Gene HUMAN41688 (SIN3B_HUMAN)

E Homo sapiens | Paired amphipathic helix protein Sin3b [SIN3B]

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General Information

DescriptionSIN3 transcription regulator family member B [Source:HGNC Symbol;Acc:HGNC:19354]; transcript_id=ENST00000379803.5
Organism HUMAN - Homo sapiens
Locus[ Chromosome 19 ]: 16829421 ... 16878727
Number of exons20
Exonsjoin(16829421..16829540, 16829791..16829897, 16831494..16831647, 16841768..16841968, 16846970..16847113, 16851412..16851534, 16853069..16853158, 16854143..16854261, 16862352..16862559, 16862884..16862979, 16863680..16863796, 16865410..16865648, 16866373..16866556, 16869460..16870075, 16871229..16871398, 16876055..16876228, 16876486..16876578, 16877545..16877639, 16878183..16878390, 16878497..16878727)

IDs and Cross-references

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