ZMP
cx47.1
Ensembl ID:
ZFIN ID:
Description:
connexin 47.1 [Source:RefSeq peptide;Acc:NP_001004574]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25746 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11554 | Nonsense | Available for shipment | Available now |
sa39750 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa540 | Nonsense | F2 line generated | Not yet available |
sa32830 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25746
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115278 | Nonsense | 123 | 409 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 3991208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3665734 |
GRCz11 | 2 | 3496913 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGACACAAGAACCAGATTTACCAGAAGAGGAGGCACCACAGTCGCTGG[A/T]GAAACGGACACCATCTAGAGGACGCTTTAGAGGAGGAAGATGAGGACGCG
Long Flanking Sequence:
GTTGCAACTAAAATTTGCAGAAAGGTAGCTCTCCTAGAACAAGGTTAGGGACCCCTGATGTAGACTGTACCTCAACACTTACCTCATTTTCCCTCTGTTTTTCAGATCCTAAATAAAGAGCCTCTGTCACCAACATGAGCTGGAGCTTTCTCACTCGACTCTTGGAGGAAATCCACAACCACTCCACATTTGTGGGGAAGGTCTGGCTGACGGTCTTGATCATCTTCCGGATCGTTCTGACCGCAGTCGGGGGCGAGTCGATCTACTCGGATGAGCAGACAAAGTTCACCTGCAACACAAAGCAGCCCGGCTGTGACAACGTCTGCTACGACGCCTTCGCACCGCTCTCACACGTCCGCTTCTGGGTCTTCCAGATAATCATGATTTCCACACCCTCCGTCATGTATCTGGGATATGCCATCCATAAGATCGCCAAAACCTCAGAGGAGGAACGACACAAGAACCAGATTTACCAGAAGAGGAGGCACCACAGTCGCTGG[A/T]GAAACGGACACCATCTAGAGGACGCTTTAGAGGAGGAAGATGAGGACGCGGAGCCAATGATCTACGAAGAAGATGCACGAGAGATCAAAGCAGAGACTGTCCGAGATCCCCTAAAACACGATGGCCGCCGCAGGATCATGCAAGAAGGTTTAATGAGGATGTATGTTCTTCAACTTTTATCCCGCGCCATCTTCGAGGTGGGATTCCTCACGGGTCAGTATCTCCTCTACGGCTTCCGCGTCAACCCTTCGTACGTCTGCAACAAGATCCCATGCCCACACAGGGTGGACTGCTTTGTTTCAAGACCCACCGAGAAGACCATCTTTTTGCTCATCATGTATGTGGTGAGCTGTCTATGTCTGCTGCTCAATGTTTGCGAGATGTTTCACTTGGGGATCGGTGCCTTTCGAGACACTCTTCGCAAACGTCGAAACCAGAATCAGCGACCTTCCTATGGCTACCCTTACTCCAGGAATATTTCCAGTTCTCCGCCAGGATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11554
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 |
---|---|---|---|---|---|
ENSDART00000115278 | Nonsense | 177 | 409 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 3991372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3665898 |
GRCz11 | 2 | 3497077 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACACGATGGCCGCCGCAGGATCATGCAAGAAGGTTTAATGAGGATGTA[T/A]GTWCTTCAACTTTTATCYCGCGCCATCTTYGAGGTGGGATTCCTCAYGGG
Long Flanking Sequence:
