Incidental Mutation 'IGL02499:Sec23ip'
ID295944
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sec23ip
Ensembl Gene ENSMUSG00000055319
Gene NameSec23 interacting protein
SynonymsD7Ertd373e, p125
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.583) question?
Stock #IGL02499
Quality Score
Status
Chromosome7
Chromosomal Location128744943-128784836 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 128776916 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Threonine at position 818 (I818T)
Ref Sequence ENSEMBL: ENSMUSP00000035610 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042942]
Predicted Effect probably damaging
Transcript: ENSMUST00000042942
AA Change: I818T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000035610
Gene: ENSMUSG00000055319
AA Change: I818T

DomainStartEndE-ValueType
low complexity region 8 26 N/A INTRINSIC
low complexity region 41 51 N/A INTRINSIC
low complexity region 79 88 N/A INTRINSIC
low complexity region 203 215 N/A INTRINSIC
low complexity region 222 230 N/A INTRINSIC
Blast:DDHD 513 585 8e-33 BLAST
SAM 637 702 2.18e-9 SMART
DDHD 777 987 1.33e-74 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104095
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 encodes a member of the phosphatidic acid preferring-phospholipase A1 family. The encoded protein is localized to endoplasmic reticulum exit sites and plays a critical role in ER-Golgi transport as part of the multimeric coat protein II complex. An orthologous gene in frogs is required for normal neural crest cell development, suggesting that this gene may play a role in Waardenburg syndrome neural crest defects. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]
PHENOTYPE: Male mice homozygous for a null allele display reduced fertility with globozoospermia and impaired fertilization. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930011G23Rik A G 5: 99,229,377 S404P probably damaging Het
A930011G23Rik G A 5: 99,229,382 P402L probably damaging Het
Abcb1a A G 5: 8,726,807 N835S possibly damaging Het
Abr A T 11: 76,509,090 F27Y probably benign Het
Adam5 C T 8: 24,781,565 probably null Het
Alas1 A T 9: 106,241,321 Y201N probably damaging Het
Aldoart1 T A 4: 72,852,239 R111W possibly damaging Het
Arhgef25 A G 10: 127,185,591 Y253H probably damaging Het
Arhgef28 G T 13: 97,953,783 A1076E possibly damaging Het
Baz2b C T 2: 59,901,496 R2066K possibly damaging Het
Bdh1 G T 16: 31,438,048 R5L possibly damaging Het
Brap A G 5: 121,679,871 Y358C probably damaging Het
Cad T C 5: 31,069,604 V1235A probably damaging Het
Cadps G T 14: 12,822,725 S5* probably null Het
Cd200r2 A G 16: 44,914,585 T220A possibly damaging Het
Cd209e T A 8: 3,854,238 M6L probably benign Het
Cdh23 G T 10: 60,385,179 T1265K probably damaging Het
Clec16a T C 16: 10,694,676 S828P probably benign Het
Dao A G 5: 114,013,941 K107E possibly damaging Het
Dnah6 T A 6: 73,021,227 M4071L probably benign Het
Dvl1 T C 4: 155,854,780 I250T probably benign Het
Dzip3 A C 16: 48,933,850 L945V probably damaging Het
Gm128 A G 3: 95,240,681 S101P possibly damaging Het
Gm4951 T C 18: 60,245,638 S82P probably damaging Het
Gphn T C 12: 78,492,300 L240P probably benign Het
Hecw2 A G 1: 53,926,488 I393T probably benign Het
Kat14 A G 2: 144,393,831 E161G probably benign Het
Kcne3 A C 7: 100,184,403 I76L probably benign Het
Kcnk18 A T 19: 59,235,182 Q253L probably benign Het
Kmt2a T C 9: 44,830,509 probably benign Het
Lrrc73 A G 17: 46,256,989 probably benign Het
Mki67 A G 7: 135,694,327 S2993P possibly damaging Het
Mto1 T A 9: 78,461,512 probably benign Het
Myo9a T A 9: 59,815,386 probably benign Het
Myt1 G A 2: 181,825,549 probably benign Het
Ncoa7 T C 10: 30,690,889 T587A probably benign Het
