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WHCR (-)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7467
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.
WHCR
SynonymsGene synonyms aliases
PRDS
ChromosomeChromosome number
4
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16
SummarySummary of gene provided in NCBI Entrez Gene.
Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features (`Greek warrior helmet` appearance of the nose, high fo
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Axenfeld anomaly Rieger eye malformation sequence rs104893857, rs1560590094, rs104893858, rs1198152064, rs104893859, rs104893860, rs121909249, rs104893862, rs104893957, rs104893951, rs104893952, rs104893953, rs121909339, rs387906810, rs372857241, rs376405759, rs886039568, rs1057519489, rs1057519488, rs1057519487, rs1057519483, rs1057519484, rs1057519471, rs1057519472, rs1057519475, rs1057519478, rs1057519479, rs1057519480, rs1057519481, rs1057519482, rs760676014, rs1085307884, rs368260972, rs1554101000, rs1553922583, rs1554100963, rs1241813534, rs1554101058, rs1183655796, rs772800095, rs1581373890, rs1581373773, rs1728998905, rs1762521548, rs1762522833, rs2230096, rs1762525473, rs1762536800
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
Hemangioma Hemangioma rs119475040, rs121917766
Unknown
Disease name Disease term dbSNP ID References
Absence of septum pellucidum Absence of septum pellucidum
Congenital anomaly of eye Congenital ectopic pupil
Congenital clubfoot Congenital clubfoot
Congenital epicanthus Congenital Epicanthus

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