Incidental Mutation 'R9781:Cntn5'
ID |
734058 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cntn5
|
Ensembl Gene |
ENSMUSG00000039488 |
Gene Name |
contactin 5 |
Synonyms |
A830025P08Rik, 6720426O10Rik, NB-2, LOC244683 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R9781 (G1)
|
Quality Score |
214.009 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
9660896-10904780 bp(-) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
A to C
at 10048686 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124214
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000074133]
[ENSMUST00000160216]
[ENSMUST00000162484]
[ENSMUST00000179049]
|
AlphaFold |
P68500 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000074133
|
SMART Domains |
Protein: ENSMUSP00000073769 Gene: ENSMUSG00000039488
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
IGc2
|
113 |
179 |
1.11e-10 |
SMART |
IG
|
201 |
289 |
4.82e-6 |
SMART |
IGc2
|
312 |
375 |
1.4e-16 |
SMART |
IGc2
|
401 |
464 |
8.97e-15 |
SMART |
IGc2
|
493 |
557 |
4.96e-8 |
SMART |
IG
|
577 |
667 |
2.13e-7 |
SMART |
FN3
|
670 |
756 |
1.01e-11 |
SMART |
FN3
|
773 |
859 |
9.19e-1 |
SMART |
FN3
|
875 |
958 |
3.99e-10 |
SMART |
FN3
|
974 |
1053 |
1.68e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000160216
|
SMART Domains |
Protein: ENSMUSP00000124327 Gene: ENSMUSG00000039488
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
IGc2
|
113 |
179 |
1.11e-10 |
SMART |
IG
|
201 |
289 |
4.82e-6 |
SMART |
IGc2
|
312 |
375 |
1.4e-16 |
SMART |
IGc2
|
401 |
464 |
8.97e-15 |
SMART |
IGc2
|
493 |
557 |
4.96e-8 |
SMART |
IG
|
577 |
667 |
2.13e-7 |
SMART |
FN3
|
670 |
756 |
1.01e-11 |
SMART |
FN3
|
773 |
859 |
9.19e-1 |
SMART |
FN3
|
875 |
958 |
3.99e-10 |
SMART |
FN3
|
974 |
1053 |
1.68e-3 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000162484
|
SMART Domains |
Protein: ENSMUSP00000124214 Gene: ENSMUSG00000039488
Domain | Start | End | E-Value | Type |
IG_like
|
10 |
84 |
1.12e2 |
SMART |
IGc2
|
107 |
170 |
1.4e-16 |
SMART |
IGc2
|
196 |
259 |
8.97e-15 |
SMART |
IGc2
|
288 |
352 |
4.96e-8 |
SMART |
IG
|
372 |
462 |
2.13e-7 |
SMART |
FN3
|
465 |
551 |
1.01e-11 |
SMART |
FN3
|
568 |
654 |
9.19e-1 |
SMART |
FN3
|
670 |
753 |
3.99e-10 |
SMART |
FN3
|
769 |
848 |
1.68e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000179049
|
SMART Domains |
Protein: ENSMUSP00000135903 Gene: ENSMUSG00000039488
Domain | Start | End | E-Value | Type |
IG_like
|
10 |
84 |
1.12e2 |
SMART |
IGc2
|
107 |
170 |
1.4e-16 |
SMART |
IGc2
|
196 |
259 |
8.97e-15 |
SMART |
IGc2
|
288 |
352 |
4.96e-8 |
SMART |
IG
|
372 |
462 |
2.13e-7 |
SMART |
FN3
|
465 |
551 |
1.01e-11 |
SMART |
FN3
|
568 |
654 |
9.19e-1 |
SMART |
FN3
|
670 |
753 |
3.99e-10 |
SMART |
FN3
|
769 |
848 |
1.68e-3 |
SMART |
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.3%
- 20x: 98.1%
|
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 immunoglobulin superfamily, and contactin family, which mediate cell surface interactions during nervous system development. This protein is a glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein that functions as a cell adhesion molecule. It may play a role in the formation of axon connections in the developing nervous system. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011] PHENOTYPE: Homozygous null mice are viable, fertile, and less susceptible to audiogenic seizures. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
