LMCD1
LIM and cysteine rich domains 1
Summary
This gene encodes a member of the LIM-domain family of zinc finger proteins. The encoded protein contains an N-terminal cysteine-rich domain and two C-terminal LIM domains. The presence of LIM domains suggests involvement in protein-protein interactions. The protein may act as a co-regulator of transcription along with other transcription factors. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1873944 | 3:8,553,087 | T/C | intron variant | — |
| rs375585532 | 3:8,574,443 | G/T | — | uncertain significance |
| rs199766095 | 3:8,574,451 | G/C | — | uncertain significance |
| rs2469974343 | 3:8,574,480 | A/G | — | uncertain significance |
| rs748271539 | 3:8,578,938 | C/T | — | uncertain significance |
| rs143907741 | 3:8,578,948 | G/C | — | uncertain significance |
| rs761332410 | 3:8,578,989 | C/T | — | uncertain significance |
| rs534848078 | 3:8,579,013 | C/T | — | uncertain significance |
| rs771067474 | 3:8,579,031 | C/T | — | uncertain significance |
| rs139605755 | 3:8,579,093 | C/T | — | likely benign |
| rs11707002 | 3:8,580,237 | C/G | intron variant | — |
| rs7629532 | 3:8,584,999 | G/A | — | — |
| rs2469991586 | 3:8,590,258 | T/C | — | uncertain significance |
| rs143268894 | 3:8,590,292 | G/T | — | uncertain significance |
| rs2469991676 | 3:8,590,305 | A/C | — | uncertain significance |
| rs531699233 | 3:8,590,306 | C/T | — | uncertain significance |
| rs753760540 | 3:8,590,326 | C/T | — | uncertain significance |
| rs566518812 | 3:8,590,380 | C/T | — | uncertain significance |
| rs200280069 | 3:8,590,381 | G/A | — | uncertain significance |
| rs2469991962 | 3:8,590,408 | T/A | — | uncertain significance |
| rs767714444 | 3:8,590,440 | G/A | — | uncertain significance |
| rs143760169 | 3:8,590,471 | C/T | — | uncertain significance |
| rs773172230 | 3:8,590,482 | G/T | — | uncertain significance |
| rs540916401 | 3:8,602,617 | T/C | — | — |
| rs908227942 | 3:8,607,137 | G/A | — | uncertain significance |
| rs2470009829 | 3:8,607,157 | C/T | — | uncertain significance |
| rs1000714171 | 3:8,607,272 | C/T | — | uncertain significance |
| rs138139932 | 3:8,607,310 | C/T | — | uncertain significance |
| rs2470010158 | 3:8,607,314 | G/A | — | likely benign |
| rs760177538 | 3:8,607,328 | G/A | — | uncertain significance |
| rs762826592 | 3:8,609,135 | G/A | — | uncertain significance |
| rs1695148047 | 3:8,609,136 | C/T | — | uncertain significance |
| rs141817419 | 3:8,609,151 | G/A | — | uncertain significance |
| rs768281560 | 3:8,609,191 | T/G | — | uncertain significance |
| rs772016331 | 3:8,609,226 | A/G | — | uncertain significance |
| rs375120817 | 3:8,609,231 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.