ZMP
si:dkey-91f15.1
Ensembl ID:
ZFIN ID:
Description:
gap junction protein, gamma 2, 47kDa [Source:RefSeq peptide;Acc:NP_001076577]
Human Orthologue:
GJC2
Human Description:
gap junction protein, gamma 2, 47kDa [Source:HGNC Symbol;Acc:17494]
Mouse Orthologue:
Gjc2
Mouse Description:
gap junction protein, gamma 2 Gene [Source:MGI Symbol;Acc:MGI:2153060]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33861 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18841 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9858 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33861
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000141643 | Nonsense | 248 | 391 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 22747521)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19002967 |
GRCz11 | 6 | 21063189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGAAAAAACCATCTTTCTGCTCATCATGTATGTTGTCAGTGTACTCTG[T/A]CTGGCACTGACTGTATTGGAAATCCTGCATCTGGGAATTGGTGGCTTGAG
Long Flanking Sequence:
ATTATGATAAGCACCCCGTCTGTTATGTACCTCGGCTTTGCCATGCACAAAATTGCTCGAATGGCCGATAATGAATACCAACCACGCAAACACAAAATGCTGTCTACGGTACATCAGAGAATGAATCGTGACTACGACATGGTGGACGAGATGACTGAAGAAGTTCCCATGATCCCAGAAGAGATTGAGCCATCAGAGAAGGACAACAAATCAGCAGCTTCAACCAAGACTACCGCTGCTTCTGATGCTGCCGTGAAACATGATGGCCGACGCCGCATCAAGAGAGATGGTCTCATGAAGGTGTACGTGTTACAGTTGATCTCTCGTGTTGCCTTTGAGATAGCCTTCCTCTTTGGCCAATGTATTCTTTATGGTTTTGAGGTCTCTCCATCCTACATTTGCACCCGAAGCCCTTGCCCACACACAGTGGATTGCTTTGTCTCACGTCCCACTGAAAAAACCATCTTTCTGCTCATCATGTATGTTGTCAGTGTACTCTG[T/A]CTGGCACTGACTGTATTGGAAATCCTGCATCTGGGAATTGGTGGCTTGAGGGACTCATTTCGTAGTCGAGCAAATCGGAGACTCCCTGTTCATAGGCCATCCACGTCCACCATCTGTCACCGCCTTTCCAGTGCTCCACCTGGATATCAGGCTGTCCAGAAAAAGTACTCCTCAGGCAAGCTAAAGGCTGAGTTCCTGTCAGACTCAGGACGGGAGTCACTGGCTGATGACAACACTACTCGTGATCTAGACCGTCTGCGGAGGCATCTGAAAATTGCACAGCAACACCTGGACCAGGCCTACCACACTGAGGAAGTAGGGGCTTCACACAACAGCGGGCCTGACTCTAAAAGCATCGCTGCTGAGCAAAACCGACTCAACCAGGCGCAGGGAGGCTTTGGCAGCACTGAGGAGAAAGGTTAGTTTGAGATGCACTTCATTCCCTCACTTAAACCCAGTCGAGTAATCAGGGTTAGATATTTACTAGGAATGTGACGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18841
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000141643 | Nonsense | 297 | 391 | 1 | 2 |
ENSDART00000141643 | Nonsense | 297 | 391 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 22747668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19003114 |
GRCz11 | 6 | 21063336 |
KASP Assay ID:
2259-7479.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCCACGTCCACCATCTGTCACCGCCTTTCCAGTGCTCCACCTGGATA[T/A]CAGGCTGTCCAGAAAAAGTACTCCTCAGGCAAGCTAAAGGCTGAGTTCCT
Long Flanking Sequence:
GAGATGACTGAAGAAGTTCCCATGATCCCAGAAGAGATTGAGCCATCAGAGAAGGACAACAAATCAGCAGCTTCAACCAAGACTACCGCTGCTTCTGATGCTGCCGTGAAACATGATGGCCGACGCCGCATCAAGAGAGATGGTCTCATGAAGGTGTACGTGTTACAGTTGATCTCTCGTGTTGCCTTTGAGATAGCCTTCCTCTTTGGCCAATGTATTCTTTATGGTTTTGAGGTCTCTCCATCCTACATTTGCACCCGAAGCCCTTGCCCACACACAGTGGATTGCTTTGTCTCACGTCCCACTGAAAAAACCATCTTTCTGCTCATCATGTATGTTGTCAGTGTACTCTGTCTGGCACTGACTGTATTGGAAATCCTGCATCTGGGAATTGGTGGCTTGAGGGACTCATTTCGTAGTCGAGCAAATCGGAGACTCCCTGTTCATAGGCCATCCACGTCCACCATCTGTCACCGCCTTTCCAGTGCTCCACCTGGATA[T/A]CAGGCTGTCCAGAAAAAGTACTCCTCAGGCAAGCTAAAGGCTGAGTTCCTGTCAGACTCAGGACGGGAGTCACTGGCTGATGACAACACTACTCGTGATCTAGACCGTCTGCGGAGGCATCTGAAAATTGCACAGCAACACCTGGACCAGGCCTACCACACTGAGGAAGTAGGGGCTTCACACAACAGCGGGCCTGACTCTAAAAGCATCGCTGCTGAGCAAAACCGACTCAACCAGGCGCAGGGAGGCTTTGGCAGCACTGAGGAGAAAGGTTAGTTTGAGATGCACTTCATTCCCTCACTTAAACCCAGTCGAGTAATCAGGGTTAGATATTTACTAGGAATGTGACGAGATCTCGAGCTACTAGATATCGCAAGACTAAATCAAGATTTCTTGTTGTGGTGAAAAGTTGTCTCGTGAGTTGTGATGTTATGATGGAGCGTGAGGGTAAATTTAGCACTGAAGATTGAAGGCAGGATTGGATTAGAACCGCACAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9858
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000141643 | Nonsense | 297 | 391 | 1 | 2 |
ENSDART00000141643 | Nonsense | 297 | 391 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 22747668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19003114 |
GRCz11 | 6 | 21063336 |
KASP Assay ID:
2259-7479.1 (used for ordering genotyping assays)
KASP Sequence:
CCATCCACGTCCACCATCTGTCACCGCCTTTCCAGTGCTCCACCTGGATA[T/A]CAGGCTKTCCAGAAAAAGTACTCCTCAGGCAAGCTAAAGGCTGAGTTCCT
Long Flanking Sequence:
GAGATGACTGAAGAAGTTCCCATGATCCCAGAAGAGATTGAGCCATCAGAGAAGGACAACAAATCAGCAGCTTCAACCAAGACTACCGCTGCTTCTGATGCTGCCGTGAAACATGATGGCCGACGCCGCATCAAGAGAGATGGTCTCATGAAGGTGTACGTGTTACAGTTGATCTCTCGTGTTGCCTTTGAGATAGCCTTCCTCTTTGGCCAATGTATTCTTTATGGTTTTGAGGTCTCTCCATCCTACATTTGCACCCGAAGCCCTTGCCCACACACAGTGGATTGCTTTGTCTCACGTCCCACTGAAAAAACCATCTTTCTGCTCATCATGTATGTTGTCAGTGTACTCTGTCTGGCACTGACTGTATTGGAAATCCTGCATCTGGGAATTGGTGGCTTGAGGGACTCATTTCGTAGTCGAGCAAATCGGAGACTCCCTGTTCATAGGCCATCCACGTCCACCATCTGTCACCGCCTTTCCAGTGCTCCACCTGGATA[T/A]CAGGCTGTCCAGAAAAAGTACTCCTCAGGCAAGCTAAAGGCTGAGTTCCTGTCAGACTCAGGACGGGAGTCACTGGCTGATGACAACACTACTCGTGATCTAGACCGTCTGCGGAGGCATCTGAAAATTGCACAGCAACACCTGGACCAGGCCTACCACACTGAGGAAGTAGGGGCTTCACACAACAGCGGGCCTGACTCTAAAAGCATCGCTGCTGAGCAAAACCGACTCAACCAGGCGCAGGGAGGCTTTGGCAGCACTGAGGAGAAAGGTTAGTTTGAGATGCACTTCATTCCCTCACTTAAACCCAGTCGAGTAATCAGGGTTAGATATTTACTAGGAATGTGACGAGATCTCGAGCTACTAGATATCGCAAGACTAAATCAAGATTTCTTGTTGTGGTGAAAAGTTGTCTCGTGAGTTGTGATGTTATGATGGAGCGTGAGGGTAAATTTAGCACTGAAGATTGAAGGCAGGATTGGATTAGAACCGCACAACAT
Associated Phenotype:
Not determined