G |
6: 128,519,860 (GRCm39) |
F1386L |
probably benign |
Het |
Aoc1l2 |
G |
A |
6: 48,907,660 (GRCm39) |
S220N |
possibly damaging |
Het |
Ap3d1 |
A |
C |
10: 80,545,609 (GRCm39) |
L1040R |
possibly damaging |
Het |
Bag4 |
T |
A |
8: 26,259,564 (GRCm39) |
N212Y |
probably damaging |
Het |
Bop1 |
A |
T |
15: 76,338,041 (GRCm39) |
S610T |
probably damaging |
Het |
Car12 |
T |
G |
9: 66,624,844 (GRCm39) |
S30A |
probably benign |
Het |
Ccdc14 |
A |
T |
16: 34,543,984 (GRCm39) |
T829S |
possibly damaging |
Het |
Ccn6 |
T |
A |
10: 39,027,167 (GRCm39) |
*355L |
probably null |
Het |
Cdc14a |
A |
T |
3: 116,122,274 (GRCm39) |
I231N |
probably benign |
Het |
Ceacam14 |
A |
T |
7: 17,549,082 (GRCm39) |
I158F |
possibly damaging |
Het |
Clca4a |
G |
T |
3: 144,667,713 (GRCm39) |
S419R |
probably benign |
Het |
Clec2g |
A |
G |
6: 128,960,012 (GRCm39) |
N258D |
probably benign |
Het |
Col5a3 |
T |
A |
9: 20,721,272 (GRCm39) |
S72C |
unknown |
Het |
Dmbt1 |
G |
C |
7: 130,639,599 (GRCm39) |
V46L |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,376,754 (GRCm39) |
|
probably null |
Het |
Dnase1 |
T |
C |
16: 3,857,054 (GRCm39) |
S204P |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,352,917 (GRCm39) |
E2690G |
probably benign |
Het |
Dst |
T |
C |
1: 34,218,075 (GRCm39) |
L1505P |
probably benign |
Het |
Dzip1 |
G |
A |
14: 119,148,834 (GRCm39) |
L282F |
probably benign |
Het |
E330034G19Rik |
A |
G |
14: 24,359,528 (GRCm39) |
E313G |
unknown |
Het |
Epc1 |
A |
T |
18: 6,455,187 (GRCm39) |
|
probably null |
Het |
Herc1 |
T |
C |
9: 66,280,004 (GRCm39) |
M304T |
probably benign |
Het |
Herc2 |
A |
T |
7: 55,750,096 (GRCm39) |
I594F |
possibly damaging |
Het |
Hivep2 |
T |
A |
10: 14,005,828 (GRCm39) |
S809T |
probably benign |
Het |
Hnrnph3 |
A |
T |
10: 62,853,861 (GRCm39) |
M132K |
unknown |
Het |
Hrnr |
A |
T |
3: 93,239,696 (GRCm39) |
R3311S |
unknown |
Het |
Jph3 |
T |
C |
8: 122,457,380 (GRCm39) |
F7L |
probably damaging |
Het |
Med13l |
C |
T |
5: 118,868,032 (GRCm39) |
T732M |
possibly damaging |
Het |
Mocos |
A |
T |
18: 24,828,939 (GRCm39) |
H748L |
probably benign |
Het |
Mrc1 |
A |
G |
2: 14,249,100 (GRCm39) |
H212R |
probably benign |
Het |
Mrc1 |
A |
T |
2: 14,310,175 (GRCm39) |
Y812F |
possibly damaging |
Het |
Mthfr |
T |
C |
4: 148,132,710 (GRCm39) |
I296T |
probably damaging |
Het |
Ncdn |
G |
A |
4: 126,642,467 (GRCm39) |
R397W |
probably damaging |
Het |
Nefh |
G |
A |
11: 4,895,271 (GRCm39) |
T306I |
probably damaging |
Het |
Nme7 |
C |
A |
1: 164,155,890 (GRCm39) |
A30E |
possibly damaging |
Het |
Or52z15 |
T |
A |
7: 103,332,246 (GRCm39) |
M97K |
probably damaging |
Het |
Pappa |
T |
A |
4: 65,043,104 (GRCm39) |
L109Q |
possibly damaging |
Het |
Pcdha2 |
A |
G |
18: 37,074,102 (GRCm39) |
S578G |
probably benign |
Het |
Pcf11 |
A |
T |
7: 92,297,228 (GRCm39) |
D1361E |
possibly damaging |
Het |
Pcm1 |
T |
C |
8: 41,720,398 (GRCm39) |
S320P |
probably damaging |
Het |
Pex19 |
T |
A |
1: 171,956,855 (GRCm39) |
F105Y |
probably damaging |
