ZMP
si:dkey-61p9.6
Ensembl ID:
Description:
hypothetical protein LOC558896 [Source:RefSeq peptide;Acc:NP_001038342]
Human Orthologues:
HSPA12A, HSPA12B
Human Descriptions:
heat shock 70kD protein 12B [Source:HGNC Symbol;Acc:16193]
heat shock 70kDa protein 12A [Source:HGNC Symbol;Acc:19022]
heat shock 70kDa protein 12A [Source:HGNC Symbol;Acc:19022]
Mouse Orthologues:
Hspa12a, Hspa12b
Mouse Descriptions:
heat shock protein 12A Gene [Source:MGI Symbol;Acc:MGI:1920692]
heat shock protein 12B Gene [Source:MGI Symbol;Acc:MGI:1919880]
heat shock protein 12B Gene [Source:MGI Symbol;Acc:MGI:1919880]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12979 | Nonsense | Available for shipment | Available now |
sa33515 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40343 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26366 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20322 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12979
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099739 | Nonsense | 202 | 571 | 3 | 4 |
ENSDART00000099750 | None | None | 571 | None | 4 |
Genomic Location (Zv9):
Chromosome 4 (position 61416397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 76203509 |
GRCz11 | 4 | 77678028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCCTTGGAGCCTGAGGCTGCATCTATTTACTGCAAACAWCTGCYAAGT[G/T]AAGGCTAMATATCAGAGGAGGCCTGTCGAGACACACTGGAACAWAAACCT
Long Flanking Sequence:
CATTCGAATCCATCATCGAATTTCCTCCAGGAACCGTCTGCCTTCAAACAAAGCACAAACACACAGAGAGAACACCAGAGGGCAGCATAGATCCAAACACATTAACTAAAGGTCTTAACACCCCCACCCTTAAAAACAAAACTTGAGCAAATCGCTGCTACATTCTAGTGGCCACGAAATGTTATTACAATGCAAACTCGTGCTTAAAACCTAAGAAGTCTGGTCAGCCTTAACGCTGCTGAAAAATGCAGTGTTGCGCCCATATGAGCTAATTCCTGAGACTTACCGGCAAAAGTTTCTAAATCTTGTGAAAATGTTTATTATATACTTGTTGACATAATAACAATGCCTGTTTCTATTGTAATATTATTATCTTGCTTATCATCAATTTTCTTTTAAATGATTTTCAGGCAGGTCTAGTGATAGAGTCTGAGCCAGAGAGGCTCGTCTTTGCCTTGGAGCCTGAGGCTGCATCTATTTACTGCAAACATCTGCCAAGT[G/T]AAGGCTACATATCAGAGGAGGCCTGTCGAGACACACTGGAACAAAAACCTGGAACCCAGTATATGGTTGTGGATTGTGGAGGTACATCTCTAGCATTTCTCTTACATTGCTGTTTCATTTTGTACAGACATCAAGTTTATTTAGCAATAAGAACCACAACAAGATTTTAAAAATGAATGCACCACAGCAACTGCTCAGGATACGGGCCGGGTCCAGGATTATGGAGACCTTGTGATAAGGAGAAAAAGACTAACATAAGCTTAGATGCCTTTCAAATTATAATGTCTTTTGGCAAAGTGTTCCCGGCTCCGGTTGCTCTAATTCATGATACAAACAGTATCATGAGGGTAATCCAAAAATGTAGTCGTGGTCACAGGCAAAGAGTTCAACGTAAGCAGCAAAACAACACAAACCTGAAACAAAACAAGATTCAGGAAACACGGCAAGACTAGATTATAGAACAACCTGAAATGTTACAGCAAACAAGACTCAGCAATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33515
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 |
---|---|---|---|---|---|
ENSDART00000099739 | Essential Splice Site | 228 | 571 | 3 | 4 |
ENSDART00000099750 | None | None | 571 | None | 4 |
Genomic Location (Zv9):
Chromosome 4 (position 61416315)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 76203591 |
GRCz11 | 4 | 77677946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACTGGAACAAAAACCTGGAACCCAGTATATGGTTGTGGATTGTGGAG[G/A]TACATCTCTAGCATTTCTCTTACATTGCTGTTTCATTTTGTACAGACATC
