NUBP2
NUBP iron-sulfur cluster assembly factor 2, cytosolic
Summary
This gene encodes an adenosine triphosphate (ATP) and metal-binding protein that is required for the assembly of cyotosolic iron-sulfur proteins. The encoded protein functions in a heterotetramer with nucleotide-binding protein 1 (NUBP1). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2013]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2575352 | 16:1,835,393 | A/G | upstream gene variant | — |
| rs2548150336 | 16:1,836,616 | C/T | — | uncertain significance |
| rs145549922 | 16:1,836,619 | C/T | — | uncertain significance |
| rs138470873 | 16:1,836,839 | G/A | — | uncertain significance |
| rs1896998833 | 16:1,836,864 | T/G | — | uncertain significance |
| rs375596127 | 16:1,836,869 | C/T | — | uncertain significance |
| rs2548150681 | 16:1,836,872 | G/C | — | uncertain significance |
| rs150668442 | 16:1,836,883 | C/G | — | uncertain significance |
| rs1395127914 | 16:1,836,894 | C/G | — | uncertain significance |
| rs752514400 | 16:1,836,896 | G/C | — | uncertain significance |
| rs767143434 | 16:1,836,917 | C/T | — | uncertain significance |
| rs1232699640 | 16:1,836,923 | G/A | — | uncertain significance |
| rs543159832 | 16:1,836,929 | G/A | — | uncertain significance |
| rs1196912584 | 16:1,836,935 | T/C | — | uncertain significance |
| rs562994729 | 16:1,836,956 | G/A | — | uncertain significance |
| rs2235649 | 16:1,837,406 | C/G | — | — |
| rs149434317 | 16:1,837,683 | A/G | — | uncertain significance |
| rs1158172880 | 16:1,837,691 | G/C | — | uncertain significance |
| rs776999506 | 16:1,837,704 | G/A | — | uncertain significance |
| rs1031941940 | 16:1,837,741 | C/T | — | uncertain significance |
| rs1441796995 | 16:1,837,777 | T/C | — | uncertain significance |
| rs371544634 | 16:1,837,943 | C/T | — | uncertain significance |
| rs111886912 | 16:1,837,991 | C/T | — | benign |
| rs140058906 | 16:1,838,051 | C/T | — | uncertain significance |
| rs149804454 | 16:1,838,150 | C/T | — | benign |
| rs749090089 | 16:1,838,166 | G/A | — | uncertain significance |
| rs773854014 | 16:1,838,169 | G/A | — | uncertain significance |
| rs778420175 | 16:1,838,630 | A/G | — | likely benign |
| rs369792650 | 16:1,838,641 | G/A | — | uncertain significance |
| rs756912126 | 16:1,838,649 | C/T | — | likely benign |
| rs779333563 | 16:1,838,657 | C/G | — | uncertain significance |
| rs1408585932 | 16:1,838,699 | C/G | — | uncertain significance |
| rs1065656 | 16:1,838,836 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.