Abstract is: DNA repair protein XRCC2 is a protein that in humans is encoded by the XRCC2 gene.
P594 | Ensembl gene ID | ENSG00000196584 |
P704 | Ensembl transcript ID | ENST00000359321 |
ENST00000495707 | ||
P351 | Entrez Gene ID | 7516 |
P2888 | exact match | http://identifiers.org/ncbigene/7516 |
P646 | Freebase ID | /m/03gxll2 |
P353 | HGNC gene symbol | XRCC2 |
P354 | HGNC ID | 12829 |
P593 | HomoloGene ID | 3964 |
P6366 | Microsoft Academic ID | 2780301538 |
P492 | OMIM ID | 600375 |
600375 | ||
P639 | RefSeq RNA ID | NM_005431 |
P2892 | UMLS CUI | C1337031 |
P1057 | chromosome | human chromosome 7 | Q657319 |
P4196 | cytogenetic location | 7q36.1 | |
P688 | encodes | X-ray repair cross complementing 2 | Q21124977 |
P5572 | expressed in | pylorus | Q290248 |
ventral tegmental area | Q640562 | ||
tendon of biceps brachii | Q66527398 | ||
buccal mucosa cell | Q116529247 | ||
sperm | Q17145 | ||
cardia | Q1542842 | ||
subthalamic nucleus | Q2270424 | ||
inferior ganglion of vagus nerve | Q6029330 | ||
external globus pallidus | Q6495612 | ||
pars reticulata | Q7139918 | ||
P703 | found in taxon | Homo sapiens | Q15978631 |
P2293 | genetic association | Fanconi anemia complementation group U | Q32146921 |
P645 | genomic end | 152373250 | |
152676141 | |||
P644 | genomic start | 152341864 | |
152644776 | |||
P684 | ortholog | xrcc2 | Q29747400 |
Xrcc2 | Q18258754 | ||
Xrcc2 | Q24414587 | ||
P2548 | strand orientation | reverse strand | Q22809711 |
FileName: PBB GE XRCC2 207598 x at fs.png
Description: Gene expression pattern of the XRCC2 gene.
Artist: AndrewGNF at English Wikipedia
Work is copyrighted.
License: CC BY-SA 3.0
Attribution is required.
Q27594338 | hsa-miR-124-3p |
Q27593854 | hsa-miR-1250-3p |
Q27594174 | hsa-miR-1285-3p |
Q27593154 | hsa-miR-1304-3p |
Q27594383 | hsa-miR-1306-5p |
Q27593064 | hsa-miR-1343-3p |
Q27593978 | hsa-miR-1470 |
Q27592804 | hsa-miR-186-5p |
Q27593695 | hsa-miR-212-5p |
Q27593965 | hsa-miR-23a-5p |
Q27595117 | hsa-miR-23b-5p |
Q27593961 | hsa-miR-24-3p |
Q27594628 | hsa-miR-302c-5p |
Q27592801 | hsa-miR-3117-3p |
Q27594281 | hsa-miR-3133 |
Q27593316 | hsa-miR-3169 |
Q27593913 | hsa-miR-3187-3p |
Q27593914 | hsa-miR-3187-5p |
Q27593980 | hsa-miR-3189-3p |
Q27593852 | hsa-miR-338-3p |
Q27594692 | hsa-miR-3607-3p |
Q27595033 | hsa-miR-3686 |
Q27594818 | hsa-miR-4282 |
Q27594889 | hsa-miR-4284 |
Q27594182 | hsa-miR-4435 |
Q27594994 | hsa-miR-4469 |
Q27595085 | hsa-miR-4667-3p |
Q27595132 | hsa-miR-4668-5p |
Q27593202 | hsa-miR-4701-5p |
Q27594142 | hsa-miR-4757-5p |
Q27594360 | hsa-miR-4759 |
Q27594189 | hsa-miR-4772-3p |
Q27594170 | hsa-miR-4778-5p |
Q27593437 | hsa-miR-495-3p |
Q27595322 | hsa-miR-508-5p |
Q27593685 | hsa-miR-5189-5p |
Q27594137 | hsa-miR-548s |
Q27594394 | hsa-miR-5571-3p |
Q27593078 | hsa-miR-5582-3p |
Q27594511 | hsa-miR-5688 |
Q27594830 | hsa-miR-588 |
Q27593116 | hsa-miR-612 |
Q27594224 | hsa-miR-6512-3p |
Q27595220 | hsa-miR-660-3p |
Q27595048 | hsa-miR-661 |
Q27594756 | hsa-miR-6720-5p |
Q27592921 | hsa-miR-6742-3p |
Q27593037 | hsa-miR-6744-3p |
Q27593111 | hsa-miR-6749-3p |
Q27593123 | hsa-miR-6752-3p |
Q27593728 | hsa-miR-6778-3p |
Q27593789 | hsa-miR-6783-3p |
Q27595062 | hsa-miR-6849-3p |
Q27595086 | hsa-miR-6852-5p |
Q27593121 | hsa-miR-6860 |
Q27592831 | hsa-miR-6878-3p |
Q27594487 | hsa-miR-6890-3p |
Q27595099 | hsa-miR-7-1-3p |
Q27593583 | hsa-miR-7-2-3p |
Q27593582 | hsa-miR-7-5p |
Q27595274 | hsa-miR-766-3p |
Q27594008 | hsa-miR-769-5p |
Q27592834 | hsa-miR-8083 |
Q27595059 | hsa-miR-939-3p |
Q32146921 | Fanconi anemia complementation group U | genetic association | P2293 |
Q102743759 | Male infertility | has part(s) | P527 |
Q21124977 | X-ray repair cross complementing 2 | encoded by | P702 |
XRCC2 | wikipedia | |
Persian (fa / Q9168) | XRCC2 | wikipedia |
Tatar language (tt / Q25285) | XRCC2 | wikipedia |
XRCC2 | wikipedia |
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