JAKMIP1
janus kinase and microtubule interacting protein 1
Summary
Enables GABA receptor binding activity and RNA binding activity. Involved in cognition. Located in membrane. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs193101356 | 4:6,030,498 | G/A | intron variant | — |
| rs752154686 | 4:6,031,452 | C/T | — | likely benign |
| rs146662557 | 4:6,037,784 | C/T | — | benign |
| rs61734119 | 4:6,037,799 | C/T | — | benign |
| rs113514072 | 4:6,043,925 | G/A | — | benign |
| rs61747882 | 4:6,055,825 | G/A | — | benign |
| rs1114167350 | 4:6,055,827 | C/G | — | pathogenic |
| rs2474410131 | 4:6,058,453 | T/C | — | uncertain significance |
| rs16838131 | 4:6,058,497 | G/A | intron variant | — |
| rs1321615842 | 4:6,062,231 | G/A | — | uncertain significance |
| rs140800814 | 4:6,064,057 | G/A | — | likely benign |
| rs369235121 | 4:6,064,123 | G/C | — | likely benign |
| rs547846737 | 4:6,064,128 | G/T | — | uncertain significance |
| rs145453817 | 4:6,064,135 | G/A | — | benign |
| rs1135401781 | 4:6,064,169 | T/C | — | uncertain significance |
| rs995849470 | 4:6,066,647 | G/A | — | uncertain significance |
| rs1578134381 | 4:6,066,718 | T/C | — | likely benign |
| rs369897699 | 4:6,066,744 | C/T | — | likely benign |
| rs374764524 | 4:6,080,673 | G/A | — | uncertain significance |
| rs751046894 | 4:6,080,706 | C/T | — | uncertain significance |
| rs375128464 | 4:6,081,910 | C/T | — | uncertain significance |
| rs199727362 | 4:6,082,024 | C/T | — | uncertain significance |
| rs61731760 | 4:6,083,345 | G/A | — | benign |
| rs113369415 | 4:6,083,399 | C/G | — | benign |
| rs756138238 | 4:6,083,424 | C/T | — | uncertain significance |
| rs200686241 | 4:6,083,452 | G/C | — | uncertain significance |
| rs973744592 | 4:6,086,673 | C/T | — | uncertain significance |
| rs758012106 | 4:6,086,685 | T/C | — | uncertain significance |
| rs61753516 | 4:6,087,174 | C/T | — | likely benign |
| rs761128103 | 4:6,087,182 | C/T | — | uncertain significance |
| rs763794567 | 4:6,087,190 | A/T | — | uncertain significance |
| rs73196084 | 4:6,087,371 | G/A | — | benign |
| rs765078893 | 4:6,107,247 | C/G | — | uncertain significance |
| rs570283889 | 4:6,107,271 | C/A | — | uncertain significance |
| rs746565087 | 4:6,107,278 | G/C | — | uncertain significance |
| rs369991878 | 4:6,107,310 | A/T | — | conflicting classifications of pathogenicity |
| rs1713792355 | 4:6,107,346 | C/A | — | uncertain significance |
| rs1560193696 | 4:6,107,410 | C/G | — | uncertain significance |
| rs141800203 | 4:6,107,416 | C/T | — | benign |
| rs2474516894 | 4:6,107,424 | T/C | — | likely benign |
| rs750499928 | 4:6,107,433 | C/T | — | uncertain significance |
| rs771019447 | 4:6,107,663 | G/A | — | uncertain significance |
| rs1334180094 | 4:6,114,511 | T/G | — | uncertain significance |
| rs373856583 | 4:6,114,525 | G/A | — | uncertain significance |
| rs141392058 | 4:6,114,573 | G/A | — | uncertain significance |
| rs13102430 | 4:6,179,713 | G/A | regulatory region variant | — |
| rs10937705 | 4:6,183,184 | T/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.