Long Flanking Sequence:
CAGCATAGATCCAAACACATTAACTAAAGGTCTTAACACCCCCACCCTTAAAAACAAAACTTGAGCAAATCGCTGCTACATTCTAGTGGCCACGAAATGTTATTACAATGCAAACTCGTGCTTAAAACCTAAGAAGTCTGGTCAGCCTTAACGCTGCTGAAAAATGCAGTGTTGCGCCCATATGAGCTAATTCCTGAGACTTACCGGCAAAAGTTTCTAAATCTTGTGAAAATGTTTATTATATACTTGTTGACATAATAACAATGCCTGTTTCTATTGTAATATTATTATCTTGCTTATCATCAATTTTCTTTTAAATGATTTTCAGGCAGGTCTAGTGATAGAGTCTGAGCCAGAGAGGCTCGTCTTTGCCTTGGAGCCTGAGGCTGCATCTATTTACTGCAAACATCTGCCAAGTGAAGGCTACATATCAGAGGAGGCCTGTCGAGACACACTGGAACAAAAACCTGGAACCCAGTATATGGTTGTGGATTGTGGAG[G/A]TACATCTCTAGCATTTCTCTTACATTGCTGTTTCATTTTGTACAGACATCAAGTTTATTTAGCAATAAGAACCACAACAAGATTTTAAAAATGAATGCACCACAGCAACTGCTCAGGATACGGGCCGGGTCCAGGATTATGGAGACCTTGTGATAAGGAGAAAAAGACTAACATAAGCTTAGATGCCTTTCAAATTATAATGTCTTTTGGCAAAGTGTTCCCGGCTCCGGTTGCTCTAATTCATGATACAAACAGTATCATGAGGGTAATCCAAAAATGTAGTCGTGGTCACAGGCAAAGAGTTCAACGTAAGCAGCAAAACAACACAAACCTGAAACAAAACAAGATTCAGGAAACACGGCAAGACTAGATTATAGAACAACCTGAAATGTTACAGCAAACAAGACTCAGCAATGTGTGTGAGAATGTGAGGTGCATATGTAGTCCATCTAGTCAGTCTTTCTACAGATGTGTGCAAGTAATCAGGGGTGATCTGGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40343
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 |
---|---|---|---|---|---|
ENSDART00000099739 | Nonsense | 387 | 571 | 4 | 4 |
ENSDART00000099750 | Nonsense | 387 | 571 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 4 (position 61391467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 76228439 |
GRCz11 | 4 | 77653098 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGCTGAACATCGAGTACATGCTGTTAGTCGGAGGCTTTGCTGAATGT[A/T]AAATTCTGAAGAAGTTTCTGAAGGAGCGCTTTGATAAATGCAAGATAGTC
Long Flanking Sequence:
GATTTAAACGTCATTCTTATTTTGCAGGTGGCACTATTGATATAACGGTACACGAGGTGGTCGAGGACGGCAAACTGAAAGAACTGAACGCCGCTTCCGGAAATGACATGGGTGGACAGACCGTAGACAGGAAGTTCATCTCTTTTCTGAAAGAGATATTTTCAGAGAAAATTTACAACAAGTTTGAACAAGATTTCCCAGCAGAGGCGCTGAAATTAAAATATGACATTGCTCTAGCTAAATCTTGTGATCAACTTGTGCTGATCCAGTGCCCAGTGACCTTGCAGGATCTGGCCAAGAAAGAAAAGGCAATCGAGAGTTACTTTGAGGGTGTTGAGGGAGCGGAATGGGACGAGGGGTCGATCATAATCAAAGAGGATAAACTGCAGAGCTTTTTTGATGAAAGTCTCAAGACAACAGCAGAGAAACTAGAGAAGATCATGAGCAACCCTGAGCTGAACATCGAGTACATGCTGTTAGTCGGAGGCTTTGCTGAATGT[A/T]AAATTCTGAAGAAGTTTCTGAAGGAGCGCTTTGATAAATGCAAGATAGTCTGCCCTGTTGAGCCCCAGGTAGTAATAATCAAAGGAGCGATCAGATACGCCAAACAGCCCAAAGTGGTCAAATCCCGTATGAGTGCTCTAACATACGGGATCAGAATAGATGCGCCCTTCGATAAGGTCTTACACAAAGGCAAGACTAGCTATGTGAACAGTGAGGGACAGACGTACTGTGATGTCTGTTTCGAAACATTCGTTAGAAAGGGAGAGTCGGTCAACTGCGATGAAGTTCGACAGTTCTTTTTTAATCCATCAGACACCAATCAAACATTTGCCACCTTCCAGTTCTTCAGCACAAATGAAAAACAGGTGCAGTTTATCGATGAGCCGGGGGTTGAGTCGGTTGGGGTTTTTCAAGTGGGAATGCCCAAAACTGATGGAGGCTTGAGTCGTGAAATTAAATTGGAAATAAAATTTGGCTCCACTGAAATGAAGGCAACTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26366
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 |
---|---|---|---|---|---|
ENSDART00000099739 | Nonsense | 390 | 571 | 4 | 4 |
