Incidental Mutation 'R0766:Tex22'
ID 69514
Institutional Source Beutler Lab
Gene Symbol Tex22
Ensembl Gene ENSMUSG00000012211
Gene Name testis expressed gene 22
Synonyms Tep22, 1700028O09Rik
MMRRC Submission 038946-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # R0766 (G1)
Quality Score 192
Status Validated
Chromosome 12
Chromosomal Location 113038122-113052537 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 113052143 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 67 (N67S)
Ref Sequence ENSEMBL: ENSMUSP00000116272 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000012355] [ENSMUST00000109729] [ENSMUST00000146107]
AlphaFold Q9D9U4
Predicted Effect possibly damaging
Transcript: ENSMUST00000012355
AA Change: N67S

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000012355
Gene: ENSMUSG00000012211
AA Change: N67S

DomainStartEndE-ValueType
low complexity region 14 24 N/A INTRINSIC
low complexity region 103 120 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000109729
AA Change: N67S

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000105351
Gene: ENSMUSG00000012211
AA Change: N67S

DomainStartEndE-ValueType
low complexity region 14 24 N/A INTRINSIC
low complexity region 103 120 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000146107
AA Change: N67S

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000116272
Gene: ENSMUSG00000012211
AA Change: N67S

DomainStartEndE-ValueType
low complexity region 14 24 N/A INTRINSIC
low complexity region 103 120 N/A INTRINSIC
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.0%
  • 20x: 93.4%
Validation Efficiency 100% (37/37)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921539E11Rik A T 4: 103,127,994 (GRCm39) F44I probably damaging Het
A2m T C 6: 121,653,849 (GRCm39) probably benign Het
Card14 T C 11: 119,215,002 (GRCm39) S241P probably damaging Het
Cdh15 G A 8: 123,588,188 (GRCm39) probably benign Het
Dnah5 A C 15: 28,448,633 (GRCm39) K4232T probably null Het
Eml6 A G 11: 29,781,219 (GRCm39) probably benign Het
Esd T C 14: 74,979,561 (GRCm39) S122P probably damaging Het
Frem3 G A 8: 81,341,951 (GRCm39) V1415I probably benign Het
Fry T C 5: 150,326,897 (GRCm39) probably benign Het
Gp1ba C T 11: 70,532,253 (GRCm39) P673L probably damaging Het
Herc1 C T 9: 66,412,122 (GRCm39) P4781S probably damaging Het
Ift70a2 A T 2: 75,806,676 (GRCm39) V612D probably benign Het
Iqch G A 9: 63,389,965 (GRCm39) S738L probably benign Het
Itih2 T A 2: 10,102,735 (GRCm39) T800S probably benign Het
Itpr1 A G 6: 108,387,861 (GRCm39) E1533G probably damaging Het
Klrg1 T C 6: 122,256,622 (GRCm39) M55V probably benign Het
Lrrk2 A G 15: 91,584,098 (GRCm39) N286S probably damaging Het
Mkx T A 18: 6,937,192 (GRCm39) D284V probably benign Het
Mroh2a C T 1: 88,158,402 (GRCm39) R150* probably null Het
Otos A C 1: 92,573,073 (GRCm39) L14R probably damaging Het
Plch2 C T 4: 155,074,256 (GRCm39) V765M probably damaging Het
Ppp4r3b A T 11: 29,123,358 (GRCm39) Q18L probably benign Het
Psme4 T A 11: 30,757,687 (GRCm39) probably null Het
Pwp1 G A 10: 85,715,173 (GRCm39) D220N probably damaging Het
Rel G A 11: 23,707,010 (GRCm39) T64I probably damaging Het
Snai2 T A 16: 14,526,111 (GRCm39) M254K possibly damaging Het
Sntb2 A G 8: 107,728,209 (GRCm39) T386A probably damaging Het
Tedc2 T A 17: 24,435,291 (GRCm39) E366V probably damaging Het
Tedc2 C A 17: 24,435,292 (GRCm39) E366* probably null Het
Trank1 T G 9: 111,176,537 (GRCm39) S270A probably benign Het
Vcp T C 4: 42,988,728 (GRCm39) T249A possibly damaging Het
Vmn1r167 A G 7: 23,204,548 (GRCm39) F156S probably benign Het
Vrk2 G A 11: 26,485,522 (GRCm39) probably benign Het
Wdfy4 T C 14: 32,862,569 (GRCm39) E601G probably damaging Het
Zfp407 C T 18: 84,577,898 (GRCm39) A1072T probably benign Het
Zfp638 A G 6: 83,906,023 (GRCm39) N63D probably damaging Het
Other mutations in Tex22
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0100:Tex22 UTSW 12 113,052,392 (GRCm39) missense probably benign 0.15
R0100:Tex22 UTSW 12 113,052,392 (GRCm39) missense probably benign 0.15
R1497:Tex22 UTSW 12 113,039,000 (GRCm39) missense probably benign 0.00
R4761:Tex22 UTSW 12 113,052,386 (GRCm39) missense possibly damaging 0.54
R5013:Tex22 UTSW 12 113,052,104 (GRCm39) missense probably damaging 0.97
R7859:Tex22 UTSW 12 113,052,103 (GRCm39) missense possibly damaging 0.92
R8221:Tex22 UTSW 12 113,038,696 (GRCm39) splice site probably null
R9732:Tex22 UTSW 12 113,052,196 (GRCm39) missense possibly damaging 0.94
Z1177:Tex22 UTSW 12 113,052,239 (GRCm39) frame shift probably null
Predicted Primers PCR Primer
(F):5'- ACCATGTCGGGCTACTGTGAGAAG -3'
(R):5'- GCCAAGAAGTCCTGGAAGGCATTAG -3'

Sequencing Primer
(F):5'- CTACTGTGAGAAGGTACTGCTTCC -3'
(R):5'- GGGATCAGCCATAGTCTCACAG -3'
Posted On 2013-09-30