ZMP
LOC560086
Ensembl ID:
Human Orthologues:
KLK14, KLK6, PRSS1, PRSS3, PRSS37, U66059.56
Human Descriptions:
Trypsin-X3 [Source:UniProtKB/Swiss-Prot;Acc:Q8IYP2]
kallikrein-related peptidase 14 [Source:HGNC Symbol;Acc:6362]
kallikrein-related peptidase 6 [Source:HGNC Symbol;Acc:6367]
protease, serine, 1 (trypsin 1) [Source:HGNC Symbol;Acc:9475]
protease, serine, 3 [Source:HGNC Symbol;Acc:9486]
protease, serine, 37 [Source:HGNC Symbol;Acc:29211]
kallikrein-related peptidase 14 [Source:HGNC Symbol;Acc:6362]
kallikrein-related peptidase 6 [Source:HGNC Symbol;Acc:6367]
protease, serine, 1 (trypsin 1) [Source:HGNC Symbol;Acc:9475]
protease, serine, 3 [Source:HGNC Symbol;Acc:9486]
protease, serine, 37 [Source:HGNC Symbol;Acc:29211]
Mouse Orthologues:
1700074P13Rik, 1810009J06Rik, 2210010C04Rik, AC161768.1, BC048599, Gm10334, Gm4744, Gm5771, Klk14, Klk6, Prss1, Prss2, Prss3, Prss37, Try10, Try4, Try5
Mouse Descriptions:
RIKEN cDNA 1700074P13 gene Gene [Source:MGI Symbol;Acc:MGI:1920731]
RIKEN cDNA 1810009J06 gene Gene [Source:MGI Symbol;Acc:MGI:1920876]
RIKEN cDNA 2210010C04 gene Gene [Source:MGI Symbol;Acc:MGI:1914623]
cDNA sequence BC048599 Gene [Source:MGI Symbol;Acc:MGI:3608323]
kallikrein related-peptidase 14 Gene [Source:MGI Symbol;Acc:MGI:2447564]
kallikrein related-peptidase 6 Gene [Source:MGI Symbol;Acc:MGI:1343166]
predicted gene 10334 Gene [Source:MGI Symbol;Acc:MGI:3641889]
predicted gene 4744 Pseudogene [Source:MGI Symbol;Acc:MGI:3643181]
predicted gene 5771 Gene [Source:MGI Symbol;Acc:MGI:3646222]
protease, serine, 1 (trypsin 1) Gene [Source:MGI Symbol;Acc:MGI:98839]
protease, serine, 2 Gene [Source:MGI Symbol;Acc:MGI:102759]
protease, serine, 3 Gene [Source:MGI Symbol;Acc:MGI:102758]
protease, serine, 37 Gene [Source:MGI Symbol;Acc:MGI:1914940]
trypsin 10 Gene [Source:MGI Symbol;Acc:MGI:3687012]
trypsin 4 Gene [Source:MGI Symbol;Acc:MGI:102757]
trypsin 5 Gene [Source:MGI Symbol;Acc:MGI:102756]
trypsinogen 4 [Source:RefSeq peptide;Acc:NP_001096130]
RIKEN cDNA 1810009J06 gene Gene [Source:MGI Symbol;Acc:MGI:1920876]
RIKEN cDNA 2210010C04 gene Gene [Source:MGI Symbol;Acc:MGI:1914623]
cDNA sequence BC048599 Gene [Source:MGI Symbol;Acc:MGI:3608323]
kallikrein related-peptidase 14 Gene [Source:MGI Symbol;Acc:MGI:2447564]
kallikrein related-peptidase 6 Gene [Source:MGI Symbol;Acc:MGI:1343166]
predicted gene 10334 Gene [Source:MGI Symbol;Acc:MGI:3641889]
predicted gene 4744 Pseudogene [Source:MGI Symbol;Acc:MGI:3643181]
predicted gene 5771 Gene [Source:MGI Symbol;Acc:MGI:3646222]
protease, serine, 1 (trypsin 1) Gene [Source:MGI Symbol;Acc:MGI:98839]
protease, serine, 2 Gene [Source:MGI Symbol;Acc:MGI:102759]
protease, serine, 3 Gene [Source:MGI Symbol;Acc:MGI:102758]
protease, serine, 37 Gene [Source:MGI Symbol;Acc:MGI:1914940]
trypsin 10 Gene [Source:MGI Symbol;Acc:MGI:3687012]
trypsin 4 Gene [Source:MGI Symbol;Acc:MGI:102757]
trypsin 5 Gene [Source:MGI Symbol;Acc:MGI:102756]
trypsinogen 4 [Source:RefSeq peptide;Acc:NP_001096130]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17320 | Essential Splice Site | Available for shipment | Available now |
