|Institutional Source||Beutler Lab|
|Gene Name||neuropilin 1|
|Synonyms||Neuropilin-1, NP-1, NPN-1, Npn1|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R1733 (G1)|
|Chromosomal Location||128358604-128503363 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||C to T at 128468493 bp|
|Amino Acid Change||Proline to Serine at position 477 (P477S)|
|Ref Sequence||ENSEMBL: ENSMUSP00000026917 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000026917]|
Mouse Neuropilin-1, extracellular domains 1-4 (a1a2b1b2) [X-RAY DIFFRACTION]
Complex of mouse Plexin A2 - Semaphorin 3A - Neuropilin-1 [X-RAY DIFFRACTION]
|Predicted Effect||probably benign
AA Change: P477S
PolyPhen 2 Score 0.022 (Sensitivity: 0.95; Specificity: 0.81)
AA Change: P477S
|Meta Mutation Damage Score||0.0762|
|Coding Region Coverage||
|Validation Efficiency||95% (95/100)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of two neuropilins, which contain specific protein domains which allow them to participate in several different types of signaling pathways that control cell migration. Neuropilins contain a large N-terminal extracellular domain, made up of complement-binding, coagulation factor V/VIII, and meprin domains. These proteins also contains a short membrane-spanning domain and a small cytoplasmic domain. Neuropilins bind many ligands and various types of co-receptors; they affect cell survival, migration, and attraction. Some of the ligands and co-receptors bound by neuropilins are vascular endothelial growth factor (VEGF) and semaphorin family members. Several alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2011]
PHENOTYPE: Homozygous null mice show embryonic death, impaired neuronal migration and axon guidance, and vascular defects including a disorganized yolk sac vascular plexus, and malformed brachial arch arteries and great vessels. Mice lacking the cytoplasmic domain show altered retinal arteriovenous patterning. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Nrp1||
(F):5'- GTGTCTCTGAGAAAATAACCTCAGCCC -3'
(R):5'- AGAAACGTCTTCCTAGTGAGCTAGTGG -3'
(F):5'- AAATAACCTCAGCCCATCTGTTTC -3'
(R):5'- GTCATGTCCCCAGACTGTG -3'