| Gene Symbol |
ALX4
|
| Entrez Gene |
60529
|
| Alt Symbol |
CRS5, FND2
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
ALX homeobox 4
|
| Other Description |
aristaless-like homeobox 4|homeobox protein aristaless-like 4|homeodomain transcription factor ALX4
|
| Swissprots |
Q9HAY9 Q9H198 Q9H161 Q96JN7
|
| Accessions |
AAK38835 CAC15120 EAW68066 Q9H161 AB058691 BAB47417 AF294629 AAG23961 AJ404888 CAC15060 AK092346 BC166622 AAI66622 XM_011520264 XP_011518566 XM_011520265 XP_011518567 XM_011520266 XP_011518568 NM_021926 NP_068745
|
| Function |
Transcription factor involved in skull and limb development. Plays an essential role in craniofacial development, skin and hair follicle development. {ECO:0000269|PubMed:19692347}.
|
| Subcellular Location |
Nucleus {ECO:0000255|PROSITE- ProRule:PRU00108, ECO:0000255|PROSITE-ProRule:PRU00138, ECO:0000269|PubMed:19692347}.
|
| Tissue Specificity |
Expression is likely to be restricted to bone. Found in parietal bone.
|