|
341
|
|
|
Ninein |
SCKL7 |
Breast carcinoma, Camptodactyly of fingers, Central hypothyroidism, Clinodactyly, Developmental delay, Dwarfism, Mental retardation, Lumbar scoliosis, Lupus erythematosus, Lupus nephritis, Madelung deformity, Microcephalic primordial dwarfism, Microcephaly, Microtia, Obesity, Physiologic amenorrhea, Seckel syndromeView all (2 more) |
|
342
|
|
|
Nucleolar and spindle associated protein 1 |
ANKT, BM037, LNP, NUSAP, PRO0310p1, Q0310, SAPL |
|
|
343
|
|
|
5'-nucleotidase, cytosolic IIIA |
CNSHA8, NT5C3, P5'N-1, P5N-1, PN-I, POMP, PSN1, UMPH, UMPH1, cN-III, hUMP1, p36 |
|
|
344
|
|
|
Neuritin 1 |
NRN, dJ380B8.2 |
|
|
345
|
|
|
NME/NM23 family member 8 |
CILD6, DNAI8, HEL-S-99, NM23-H8, SPTRX2, TXNDC3, sptrx-2 |
Asthenozoospermia, Asthma, Breast cancer, Bronchiectasis, Ciliary dyskinesia, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Hearing loss, Hydrocephalus, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (3 more) |
|
346
|
|
|
Nucleolar pre-rRNA processing protein NIP7 |
CGI-37, HSPC031, KD93 |
|
|
347
|
|
|
NOP16 nucleolar protein |
HSPC111, HSPC185 |
|
|
348
|
|
|
NCK interacting protein with SH3 domain |
AF3P21, DIP, DIP1, ORF1, SPIN90, VIP54, WASLBP, WISH |
|
|
349
|
|
|
NBAS subunit of NRZ tethering complex |
ILFS2, NAG, SOPH |
Achromatopsia, Blood coagulation disorders, Brachycephaly, Brachydactyly, Congenital epicanthus, Cutis laxa, Developmental delay, Dwarfism, Gastric cancer, Hepatic encephalopathy, Hypoglycemia, Immunologic deficiency syndromes, Liver failure, Mental depression, Micromelia, Optic atrophy, Proptosis, Short stature, optic nerve atrophy, and pelger-huet anomaly, Short stature-optic atrophy-pelger-huet anomaly syndrome, Stomach neoplasmsView all (5 more) |
|
350
|
|
|
NOP58 ribonucleoprotein |
HSPC120, NOP5, NOP5/NOP58 |
|
