Incidental Mutation 'IGL03062:Fam83a'
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ID409522
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam83a
Ensembl Gene ENSMUSG00000051225
Gene Namefamily with sequence similarity 83, member A
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.051) question?
Stock #IGL03062
Quality Score
Status
Chromosome15
Chromosomal Location57985419-58011009 bp(+) (GRCm38)
Type of Mutationsplice site (3 bp from exon)
DNA Base Change (assembly) A to T at 57993077 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000125464 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050374] [ENSMUST00000160942]
Predicted Effect probably null
Transcript: ENSMUST00000050374
SMART Domains Protein: ENSMUSP00000050051
Gene: ENSMUSG00000051225

DomainStartEndE-ValueType
Pfam:DUF1669 14 258 6e-85 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000160942
SMART Domains Protein: ENSMUSP00000125464
Gene: ENSMUSG00000051225

DomainStartEndE-ValueType
Pfam:DUF1669 19 295 3.6e-102 PFAM
low complexity region 350 361 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik T C 3: 37,038,517 probably benign Het
Abcb10 C T 8: 123,954,315 R714Q possibly damaging Het
Abcb5 T A 12: 118,936,087 I282L probably benign Het
Aox1 A T 1: 58,078,465 E835D probably benign Het
Arhgap17 C T 7: 123,321,874 probably null Het
Calcr C T 6: 3,693,718 V359I probably benign Het
Chd9 T A 8: 91,015,267 probably benign Het
Col28a1 T C 6: 8,017,029 probably benign Het
Dnajc11 A G 4: 151,970,861 E171G possibly damaging Het
Efhd1 T C 1: 87,264,684 F79L possibly damaging Het
Fam98a A G 17: 75,540,105 probably benign Het
Ficd A G 5: 113,738,253 Y163C probably damaging Het
Filip1l T C 16: 57,506,804 S66P probably damaging Het
Fmo5 A G 3: 97,635,593 Y73C probably damaging Het
Galnt12 C A 4: 47,122,566 R574S possibly damaging Het
Klc3 C A 7: 19,395,062 G461W probably damaging Het
Lmo7 A T 14: 101,912,079 T973S possibly damaging Het
Loxl1 C A 9: 58,311,910 G326V possibly damaging Het
Lrrc24 A G 15: 76,718,304 V127A probably benign Het
Lyrm1 T C 7: 119,916,131 probably benign Het
Med28 G A 5: 45,522,469 V65I probably damaging Het
Mgat4c T C 10: 102,388,461 Y179H probably damaging Het
Micall1 A C 15: 79,114,681 N58T probably damaging Het
Ncoa4 T A 14: 32,173,420 M72K possibly damaging Het
Nutm1 T C 2: 112,248,933 Q879R probably benign Het
Olfr1428 C T 19: 12,109,148 V133I probably benign Het
Olfr870 T A 9: 20,171,167 I135F probably damaging Het
Olfr965 T A 9: 39,720,035 D269E probably benign Het
Phf11b T C 14: 59,324,924 I177M probably damaging Het
Pin1rt1 T G 2: 104,714,707 I27L probably benign Het
Plxna2 T C 1: 194,762,550 V750A possibly damaging Het
Pou5f1 A T 17: 35,510,039 N126I possibly damaging Het
Ptprn A T 1: 75,247,873 H946Q possibly damaging Het
Rnf43 G T 11: 87,732,304 G744* probably null Het
Rsbn1 C A 3: 103,953,629 probably benign Het
Sars2 T A 7: 28,746,781 I145N possibly damaging Het
Sh3tc2 A T 18: 62,011,880 E1135V probably damaging Het
Shroom1 A G 11: 53,463,379 D42G probably benign Het
Sidt2 A G 9: 45,942,683 probably null Het
Slc39a8 T C 3: 135,886,797 probably benign Het
Slc9c1 T C 16: 45,599,758 S1059P probably benign Het
Socs6 A T 18: 88,869,846 M315K probably benign Het
Soga3 T A 10: 29,198,949 F911Y probably damaging Het
Speer2 T C 16: 69,857,977 E200G probably damaging Het
Sult2a5 T A 7: 13,624,182 probably null Het
Tmbim1 A T 1: 74,291,699 I168N possibly damaging Het
Trim38 T C 13: 23,782,963 V131A probably damaging Het
Ube2o A G 11: 116,541,642 S833P probably damaging Het
Uggt2 T C 14: 119,075,346 I350M probably damaging Het
Unc80 A G 1: 66,509,489 D640G probably damaging Het
Vmn2r13 A G 5: 109,156,282 F761S probably damaging Het
Vmn2r54 C T 7: 12,632,428 C193Y probably damaging Het
Other mutations in Fam83a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01061:Fam83a APN 15 57986375 missense possibly damaging 0.91
IGL01328:Fam83a APN 15 57986505 missense probably damaging 1.00
IGL01590:Fam83a APN 15 58009777 missense probably damaging 1.00
IGL02306:Fam83a APN 15 57995308 missense probably damaging 1.00
R0110:Fam83a UTSW 15 58009926 missense probably benign 0.09
R0450:Fam83a UTSW 15 58009926 missense probably benign 0.09
R0469:Fam83a UTSW 15 58009926 missense probably benign 0.09
R0533:Fam83a UTSW 15 58009811 missense probably benign 0.43
R1210:Fam83a UTSW 15 57995248 missense possibly damaging 0.95
R1386:Fam83a UTSW 15 57986503 missense probably damaging 1.00
R1474:Fam83a UTSW 15 58009876 missense probably benign 0.02
R1476:Fam83a UTSW 15 58009945 missense probably benign 0.00
R1969:Fam83a UTSW 15 57986102 missense probably damaging 1.00
R4463:Fam83a UTSW 15 57995259 missense probably damaging 1.00
R5088:Fam83a UTSW 15 58009800 missense probably benign 0.00
R5961:Fam83a UTSW 15 58009596 missense possibly damaging 0.90
R6307:Fam83a UTSW 15 57986111 missense possibly damaging 0.93
R6524:Fam83a UTSW 15 57995340 critical splice donor site probably null
R6676:Fam83a UTSW 15 57993043 missense possibly damaging 0.91
R7412:Fam83a UTSW 15 57986425 missense probably benign
R7447:Fam83a UTSW 15 58009690 missense probably benign 0.00
R7493:Fam83a UTSW 15 57986173 missense probably damaging 1.00
X0023:Fam83a UTSW 15 58009605 missense possibly damaging 0.72
Posted On2016-08-02