Incidental Mutation 'IGL01325:Fam169a'
ID 74234
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam169a
Ensembl Gene ENSMUSG00000041817
Gene Name family with sequence similarity 169, member A
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.103) question?
Stock # IGL01325
Quality Score
Status
Chromosome 13
Chromosomal Location 97067286-97131013 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to A at 97122699 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Alanine to Glutamic Acid at position 421 (A421E)
Ref Sequence ENSEMBL: ENSMUSP00000126209 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042517] [ENSMUST00000169863]
AlphaFold Q5XG69
Predicted Effect probably benign
Transcript: ENSMUST00000042517
AA Change: A421E

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000043738
Gene: ENSMUSG00000041817
AA Change: A421E

DomainStartEndE-ValueType
low complexity region 374 386 N/A INTRINSIC
low complexity region 602 619 N/A INTRINSIC
low complexity region 630 642 N/A INTRINSIC
low complexity region 650 663 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000169863
AA Change: A421E

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000126209
Gene: ENSMUSG00000041817
AA Change: A421E

DomainStartEndE-ValueType
low complexity region 374 386 N/A INTRINSIC
low complexity region 602 619 N/A INTRINSIC
low complexity region 630 642 N/A INTRINSIC
low complexity region 650 663 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930486L24Rik T C 13: 60,853,533 T127A probably damaging Het
Acrv1 T A 9: 36,698,514 M227K probably benign Het
Adam22 T C 5: 8,127,333 N592S probably benign Het
Adamts15 T A 9: 30,921,688 I184F possibly damaging Het
Adcy1 T C 11: 7,064,102 V168A possibly damaging Het
Arl6ip5 T C 6: 97,232,540 F179L probably benign Het
Asxl2 G T 12: 3,427,172 R6L probably damaging Het
Btaf1 T A 19: 37,004,649 probably benign Het
Ccdc136 T C 6: 29,412,950 F445L probably benign Het
Cpne3 T C 4: 19,535,229 S268G probably benign Het
Crtc3 C T 7: 80,677,368 R70Q probably damaging Het
Fhod1 A T 8: 105,331,649 M825K probably benign Het
Gjb2 T C 14: 57,100,221 T177A probably benign Het
Gm6576 A G 15: 27,025,884 noncoding transcript Het
Herpud2 A G 9: 25,113,911 V175A probably benign Het
Hmgxb3 T C 18: 61,134,006 D1052G probably damaging Het
Itpr1 T A 6: 108,381,208 F578L probably benign Het
Kdm7a T G 6: 39,158,309 probably benign Het
Krt76 A T 15: 101,884,888 S572T unknown Het
Lrrcc1 T C 3: 14,536,541 probably null Het
March9 A C 10: 127,057,590 V183G probably damaging Het
Mkl2 T C 16: 13,401,224 V578A probably damaging Het
Ndufaf6 A T 4: 11,070,251 D123E probably benign Het
Nhlh2 T G 3: 102,013,026 Y125D probably damaging Het
Nol4l A G 2: 153,436,351 probably benign Het
Npas1 C T 7: 16,463,322 G206D probably benign Het
Olfr651 T C 7: 104,553,689 F257L probably damaging Het
Olfr994 C A 2: 85,430,295 C178F possibly damaging Het
Pcdhb4 T A 18: 37,309,623 V662E probably damaging Het
Plxna3 G A X: 74,335,794 G758S probably damaging Het
Prdm15 T A 16: 97,806,517 N709Y probably damaging Het
Pygo2 C T 3: 89,432,446 probably benign Het
Ranbp2 T A 10: 58,476,298 S947T probably damaging Het
Rasgrp1 T A 2: 117,298,529 H203L probably damaging Het
