ZMP
mtrr
Ensembl ID:
ZFIN ID:
Description:
LOC560667 protein [Source:UniProtKB/TrEMBL;Acc:Q4V8W4]
Human Orthologue:
MTRR
Human Description:
5-methyltetrahydrofolate-homocysteine methyltransferase reductase [Source:HGNC Symbol;Acc:7473]
Mouse Orthologue:
Mtrr
Mouse Description:
5-methyltetrahydrofolate-homocysteine methyltransferase reductase Gene [Source:MGI Symbol;Acc:MGI:18
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10422 | Nonsense | Available for shipment | Available now |
sa24469 | Essential Splice Site | Available for shipment | Available now |
sa37856 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37855 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8432 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10422
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066759 | Nonsense | 8 | 713 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 17453882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16760358 |
GRCz11 | 24 | 16904777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGTGTGGRTTKCAGTATGTTRCAYGACCGAAGAGGCTGTTKGTGTTGT[T/A]ATTTGCAAAAGCAAGGTGACTTTTTTNNCTCTCTCCATCATTTACGTTTTAC
Long Flanking Sequence:
AGAATTTAATCCTCTAGCTGCGCACCTCACCGCGCGGATCTGCCGGCTAGTTCTGGAAGAATCTCGGGGAGGGACGGACCAAACCAAGTTGACAATGTTAAAACATCCACATTTTTGTACATTACATTACCATTTAATCCCTAATTAAATAACAATATTAAACATTTAAGACAATTATGAAGGAGAAAAAGCAATTAACGAATCTTTAAATAATTTTTTTAAATTGAAGCATATTAATGGTTTATTCCATTCTCGCGATAACGACAACAAATAACGCGAGTGCGGGTACAGATTTATAATTCATGCAGATTGACTAACAAATAGACGTTACAAAATTGATTTGTGTATGTGCACACGTACAACTTGTGTATTTGAGAAAGGCCATGTGCTCGTCGTTGGTAACGTAATTTCCGATTACCTGTTCCTCCCGTTCATGCTTCTGACAGCACACCAGTGTGGATTTCAGTATGTTACATGACCGAAGAGGCTGTTTGTGTTGT[T/A]ATTTGCAAAAGCAAGGTGACTTTTTTCTCTCTCCATCATTTACGTTTTACATTTGTGACCGACATTTGTTTTTGAAGTGTCTTTGTGAGGTCTACATGACTTTAAAGTTAGACTTGGTGAAGCTACAGCTTGTTTTGATATCTTTTTGGATATCTCTTATAAAACTTATGCAACATTCACATGATCAGGGTTGCTTGATTTCCGTTTGCACCTGTATATTATAATGATTCTTTTTACATTACAAACGTACACAGATTAGGTCATATTTAAAGTAAATTGTTTCATTATATCATACAGTACATACGTGTAATAAACTAAAAGAACTTCTCACAATCACAAAATGTAAATACAGAGGTTCCTTTAAAAAAACGAAGCTCATAAATAAACATTTCAATGAAAAAAAAGGTTAATTGAACATAAATGATCATATGCTATGCAACCTTCTTTTGGAATTTATTTATGTTTTGAATAATATATTTTATTGAATAATAATTATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24469
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 |
---|---|---|---|---|---|
ENSDART00000066759 | Essential Splice Site | 396 | 713 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 17447003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16753479 |
GRCz11 | 24 | 16897898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTTTATTCTCACCTGGTGTTTAGAGATAAGGAGCACTCCGAAAAAA[G/A]TAATTTTGTGTTGTTATTAACCTTATTTAATGTAATAGTTGCTGTGCTGT
Long Flanking Sequence:
