ZMP
zgc:111986
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC553664 [Source:RefSeq peptide;Acc:NP_001018473]
Human Orthologue:
C6orf62
Human Description:
chromosome 6 open reading frame 62 [Source:HGNC Symbol;Acc:20998]
Mouse Orthologue:
BC005537
Mouse Description:
cDNA sequence BC005537 Gene [Source:MGI Symbol;Acc:MGI:2441726]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17934 | Nonsense | Available for shipment | Available now |
| sa43306 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17934
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000052183 | Nonsense | 12 | 230 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 32828352)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 31995641 |
| GRCz11 | 19 | 31582954 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGTACTGTCCGTAAAAATGGRTGACCCAAATTCTCGACGGAATCAAACA[C/T]GAAACCGACTCCGTGCCCAGCTACGGAAGAAACGGGAATCTCTGGCTGAT
Long Flanking Sequence:
AATCCAGGGATCTGTCCCCTCACACATACACGGACGCACACACAAAATTGTCAGTATGGATTTTCAGTGTAGCAGGCATTTGTGTTTCCTGTCTTTTGTTCAGTGATACAATACAGACTCTCATTTAAAAAAAAAAAAGACTAACCAGGTCGTGTTATATGAGTGGTTTCTTTTAGTTTACCCTTAGCCTTGACTTGATGTTTTAAAAAAATGGTGTCACGCATCAAAACTTAGACAAGTGCAAACTTACTTGGCCCAAGTGCACTACCGATATTGATTAAAAATGAGTTGATTTGATTATTGCTAACTTTCTTTAATTCAAATTGGTATGTAGTGCTTGGTTATAGCTTCTTTAGTTTTTAAAAGGGTTTGAAAACAAAATAGTCTACAGTCGAGACAATAAAAAGTCAAAGAAATATTTAATAAAAAAAAAAGTCTGCATAAGGAAAATAGTACTGTCCGTAAAAATGGGTGACCCAAATTCTCGACGGAATCAAACA[C/T]GAAACCGACTCCGTGCCCAGCTACGGAAGAAACGGGAATCTCTGGCTGATCAGTTTGACTTCAAGATCTACATTGCCTTTGTATTTAAGGAAAAGGTATGTACATCTAAACGATATGAATTTGTTTGGAAAATGGACTGGCGTGGTTCTAATATCTCACTTTTTTGCAGAAAAAGAAGTCCGCACTCTTTGAAGTAGCTGAGGTTGTACCTGTGATGACCAACAACTATGAGGAAAATATCCTTAAAGGCGTGAAGGATTCGAGCTACTCCTTGGAGAGTTCTCTAGAGCTTCTCCAGAAAGATGTGGTGCAGTTACACGCGCTGCGTTACCAGTCGATGCGTAGAGTAAGTGTCCACACAAATGCTGTGCACTTTCAACATAGGCAGTTGAAGATTAAACCGCCATCGTAATTGTCTGTGTTGTCTAACTACACCATATCATGTCATTTGAGATCATTTTGTTTCTAAATTTGTCCAGGATGTGATAGGTTGTACCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43306
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 |
|---|---|---|---|---|---|
| ENSDART00000052183 | Essential Splice Site | 43 | 230 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 32828256)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 31995545 |
| GRCz11 | 19 | 31582858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATCAGTTTGACTTCAAGATCTACATTGCCTTTGTATTTAAGGAAAAG[G/A]TATGTACATCTAAACGATATGAATTTGTTTGGAAAATGGACTGGCGTGGT
Long Flanking Sequence:
TGTTCAGTGATACAATACAGACTCTCATTTAAAAAAAAAAAAGACTAACCAGGTCGTGTTATATGAGTGGTTTCTTTTAGTTTACCCTTAGCCTTGACTTGATGTTTTAAAAAAATGGTGTCACGCATCAAAACTTAGACAAGTGCAAACTTACTTGGCCCAAGTGCACTACCGATATTGATTAAAAATGAGTTGATTTGATTATTGCTAACTTTCTTTAATTCAAATTGGTATGTAGTGCTTGGTTATAGCTTCTTTAGTTTTTAAAAGGGTTTGAAAACAAAATAGTCTACAGTCGAGACAATAAAAAGTCAAAGAAATATTTAATAAAAAAAAAAGTCTGCATAAGGAAAATAGTACTGTCCGTAAAAATGGGTGACCCAAATTCTCGACGGAATCAAACACGAAACCGACTCCGTGCCCAGCTACGGAAGAAACGGGAATCTCTGGCTGATCAGTTTGACTTCAAGATCTACATTGCCTTTGTATTTAAGGAAAAG[G/A]TATGTACATCTAAACGATATGAATTTGTTTGGAAAATGGACTGGCGTGGTTCTAATATCTCACTTTTTTGCAGAAAAAGAAGTCCGCACTCTTTGAAGTAGCTGAGGTTGTACCTGTGATGACCAACAACTATGAGGAAAATATCCTTAAAGGCGTGAAGGATTCGAGCTACTCCTTGGAGAGTTCTCTAGAGCTTCTCCAGAAAGATGTGGTGCAGTTACACGCGCTGCGTTACCAGTCGATGCGTAGAGTAAGTGTCCACACAAATGCTGTGCACTTTCAACATAGGCAGTTGAAGATTAAACCGCCATCGTAATTGTCTGTGTTGTCTAACTACACCATATCATGTCATTTGAGATCATTTTGTTTCTAAATTTGTCCAGGATGTGATAGGTTGTACCCAGGAGATGGACTTTATCCTCTGGCCCCGCAACGATATTGAGAAAGTTGTCTGTCTCCTGTTCTCCAGATGGAAAGGGGCTGAACATGAACCATTCAGG
Associated Phenotype:
Not determined