Busch Lab

ZMP

si:dkey-25e12.6

Ensembl ID:
ENSDARG00000091891
ZFIN ID:
ZDB-GENE-041001-134
Description:
Novel protein similar to methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahyd
Human Orthologues:
AL445665.1, MTHFD2, MTHFD2L
Human Descriptions:
methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase
methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like [Source:HGNC Symbol;Acc:31865]
Mouse Orthologues:
Mthfd2, Mthfd2l
Mouse Descriptions:
methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase Ge
methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like Gene [Source:MGI Symbol;Acc:MGI:191

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa17397 Essential Splice Site Available for shipment Available now
sa915 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa17397
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000147154 Essential Splice Site 6 122 None 5
ENSDART00000147154 Essential Splice Site 6 122 None 5

The following transcripts of ENSDARG00000091891 do not overlap with this mutation:

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 26521155)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 26592458
GRCz11 20 26491548
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAGTTGCTGCTCAGGGAAGCCGTTTTCAGTTCCTGTATAACTTGCAGG[T/C]GAGAACAGACGCAAGTAGTTACAGTGTAGAAGAAAACAAACAAAATGATC
Long Flanking Sequence:
ATGTTCATGACAGATTTATGACAAGTTATGTTGCATTGGTTATGTTAAATTGTCATGACAAGGACATCTCAAACAGCATCTTGGATTTTAAATGACAACTTAGCGAATAAGCATGCATAAAATCTCCTTCATGTTCATGACGTGTCATGTCATAATTATTAAGGTGTCGTAATGGTCTTATGAACATCCCCTTCAAGTTAAGTGTTACCCATCTGTCTTTCTAGCATGCTTTAATTTTTTTCTCAAAATTTTTGATTAATATCCATGTTTAGCCAGAGTGTTGTCTGCCCTGTGCCCAAGTATGTTTTTCTTTAAATCAAGGACAGACACTCAAGCAGAGATTGACCTGGTTTGTCGCATTGCAAAGGCTTCTGGGGCGTCCGCTGCAGTGCCATGTCATCATTGGTCCAGAGGTGGACGGGGCTCTCTTGAACTGGCACACGCTGTAAAGGAAGTTGCTGCTCAGGGAAGCCGTTTTCAGTTCCTGTATAACTTGCAGG[T/C]GAGAACAGACGCAAGTAGTTACAGTGTAGAAGAAAACAAACAAAATGATCTCGTGTAAACCAAATTTAATCTAAGACCAGGCCAGGCAGACTCAGAGTGATGAATTAAACATGATTGTATCTGAAAGGGAGTCTTCTATAATGTGCTAATGGTTTTTTCCCTCCAGTCTGAGCATGTCAGGTTTAAGGAGGGTCTGTGGAGGCATCAGCTGGTTTGAGTTAACCTTAGTGAGTTTGGAGGTTGTGACATTGATTAAACAATGCTATGAAAGGAGCTGTAATCTCTGCCCTTGGCTCTGGCTGGTCTCTATTATCCTATTAGAGGTCTGAACACTTGCTATCCCAATCATCTGCCCAGAGAAATGACTGGGGTGATTTTATGGCCATCAGATTGGCGGAAGCTTCAATTCAGAACTGATAATGAGGTTAAAGTGTTTTTAAATTCTTCCCGCTTTTATCTGCATGCCTTTTATTTCAAGGAATTAGCGTGTCCTGTGCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa915
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000147154 Nonsense 103 122 4 5

The following transcripts of ENSDARG00000091891 do not overlap with this mutation:

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 26510614)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 26581917
GRCz11 20 26481007
KASP Assay ID:
554-0821.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTCTTTTCTCTTGTCTTTCAGATGAGCACTATGCCAGGCTTGCCTACA[C/T]GACCCTGTTTCTATGACATTGACCTTGATCCTGTGACCGAGGAGATAAAA
Long Flanking Sequence:
GGGAAAACATAATGAATGCAGACTGCCTTAATGACAGATCATCTTACACCGTTGTATTTTAAAAATAAAACATTCGTTTTAAGAAAGAGCACTCATTGGATGATTTGGGTTTGGCTTTTCTGGCTCCAGCGTTAATTTCTGTTTACAGTTTAGATTTGTCTGACAGTGAAGTCCTTTGGTTTTAACAAGATTTGCCTAGAAAAGACATTTTGCAAGAAAATTTCTTCAACATACTTCAGCATCTTTGAAACAACTTCTTGTTTTAGACTGAATTTATGATCCTTCCTACTAAGTGAATCTAAACCTGAGTTCCCTTGTGACTCCATTACACTGTTTCCTCTGATGTTTTGTGGGCATACAATATATTTGCCTTTTTGTTTTGATACCTGTGTCAAATAAAACTGAGCACTGATTCTGTTTTGTGCTATGTATACACTTTAGGTACTCCCTTCTTCTTTTCTCTTGTCTTTCAGATGAGCACTATGCCAGGCTTGCCTACA[C/T]GACCCTGTTTCTATGACATTGACCTTGATCCTGTGACCGAGGAGATAAAAGGCCTTTTCTGAGGACACACTCTTCACCAGTGCGAACTCAACTAGGTCTTAATTCACACTGCAAACATTTGTGCTGAGTTACAATGTTTCGATTGGCTTTACTTAGTATTTCGTTAAACTATGTAAAATTTCTAATTCTGTTCTATTGAGTCTGCAGACTGAGGTTGTATTACAAAACATGAAGTTTATATGATTAAAGGAATAGTTCACTTCTAATGACTGGTAACCATTGAGTTCCACTTAAGTTCCAGTTGAGGCTCTCCATTGACTTCCATAGTATTTAGTTTTGATGGCATCAATTTTAAAGACATCTTTTGTGATTAACATTAGAAAGAAACTCATACAAGTTTGAAACAAGTTGGGAGTGAGTACATGAAGTGAACTACTCCTTTAAGGATCACGTATGAGTCAAATTTTTTTTTTCATTTGGTAAAAAAGTGACACATGACA
Associated Phenotype:
Not determined