Accession: | NM_001101801 |
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基因名称: | FAM13B |
基因别名: | N61; KHCHP; C5orf5; FAM13B1; ARHGAP49 |
基因描述: | Homo sapiens family with sequence similarity 13, member B (FAM13B), transcript variant 3, mRNA. |
种属: | Human |
CDS区长度: | 2376 (查看编码区序列) |
翻译后氨基酸长度: | 791 (查看氨基酸序列) |
Transcript Variant: | This variant (3) has a distinct 5' UTR, lacks an in-frame portion of the 5' coding region, contains an alternate in-frame exon in the mid-coding region, and lacks an alternate in-frame exon in the 3' coding region, as compared to variant 1. This results in a shorter isoform (3) that has a truncated N-terminus, compared to isoform 1. |
人 FAM13B (NM_016603) cDNA克隆 | transcript variant 1 |
人 FAM13B (NM_001101800) cDNA克隆 | transcript variant 2 |
人 FAM13B (NM_001101801) cDNA克隆 | transcript variant 3 |