Incidental Mutation 'IGL02466:Cblif'
| ID |
294601 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Cblif
|
| Ensembl Gene |
ENSMUSG00000024682 |
| Gene Name |
cobalamin binding intrinsic factor |
| Synonyms |
Gif |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02466
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
19 |
| Chromosomal Location |
11724918-11740811 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 11729596 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Isoleucine
at position 185
(N185I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000025585
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025585]
|
| AlphaFold |
P52787 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000025585
AA Change: N185I
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000025585
Gene: ENSMUSG00000024682
AA Change: N185I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Cobalamin_bind
|
8 |
308 |
2.6e-110 |
PFAM |
|
Pfam:DUF4430
|
340 |
416 |
7.7e-9 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the cobalamin transport protein family. It encodes a glycoprotein secreted by parietal cells of the gastric mucosa and is required for adequate absorption of vitamin B12. Vitamin B12 is necessary for erythrocyte maturation and mutations in this gene may lead to congenital pernicious anemia. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit vitamin B12-sensitive susceptibility to bacterial infection and reduced body weight and altered blood chemistry that can be compensated by maternal effect. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
T |
C |
11: 9,247,527 (GRCm39) |
F2425L |
probably benign |
Het |
| Adgre4 |
A |
T |
17: 56,121,188 (GRCm39) |
Y418F |
probably benign |
Het |
| Adra1a |
G |
T |
14: 66,875,322 (GRCm39) |
C99F |
probably damaging |
Het |
| Aox3 |
C |
A |
1: 58,197,431 (GRCm39) |
H592Q |
probably benign |
Het |
| Cacna1f |
A |
G |
X: 7,495,644 (GRCm39) |
|
probably null |
Het |
| Cacna2d2 |
T |
A |
9: 107,342,753 (GRCm39) |
I100N |
probably damaging |
Het |
| Ccr9 |
T |
A |
9: 123,608,911 (GRCm39) |
C198S |
probably damaging |
Het |
| Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
| Col4a3 |
T |
A |
1: 82,647,913 (GRCm39) |
C475S |
unknown |
Het |
| Csnk2a2 |
T |
C |
8: 96,203,859 (GRCm39) |
D100G |
possibly damaging |
Het |
| Cstf2t |
G |
A |
19: 31,061,277 (GRCm39) |
G271E |
possibly damaging |
Het |
| Fbxw22 |
T |
C |
9: 109,214,160 (GRCm39) |
R219G |
probably damaging |
Het |
| Homez |
A |
G |
14: 55,095,559 (GRCm39) |
F50L |
probably damaging |
Het |
| Hspa4l |
C |
T |
3: 40,707,657 (GRCm39) |
Q81* |
probably null |
Het |
| Ifi202b |
T |
C |
1: 173,799,875 (GRCm39) |
D202G |
possibly damaging |
Het |
| Inava |
T |
C |
1: 136,144,173 (GRCm39) |
|
probably null |
Het |
| Mansc1 |
T |
A |
6: 134,587,814 (GRCm39) |
D121V |
probably damaging |
Het |
| Or13a24 |
A |
G |
7: 140,154,684 (GRCm39) |
Y206C |
probably benign |
Het |
| Or4a27 |
T |
G |
2: 88,559,739 (GRCm39) |
D68A |
probably damaging |
Het |
| Or51h5 |
T |
A |
7: 102,577,723 (GRCm39) |
V296E |
possibly damaging |
Het |
| P2rx1 |
A |
T |
11: 72,900,410 (GRCm39) |
|
probably null |
Het |
| Phactr4 |
A |
G |
4: 132,104,483 (GRCm39) |
|
probably benign |
Het |
| Pus10 |
C |
T |
11: 23,675,574 (GRCm39) |
T482I |
probably damaging |
Het |
| Scyl2 |
G |
T |
10: 89,488,871 (GRCm39) |
Y206* |
probably null |
Het |
| Sell |
G |
A |
1: 163,896,632 (GRCm39) |
|
probably null |
Het |
| Slfn10-ps |
C |
T |
11: 82,921,090 (GRCm39) |
|
noncoding transcript |
Het |
| Ssh2 |
T |
C |
11: 77,307,233 (GRCm39) |
|
probably benign |
Het |
| Tas2r117 |
A |
G |
6: 132,779,963 (GRCm39) |
M34V |
probably benign |
Het |
| Vmn2r103 |
A |
T |
17: 19,993,631 (GRCm39) |
T3S |
probably benign |
Het |
| Vmn2r73 |
A |
T |
7: 85,522,084 (GRCm39) |
I85K |
probably damaging |
Het |
| Vps13b |
T |
C |
15: 35,770,887 (GRCm39) |
V2110A |
possibly damaging |
Het |
| Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
probably benign |
Het |
| Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
| Zfp592 |
G |
A |
7: 80,673,746 (GRCm39) |
G237R |
probably damaging |
Het |
| Zkscan7 |
A |
G |
9: 122,717,950 (GRCm39) |
E115G |
probably damaging |
Het |
| Zranb3 |
G |
A |
1: 127,943,829 (GRCm39) |
T306M |
probably benign |
Het |
|
| Other mutations in Cblif |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01604:Cblif
|
APN |
19 |
11,735,126 (GRCm39) |
missense |
probably benign |
0.40 |
|
IGL02678:Cblif
|
APN |
19 |
11,725,839 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02955:Cblif
|
APN |
19 |
11,725,027 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R0048:Cblif
|
UTSW |
19 |
11,727,120 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0048:Cblif
|
UTSW |
19 |
11,727,120 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0135:Cblif
|
UTSW |
19 |
11,735,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0606:Cblif
|
UTSW |
19 |
11,729,658 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R1758:Cblif
|
UTSW |
19 |
11,735,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1885:Cblif
|
UTSW |
19 |
11,729,688 (GRCm39) |
missense |
probably benign |
|
|
R2054:Cblif
|
UTSW |
19 |
11,736,370 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3087:Cblif
|
UTSW |
19 |
11,737,737 (GRCm39) |
nonsense |
probably null |
|
|
R4004:Cblif
|
UTSW |
19 |
11,736,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4601:Cblif
|
UTSW |
19 |
11,729,554 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4888:Cblif
|
UTSW |
19 |
11,729,583 (GRCm39) |
missense |
probably benign |
0.16 |
|
R5546:Cblif
|
UTSW |
19 |
11,725,859 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5795:Cblif
|
UTSW |
19 |
11,737,740 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6136:Cblif
|
UTSW |
19 |
11,727,649 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6147:Cblif
|
UTSW |
19 |
11,724,936 (GRCm39) |
start gained |
probably benign |
|
|
R7342:Cblif
|
UTSW |
19 |
11,740,587 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7814:Cblif
|
UTSW |
19 |
11,727,551 (GRCm39) |
missense |
probably benign |
0.14 |
|
R8382:Cblif
|
UTSW |
19 |
11,727,090 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8792:Cblif
|
UTSW |
19 |
11,727,599 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9227:Cblif
|
UTSW |
19 |
11,737,748 (GRCm39) |
nonsense |
probably null |
|
|
R9230:Cblif
|
UTSW |
19 |
11,737,748 (GRCm39) |
nonsense |
probably null |
|
|
R9428:Cblif
|
UTSW |
19 |
11,735,102 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation