferred Names Protein Names

neurite extension and migration factor

XLMR protein related to neurite extension

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, X-Linked 98

X-Linked Intellectual Disability, Cantagrel Type

XLID98

Mental Retardation, X-Linked 98

Mrx98

Mental Retardation, X-Linked, Type 98

Continuous Spike-Wave During Slow Sleep Syndrome

Csws

Cswss Syndrome

Continuous Spikes And Waves During Sleep

Continuous Spikes And Waves During Slow-Wave Sleep

Epileptic Encephalopathy With Continuous Spike-And-Wave During Slow Sleep

Continuous Spike And Waves During Slow Sleep

Continuous Spike And Waves During Slow-Wave Sleep Syndrome

Epilepsy, Focal, With Speech Disorder And With Or Without Impaired Intellectual Development

Continuous Spike And Waves During Slow-Wave Sleep Syndrome

FESD

Epilepsy, Focal, With Speech Disorder And With Or Without Mental Retardation

Aphasia, Acquired, With Epilepsy

Landau-Kleffner Syndrome

Acquired Aphasia With Epilepsy

Adresd

Bects

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Csws

Cswss

Lks

Resdad

Epilepsy, Focal, With Speech Disorder With/Without Mental Retardation

Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant

Benign Rolandic Epilepsy

Aphasia

Epilepsy With Myoclonic-Atonic Seizures

Myoclonic Astatic Epilepsy

Doose Syndrome

Epilepsy With Myoclonic-Astatic Seizures

Epilepsy With Myoclono-Astatic Crisis

Myoclonic-Astatic Epilepsy

Emas

Mae

Myoclonic Atonic Epilepsy

Myoclonic-Astatic Epilepsy In Early Childhood

Non-Syndromic X-Linked Intellectual Disability

X-Linked Non-Syndromic Intellectual Disability

Non-Specific X-Linked Mental Retardation

X-Linked Non-Specific Intellectual Disability

Non-Syndromic X-Linked Intellectual Disability 98

Mrx98

X-Linked Mental Retardation 98

Non-Syndromic X-Linked Intellectual Disability 91

Mrx91

Xia-Gibbs Syndrome

Ahdc1-Related Intellectual Disability-Obstructive Sleep Apnea-Mild Dysmorphism Syndrome

XIGIS

Mrd25

Ahdc1-Related Intellectual Disability - Obstructive Sleep Apnea - Mild Dysmorphism Syndrome

Mental Retardation, Autosomal Dominant 25, Formerly

Mrd25, Formerly

Autosomal Dominant Mental Retardation 25

Autosomal Dominant Intellectual Disability 25

Xgs

Non-Syndromic X-Linked Intellectual Disability 58

Mrx58

Developmental And Epileptic Encephalopathy 26

DEE26

Epileptic Encephalopathy, Early Infantile, 26

Eiee26

Early Infantile Epileptic Encephalopathy 26

Developmental And Epileptic Encephalopathy, 26

Encephalopathy, Epileptic, Early Infantile, Type 26

Tonne-Kalscheuer Syndrome

TOKAS

Mrx61

Intellectual Developmental Disorder With Or Without Hand And Foot Anomalies, Genital Anomalies, Or Congenital Diaphragmatic Hernia

