Incidental Mutation 'R7399:Spert'
ID574059
Institutional Source Beutler Lab
Gene Symbol Spert
Ensembl Gene ENSMUSG00000034913
Gene Namespermatid associated
Synonyms1700086N05Rik, Nurit
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.070) question?
Stock #R7399 (G1)
Quality Score225.009
Status Validated
Chromosome14
Chromosomal Location75582877-75593116 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 75592637 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 39 (S39P)
Ref Sequence ENSEMBL: ENSMUSP00000127439 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035243] [ENSMUST00000164082] [ENSMUST00000165569] [ENSMUST00000169658]
Predicted Effect probably benign
Transcript: ENSMUST00000035243
SMART Domains Protein: ENSMUSP00000046259
Gene: ENSMUSG00000034913

DomainStartEndE-ValueType
Pfam:Chibby 40 176 1e-13 PFAM
coiled coil region 200 228 N/A INTRINSIC
coiled coil region 317 361 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000164082
AA Change: S39P

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000127439
Gene: ENSMUSG00000034913
AA Change: S39P

DomainStartEndE-ValueType
Pfam:Chibby 77 200 4.9e-15 PFAM
coiled coil region 236 264 N/A INTRINSIC
coiled coil region 353 397 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000165569
SMART Domains Protein: ENSMUSP00000131347
Gene: ENSMUSG00000034913

DomainStartEndE-ValueType
Pfam:Chibby 1 135 2.1e-13 PFAM
coiled coil region 158 186 N/A INTRINSIC
coiled coil region 275 319 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000169658
SMART Domains Protein: ENSMUSP00000129616
Gene: ENSMUSG00000034913

