Incidental Mutation 'IGL01761:Fam169a'
ID 153578
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 # IGL01761
Quality Score
Status
Chromosome 13
Chromosomal Location 97203795-97266801 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 97228426 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 33 (E33G)
Ref Sequence ENSEMBL: ENSMUSP00000126209 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042517] [ENSMUST00000169863]
AlphaFold Q5XG69
Predicted Effect possibly damaging
Transcript: ENSMUST00000042517
AA Change: E33G

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000043738
Gene: ENSMUSG00000041817
AA Change: E33G

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 possibly damaging
Transcript: ENSMUST00000169863
AA Change: E33G

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000126209
Gene: ENSMUSG00000041817
AA Change: E33G

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: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2410137M14Rik T C 17: 37,289,699 (GRCm39) T44A probably damaging Het
A2ml1 T A 6: 128,523,300 (GRCm39) Q1212L possibly damaging Het
A530064D06Rik T C 17: 48,460,127 (GRCm39) S190G possibly damaging Het
AA986860 A G 1: 130,670,459 (GRCm39) H227R possibly damaging Het
Ace C A 11: 105,870,319 (GRCm39) A826E possibly damaging Het
Amigo3 G A 9: 107,930,601 (GRCm39) G8D possibly damaging Het
Angpt1 A T 15: 42,339,863 (GRCm39) F283I possibly damaging Het
Arhgef5 T C 6: 43,251,538 (GRCm39) L763P probably benign Het
Atr T C 9: 95,833,501 (GRCm39) probably benign Het
C4b T A 17: 34,958,912 (GRCm39) M506L possibly damaging Het
Cdc25a T C 9: 109,720,933 (GRCm39) probably benign Het
Dcaf17 T C 2: 70,886,881 (GRCm39) S57P probably damaging Het
Dph5 T A 3: 115,693,362 (GRCm39) D93E probably damaging Het
Fam193b G A 13: 55,697,070 (GRCm39) T340I probably benign Het
Glod4 T C 11: 76,134,428 (GRCm39) N15D probably benign Het
Hrob T C 11: 102,146,422 (GRCm39) C233R probably benign Het
Inpp5k A G 11: 75,538,503 (GRCm39) E102G possibly damaging Het
Kif27 A T 13: 58,485,459 (GRCm39) D500E probably benign Het
Lmntd1 A G 6: 145,379,448 (GRCm39) I15T possibly damaging Het
Lrp2 C T 2: 69,311,579 (GRCm39) R2633H possibly damaging Het
Lrp4 G A 2: 91,312,326 (GRCm39) probably null Het
Lrrc3b A C 14: 15,358,098 (GRCm38) N169K probably benign Het
Marchf7 T C 2: 60,064,539 (GRCm39) S272P probably benign Het
Mier2 A G 10: 79,384,186 (GRCm39) probably null Het
Myo9b G A 8: 71,801,796 (GRCm39) S1307N probably damaging Het
Or4c115 G T 2: 88,927,888 (GRCm39) P128T probably damaging Het
Or5p69 T G 7: 107,967,525 (GRCm39) V276G probably damaging Het
Phkb A T 8: 86,745,693 (GRCm39) M629L probably benign Het
Rergl C A 6: 139,478,863 (GRCm39) V4F probably damaging Het
Rgs22 A T 15: 36,103,897 (GRCm39) I188N probably damaging Het
Rgs3 G T 4: 62,570,946 (GRCm39) probably benign Het
Rpl4 T A 9: 64,082,221 (GRCm39) V40D probably damaging Het
Sox4 A T 13: 29,136,790 (GRCm39) I72N possibly damaging Het
Syne1 A C 10: 5,355,456 (GRCm39) V375G probably damaging Het
Tfrc G T 16: 32,447,369 (GRCm39) D662Y probably damaging Het
Ubqln5 T C 7: 103,777,634 (GRCm39) R397G possibly damaging Het
Unc13d T C 11: 115,964,695 (GRCm39) D257G probably damaging Het
Vmn1r160 A T 7: 22,570,868 (GRCm39) N74Y probably damaging Het
Vmn1r168 T A 7: 23,241,070 (GRCm39) I309N possibly damaging Het
Vmn1r20 T C 6: 57,408,725 (GRCm39) L17P probably damaging Het
Wdr19 A G 5: 65,373,163 (GRCm39) I142V possibly damaging Het
Zan A T 5: 137,423,859 (GRCm39) I2680N unknown Het
Zbtb20 T C 16: 43,431,024 (GRCm39) F512L possibly 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
IGL02628:Fam169a APN 13 97,247,796 (GRCm39) splice site probably benign
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 2014-02-04