BLVRB
biliverdin reductase B
Summary
Enables biliverdin reductase [NAD(P)+] activity; peptidyl-cysteine S-nitrosylase activity; and riboflavin reductase (NADPH) activity. Involved in heme catabolic process; megakaryocyte differentiation; and negative regulation of insulin receptor signaling pathway. Located in cytosol; nucleoplasm; and plasma membrane. Is active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants24 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747103556 | 19:40,953,858 | G/A | — | uncertain significance |
| rs2514852854 | 19:40,953,881 | T/C | — | uncertain significance |
| rs368720101 | 19:40,953,891 | T/C | — | uncertain significance |
| rs770238288 | 19:40,953,895 | C/A | — | uncertain significance |
| rs145609085 | 19:40,957,316 | G/C | — | likely benign |
| rs534754752 | 19:40,957,333 | C/T | — | uncertain significance |
| rs139843463 | 19:40,957,370 | G/A | — | uncertain significance |
| rs757578768 | 19:40,957,393 | A/G | — | uncertain significance |
| rs149698066 | 19:40,964,064 | G/A | missense variant | — |
| rs1050862630 | 19:40,964,077 | C/T | — | uncertain significance |
| rs145500296 | 19:40,964,121 | C/T | — | likely benign |
| rs200026690 | 19:40,964,122 | G/A | — | uncertain significance |
| rs201096602 | 19:40,964,125 | C/T | — | uncertain significance |
| rs1599689344 | 19:40,964,128 | C/T | — | uncertain significance |
| rs142505402 | 19:40,964,144 | C/G | — | benign |
| rs865805057 | 19:40,964,299 | C/T | — | uncertain significance |
| rs150228804 | 19:40,964,354 | C/T | — | uncertain significance |
| rs747352017 | 19:40,964,385 | G/A | — | likely benign |
| rs945697656 | 19:40,964,387 | G/C | — | uncertain significance |
| rs949506555 | 19:40,964,392 | G/A | — | uncertain significance |
| rs11547746 | 19:40,964,395 | C/T | — | likely benign |
| rs1038324392 | 19:40,964,440 | G/C | — | uncertain significance |
| rs148777635 | 19:40,971,531 | T/C | — | uncertain significance |
| rs763134254 | 19:40,971,568 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.