TTAATGTTTGGATTGGCTCAGATAGACCTGTTTGTTTATATTTTAAAAAAATCCAGTAAAATGTATCTTTTTAAAAGCGTACATTGTCTCTTCAGCAGCAGCAGGAGCAGGTTTATCAGCCTGGAGACGCTTTTGATATTCTCTGTCCAAACAGAGACAGTGAGGTTGAAGAGCTGCTGCTCAAACTGGATCTGCAAATGCAAAAGAACTGCACCGTTCAAGTTAATCTGCTTAAAAACACCAGCAAGAAAGGTATCACAACCTTTGTTGACACAATCTGTGACACCAAGAACAAACTGTCCTAGAAAAGAGATAAAATAATGTATTCTGGCCAACAAGTCAGACACCAGATTAAGATTAAACAACTTGAAACGTTGAATAAATGCATAGCAATTTTTTTTTCTTTTACAGCAGCAAAAGTTCCACTTCACATCCCACAGAATGGCTCTTTGCAGTTTATTCTCACCTGGTGTTTAGAGATAAGGAGCACTCCGAAAAAA[G/A]TAATTTTGTGTTGTTATTAACCTTATTTAATGTAATAGTTGCTGTGCTGTTGAAGTTGTGCACCTTTGAGTTAGCTCTAGCGCACTTACATTATACACAGTGCTTTTGATGGTTTATTTTGCTTTCTTGTCACTGACATACTTTGTTAGTTTAACTTCTACTGTTTTTAAAGGAATAGTTCACCCAAAACTATCTGTTATCATTTTATATTAATTTCAAAACTGAACAGACCGCATTGAGCATTTTAAGTCAACAACTCCTCTATTCAAAAGATCTAATTAAAAAAAAGAGTTTCTTTGATTAAATGACTCACAAATGATTCAGTCAGACTGATTCAGATTCAGCGAATTTTCAAATAAAAATCATATGTAGGTTAAATATGTCAGCTGTTGAAATACTGTTCACTCTATGAAGTGCATAAAGTAATTTCTATTTTTTGTTTATTATTGTCTGAATGTGGTAGATTTTATATAAAAATAAGCTTTAATTTAGTTAAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37856
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066759 | Nonsense | 572 | 713 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 17435324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16741800 |
GRCz11 | 24 | 16886219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGGTTGGACCTGGGACTGGTGTTGCACCTTTTATTGGATTTCTCCAA[C/T]AGAGGTACGTTCAGGAGTTTTTTTTAAACTATGCTTTTTACCCCCTTCAC
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATTAGTTTAACTTTTTTGTGAAATAAAATGTAGAATCAAGGCAAGGCAAGTTTATTTATATAGCACATTTCATAAAATTGAATAAAATAATTTTTAAAAAATCGATAAAAGGGGACAAAAGAAACGCTTAATGTCTTTTCTTTCCATTAGTCTGAAAACAACAACTACAAAACACTTTATTAGAAGTCAAAAACCCAACATCTCAAAATAGACAATGTTTGTTTTTGTAAAAGAAAATAGTTTCTGCCTACAACCTTAAATGGATGTTATGTGGGGGATTTGAGACTATAGATGTCCCATCTGCACTTAAAATTGATTGTATCTAAATGTCACATTCAGGTACATGTCAGAGCTCGTCCCAGCAGCACCTTCCACTTACCATCCGACCCCTGTGTTCCTGTAGTCATGGTTGGACCTGGGACTGGTGTTGCACCTTTTATTGGATTTCTCCAA[C/T]AGAGGTACGTTCAGGAGTTTTTTTTAAACTATGCTTTTTACCCCCTTCACCCTTTTGTTTTGTTGACTCTGTAACTGTATTATTTTCTTAATGTTTTATTTATTTATTGTAGTTGCCAGGATATTTAATAGTCATTGTTGTGCAATGGGATAACATTTTTGCACAGATATCAAAATCGGGCCTGATAAAACAATAAGCGGAAAAATTATGTTAATGTAACGGCCATTAAGGTAACTTGAAAATGCTAACCAATCACTGCTAAATGCTACTGAAAGTAATGATCAAATTCTGAAACAAACACACAAAATGAGTAATTATTGTGTTAATGAAAATCAAGTAGACGAGTATAAAAAAAGTAGACATTGAATCATAAATTCACCTTATTCGTTTAAAGGATTTGTTCATTTATTCAGCAATGAAGTAAAGCACTCCTTACTTGAATGGCATTGAATCATTGGCTCACTCAGTTAATTCAATACAACTGATTCAGTCAGAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37855
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066759 | Essential Splice Site | 666 | 713 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 17408988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16715464 |
