| Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
10108 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
- |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
MKRN3-AS1 |
SynonymsGene synonyms aliases
|
FNZ127, MKRN3-AS, MKRN3AS, NCRNA00009, ZNF127-AS, ZNF127AS |
ChromosomeChromosome number
|
15 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
15q11-q13 |
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|
| Interactions |
View interactions |
| Associated diseases
|
| Causal |
| Disease name |
Disease term |
dbSNP ID |
References |
| Acromicric dysplasia |
Acromicric Dysplasia |
rs387906622, rs387906623, rs387906624, rs1131692052, rs387906626, rs587776863, rs1064797059, rs363806, rs1060501041, rs1555400049 |
|
| Attention deficit hyperactivity disorder |
Attention deficit hyperactivity disorder |
rs120074176, rs786205019 |
|
| Cryptorchidism |
Cryptorchidism |
rs121912555, rs104894697, rs104894698, rs398122886 |
|
| Developmental delay |
Global developmental delay |
rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291, rs886041382, rs1057518991, rs1057518699, rs753254213, rs748294403, rs762552974, rs1135401795, rs1553121073, rs1553122926, rs1364690005, rs1554086554, rs1554210415, rs1554168326, rs1554776342, rs1553873247, rs1567860112, rs779009256, rs1557447255, rs1564568350, rs780011005, rs1597464953, rs1200336864, rs1569513017, rs1587459606, rs1570332505, rs748888652, rs1575155995, rs2087029320, rs1589669105, rs1601769604, rs1184981709, rs749201074 |
|
| Hyperinsulinism |
Hyperinsulinism |
rs387906407, rs151344623, rs121913156, rs137853245, rs80356655, rs104894010, rs104894012, rs104894014, rs104894015, rs137852676, rs587783169, rs72559716, rs541269678, rs151344624, rs797045209, rs761749884, rs797045624, rs863225280, rs139964066, rs1057516281, rs1057516317, rs576684889, rs201682634, rs1350717554, rs768951263, rs1260178539, rs200670692, rs72559734, rs1400535021, rs372307320, rs1554923999, rs751279984, rs1008906426, rs367850779, rs1382448285, rs1564977373, rs750586210, rs1599937180 |
|
| Hypogonadotropic hypogonadism |
Hypogonadotropic hypogonadism |
rs104894702, rs104893836, rs104893837, rs104893842, rs121909628, rs138249161, rs1601946139 |
|
| Isolated somatotropin deficiency |
Isolated somatotropin deficiency |
rs797044450, rs71640277, rs863223306, rs2144738731, rs863223307, rs2144739370, rs863223309, rs863223310, rs137853223, rs2144739380, rs2144739391 |
|
| Hypotonia |
Neonatal Hypotonia |
rs141138948, rs397517172, rs869312824, rs1583169151 |
|
| Scoliosis |
Scoliosis, unspecified |
rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085 |
|
|
| Unknown |
| Disease name |
Disease term |
dbSNP ID |
References |
| Acromicria |
Acromicria |
|
|
| Clinodactyly |
Clinodactyly of fingers, Clinodactyly |
|
|
| Dolichocephaly |
Long narrow head |
|
|
| Dwarfism |
Dwarfism |
|
|
| Hyperopia |
Hyperopia |
|
|
| Motor delay |
Clumsiness - motor delay |
|
|
| Penis agenesis |
Penis agenesis |
|
|
| Physiologic amenorrhea |
Primary physiologic amenorrhea |
|
|
| Prader-willi syndrome |
Prader-Willi Syndrome |
rs188762916, rs1555376130, rs35667483, rs74942536 |
|
| Royer syndrome |
Royer Syndrome |
|
|
| Sleep apnea |
Sleep Apnea Syndromes |
|
|
| Somatotropin deficiency |
Somatotropin deficiency |
|
|
| Specific learning disorder |
Specific learning disability |
rs1057519497 |
|
|
|
|
| © 2021, Biomedical Informatics Centre, NIRRH |
ICMR-National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400012
Tel: +91-22-24192104, Fax No: +91-22-24139412 |
