ZMP
si:ch211-286o21.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens C10orf132, chromosome 10 open reading frame 132 (C10orf132) [Sour
Human Orthologue:
GOLGA7B
Human Description:
golgin A7 family, member B [Source:HGNC Symbol;Acc:31668]
Mouse Orthologue:
Golga7b
Mouse Description:
golgi autoantigen, golgin subfamily a, 7B Gene [Source:MGI Symbol;Acc:MGI:1918396]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45498 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45498
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039676 | Essential Splice Site | 60 | 214 | 1 | 5 |
| ENSDART00000146456 | Essential Splice Site | 4 | 158 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 40860282)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 39893354 |
| GRCz11 | 13 | 40019244 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGCACCGGGACAGATCCTTCACCGTCTCAGGCATCATGGGGACAGAG[G/A]TAAGATCCACTAACCTTCATATGAGCTTCAAGCGAGATGAAAAGCGGCTC
Long Flanking Sequence:
CAGGGAATAAGCCAAAAAGAAAATGAATGAATGAATATATAAATTGCACTTCAAGCTAAAAACTAGTATCCTGAAAAATATCTAGTAAAATATTATTTATTGTCATCATTGCAAAGATAAAAGAAATCAGTTATTAGAAATTAGTCAGTTAGTTATGTTTAGGAATGTGTTTTAAAAAGTCTTTGAAAGTATAGTTATTGACGAGACACTCATTTAAATAGTTATTGACGAGATATTCTTTCACGACTCACGAGACACTTTTTAACCTCGTTGTTTAAGTGTTAATCAGGTGCTCCTGCTCCCCCTTTCTCAGAAGATGCATGTACAATCCTGAAGTGAAGCACAACTGTTGTAGTCACTCCTCCTCCGTCAGCGGGAGTCGGATGCTGCTCCACCCTCTCCAGCGCCTTCATCTCACCGTCCGTTCTCTGTCCCGCGAGTGGAGAGGATTTCAGCACCGGGACAGATCCTTCACCGTCTCAGGCATCATGGGGACAGAG[G/A]TAAGATCCACTAACCTTCATATGAGCTTCAAGCGAGATGAAAAGCGGCTCCGTTTATGCGCACGGCTTGTATGAAGTTATTTTGACACCTGCTGTACGAAATCACGACAATTCCTATGGACGCGTTCAGGGAATCCAGTTCGCACACGGTGTTTCAAGACAAGATTTCGTCGACGTGACACGGGGTTTTCCCATTTAAATCCGCCAAAAGAATATCTTGTGGTCAAAGCTAAGGAATCTGCGGTAAGAAAGAGTGAGTGATACAGACTGATGTTTTATTCAGCACCCTGGACAGAGACGAAAACATGTAAGACTGAATAAAGACGCTGAAGTTAAAGTATTTGTTACGCGGCTTTCTGTGATACTTGATTCTGATTGGTTAGTTGCGCAATTCATTTATTAATAACAATGGGAACACTGTGTGACTGAATGGAGATCGGGGAAACCCGTGTCTCTAACTGTGCTCCTGCCTCTGAATTGCTTAATAAAACATTTTAACTC
Associated Phenotype:
Not determined