ENSDART00000099750 | Nonsense | 390 | 571 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 4 (position 61391458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 76228448 |
GRCz11 | 4 | 77653089 |
KASP Assay ID:
2259-5264.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCGAGTACATGCTGTTAGTCGGAGGCTTTGCTGAATGTAAAATTCTG[A/T]AGAAGTTTCTGAAGGAGCGCTTTGATAAATGCAAGATAGTCTGCCCTGTT
Long Flanking Sequence:
GTCATTCTTATTTTGCAGGTGGCACTATTGATATAACGGTACACGAGGTGGTCGAGGACGGCAAACTGAAAGAACTGAACGCCGCTTCCGGAAATGACATGGGTGGACAGACCGTAGACAGGAAGTTCATCTCTTTTCTGAAAGAGATATTTTCAGAGAAAATTTACAACAAGTTTGAACAAGATTTCCCAGCAGAGGCGCTGAAATTAAAATATGACATTGCTCTAGCTAAATCTTGTGATCAACTTGTGCTGATCCAGTGCCCAGTGACCTTGCAGGATCTGGCCAAGAAAGAAAAGGCAATCGAGAGTTACTTTGAGGGTGTTGAGGGAGCGGAATGGGACGAGGGGTCGATCATAATCAAAGAGGATAAACTGCAGAGCTTTTTTGATGAAAGTCTCAAGACAACAGCAGAGAAACTAGAGAAGATCATGAGCAACCCTGAGCTGAACATCGAGTACATGCTGTTAGTCGGAGGCTTTGCTGAATGTAAAATTCTG[A/T]AGAAGTTTCTGAAGGAGCGCTTTGATAAATGCAAGATAGTCTGCCCTGTTGAGCCCCAGGTAGTAATAATCAAAGGAGCGATCAGATACGCCAAACAGCCCAAAGTGGTCAAATCCCGTATGAGTGCTCTAACATACGGGATCAGAATAGATGCGCCCTTCGATAAGGTCTTACACAAAGGCAAGACTAGCTATGTGAACAGTGAGGGACAGACGTACTGTGATGTCTGTTTCGAAACATTCGTTAGAAAGGGAGAGTCGGTCAACTGCGATGAAGTTCGACAGTTCTTTTTTAATCCATCAGACACCAATCAAACATTTGCCACCTTCCAGTTCTTCAGCACAAATGAAAAACAGGTGCAGTTTATCGATGAGCCGGGGGTTGAGTCGGTTGGGGTTTTTCAAGTGGGAATGCCCAAAACTGATGGAGGCTTGAGTCGTGAAATTAAATTGGAAATAAAATTTGGCTCCACTGAAATGAAGGCAACTGCCACTGATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20322
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099739 | Nonsense | 400 | 571 | 4 | 4 |
ENSDART00000099750 | Nonsense | 400 | 571 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 4 (position 61391426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 76228480 |
GRCz11 | 4 | 77653057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGAATGTAAAATTCTGAAGAAGTTTCTGAAGGAGCGCTTTGATAAATG[C/A]AAGATAGTCTGCCCTGTTGAGCCCCAGGTAGTAATAATCAAAGGAGCGAT
Long Flanking Sequence:
ATAACGGTACACGAGGTGGTCGAGGACGGCAAACTGAAAGAACTGAACGCCGCTTCCGGAAATGACATGGGTGGACAGACCGTAGACAGGAAGTTCATCTCTTTTCTGAAAGAGATATTTTCAGAGAAAATTTACAACAAGTTTGAACAAGATTTCCCAGCAGAGGCGCTGAAATTAAAATATGACATTGCTCTAGCTAAATCTTGTGATCAACTTGTGCTGATCCAGTGCCCAGTGACCTTGCAGGATCTGGCCAAGAAAGAAAAGGCAATCGAGAGTTACTTTGAGGGTGTTGAGGGAGCGGAATGGGACGAGGGGTCGATCATAATCAAAGAGGATAAACTGCAGAGCTTTTTTGATGAAAGTCTCAAGACAACAGCAGAGAAACTAGAGAAGATCATGAGCAACCCTGAGCTGAACATCGAGTACATGCTGTTAGTCGGAGGCTTTGCTGAATGTAAAATTCTGAAGAAGTTTCTGAAGGAGCGCTTTGATAAATG[C/A]AAGATAGTCTGCCCTGTTGAGCCCCAGGTAGTAATAATCAAAGGAGCGATCAGATACGCCAAACAGCCCAAAGTGGTCAAATCCCGTATGAGTGCTCTAACATACGGGATCAGAATAGATGCGCCCTTCGATAAGGTCTTACACAAAGGCAAGACTAGCTATGTGAACAGTGAGGGACAGACGTACTGTGATGTCTGTTTCGAAACATTCGTTAGAAAGGGAGAGTCGGTCAACTGCGATGAAGTTCGACAGTTCTTTTTTAATCCATCAGACACCAATCAAACATTTGCCACCTTCCAGTTCTTCAGCACAAATGAAAAACAGGTGCAGTTTATCGATGAGCCGGGGGTTGAGTCGGTTGGGGTTTTTCAAGTGGGAATGCCCAAAACTGATGGAGGCTTGAGTCGTGAAATTAAATTGGAAATAAAATTTGGCTCCACTGAAATGAAGGCAACTGCCACTGATGTTGATTCTGGAGAGACTACATCAGTCAAGCTTGA
Associated Phenotype:
Not determined