ZMP
mmp14b
Ensembl ID:
ZFIN ID:
Description:
matrix metalloproteinase 14b (membrane-inserted) [Source:RefSeq peptide;Acc:NP_919395]
Human Orthologue:
MMP14
Human Description:
matrix metallopeptidase 14 (membrane-inserted) [Source:HGNC Symbol;Acc:7160]
Mouse Orthologue:
Mmp14
Mouse Description:
matrix metallopeptidase 14 (membrane-inserted) Gene [Source:MGI Symbol;Acc:MGI:101900]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39891 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5721 | Nonsense | F2 line generated | Not yet available |
sa2034 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa39891
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044264 | Essential Splice Site | 332 | 621 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 37880755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38195669 |
GRCz11 | 2 | 38177997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATTTTGACACCATTGGCATTTTCAGAGGAGAAATGTTTGTGTTTAAG[G/A]TACTGATGGAGTATGTGCTGCATTATTTTTGGAATAATGACTAGGAGATT
Long Flanking Sequence:
AAACGTTCAAGTTTGCGATGCAGTTTGCAAATTTTTATTGTATTGATGGATATGGGAAACACCAAATCAACGAACTATGTTTGTAATGACGCAACTTGCGACCTTAGTTGGCTAGCGATGGTTTTCAGAAACGCACCCCTGTATAGTAAAATCCAATAATAGAGCAGTATACCATTTCCAATTAATTTTCAGTTCAACTAGAGTGAAAAATAATAGTCAAGTACAGCATTTAATTACATATTAAGATGCTTTTGTCAATCAGTTATTTACACAGACCAATGCAAATAAGCTAATTCACTAAAATATTTATATATTTTGATTTAATCTCTGTAGGACCAGGATCTGGAGGACACCCTCGAACCCCTGTCACCCCTGAGACGCCCCATCACACTCCATACCCCACACCGTACAGGCCAGGAGGACCCTCCTATGGTCCCAACATCTGCGAGGGTCATTTTGACACCATTGGCATTTTCAGAGGAGAAATGTTTGTGTTTAAG[G/A]TACTGATGGAGTATGTGCTGCATTATTTTTGGAATAATGACTAGGAGATTGTTTGTTCATTATGGTTCCTGTCTCTGTGTTTTAGGGTAAGTGGTTCTGGCGTGTTCGAAATAATCAAGTTATGGAAAACTACCCCATGCCAATTGGACACTTCTGGAGAGGTCTGCCTACTGACATTAATGCTGCATATGAAAGAGAAGATGGCAAATTTGTCTTCTTTAAAGGTACTAGATCTATCTTATCGCATGAATTCAGTGGAGAATTTGCTTATTGACCCTGAAATACTACATTTGACATGTCTGGTTTGCAGGGGACAGGCATTGGGTGTTCACTGAGTCCAACTTAGAGCCAGGATACCCGAAGGTTTTAGGAGAACTGGGATCTGGTGTACCAAAGGACAAACTGGATGCAGCTCTTCTCTACACGCCTACAGGCTACACTTACTTCTTCAGAGGAAACAAGTCAGTAGCTTTGATGTCCCATAACATAAAGCACGAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5721
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044264 | Nonsense | 335 | 621 | 7 | 10 |
ENSDART00000044264 | Nonsense | 335 | 621 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 37880849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38195763 |
GRCz11 | 2 | 38178091 |
KASP Assay ID:
554-2622.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGATTGTTTGTTCATTATGGTTCCTGTCTCTGTGTTTTAGGGTAAGTG[G/A]TTCTGGCGTGTTCGWAATAATCAAGTTATGGAAAACTACCCCATGCCAAT
Long Flanking Sequence:
