ZMP
LOC559645
Ensembl ID:
Human Orthologue:
SLC35F2
Human Description:
solute carrier family 35, member F2 [Source:HGNC Symbol;Acc:23615]
Mouse Orthologue:
Slc35f2
Mouse Description:
solute carrier family 35, member F2 Gene [Source:MGI Symbol;Acc:MGI:1919272]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11796 | Nonsense | Available for shipment | Available now |
sa24986 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28457 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11796
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 |
---|---|---|---|---|---|
ENSDART00000128267 | Nonsense | 49 | 332 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 24511798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25222985 |
GRCz11 | 15 | 25158250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCCTATGCTGCAGAGCTTTAKTAACTACACACTCCTGGGCATCACTTA[C/A]ACCATGGCACTTATCTTCAGAAGAGGTATTTGATCACGAATCATCAGATT
Long Flanking Sequence:
CTTTTGGTGCTGAATCTAAGTAAGAGGTTCTAAATATTCATGAATTTATTTCTCCTGTTGAACGCAAAACAAGACATTATGAAGAATGTTGGGAAAAAATTTCCATTGACATCCAAAAAAATGCTATGGAAGTCAATGGCTATTTATTCCAACAGTCTTCAGTATATCTTCCTTTGTGCTCAACAGAAAAAAAATCCTCAAACAGGCTCTGAACAATTAGAGAATGAGCAATGGTGACAGAATTTATCCATGTCCGTGTGTGAACTATCCCTTTAAAAATGTCATTAGAAAAGAATCGTCTCAAAACCTTGATAAAAGATTGCAATGATTCCAGTGGATGTTGATTGCAGGCAGCTGTTGAAGATTCTGCTGATGGGACAAGGCCTCTCAGCTCTGATCTGTGGCACTGCTGTAACATCACAGTATCTGGCATCCGTTTACTATCTGAATACCCCTATGCTGCAGAGCTTTATTAACTACACACTCCTGGGCATCACTTA[C/A]ACCATGGCACTTATCTTCAGAAGAGGTATTTGATCACGAATCATCAGATTTTCAATGAATTTCAATCTCTTGTTTCAATCTTGTTCATTATTTAAAGCTCTTCAGATATCTGACACTTTCTGGCATGCGATATTCAGGATGCCTCTCTTTTAATGTAGGTGATGGAAATATTTTGCAGATATTAAAGACAAAATGGTGGAAGTATCTATTGTTGGCGGTGGCAGATGTGGAGGCAAATTATGCAGTGGTGAAAGCATACCAGTACACCACATTAACCAGCATACAGGTCAGATTAGATCATATACAGTATCATTATCATTCTCTCATGCTCACTAGGTGTGCTGATTAAAATACAGTAAAAACAGTAATATTGTGAAATAATAGTAGATTTGATATTAGTATTTTCTGTTTGAATATATTTTAAAATTGTCATTTATTCCTGTGATTTCCATCTGAATTGTCAGCATTTTTAGTCTGGATCAGTCTGGATATTTAAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24986
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 |
---|---|---|---|---|---|
ENSDART00000128267 | Nonsense | 205 | 332 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 24515463)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25226650 |
GRCz11 | 15 | 25161915 |
KASP Assay ID:
554-7494.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGTTTCTGGGGATGGTTGGCCTCTTTGGGTCTATTATCAGCGCAATC[C/T]AACTGTGAGTTTGGTTCTGAAAAATTACAAAATACTCCCTAAAGCGATAG
Long Flanking Sequence:
