Incidental Mutation 'R4557:Smok4a'
ID 341926
Institutional Source Beutler Lab
Gene Symbol Smok4a
Ensembl Gene ENSMUSG00000079711
Gene Name sperm motility kinase 4A
Synonyms
MMRRC Submission 041784-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # R4557 (G1)
Quality Score 83
Status Validated
Chromosome 17
Chromosomal Location 13746453-13747907 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 13746643 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000074512
SMART Domains Protein: ENSMUSP00000074106
Gene: ENSMUSG00000060417

DomainStartEndE-ValueType
S_TKc 8 256 5.81e-84 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135850
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137459
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144015
SMART Domains Protein: ENSMUSP00000119597
Gene: ENSMUSG00000079711

DomainStartEndE-ValueType
S_TKc 8 256 2.17e-83 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185626
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.4%
Validation Efficiency 98% (49/50)
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830005F24Rik T C 13: 48,667,937 (GRCm39) probably benign Het
Acad11 T C 9: 103,960,038 (GRCm39) F219L probably benign Het
Adamts16 G A 13: 70,927,637 (GRCm39) probably benign Het
Adamts17 A T 7: 66,677,641 (GRCm39) E518D probably damaging Het
Adamts3 A G 5: 89,848,346 (GRCm39) Y659H probably benign Het
Adgrb3 T C 1: 25,123,360 (GRCm39) R1414G probably damaging Het
Apba1 T A 19: 23,894,956 (GRCm39) I464N probably damaging Het
Bahcc1 A G 11: 120,165,914 (GRCm39) T1057A probably damaging Het
Bcl11a A G 11: 24,114,004 (GRCm39) E449G probably damaging Het
Ccdc162 T A 10: 41,463,384 (GRCm39) I1453L probably benign Het
Ccdc175 T A 12: 72,175,080 (GRCm39) E531V probably benign Het
Cep68 A T 11: 20,189,113 (GRCm39) probably benign Het
Dlgap1 C A 17: 70,823,684 (GRCm39) T223K probably benign Het
Exoc1 G A 5: 76,709,290 (GRCm39) V24M probably damaging Het
Fbxo4 A G 15: 3,995,187 (GRCm39) *386R probably null Het
Gm10100 G A 10: 77,562,365 (GRCm39) probably benign Het
Gpr149 A G 3: 62,438,291 (GRCm39) V622A probably damaging Het
Gpr149 A C 3: 62,511,918 (GRCm39) M27R probably benign Het
Ighv3-6 T C 12: 114,251,818 (GRCm39) N101D probably benign Het
Igkv4-78 A G 6: 69,036,755 (GRCm39) S93P possibly damaging Het
Kmt2c A T 5: 25,505,313 (GRCm39) W3332R probably damaging Het
Marf1 T C 16: 13,971,841 (GRCm39) probably benign Het
Mcrs1 A G 15: 99,141,028 (GRCm39) I459T probably benign Het
Mdn1 G T 4: 32,754,437 (GRCm39) C4646F probably damaging Het
Med17 T C 9: 15,182,993 (GRCm39) K351E possibly damaging Het
Nalcn T C 14: 123,558,647 (GRCm39) probably benign Het
Or14j8 C A 17: 38,263,142 (GRCm39) A258S probably benign Het
Or1e29 G A 11: 73,667,307 (GRCm39) T282I possibly damaging Het
Or1r1 A T 11: 73,875,425 (GRCm39) V3E probably benign Het
Or6c69 A G 10: 129,747,398 (GRCm39) Y250H probably damaging Het
Phrf1 C T 7: 140,838,842 (GRCm39) probably benign Het
Pitpnm1 A G 19: 4,153,085 (GRCm39) Q135R probably benign Het
Prdm16 T A 4: 154,613,284 (GRCm39) M48L probably benign Het
Ptpn13 A G 5: 103,688,976 (GRCm39) E923G probably damaging Het
Rp1 A T 1: 4,414,886 (GRCm39) S2075R possibly damaging Het
Sft2d2 A G 1: 165,011,553 (GRCm39) C114R probably damaging Het
Sipa1l2 T G 8: 126,191,154 (GRCm39) R945S probably damaging Het
Slc12a1 A G 2: 125,028,561 (GRCm39) N517S probably damaging Het
Slc44a2 T G 9: 21,258,079 (GRCm39) L443R possibly damaging Het
Snx18 A G 13: 113,754,364 (GRCm39) S190P probably damaging Het
Thap12 A G 7: 98,365,052 (GRCm39) N407D probably benign Het
Tmc5 T C 7: 118,269,956 (GRCm39) I902T probably benign Het
Ttc27 T G 17: 75,136,544 (GRCm39) S584A probably benign Het
Ttn A T 2: 76,779,359 (GRCm39) Y1174N probably damaging Het
Zbtb44 T G 9: 30,975,544 (GRCm39) S391R probably damaging Het
Other mutations in Smok4a
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5511:Smok4a UTSW 17 13,746,474 (GRCm39) intron noncoding transcript
Predicted Primers PCR Primer
(F):5'- TCTGACATGGAGAAATTTCATGCTC -3'
(R):5'- ATTGTCAGGTGTCAGGTCCC -3'

Sequencing Primer
(F):5'- CATGCTCAATATGAAATGCTAGAGAC -3'
(R):5'- GTGTCAGGTCCCTGTGAACTATAC -3'
Posted On 2015-09-24