Busch Lab

ZMP

jam3b

Ensembl ID:
ENSDARG00000061794
ZFIN ID:
ZDB-GENE-030131-441
Description:
junctional adhesion molecule 3b [Source:RefSeq peptide;Acc:NP_001076332]
Human Orthologue:
JAM3
Human Description:
junctional adhesion molecule 3 [Source:HGNC Symbol;Acc:15532]
Mouse Orthologue:
Jam3
Mouse Description:
junction adhesion molecule 3 Gene [Source:MGI Symbol;Acc:MGI:1933825]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa14980 Essential Splice Site Available for shipment Available now
sa37 Missense Confirmed mutation in F2 line Not yet available
sa16151 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa14980
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088546 Essential Splice Site 71 333 2 9
ENSDART00000128297 Essential Splice Site 26 288 2 9
ENSDART00000128795 Essential Splice Site 52 314 2 9
Genomic Location (Zv9):
Chromosome 21 (position 24312444)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 24998118
GRCz11 21 25034723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCCTCCTGAAGTCGACGAATTCTAAACCGTGGGTCAACGAGTTTGAATG[T/G]AAGGCTGARTAATTTAACTCCTGCAGTCTGATTTTAACATTAAACAGGCC
Long Flanking Sequence:
TGTTTGTTGTGAGAGTGAAACTAAAGATGGCTGGTAACATATCCGTTCACAGCTCACAGAGATGCGAGGAATGTGTGCCGTCAGGGTGGAGGCGTTGGACGCTGGGCTCGTCTGTTAATTGAGTTTCATGAATCTTTACTGTCACGTGTGCTTGAGACTATAATAACACCACCTGAAATGTTACTGCGAGTTATTCAAGTTGTTCAAGCAATGGTTCGTCCATAATTTCATCCTTTTCTCACCCTCCACTTCTTTCAAATCCGATTTTCTGTTCAACACAGAATATATTTTGAAGAAATTTGAAAATCGGTAGCCATTTTTATTCATATGAACCTGAACCACTTGAATTCGTAAATGAATTTTTGTGTGAACTAAAAAGCTCTCTTTAATTTCTCTTAAAACTGACTTTGTGTCTCTCTTCTCATTGCAGGTTACATCAGCACCTTGGCAGTCCTCCTGAAGTCGACGAATTCTAAACCGTGGGTCAACGAGTTTGAATG[T/G]AAGGCTGAGTAATTTAACTCCTGCAGTCTGATTTTAACATTAAACAGGCCATTGGAATGGTTTGTGAGCTCTGGCTTTGTTTCCCCATGCAGCAATCGAGCTGTCCTGCATGATCGAGTCCATCACCACCACTAAACCCAGAATAGAGTGGAAGAAGATTAAGAATGGAGACCCAAGCTATGTGTATTTTGATAATCAAATATCAGGTAACACACTAATAAACACTGTGAGACACACAACACAATAATGCAATGCTTACCAAGAAATAATAGTGAATAAAACTTCTACAGTATGTAGTAATGTAGGTTGTTCATTTTTACATTTAATGTGTCTGAAAGAAGATTAGGTCTAGAAGTTTAGTTGGTGAATAATTCAATTGATTCATTCAAAACAGATGATTCATTCTGAAAGCAAGTAAATGGCTTTATCAATTGATCACTGAATCCTAAATTCATAAATTCGTTCAAAAAGTTAATTTTAGGGACAAAATATGTCCTGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088546 Missense 167 333 5 9
ENSDART00000128297 Missense 122 288 5 9
ENSDART00000128795 Missense 148 314 5 9
Genomic Location (Zv9):
Chromosome 21 (position 24315130)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 25000804
GRCz11 21 25037409
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGATGATTCTCTTGTATGTCATGCAGTGAAGCCAGTCGTGCCAAGAT[G/A]CTCTGTGCCCAAGTCTATCCCGGTGGGCAAACCAGCAGAGCTGCATTGCC
