ZMP
jam2a
Ensembl ID:
ZFIN ID:
Description:
junctional adhesion molecule 2a [Source:RefSeq peptide;Acc:NP_001091734]
Human Orthologue:
JAM2
Human Description:
junctional adhesion molecule 2 [Source:HGNC Symbol;Acc:14686]
Mouse Orthologue:
Jam2
Mouse Description:
junction adhesion molecule 2 Gene [Source:MGI Symbol;Acc:MGI:1933820]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| hu3319 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa39528 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu3319
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081989 | Nonsense | 40 | 307 | 3 | 13 |
| ENSDART00000133165 | None | None | 98 | None | 4 |
| ENSDART00000135944 | Nonsense | 40 | 185 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 476576)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 606700 |
| GRCz11 | 1 | 601879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGATGAGCTCTAAAATCTGTCTCTGTCCACAGACGCAGAGCTCTCCTG[C/A]GAGTTCAAGACTGAGAAAGACACCAACCCTCGCATCGAGTGGAAGAGGAA
Long Flanking Sequence:
TTGTCTGAAACATACAACAAAACATTCCCTAAGTTACTTATTACAGACTTACAAAACAGTAGACAGCGCCCTCTCTGGGGTTTGTTTTTTGAAATTACGAAGAAAAAAATCAAAGATAGTGTTATCAAGAGTTTTAGAAAGAGGAAAAAATTGTAAAAGACTTATAACGGCAGCCAGAAGACACAACGTGTTGTAACGTAACATTCGTTTTTCTGTAATTTGCTGCAACGATACAGCTTTTATAAACGTACACACATTTCTATTATTACAGTTGCTGATGACCGTTAAACACATCACAACCGTCCATCTGTGTGCATTCATCCTCATGATGTGTGTTTCAGGCGTCCCTGTGTCTCCCGTCACCGTCAGCAGTCGCAATCCTAAAGTGGAGGTGCACGAGTTCTCAGGTGAGTTTGAGTCAGTTTTCCATGCAGACGTCAGTCATACCTGCAGGATGAGCTCTAAAATCTGTCTCTGTCCACAGACGCAGAGCTCTCCTG[C/A]GAGTTCAAGACTGAGAAAGACACCAACCCTCGCATCGAGTGGAAGAGGAAAGACAAGGAAAAAGACGTGTCCTTCGTCTACTATGGAGAACGATTCGTAGGTAACTGATAAAACACTTCATTGCTTAAGACATGGGGTATGTTGAGGACAGGCTCGCTGTTACTCTAATGAAGTGACCACTTGTAGCATGTGAATAGCATAGCAACACCCTAGCAACCTCATTCCTACACTCTCAACACCCTAGCAACCACATTTCACTGGCAATAACACCCTAGCAATCACATTCCAAACACTCATAACCCTTAGCAACCACATTCCAATGTCAATAACACCCTAGCAACCACATTCCAACACCCTTTAACACCTTAGCAACTGCATTCCAACATATAACAGCCTAGCAACGTCAATTCAAACAGTCATATTACCCTAGCAACCACATTTCAATGTCAACCACACCCTAGCAACCACATTTCAAACACTCATAACCCTTGGCAACCCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39528
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081989 | Essential Splice Site | 215 | 307 | 8 | 13 |
| ENSDART00000133165 | None | None | 98 | None | 4 |
| ENSDART00000135944 | None | None | 185 | None | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 478673)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 608797 |
| GRCz11 | 1 | 603976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTAAAGCACCCTAGCAACCACATTCTGAAAACTCAGAACATTCGTTTA[T/A]ATTCATATGATAATAAAGGCCTGTGCTGCGTTTTGGAATCAACAGAATGC
Long Flanking Sequence:
TCCAAACACTCATAACACTATAGCAACTAAAGTCCTAATCTCAGAACACCCAATCAACCAGATTCCACAGTCTCATTACAACCCAGGAACTGTATGTCAACACTGTATGTATCACCCTAACTACCACATTCCAAACACTCATAACATCATAGCAACCACAGTCCTATGCTTAAAGCACCCTAGCAACCACAACCCAAAAACTCATAACAACTTAACAACCGTCTTCCAACAGTCGTATCACCCTAACTACAACATTCCAAACACACTTAATGCCAAAGCAACCACACTCCTATGCTCATAACACCCTAGCAACCACAGTCCTATGCTCATAACACCCTAGCAACCACACTTCAAAATCTCATAACAACCCAGGAACAATATATCAACACTTGTTTCAGGCTAACAACAACATTCCAAACACGTATAATACCATAGCAACCGCCGTCCTATGCTTAAAGCACCCTAGCAACCACATTCTGAAAACTCAGAACATTCGTTTA[T/A]ATTCATATGATAATAAAGGCCTGTGCTGCGTTTTGGAATCAACAGAATGCTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGATGACCTGAACGTGGCGGCGGTGGTCTCAGCTGTGGTTCTGGTGTGTGTGATCCTCTTCCTCTGTGCGTTTGGAGTGTGTTTGGCTCATCGACAGGGATATTTCAGCCGTGAGTCTCTGCTTTTCTCCCTCCTCCAGAAACAGAGTGTGTTTAAGGTTTCGTTCCCACAAAATTCTGCATTGCCTGTTCGTTCACTCTGGTGAGCTCCTGCGGGAGCCAGAGCCGGGGTGGGCGGGGTTTCCGTGGGAGTCAGGAAAGGTTTTTGGGCGGAGTTAACTCCGGCGGAAAAGGGGTGTGAGTTAGAGGGGGGGGGGATATATATATAACCTTATAGCCGCCTTTCCACTGCA
Associated Phenotype:
Not determined