Het |
Pgap4 |
C |
T |
4: 49,586,890 (GRCm39) |
V93I |
probably benign |
Het |
Pggt1b |
A |
T |
18: 46,392,779 (GRCm39) |
M124K |
probably damaging |
Het |
Phkg1 |
T |
A |
5: 129,895,807 (GRCm39) |
H148L |
probably damaging |
Het |
Phlpp2 |
G |
T |
8: 110,662,178 (GRCm39) |
R855L |
possibly damaging |
Het |
Pkhd1 |
T |
A |
1: 20,187,665 (GRCm39) |
I3548L |
possibly damaging |
Het |
Plce1 |
T |
G |
19: 38,513,654 (GRCm39) |
S318A |
probably damaging |
Het |
Plcxd2 |
A |
G |
16: 45,830,117 (GRCm39) |
W35R |
probably benign |
Het |
Prl2b1 |
T |
A |
13: 27,569,129 (GRCm39) |
E156D |
possibly damaging |
Het |
Ptpn21 |
A |
G |
12: 98,655,170 (GRCm39) |
V599A |
probably damaging |
Het |
Raly |
T |
C |
2: 154,699,265 (GRCm39) |
V23A |
probably damaging |
Het |
Rapgef3 |
T |
C |
15: 97,643,479 (GRCm39) |
I911V |
probably damaging |
Het |
Rhbdl1 |
A |
G |
17: 26,055,443 (GRCm39) |
V48A |
probably benign |
Het |
Rhpn1 |
C |
T |
15: 75,582,543 (GRCm39) |
Q212* |
probably null |
Het |
Sec24b |
G |
T |
3: 129,789,742 (GRCm39) |
P760T |
probably damaging |
Het |
Septin8 |
C |
A |
11: 53,422,889 (GRCm39) |
Q33K |
probably damaging |
Het |
Serpinb6a |
T |
C |
13: 34,109,346 (GRCm39) |
T150A |
probably benign |
Het |
Shmt1 |
A |
T |
11: 60,692,329 (GRCm39) |
H142Q |
probably damaging |
Het |
Slc27a3 |
G |
A |
3: 90,296,591 (GRCm39) |
S127L |
|
Het |
Slc4a5 |
G |
A |
6: 83,239,466 (GRCm39) |
A242T |
probably benign |
Het |
Sphkap |
G |
A |
1: 83,255,772 (GRCm39) |
T659I |
possibly damaging |
Het |
Ssbp3 |
T |
C |
4: 106,905,224 (GRCm39) |
S381P |
probably damaging |
Het |
Stxbp5l |
C |
T |
16: 37,165,485 (GRCm39) |
D78N |
probably benign |
Het |
Suv39h2 |
G |
T |
2: 3,463,631 (GRCm39) |
Q362K |
probably benign |
Het |
Tcerg1 |
G |
A |
18: 42,701,030 (GRCm39) |
R828Q |
probably damaging |
Het |
Tgm2 |
T |
G |
2: 157,971,321 (GRCm39) |
D306A |
probably damaging |
Het |
Tmem79 |
A |
G |
3: 88,239,931 (GRCm39) |
C260R |
possibly damaging |
Het |
Ubn2 |
C |
A |
6: 38,466,190 (GRCm39) |
A508E |
probably benign |
Het |
Uggt2 |
T |
A |
14: 119,232,384 (GRCm39) |
H1489L |
possibly damaging |
Het |
Wnt16 |
T |
C |
6: 22,291,114 (GRCm39) |
F181L |
probably damaging |
Het |
Zfp326 |
T |
C |
5: 106,062,825 (GRCm39) |
F565L |
unknown |
Het |
Zfp62 |
T |
A |
11: 49,106,297 (GRCm39) |
C129* |
probably null |
Het |
|
Other mutations in Cntn5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00742:Cntn5
|
APN |
9 |
9,976,302 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01118:Cntn5
|
APN |
9 |
9,831,565 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01328:Cntn5
|
APN |
9 |
9,781,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01445:Cntn5
|
APN |
9 |
9,693,489 (GRCm39) |
splice site |
probably benign |
|
IGL01505:Cntn5
|
APN |
9 |
9,706,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01556:Cntn5
|
APN |
9 |
9,673,913 (GRCm39) |
missense |
probably benign |
|
IGL01804:Cntn5
|
APN |
9 |
9,831,542 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02173:Cntn5
|
APN |
9 |
9,748,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02250:Cntn5
|
APN |
9 |
10,145,336 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02366:Cntn5
|
APN |
9 |
9,984,060 (GRCm39) |
splice site |
probably benign |
|
IGL02565:Cntn5
|
APN |
9 |
10,145,343 (GRCm39) |
nonsense |
probably null |
|
IGL02593:Cntn5
|
APN |
9 |
9,833,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02743:Cntn5
|
APN |
9 |
9,984,115 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02976:Cntn5
|
APN |
9 |
10,419,104 (GRCm39) |
unclassified |
probably benign |
|
IGL03103:Cntn5
|
APN |
9 |
9,972,817 (GRCm39) |
splice site |
probably benign |
|
IGL03114:Cntn5
|
APN |
9 |
9,748,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03156:Cntn5
|
APN |
9 |
9,673,882 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02802:Cntn5
|
UTSW |
9 |
10,048,683 (GRCm39) |
splice site |
probably null |
|
R0243:Cntn5
|
UTSW |
9 |
9,781,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R0385:Cntn5
|
UTSW |
9 |
9,972,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R0541:Cntn5
|
UTSW |
9 |
9,673,407 (GRCm39) |
splice site |
probably benign |
|
R0827:Cntn5
|
UTSW |
9 |
9,666,943 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1029:Cntn5
|
UTSW |
9 |
9,831,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Cntn5
|
UTSW |
9 |
10,145,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Cntn5
|
UTSW |
9 |
9,673,801 (GRCm39) |
critical splice donor site |
probably null |
|
R1536:Cntn5
|
UTSW |
9 |
9,976,321 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1746:Cntn5
|
UTSW |
9 |
9,831,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Cntn5
|
UTSW |
9 |
10,172,059 (GRCm39) |
missense |
probably benign |
0.01 |
R1764:Cntn5
|
UTSW |
9 |
9,673,988 (GRCm39) |
missense |
probably benign |
|
R1859:Cntn5
|
UTSW |
9 |
9,972,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Cntn5
|
UTSW |
9 |
9,984,082 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1888:Cntn5
|
UTSW |
9 |
9,984,082 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1950:Cntn5
|
UTSW |
9 |
9,781,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Cntn5
|
UTSW |
9 |
9,748,420 (GRCm39) |
missense |
probably damaging |
0.98 |
R2145:Cntn5
|
UTSW |
9 |
9,748,420 (GRCm39) |
missense |
probably damaging |
0.98 |
R2437:Cntn5
|
UTSW |
9 |
10,048,758 (GRCm39) |
nonsense |
probably null |
|
R2440:Cntn5
|
UTSW |
9 |
10,171,960 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2504:Cntn5
|
UTSW |
9 |
10,172,126 (GRCm39) |
missense |
probably benign |
|
R3054:Cntn5
|
UTSW |
9 |
10,419,076 (GRCm39) |
missense |
probably benign |
0.30 |
R3056:Cntn5
|
UTSW |
9 |
10,419,076 (GRCm39) |
missense |
probably benign |
0.30 |
R3804:Cntn5
|
UTSW |
9 |
9,781,668 (GRCm39) |
splice site |
probably benign |
|
R4164:Cntn5
|
UTSW |
9 |
9,781,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R4444:Cntn5
|
UTSW |
9 |
9,704,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Cntn5
|
UTSW |
9 |
10,048,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Cntn5
|
UTSW |
9 |
9,673,297 (GRCm39) |
missense |
probably benign |
0.10 |
R4624:Cntn5
|
UTSW |
9 |
9,704,809 (GRCm39) |
nonsense |
probably null |
|
R4652:Cntn5
|
UTSW |
9 |
9,704,917 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4664:Cntn5
|
UTSW |
9 |
10,144,214 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4679:Cntn5
|
UTSW |
9 |
9,970,536 (GRCm39) |
missense |
probably benign |
0.09 |
R4829:Cntn5
|
UTSW |
9 |
9,976,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4929:Cntn5
|
UTSW |
9 |
9,976,400 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5211:Cntn5
|
UTSW |
9 |
9,704,894 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5406:Cntn5
|
UTSW |
9 |
9,833,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Cntn5
|
UTSW |
9 |
9,743,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R5584:Cntn5
|
UTSW |
9 |
9,661,457 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5688:Cntn5
|
UTSW |
9 |
9,748,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5762:Cntn5
|
UTSW |
9 |
9,748,394 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6141:Cntn5
|
UTSW |
9 |
10,144,162 (GRCm39) |
missense |
probably benign |
|
R6147:Cntn5
|
UTSW |
9 |
10,012,894 (GRCm39) |
missense |
probably damaging |
0.98 |
R6325:Cntn5
|
UTSW |
9 |
10,144,328 (GRCm39) |
splice site |
probably null |
|
R6377:Cntn5
|
UTSW |
9 |
9,743,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:Cntn5
|
UTSW |
9 |
10,144,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Cntn5
|
UTSW |
9 |
10,904,704 (GRCm39) |
start gained |
probably benign |
|
R7252:Cntn5
|
UTSW |
9 |
9,831,640 (GRCm39) |
missense |
probably benign |
0.00 |
R7363:Cntn5
|
UTSW |
9 |
10,172,021 (GRCm39) |
missense |
probably benign |
0.00 |
R7401:Cntn5
|
UTSW |
9 |
9,833,466 (GRCm39) |
missense |
probably benign |
0.13 |
R7488:Cntn5
|
UTSW |
9 |
9,970,570 (GRCm39) |
missense |
probably damaging |
0.99 |
R7548:Cntn5
|
UTSW |
9 |
9,673,415 (GRCm39) |
splice site |
probably null |
|
R7662:Cntn5
|
UTSW |
9 |
9,661,390 (GRCm39) |
missense |
probably benign |
0.17 |
R7718:Cntn5
|
UTSW |
9 |
9,984,133 (GRCm39) |
missense |
probably benign |
|
R7719:Cntn5
|
UTSW |
9 |
9,704,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R7788:Cntn5
|
UTSW |
9 |
9,704,934 (GRCm39) |
missense |
probably benign |
0.01 |
R7864:Cntn5
|
UTSW |
9 |
9,984,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R7937:Cntn5
|
UTSW |
9 |
9,748,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R8117:Cntn5
|
UTSW |
9 |
9,673,955 (GRCm39) |
missense |
probably benign |
0.33 |
R8159:Cntn5
|
UTSW |
9 |
10,145,386 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8349:Cntn5
|
UTSW |
9 |
9,666,840 (GRCm39) |
critical splice donor site |
probably null |
|
R8449:Cntn5
|
UTSW |
9 |
9,666,840 (GRCm39) |
critical splice donor site |
probably null |
|
R8779:Cntn5
|
UTSW |
9 |
10,171,920 (GRCm39) |
missense |
probably benign |
|
R8789:Cntn5
|
UTSW |
9 |
9,673,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R8985:Cntn5
|
UTSW |
9 |
10,171,960 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9370:Cntn5
|
UTSW |
9 |
9,833,520 (GRCm39) |
missense |
probably benign |
0.19 |
R9382:Cntn5
|
UTSW |
9 |
9,673,817 (GRCm39) |
missense |
probably benign |
|
Z1177:Cntn5
|
UTSW |
9 |
10,090,241 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cntn5
|
UTSW |
9 |
9,673,967 (GRCm39) |
nonsense |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- GCCAGAGGTTGACATCATGTG -3'
(R):5'- GAGTTCCCTTCCTTTGTGGCAG -3'
Sequencing Primer
(F):5'- CTAGCAAGCTCCAGAGATGTTCATG -3'
(R):5'- CCTTCCTTTGTGGCAGAGGAC -3'
|
Posted On |
2022-11-14 |