Long Flanking Sequence:
CTTGGAAAGGAGAGCAAAAATTCGAGAGCCTGCAACCCTGGTCATTCTCAATGCCACAAGATCGGACAGCGCTGACTACCGCTGTGAGGTCACAGCACCCAATGACCAGAAATCCTTCGATGAGATCTTGATATCACTCACTGTACGAGGTGAGAACTCTAACAACTCTACATCTATTGATGGATAACTTTTGAAACGGTTGTAGACGTAGCATTATTAGTTTTTCCCAACTGCTACGATGTAAGATGAGAAGGAGCGCCGAGCCAATGATCCCACCCTTGGCGCACATGCAGGATGCATGCAGGGCGTGACCAGGGCTAAATGAGGAAACCTCTGAAACTGCATCTGAATTCAATCTGGGGTCTAAAAGGGGAAAGAGCAGTGTGTTCAGCTGTAGACTGAGTCGCTGTAATGGTGCATGTGTGTGAGGATGCGATCTTCGGAATGACGTTAAGATGATTCTCTTGTATGTCATGCAGTGAAGCCAGTCGTGCCAAGAT[G/A]CTCTGTGCCCAAGTCTATCCCGGTGGGCAAACCAGCAGAGCTGCATTGCCTGGAGGATGAAGGCTACCCAAAATCTCAATACCAGTGGTTCCGCAACAAGGAGGAAATCCCGCTAGATCCCAAGAGCAGCCCAAAGTTCTTCAACTCCACTTACACCCTAGATGGGGAAATGGGCACGCTGGTGAGTTGGGGTAGACGGAGGGATATTTTTGGGTAGTGATGGGCTCAGACATGAGGAGAATCTGCTGCCCTCATTTGCACATTCCAGAGTGCCATTCTCCACCATTTGTACTCAGTGCCCTTGTCAACCTTCACACCGATTTTAAAGCCCCCATGAAATCAAAGTAAAAATTTTTTTAAGTATTAGTATTAGTATATTAGTCTTAAGGATATCTGTAACCTACTATGCTTCAAAATAGTGACAACATTTGCATTAAGATATAAGCATCCAAAACCTGCAGTTTGTCACTTCCTCTTAAATGAATCAATGATTTTTTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16151
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088546 Nonsense 218 333 5 9
ENSDART00000128297 Nonsense 173 288 5 9
ENSDART00000128795 Nonsense 199 314 5 9
Genomic Location (Zv9):
Chromosome 21 (position 24315284)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 25000958
GRCz11 21 25037563
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAATCCCRCTAGATCCCAAGAGCAGCCCAAAGTTCTTCAACTCMACTTA[C/A]ACCCTAGAYGGGGAAATGGGCACGCTGGTGAGTTGGGGTAGACGGAGGGA
Long Flanking Sequence:
AACTCTAACAACTCTACATCTATTGATGGATAACTTTTGAAACGGTTGTAGACGTAGCATTATTAGTTTTTCCCAACTGCTACGATGTAAGATGAGAAGGAGCGCCGAGCCAATGATCCCACCCTTGGCGCACATGCAGGATGCATGCAGGGCGTGACCAGGGCTAAATGAGGAAACCTCTGAAACTGCATCTGAATTCAATCTGGGGTCTAAAAGGGGAAAGAGCAGTGTGTTCAGCTGTAGACTGAGTCGCTGTAATGGTGCATGTGTGTGAGGATGCGATCTTCGGAATGACGTTAAGATGATTCTCTTGTATGTCATGCAGTGAAGCCAGTCGTGCCAAGATGCTCTGTGCCCAAGTCTATCCCGGTGGGCAAACCAGCAGAGCTGCATTGCCTGGAGGATGAAGGCTACCCAAAATCTCAATACCAGTGGTTCCGCAACAAGGAGGAAATCCCGCTAGATCCCAAGAGCAGCCCAAAGTTCTTCAACTCCACTTA[C/A]ACCCTAGATGGGGAAATGGGCACGCTGGTGAGTTGGGGTAGACGGAGGGATATTTTTGGGTAGTGATGGGCTCAGACATGAGGAGAATCTGCTGCCCTCATTTGCACATTCCAGAGTGCCATTCTCCACCATTTGTACTCAGTGCCCTTGTCAACCTTCACACCGATTTTAAAGCCCCCATGAAATCAAAGTAAAAATTTTTTTAAGTATTAGTATTAGTATATTAGTCTTAAGGATATCTGTAACCTACTATGCTTCAAAATAGTGACAACATTTGCATTAAGATATAAGCATCCAAAACCTGCAGTTTGTCACTTCCTCTTAAATGAATCAATGATTTTTTATGTCATCAAATCTTATGACCAATCAAATGCTCTCTATCATCTAACATGTCCCATTCCCTTCAAGAAGCTACTGCTATATACACTTGAGCTCAATCACTTTCACTGGCAGTGAATAAAAACTAAATGCTATTGGCTGTTATTTTAAAGGGGGAGGCG
Associated Phenotype:
Not determined