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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
小鼠
Rpgrip1l - Rpgrip1-like
Alias:
Ftm
Nphp8
4931437C01
1700047E16Rik
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Basic Information
Sequence Homology
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
References Literature
预测能够激活血栓素A2受体结合活性。在几个过程的上游或内部发挥作用,包括动物器官发育;脊索动物胚胎发育;和胚胎肢芽形态发生。位于纤毛基体;纤毛过渡区;和细胞质中。在耳蜗器官;卵巢;和睾丸中表达。用于研究Joubert综合征7和Meckel综合征。这个基因的人类同源物涉及几种疾病,包括Joubert综合征7;Meckel综合征5;无脑畸形;视网膜色素变性3;和血管性痴呆。与人类RPGRIP1L(类似于RPGRIP1)正交。[由基因组资源联盟,2022年4月提供]
Related ID:
NCBI:244585
ENSEMBL:ENSMUSG00000033282
UNIPROT:Q8CG73
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Related Mouse Models
Reference
244585
11
26
96262 bp
145.00
5
6
Rpgrip1l Genetics information (-)
GRCm39
Sequence Homology
Transcripts & Proteins
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Transcript
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* This data comes from NCBI.
Gene Expression
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Type
Name
MGI
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IF
No Data Found!
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