sa9267 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17320
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016249 | Essential Splice Site | 72 | 263 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 37519493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 37318721 |
GRCz11 | 23 | 37421383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCATCTGGAGTYATTCATTGGGAMAATAATMACTGTTTRTGTGTCTCC[A/T]GGGAAGCCAACATGAGGATCGTGGCTGGAGATTATTCAGTGGGATTATAT
Long Flanking Sequence:
AGAGGGTCGCTGGTTCGAGTCCCGGCTGGGCCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTGTCTGTGTTTCCTCTGGGTGCACAGTCCAAAGACAAGTGCTATAAGTGAATTGGGTACAGTTAATCAATTTGAAAGCCACTTAATAAATAGGAGTTTATAACAATAAGCGGCCTGTCCAAAACAATGGTCAATACTTGTAATACAGATTAAAAAAACTAAGAAAAATGTTTATCATAATCATGTTATGTGCCATACAGACACTTCAGAGAATACATCCTTACCTTTTATTAATGACAATAATATTATATAGTATAGTACATCCTACAATACCCATAATAGAATTATTTTACCTTTACATTTTTTGCACATTCAGGCCTTAACAGTGTACTCTAAAGATGAATAATGGTGAAACATAACAAAAGCACATTTACACAGTTACAGTAGGTGCATCTGGAGTCATTCATTGGGACAATAATCACTGTTTATGTGTCTCC[A/T]GGGAAGCCAACATGAGGATCGTGGCTGGAGATTATTCAGTGGGATTATATGAGGGGATGGAGCAGTTTCGCAGGCCTCATATGTTGATACCTCACCCACAATACGACAGAAGCACCAATAACGCAGACATCATGCTCATTAAGGTGAGACGTTTCAATCAATGCTCCTATGTTACACCAACTGACCGTCAGAGCCGTGAATCATTAATTCCTTTCATGCATACCAAATGAACACAATGATCCAGCATCAAATCACGTTACAGGAAGTGACAAGTACTTGTCTTGGTGCATTAATTTTTCATTTCGTTTGCTATTTATACTACAGCATTTTGGCCATTTTTATTAGCTAATTATATATCATTAATATGCATGAGTTGAAATCAACGAACAATTAAAAGATTTAATCAACTTCTGACTAAATTATATTGTAACATGTATTTTGCTACCTTTTTAAGGTAACTGTAGTGCAAAAAGCTTCAATTTTATTACACATGTAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9267
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 |
---|---|---|---|---|---|
ENSDART00000016249 | Nonsense | 170 | 263 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 37517136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 37316364 |
GRCz11 | 23 | 37419026 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGGCTTTACCACTTCAACCGGAGGCATCTCTTCAATCCTGCGCACAGTA[A/T]AGCTGCCCATCGTGTCCACYGCTGTGTGTAACGGMACAGACTCATTCAAT
Long Flanking Sequence:
TCTATGGAGGATGAGAGAGCTCTGGGATTTCATATAAAATATCTTCATTTGTGTTCTCAAGATTAAAAAAAAACATTGTCAAACCATTCCATCTGACTGCAGTGGTTTGTGCGTGTGGTTTGACTTTAAGGTGCTATATAAATAAATATTGTATTGCATTGTATTGTTTTGAGGCCAGTGCGGTCTATGGAGGATGAGAGAGCTCTAGGATTTCATCTAAAAGCATCTTAATTTGTGTTCTGAAGATGGACAAAGGTCTTAGGGATTTGTAACAACATGAGTATTTAATAACAGCTTTTTTTATTTCTGGTTGAACAAGCCCTTAAATTGTTTCTTGCTCACCTGCGCAGCTGCAGTCTCCAGTCTATCTGAACAGCTACGTGTCTCTGGTGCCGCTGCCACGTCAGGACGCAATGGTGGCCGTGGGTCGCCTATGCAGCGTCTCCGGCTGGGGCTTTACCACTTCAACCGGAGGCATCTCTTCAATCCTGCGCACAGTA[A/T]AGCTGCCCATCGTGTCCACCGCTGTGTGTAACGGCACAGACTCATTCAATGGAAACATCACCGAGAACATGATCTGTGCAGGATACAGTACAGGAGGAAAAGACGCATGCAAGGTGAGACAACTGATACACTTATAATGTGCTGTAATACTATTAAAACCATGATTATAATGTGTAAACCTGAATCCTGATATCAGATGGTCACAGTCTACATCATGATTTAGTAAAAGATTTGGTATACTGTGGGATATTGTGGTCATTAATTGCATTTTTCTAATGAGCAGAGGTTTGAACTAAGAAACAGTGACCCATACAATACAACTTCACCTGAATAAGGAATAAATTAATAAAAAGCGAAACATTTACACAGAATAAACCACTGGGGACTATTACCACTACAGAATTAAAGGGATTTACTGGACTGTGACCTTTTTTCAGCCATTATGTGGGTGTCACATTGGTTTAGCAAGCTGTTTAATTCCTTGTGCTATTTGCTGCTGT
Associated Phenotype:
Not determined