ZMP
zgc:113307
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC553753 [Source:RefSeq peptide;Acc:NP_001018560]
Human Orthologues:
FMOD, LUM
Human Descriptions:
fibromodulin [Source:HGNC Symbol;Acc:3774]
lumican [Source:HGNC Symbol;Acc:6724]
lumican [Source:HGNC Symbol;Acc:6724]
Mouse Orthologues:
Fmod, Lum
Mouse Descriptions:
fibromodulin Gene [Source:MGI Symbol;Acc:MGI:1328364]
lumican Gene [Source:MGI Symbol;Acc:MGI:109347]
lumican Gene [Source:MGI Symbol;Acc:MGI:109347]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2608 | Nonsense | F2 line generated | Not yet available |
sa5594 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa2608
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000065984 | Nonsense | 60 | 343 | 2 | 4 |
ENSDART00000065984 | Nonsense | 60 | 343 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 21886869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 20893100 |
GRCz11 | 11 | 21053668 |
KASP Assay ID:
554-3141.1 (used for ordering genotyping assays)
KASP Sequence:
TGGAGTGCGACTGCCCAATTCAGTGGCCRACAGCCATTTATTGTGACCAC[A/T]GAGGCCTTAACCAGCTTCCCTCTGGCCTTCCCTTCCGCCTGCAGTACCTG
Long Flanking Sequence:
CTAGTTATCATTGTGAAGATTGCTACTGTATTATTTCAATATTATATATATATATATATATATATATATATAGTATCAATGTTGACATGGTTTTATCATCCGTTTGCCTTATTTTGTGAAAAAAATACCTGTTATCTTTTTGTAAACAGCTTCTTTGGAGTTTTTAATTTATTGCTGCTAGACAAAAAAGCTTCCTAAACTCTATTAAGAATTACAAATATGTTTATATACCTATTTGTGTGTTCATCTAGGTAGGCGGACGAATGGATTATAGGTCAGTTTTTTTGTTACTCTCTGTGTGTGGGCTGACTCGGGCCTTCACAATGGATTTGGACTATGGAGGTGTACCCCTCTGGATCAACCGTTTTCTAGGAGAGCCGAGCGTGTTGACTTTGAAAGACCGGATAGATCCAGGCTGGTATCGGGCTGTGAACACACAAAGTTGTCCTTTGGAGTGCGACTGCCCAATTCAGTGGCCGACAGCCATTTATTGTGACCAC[A/T]GAGGCCTTAACCAGCTTCCCTCTGGCCTTCCCTTCCGCCTGCAGTACCTGTTCCTCCAAGGCAATAATATTACTTCCCTTGGATCCAGAGCGTTTGACAATACCACCTACTTGCGCTGGTTGATCTTGGACCACAATCAACTATTGAGTGAGCAACTTGATAATGTGTTGTTCTCCAGTCTGACCCGCTTGGTAAATCTGTTCATAAATCATAATAACCTGACTAAAGTGCCAGCCGGACTGCCAAGCGGACTGAAACAGCTGCGACTCGCATACAATCACATTGAAAAGATTTCTGAAGGTGATTTCCAAAATCTGGACAGTTTGACGTTAATTTTGTTACAAGGCAATCGTCTGAAGACTATCGAAGAGGGGGATTTCAAAGGTATGCAATATTTTCCTTTGTTGGTTTTTCCTAGATCCCAAATTTTCTAAAGATAAACCTAGAAATAAACTAATTTATTATCCACTAACCAATAAATTACTTATTTAAATATGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5594
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000065984 | Nonsense | 60 | 343 | 2 | 4 |
ENSDART00000065984 | Nonsense | 60 | 343 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 21886869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 20893100 |
GRCz11 | 11 | 21053668 |
KASP Assay ID:
554-3141.1 (used for ordering genotyping assays)
KASP Sequence:
TGGAGTGCGACTGCCCAATTCAGTGGCCRACAGCCATTTATTGTGACCAC[A/T]GAGGCCTTAACCAGCTTCCCTCTGGCCTTCCCTTCCGCCTGCAGTACCTG
Long Flanking Sequence:
CTAGTTATCATTGTGAAGATTGCTACTGTATTATTTCAATATTATATATATATATATATATATATATATATAGTATCAATGTTGACATGGTTTTATCATCCGTTTGCCTTATTTTGTGAAAAAAATACCTGTTATCTTTTTGTAAACAGCTTCTTTGGAGTTTTTAATTTATTGCTGCTAGACAAAAAAGCTTCCTAAACTCTATTAAGAATTACAAATATGTTTATATACCTATTTGTGTGTTCATCTAGGTAGGCGGACGAATGGATTATAGGTCAGTTTTTTTGTTACTCTCTGTGTGTGGGCTGACTCGGGCCTTCACAATGGATTTGGACTATGGAGGTGTACCCCTCTGGATCAACCGTTTTCTAGGAGAGCCGAGCGTGTTGACTTTGAAAGACCGGATAGATCCAGGCTGGTATCGGGCTGTGAACACACAAAGTTGTCCTTTGGAGTGCGACTGCCCAATTCAGTGGCCGACAGCCATTTATTGTGACCAC[A/T]GAGGCCTTAACCAGCTTCCCTCTGGCCTTCCCTTCCGCCTGCAGTACCTGTTCCTCCAAGGCAATAATATTACTTCCCTTGGATCCAGAGCGTTTGACAATACCACCTACTTGCGCTGGTTGATCTTGGACCACAATCAACTATTGAGTGAGCAACTTGATAATGTGTTGTTCTCCAGTCTGACCCGCTTGGTAAATCTGTTCATAAATCATAATAACCTGACTAAAGTGCCAGCCGGACTGCCAAGCGGACTGAAACAGCTGCGACTCGCATACAATCACATTGAAAAGATTTCTGAAGGTGATTTCCAAAATCTGGACAGTTTGACGTTAATTTTGTTACAAGGCAATCGTCTGAAGACTATCGAAGAGGGGGATTTCAAAGGTATGCAATATTTTCCTTTGTTGGTTTTTCCTAGATCCCAAATTTTCTAAAGATAAACCTAGAAATAAACTAATTTATTATCCACTAACCAATAAATTACTTATTTAAATATGTAT
Associated Phenotype:
Not determined