Incidental Mutation 'R5139:Trf'
| ID |
396353 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Trf
|
| Ensembl Gene |
ENSMUSG00000032554 |
| Gene Name |
transferrin |
| Synonyms |
HP, Tfn |
| MMRRC Submission |
042725-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R5139 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
103086075-103107485 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (1 bp from exon) |
| DNA Base Change (assembly) |
C to T
at 103100133 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000127808
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035158]
[ENSMUST00000112645]
[ENSMUST00000126359]
[ENSMUST00000164377]
[ENSMUST00000165296]
[ENSMUST00000166836]
[ENSMUST00000170904]
|
| AlphaFold |
Q921I1 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000035158
|
| SMART Domains |
Protein: ENSMUSP00000035158
Gene: ENSMUSG00000032554
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
TR_FER
|
25 |
352 |
5.04e-194 |
SMART |
|
TR_FER
|
360 |
686 |
8.64e-193 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000112503
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000112645
|
| SMART Domains |
Protein: ENSMUSP00000108264
Gene: ENSMUSG00000032554
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
TR_FER
|
25 |
352 |
5.04e-194 |
SMART |
|
TR_FER
|
360 |
686 |
8.64e-193 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000126359
|
| SMART Domains |
Protein: ENSMUSP00000120472
Gene: ENSMUSG00000032554
| Domain | Start | End | E-Value | Type |
|---|
|
TR_FER
|
22 |
237 |
2.25e-77 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000164377
|
| SMART Domains |
Protein: ENSMUSP00000128647
Gene: ENSMUSG00000032554
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
Pfam:Transferrin
|
25 |
72 |
6.6e-15 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000165296
|
| SMART Domains |
Protein: ENSMUSP00000129013
Gene: ENSMUSG00000032554
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
TR_FER
|
25 |
171 |
5.58e-15 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000166836
|
| SMART Domains |
Protein: ENSMUSP00000127808
Gene: ENSMUSG00000090639
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
19 |
N/A |
INTRINSIC |
|
TR_FER
|
25 |
338 |
4.98e-175 |
SMART |
|
TR_FER
|
346 |
672 |
8.64e-193 |
SMART |
|
Pfam:Arf
|
758 |
928 |
1.5e-15 |
PFAM |
|
Pfam:SRPRB
|
769 |
948 |
1.4e-73 |
PFAM |
|
Pfam:MMR_HSR1
|
773 |
888 |
7.8e-8 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000170904
|
| SMART Domains |
Protein: ENSMUSP00000128390
Gene: ENSMUSG00000032554
| Domain | Start | End | E-Value | Type |
|---|
|
TR_FER
|
15 |
275 |
7.6e-139 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000168142
|
| SMART Domains |
Protein: ENSMUSP00000128609
Gene: ENSMUSG00000032554
| Domain | Start | End | E-Value | Type |
|---|
|
TR_FER
|
2 |
249 |
1.87e-115 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 96.9%
- 20x: 94.0%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009]
PHENOTYPE: Homozygotes for a spontaneous mutation exhibit refractory iron-deficient, hypochromic, microcytic anemia with iron-loading in the liver, pancreas, heart and brain. Mutants usually die by two weeks of age. Heterozygotes show minor increases in iron stores. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2510039O18Rik |
T |
C |
4: 148,029,905 (GRCm39) |
L625P |
probably damaging |
Het |
| Agtpbp1 |
A |
G |
13: 59,648,027 (GRCm39) |
S598P |
probably damaging |
Het |
| Ahnak |
A |
C |
19: 8,982,019 (GRCm39) |
D1101A |
probably damaging |
Het |
| Aoah |
T |
C |
13: 21,207,407 (GRCm39) |
V542A |
possibly damaging |
Het |
| Aox1 |
