FGFR3
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FGFR3
Summary
FGFR3 is a gene[1]. FGFR3 ranks in the top 1% of gene entities by monthly Wikipedia readership (101 views/month).[2]
Key Facts
- FGFR3's instance of is recorded as gene[3].
- FGFR3 is a type of protein-coding gene[4].
- FGFR3's Commons category is recorded as Fibroblast growth factor receptor 3[5].
- FGFR3's HomoloGene ID is recorded as 55437[6].
- FGFR3's genomic start is recorded as 1795034[7].
- FGFR3's genomic start is recorded as 1793293[8].
- FGFR3's genomic end is recorded as 1808872[9].
- FGFR3's genomic end is recorded as 1810599[10].
- FGFR3's ortholog is recorded as Fgfr3[11].
- FGFR3's ortholog is recorded as Fgfr3[12].
- FGFR3's ortholog is recorded as htl[13].
- FGFR3's ortholog is recorded as egl-15[14].
- FGFR3's ortholog is recorded as fgfr3[15].
- FGFR3's encodes is recorded as fibroblast growth factor receptor 3[16].
- FGFR3's found in taxon is recorded as Homo sapiens[17].
- FGFR3's chromosome is recorded as human chromosome 4[18].
- FGFR3's genetic association is recorded as crouzonodermoskeletal syndrome[19].
- FGFR3's genetic association is recorded as thanatophoric dysplasia type 2[20].
- FGFR3's genetic association is recorded as bladder cancer[21].
- FGFR3's genetic association is recorded as camptodactyly-tall stature-scoliosis-hearing loss syndrome[22].
- FGFR3's genetic association is recorded as LADD syndrome[23].
- FGFR3's genetic association is recorded as Muenke syndrome[24].
- FGFR3's genetic association is recorded as seborrheic keratosis[25].
- FGFR3's genetic association is recorded as SADDAN[26].
- FGFR3's genetic association is recorded as thanatophoric dysplasia type 1[27].
Why It Matters
FGFR3 ranks in the top 1% of gene entities by monthly Wikipedia readership (101 views/month).[2] FGFR3 has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] FGFR3 is known by 6 alternative names across languages and contexts.[29]