Rbbp6 G A 7: 122,988,618 G270R probably damaging Het
Rcl1 A G 19: 29,121,262 probably null Het
Rpl23a-ps1 T C 1: 45,981,633 noncoding transcript Het
Serpinb7 T G 1: 107,435,380 H91Q probably damaging Het
Shd C T 17: 55,972,839 P111S possibly damaging Het
Slc35e1 G T 8: 72,483,758 probably benign Het
Srgap3 C T 6: 112,775,686 R279H probably damaging Het
Sstr4 G A 2: 148,395,552 E28K probably benign Het
Stip1 T C 19: 7,021,096 probably benign Het
Syne2 A G 12: 75,926,514 E1097G probably benign Het
Tbcd T A 11: 121,540,993 V489E probably damaging Het
Tnks2 T A 19: 36,871,633 S516R probably benign Het
Trmt44 T A 5: 35,568,803 R343S possibly damaging Het
Trps1 A G 15: 50,846,814 S47P probably benign Het
Ubr3 A C 2: 69,917,097 K235Q possibly damaging Het
Uckl1 G A 2: 181,574,961 Q48* probably null Het
Vat1 T C 11: 101,465,715 D140G probably benign Het
Vmn2r80 A G 10: 79,194,247 T636A possibly damaging Het
Zfp423 A T 8: 87,781,611 probably null Het
Zfp667 C A 7: 6,290,546 T15N probably damaging Het
Other mutations in Fam169a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01380:Fam169a APN 13 97091951 missense probably damaging 0.97
IGL01761:Fam169a APN 13 97091918 missense possibly damaging 0.92
IGL02628:Fam169a APN 13 97111288 splice site probably benign
IGL02739:Fam169a APN 13 97094055 splice site probably benign
IGL03171:Fam169a APN 13 97110014 splice site probably benign
IGL03306:Fam169a APN 13 97106989 missense possibly damaging 0.66
IGL03377:Fam169a APN 13 97091873 missense probably benign 0.04
IGL02980:Fam169a UTSW 13 97113680 critical splice donor site probably null
R0282:Fam169a UTSW 13 97097715 splice site probably benign
R1319:Fam169a UTSW 13 97097562 missense probably damaging 1.00
R1468:Fam169a UTSW 13 97118530 missense probably benign 0.01
R1468:Fam169a UTSW 13 97118530 missense probably benign 0.01
R2037:Fam169a UTSW 13 97107092 missense probably benign 0.37
R2380:Fam169a UTSW 13 97118535 splice site probably benign
R3805:Fam169a UTSW 13 97097684 missense probably benign 0.00
R4434:Fam169a UTSW 13 97126740 missense probably damaging 1.00
R4435:Fam169a UTSW 13 97126740 missense probably damaging 1.00
R4437:Fam169a UTSW 13 97126740 missense probably damaging 1.00
R4590:Fam169a UTSW 13 97097585 missense probably benign 0.02
R4896:Fam169a UTSW 13 97097592 missense probably damaging 1.00
R5004:Fam169a UTSW 13 97097592 missense probably damaging 1.00
R5276:Fam169a UTSW 13 97118496 missense probably benign 0.01
R5370:Fam169a UTSW 13 97106962 missense probably damaging 1.00
R5687:Fam169a UTSW 13 97093618 missense probably damaging 1.00
R6151:Fam169a UTSW 13 97093630 missense probably damaging 1.00
R7711:Fam169a UTSW 13 97126688 nonsense probably null
R8322:Fam169a UTSW 13 97122752 missense probably benign 0.00
R8493:Fam169a UTSW 13 97122859 missense probably benign 0.00
R8698:Fam169a UTSW 13 97107070 missense probably damaging 1.00
R8794:Fam169a UTSW 13 97114120 missense possibly damaging 0.85
R9231:Fam169a UTSW 13 97118459 missense probably benign 0.08
R9479:Fam169a UTSW 13 97110035 missense possibly damaging 0.68
R9479:Fam169a UTSW 13 97114187 missense possibly damaging 0.94
Posted On 2013-10-07