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  2. KLLN - killin, p53 regulated DNA replication inhibitor Gene

KLLN - killin, p53 regulated DNA replication inhibitor Gene

中文名称:killin,p53 调节的 DNA 复制抑制因子

种属: Homo sapiens

同用名: CWS4; KILLIN

基因 ID: 100144748 | 基因类型: protein coding

关于 KLLN

Cytogenetic location: 10q23.31 Genomic coordinates (GRCh38): 10:87,859,158-87,863,533 (from NCBI)

This gene has 1 transcript (splice variant), 1 gene allele, 13 orthologues and is associated with 3 phenotypes.

功能概要

由这种无内含子基因编码的蛋白质存在于细胞核中,在那里它可以抑制 DNA 合成并促进与细胞凋亡相关的 S 期停滞。这种 DNA 结合蛋白的表达被转录因子 p53 上调。[RefSeq 提供,2012 年 12 月]

The protein encoded by this intronless gene is found in the nucleus, where it can inhibit DNA synthesis and promote S phase arrest coupled to Apoptosis. The expression of this DNA binding protein is upregulated by transcription factor p53. [provided by RefSeq, Dec 2012]

KLLN 基因产物(1)

mRNA Protein Name
NM_001126049.2 NP_001119521.1 killin
蛋白主名 其他名称

killin

关联疾病

疾病名称 别名
Cowden Syndrome 4

CWS4

Cowden Syndrome, Type 4

Cowden Syndrome

Cowden Disease

Multiple Hamartoma Syndrome

Cowden'S Disease

Lhermitte-Duclos Disease

Cd

Cs

Mham

Dysplastic Gangliocytoma Of Cerebellum

Cowden'S Syndrome

Hamartoma Syndrome, Multiple

Hereditary Breast Cancer

Familial Breast Cancer

Familial Breast Carcinoma

Hereditary Breast Carcinoma

Cowden Syndrome 1

Bannayan-Riley-Ruvalcaba Syndrome

Pten Hamartoma Tumor Syndrome

Lhermitte-Duclos Disease

Bannayan-Zonana Syndrome

Phts

Riley-Smith Syndrome

Bzs

Ruvalcaba-Myhre-Smith Syndrome

Multiple Hamartoma Syndrome

Rmss

Brrs

Dysplastic Gangliocytoma Of The Cerebellum

CWS1

Cs

Cd

Mham

Pten Hamartoma Tumor Syndrome With Granular Cell Tumor

Macrocephaly Multiple Lipomas And Hemangiomata

Bannayan-Ruvalcaba-Riley Syndrome

Myhre-Riley-Smith Syndrome

LDD

Cerebelloparenchymal Disorder Vi

Hamartoma Syndrome, Multiple

Bbrs

Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata

Macrocephaly, Multiple Lipomas, And Hemangiomata

Macrocephaly Pseudopapilledema And Multiple Hemangiomas

Ruvalcaba -Myhre-Smith Syndrome

Ruvalcaba-Myhre Syndrome

Cowden Disease

Macrocephaly Pseudopapilledema And Multiple Hemangiomata

Cerebellar Granule Cell Hypertrophy And Megalencephaly

Cpd6

Pten Hamartoma Tumor Syndromes

Cowden Syndrome, Type 1

Infiltrating Angiolipoma

Angiolipoma, Infiltrating

Gangliocytoma

Ganglioneuroma

Gangliocytoma Of Central Nervous System

Liver Inflammatory Pseudotumor

Inflammatory Pseudotumor Of The Liver

Liver Inflammatory Myofibroblastic Tumor

Multinodular Goiter
疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus KLLN RGD RGD:7720631