2. Gene
  3. TEN1 - TEN1 subunit of CST complex Gene

TEN1 - TEN1 subunit of CST complex Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：CST 复合物的 TEN1 亚基

种属: Homo sapiens

同用名: C17orf106

基因 ID: 100134934 | 基因类型: protein coding

关于 TEN1

Cytogenetic location: 17q25.1 Genomic coordinates (GRCh38): 17:75,979,240-76,000,586 (from NCBI)

This gene has 5 transcripts (splice variants) and 182 orthologues. Ubiquitous expression in small intestine (RPKM 13.6), fat (RPKM 12.7) and 25 other tissues.

功能概要

C17ORF106 或 TEN1 似乎在与 STN1 (OBFC1；MIM 613128) 和 CTC1 (C17ORF68；MIM 613129) 的端粒相关复合体中起作用 (Miyake 等人，2009 [PubMed 19854130]) 。[OMIM 提供，2009 年 11 月] ]

C17ORF106, or TEN1, appears to function in a telomere-associated complex with STN1 (OBFC1; MIM 613128) and CTC1 (C17ORF68; MIM 613129) (Miyake et al., 2009 [PubMed 19854130]).[supplied by OMIM, Nov 2009]

TEN1 基因产物(1)

mRNA Protein Name
NM_001113324.3 NP_001106795.2 CST complex subunit TEN1

TEN1 蛋白结构

Ten1_2

Ten1_2: Telomere-capping, CST complex subunit (4 - 119)

  • 0
  • 100
  • 123 a.a.
蛋白主名 其他名称

CST complex subunit TEN1

TEN1 telomerase capping complex subunit homolog

关联疾病

疾病名称 别名
Dyskeratosis Congenita, Autosomal Recessive 6

DKCB6

Autosomal Recessive Dyskeratosis Congenita 6

Dyskeratosis Congenita, Autosomal Recessive, 6

Dyskeratosis Congenita, Autosomal Recessive, Type 6
Dyskeratosis Congenita, Autosomal Recessive 1

DKCB1

Autosomal Recessive Dyskeratosis Congenita 1

Dyskeratosis Congenita, Autosomal Recessive, 1

Dyskeratosis Congenita, Autosomal Recessive, Type 1
Dyskeratosis Congenita, Autosomal Recessive 3

DKCB3

Autosomal Recessive Dyskeratosis Congenita 3

Dyskeratosis Congenita, Autosomal Recessive, 3

Dyskeratosis Congenita, Autosomal Recessive, Type 3
Immunodeficiency 26

Severe Combined Immunodeficiency Due To Dna-Pkcs Deficiency

Scid Due To Dna-Pkcs Deficiency

Imd26

Immunodeficiency 26, With Or Without Neurologic Abnormalities
Retinal Telangiectasia
Revesz Syndrome

Exudative Retinopathy With Bone Marrow Failure

DKCA5

Dyskeratosis Congenita, Autosomal Dominant 5

Dyskeratosis Congenita With Bilateral Exudative Retinopathy

Retinopathy-Anemia-Central Nervous System Anomalies Syndrome

Revesz-Debuse Syndrome

Dyskeratosis Congenita, Autosomal Dominant, 5

Revesz Debuse Syndrome
Glioblastoma Mesenchymal Subtype
Coats Disease

Exudative Retinopathy

Retinal Telangiectasis

Coats' Disease

Leber Miliary Aneurysm

Coats' Syndrome

Congenital Retinal Telangiectasia
Dyskeratosis Congenita

Dyskeratosis Congenita Autosomal Dominant

Dc

Dkc

Zinsser-Engman-Cole Syndrome

Dyskeratosis Congenita, Autosomal Dominant

Autosomal Dominant Dyskeratosis Congenita

Dkca

Dyskeratosis Congenita Scoggins Type

Zinsser-Cole-Engman Syndrome

X-Linked Dyskeratosis Congenita

Hoyeraal-Hreidarsson Syndrome
Melanoma, Cutaneous Malignant 1

Familial Melanoma

Melanoma, Cutaneous Malignant, Susceptibility To, 1

Melanoma, Malignant

CMM1

Melanoma, Cutaneous Malignant

Cmm

Familial Atypical Mole-Malignant Melanoma Syndrome

Fammm

Melanoma, Familial

Mlm

Dysplastic Nevus Syndrome, Hereditary

Dns

B-K Mole Syndrome

Melanoma, Cutaneous Malignant, 1

Malignant Melanoma, Cutaneous

Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1

Dysplastic Nevus Syndrome

Cutaneous Melanoma

Familial Atypical Mole Melanoma Syndrome

Hereditary Melanoma
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS14361 TEN1 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus TEN1 RGD RGD:1311078
Bos taurus TEN1 VGNC VGNC:54498
Canis familiaris TEN1 VGNC VGNC:54372
Mus musculus TEN1 MGD MGI:1916785
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