Incidental Mutation 'R6748:Sec23b'
ID |
530632 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sec23b
|
Ensembl Gene |
ENSMUSG00000027429 |
Gene Name |
SEC23 homolog B, COPII coat complex component |
Synonyms |
|
MMRRC Submission |
044865-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R6748 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
144398165-144432673 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 144408714 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Cysteine
at position 133
(Y133C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000120972
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028916]
[ENSMUST00000143573]
[ENSMUST00000149697]
[ENSMUST00000155876]
|
AlphaFold |
Q9D662 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000028916
AA Change: Y133C
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000028916 Gene: ENSMUSG00000027429 AA Change: Y133C
Domain | Start | End | E-Value | Type |
Pfam:zf-Sec23_Sec24
|
58 |
98 |
4.3e-17 |
PFAM |
Pfam:Sec23_trunk
|
126 |
392 |
2.3e-82 |
PFAM |
Pfam:Sec23_BS
|
403 |
506 |
7.2e-33 |
PFAM |
Pfam:Sec23_helical
|
522 |
620 |
1.1e-28 |
PFAM |
Pfam:Gelsolin
|
631 |
720 |
1e-18 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128210
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000143573
AA Change: Y133C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000120972 Gene: ENSMUSG00000027429 AA Change: Y133C
Domain | Start | End | E-Value | Type |
Pfam:zf-Sec23_Sec24
|
57 |
98 |
3.7e-18 |
PFAM |
Pfam:Sec23_trunk
|
126 |
278 |
1.3e-41 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000149697
|
SMART Domains |
Protein: ENSMUSP00000122819 Gene: ENSMUSG00000027429
Domain | Start | End | E-Value | Type |
Pfam:zf-Sec23_Sec24
|
57 |
98 |
8.7e-19 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000155876
AA Change: Y133C
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000122884 Gene: ENSMUSG00000027429 AA Change: Y133C
Domain | Start | End | E-Value | Type |
Pfam:zf-Sec23_Sec24
|
57 |
98 |
1.1e-18 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.2%
- 20x: 94.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The function of this gene product has been implicated in cargo selection and concentration. Multiple alternatively spliced transcript variants have been identified in this gene. [provided by RefSeq, Feb 2010] PHENOTYPE: Mice homozygous for a null mutation display complete neonatal lethality, fail to suckle, and show degeneration of the secretory tissues in the pancreas, salivary gland, and gastric glands. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aff3 |
C |
A |
1: 38,574,327 (GRCm39) |
R178I |
probably damaging |
Het |
Agr3 |
A |
G |
12: 35,997,594 (GRCm39) |
|
probably null |
Het |
Aoc1 |
C |
T |
6: 48,883,228 (GRCm39) |
T368I |
possibly damaging |
Het |
Aph1c |
A |
G |
9: 66,740,577 (GRCm39) |
S50P |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,232,378 (GRCm39) |
E341G |
possibly damaging |
Het |
Atp8b3 |
A |
T |
10: 80,361,058 (GRCm39) |
M926K |
possibly damaging |
Het |
C1qtnf9 |
A |
G |
14: 61,017,276 (GRCm39) |
N269D |
probably damaging |
Het |
Cdc42bpb |
T |
C |
12: 111,261,273 (GRCm39) |
|
probably benign |
Het |
Clec4a1 |
T |
C |
6: 122,910,856 (GRCm39) |
I237T |
possibly damaging |
Het |
Clpx |
A |
G |
9: 65,217,441 (GRCm39) |
N3S |
probably benign |
Het |
Col19a1 |
A |
G |
1: 24,573,151 (GRCm39) |
I207T |
unknown |
Het |
Cyp2j8 |
T |
A |
4: 96,363,782 (GRCm39) |
T294S |
probably benign |
Het |
Dnah1 |
A |
G |
14: 31,021,945 (GRCm39) |
I1186T |
probably damaging |
Het |
Dnhd1 |
T |
G |
7: 105,369,844 (GRCm39) |
V4423G |
