|Institutional Source||Beutler Lab|
|Gene Name||teashirt zinc finger family member 1|
|Synonyms||Mtsh1, teashirt1, Sdccag33, D18Bwg1409e, Tsh1, NY-CO-33, 5730407I04Rik|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R4119 (G1)|
|Chromosomal Location||84011627-84086404 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to G at 84014189 bp (GRCm38)|
|Amino Acid Change||Lysine to Threonine at position 698 (K698T)|
|Ref Sequence||ENSEMBL: ENSMUSP00000089388 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000060303]|
AA Change: K698T
PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
AA Change: K698T
|Meta Mutation Damage Score||0.0714|
|Coding Region Coverage||
|Validation Efficiency||98% (46/47)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012]
PHENOTYPE: Mice homozygous for a null allele die shortly after birth of respiratory distress, have defects in soft palate formation, have altered axial skeleton and have middle ear defects. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Tshz1||
(F):5'- CAGAGCGCTTAGAGGGTTGATG -3'
(R):5'- GTCCTCCACAGAGCACAATG -3'
(F):5'- TTGATGAAAGAAGGCTCCGGC -3'
(R):5'- CCATAAGAGCAATGTGTCTGCCATG -3'