Incidental Mutation 'IGL02980:Fam169a'
ID 392153
Institutional Source Beutler Lab
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 # IGL02980 (G1)
Quality Score 92
Status Validated
Chromosome 13
Chromosomal Location 97203795-97266801 bp(+) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 97250188 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 null
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 null
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
Meta Mutation Damage Score 0.9490 question?
Coding Region Coverage
  • 1x: 0.0%
  • 3x: 0.0%
  • 10x: 0.0%
  • 20x: 0.0%
Validation Efficiency 97% (35/36)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr1b A G 15: 101,100,959 (GRCm39) R374G probably damaging Het
Adam28 A T 14: 68,857,255 (GRCm39) S584T probably benign Het
Akap1 A T 11: 88,735,990 (GRCm39) I224N probably benign Het
Ankdd1b C T 13: 96,572,448 (GRCm39) R214Q probably benign Het
Armt1 A G 10: 4,400,643 (GRCm39) probably benign Het
C1rl T C 6: 124,485,487 (GRCm39) I286T probably benign Het
Cdh23 T C 10: 60,150,399 (GRCm39) T2528A probably damaging Het
Col4a4 A G 1: 82,447,198 (GRCm39) probably null Het
Dag1 A G 9: 108,095,237 (GRCm39) I85T probably benign Het
Elf2 A G 3: 51,172,379 (GRCm39) V86A possibly damaging Het
Emsy T C 7: 98,268,587 (GRCm39) T485A probably damaging Het
Hsd17b4 A G 18: 50,279,585 (GRCm39) H188R probably benign Het
Ighv9-2 C T 12: 114,072,839 (GRCm39) V45M probably damaging Het
Kifbp A C 10: 62,394,947 (GRCm39) L565W probably damaging Het
Lama3 C T 18: 12,686,288 (GRCm39) L2784F probably benign Het
Ms4a4c G T 19: 11,393,747 (GRCm39) A64S probably benign Het
Nudt22 A G 19: 6,970,500 (GRCm39) L280P probably damaging Het
Oscar T C 7: 3,614,062 (GRCm39) probably benign Het
Paics A G 5: 77,114,102 (GRCm39) I321V probably benign Het
Pappa A T 4: 65,226,011 (GRCm39) H1288L probably benign Het
Pla2r1 T C 2: 60,345,390 (GRCm39) E322G possibly damaging Het
Poldip2 T A 11: 78,412,054 (GRCm39) M330K probably damaging Het
Potefam1 G A 2: 110,994,818 (GRCm39) H232Y unknown Het
Recql5 T C 11: 115,784,770 (GRCm39) probably null Het
Rnf145 A G 11: 44,452,484 (GRCm39) M488V probably benign Het
Rrp1b T A 17: 32,269,013 (GRCm39) D170E possibly damaging Het
Slamf7 T C 1: 171,468,566 (GRCm39) S109G possibly damaging Het
Slf1 A G 13: 77,192,123 (GRCm39) S904P possibly damaging Het
St7 C A 6: 17,749,545 (GRCm39) probably benign Het
Stk25 A G 1: 93,555,390 (GRCm39) S102P probably damaging Het
Supt6 C T 11: 78,116,548 (GRCm39) A659T probably damaging Het
Tdrp A C 8: 14,003,918 (GRCm39) S140A probably damaging Het
Thbs3 A G 3: 89,130,451 (GRCm39) N527D probably benign Het
Tsnaxip1 G T 8: 106,568,842 (GRCm39) V444L probably damaging Het
U2af2 A G 7: 5,071,042 (GRCm39) I116V probably benign Het
Zfp931 C A 2: 177,711,409 (GRCm39) probably null 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
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
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
Predicted Primers PCR Primer
(F):5'- TTAGGCTTATAATGAACCAAGGGC -3'
(R):5'- GGGTCACTGTGTCTACACTCTC -3'

Sequencing Primer
(F):5'- GCTTATAATGAACCAAGGGCTATAAC -3'
(R):5'- CCATGTTCTCTCTTACTGTTGTTGGG -3'
Posted On 2016-06-09