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)
|
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
Domain | Start | End | E-Value | Type |
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
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
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 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |