ZMP
zgc:110222
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC550336 [Source:RefSeq peptide;Acc:NP_001017643]
Human Orthologues:
CXorf40A, CXorf40B
Human Descriptions:
chromosome X open reading frame 40A [Source:HGNC Symbol;Acc:28089]
chromosome X open reading frame 40B [Source:HGNC Symbol;Acc:17402]
chromosome X open reading frame 40B [Source:HGNC Symbol;Acc:17402]
Mouse Orthologue:
1110012L19Rik
Mouse Description:
RIKEN cDNA 1110012L19 gene Gene [Source:MGI Symbol;Acc:MGI:1915868]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25164 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa37353 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25164
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000065318 | Nonsense | 47 | 173 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 33045174)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 34044867 |
| GRCz11 | 21 | 34079357 |
KASP Assay ID:
554-7384.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCCTGCTGTCAGAGATGCAGAACAGCACTCTAGCTGTTCATATTGCTT[G/A]GAAAAGCTGGGAAGGAGAGGACTGGAGGCTCATTCTCACTGAAAGACTGG
Long Flanking Sequence:
TGCTGGATAAGTTGGCGATTCATTCCGCTGTGGCGACCCTAGATTAATAAAGGGACTAAGTCCAAAAGAAAATTTATGAATACAAAGCAGTCTACTGTGTAGCGTTTCCTGCAATGGTTGGTCTCTTTCACTAGTCGGCGCTCTTTCTTTTACGAGTTATTTTGTTTGTTAAGTGTCTCCTCTTTTTCTGGCGAATTTAAAAAAACAGGAAATGTATAACCAGTAGTTTACGAACGTGTATGACGGCTTGGCTGTTAACAACAGTTTAGGCGTAAGACTTTATCTGTTTGGTAAAGTAATTAGATTATTGTGATATTCACATTTTTTTCTGCTAAATAAATCGTTTAATATTGTTCTCGGTATGAGTTTAGAGGTGCATTGTTTGTCATTTCGTCAGCCGTACGCTACTCTTGTGTTAAATGGTGTTAAAACAATAGAAAGTCGCTGGCGACCCCTGCTGTCAGAGATGCAGAACAGCACTCTAGCTGTTCATATTGCTT[G/A]GAAAAGCTGGGAAGGAGAGGACTGGAGGCTCATTCTCACTGAAAGACTGGGAATGACATCCAAACAAACGGAGGAACTCCTGGAGTCGGGAGAAAGGTTCGGGCGGAGTGTTATAGCAGGTGAAGTTTAAATTAAATTGTTATTAATTATATTATTCAAAACTGTAAAACTGAAGTATTTAATGATTATGAACATAGAAAATAAAACAAATTTGTTTCCATATTTTGTGTCGTAGACATAAAATGATTTGATGGGATAACATCTAGATATAGACCCTATTATAAAAATCAAGGATTCTTATTGGTTTGTAATCCCATCTTATTTGTTTAAAAAAAACAGAGGTATAAAGTTTTTTCCGTTAAAGTTTTACTGAAACTTTCCAAATTTCATAAGCAGGTTTGTTGTATTGGAAAATGCTGTACAAACGTAACTCATAATGTGACATTATGGAACAATCACTGTATAATAATGCAACGTAAATCTTTTTTTTTTTTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37353
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 |
|---|---|---|---|---|---|
| ENSDART00000065318 | Nonsense | 69 | 173 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 33045239)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 34044932 |
| GRCz11 | 21 | 34079422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGGACTGGAGGCTCATTCTCACTGAAAGACTGGGAATGACATCCAAA[C/T]AAACGGAGGAACTCCTGGAGTCGGGAGAAAGGTTCGGGCGGAGTGTTATA
Long Flanking Sequence:
AAGAAAATTTATGAATACAAAGCAGTCTACTGTGTAGCGTTTCCTGCAATGGTTGGTCTCTTTCACTAGTCGGCGCTCTTTCTTTTACGAGTTATTTTGTTTGTTAAGTGTCTCCTCTTTTTCTGGCGAATTTAAAAAAACAGGAAATGTATAACCAGTAGTTTACGAACGTGTATGACGGCTTGGCTGTTAACAACAGTTTAGGCGTAAGACTTTATCTGTTTGGTAAAGTAATTAGATTATTGTGATATTCACATTTTTTTCTGCTAAATAAATCGTTTAATATTGTTCTCGGTATGAGTTTAGAGGTGCATTGTTTGTCATTTCGTCAGCCGTACGCTACTCTTGTGTTAAATGGTGTTAAAACAATAGAAAGTCGCTGGCGACCCCTGCTGTCAGAGATGCAGAACAGCACTCTAGCTGTTCATATTGCTTGGAAAAGCTGGGAAGGAGAGGACTGGAGGCTCATTCTCACTGAAAGACTGGGAATGACATCCAAA[C/T]AAACGGAGGAACTCCTGGAGTCGGGAGAAAGGTTCGGGCGGAGTGTTATAGCAGGTGAAGTTTAAATTAAATTGTTATTAATTATATTATTCAAAACTGTAAAACTGAAGTATTTAATGATTATGAACATAGAAAATAAAACAAATTTGTTTCCATATTTTGTGTCGTAGACATAAAATGATTTGATGGGATAACATCTAGATATAGACCCTATTATAAAAATCAAGGATTCTTATTGGTTTGTAATCCCATCTTATTTGTTTAAAAAAAACAGAGGTATAAAGTTTTTTCCGTTAAAGTTTTACTGAAACTTTCCAAATTTCATAAGCAGGTTTGTTGTATTGGAAAATGCTGTACAAACGTAACTCATAATGTGACATTATGGAACAATCACTGTATAATAATGCAACGTAAATCTTTTTTTTTTTTTTTTTTGGAGGATTGGTGGCAAAATGTAGGTTGGTCAGTACTACATATTTTGGATACGAATGCTTGTTTTG
Associated Phenotype:
Not determined