ZMP
cx52.6
Ensembl ID:
ZFIN ID:
Description:
connexin 52.6 [Source:RefSeq peptide;Acc:NP_997984]
Human Orthologues:
GJA10, GJA9
Human Descriptions:
gap junction protein, alpha 10, 62kDa [Source:HGNC Symbol;Acc:16995]
gap junction protein, alpha 9, 59kDa [Source:HGNC Symbol;Acc:19155]
gap junction protein, alpha 9, 59kDa [Source:HGNC Symbol;Acc:19155]
Mouse Orthologue:
Gja10
Mouse Description:
gap junction protein, alpha 10 Gene [Source:MGI Symbol;Acc:MGI:1339969]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu2504 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa43436 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu2504
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042123 | Nonsense | 329 | 466 | 1 | 1 |
ENSDART00000121815 | Nonsense | 329 | 474 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 23943849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24062650 |
GRCz11 | 20 | 23961750 |
KASP Assay ID:
554-0065.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCTGTGCAGCCTCTGAGACAGGACCGTCTTCCAAGCCAACCCGAAATT[C/T]AAGTTCTTCAACAACTGGGAATCAAAGAACGAAGGTCCATTCCAGACAAC
Long Flanking Sequence:
CCAGGTCAGTGGTGGAGGTGGGATTCATAGTGGGGCAGTACATGCTCTACGGTATCGGACTGACGCCGCTGTACAAGTGTGAGCGTGATCCTTGCCCCAACAGTGTAGACTGCTTTGTTTCTCGGCCGACAGAGAAGAACATCTTCATGATTTTCATGCTGGTCATATCAGGAGTGTCCTTGTTCCTCAATCTCCTGGAGATTTTCCACCTTGGTGTGAAAAAGATCAAGCAGACCATATATGGATCCATGTACAGCGACGACGACAGCATTTGCAGGTCAAAGAAAAACTCCATGGTCCAACAAGTGTGCTTCCTTACAAATTCCTCACCACAAAAACAGTTGCATTTGACACACACTTCCCTTGCCATGGCACCTGATGGACAGATGGTACCTTTGCCTATCTATATGCAGACAGCTGGTCATGTAGTGTCCAACATTAACCCAAATGGATCTGTGCAGCCTCTGAGACAGGACCGTCTTCCAAGCCAACCCGAAATT[C/T]AAGTTCTTCAACAACTGGGAATCAAAGAACGAAGGTCCATTCCAGACAACCGTCTGCAATCCTGCAGCAGTGAGGATTCTGGCCCCAAAGGTTCCGAACCACCGAAATATTCTCAGCAGCCCCGAGCTTCATTCAGAGCCAGTCATATAGAAATACCAGCAGCATTAAGGAAACACAGCCGTGTTAGTCAGTGTAAAGACTTCAGTGAGGAGAGTGATTCGGTGGAAAGTGGGAACTATCCTACTGCCAGGAAAGCCAGCTTCATGTCAAGGGGACTTTCAGAGAGCCCGTCTGAGAGTGCAGCCTCCAAGAGTGGATCAGACACAGAGGCCAACCGTATCACTCAAGGGGAGAGTCCCGCTATGACACCACCCCCTGCAGCAGGACGTAGAATGTCAATGGTAAGAAAATTCTGATAAAATCCATTATATACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa43436
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 |
---|---|---|---|---|---|
ENSDART00000042123 | Nonsense | 384 | 466 | 1 | 1 |
ENSDART00000121815 | Nonsense | 384 | 474 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 23944015)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24062816 |
GRCz11 | 20 | 23961916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCCCCGAGCTTCATTCAGAGCCAGTCATATAGAAATACCAGCAGCAT[T/A]AAGGAAACACAGCCGTGTTAGTCAGTGTAAAGACTTCAGTGAGGAGAGTG
Long Flanking Sequence:
ATCAGGAGTGTCCTTGTTCCTCAATCTCCTGGAGATTTTCCACCTTGGTGTGAAAAAGATCAAGCAGACCATATATGGATCCATGTACAGCGACGACGACAGCATTTGCAGGTCAAAGAAAAACTCCATGGTCCAACAAGTGTGCTTCCTTACAAATTCCTCACCACAAAAACAGTTGCATTTGACACACACTTCCCTTGCCATGGCACCTGATGGACAGATGGTACCTTTGCCTATCTATATGCAGACAGCTGGTCATGTAGTGTCCAACATTAACCCAAATGGATCTGTGCAGCCTCTGAGACAGGACCGTCTTCCAAGCCAACCCGAAATTCAAGTTCTTCAACAACTGGGAATCAAAGAACGAAGGTCCATTCCAGACAACCGTCTGCAATCCTGCAGCAGTGAGGATTCTGGCCCCAAAGGTTCCGAACCACCGAAATATTCTCAGCAGCCCCGAGCTTCATTCAGAGCCAGTCATATAGAAATACCAGCAGCAT[T/A]AAGGAAACACAGCCGTGTTAGTCAGTGTAAAGACTTCAGTGAGGAGAGTGATTCGGTGGAAAGTGGGAACTATCCTACTGCCAGGAAAGCCAGCTTCATGTCAAGGGGACTTTCAGAGAGCCCGTCTGAGAGTGCAGCCTCCAAGAGTGGATCAGACACAGAGGCCAACCGTATCACTCAAGGGGAGAGTCCCGCTATGACACCACCCCCTGCAGCAGGACGTAGAATGTCAATGGTAAGAAAATTCTGATAAAATCCATTATATACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTTGAGATCAAAATTATTAGCCCCCCTGAATTATTACCCCTCTGTTGATTGTTTCCCCAATTTCTACAGTAATTTCAAATTTTCTTTAATAGAGAGATGATTTTTTTCATCACACTTGTCAACATAACACACACATAT
Associated Phenotype:
Not determined