ZMP
zgc:152953
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC571919 [Source:RefSeq peptide;Acc:NP_001073526]
Human Orthologue:
KIAA0649
Human Description:
KIAA0649 [Source:HGNC Symbol;Acc:29089]
Mouse Orthologue:
Gm347
Mouse Description:
predicted gene 347 Gene [Source:MGI Symbol;Acc:MGI:2685193]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35144 | Nonsense | Available for shipment | Available now |
| sa41898 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16533 | Nonsense | Available for shipment | Available now |
| sa24894 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45437 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35144
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 |
|---|---|---|---|---|---|
| ENSDART00000099351 | Nonsense | 69 | 1004 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 38626991)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 7547815 |
| GRCz11 | 21 | 7109306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTGAGAGCCTTCACAGTACCCAGTCTTCGGGCATGAGTGAAAACGAG[C/T]AGGCTGAAAAGGCTGCTCATTCCAGTCACGAGGCTGGCTACAAGGGTCAG
Long Flanking Sequence:
TTTCTTGTGCGCTCTCAAATAAATGCGGCTGAAGGGCGATTTAGTGTGCATGGATATAAGGGGTATGTCTCCAACATGTATTAAATCAGCACTACTAAGATTACAGAAAAGTTTGCTCAAAAACATTTTGATGCATTTATAACCCGCTGCAAAAGAAAAAACATCACAACTGAAGGAATGTTTTTACAATTACATGTTTTAAATGAAGATTTCTGCTTCTTTCTTTCAGGATGTAAACAAGATCACTGGTGGAGCTTCCCCATGCACCTGCATCCCTTCCATTCTGACTATCTAGAATGTTCCTGAAGACAGTTCCTCCGGCTGTGGCTATTCATTCAGAATGGAGGTCCAGTAAGAGCTGCAGCCTGCCTCTCTATTTCAATGACAGTGCCTCCGACAGCGACCTTGCCTCAGTTAGTGGCACCCCGTTCCCACAGAAGATCCAGATGATAATTGAGAGCCTTCACAGTACCCAGTCTTCGGGCATGAGTGAAAACGAG[C/T]AGGCTGAAAAGGCTGCTCATTCCAGTCACGAGGCTGGCTACAAGGGTCAGATGCGACTCATGGACATGTCGGCGAGAACCCGGCGATCAGGGTCAGACGCTAAGCTGCAGAACAACAGGTCTGATACTGGAGATGATTCAGATAGTGATGACTCTGTGGACAGAGGCATTGAGGAGGCCATACAGGAGTATTTAAAGGAGAAGGTGGACCACAAGCGCAAAGGGGATCCAGTGACAAGTTCACCCCCAGCGCCCAAACTTCAGCGAAGGGAACTAGATGCTCCGAAACAACAGACACATTCCAGCAGTGCTAAGGTGCTGACTGCTAGCAATCATATCCAGAGACTCTCAAGCGGGATGGTGGCCTTAAAAAAGAAAGTCAAAAAGAAGCAGCTGAGCAAAGAAAATCCCTTTAAGAAAGCAGACGCGAGTAAAGTTTCGCCTTTAAAAAGTCTTCCTCCACCCAGAGCTAAAAAAGGATCCTCCTCGTCTTCTGAGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41898
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099351 | Nonsense | 588 | 1004 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 38625106)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 7549700 |
| GRCz11 | 21 | 7111191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCGAGCAGAAGTGTATCCCACTCAACAGGCTTGTTAAATCTAGCATCT[T/A]GAAAGGTGGGAAAGAATCCCTGAACATTCAGGCTAAAAATGACAAGGTGC
Long Flanking Sequence:
CAAGTTCAAAGAGGAACAATGCAAACTTTCCAGAGATCAAGACATGGTTTTGAATGTTAAAGAGGAGCCTCCTGGGACACCTCTGATCCACAGTGACTCCACCAGACTTGAACTTTCTACCACTCCCACTGCGATTTCACATTCAAGTAGTGTGAAAAATAGCAAACTGAAACAGAACTCTCCTCCTCGCAAGGGTGCAGATCATGTAACTAAAGACAACGTTTCCTCTTGTAGTGCATCCAGCCCAAAGGCTGCGATCGGCTCTGAGAGAAACGACAGCAGTGACAAAAGCAGCTCCTTGGACAGTGACGAGGATTTAGATGCAGCAATTAAAGACCTACTCAAGACGAAGAAAAAAGTCAAGAAGAAGGTAAGGGACTTGAAGGCGAGAAAAAGTGACAAACCTTTTGAGGCGTCATCTTTGGATGCCATAAAAAAGCAGAAGCCTTTAACCGAGCAGAAGTGTATCCCACTCAACAGGCTTGTTAAATCTAGCATCT[T/A]GAAAGGTGGGAAAGAATCCCTGAACATTCAGGCTAAAAATGACAAGGTGCCTAAAAGCAAACCAGCTAAAGGCAAATGTGAGGTTCAAAACTTCAAGCCTTCTAAAAGCTTTGCGCAGACTGACAAGGTGACCGGGAATGGAGGGATTTCCTCAGCCCCAGGTGGAGACACACTTTCACCAAGTCTGCATGCAGATGACGACAGTGATGTGGACAGCGATGACAGCATTGAGCGAGAGATCAGGAGATTTCTAGCTGAAAGAGCTAAGGTGTCCGCACCTGTAACCACAAACATTAAAAGTGAGGAGAAGGGCATCAACTCCTCATCTGCAGAGACTGAGGAAAATCCAGATCTTCAAAAGACTCAAACTGAAACTCCAGTATCTGCTGCGACATCAACCTCCGGGAGACTCTGGAAGACTGAACTCACAGGTACGTCCACAAAATCTACAGAAACACCTGCAGAACTCAACAAGGGACCAGTCCTGACACCAGGCAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16533
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 |
|---|---|---|---|---|---|
| ENSDART00000099351 | Nonsense | 627 | 1004 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 38624990)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 7549816 |
| GRCz11 | 21 | 7111307 |
KASP Assay ID:
2260-4595.1 (used for ordering genotyping assays)
KASP Sequence:
CTAAAGGCAAATGYGAGGTTCAAAACTTCAAGCCTTCTAAAAGCYTTGCG[C/T]AGACTGACAAGGTGACCGGGAATGGAGGRATTTCCTCAGCCCCAGGTGGA
Long Flanking Sequence:
CTACCACTCCCACTGCGATTTCACATTCAAGTAGTGTGAAAAATAGCAAACTGAAACAGAACTCTCCTCCTCGCAAGGGTGCAGATCATGTAACTAAAGACAACGTTTCCTCTTGTAGTGCATCCAGCCCAAAGGCTGCGATCGGCTCTGAGAGAAACGACAGCAGTGACAAAAGCAGCTCCTTGGACAGTGACGAGGATTTAGATGCAGCAATTAAAGACCTACTCAAGACGAAGAAAAAAGTCAAGAAGAAGGTAAGGGACTTGAAGGCGAGAAAAAGTGACAAACCTTTTGAGGCGTCATCTTTGGATGCCATAAAAAAGCAGAAGCCTTTAACCGAGCAGAAGTGTATCCCACTCAACAGGCTTGTTAAATCTAGCATCTTGAAAGGTGGGAAAGAATCCCTGAACATTCAGGCTAAAAATGACAAGGTGCCTAAAAGCAAACCAGCTAAAGGCAAATGTGAGGTTCAAAACTTCAAGCCTTCTAAAAGCTTTGCG[C/T]AGACTGACAAGGTGACCGGGAATGGAGGGATTTCCTCAGCCCCAGGTGGAGACACACTTTCACCAAGTCTGCATGCAGATGACGACAGTGATGTGGACAGCGATGACAGCATTGAGCGAGAGATCAGGAGATTTCTAGCTGAAAGAGCTAAGGTGTCCGCACCTGTAACCACAAACATTAAAAGTGAGGAGAAGGGCATCAACTCCTCATCTGCAGAGACTGAGGAAAATCCAGATCTTCAAAAGACTCAAACTGAAACTCCAGTATCTGCTGCGACATCAACCTCCGGGAGACTCTGGAAGACTGAACTCACAGGTACGTCCACAAAATCTACAGAAACACCTGCAGAACTCAACAAGGGACCAGTCCTGACACCAGGCAGCTCTTGCATAATGGGATTCAGGAGGACTGAAAGTCAAAAACCTGAGAACTCTGCTCCAAGAGATCCAACGAATGGCAGCTGCCAGACAGGCAAGGACACTCCGACAGGTCATGTCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24894
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099351 | Nonsense | 708 | 1004 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 38624747)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 7550059 |
| GRCz11 | 21 | 7111550 |
KASP Assay ID:
554-7605.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGCATCAACTCCTCATCTGCAGAGACTGAGGAAAATCCAGATCTTCAA[A/T]AGACTCAAACTGAAACTCCAGTATCTGCTGCGACATCAACCTCCGGGAGA
Long Flanking Sequence:
TCAAGAAGAAGGTAAGGGACTTGAAGGCGAGAAAAAGTGACAAACCTTTTGAGGCGTCATCTTTGGATGCCATAAAAAAGCAGAAGCCTTTAACCGAGCAGAAGTGTATCCCACTCAACAGGCTTGTTAAATCTAGCATCTTGAAAGGTGGGAAAGAATCCCTGAACATTCAGGCTAAAAATGACAAGGTGCCTAAAAGCAAACCAGCTAAAGGCAAATGTGAGGTTCAAAACTTCAAGCCTTCTAAAAGCTTTGCGCAGACTGACAAGGTGACCGGGAATGGAGGGATTTCCTCAGCCCCAGGTGGAGACACACTTTCACCAAGTCTGCATGCAGATGACGACAGTGATGTGGACAGCGATGACAGCATTGAGCGAGAGATCAGGAGATTTCTAGCTGAAAGAGCTAAGGTGTCCGCACCTGTAACCACAAACATTAAAAGTGAGGAGAAGGGCATCAACTCCTCATCTGCAGAGACTGAGGAAAATCCAGATCTTCAA[A/T]AGACTCAAACTGAAACTCCAGTATCTGCTGCGACATCAACCTCCGGGAGACTCTGGAAGACTGAACTCACAGGTACGTCCACAAAATCTACAGAAACACCTGCAGAACTCAACAAGGGACCAGTCCTGACACCAGGCAGCTCTTGCATAATGGGATTCAGGAGGACTGAAAGTCAAAAACCTGAGAACTCTGCTCCAAGAGATCCAACGAATGGCAGCTGCCAGACAGGCAAGGACACTCCGACAGGTCATGTCATCAAACCTAATTCCTTCACACCACCATGTGTGAACTCAGAAACTGCTCGGCCGTTGGGTCACCAGCACCAGAACCTGTTCCTGATGAGGCCTGTTAACAACAGAATGAGTGAATCTTCCTCAAGAAACAGTAATGACATTCCCATCAGCCACCAGAGTAGATCAGCCCCAAGGATACCTTTGAGGGAAGTCATTACTTCCCTTTGTCCCTCGCCTCTCTCGAAAACTCAGATTAATTCCCCTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45437
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 |
|---|---|---|---|---|---|
| ENSDART00000099351 | Nonsense | 985 | 1004 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 38623915)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 7550891 |
| GRCz11 | 21 | 7112382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCAAGGAAGATGAGGAAGAGAAATGTATTGATGAGACAGATGTAGAGT[C/A]AGATGAGGAAAGGAAAGATCAGAAGACAAAAGACACGAGCAAGCAGACCA
Long Flanking Sequence:
GTTCCTGATGAGGCCTGTTAACAACAGAATGAGTGAATCTTCCTCAAGAAACAGTAATGACATTCCCATCAGCCACCAGAGTAGATCAGCCCCAAGGATACCTTTGAGGGAAGTCATTACTTCCCTTTGTCCCTCGCCTCTCTCGAAAACTCAGATTAATTCCCCTGCTGTTGACCTTTCAACCTCTGTACCTCCGTTGAGCAGGACAGAGGGCGTTTACATGCATAACCGCCTGAAAAGGGACCGACATTTCTCTGATAGACCACACATATCCTTCAGCACCTCACATCTGTGCCAGCCCTCGCCAGAACTGCAGTCCCACCAGGGCGTTAGTGTAATTCAGGTTCAACGGGACCAGGCTGTGTTATTTCAGGCTACGAATCGCCTGCAGGTCAGCCAAACTGAGGTCACTGCAAGTTTAGGAGAAACACAAAGGGAGGGAGGAAGTGTTAGCAAGGAAGATGAGGAAGAGAAATGTATTGATGAGACAGATGTAGAGT[C/A]AGATGAGGAAAGGAAAGATCAGAAGACAAAAGACACGAGCAAGCAGACCAATAATCAGTGAGTACCTATATTTGTTCTTTCCAAATACACACACATATCAGTGATCGGGATGGGGGGAATCCCAATGCATATCCATGCTGTTGATCCATCTAAGATGCAAAAAACTTTCTGAACAAATTGTCTTTGATTGAGGTGATTTAATGAGTGTGTTGGTCATTAGTTCGGATGGATTTATTGATGACCCACAGGTATTTTGAAAGATCTTTCCAAACATTCAGCCGAAATTTTCCTTCGGCGTTAAACATTAGCTGATTATTTTAGCATTAGCCTGACGGACTGCGGCGCTGGAGTTCATCCTGCATTATCATCATTTCTGTCTTTTTGTACTGTATTGTTTAGGTTCCAAGGGACGTCATGTAGGAGTCTTTAAGTGTACCACATCCTCTCTTTTTTTTTTGTATGTTTGTACATTTATAAATATATTTAAAAGCAGACGCGAT
Associated Phenotype:
Not determined