ZMP
stm
Ensembl ID:
ZFIN ID:
Description:
Protein starmaker [Source:UniProtKB/Swiss-Prot;Acc:A2VD23]
Human Orthologues:
AC010606.5, AC137896.1, AL008728.1, AL138918.1, DMP1
Human Description:
dentin matrix acidic phosphoprotein 1 [Source:HGNC Symbol;Acc:2932]
Mouse Orthologue:
Dmp1
Mouse Description:
dentin matrix protein 1 Gene [Source:MGI Symbol;Acc:MGI:94910]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15436 | Essential Splice Site | Available for shipment | Available now |
sa36758 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15436
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051768 | Essential Splice Site | 44 | 468 | 5 | 19 |
ENSDART00000074620 | Essential Splice Site | 44 | 212 | 5 | 15 |
ENSDART00000105174 | Essential Splice Site | 44 | 613 | 5 | 26 |
ENSDART00000110763 | Essential Splice Site | 33 | 231 | 4 | 16 |
ENSDART00000145710 | Essential Splice Site | 44 | 217 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 19 (position 3726140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3222713 |
GRCz11 | 19 | 3163611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TRAAGAGAAAAACAAACAAAGAATTAAACATGTTTTTCTCTTTYTTTTTC[A/G]GTTCAGTTTAATKTTGGTACTCCAGCGCCTGCAGATGGAGACTCAGGTTG
Long Flanking Sequence:
ATGTACATAAATTCATGTTAAAAAGGAAGACTTATTGTATATTAAAATTATTATTAGATTTTCCCAATGAGCCTCTGCACTCTCAGAAATAAAGGTAATTGAGCTGTCATTGAGGCAGTAACTTTTTAAAAGGTCCATATTTGTACCTGAAGGGTCCATAATGGTACCTTAAAGGTACTTTTTAGGTACATTTGGGTACTAATGTGCACCTTTTAGGTACCACTGTGGACTATTTGGGTGCAAATATGTACCTTTTAAGAAGGTGCTGCCCCAGTGACAGCTCCAGTACCTTCATTTCTGAGTGTGTAGTAAATGAATGTGCTCTGGTTATCTGACTGATTGTGTTTTCTATGTTATTCCTCTCAGAATCAGCTGCAGACCAGCGACACATCTTTACTGGTAGGTCACAATGACTTTAAATCAGTTCTTTTCCATGAATCAAAGTGCCATTGAAGAGAAAAACAAACAAAGAATTAAACATGTTTTTCTCTTTCTTTTTC[A/G]GTTCAGTTTAATGTTGGTACTCCAGCGCCTGCAGATGGAGACTCAGGTTGGTTCAGCTCACATAAATCCAATCTCACTCAAGCATTCATTCTAAAACTGCAGGAAGGTTAAATGGCTTGGGTGTGTGTTTATTTGGAATATCATATTTAAGCAGGTTTTATATGGTAACTAGAAGTATTTACAAAGAAAACTGATGCATTGAAAGCTAGACAGATAAACAGACAGACAAAGAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACAGACAGATAAACAGATAAACAGATTAACAAAGACAGATATTTAGACAGACATATGGTCAGACAGACAGATGCATAGATTGACAGACAGACCAATAGACTGACAGACAGACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36758
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051768 | Essential Splice Site | 83 | 468 | 7 | 19 |
ENSDART00000074620 | Essential Splice Site | 83 | 212 | 7 | 15 |
ENSDART00000105174 | Essential Splice Site | 83 | 613 | 7 | 26 |
ENSDART00000110763 | Essential Splice Site | 72 | 231 | 6 | 16 |
ENSDART00000145710 | Essential Splice Site | 83 | 217 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 19 (position 3723736)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3220309 |
GRCz11 | 19 | 3161207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGTGCTTTTAGCTCCCGGTGACTCGTCTGACACCACTGAAAAACCAG[G/A]TCAGTGTCTGCTATCACCACTCATTCAGTCTAACATTCACAAAGACCTGA
Long Flanking Sequence:
ATAGACAGACAGGCATGTAGACTGACAGACAAATGGATAGACAGACAGAGAGATGTACAGAAAGAAAAAGAGACAGATGAACAGGCAGACAGAAAGACAGATAGACAGGCAGATAGATAGCAGACAGACGGACGGACAGACGGATGGCTGGCTGGATGGATAGACAGACAGACAGACATACAAACAGAAAGACAAACAGACGGATATATAAAAAGACAGACAGACAGGAGGATAGAAAGACAGACAGAACAGATGAATAGACAGGTAGACGGGCAGACGTACAAGTGGAAGTAACTCTGGAAATCTTCTTTTAATAGTAACTACAGACGGCAAAGACTCCGCAGAGAAAAATGAAGGTAAGCATGACAAATGAACTCAAAATCCCAAACTGGAACACACACAACGAGCAGACGTGAAGAGAACAGACGATAGTAATAAACACACGTGACCCTCTGTGCTTTTAGCTCCCGGTGACTCGTCTGACACCACTGAAAAACCAG[G/A]TCAGTGTCTGCTATCACCACTCATTCAGTCTAACATTCACAAAGACCTGATACACGAGCTGAAGAATTTCACAAGCGCACACACACACACACACACACACACACACACACAGAGCACTGATATCACCACAATGATGATAACACACCAATGAATGAATGAACGAGAGTGATAACACATTACACACGGATTAATGTTTAACCGCTGTGTGTTCGGCATCAATGAGCTCAGAGAATCAGTGTTAGATTGCCGAGCAGGAGACACTCAGTCAACAGGAAAAGATTACAGGAGTTACAGCAGCAGATAAAGCTGAACAGCTCAGGATTGTGAAAAGTCGTCACACTCCATCAAATCCCAGCATGAATTCATGAGACGCATTGTTCAGGAAGGAAAGGCTGTTCATTTATGAATAATATGAAGAGTGTGTGGTCACGCTGGCAATGTTTGATGTATTTTCGGCTGCTCATTTAAGTGACGACAGCATTTTGGAAGACTGAAAATCC
Associated Phenotype:
Not determined