Incidental Mutation 'IGL02605:Fam91a1'
ID 300252
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 # IGL02605
Quality Score
Status
Chromosome 15
Chromosomal Location 58287317-58329589 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 58303045 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: ENSMUST00000227770
Predicted Effect noncoding transcript
Transcript: ENSMUST00000227796
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abtb2 A T 2: 103,547,602 (GRCm39) Y992F probably benign Het
Adgrg6 T A 10: 14,342,976 (GRCm39) N324Y probably damaging Het
Ampd3 T C 7: 110,394,965 (GRCm39) F305L probably benign Het
Ankrd35 A G 3: 96,588,388 (GRCm39) probably null Het
Api5 A G 2: 94,260,064 (GRCm39) I64T possibly damaging Het
Arhgap21 A G 2: 20,860,399 (GRCm39) I1165T probably damaging Het
Bdp1 T C 13: 100,214,623 (GRCm39) probably null Het
Capn3 T A 2: 120,326,518 (GRCm39) I570N probably damaging Het
Catsperg2 T C 7: 29,418,990 (GRCm39) H232R possibly damaging Het
Clcn7 T C 17: 25,365,792 (GRCm39) L156P possibly damaging Het
Cpa3 C A 3: 20,276,376 (GRCm39) V286F probably benign Het
Csrnp3 G A 2: 65,853,153 (GRCm39) C527Y probably damaging Het
Dock5 A T 14: 68,065,887 (GRCm39) V372E probably benign Het
Elmo1 T C 13: 20,789,372 (GRCm39) L696P probably damaging Het
Gm12695 T A 4: 96,650,988 (GRCm39) D155V probably null Het
Hspa4l A G 3: 40,736,055 (GRCm39) I559V probably benign Het
Kdm1a G T 4: 136,278,348 (GRCm39) probably benign Het
Lrrc8d A T 5: 105,974,683 (GRCm39) noncoding transcript Het
Minpp1 A T 19: 32,475,815 (GRCm39) Y316F possibly damaging Het
Neto2 T C 8: 86,390,064 (GRCm39) probably benign Het
Nrxn2 T A 19: 6,500,610 (GRCm39) D277E probably benign Het
Ola1 A G 2: 72,972,644 (GRCm39) probably benign Het
Or4k48 A G 2: 111,475,850 (GRCm39) V164A probably benign Het
Or51r1 T C 7: 102,228,602 (GRCm39) I300T probably damaging Het
Or8c15 T A 9: 38,120,532 (GRCm39) M61K probably damaging Het
Pam A G 1: 97,768,064 (GRCm39) V722A possibly damaging Het
Pfdn6 T C 17: 34,158,077 (GRCm39) Y90C probably benign Het
Pkhd1 T A 1: 20,621,126 (GRCm39) H844L possibly damaging Het
Plk5 G A 10: 80,198,896 (GRCm39) V422M probably damaging Het
Psmc1 G T 12: 100,085,386 (GRCm39) R249L probably damaging Het
Ptpro C T 6: 137,357,316 (GRCm39) P269L probably benign Het
Ralgapa1 G T 12: 55,759,450 (GRCm39) H1480Q possibly damaging Het
Rars1 G A 11: 35,715,353 (GRCm39) probably benign Het
Rbm48 G A 5: 3,640,600 (GRCm39) R260C possibly damaging Het
Smarcc1 C T 9: 110,051,068 (GRCm39) H963Y possibly damaging Het
Spef2 T C 15: 9,725,238 (GRCm39) E230G probably damaging Het
Spg11 A G 2: 121,922,741 (GRCm39) S903P probably benign Het
Tas2r122 T C 6: 132,688,572 (GRCm39) Y107C probably damaging Het
Tpm3 C A 3: 89,995,753 (GRCm39) N204K probably benign Het
Wdr36 T C 18: 32,985,044 (GRCm39) I450T possibly damaging 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
IGL02882:Fam91a1 APN 15 58,324,910 (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 2015-04-16