PDXDC1
pyridoxal dependent decarboxylase domain containing 1
Summary
Enables cadherin binding activity. Predicted to be involved in carboxylic acid metabolic process. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants109 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4985167 | 16:15,082,865 | C/G | coding sequence variant | — |
| rs56252725 | 16:15,089,676 | G/A | intron variant | — |
| rs28545123 | 16:15,091,601 | G/A | — | — |
| rs1390048037 | 16:15,095,673 | C/T | — | uncertain significance |
| rs11549900 | 16:15,098,047 | C/G | — | benign |
| rs768074533 | 16:15,098,051 | A/G | — | uncertain significance |
| rs545192333 | 16:15,098,067 | G/A | — | uncertain significance |
| rs770650652 | 16:15,098,112 | C/T | — | uncertain significance |
| rs2544037077 | 16:15,100,402 | G/T | — | uncertain significance |
| rs150502355 | 16:15,102,670 | C/A | — | conflicting classifications of pathogenicity |
| rs780031901 | 16:15,103,575 | T/C | — | uncertain significance |
| rs11645958 | 16:15,104,807 | C/T | — | — |
| rs11648118 | 16:15,108,287 | A/G | — | — |
| rs753481478 | 16:15,110,007 | C/T | — | uncertain significance |
| rs4262938 | 16:15,110,077 | C/T | — | benign |
| rs2544324130 | 16:15,111,181 | G/A | — | uncertain significance |
| rs142502352 | 16:15,111,231 | G/A | — | likely benign |
| rs142060473 | 16:15,111,245 | C/T | — | uncertain significance |
| rs2544326623 | 16:15,111,250 | A/G | — | uncertain significance |
| rs762163407 | 16:15,112,701 | T/C | — | uncertain significance |
| rs2544370062 | 16:15,112,772 | T/C | — | uncertain significance |
| rs4985127 | 16:15,116,156 | T/C | — | — |
| rs79303621 | 16:15,117,386 | C/T | upstream gene variant | — |
| rs4985126 | 16:15,118,254 | T/C | — | — |
| rs369278385 | 16:15,118,939 | G/T | — | — |
| rs8059755 | 16:15,119,607 | T/C | — | — |
| rs181648237 | 16:15,120,088 | C/G | intron variant | — |
| rs1409538615 | 16:15,120,525 | T/C | — | uncertain significance |
| rs772887191 | 16:15,122,738 | C/T | — | uncertain significance |
| rs143237387 | 16:15,122,745 | T/A | — | likely benign |
| rs745935811 | 16:15,122,808 | C/G | — | uncertain significance |
| rs2042934713 | 16:15,123,820 | C/G | — | uncertain significance |
| rs771343046 | 16:15,123,901 | A/G | — | uncertain significance |
| rs77927814 | 16:15,124,327 | T/G | — | — |
| rs77031093 | 16:15,125,627 | G/A | — | likely benign |
| rs1055965952 | 16:15,125,676 | T/C | — | uncertain significance |
| rs766601678 | 16:15,126,728 | G/A | — | uncertain significance |
| rs140715398 | 16:15,126,744 | G/A | — | benign |
| rs1181216209 | 16:15,127,137 | C/T | — | uncertain significance |
| rs2544704151 | 16:15,127,168 | A/G | — | uncertain significance |
| rs2544704549 | 16:15,127,177 | T/C | — | uncertain significance |
| rs761085473 | 16:15,127,190 | C/T | — | likely benign |
| rs776844796 | 16:15,127,192 | T/C | — | uncertain significance |
| rs1435091940 | 16:15,127,249 | A/G | — | uncertain significance |
| rs1157025185 | 16:15,127,251 | T/G | — | uncertain significance |
| rs573475420 | 16:15,127,252 | C/T | — | uncertain significance |
| rs559829048 | 16:15,127,470 | A/G | — | — |