T |
C |
1: 58,100,456 (GRCm39) |
S418P |
probably benign |
Het |
| Appl1 |
A |
G |
14: 26,669,112 (GRCm39) |
I354T |
probably benign |
Het |
| BC035947 |
T |
C |
1: 78,475,884 (GRCm39) |
E216G |
possibly damaging |
Het |
| Bnip3l |
A |
G |
14: 67,237,064 (GRCm39) |
S63P |
probably damaging |
Het |
| Cckar |
T |
C |
5: 53,860,265 (GRCm39) |
N188S |
probably benign |
Het |
| Ccl24 |
C |
T |
5: 135,601,775 (GRCm39) |
A18T |
probably benign |
Het |
| Cmya5 |
A |
G |
13: 93,232,569 (GRCm39) |
C840R |
probably benign |
Het |
| Copa |
C |
T |
1: 171,948,896 (GRCm39) |
R1183W |
probably damaging |
Het |
| Dnah10 |
T |
C |
5: 124,876,024 (GRCm39) |
V2621A |
probably damaging |
Het |
| Fryl |
A |
G |
5: 73,248,061 (GRCm39) |
Y1019H |
probably damaging |
Het |
| Hira |
T |
C |
16: 18,773,508 (GRCm39) |
Y943H |
probably damaging |
Het |
| Ighv3-8 |
T |
C |
12: 114,285,994 (GRCm39) |
Y116C |
probably damaging |
Het |
| Igkv4-70 |
G |
A |
6: 69,245,089 (GRCm39) |
T44I |
probably damaging |
Het |
| Lce3c |
G |
A |
3: 92,852,778 (GRCm39) |
G80S |
unknown |
Het |
| Ldhb |
A |
T |
6: 142,439,921 (GRCm39) |
N206K |
probably damaging |
Het |
| Mical1 |
T |
A |
10: 41,354,411 (GRCm39) |
|
probably null |
Het |
| Myh2 |
T |
C |
11: 67,070,174 (GRCm39) |
L402P |
probably damaging |
Het |
| Naa15 |
T |
A |
3: 51,351,261 (GRCm39) |
L144I |
probably damaging |
Het |
| Nbea |
T |
A |
3: 55,534,384 (GRCm39) |
I2918F |
possibly damaging |
Het |
| Or5w11 |
C |
A |
2: 87,459,000 (GRCm39) |
H64Q |
probably benign |
Het |
| Pdcd11 |
C |
A |
19: 47,095,554 (GRCm39) |
S625R |
probably benign |
Het |
| Pdlim7 |
A |
G |
13: 55,654,869 (GRCm39) |
S214P |
probably damaging |
Het |
| Polg |
T |
C |
7: 79,099,773 (GRCm39) |
D49G |
probably damaging |
Het |
| Polr2f |
C |
A |
15: 79,035,858 (GRCm39) |
D106E |
possibly damaging |
Het |
| Ppp6r3 |
A |
C |
19: 3,514,610 (GRCm39) |
N766K |
probably damaging |
Het |
| Prl8a1 |
T |
A |
13: 27,758,049 (GRCm39) |
D220V |
probably damaging |
Het |
| Qrfprl |
A |
T |
6: 65,433,203 (GRCm39) |
N341I |
probably damaging |
Het |
| Septin9 |
A |
G |
11: 117,247,511 (GRCm39) |
K497E |
possibly damaging |
Het |
| Sfswap |
T |
G |
5: 129,648,073 (GRCm39) |
M927R |
possibly damaging |
Het |
| Smad9 |
T |
G |
3: 54,704,827 (GRCm39) |
W400G |
possibly damaging |
Het |
| St13 |
G |
C |
15: 81,283,786 (GRCm39) |
R4G |
probably benign |
Het |
| Tcaf3 |
A |
G |
6: 42,573,867 (GRCm39) |
V115A |
probably benign |
Het |
| Tesmin |
A |
G |
19: 3,456,934 (GRCm39) |
I238V |
probably damaging |
Het |
| Trpc3 |
A |
T |
3: 36,725,706 (GRCm39) |
M90K |
possibly damaging |
Het |
| Tshz3 |
C |
T |
7: 36,470,450 (GRCm39) |
T813I |
probably benign |
Het |
| Tub |
T |
A |
7: 108,610,309 (GRCm39) |
M1K |
probably null |
Het |
| Wdfy3 |
A |
T |
5: 101,997,133 (GRCm39) |
|
probably null |
Het |
| Zfp853 |
T |
C |
5: 143,274,570 (GRCm39) |
Q350R |
unknown |
Het |
|
| Other mutations in Trf |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00156:Trf
|
APN |
9 |
103,098,156 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00424:Trf
|
APN |
9 |
103,104,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00793:Trf
|
APN |
9 |
103,103,342 (GRCm39) |
unclassified |
probably benign |
|
|
IGL01139:Trf
|
APN |
9 |
103,100,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01658:Trf
|
APN |
9 |
103,104,055 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02671:Trf
|
APN |
9 |
103,089,181 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02996:Trf
|
APN |
9 |
103,098,102 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0060:Trf
|
UTSW |
9 |
103,098,121 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0060:Trf