Mental Retardation, X-Linked 61

X-Linked Mental Retardation 61

Epilepsy

Epilepsy Syndrome

Epileptic Syndrome

Epilepsies

Symptomatic Epilepsies

Post Traumatic Epilepsy

Traumatic Epilepsy

Traumatic Epileptic

Epilepsy Due To Hippocampal Sclerosis

Epilepsy With Ammon'S Horn Sclerosis

Epilepsy Due To Cortical Dysplasia

Epilepsy Due To Neuronal Migration Disorders

Cardiomyopathy, Dilated, 1hh

Dilated Cardiomyopathy 1hh

CMD1HH

Cardiomyopathy, Dilated 1hh

Cardiomyopathy, Dilated, Type 1hh

Borjeson-Forssman-Lehmann Syndrome

BFLS

Borj

Borjeson Syndrome

Mrxsbfl

Intellectual Deficiency-Epilepsy-Endocrine Disorders Syndrome

Intellectual Disability-Epilepsy-Endocrine Disorders Syndrome

Mental Retardation, X-Linked, Syndromic, Borjeson-Forssman-Lehmann Type

Mental Retardation, Epilepsy, And Endocrine Disorders

Mental Retardation, Epilepsy, And Endocrine Disorder

Syndromic X-Linked Mental Retardation Borjeson-Forssman-Lehmann Type

Mental Deficiency, Epilepsy And Endocrine Disorders

Boerjeson-Forssman-Lehmann Syndrome

Borjeson-Forssman Syndrome

Mental Deficiency-Epilepsy- Endocrine Disorders

Photosensitive Epilepsy

Pse

Photogenic Epilepsy

Photoparoxysmal Response

Reflex Epilepsy, Photosensitive

Photoparoxysmal Response 1

Partington Syndrome

X-Linked Reticulate Pigmentary Disorder

PRTS

Partington X-Linked Mental Retardation Syndrome

Mrxs1

Mrx36

Intellectual Developmental Disorder, X-Linked, Syndromic 1

Partington Disease

Pdr

Partington-Mulley Syndrome

Russell-Silver Syndrome, X-Linked

Mental Retardation, X-Linked, Syndromic 1

Mental Retardation, X-Linked, With Dystonic Movements, Ataxia, And Seizures

Mental Retardation, X-Linked 36

X-Linked Reticulate Pigmentary Disorder With Systemic Manifestations

X-Linked Russell-Silver Syndrome

Intelectual Disability-Dystonic Movements-Ataxia-Seizures Syndrome

Intellectual Disability, X-Linked, Syndromic 1

Intellectual Disability, X-Linked, With Dystonic Movements, Ataxia, And Seizures

Partington X-Linked Intellectual Disability Syndrome

X-Linked Intellectual Deficit-Dystonia-Dysarthria

X-Linked Mental Retardation With Dystonic Movements, Ataxia, And Seizures

Familial Cutaneous Amyloidosis

X-Linked Cutaneous Amyloidosis

Xlpdr

X-Linked Intellectual Disability-Dystonia-Dysarthria Syndrome

Pigmentary Disorder, Reticulate, With Systemic Manifestations

Gastroesophageal Reflux

Gastroesophageal Reflux Disease

Gerd

GER

Gastroesophageal Reflux, Pediatric

Acid Reflux

Gastresophageal Reflux

Gastro-Esophageal Reflux

Gerd - Gastro-Esophageal Reflux Disease

Autism Spectrum Disorder

Asd

Autism Spectrum Disorders

Autistic Continuum

Pervasive Developmental Disorder

Pervasive Development Disorder

Autistic Behavior

Autistic Disorder

Autistic

Autistic Disorder Of Childhood Onset

Infantile Autism

Childhood Autism

Kanner Syndrome

Pervasive Developmental Delay Nos

Pervasive Developmental Disorder, Not Otherwise Specified

Kbg Syndrome

KBGS

Macrodontia, Mental Retardation, Characteristic Facies, Short Stature, And Skeletal Anomalies

Short Stature, Characteristic Facies, Macrodontia, Intellectual Disability, And Skeletal Anomalies

Short Stature, Characteristic Facies, Macrodontia, Mental Retardation, And Skeletal Anomalies

Short Stature-Characteristic Facies-Mental Retardation-Macrodontia-Skeletal Anomalies Syndrome

Short Stature-Facial And Skeletal Anomalies-Intellectual Disability-Macrodontia Syndrome

Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Childhood Absence Epilepsy

Pyknolepsy

Petit Mal Epilepsy

Absence Seizures

Absence Seizure

Petit Mal Seizure

Absence Epilepsy, Childhood

Pykno-Epilepsy

Epilepsy, Absence

Absence Epilepsy

Pycnolepsy

Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly

Developmental And Epileptic Encephalopathy

Encephalopathy, Developmental And Epileptic

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus NEXMIF VGNC VGNC:63786
Canis familiaris NEXMIF VGNC VGNC:43759
Macaca mulatta NEXMIF VGNC VGNC:75274
Rattus norvegicus NEXMIF RGD RGD:1561931
Bos taurus NEXMIF VGNC VGNC:32024
Mus musculus NEXMIF MGD MGI:2148050