ZMP
si:ch211-232m10.6
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC572203 [Source:RefSeq peptide;Acc:NP_001092222]
Human Orthologue:
AC027045.1
Human Description:
Putative germ cell-specific gene 1-like protein 2 [Source:UniProtKB/Swiss-Prot;Acc:A8MUP6]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39234 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43238 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39234
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 |
---|---|---|---|---|---|
ENSDART00000104548 | Nonsense | 64 | 205 | 2 | 3 |
ENSDART00000126547 | Nonsense | 203 | 242 | 5 | 6 |
ENSDART00000131517 | Nonsense | 228 | 369 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 19 (position 10979842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10438381 |
GRCz11 | 19 | 10357306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAGTATTCCAGATGACTGTCAGCATTGGGCCCAAAGACTGGAGACCT[C/T]AGACCTGGGACTACGGCTGGTCATTTGCGTGAGTATCCTTATACCTTTGT
Long Flanking Sequence:
AAAAAAGAAGGGTGCTGCAAGATTTCAACCTTTGGGAACCGATTGGATTGTTTGAAGGAGGGTAATGCCAACAAAACAGAGAAAGATTATTAAATGGACAAAATCAGGCTAAAAACAAAACATGCCCTAATAGCCCTTAAAAGACTGATAGCCCCGCCCTCAATGCACTCCATGTGACCAAAAGTAAAGAAAAGTCATTTTGATGGGGGAGGGAAGGTTACGAGATTTGATTAAAGATTATTAAAGAATGTTTAGAAAATAATGTGCACAGACGCATCATTTATAACAAGCACTACTATATGCATAGAAAAATAAGAATAGAACATATTTCTTTCATGCCAACTTTAAGAAAATGTTATTCATAATCGATATTTAACAGAATTAAACTAGCAGAATAATAACCTTTCTCCATTTTAGGCATGATGGGAATGGTGGCGCATATGATGTACACAACAGTATTCCAGATGACTGTCAGCATTGGGCCCAAAGACTGGAGACCT[C/T]AGACCTGGGACTACGGCTGGTCATTTGCGTGAGTATCCTTATACCTTTGTCTAGTGCTATATTAATATACGCCTGGGGATGGATGGATGGATGGATGGATGGATGGATGGATAGATGGATGTACGGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGATAGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGTTGGGTTGGATGGATGGATGGATGGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGAGATTATGAATCTGAATATTAATTTCCATTTCTTCTTCTTCCACAGAATGGCCTGGATCTCCTTCAGCTGTTGCATGGCGGCGGCCGTATTCACACTAAACTCTTACACCAAAACATTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43238
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104548 | Nonsense | 93 | 205 | 3 | 3 |
ENSDART00000126547 | Nonsense | 232 | 242 | 6 | 6 |
ENSDART00000131517 | Nonsense | 257 | 369 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 19 (position 10979357)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10437896 |
GRCz11 | 19 | 10356821 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCCTTCAGCTGTTGCATGGCGGCGGCCGTATTCACACTAAACTCTTA[C/A]ACCAAAACATTGATTGAGATGAAACACCGTGCCCGTGTCCGTCTGGAGGA
Long Flanking Sequence:
AAAGACTGGAGACCTCAGACCTGGGACTACGGCTGGTCATTTGCGTGAGTATCCTTATACCTTTGTCTAGTGCTATATTAATATACGCCTGGGGATGGATGGATGGATGGATGGATGGATGGATGGATAGATGGATGTACGGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGATAGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGTTGGGTTGGATGGATGGATGGATGGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGAGATTATGAATCTGAATATTAATTTCCATTTCTTCTTCTTCCACAGAATGGCCTGGATCTCCTTCAGCTGTTGCATGGCGGCGGCCGTATTCACACTAAACTCTTA[C/A]ACCAAAACATTGATTGAGATGAAACACCGTGCCCGTGTCCGTCTGGAGGAAGCCCGAGCTGCCAACCACGCACCTCCCTATGATGAGGTGATCACAAGCGGCGGAGAGAGCCTGTACTCGGTCAGCCGGCTGGTTCAGCAAAGCCAGCAGGGAGCGTACATCGACAACATGTGGATGCCCAGAGACGAAGGGTCCATTGGGGGAATGGTGGGCACCAAGAGTCCTCATGGGCTGGTGCTATTGGGGGGCTGTGGGAGAGAGGGATGCGAGGATTGCGAGAGAGAAATGGATGAGATGGAGGAAGCGTTGGAGAGGGAGAGAAACGATGAAATGTGCTGAGGAGACTCTAATGGGAAATGACATTTGGAGAAAGAAAAAAAAACAACGAAGCTTTTCGTCATCAGTACCATCAGTGATCACATTTGCATATCTTTTTTTTTAATTAAAGGGATAGTTCAAACAAGAAAGAAAGAAAATTCTGTCATCATTTACTCGCCTTT
Associated Phenotype:
Not determined