Nemf T A 12: 69,322,129 I771F probably damaging Het
Olfr180 A G 16: 58,916,251 L130P probably damaging Het
Olfr250 A T 9: 38,367,681 Y45F probably benign Het
Olfr370 T A 8: 83,541,183 V13D possibly damaging Het
Papln T C 12: 83,780,671 V761A probably benign Het
Pask A T 1: 93,321,095 L861* probably null Het
Pcdh18 T A 3: 49,753,447 R859S probably benign Het
Ppip5k1 C T 2: 121,331,553 probably null Het
Ptprs A G 17: 56,437,884 V284A probably damaging Het
Rasgrp4 A T 7: 29,151,503 probably benign Het
Rp1 T C 1: 4,349,048 I614V probably benign Het
Skint11 G A 4: 114,194,604 A50T probably benign Het
Sqor T A 2: 122,808,087 M417K possibly damaging Het
Tbc1d24 T C 17: 24,207,619 probably null Het
Tbc1d8b A T X: 139,712,424 D333V probably damaging Het
Tbx2 T C 11: 85,840,913 S679P possibly damaging Het
Thbs2 A G 17: 14,684,066 probably benign Het
Ttn T C 2: 76,859,451 probably benign Het
Vmn2r28 A T 7: 5,490,569 I126N probably damaging Het
Zbtb10 G T 3: 9,251,740 G204V probably damaging Het
Zfp426 A C 9: 20,473,118 probably benign Het
Other mutations in Sec23ip
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00825:Sec23ip APN 7 128767609 missense probably damaging 1.00
IGL01347:Sec23ip APN 7 128762405 missense probably benign 0.08
IGL01358:Sec23ip APN 7 128752797 missense possibly damaging 0.68
IGL01656:Sec23ip APN 7 128750245 missense probably damaging 1.00
IGL01835:Sec23ip APN 7 128755311 splice site probably null
IGL02233:Sec23ip APN 7 128779179 missense probably damaging 1.00
IGL03381:Sec23ip APN 7 128750305 missense probably damaging 0.97
R0053:Sec23ip UTSW 7 128745167 missense probably damaging 1.00
R0147:Sec23ip UTSW 7 128779051 splice site probably benign
R0360:Sec23ip UTSW 7 128761405 splice site probably benign
R1427:Sec23ip UTSW 7 128776885 missense probably damaging 0.99
R1442:Sec23ip UTSW 7 128776786 missense probably benign 0.10
R1462:Sec23ip UTSW 7 128766138 missense probably benign
R1462:Sec23ip UTSW 7 128766138 missense probably benign
R1564:Sec23ip UTSW 7 128766281 splice site probably null
R1876:Sec23ip UTSW 7 128752851 missense probably benign
R1966:Sec23ip UTSW 7 128755353 missense probably damaging 0.98
R1977:Sec23ip UTSW 7 128766273 missense probably damaging 1.00
R2115:Sec23ip UTSW 7 128762461 missense probably benign 0.00
R2847:Sec23ip UTSW 7 128754073 missense probably benign 0.00
R3958:Sec23ip UTSW 7 128776850 missense probably benign 0.35
R3959:Sec23ip UTSW 7 128776850 missense probably benign 0.35
R3960:Sec23ip UTSW 7 128776850 missense probably benign 0.35
R4287:Sec23ip UTSW 7 128777333 missense probably benign 0.37
R4510:Sec23ip UTSW 7 128779176 missense probably damaging 1.00
R4511:Sec23ip UTSW 7 128779176 missense probably damaging 1.00
R4612:Sec23ip UTSW 7 128750502 nonsense probably null
R4660:Sec23ip UTSW 7 128750286 missense probably null 0.00
R4890:Sec23ip UTSW 7 128752910 missense probably damaging 0.98
R5287:Sec23ip UTSW 7 128766136 missense probably benign
R5587:Sec23ip UTSW 7 128750427 missense probably benign
R5625:Sec23ip UTSW 7 128744983 unclassified probably benign
R5656:Sec23ip UTSW 7 128776784 missense probably damaging 1.00
R5808:Sec23ip UTSW 7 128772184 missense probably benign 0.00
R6034:Sec23ip UTSW 7 128750203 missense possibly damaging 0.66
R6034:Sec23ip UTSW 7 128750203 missense possibly damaging 0.66
R6145:Sec23ip UTSW 7 128778484 missense probably damaging 0.99
R6747:Sec23ip UTSW 7 128752849 synonymous silent
R6953:Sec23ip UTSW 7 128752796 nonsense probably null
R6992:Sec23ip UTSW 7 128765440 missense probably benign
R7131:Sec23ip UTSW 7 128779640 missense probably damaging 1.00
R7163:Sec23ip UTSW 7 128762533 critical splice donor site probably null
R7387:Sec23ip UTSW 7 128745003 unclassified probably benign
Posted On2015-04-16