Efcab5-KO Mouse
Common Name
Efcab5-KO
제품 ID
S-KO-18127
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-319634-Efcab5-B6J-VB
상태
이 마우스 계통을 논문에서 사용할 경우, “Efcab5-KO Mouse (카탈로그 번호 S-KO-18127)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
기본 정보
품종 계통
Efcab5-KO
품종 계통계통 ID
KOCMP-319634-Efcab5-B6J-VB
유전자명
제품 ID
S-KO-18127
유전자 별칭
4930563A03Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 11
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000108400
NCBI 전사체 ID
XM_017314601
타겟 영역
Exon 4~9
유효 영역 크기
~11.1 kb
유전자 연구 개요
Efcab5, short for EF-hand calcium binding domain 5, likely plays a role in calcium-related functions considering its name indicates an EF-hand calcium-binding domain. Calcium-binding proteins are often involved in signal transduction pathways and various cellular processes, highlighting its potential importance in normal biological function [3].
In genetic studies, Efcab5 has been associated with multiple conditions. In a GWAS for assessing the brain glymphatic system (GS) function, Efcab5 was among 58 genes prioritized in DTI-ALPS index subtypes and associated with neurodegenerative diseases [1]. In whole-exome sequencing of biliary tract cancers in primary sclerosing cholangitis, Efcab5 was identified as one of the candidate cancer genes, suggesting its possible role in cancer development [2]. In a family with a monozygotic twin pair concordant for autism spectrum disorder (ASD), a truncating variation in Efcab5 was found, hinting at its potential role in the genetic etiology of ASD, at least in some patients [4]. In skin cutaneous melanoma, Efcab5 was significantly associated with prognosis, indicating its importance in this cancer [5].
In conclusion, Efcab5 is potentially involved in a range of biological processes related to neurodegenerative diseases, cancer, and ASD. Its associations with these disease conditions suggest that understanding its function could provide insights into the underlying disease mechanisms, potentially leading to new diagnostic or therapeutic strategies.
References:
1. Ran, Lusen, Fang, Yuanyuan, Cheng, Chang, Hao, Xingjie, Wang, Minghuan. 2025. Genome-wide and phenome-wide studies provided insights into brain glymphatic system function and its clinical associations. In Science advances, 11, eadr4606. doi:10.1126/sciadv.adr4606. https://pubmed.ncbi.nlm.nih.gov/39823331/
2. Grimsrud, Marit M, Forster, Michael, Goeppert, Benjamin, Roessler, Stephanie, Folseraas, Trine. 2024. Whole-exome sequencing reveals novel cancer genes and actionable targets in biliary tract cancers in primary sclerosing cholangitis. In Hepatology communications, 8, . doi:10.1097/HC9.0000000000000461. https://pubmed.ncbi.nlm.nih.gov/38967597/
3. Sani, Morteza Bitaraf, Roudbari, Zahra, Karimi, Omid, Shafei Naderi, Ali, Burger, Pamela Anna. 2022. Gene-Set Enrichment Analysis for Identifying Genes and Biological Activities Associated with Growth Traits in Dromedaries. In Animals : an open access journal from MDPI, 12, . doi:10.3390/ani12020184. https://pubmed.ncbi.nlm.nih.gov/35049806/
4. Egawa, Jun, Watanabe, Yuichiro, Sugimoto, Atsunori, Sugiyama, Toshiro, Someya, Toshiyuki. 2015. Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study. In Psychiatry research, 229, 599-601. doi:10.1016/j.psychres.2015.07.018. https://pubmed.ncbi.nlm.nih.gov/26189338/
5. Wang, Shaoxi, Wang, Qiaoqi, Zheng, Jiayu, He, Zhiyi, Chen, Quanfang. 2025. Clinical implications and molecular mechanism of long noncoding RNA LINC00518 and protein-coding genes in skin cutaneous melanoma by genome‑wide investigation. In Archives of dermatological research, 317, 454. doi:10.1007/s00403-025-03961-1. https://pubmed.ncbi.nlm.nih.gov/39987414/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
Cyagen문의하기
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