Gene Gene information from NCBI Gene database.
Entrez ID 8603
Gene name Family with sequence similarity 193 member A
Gene symbol FAM193A
Synonyms (NCBI Gene)
C4orf8RES4-22
Chromosome 4
Chromosome location 4p16.3
miRNA miRNA information provided by mirtarbase database.
117
miRTarBase ID miRNA Experiments Reference
MIRT030136 hsa-miR-26b-5p Microarray 19088304
MIRT720772 hsa-miR-6856-3p HITS-CLIP 19536157
MIRT720771 hsa-miR-29a-3p HITS-CLIP 19536157
MIRT720770 hsa-miR-29b-3p HITS-CLIP 19536157
MIRT720769 hsa-miR-29c-3p HITS-CLIP 19536157
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620037 16822 ENSG00000125386
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P78312
Protein name Protein FAM193A (Protein IT14)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15914 FAM193_C 1208 1264 FAM193 family C-terminal Family
Sequence
MKVRLLRQLSAAAKVKAPSGLQGPPQAHQFISLLLEEYGALCQAARSISTFLGTLENEHL
KKFQVTWELHNKHLFENLVFSEPLLQSNLPALVSQIRLGTTTHDTCSEDTYSTLLQRYQR
SEEELRRVAEEWLECQKRIDAYVDEQMTMKTKQRMLTEDWELFKQRRFIEEQLTNKKAVT
GENNFTDTMRHMLSSRLSMPDCPNCNYRRRCACDDCSLSHILTCGIMDPPVTDDIHIHQL
PLQVDPAPDYLAERSPPSVSSASSGSGSSSPITIQQHPRLILTDSGSAPTFCSDDEDVAP
LSAKFADIYPLSNYDDTEVVANMNGIHSELNGGGENMALKDESPQISSTSSSSSEADDEE
ADGESSGEPPGAPKEDGVLGSRSPRTEESKADSPPPSYPTQQAEQAPNTCECHVCKQEAS
GLTPSAMTAGALPPGHQFLSPEKPTHPALHLYPHIHGHVPLHTVPHLPRPLIHPTLYATP
PFTHSKALPPAPVQNHTNKHQVFNASLQDHIYPSCFGNTPEWNSSKFISLWGSEVMNDKN
WNPGTFLPDTISGSEILGPTLSETRPEALPPPSSNETPAVSDSKEKKNAAKKKCLYNFQD
AFMEANKVVMATSSATSSVSCTATTVQSSNSQFRVSSKRPPSVGDVFHGISKEDHRHSAP
AAPRNSPTGLAPLPALSPAALSPAALSPASTPHLANLAAPSFPKTATTTPGFVDTRKSFC
PAPLPPATDGSISAPPSVCSDPDCEGHRCENGVYDPQQDDGDESADEDSCSEHSSSTSTS
TNQKEGKYCDCCYCEFFGHGGPPAAPTSRNYAEMREKLRLRLTKRKEEQPKKMDQISERE
SVVDHRRVEDLLQFINSSETKPVSSTRAAKRARHKQRKLEEKARLEAEARAREHLHLQEE
QRRREEEEDEEEEEDRFKEEFQRLQELQKLRAVKKKKKERPSKDCPKLDMLTRNFQAATE
SVPNSGNIHNGSLEQTEEPETSSHSPSRHMNHSEPRPGLGADGDAADPVDTRDSKFLLPK
EVNGKQHEPLSFFFDIMQHHKEGNGKQKLRQTSKASSEPARRPTEPPKATEGQSKPRAQT
ESKAKVVDLMSITEQKREERKVNSNNNNKKQLNHIKDEKSNPTPMEPTSPGEHQQNSKLV
LAESPQPKGKNKKNKKKKGDRVNNSIDGVSLLLPSLGYNGAILAHCNLRLPGSSDCAASA
SQVVGITDDVFLPKDIDLDSVDMDETEREVEYFKRFCLDSARQTRQRLSINWSNFSLKKA
TFAA
H
Sequence length 1265
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
EBV-positive nodal T- and NK-cell lymphoma Likely benign rs534197687 RCV004560262
Malignant tumor of esophagus Benign rs79752154 RCV005907894
Uterine corpus endometrial carcinoma Benign rs79752154 RCV005907895
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Brain Ischemia Associate 11169226
Heredodegenerative Disorders Nervous System Associate 11169226
Huntington Disease Associate 11169226, 9734812
Neoplasms Associate 36897777, 38111983
Neurologic Manifestations Associate 11169226
Osteoporosis Associate 31747953