CTTGCGACCTTAGTTGGCTAGCGATGGTTTTCAGAAACGCACCCCTGTATAGTAAAATCCAATAATAGAGCAGTATACCATTTCCAATTAATTTTCAGTTCAACTAGAGTGAAAAATAATAGTCAAGTACAGCATTTAATTACATATTAAGATGCTTTTGTCAATCAGTTATTTACACAGACCAATGCAAATAAGCTAATTCACTAAAATATTTATATATTTTGATTTAATCTCTGTAGGACCAGGATCTGGAGGACACCCTCGAACCCCTGTCACCCCTGAGACGCCCCATCACACTCCATACCCCACACCGTACAGGCCAGGAGGACCCTCCTATGGTCCCAACATCTGCGAGGGTCATTTTGACACCATTGGCATTTTCAGAGGAGAAATGTTTGTGTTTAAGGTACTGATGGAGTATGTGCTGCATTATTTTTGGAATAATGACTAGGAGATTGTTTGTTCATTATGGTTCCTGTCTCTGTGTTTTAGGGTAAGTG[G/A]TTCTGGCGTGTTCGAAATAATCAAGTTATGGAAAACTACCCCATGCCAATTGGACACTTCTGGAGAGGTCTGCCTACTGACATTAATGCTGCATATGAAAGAGAAGATGGCAAATTTGTCTTCTTTAAAGGTACTAGATCTATCTTATCGCATGAATTCAGTGGAGAATTTGCTTATTGACCCTGAAATACTACATTTGACATGTCTGGTTTGCAGGGGACAGGCATTGGGTGTTCACTGAGTCCAACTTAGAGCCAGGATACCCGAAGGTTTTAGGAGAACTGGGATCTGGTGTACCAAAGGACAAACTGGATGCAGCTCTTCTCTACACGCCTACAGGCTACACTTACTTCTTCAGAGGAAACAAGTCAGTAGCTTTGATGTCCCATAACATAAAGCACGAGCACAAAGAGAGCATAGATCTGAAACTGCTGCTTATCTTTCATCAGATATTATCGTTACAATGAAGACACGCACTCAGTGGATCCAGATTATCCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2034
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044264 | Nonsense | 335 | 621 | 7 | 10 |
ENSDART00000044264 | Nonsense | 335 | 621 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 37880849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38195763 |
GRCz11 | 2 | 38178091 |
KASP Assay ID:
554-2622.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGATTGTTTGTTCATTATGGTTCCTGTCTCTGTGTTTTAGGGTAAGTG[G/A]TTCTGGCGTGTTCGWAATAATCAAGTTATGGAAAACTACCCCATGCCAAT
Long Flanking Sequence:
CTTGCGACCTTAGTTGGCTAGCGATGGTTTTCAGAAACGCACCCCTGTATAGTAAAATCCAATAATAGAGCAGTATACCATTTCCAATTAATTTTCAGTTCAACTAGAGTGAAAAATAATAGTCAAGTACAGCATTTAATTACATATTAAGATGCTTTTGTCAATCAGTTATTTACACAGACCAATGCAAATAAGCTAATTCACTAAAATATTTATATATTTTGATTTAATCTCTGTAGGACCAGGATCTGGAGGACACCCTCGAACCCCTGTCACCCCTGAGACGCCCCATCACACTCCATACCCCACACCGTACAGGCCAGGAGGACCCTCCTATGGTCCCAACATCTGCGAGGGTCATTTTGACACCATTGGCATTTTCAGAGGAGAAATGTTTGTGTTTAAGGTACTGATGGAGTATGTGCTGCATTATTTTTGGAATAATGACTAGGAGATTGTTTGTTCATTATGGTTCCTGTCTCTGTGTTTTAGGGTAAGTG[G/A]TTCTGGCGTGTTCGAAATAATCAAGTTATGGAAAACTACCCCATGCCAATTGGACACTTCTGGAGAGGTCTGCCTACTGACATTAATGCTGCATATGAAAGAGAAGATGGCAAATTTGTCTTCTTTAAAGGTACTAGATCTATCTTATCGCATGAATTCAGTGGAGAATTTGCTTATTGACCCTGAAATACTACATTTGACATGTCTGGTTTGCAGGGGACAGGCATTGGGTGTTCACTGAGTCCAACTTAGAGCCAGGATACCCGAAGGTTTTAGGAGAACTGGGATCTGGTGTACCAAAGGACAAACTGGATGCAGCTCTTCTCTACACGCCTACAGGCTACACTTACTTCTTCAGAGGAAACAAGTCAGTAGCTTTGATGTCCCATAACATAAAGCACGAGCACAAAGAGAGCATAGATCTGAAACTGCTGCTTATCTTTCATCAGATATTATCGTTACAATGAAGACACGCACTCAGTGGATCCAGATTATCCCAA
Associated Phenotype:
Not determined