CATTTTAATTTGCATTTCACAATGTAACACATTAACAAAAGCATTGAAATACTTAAAGCAAACAGTTATTTCATCAACCAACCTTCTTGTCTGTGTTTCAGCTGCTGGACTGCTTTATTATCCCAGTTTTAATGATCTTGTCCTGGTTCTTCCTGAAGACCCGCTACAGGATCATTCATTATGCAGCTGTAGGCATCTGTCTGGCCGGGGTGGGAGCCATGGTGGGAGCAGACATCCTCGCTGGACAAGACCAGGGATCATGTGAGGAGCAAGATGCTTCTCTGGAACAAAATCAGCTACAAAACTTTGTATAAGTCAAACCATAATCATTCCTGTGTCTGTCAACAGCCAGTGACGTGCTCCTGGGTGATGGTCTGGTTTTAGTTAGTGCCACTCTGTATGCCATCTCTAATGTGTGCCAGGAATACACAGTGAAGAATCTGAGCCGGGTGGAGTTTCTGGGGATGGTTGGCCTCTTTGGGTCTATTATCAGCGCAATC[C/T]AACTGTGAGTTTGGTTCTGAAAAATTACAAAATACTCCCTAAAGCGATAGTTCACCCAAAACCGAAAATTTTATCATGGTTTATTCTCAGGTTGCAAAGATATTTAAAGGTGCTGTATGTAGTTTTTGACTCATCTAAAGAATGAAAAATAATATAATATTTTTGCAGATATTTAAGATACATGAACATACTTGTTTATCTTAAAAACAAAGCTAAAGTCAAATATTTTGCTTTAAAAATGTGTTTTCCGTGTCAGAACGAAATGGTAAGGGTTATAATCTATTTAATACATATAAACCCACTTTAGCATTACTAAATTTACATGCTGAATCACTCATATGTGTTTAGTTCTAAAGTTTAATTTCAAACAGTTTATTTTATTTTCAAAACCTGAGGTGAACTATCTGCTGCTGCTTTCAGTAGTATGGCAATAAATGTCATGTAAAATGGCATTCAAACTCACATTGTTACGCCTGTTTCACACCGCAAGCGTCAGCGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28457
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 |
---|---|---|---|---|---|
ENSDART00000128267 | Nonsense | 260 | 332 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 24519404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25230591 |
GRCz11 | 15 | 25165856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGATAAAAAGGAGCAGTGCCACAGCGGTTAACCTTTCCTTACTCACC[G/T]GAGACCTCTTCAGCCTGTTCTTTGGGCTCTTTTTGTTCCATTATAACGTG
Long Flanking Sequence:
GGATTGTCCATCAGTTTTTGATTCATCAGGTCATCATCAGATTGTCTCTTTAGTATTTTTTGTTCCTAATATGGTTGTCAATGGTTACTTTTTAAACATTCTTCAGAATATCTTGTTTTGTGTTTAACATGCAGAAAATAAAAATTAAGATAAAACATTACAACAACTTGACCGTGAGTAAATGAGGACATTTTTATATTTTTGGGGTGAACTGTCCCCTCAAGTCAACACCACATCATTTGTTTAATTTGGTCACTTGCAGAGGGATTCTAGAACATAAAGAAGTGGCTAACATTCAGTGGACATGGGAAAAGGGTAAAGTATGGGTTCTAATGCCATATGAAAATGCTTACCCGTTGTGTCAGTGATGTCATTTTATTGTTTTTCTCTCAGCTCTTCTCTTGTCTGGATATGCGCTCTGTATGTACGGCTTCTATAGCTTCATGCCTGTGGTGATAAAAAGGAGCAGTGCCACAGCGGTTAACCTTTCCTTACTCACC[G/T]GAGACCTCTTCAGCCTGTTCTTTGGGCTCTTTTTGTTCCATTATAACGTGAGTAAAGTAATTTATTCAGATTGTCTTTGATCAGTCTGCTTACTTAAATAAAAGTTGCTTCTGATTGGCTGATAGGGATATTTCTTAACTTAACAGAGGATCTGATGTTCGGAAACTTTGTAAAAGGGTTTTGTTAAATATACACAATGGGGGAAATAAGTTTTAAATATGTCAAGTTTTTTCCTAGTGGACAAGTACAGATTTTGGTAAAAACCCATACAATACAAACATAAAAAATAATACAAAACAAAAAATAAATACATAAATTGTGTTATAATAGTGTATGTGTAATAATGAAATGACAAGGAGAAAGTGCTGAACTACTGAAATGTATTTAATATTTTATATAAATGGCTTTTTTGGTGATGGCAGCTTAAAGACGCCTCTCATTGGGAGAATGTGGTCACATGCTCAGGTGTGATGTTTTTACAGACTTCAACAGACTTCAGT
Associated Phenotype:
Not determined