ZMP
zgc:77713
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC402894 [Source:RefSeq peptide;Acc:NP_991165]
Human Orthologue:
C4orf34
Human Description:
chromosome 4 open reading frame 34 [Source:HGNC Symbol;Acc:27321]
Mouse Orthologue:
1110003E01Rik
Mouse Description:
RIKEN cDNA 1110003E01 gene Gene [Source:MGI Symbol;Acc:MGI:1915802]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16849 | Nonsense | Available for shipment | Available now |
sa17683 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16849
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008201 | None | None | 103 | 1 | 5 |
ENSDART00000137567 | Nonsense | 18 | 142 | 1 | 5 |
The following transcripts of ENSDARG00000005799 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 22082268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 22617435 |
GRCz11 | 1 | 23308174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTTGCACTGGGYTTKGTCTGTCCAACCGGAGTCTCTCAAGGATCGATA[T/G]AAACATATCAGAGCTGCTTANNNNAAGYGAAKGCTTTTAAATCTCTTCGA
Long Flanking Sequence:
ATTTAATATTTTAAATTGTACTTCTTTTGCCTTGGGTAGACTGATATTGTATGGTAAGCCTTTTTTCGTCCTCACAGAATGATCTCAGAGTCTGCGACATTTCACGTCAGCGACGTGGCTCTCCATGTTAATTCCTCTACACGAACGAGTAAATATTACTATGCTAAAGGATGATCTCATGTATATTAATTACCAGGCGTTCTCTGCGGCCAGTCGGCCTTGTTGATTTGTTTAAATCTACAGATGACTTATCTCTTTAATATTAATTACGTCTGCAATTGGACGCCCCACGAAGGATACAAATCAACGTCAGCACAGGTGTTTACCATTCATGAACCAAGCCTTCGCCATAGTAACATTCCTAATTTTGCTTTGCCGATCCTATCAAAACACAGACGGAACATCAGCCGGAGGTGCAGCTCTTTGCCAAACGCCAGTGTACACAGGGATCATTTGCACTGGGTTTTGTCTGTCCAACCGGAGTCTCTCAAGGATCGATA[T/G]AAACATATCAGAGCTGCTTATTTAAAGCGAATGCTTTTAAATCTCTTCGAGTGAGTTGTCCAAATCATTGGTAAGATATCTAAATACTGTTTGATTTGCATTGTAGTTTAACATATCATTCTTATATTTCATAATTGCCTTTTTTAACGTTGCCTTCGTTCAAATATTTTGTCTTGGTTAATGAATTTAAGTAAATTTTGCATCCTTGAGGATAGGATTGCAATTAATGCTTACTTATGATTTACAATAGCTTTTAAAAATGTGTTTTTTATTCTTTGTTTATTTTGTAAAAGTTACCTTAAATTATATTGATTGCGTGCTTTTAGAAGCAGTTAGTAACTTTTTAGTGCTTGTCGCTAGGTTGAGTGTAAAGTTTCTCGAAAGGAAGGTATCCACGACAAATTAACGTAGTAAAATAAGACATTTACAATTGCATCGAATCTATCTAGGTATCTTTAAGATGTGTAGTATTACTTTTTTAAATAAGTAAACGCATCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17683
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 |
---|---|---|---|---|---|
ENSDART00000008201 | None | None | 103 | 1 | 5 |
ENSDART00000137567 | Nonsense | 28 | 142 | 1 | 5 |
The following transcripts of ENSDARG00000005799 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 22082240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 22617407 |
GRCz11 | 1 | 23308146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGAGTCTCTCAAGGATCGATAKAAACATATCAGAGCTGCTTANNNNAAG[C/T]GAAKGCTTTTAAATCTCTTCGAGTGAGTTGTCCAAATCATTGGTAAGATA
Long Flanking Sequence:
GCCTTGGGTAGACTGATATTGTATGGTAAGCCTTTTTTCGTCCTCACAGAATGATCTCAGAGTCTGCGACATTTCACGTCAGCGACGTGGCTCTCCATGTTAATTCCTCTACACGAACGAGTAAATATTACTATGCTAAAGGATGATCTCATGTATATTAATTACCAGGCGTTCTCTGCGGCCAGTCGGCCTTGTTGATTTGTTTAAATCTACAGATGACTTATCTCTTTAATATTAATTACGTCTGCAATTGGACGCCCCACGAAGGATACAAATCAACGTCAGCACAGGTGTTTACCATTCATGAACCAAGCCTTCGCCATAGTAACATTCCTAATTTTGCTTTGCCGATCCTATCAAAACACAGACGGAACATCAGCCGGAGGTGCAGCTCTTTGCCAAACGCCAGTGTACACAGGGATCATTTGCACTGGGTTTTGTCTGTCCAACCGGAGTCTCTCAAGGATCGATATAAACATATCAGAGCTGCTTATTTAAAG[C/T]GAATGCTTTTAAATCTCTTCGAGTGAGTTGTCCAAATCATTGGTAAGATATCTAAATACTGTTTGATTTGCATTGTAGTTTAACATATCATTCTTATATTTCATAATTGCCTTTTTTAACGTTGCCTTCGTTCAAATATTTTGTCTTGGTTAATGAATTTAAGTAAATTTTGCATCCTTGAGGATAGGATTGCAATTAATGCTTACTTATGATTTACAATAGCTTTTAAAAATGTGTTTTTTATTCTTTGTTTATTTTGTAAAAGTTACCTTAAATTATATTGATTGCGTGCTTTTAGAAGCAGTTAGTAACTTTTTAGTGCTTGTCGCTAGGTTGAGTGTAAAGTTTCTCGAAAGGAAGGTATCCACGACAAATTAACGTAGTAAAATAAGACATTTACAATTGCATCGAATCTATCTAGGTATCTTTAAGATGTGTAGTATTACTTTTTTAAATAAGTAAACGCATCCTTTCCTGAAACTATTCGTTTTGTTTGTTTG
Associated Phenotype:
Not determined