2. Gene
  3. NAALADL2 - N-acetylated alpha-linked acidic dipeptidase like 2 Gene

NAALADL2 - N-acetylated alpha-linked acidic dipeptidase like 2 Gene

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

中文名称：N-乙酰化α连接的酸性二肽酶样 2

种属: Homo sapiens

基因 ID: 254827 | 基因类型: protein coding

关于 NAALADL2

Cytogenetic location: 3q26.31 Genomic coordinates (GRCh38): 3:174,440,982-175,810,548 (from NCBI)

This gene has 12 transcripts (splice variants), 184 orthologues and 5 paralogues. Ubiquitous expression in prostate (RPKM 1.4), gall bladder (RPKM 1.0) and 24 other tissues.

功能概要

预测可启用金属外肽酶活性。预计参与蛋白水解。预计在对细菌的反应上游或反应内起作用。位于核质中。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable metalloexopeptidase activity. Predicted to be involved in proteolysis. Predicted to act upstream of or within response to bacterium. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

NAALADL2 基因产物(1)

mRNA Protein Name
NM_207015.3 NP_996898.2 inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2

NAALADL2 蛋白结构

Peptidase_M28

Peptidase_M28: Peptidase family M28 (463 - 595)

  • 0
  • 200
  • 400
  • 600
  • 795 a.a.
蛋白主名 其他名称

inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2

N-acetylated alpha-linked acidic dipeptidase 2

重组 NAALADL2 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71559 NAALADL2 Protein, Human (His-SUMO) Q58DX5 (143G-795N) ≥95%

关联疾病

疾病名称 别名
Cornelia De Lange Syndrome

De Lange Syndrome

Brachmann De Lange Syndrome

Brachmann-De Lange Syndrome

Cdls

Bdls

Typus Degenerativus Amstelodamensis
Chromosome 6pter-P24 Deletion Syndrome

6p Subtelomeric Deletion Syndrome

6p25 Microdeletion Syndrome

Distal Monosomy 6p

Distal Deletion 6p

Monosomy 6p25
Facial Clefting, Oblique, 1

Oculomaxillofacial Dysostosis

Oculomaxillofacial Dysplasia With Oblique Facial Clefts

OBLFC1

Oblique Facial Clefting 1

Tessier Number 4 Facial Cleft

Oblique Facial Cleft

Orbitofacial Cleft

Oblique Facial Clefts

Richieri Costa Gorlin Syndrome

Richieri-Costa-Gorlin Syndrome

Facial Clefting, Oblique, Type 1
Teebi Hypertelorism Syndrome 1

Teebi Hypertelorism Syndrome

Brachycephalofrontonasal Dysplasia

Hypertelorism, Teebi Type

TBHS1

Tbhs

Chromosome 22q11.2 Deletion Syndrome, Opitz Phenotype

Opitz Gbbb Syndrome Type Ii

Specc1l-Related Hypertelorism Syndrome

Opitz Gbbb Syndrome, Type Ii, Formerly

Gbbb2, Formerly

Opitz Bbbg Syndrome, Type Ii, Formerly

Bbbg2, Formerly

Opitz-G Syndrome, Type Ii, Formerly

Ogs2, Formerly

Opitz Bbb Syndrome, Type Ii, Formerly

Hypertelorism-Hypospadias Syndrome, Formerly

Hypertelorism With Esophageal Abnormality And Hypospadias, Formerly

Opitz Oculogenitolaryngeal Syndrome, Type Ii, Formerly

Opitz-Frias Syndrome, Formerly

Teebi Hypertelorism Syndrome-1

Craniofrontonasal Dysplasia, Teebi Type

Bbb Syndrome

Gbbb Syndrome

G Syndrome

Hypertelorism-Hypospadias Syndrome

Hypertelorism With Esophageal Abnormality And Hypospadias

Hypospadias-Dysphagia Syndrome

Ogs2

Opitz Bbbg Syndrome

Opitz-Frias Syndrome

Opitz Gbbb Syndrome, Autosomal Dominant

Opitz-G Syndrome, Type Ii

Opitz Oculogenitolaryngeal Syndrome, Type Ii

Opitz Gbbb Syndrome, Type Ii

Teebi Syndrome

Opitz-G Syndrome, Type 2

Opitz Gbbb Syndrome, X-Linked

Digeorge Syndrome
Heart Aneurysm

Cardiac Aneurysm
Chromosome 1p36 Deletion Syndrome

1p36 Deletion Syndrome

Deletion 1p36

Monosomy 1p36

Subtelomeric 1p36 Deletion

Monosomy 1p36 Syndrome

Distal Monosomy 1p36

Del(1)(P36)

Deletion 1pter

Monosomy 1pter
Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly
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-RS08995 NAALADL2 Human Pre-designed siRNA Set A / 否

直系同源

种属 基因名 来源 基因 ID
Canis familiaris NAALADL2 VGNC VGNC:43599
Felis catus NAALADL2 VGNC VGNC:102784
Bos taurus NAALADL2 VGNC VGNC:106832
Rattus norvegicus NAALADL2 RGD RGD:1565147
Mus musculus NAALADL2 MGD MGI:2685867
Macaca mulatta NAALADL2 VGNC VGNC:83927
Others NAALADL2 NCBI
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