|
UTSW |
9 |
103,098,121 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0096:Trf
|
UTSW |
9 |
103,099,358 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0096:Trf
|
UTSW |
9 |
103,099,358 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0112:Trf
|
UTSW |
9 |
103,104,155 (GRCm39) |
unclassified |
probably benign |
|
|
R0234:Trf
|
UTSW |
9 |
103,104,078 (GRCm39) |
splice site |
probably null |
|
|
R0234:Trf
|
UTSW |
9 |
103,104,078 (GRCm39) |
splice site |
probably null |
|
|
R0411:Trf
|
UTSW |
9 |
103,094,700 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0456:Trf
|
UTSW |
9 |
103,104,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0601:Trf
|
UTSW |
9 |
103,100,132 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1419:Trf
|
UTSW |
9 |
103,103,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1606:Trf
|
UTSW |
9 |
103,102,335 (GRCm39) |
splice site |
probably null |
|
|
R3943:Trf
|
UTSW |
9 |
103,100,151 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4431:Trf
|
UTSW |
9 |
103,089,075 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4609:Trf
|
UTSW |
9 |
103,089,184 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4658:Trf
|
UTSW |
9 |
103,100,807 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4830:Trf
|
UTSW |
9 |
103,105,114 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4925:Trf
|
UTSW |
9 |
103,096,445 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4929:Trf
|
UTSW |
9 |
103,105,074 (GRCm39) |
intron |
probably benign |
|
|
R4931:Trf
|
UTSW |
9 |
103,105,247 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5272:Trf
|
UTSW |
9 |
103,105,177 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5692:Trf
|
UTSW |
9 |
103,103,324 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6227:Trf
|
UTSW |
9 |
103,107,504 (GRCm39) |
start gained |
probably benign |
|
|
R6365:Trf
|
UTSW |
9 |
103,099,327 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6928:Trf
|
UTSW |
9 |
103,099,307 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R7127:Trf
|
UTSW |
9 |
103,102,326 (GRCm39) |
missense |
probably benign |
|
|
R7231:Trf
|
UTSW |
9 |
103,102,347 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7648:Trf
|
UTSW |
9 |
103,105,168 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8088:Trf
|
UTSW |
9 |
103,089,130 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8095:Trf
|
UTSW |
9 |
103,087,735 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8317:Trf
|
UTSW |
9 |
103,094,715 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8443:Trf
|
UTSW |
9 |
103,094,675 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8735:Trf
|
UTSW |
9 |
103,087,723 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8854:Trf
|
UTSW |
9 |
103,107,529 (GRCm39) |
unclassified |
probably benign |
|
|
R9131:Trf
|
UTSW |
9 |
103,089,087 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9360:Trf
|
UTSW |
9 |
103,094,734 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R9499:Trf
|
UTSW |
9 |
103,099,283 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9526:Trf
|
UTSW |
9 |
103,104,130 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9551:Trf
|
UTSW |
9 |
103,099,283 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9552:Trf
|
UTSW |
9 |
103,099,283 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9710:Trf
|
UTSW |
9 |
103,103,217 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTGACGGAGATTCTCTTTCC -3'
(R):5'- TAGAGGTCTTGCCGGAGAAG -3'
Sequencing Primer
(F):5'- CCTTGAGGGCCTAATTCAGATG -3'
(R):5'- GGCTGACAGGGACCAATATG -3'
|
| Posted On |
2016-06-21 |
Incidental Mutation