probably benign |
Het |
Dock4 |
A |
T |
12: 40,754,465 (GRCm39) |
I485F |
probably benign |
Het |
Drd2 |
T |
A |
9: 49,314,502 (GRCm39) |
C244* |
probably null |
Het |
Frmpd1 |
T |
A |
4: 45,274,397 (GRCm39) |
I435K |
probably benign |
Het |
Fzd5 |
A |
G |
1: 64,774,723 (GRCm39) |
M346T |
possibly damaging |
Het |
Gc |
T |
C |
5: 89,583,431 (GRCm39) |
T371A |
probably benign |
Het |
Gm12185 |
T |
A |
11: 48,807,123 (GRCm39) |
T23S |
possibly damaging |
Het |
Hbq1a |
A |
G |
11: 32,250,169 (GRCm39) |
|
probably null |
Het |
Herc1 |
TCCC |
TCC |
9: 66,408,470 (GRCm39) |
|
probably null |
Het |
Il1rap |
A |
T |
16: 26,541,106 (GRCm39) |
N449I |
probably benign |
Het |
Itgb5 |
T |
A |
16: 33,719,667 (GRCm39) |
D279E |
probably damaging |
Het |
Mat2b |
T |
A |
11: 40,571,021 (GRCm39) |
I268F |
probably benign |
Het |
Mtor |
T |
C |
4: 148,634,641 (GRCm39) |
F2421L |
probably damaging |
Het |
Myo5b |
G |
A |
18: 74,834,574 (GRCm39) |
R878Q |
possibly damaging |
Het |
Nkx2-6 |
A |
G |
14: 69,412,555 (GRCm39) |
D241G |
probably benign |
Het |
Or4f14 |
T |
A |
2: 111,742,702 (GRCm39) |
N191I |
possibly damaging |
Het |
Or5h23 |
T |
A |
16: 58,906,253 (GRCm39) |
M198L |
probably benign |
Het |
Pcdhb22 |
A |
C |
18: 37,651,799 (GRCm39) |
D89A |
probably damaging |
Het |
Pcnx2 |
C |
T |
8: 126,577,074 (GRCm39) |
R986Q |
probably damaging |
Het |
Plxna2 |
A |
G |
1: 194,476,490 (GRCm39) |
|
probably null |
Het |
Ppwd1 |
A |
T |
13: 104,344,538 (GRCm39) |
Y527* |
probably null |
Het |
Pramel35 |
T |
C |
5: 94,000,072 (GRCm39) |
W38R |
probably benign |
Het |
Rnf126 |
A |
G |
10: 79,597,970 (GRCm39) |
L131P |
probably benign |
Het |
Rsl1 |
T |
A |
13: 67,330,688 (GRCm39) |
C379S |
probably benign |
Het |
Slc25a24 |
T |
A |
3: 109,056,823 (GRCm39) |
V112D |
possibly damaging |
Het |
Slc35f3 |
A |
T |
8: 127,121,377 (GRCm39) |
R413* |
probably null |
Het |
Tas1r2 |
T |
C |
4: 139,396,922 (GRCm39) |
F754L |
probably damaging |
Het |
Tbc1d14 |
A |
G |
5: 36,652,598 (GRCm39) |
S615P |
probably damaging |
Het |
Ttc17 |
T |
C |
2: 94,216,447 (GRCm39) |
K80R |
probably benign |
Het |
Ttn |
T |
C |
2: 76,576,428 (GRCm39) |
T24822A |
possibly damaging |
Het |
Vmn1r222 |
C |
A |
13: 23,417,117 (GRCm39) |
R32L |
probably benign |
Het |
Zfp354b |
G |
A |
11: 50,813,659 (GRCm39) |
T422M |
probably damaging |
Het |
Zfp407 |
G |
A |
18: 84,226,955 (GRCm39) |
T2218M |
probably damaging |
Het |
|
Other mutations in Sec23b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:Sec23b
|
APN |
2 |
144,425,690 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00668:Sec23b
|
APN |
2 |
144,401,138 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL00714:Sec23b
|
APN |
2 |
144,401,145 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00914:Sec23b
|
APN |
2 |
144,408,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Sec23b
|
APN |
2 |
144,406,509 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01341:Sec23b
|
APN |
2 |
144,427,653 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01377:Sec23b
|
APN |
2 |
144,401,157 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01634:Sec23b
|
APN |
2 |
144,401,150 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02321:Sec23b
|
APN |
2 |
144,421,325 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03027:Sec23b
|
APN |
2 |
144,429,465 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03064:Sec23b
|
APN |
2 |
144,423,952 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03105:Sec23b
|
APN |
2 |
144,423,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03240:Sec23b
|
APN |
2 |
144,408,679 (GRCm39) |
splice site |
probably benign |
|
