Incidental Mutation 'IGL02628:Fam169a'
ID 301181
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam169a
Ensembl Gene ENSMUSG00000041817
Gene Name family with sequence similarity 169, member A
Synonyms B230112C05Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # IGL02628
Quality Score
Status
Chromosome 13
Chromosomal Location 97203795-97266801 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 97247796 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000126209 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042517] [ENSMUST00000169863]
AlphaFold Q5XG69
Predicted Effect probably benign
Transcript: ENSMUST00000042517
SMART Domains Protein: ENSMUSP00000043738
Gene: ENSMUSG00000041817

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
SMART Domains Protein: ENSMUSP00000126209
Gene: ENSMUSG00000041817

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: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr10 T A 12: 71,001,430 (GRCm39) probably null Het
Ankhd1 T C 18: 36,780,756 (GRCm39) V1936A probably benign Het
Ap3m1 C A 14: 21,095,588 (GRCm39) E81* probably null Het
Camkk1 T C 11: 72,919,995 (GRCm39) probably benign Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cmc1 A G 9: 117,894,376 (GRCm39) Y33H probably damaging Het
Cntnap5b A T 1: 99,999,794 (GRCm39) D184V probably damaging Het
F5 A T 1: 164,021,644 (GRCm39) D1373V probably damaging Het
Fem1c G A 18: 46,639,019 (GRCm39) R328W probably damaging Het
Gba2 T C 4: 43,568,919 (GRCm39) R579G probably benign Het
Gm42641 G A 9: 108,887,698 (GRCm39) Q98* probably null Het
Hsd17b7 A G 1: 169,792,058 (GRCm39) F117L possibly damaging Het
Itsn1 A G 16: 91,696,511 (GRCm39) D38G possibly damaging Het
Map1a T C 2: 121,130,585 (GRCm39) I467T probably damaging Het
Map2k4 T A 11: 65,581,567 (GRCm39) I382F possibly damaging Het
Myh1 T G 11: 67,097,088 (GRCm39) probably benign Het
Nr1h4 C T 10: 89,309,701 (GRCm39) A339T probably damaging Het
Opn4 T A 14: 34,315,014 (GRCm39) T420S probably benign Het
Or5h22 A C 16: 58,895,155 (GRCm39) M96R probably benign Het
Or6n1 A G 1: 173,916,756 (GRCm39) Y50C probably benign Het
Rnf123 G A 9: 107,945,501 (GRCm39) R390* probably null Het
Slc17a3 T A 13: 24,026,434 (GRCm39) M1K probably null Het
T T A 17: 8,654,190 (GRCm39) I125N probably damaging Het
Tns2 T A 15: 102,020,263 (GRCm39) S710T probably benign Het
Trav3-1 T A 14: 52,818,551 (GRCm39) V75E probably benign Het
U2surp A G 9: 95,354,143 (GRCm39) Y832H possibly damaging Het
Zng1 T A 19: 24,935,269 (GRCm39) E78D probably damaging Het
Other mutations in Fam169a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01325:Fam169a APN 13 97,259,207 (GRCm39) missense probably benign 0.00
IGL01380:Fam169a APN 13 97,228,459 (GRCm39) missense probably damaging 0.97
IGL01761:Fam169a APN 13 97,228,426 (GRCm39) missense possibly damaging 0.92
IGL02739:Fam169a APN 13 97,230,563 (GRCm39) splice site probably benign
IGL03171:Fam169a APN 13 97,246,522 (GRCm39) splice site probably benign
IGL03306:Fam169a APN 13 97,243,497 (GRCm39) missense possibly damaging 0.66
IGL03377:Fam169a APN 13 97,228,381 (GRCm39) missense probably benign 0.04
IGL02980:Fam169a UTSW 13 97,250,188 (GRCm39) critical splice donor site probably null
R0282:Fam169a UTSW 13 97,234,223 (GRCm39) splice site probably benign
R1319:Fam169a UTSW 13 97,234,070 (GRCm39) missense probably damaging 1.00
R1468:Fam169a UTSW 13 97,255,038 (GRCm39) missense probably benign 0.01
R1468:Fam169a UTSW 13 97,255,038 (GRCm39) missense probably benign 0.01
R2037:Fam169a UTSW 13 97,243,600 (GRCm39) missense probably benign 0.37
R2380:Fam169a UTSW 13 97,255,043 (GRCm39) splice site probably benign
R3805:Fam169a UTSW 13 97,234,192 (GRCm39) missense probably benign 0.00
R4434:Fam169a UTSW 13 97,263,248 (GRCm39) missense probably damaging 1.00
R4435:Fam169a UTSW 13 97,263,248 (GRCm39) missense probably damaging 1.00
R4437:Fam169a UTSW 13 97,263,248 (GRCm39) missense probably damaging 1.00
R4590:Fam169a UTSW 13 97,234,093 (GRCm39) missense probably benign 0.02
R4896:Fam169a UTSW 13 97,234,100 (GRCm39) missense probably damaging 1.00
R5004:Fam169a UTSW 13 97,234,100 (GRCm39) missense probably damaging 1.00
R5276:Fam169a UTSW 13 97,255,004 (GRCm39) missense probably benign 0.01
R5370:Fam169a UTSW 13 97,243,470 (GRCm39) missense probably damaging 1.00
R5687:Fam169a UTSW 13 97,230,126 (GRCm39) missense probably damaging 1.00
R6151:Fam169a UTSW 13 97,230,138 (GRCm39) missense probably damaging 1.00
R7711:Fam169a UTSW 13 97,263,196 (GRCm39) nonsense probably null
R8322:Fam169a UTSW 13 97,259,260 (GRCm39) missense probably benign 0.00
R8493:Fam169a UTSW 13 97,259,367 (GRCm39) missense probably benign 0.00
R8698:Fam169a UTSW 13 97,243,578 (GRCm39) missense probably damaging 1.00
R8794:Fam169a UTSW 13 97,250,628 (GRCm39) missense possibly damaging 0.85
R9231:Fam169a UTSW 13 97,254,967 (GRCm39) missense probably benign 0.08
R9479:Fam169a UTSW 13 97,250,695 (GRCm39) missense possibly damaging 0.94
R9479:Fam169a UTSW 13 97,246,543 (GRCm39) missense possibly damaging 0.68
Posted On 2015-04-16