ZMP
ENSDARG00000088660
Ensembl ID:
Human Orthologues:
EFEMP1, EFEMP2, FBLN5
Human Descriptions:
EGF-containing fibulin-like extracellular matrix protein 1 [Source:HGNC Symbol;Acc:3218]
EGF-containing fibulin-like extracellular matrix protein 2 [Source:HGNC Symbol;Acc:3219]
fibulin 5 [Source:HGNC Symbol;Acc:3602]
EGF-containing fibulin-like extracellular matrix protein 2 [Source:HGNC Symbol;Acc:3219]
fibulin 5 [Source:HGNC Symbol;Acc:3602]
Mouse Orthologues:
Efemp1, Efemp2, Fbln5
Mouse Descriptions:
epidermal growth factor-containing fibulin-like extracellular matrix protein 1 Gene [Source:MGI Symb
epidermal growth factor-containing fibulin-like extracellular matrix protein 2 Gene [Source:MGI Symb
fibulin 5 Gene [Source:MGI Symbol;Acc:MGI:1346091]
epidermal growth factor-containing fibulin-like extracellular matrix protein 2 Gene [Source:MGI Symb
fibulin 5 Gene [Source:MGI Symbol;Acc:MGI:1346091]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24063 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24063
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 |
---|---|---|---|---|---|
ENSDART00000125020 | Nonsense | 147 | 193 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 22 (position 4162761)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 4196021 |
GRCz11 | 22 | 4581386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGTTGTGTTTCGCACAGATCATCGGATCGGGACGTGCTTCTCGTCTT[T/A]GGCGAACGGCCGCTGTGCGAGTGAACTGTCTGGTCAGTACACCAAGATGC
Long Flanking Sequence:
GTCTGGAGGTTCCAGGCGCACACTCCTGAACTGCAACCTCTTGGGATCGACCCGGCTGTAGGCTTTCGCAAGCGTGCTGATGGGAACGCTGGCTTCAATTGCAACCAGACCTACTATTGGGCCTCAAAGTGAGATTTCTTGTGTTCGCGCGGGGCCTAACAACGCATTAGTGCTGATTAGCATCANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNACCAGCCTAGGCTGGTTTAAGCTGGATTTTACAGCAGGGTTTCCATAACATCCACGTGTTGTTACTTGTTCTGGTAATTTGAAGTGCTTCTTTTATACGTATTTGTACATGGCTTTGGATAAAAGTGTCTGCTAAGTGAATAAATGTAAATACTCATATATTTTCTCTGGTTGTGTTTCGCACAGATCATCGGATCGGGACGTGCTTCTCGTCTT[T/A]GGCGAACGGCCGCTGTGCGAGTGAACTGTCTGGTCAGTACACCAAGATGCAGTGCTGCTGCGACACAGGCCGCTGCTGGGCCCTCGGACACATACCTGAGATGTGCCCCGTCAGAGGATCCGGTGAGTATGCTAATAGCTAATAGCTAACAATGTTTACCAAGTCAAGAATCGTTGAATGACAAGAATCATTGCTAATACAACTAATTTCAACTTTAATTGTATGGCTTTAAGACCATTCTGTTTGTTAGCTTTGAGGCTAACGTCTGTATGCTTACATTTACGATACGCGCAATTAAAAAATGATTTTCCAAAAATAATCCTAACATTATATTAAATGTTTCAATAATGTTAAAAATATTTGACAGACATAGGCACAATTAAAATGAGTTTATTTTTCCAAAATTATTTATGACAATGAAAATTAACGTAGCCTATATGAGGACGTGGTGAGTATGCTAATCACTAACAATGTTGCTAAGTCAGACACCTTATATTACA
Associated Phenotype:
Not determined