Incidental Mutation 'IGL02882:Fam91a1'
ID 362857
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam91a1
Ensembl Gene ENSMUSG00000037119
Gene Name family with sequence similarity 91, member A1
Synonyms D15Ertd621e
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02882
Quality Score
Status
Chromosome 15
Chromosomal Location 58287317-58329589 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 58324910 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000036524 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037270]
AlphaFold Q3UVG3
Predicted Effect probably benign
Transcript: ENSMUST00000037270
SMART Domains Protein: ENSMUSP00000036524
Gene: ENSMUSG00000037119

DomainStartEndE-ValueType
Pfam:FAM91_N 8 312 2.8e-149 PFAM
Pfam:FAM91_C 374 821 3.8e-182 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228576
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit male infertility. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg4 A T 9: 44,188,786 (GRCm39) L469* probably null Het
Calr3 T A 8: 73,188,665 (GRCm39) Y46F probably damaging Het
Clcn4 A G 7: 7,293,464 (GRCm39) C491R probably damaging Het
Col6a5 G T 9: 105,811,520 (GRCm39) D666E unknown Het
D130052B06Rik G A 11: 33,573,780 (GRCm39) V126M probably damaging Het
Ddx27 A G 2: 166,869,833 (GRCm39) I389M possibly damaging Het
Dgka T C 10: 128,569,253 (GRCm39) I160V possibly damaging Het
Enpp6 T C 8: 47,483,567 (GRCm39) S120P probably damaging Het
Ezh1 A G 11: 101,094,115 (GRCm39) I459T probably benign Het
Foxn2 T C 17: 88,770,375 (GRCm39) L74P probably damaging Het
Fscn2 T C 11: 120,253,325 (GRCm39) V264A probably benign Het
Gmeb2 G A 2: 180,907,676 (GRCm39) T54I probably damaging Het
Hmcn2 A T 2: 31,303,379 (GRCm39) K3007* probably null Het
Ice1 A T 13: 70,772,593 (GRCm39) probably benign Het
Lgi1 A G 19: 38,272,453 (GRCm39) D84G probably benign Het
Mier2 T C 10: 79,383,555 (GRCm39) I196V probably damaging Het
Nipal2 T C 15: 34,600,223 (GRCm39) Y198C probably damaging Het
Npas2 A C 1: 39,352,077 (GRCm39) S176R probably benign Het
Or8b50 A T 9: 38,518,234 (GRCm39) I158F probably benign Het
Pam A C 1: 97,768,092 (GRCm39) C713G probably damaging Het
Pcdh17 C A 14: 84,684,101 (GRCm39) D189E probably damaging Het
Pcdhb8 T A 18: 37,489,276 (GRCm39) I318N possibly damaging Het
Pcyt2 A G 11: 120,502,233 (GRCm39) S300P possibly damaging Het
Pkdrej A G 15: 85,701,497 (GRCm39) S1480P probably damaging Het
Plekhd1 G A 12: 80,765,781 (GRCm39) probably null Het
Plxna2 A T 1: 194,444,878 (GRCm39) S757C probably damaging Het
Prkdc A T 16: 15,469,383 (GRCm39) K163* probably null Het
Serpina3f A T 12: 104,183,263 (GRCm39) T42S probably damaging Het
Sesn2 T C 4: 132,221,104 (GRCm39) N456D probably benign Het
Tas2r105 A T 6: 131,664,143 (GRCm39) L95Q possibly damaging Het
Tln1 A G 4: 43,539,522 (GRCm39) V1600A probably benign Het
Zfp764l1 A G 7: 126,991,424 (GRCm39) Y188H probably damaging Het
Zfp808 A G 13: 62,320,994 (GRCm39) K741R probably benign Het
Other mutations in Fam91a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00090:Fam91a1 APN 15 58,302,584 (GRCm39) missense probably damaging 0.99
IGL00590:Fam91a1 APN 15 58,287,565 (GRCm39) missense possibly damaging 0.66
IGL01301:Fam91a1 APN 15 58,314,720 (GRCm39) missense probably damaging 0.99
IGL01372:Fam91a1 APN 15 58,301,911 (GRCm39) missense probably damaging 1.00
IGL01979:Fam91a1 APN 15 58,304,433 (GRCm39) missense probably damaging 1.00
IGL02085:Fam91a1 APN 15 58,313,505 (GRCm39) missense possibly damaging 0.95
IGL02553:Fam91a1 APN 15 58,304,831 (GRCm39) critical splice donor site probably null
IGL02605:Fam91a1 APN 15 58,303,045 (GRCm39) splice site probably benign
IGL02894:Fam91a1 APN 15 58,315,080 (GRCm39) missense probably benign 0.09
ANU18:Fam91a1 UTSW 15 58,314,720 (GRCm39) missense probably damaging 0.99
H8562:Fam91a1 UTSW 15 58,298,970 (GRCm39) splice site probably null
R0395:Fam91a1 UTSW 15 58,326,641 (GRCm39) missense probably benign
R1165:Fam91a1 UTSW 15 58,302,518 (GRCm39) missense possibly damaging 0.90
R1699:Fam91a1 UTSW 15 58,304,797 (GRCm39) missense probably benign 0.04
R1749:Fam91a1 UTSW 15 58,298,443 (GRCm39) missense probably benign 0.02
R1997:Fam91a1 UTSW 15 58,296,044 (GRCm39) critical splice acceptor site probably null
R2042:Fam91a1 UTSW 15 58,298,443 (GRCm39) missense probably benign 0.02
R2188:Fam91a1 UTSW 15 58,302,512 (GRCm39) missense probably damaging 0.98
R2518:Fam91a1 UTSW 15 58,322,449 (GRCm39) missense possibly damaging 0.92
R3124:Fam91a1 UTSW 15 58,293,738 (GRCm39) missense probably benign 0.34
R3916:Fam91a1 UTSW 15 58,302,583 (GRCm39) missense probably damaging 1.00
R4810:Fam91a1 UTSW 15 58,306,589 (GRCm39) missense probably damaging 1.00
R4959:Fam91a1 UTSW 15 58,303,059 (GRCm39) missense probably benign 0.16
R4973:Fam91a1 UTSW 15 58,303,059 (GRCm39) missense probably benign 0.16
R5288:Fam91a1 UTSW 15 58,320,243 (GRCm39) missense probably benign
R5385:Fam91a1 UTSW 15 58,320,243 (GRCm39) missense probably benign
R5386:Fam91a1 UTSW 15 58,320,243 (GRCm39) missense probably benign
R5941:Fam91a1 UTSW 15 58,303,166 (GRCm39) missense probably benign 0.01
R6415:Fam91a1 UTSW 15 58,314,766 (GRCm39) missense probably damaging 1.00
R6869:Fam91a1 UTSW 15 58,303,117 (GRCm39) missense probably benign 0.00
R7175:Fam91a1 UTSW 15 58,302,527 (GRCm39) missense probably benign 0.06
R7872:Fam91a1 UTSW 15 58,320,209 (GRCm39) missense probably benign 0.01
X0024:Fam91a1 UTSW 15 58,302,038 (GRCm39) missense probably damaging 0.98
Z1177:Fam91a1 UTSW 15 58,304,397 (GRCm39) missense possibly damaging 0.68
Posted On 2015-12-18