GRCz11 | 24 | 16859883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTGCCAAAATTCTCCTGGAAGACAAAGGCTGCCTTTATGTCTGTGGG[T/C]GGGTACAAAAACACATTTTTAGGCTTTGTTTAACAATCATTAGCCCCTTT
Long Flanking Sequence:
AAAGCAGCCAAACTTGTGTGAGGAGCTAGAAAATAAAAGCTGCTACAGAAGCAATTTACACCAATAGCCTTGAGGTTTTTATAAACTCCTTGCCAGATGGATGAGGGAGACGAAAATCTGAGTTTCAAATGCAACACTAATGAGCTCAATTGTTTGCTACTTCACTGCAAAATCTCAGAGAATCTAATTTGCCATTTGTACCATTCGTATGTTTTAATGCGCAAGTTTAGTTTAACCACCGCAAAAAACAACCACAGACTGATGAAATAGCAATGAAACATTGTAGTAAGAGCATCTTTTTTTTTATTTTCAGAGAGGAGCTGGAGAAATTTGTGCATAATGGGACCCTGAGCCATCTGATTGTGTGCTTCTCCAGAGATGAACCCGATGCTGCGGAAACCGTTAACAGACCAACATATGTCCAGCATAACTTGATCCTCCATGCTAAAAATCTTGCCAAAATTCTCCTGGAAGACAAAGGCTGCCTTTATGTCTGTGGG[T/C]GGGTACAAAAACACATTTTTAGGCTTTGTTTAACAATCATTAGCCCCTTTTACGCATACAGTAGTCAACATTTGAAATAAATTACCAACTTTCATCAAAGTTGTCCTAAATTAATTGAATAACACCAGAGCTGGACTGGGACGAAAAAAAAAAAAATGGCTCTGGCATTTTGGGCCAGAGCGGCCCACTACATACAGTTAAAATGCTACCCATCTGTACACGCCCTTGAATATGTTTACCAACTTCTAATCTGCAAAAGCACAAAAGCCATATATAGAAAAACAGTGAGAGTTGACTAATTACAAACAAACAAAAAAAAGTATTATAACAATAAAATGATAATCCACACTGGATGTCTATCTTTTATGTTTTGAACGAGCCTATATTAAACAACAAAAACTGCCTGCTGATGCACACAGTTAATGTTGATTAACAAAATAAAATAATAAAAGCAAAATATCAGAGACAAAATTTTAATTTAATTCAACAGTGAAACACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8432
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066759 | Nonsense | 703 | 713 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 17405146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16711622 |
GRCz11 | 24 | 16856041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTTCAGCTTGATAAACTRGATGCAATGAAGATAGTGGCAGGACTTCGC[G/T]AGGACAAGCGGTATCTACAGGACATCTGGAGTTGAGAAAGCACACATAAA
Long Flanking Sequence:
AGAGTTGTTCACAATACCTTTCCAAAAAGACAAAAGCTGCTGCAGGAATGTGGATGTTTCAAATAAATATTAAACCTTCAACATACAAGAAACCCCACAAAAAACAGTTACATGTTAACAAATACAAACACAGCCACTTAAACTTTTTTGGGGGGGTTAGAATGTCAGAATTTACCATTATTTTGAAGGATGTGTGAGTGGTGCTTTCCAGAAACATTATGGAATGTCCTTGCCTGTGTAAATAGTAGATTTAAAAAGAAAAATACCAGTAAAGTTTTTGATTGTCATTTTACTGAGATGTACTGGTATTACTGTGTGAAAGGGGCTTTTGTTCGGTTGCTCTGCCACATTTTGTTCACCTGAAATTAAACTTTATCTTATGATTTTACAGGGATGCTAAGAACATGGCAAAGGACGTGAATGACACTTTACTGGAGATCATTGGAAACGAACTTCAGCTTGATAAACTGGATGCAATGAAGATAGTGGCAGGACTTCGC[G/T]AGGACAAGCGGTATCTACAGGACATCTGGAGTTGAGAAAGCACACATAAATTACACGAACAAACGGCATCACATTCACAGACAGATGTGCAAGCTACTTTTTTGCTCACATCTGTGACACAGGTGCCATTTAGTGATAGTCAAGCTCATTAACAACCTGCTTTTCAATATTTTTTCTCTTCTTTTCAAGTATTTAGAGAATTATCTGAGGCTCGATATGGTCGGATTAGATATGTTTGGTGGAAGTGTTTTAACTGTGCCTTTTATGCAATTATTAAAGAGGAGCACTGCATGACTGTTTCATTCTTTGAAGATCGTTTCTGTAGAGTTTAGATGCAGCTGAGGTAAAATATGCATAATGCATCAGACTCCGCAGCCAGGAGGACGCTAGACACGAGAAACCAAAACATGACAGACTGGATGAGAAAACTGTCAAAAGCTGCCAAATTGAGGATCATCTGCAGCATTTCTGGGTTCTCCAGCTCTGACTATTGTTTTTTT
Associated Phenotype:
Not determined