| rs72789541 | 16:15,127,534 | T/A | downstream gene variant | — |
| rs117719642 | 16:15,128,153 | A/C | — | likely benign |
| rs369177312 | 16:15,128,170 | C/T | — | uncertain significance |
| rs750053796 | 16:15,128,230 | G/A | — | uncertain significance |
| rs756591425 | 16:15,128,346 | C/T | — | likely benign |
| rs35811052 | 16:15,128,416 | G/A | — | benign |
| rs747080202 | 16:15,129,302 | G/A | — | likely benign |
| rs371348587 | 16:15,129,375 | C/T | — | uncertain significance |
| rs149308392 | 16:15,129,393 | C/T | — | uncertain significance |
| rs4985155 | 16:15,129,459 | A/G | downstream gene variant | — |
| rs1459075056 | 16:15,129,892 | G/T | — | uncertain significance |
| rs148061029 | 16:15,129,927 | G/A | — | likely benign |
| rs3198697 | 16:15,129,940 | C/T | synonymous variant | benign |
| rs1166424170 | 16:15,129,965 | C/T | — | uncertain significance |
| rs7200543 | 16:15,129,970 | A/G | synonymous variant | benign |
| rs2544758575 | 16:15,129,986 | C/G | — | uncertain significance |
| rs772430292 | 16:15,130,058 | G/A | — | uncertain significance |
| rs769815987 | 16:15,130,080 | C/T | — | uncertain significance |
| rs2544761572 | 16:15,130,084 | C/A | — | uncertain significance |
| rs2544761762 | 16:15,130,091 | G/T | — | uncertain significance |
| rs767344829 | 16:15,130,092 | A/G | — | uncertain significance |
| rs757982126 | 16:15,130,108 | A/G | — | likely benign |
| rs146871979 | 16:15,130,116 | C/T | — | uncertain significance |
| rs1741 | 16:15,130,351 | G/T | — | — |
| rs6498540 | 16:15,130,594 | A/G | downstream gene variant | — |
| rs111652122 | 16:15,130,728 | G/C | — | — |
| rs4985154 | 16:15,131,642 | G/T | — | — |
| rs1136001 | 16:15,131,974 | G/T | missense variant | — |
| rs2740 | 16:15,132,108 | A/G | downstream gene variant | — |
| rs34614532 | 16:15,132,908 | T/C | downstream gene variant | — |
| rs14347 | 16:15,133,889 | T/G | synonymous variant | — |
| rs16966953 | 16:15,135,854 | A/G | regulatory region variant | — |
| rs4985152 | 16:15,136,619 | T/A | intron variant | — |
| rs4985150 | 16:15,136,685 | A/G | intron variant | — |
| rs62039480 | 16:15,137,450 | G/A | regulatory region variant | — |
| rs3803575 | 16:15,138,447 | T/A | — | — |
| rs12934815 | 16:15,139,017 | A/G | intron variant | — |
| rs12934835 | 16:15,139,051 | A/G | intron variant | — |
| rs4500751 | 16:15,140,211 | C/T | intron variant | — |
| rs6498541 | 16:15,140,657 | A/G | regulatory region variant | — |
| rs16966947 | 16:15,141,045 | T/A | — | — |
| rs4985123 | 16:15,142,768 | A/T | — | — |
| rs55727637 | 16:15,145,252 | C/T | intron variant | — |
| rs7405130 | 16:15,147,725 | T/C | intron variant | — |
| rs72774845 | 16:15,147,954 | A/G | — | — |
| rs11075253 | 16:15,148,646 | C/T | — | — |
| rs76702213 | 16:15,149,086 | T/A | — | — |
| rs12928099 | 16:15,150,505 | C/A | regulatory region variant | — |
| rs2280018 | 16:15,150,833 | A/T | — | — |
| rs113936710 | 16:15,170,828 | C/A | — | — |
| rs4122352 | 16:15,174,571 | G/A | intron variant | — |
| rs56378940 | 16:15,175,112 | C/T | intron variant | — |
| rs8060236 | 16:15,177,695 | T/A | intron variant | — |
Showing 100 of 109 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.