DomainStartEndE-ValueType
Pfam:Chibby 49 185 2.4e-14 PFAM
coiled coil region 209 237 N/A INTRINSIC
coiled coil region 326 370 N/A INTRINSIC
Meta Mutation Damage Score 0.0688 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 99% (74/75)
Allele List at MGI
Other mutations in this stock
Total: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acaca T G 11: 84,260,679 V801G possibly damaging Het
Actbl2 T A 13: 111,255,593 M154K probably benign Het
Adam7 A T 14: 68,504,466 probably null Het
Arfgef1 T A 1: 10,180,897 T888S probably benign Het
AW554918 C T 18: 25,169,060 P10L possibly damaging Het
Bcap29 A G 12: 31,630,882 I35T probably damaging Het
Bhlhe40 TG TGG 6: 108,664,857 probably null Het
C87499 C A 4: 88,627,965 R380L probably benign Het
Cdc25b A G 2: 131,194,654 D458G probably damaging Het
Cdc42bpb T C 12: 111,305,667 K1104R probably benign Het
Cep89 A G 7: 35,438,378 N729S probably damaging Het
Clec4a4 T A 6: 122,991,829 M51K possibly damaging Het
Dcdc2b A G 4: 129,609,629 L270P probably damaging Het
Dennd5b G T 6: 149,036,483 H639N probably damaging Het
Dnah11 T C 12: 118,125,785 E1182G probably damaging Het
Dnah11 T G 12: 118,027,477 T2385P probably benign Het
Dok7 T C 5: 35,066,471 V81A probably damaging Het
Dtx1 T A 5: 120,682,393 M494L possibly damaging Het
Foxj1 A T 11: 116,332,254 L241Q possibly damaging Het
Gbp10 G A 5: 105,236,149 probably benign Het
Hnmt T A 2: 24,003,880 T201S probably benign Het
Jup G T 11: 100,378,351 T412K possibly damaging Het
Kcnh2 G A 5: 24,322,059 S954F probably damaging Het
Klhdc7b A C 15: 89,388,644 K585T possibly damaging Het
Klk7 T A 7: 43,812,000 S14T probably benign Het
Lama4 G A 10: 39,047,948 E451K probably damaging Het
Ldhb A G 6: 142,495,673 C164R probably damaging Het
Malrd1 G A 2: 15,610,090 D239N Het
Mgam T A 6: 40,666,854 V572E probably damaging Het
Mrgprb2 G T 7: 48,552,142 N278K probably damaging Het
Msto1 A G 3: 88,911,823 Y206H probably damaging Het
Myo6 A G 9: 80,262,291 S467G unknown Het
Mysm1 T A 4: 94,961,727 I447L probably benign Het
Nav3 T C 10: 109,852,934 E494G possibly damaging Het
Nol10 T G 12: 17,402,173 V376G probably damaging Het
Nup205 T A 6: 35,214,676 I1032N probably damaging Het
Olfr1002 T A 2: 85,647,424 D299V possibly damaging Het
Olfr1100 G A 2: 86,978,157 T213I probably benign Het
Olfr1170 A T 2: 88,225,022 Y3* probably null Het
Olfr1450 A G 19: 12,954,447 N286S probably damaging Het
Olfr449 T G 6: 42,838,746 Y288* probably null Het
Olfr455 A G 6: 42,538,728 F98S possibly damaging Het
Olfr617 A T 7: 103,584,381 I120L possibly damaging Het
Olfr782 A T 10: 129,350,557 probably benign Het
Olfr996 A G 2: 85,579,296 D19G probably benign Het
Oog2 A G 4: 144,195,281 K254E probably benign Het
Osbpl11 T A 16: 33,236,279 D694E probably benign Het
Pcm1 T A 8: 41,293,510 Y1210N probably benign Het
Pdxk T C 10: 78,440,863 M293V probably benign Het
Plcb3 T C 19: 6,962,867 I451V probably benign Het
Plekhm2 A G 4: 141,634,376 F272S probably damaging Het
Ptgdr A T 14: 44,858,232 probably null Het
Ptprf C T 4: 118,226,523 V788I probably benign Het
Ralbp1 C T 17: 65,854,148 V467I probably benign Het
Ralgds A C 2: 28,543,655 Q229P possibly damaging Het
Recql T C 6: 142,374,884 D146G probably damaging Het
Reln T C 5: 22,051,367 N493S probably damaging Het
Rfxank C T 8: 70,135,286 probably null Het
Scn5a A T 9: 119,486,530 M1704K probably damaging Het
Slc7a7 G T 14: 54,374,268 A316E possibly damaging Het
Slco1a6 A T 6: 142,091,068 C538S probably benign Het
Stard6 T C 18: 70,498,647 probably null Het
Strip2 T A 6: 29,927,613 M219K possibly damaging Het
Tcam1 T C 11: 106,284,085 V122A probably damaging Het
Tha1 A G 11: 117,869,690 V236A possibly damaging Het
Tmem201 A T 4: 149,731,097 I132N possibly damaging Het
Tnc T C 4: 64,020,657 probably benign Het
Vmn1r42 T C 6: 89,845,513 T25A probably benign Het
Vmn2r94 T A 17: 18,244,503 probably null Het
Wdfy4 A C 14: 33,068,906 V2188G Het
Zfp623 T C 15: 75,947,398 S68P probably damaging Het
Zfp950 A T 19: 61,119,155 C497S probably damaging Het
Zkscan2 C T 7: 123,480,104 E877K probably damaging Het
Zp3r C A 1: 130,577,053 V536L probably damaging Het
Other mutations in Spert
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01304:Spert APN 14 75592645 missense possibly damaging 0.69
IGL01556:Spert APN 14 75584111 missense probably damaging 1.00
IGL02653:Spert APN 14 75583157 missense probably damaging 1.00
IGL03366:Spert APN 14 75583389 missense probably benign 0.01
R0071:Spert UTSW 14 75584181 missense probably benign 0.00
R1645:Spert UTSW 14 75583649 missense probably benign 0.12
R1738:Spert UTSW 14 75593057 start codon destroyed probably null 0.98
R1844:Spert UTSW 14 75583410 missense probably benign 0.12
R4773:Spert UTSW 14 75583106 missense probably damaging 1.00
R4857:Spert UTSW 14 75593038 missense probably damaging 1.00
R5201:Spert UTSW 14 75584009 missense probably damaging 1.00
R5274:Spert UTSW 14 75583226 missense probably benign 0.00
R5880:Spert UTSW 14 75583803 missense probably benign 0.02
R6915:Spert UTSW 14 75592658 missense probably benign 0.37
R8054:Spert UTSW 14 75583899 missense probably benign 0.00
R8062:Spert UTSW 14 75592606 missense probably benign 0.13
R8172:Spert UTSW 14 75591801 splice site probably null
X0023:Spert UTSW 14 75583134 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGTCCAGAGAGACCATGTATCC -3'
(R):5'- AAGATTTCTTTCTGGTCAGGTACC -3'

Sequencing Primer
(F):5'- AGAGAGACCATGTATCCTTCCTC -3'
(R):5'- TTCACACACACCTTTACATGGAG -3'
Posted On2019-09-13