1. Gene
  2. PALMD - palmdelphin Gene

PALMD - palmdelphin Gene

中文名称:棕海豚

种属: Homo sapiens

同用名: PALML; C1orf11

基因 ID: 54873 | 基因类型: protein coding

关于 PALMD

Cytogenetic location: 1p21.2 Genomic coordinates (GRCh38): 1:99,646,113-99,694,535 (from NCBI)

This gene has 4 transcripts (splice variants), 237 orthologues and 3 paralogues. Biased expression in fat (RPKM 87.9), heart (RPKM 29.7) and 13 other tissues.

功能概要

预计参与细胞形状的调节。预测位于树突中。预计在细胞质中有活性。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to be involved in regulation of cell shape. Predicted to be located in dendrite. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

PALMD 基因产物(1)

mRNA Protein Name
NM_017734.5 NP_060204.1 palmdelphin
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

PALMD 蛋白结构

Paralemmin

Paralemmin: Paralemmin (64 - 275)

Paralemmin

Paralemmin: Paralemmin (409 - 500)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 551 a.a.
蛋白主名 其他名称

palmdelphin

paralemmin-like protein

PALMD 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
PALMD Q9NP74 WFS1 Homo sapiens O76024 32814053
种属内
PALMD Q9NP74 WFS1 Homo sapiens O76024 32814053
种属内
PALMD Q9NP74 WFS1 Homo sapiens O76024 32814053
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Aortic Valve Disease 1

Aortic Valve Disease

Bicuspid Aortic Valve

Aortic Valve Disorder

AOVD1

Bav

Bicuspid Aortic Valve Disease

Familial Bicuspid Aortic Valve

Aortic Valve Calcification

Aovd

Aortic Valve, Bicuspid

Aortic Valve, Calcification Of

Aortic Stenosis, Calcific

Familial Bav

Calcific Aortic Stenosis

Calcification Of Aortic Valve

Abnormality Of The Aortic Valve

Aortic Valve Disease, Type 1

Aortic Valve Disease 2

Bicommissural Aortic Valve

Osteopetrosis, Autosomal Dominant 2

OPTA2

Autosomal Dominant Osteopetrosis 2

Osteopetrosis Autosomal Dominant Type 2

Osteopetrosis, Autosomal Dominant, Type Ii

Albers-Schonberg Osteopetrosis

Autosomal Dominant Albers-Schonberg Disease

Osteopetrosis

Marble Bones, Autosomal Dominant

Osteosclerosis Fragilis Generalisata

Albers-Schonberg Disease, Autosomal Dominant

Autosomal Dominant Osteopetrosis Type Ii

Albers-Schönberg Osteopetrosis

Autosomal Dominant Osteopetrosis Type 2

Marble Disease Autosomal Dominant

Osteopetrosis, Autosomal Dominant, Type 2

Moebius Syndrome

Mobius Syndrome

Moebius Sequence

Oromandibular-Limb Hypogenesis Spectrum

Congenital Facial Diplegia

MBS

Moebius Congenital Oculofacial Paralysis

Absence Or Underdevelopment Of The 6th And 7th Cranial Nerves

Congenital Facial Diplegia Syndrome

Congenital Oculofacial Paralysis

Congenital Ophthalmoplegia And Facial Paresis

Moebius Spectrum

Möbius Sequence

Möbius Syndrome

Mobius Ii Syndrome

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
Canis familiaris PALMD VGNC VGNC:44249
Mus musculus PALMD MGD MGI:2148896
Macaca mulatta PALMD VGNC VGNC:75613
Bos taurus PALMD VGNC VGNC:32560
Rattus norvegicus PALMD RGD RGD:1305624
Felis catus PALMD VGNC VGNC:64029