2. Gene
  3. PNISR - PNN interacting serine and arginine rich protein Gene

PNISR - PNN interacting serine and arginine rich protein Gene

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

中文名称：PNN 相互作用的富丝氨酸和精氨酸的蛋白质

种属: Homo sapiens

同用名: SFRS18; HSPC306; SRrp130; C6orf111; bA98I9.2

基因 ID: 25957 | 基因类型: protein coding

关于 PNISR

Cytogenetic location: 6q16.2 Genomic coordinates (GRCh38): 6:99,398,050-99,425,308 (from NCBI)

This gene has 14 transcripts (splice variants) and 170 orthologues. Ubiquitous expression in lymph node (RPKM 25.8), spleen (RPKM 24.5) and 25 other tissues.

功能概要

启用 RNA 结合活性。位于胞质溶胶中；核斑点；和质膜。 [由基因组资源联盟提供，2022 年 4 月]

Enables RNA binding activity. Located in cytosol; nuclear speck; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

PNISR 基因产物(14)

mRNA Protein Name
NM_001322405.2 NP_001309334.1 arginine/serine-rich protein PNISR isoform a
NM_001322406.2 NP_001309335.1 arginine/serine-rich protein PNISR isoform a
NM_001322408.2 NP_001309337.1 arginine/serine-rich protein PNISR isoform a
NM_001322410.2 NP_001309339.1 arginine/serine-rich protein PNISR isoform b
NM_001322412.2 NP_001309341.1 arginine/serine-rich protein PNISR isoform b
NM_001322413.2 NP_001309342.1 arginine/serine-rich protein PNISR isoform b
NM_001322414.2 NP_001309343.1 arginine/serine-rich protein PNISR isoform c
NM_001322415.2 NP_001309344.1 arginine/serine-rich protein PNISR isoform c
NM_001322416.2 NP_001309345.1 arginine/serine-rich protein PNISR isoform d
NM_001322417.2 NP_001309346.1 arginine/serine-rich protein PNISR isoform e
NM_001322418.2 NP_001309347.1 arginine/serine-rich protein PNISR isoform f
NM_001322419.2 NP_001309348.1 arginine/serine-rich protein PNISR isoform f
NM_015491.3 NP_056306.1 arginine/serine-rich protein PNISR isoform a
NM_032870.4 NP_116259.2 arginine/serine-rich protein PNISR isoform a
蛋白主名 其他名称

arginine/serine-rich protein PNISR

PNN-interacting serine/arginine-rich protein

关联疾病

疾病名称 别名
Unilateral Focal Polymicrogyria
Night Blindness, Congenital Stationary, Autosomal Dominant 1

Congenital Stationary Night Blindness Autosomal Dominant 1

CSNBAD1

Rhodopsin-Related Congenital Stationary Night Blindness

Night Blindness, Congenital Stationary, Rhodopsin-Related

Blindness, Night, Stationary, Congenital, Autosomal Dominant, Type 1
Cleft Soft Palate

Cleft Velum

Cleft Velum Palatinum

Soft Cleft Palate

Soft Palate Perforation
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-RS10776 PNISR Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Felis catus PNISR VGNC VGNC:64259
Macaca mulatta PNISR VGNC VGNC:76090
Mus musculus PNISR MGD MGI:1913875
Rattus norvegicus PNISR RGD RGD:1307395
Canis familiaris PNISR VGNC VGNC:44741
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