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Q9UBW7 of Proteins MYM-type domain repeats
Uniprot ID:Q9UBW7
Protein name: Zinc finger MYM-type protein 2
Gene : ZMYM2 FIM RAMP ZNF198
Protein Family:
Squence Length : 1377
Sequnce
>Q9UBW7 1378 MDTSSVGGLELTDQTPVLLGSTAMATSLTNVGNSFSGPANPLVSRSNKFQNSSVEDDDDVVFIEPVQPPPPSVPVVADQRTITFTSSKNEELQGNDSKITPSSKELASQKGSVSETIVIDDEEDMETNQGQEKNSSNFIERRPPETKNRTNDVDFSTSSFSRSKVNAGMGNSGITTEPDSEIQIANVTTLETGVSSVNDGQLENTDGRDMNLMITHVTSLQNTNLGDVSNGLQSSNFGVNIQTYTPSLTSQTKTGVGPFNPGRMNVAGDVFQNGESATHHNPDSWISQSASFPRNQKQPGVDSLSPVASLPKQIFQPSVQQQPTKPVKVTCANCKKPLQKGQTAYQRKGSAHLFCSTTCLSSFSHKPAPKKLCVMCKKDITTMKGTIVAQVDSSESFQEFCSTSCLSLYEDKQNPTKGALNKSRCTICGKLTEIRHEVSFKNMTHKLCSDHCFNRYRMANGLIMNCCEQCGEYLPSKGAGNNVLVIDGQQKRFCCQSCVSEYKQVGSHPSFLKEVRDHMQDSFLMQPEKYGKLTTCTGCRTQCRFFDMTQCIGPNGYMEPYCSTACMNSHKTKYAKSQSLGIICHFCKRNSLPQYQATMPDGKLYNFCNSSCVAKFQALSMQSSPNGQFVAPSDIQLKCNYCKNSFCSKPEILEWENKVHQFCSKTCSDDYKKLHCIVTYCEYCQEEKTLHETVNFSGVKRPFCSEGCKLLYKQDFARRLGLRCVTCNYCSQLCKKGATKELDGVVRDFCSEDCCKKFQDWYYKAARCDCCKSQGTLKERVQWRGEMKHFCDQHCLLRFYCQQNEPNMTTQKGPENLHYDQGCQTSRTKMTGSAPPPSPTPNKEMKNKAVLCKPLTMTKATYCKPHMQTKSCQTDDTWRTEYVPVPIPVPVYIPVPMHMYSQNIPVPTTVPVPVPVPVFLPAPLDSSEKIPAAIEELKSKVSSDALDTELLTMTDMMSEDEGKTETTNINSVIIETDIIGSDLLKNSDPETQSSMPDVPYEPDLDIEIDFPRAAEELDMENEFLLPPVFGEEYEEQPRPRSKKKGAKRKAVSGYQSHDDSSDNSECSFPFKYTYGVNAWKHWVKTRQLDEDLLVLDELKSSKSVKLKEDLLSHTTAELNYGLAHFVNEIRRPNGENYAPDSIYYLCLGIQEYLCGSNRKDNIFIDPGYQTFEQELNKILRSWQPSILPDGSIFSRVEEDYLWRIKQLGSHSPVALLNTLFYFNTKYFGLKTVEQHLRLSFGTVFRHWKKNPLTMENKACLRYQVSSLCGTDNEDKITTGKRKHEDDEPVFEQIENTANPSRCPVKMFECYLSKSPQNLNQRMDVFYLQPECSSSTDSPVWYTSTSLDRNTLENMLVRVLLVKDIYDKDNYELDEDTD
MYM-type domains repeats
ZN_FING 352 386 MYM-type 1 ZN_FING 398 436 MYM-type 2 ZN_FING 445 480 MYM-type 3 ZN_FING 491 549 MYM-type 4 ZN_FING 559 597 MYM-type 5 ZN_FING 605 652 MYM-type 6 ZN_FING 660 694 MYM-type 7 ZN_FING 701 740 MYM-type 8 ZN_FING 747 781 MYM-type 9
Domin repeated regions
352 - 386 HLFCSTTCLSSFSHKPAPKKLCVMCKKDITTMKGT 398 - 436 QEFCSTSCLSLYEDKQNPTKGALNKSRCTICGKLTEIRH 445 - 480 HKLCSDHCFNRYRMANGLIMNCCEQCGEYLPSKGAG 491 - 549 KRFCCQSCVSEYKQVGSHPSFLKEVRDHMQDSFLMQPEKYGKLTTCTGCRTQCRFFDMT 559 - 597 EPYCSTACMNSHKTKYAKSQSLGIICHFCKRNSLPQYQA 605 - 652 YNFCNSSCVAKFQALSMQSSPNGQFVAPSDIQLKCNYCKNSFCSKPEI 660 - 694 HQFCSKTCSDDYKKLHCIVTYCEYCQEEKTLHETV 701 - 740 RPFCSEGCKLLYKQDFARRLGLRCVTCNYCSQLCKKGATK 747 - 781 RDFCSEDCCKKFQDWYYKAARCDCCKSQGTLKERV
Function
May function as a transcription factor
Disease
"DISEASE: Note=A chromosomal aberration involving ZMYM2 may be a cause of stem cell leukemia lymphoma syndrome (SCLL) Translocation t(8;13)(p11;q12) with FGFR1 SCLL usually presents as lymphoblastic lymphoma in association with a myeloproliferative disorder, often accompanied by pronounced peripheral eosinophilia and/or prominent eosinophilic infiltrates in the affected bone marrow"