Transcript #00017216 (NM_012293.1, PXDN gene)

Transcript name peroxidasin homolog (Drosophila)
Gene name PXDN (peroxidasin homolog (Drosophila))
Chromosome 2
Transcript - NCBI ID NM_012293.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_036425.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

127 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.3609‐1G>C r.spl p.?
+?/. - c.1A>G r.(?) p.(Met1?)
-?/. - c.19G>T r.(?) p.(Gly7Cys)
-?/. - c.19G>T r.(?) p.(Gly7Cys)
-?/. - c.165G>A r.(?) p.(Glu55=)
-/. - c.165G>A r.(?) p.(Glu55=)
-/. - c.272+18A>G r.(=) p.(=)
-?/. - c.273-17T>C r.(=) p.(=)
-?/. - c.273G>A r.(?) p.(Leu91=)
-?/. - c.455A>T r.(?) p.(Asp152Val)
-/. - c.459G>A r.(?) p.(Ser153=)
-?/. - c.488+8G>C r.(=) p.(=)
-/. - c.531A>G r.(?) p.(Thr177=)
?/. - c.631G>A r.(?) p.(Ala211Thr)
-?/. - c.646G>A r.(?) p.(Ala216Thr)
-?/. - c.648G>A r.(?) p.(Ala216=)
-?/. - c.648G>A r.(?) p.(Ala216=)
+?/. - c.693_697dup r.(?) p.(Val233Alafs*11)
?/. - c.773C>T r.(?) p.(Thr258Ile)
?/. - c.773C>T r.(?) p.(Thr258Ile)
-?/. - c.819C>T r.(?) p.(=)
+?/? 9 c.947A>C r.(?) p.(Gln316Pro)
-?/. - c.969C>T r.(?) p.(Ala323=)
-?/. - c.969C>T r.(?) p.(Ala323=)
+/. - c.1018+1G>A r.spl p.?
+?/. - c.1019-1G>T r.spl p.?
+?/? 10 c.1021C>T r.(?) p.(Arg341*)
+?/? 10 c.1021C>T r.(?) p.(Arg341*)
+?/? 10 c.1021C>T r.(?) p.(Arg341*)
-/. - c.1107C>T r.(?) p.(Pro369=)
-?/. - c.1121C>T r.(?) p.(Ser374Phe)
?/. - c.1127C>T r.(?) p.(Thr376Met)
?/. - c.1175C>T r.(?) p.(Thr392Met)
?/. - c.1175C>T r.(?) p.(Thr392Met)
-?/. - c.1176G>T r.(?) p.(Thr392=)
-?/. - c.1176G>T r.(?) p.(Thr392=)
?/. - c.1185C>T r.(?) p.(Gly395=)
+?/? 10 c.1192del r.(?) p.(Tyr398Thrfs*40)
-/. - c.1242G>A r.(?) p.(Ala414=)
-?/. - c.1495C>G r.(?) p.(Gln499Glu)
-?/. - c.1501G>A r.(?) p.(Glu501Lys)
?/. - c.1525G>A r.(?) p.(Gly509Ser)
+/. - c.1569_1570insT r.(?) p.(Thr524TyrfsTer53)
?/. - c.1603_1605del r.(?) p.(Thr535del)
?/. - c.1650C>T r.(?) p.(Gly550=)
-/. - c.1656C>T r.(?) p.(Pro552=)
?/. - c.1744A>G r.(?) p.(Asn582Asp)
?/. - c.1789C>T r.(?) p.(Arg597Trp)
-/. - c.1805C>T r.(?) p.(Ser602Leu)
-/. - c.1827C>T r.(?) p.(Leu609=)
-?/. - c.1857T>C r.(?) p.(Asn619=)
-?/. - c.1884C>T r.(?) p.(Ile628=)
-?/. - c.1896T>C r.(?) p.(Ile632=)
-?/. - c.2025G>A r.(?) p.(Ala675=)
-?/. - c.2097C>T r.(?) p.(Asn699=)
+/. 16 c.2098G>T r.(?) p.(Gly700Ter)
-?/. - c.2139C>T r.(?) p.(Tyr713=)
-/. - c.2151C>T r.(?) p.(Ile717=)
-?/. - c.2151C>T r.(?) p.(Ile717=)
?/. - c.2162C>T r.(?) p.(Ser721Leu)
-?/. - c.2178C>T r.(?) p.(=)
-?/. - c.2229G>A r.(?) p.(=)
-?/. - c.2235C>T r.(?) p.(Asp745=)
?/. 17 c.2276C>T r.(?) p.(Ser759Leu)
?/. - c.2276C>T r.(?) p.(Ser759Leu)
-?/. - c.2364C>T r.(?) p.(Asn788=)
+/. - c.2375_2397del r.(?) p.(Leu792Hisfs*67)
+?/? 17 c.2375_2397del r.(?) p.(Leu792Hisfs*67)
+?/? 17 c.2375_2397del r.(?) p.(Leu792Hisfs*67)
?/. - c.2410G>C r.(?) p.(Gly804Arg)
-?/. - c.2422G>A r.(?) p.(Val808Ile)
-?/. - c.2547C>T r.(?) p.(Asn849=)
?/. - c.2548G>A r.(?) p.(Val850Met)
+/. - c.2568del r.(?) p.(Cys857AlafsTer5)
+/. - c.2568dup r.(?) p.(Cys857LeufsTer10)
?/. - c.2620C>T r.(?) p.(Arg874Cys)
-/. - c.2640C>G r.(?) p.(Arg880=)
?/. - c.2741A>G r.(?) p.(Asn914Ser)
-?/. - c.2741A>G r.(?) p.(Asn914Ser)
-?/. - c.2748C>T r.(?) p.(Tyr916=)
?/. - c.2770C>T r.(?) p.(Arg924Cys)
?/. - c.2840C>T r.(?) p.(Pro947Leu)
-?/. - c.2919C>A r.(?) p.(Ala973=)
-?/. - c.3064G>A r.(?) p.(Val1022Met)
-?/. - c.3138G>A r.(?) p.(Thr1046=)
-/. - c.3165C>T r.(?) p.(Pro1055=)
-/. - c.3165C>T r.(?) p.(Pro1055=)
-?/. - c.3190G>A r.(?) p.(Ala1064Thr)
?/. - c.3190G>A r.(?) p.(Ala1064Thr)
-/. - c.3190G>A r.(?) p.(Ala1064Thr)
-?/. - c.3190G>A r.(?) p.(Ala1064Thr)
+/. - c.3206C>A r.(?) p.(Ala1069Asp)
?/. - c.3244T>C r.(?) p.(Tyr1082His)
-/. - c.3291C>A r.(?) p.(Pro1097=)
?/. - c.3342C>G r.(?) p.(Ile1114Met)
+?/. - c.3355_3356del r.(?) p.(Arg1119GlyfsTer72)
-/. - c.3420G>A r.(?) p.(Thr1140=)
?/. - c.3464C>A r.(?) p.(Ala1155Glu)
?/. - c.3464C>A r.(?) p.(Ala1155Glu)
-?/. - c.3483G>T r.(?) p.(Arg1161=)
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