Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes (Q24597048)

Family with sequence similarity 107, member B

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GIT ArfGAP 2

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Chromobox 7

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author

Gordon Dougan

27

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Neil J Ingham

Neil J Ingham

9

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Darren W. Logan

Darren W Logan

19

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David Tannahill

David Tannahill

18

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Natasha A Karp

Natasha A Karp

3

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Jonathan Flint

Jonathan Flint

21

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Fiona Watt

Fiona M Watt

25

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Karen Steel

31

Karen P Steel

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author name string

Jacqueline K White

1

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Anna-Karin Gerdin

2

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Ed Ryder

4

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Marija Buljan

5

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James N Bussell

6

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Jennifer Salisbury

7

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Simon Clare

8

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Christine Podrini

10

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Richard Houghton

11

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Jeanne Estabel

12

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Joanna R Bottomley

13

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David G Melvin

14

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David Sunter

15

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Niels C Adams

16

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Daniel G Macarthur

20

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Vinit B Mahajan

22

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Stephen H Tsang

23

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Ian Smyth

24

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William C Skarnes

26

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David J Adams

28

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Ramiro Ramirez-Solis

29

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Allan Bradley

Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project

30

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language of work or name

English

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publication date

18 July 2013

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published in

Cell

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volume

154

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issue

2

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page(s)

452-64

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cites work

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Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature

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Reduced body weight is a common effect of gene knockout in mice

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28 November 2018

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28 November 2018

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28 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/23870131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.CELL.2013.06.022

1 reference

1 reference

1 reference

PubMed publication ID

23870131

1 reference