R0004:Sec23b
|
UTSW |
2 |
144,406,482 (GRCm39) |
splice site |
probably benign |
|
R0092:Sec23b
|
UTSW |
2 |
144,408,830 (GRCm39) |
missense |
probably benign |
0.21 |
R0409:Sec23b
|
UTSW |
2 |
144,409,832 (GRCm39) |
missense |
probably benign |
0.22 |
R0426:Sec23b
|
UTSW |
2 |
144,410,532 (GRCm39) |
unclassified |
probably benign |
|
R0441:Sec23b
|
UTSW |
2 |
144,423,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R1034:Sec23b
|
UTSW |
2 |
144,432,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1624:Sec23b
|
UTSW |
2 |
144,409,049 (GRCm39) |
missense |
probably benign |
|
R2020:Sec23b
|
UTSW |
2 |
144,408,864 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2392:Sec23b
|
UTSW |
2 |
144,427,507 (GRCm39) |
splice site |
probably null |
|
R3946:Sec23b
|
UTSW |
2 |
144,423,893 (GRCm39) |
missense |
probably benign |
|
R4407:Sec23b
|
UTSW |
2 |
144,416,638 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4448:Sec23b
|
UTSW |
2 |
144,401,171 (GRCm39) |
missense |
probably benign |
0.43 |
R4519:Sec23b
|
UTSW |
2 |
144,423,935 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4522:Sec23b
|
UTSW |
2 |
144,420,286 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4654:Sec23b
|
UTSW |
2 |
144,414,494 (GRCm39) |
missense |
probably benign |
0.33 |
R4849:Sec23b
|
UTSW |
2 |
144,427,519 (GRCm39) |
missense |
probably damaging |
0.96 |
R4876:Sec23b
|
UTSW |
2 |
144,428,281 (GRCm39) |
splice site |
probably null |
|
R4983:Sec23b
|
UTSW |
2 |
144,423,873 (GRCm39) |
missense |
probably benign |
0.06 |
R6169:Sec23b
|
UTSW |
2 |
144,428,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Sec23b
|
UTSW |
2 |
144,401,109 (GRCm39) |
splice site |
probably null |
|
R6703:Sec23b
|
UTSW |
2 |
144,401,109 (GRCm39) |
splice site |
probably null |
|
R7238:Sec23b
|
UTSW |
2 |
144,432,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7511:Sec23b
|
UTSW |
2 |
144,432,269 (GRCm39) |
missense |
probably benign |
0.30 |
R7845:Sec23b
|
UTSW |
2 |
144,401,316 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7914:Sec23b
|
UTSW |
2 |
144,406,565 (GRCm39) |
missense |
probably benign |
|
R8177:Sec23b
|
UTSW |
2 |
144,427,543 (GRCm39) |
missense |
probably benign |
0.03 |
R8183:Sec23b
|
UTSW |
2 |
144,401,189 (GRCm39) |
missense |
probably benign |
0.08 |
R8238:Sec23b
|
UTSW |
2 |
144,406,568 (GRCm39) |
missense |
probably benign |
0.00 |
R8420:Sec23b
|
UTSW |
2 |
144,401,234 (GRCm39) |
missense |
probably benign |
0.01 |
R8488:Sec23b
|
UTSW |
2 |
144,423,983 (GRCm39) |
missense |
probably damaging |
0.98 |
R8558:Sec23b
|
UTSW |
2 |
144,428,308 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8911:Sec23b
|
UTSW |
2 |
144,401,316 (GRCm39) |
missense |
probably benign |
0.27 |
R8939:Sec23b
|
UTSW |
2 |
144,411,137 (GRCm39) |
critical splice donor site |
probably null |
|
R9058:Sec23b
|
UTSW |
2 |
144,424,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9172:Sec23b
|
UTSW |
2 |
144,401,179 (GRCm39) |
missense |
probably benign |
|
R9334:Sec23b
|
UTSW |
2 |
144,410,550 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9401:Sec23b
|
UTSW |
2 |
144,420,286 (GRCm39) |
missense |
probably benign |
0.10 |
R9561:Sec23b
|
UTSW |
2 |
144,408,728 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9593:Sec23b
|
UTSW |
2 |
144,410,564 (GRCm39) |
missense |
probably benign |
0.20 |
R9696:Sec23b
|
UTSW |
2 |
144,428,343 (GRCm39) |
missense |
probably benign |
0.03 |
|
Predicted Primers |
PCR Primer
(F):5'- TACCTGATTTGTCCTGTGGC -3'
(R):5'- TAAATCCTTGGTCCCTCGGAAG -3'
Sequencing Primer
(F):5'- TGTCCTGTGGCATGCAGC -3'
(R):5'- TTGGTCCCTCGGAAGACATAG -3'
|
Posted On |
2018-08-01 |