GAGGAAATCCACAACCACTCCACATTTGTGGGGAAGGTCTGGCTGACGGTCTTGATCATCTTCCGGATCGTTCTGACCGCAGTCGGGGGCGAGTCGATCTACTCGGATGAGCAGACAAAGTTCACCTGCAACACAAAGCAGCCCGGCTGTGACAACGTCTGCTACGACGCCTTCGCACCGCTCTCACACGTCCGCTTCTGGGTCTTCCAGATAATCATGATTTCCACACCCTCCGTCATGTATCTGGGATATGCCATCCATAAGATCGCCAAAACCTCAGAGGAGGAACGACACAAGAACCAGATTTACCAGAAGAGGAGGCACCACAGTCGCTGGAGAAACGGACACCATCTAGAGGACGCTTTAGAGGAGGAAGATGAGGACGCGGAGCCAATGATCTACGAAGAAGATGCACGAGAGATCAAAGCAGAGACTGTCCGAGATCCCCTAAAACACGATGGCCGCCGCAGGATCATGCAAGAAGGTTTAATGAGGATGTA[T/A]GTTCTTCAACTTTTATCCCGCGCCATCTTCGAGGTGGGATTCCTCACGGGTCAGTATCTCCTCTACGGCTTCCGCGTCAACCCTTCGTACGTCTGCAACAAGATCCCATGCCCACACAGGGTGGACTGCTTTGTTTCAAGACCCACCGAGAAGACCATCTTTTTGCTCATCATGTATGTGGTGAGCTGTCTATGTCTGCTGCTCAATGTTTGCGAGATGTTTCACTTGGGGATCGGTGCCTTTCGAGACACTCTTCGCAAACGTCGAAACCAGAATCAGCGACCTTCCTATGGCTACCCTTACTCCAGGAATATTTCCAGTTCTCCGCCAGGATACAACTTAGTTGTTAAATCCGACAAACCCGGTCGCATTCCCAACAGCATCGTCCTGCCTGATCAGAACATGGATAGAGAGATCGCAGAACAACACTGCACAAGTCCTGATGAGAACATCCCCACTGACCTAGCAACCTTGCACCACCATTTACGAGTAGCTCAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39750
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 |
---|---|---|---|---|---|
ENSDART00000115278 | Nonsense | 236 | 409 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 3991549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3666075 |
GRCz11 | 2 | 3497254 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTTGTTTCAAGACCCACCGAGAAGACCATCTTTTTGCTCATCATGTA[T/A]GTGGTGAGCTGTCTATGTCTGCTGCTCAATGTTTGCGAGATGTTTCACTT
Long Flanking Sequence:
CCGCTCTCACACGTCCGCTTCTGGGTCTTCCAGATAATCATGATTTCCACACCCTCCGTCATGTATCTGGGATATGCCATCCATAAGATCGCCAAAACCTCAGAGGAGGAACGACACAAGAACCAGATTTACCAGAAGAGGAGGCACCACAGTCGCTGGAGAAACGGACACCATCTAGAGGACGCTTTAGAGGAGGAAGATGAGGACGCGGAGCCAATGATCTACGAAGAAGATGCACGAGAGATCAAAGCAGAGACTGTCCGAGATCCCCTAAAACACGATGGCCGCCGCAGGATCATGCAAGAAGGTTTAATGAGGATGTATGTTCTTCAACTTTTATCCCGCGCCATCTTCGAGGTGGGATTCCTCACGGGTCAGTATCTCCTCTACGGCTTCCGCGTCAACCCTTCGTACGTCTGCAACAAGATCCCATGCCCACACAGGGTGGACTGCTTTGTTTCAAGACCCACCGAGAAGACCATCTTTTTGCTCATCATGTA[T/A]GTGGTGAGCTGTCTATGTCTGCTGCTCAATGTTTGCGAGATGTTTCACTTGGGGATCGGTGCCTTTCGAGACACTCTTCGCAAACGTCGAAACCAGAATCAGCGACCTTCCTATGGCTACCCTTACTCCAGGAATATTTCCAGTTCTCCGCCAGGATACAACTTAGTTGTTAAATCCGACAAACCCGGTCGCATTCCCAACAGCATCGTCCTGCCTGATCAGAACATGGATAGAGAGATCGCAGAACAACACTGCACAAGTCCTGATGAGAACATCCCCACTGACCTAGCAACCTTGCACCACCATTTACGAGTAGCTCAGGAGCAGCTTGACATGGCTTTTCAGACATACAACACAAAAACCACTCATATTTCAAGAGCCAGCAGCCCCGTTTCTGGTGGCACAACGACAGAGCAGAACCGCATCAACATGGCTCAGGAGAAGCAGGGCGCTCGGCCCAAAGCAAGCACCGAGAGAGCTGGGACACTAGTAAAAAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa540
Status:
F2 line generated
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115278 | Nonsense | 310 | 409 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 3991769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3666295 |
GRCz11 | 2 | 3497474 |
KASP Assay ID:
554-0450.1 (used for ordering genotyping assays)
KASP Sequence:
TTAAATCCGACAAACCCGGTCGCATTCCCAACAGCATCGTCCTGCCTGAT[C/T]AGAACATGGATAGAGAGATCGCAGAACAACACTGCACAAGTCCTGATGAG
Long Flanking Sequence:
TCTACGAAGAAGATGCACGAGAGATCAAAGCAGAGACTGTCCGAGATCCCCTAAAACACGATGGCCGCCGCAGGATCATGCAAGAAGGTTTAATGAGGATGTATGTTCTTCAACTTTTATCCCGCGCCATCTTCGAGGTGGGATTCCTCACGGGTCAGTATCTCCTCTACGGCTTCCGCGTCAACCCTTCGTACGTCTGCAACAAGATCCCATGCCCACACAGGGTGGACTGCTTTGTTTCAAGACCCACCGAGAAGACCATCTTTTTGCTCATCATGTATGTGGTGAGCTGTCTATGTCTGCTGCTCAATGTTTGCGAGATGTTTCACTTGGGGATCGGTGCCTTTCGAGACACTCTTCGCAAACGTCGAAACCAGAATCAGCGACCTTCCTATGGCTACCCTTACTCCAGGAATATTTCCAGTTCTCCGCCAGGATACAACTTAGTTGTTAAATCCGACAAACCCGGTCGCATTCCCAACAGCATCGTCCTGCCTGAT[C/T]AGAACATGGATAGAGAGATCGCAGAACAACACTGCACAAGTCCTGATGAGAACATCCCCACTGACCTAGCAACCTTGCACCACCATTTACGAGTAGCTCAGGAGCAGCTTGACATGGCTTTTCAGACATACAACACAAAAACCACTCATATTTCAAGAGCCAGCAGCCCCGTTTCTGGTGGCACAACGACAGAGCAGAACCGCATCAACATGGCTCAGGAGAAGCAGGGCGCTCGGCCCAAAGCAAGCACCGAGAGAGCTGGGACACTAGTAAAAAATGGAAAAACTTCGGTGTGGATTTAATAGAAAACTCTTCGTACCTGACTAGTCATTTTTCCTTAGAAAACATATTGCAAACTGCGTTCAGCGAGGACACAATTGATCATGTTCCTTGGGTTCTGTTGAAACTTCTTCAAATATGAAAAATAAATAAACTGTAGACGGGTAGTGTCCATTTCCGAAGCTTTCTTTGCATCGTGTCTCAGAATAACCCTTAACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32830
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115278 | Nonsense | 340 | 409 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 3991859)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3666385 |
GRCz11 | 2 | 3497564 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCTGATGAGAACATCCCCACTGACCTAGCAACCTTGCACCACCATTTA[C/T]GAGTAGCTCAGGAGCAGCTTGACATGGCTTTTCAGACATACAACACAAAA
Long Flanking Sequence:
TAATGAGGATGTATGTTCTTCAACTTTTATCCCGCGCCATCTTCGAGGTGGGATTCCTCACGGGTCAGTATCTCCTCTACGGCTTCCGCGTCAACCCTTCGTACGTCTGCAACAAGATCCCATGCCCACACAGGGTGGACTGCTTTGTTTCAAGACCCACCGAGAAGACCATCTTTTTGCTCATCATGTATGTGGTGAGCTGTCTATGTCTGCTGCTCAATGTTTGCGAGATGTTTCACTTGGGGATCGGTGCCTTTCGAGACACTCTTCGCAAACGTCGAAACCAGAATCAGCGACCTTCCTATGGCTACCCTTACTCCAGGAATATTTCCAGTTCTCCGCCAGGATACAACTTAGTTGTTAAATCCGACAAACCCGGTCGCATTCCCAACAGCATCGTCCTGCCTGATCAGAACATGGATAGAGAGATCGCAGAACAACACTGCACAAGTCCTGATGAGAACATCCCCACTGACCTAGCAACCTTGCACCACCATTTA[C/T]GAGTAGCTCAGGAGCAGCTTGACATGGCTTTTCAGACATACAACACAAAAACCACTCATATTTCAAGAGCCAGCAGCCCCGTTTCTGGTGGCACAACGACAGAGCAGAACCGCATCAACATGGCTCAGGAGAAGCAGGGCGCTCGGCCCAAAGCAAGCACCGAGAGAGCTGGGACACTAGTAAAAAATGGAAAAACTTCGGTGTGGATTTAATAGAAAACTCTTCGTACCTGACTAGTCATTTTTCCTTAGAAAACATATTGCAAACTGCGTTCAGCGAGGACACAATTGATCATGTTCCTTGGGTTCTGTTGAAACTTCTTCAAATATGAAAAATAAATAAACTGTAGACGGGTAGTGTCCATTTCCGAAGCTTTCTTTGCATCGTGTCTCAGAATAACCCTTAACATGCTCCATGTTGCATATCTTAAATGCTGCGTTTCTTTCTAATTTAAAAGAGCAAATCTGTTTCAGAAGTCAGTCTTTATTGTATCATTGTCC
Associated Phenotype:
Not determined