Incidental Mutation 'IGL03208:Fam149b'
ID 413210
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam149b
Ensembl Gene ENSMUSG00000039599
Gene Name family with sequence similarity 149, member B
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.287) question?
Stock # IGL03208
Quality Score
Status
Chromosome 14
Chromosomal Location 20398230-20433559 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 20401370 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153332 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022344] [ENSMUST00000037698] [ENSMUST00000051915] [ENSMUST00000090499] [ENSMUST00000090503] [ENSMUST00000223955] [ENSMUST00000224110] [ENSMUST00000224721] [ENSMUST00000224930] [ENSMUST00000225597] [ENSMUST00000225834] [ENSMUST00000225942] [ENSMUST00000225991] [ENSMUST00000224412]
AlphaFold Q6NSV7
Predicted Effect probably benign
Transcript: ENSMUST00000022344
SMART Domains Protein: ENSMUSP00000022344
Gene: ENSMUSG00000021810

DomainStartEndE-ValueType
Pfam:SGT1 14 597 4.4e-247 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000037698
SMART Domains Protein: ENSMUSP00000045247
Gene: ENSMUSG00000039599

DomainStartEndE-ValueType
Pfam:DUF3719 116 183 2.1e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000051915
SMART Domains Protein: ENSMUSP00000056907
Gene: ENSMUSG00000039599

DomainStartEndE-ValueType
Pfam:DUF3719 116 183 2.2e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000090499
SMART Domains Protein: ENSMUSP00000087985
Gene: ENSMUSG00000039599

DomainStartEndE-ValueType
Pfam:DUF3719 116 181 1.5e-28 PFAM
low complexity region 369 383 N/A INTRINSIC
low complexity region 404 415 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000090503
SMART Domains Protein: ENSMUSP00000087989
Gene: ENSMUSG00000039599

DomainStartEndE-ValueType
Pfam:DUF3719 116 157 5.7e-14 PFAM
low complexity region 276 290 N/A INTRINSIC
low complexity region 311 322 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000223955
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224079
Predicted Effect unknown
Transcript: ENSMUST00000224110
AA Change: I19T
Predicted Effect probably benign
Transcript: ENSMUST00000224721
Predicted Effect probably benign
Transcript: ENSMUST00000224930
Predicted Effect probably benign
Transcript: ENSMUST00000225597
Predicted Effect probably benign
Transcript: ENSMUST00000225834
Predicted Effect probably benign
Transcript: ENSMUST00000225942
Predicted Effect probably benign
Transcript: ENSMUST00000225991
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224242
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225114
Predicted Effect probably benign
Transcript: ENSMUST00000224412
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225487
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aco1 T C 4: 40,186,424 (GRCm39) V612A possibly damaging Het
Cd72 T A 4: 43,452,337 (GRCm39) T195S probably damaging Het
Cluh C A 11: 74,560,332 (GRCm39) probably null Het
Cntn3 T C 6: 102,164,060 (GRCm39) Y882C probably damaging Het
Ctnnal1 T A 4: 56,813,833 (GRCm39) K645N probably benign Het
Entpd6 T A 2: 150,610,838 (GRCm39) Y385N probably damaging Het
Epha3 T C 16: 63,431,452 (GRCm39) Y484C probably damaging Het
Exo1 G A 1: 175,723,811 (GRCm39) A386T probably benign Het
Fastkd2 G A 1: 63,778,365 (GRCm39) E413K probably damaging Het
Fbxl3 A T 14: 103,320,376 (GRCm39) L405* probably null Het
Gpr75 A T 11: 30,842,699 (GRCm39) I535F probably damaging Het
Irf2 A C 8: 47,260,340 (GRCm39) I53L probably damaging Het
Lca5l T C 16: 95,980,046 (GRCm39) E28G probably damaging Het
Mon2 A G 10: 122,853,974 (GRCm39) probably benign Het
Or10z1 A G 1: 174,077,959 (GRCm39) F178S probably damaging Het
Or52n4b T C 7: 108,144,326 (GRCm39) V196A probably benign Het
Plekhm1 T C 11: 103,267,596 (GRCm39) K792E probably benign Het
Ppp1r14c A T 10: 3,373,531 (GRCm39) D114V probably damaging Het
Rnf20 G T 4: 49,645,706 (GRCm39) probably benign Het
Srgap1 G A 10: 121,628,171 (GRCm39) P934S possibly damaging Het
Sult2b1 T C 7: 45,383,053 (GRCm39) E243G probably damaging Het
Tecta A G 9: 42,248,396 (GRCm39) probably benign Het
Tshr T C 12: 91,500,716 (GRCm39) L147P probably damaging Het
Vmn1r67 T A 7: 10,181,025 (GRCm39) S96R possibly damaging Het
Other mutations in Fam149b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01153:Fam149b APN 14 20,427,949 (GRCm39) missense possibly damaging 0.78
IGL02323:Fam149b APN 14 20,413,369 (GRCm39) missense possibly damaging 0.94
IGL02631:Fam149b APN 14 20,425,614 (GRCm39) missense probably damaging 0.97
R0334:Fam149b UTSW 14 20,413,492 (GRCm39) missense probably damaging 0.97
R2511:Fam149b UTSW 14 20,428,524 (GRCm39) missense probably damaging 1.00
R2566:Fam149b UTSW 14 20,425,578 (GRCm39) missense probably damaging 0.97
R4659:Fam149b UTSW 14 20,417,941 (GRCm39) missense probably benign 0.16
R5011:Fam149b UTSW 14 20,413,439 (GRCm39) missense possibly damaging 0.92
R5013:Fam149b UTSW 14 20,413,439 (GRCm39) missense possibly damaging 0.92
R5583:Fam149b UTSW 14 20,413,368 (GRCm39) missense possibly damaging 0.66
R5791:Fam149b UTSW 14 20,401,394 (GRCm39) missense probably damaging 0.96
R5905:Fam149b UTSW 14 20,409,978 (GRCm39) missense probably benign 0.30
R6035:Fam149b UTSW 14 20,427,985 (GRCm39) missense probably damaging 1.00
R6035:Fam149b UTSW 14 20,427,985 (GRCm39) missense probably damaging 1.00
R7180:Fam149b UTSW 14 20,431,853 (GRCm39) missense probably benign 0.01
R7210:Fam149b UTSW 14 20,428,540 (GRCm39) missense probably damaging 0.99
R7976:Fam149b UTSW 14 20,427,852 (GRCm39) missense probably damaging 0.98
R8529:Fam149b UTSW 14 20,408,370 (GRCm39) splice site probably null
R8971:Fam149b UTSW 14 20,402,777 (GRCm39) missense probably benign 0.30
R9743:Fam149b UTSW 14 20,413,411 (GRCm39) missense probably benign 0.05
Posted On 2016-08-02