ZMP
SLC44A1 (1 of 3)
Ensembl ID:
Description:
solute carrier family 44, member 1 [Source:HGNC Symbol;Acc:18798]
Human Orthologue:
SLC44A1
Human Description:
solute carrier family 44, member 1 [Source:HGNC Symbol;Acc:18798]
Mouse Orthologue:
Slc44a1
Mouse Description:
solute carrier family 44, member 1 Gene [Source:MGI Symbol;Acc:MGI:2140592]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35631 | Essential Splice Site | Available for shipment | Available now |
| sa38978 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35631
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000121552 | Essential Splice Site | 35 | 282 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 14 (position 6371237)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6058234 |
| GRCz11 | 14 | 6365068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGCAGATGACCGTCGCCGGAGCTGTGGTGACCTACTATTTCACAAG[G/T]TCGGTGTTTCTAGAGGAAAACTCTCATATGCTACTGGTCAACCTTTATTT
Long Flanking Sequence:
ATTTTGCGTTAACGAGCAGCAGGACAGGTGTACCTAATAAAGTGGCCGGTGAGTGTATATTAGGTCAATATCCCTTAAATCGCTCATGAAAAGTTAATTGAACTCATGAATTGTTTTGCTTCTATTTTTCCTCCGACATAATGTGTACAAGGCTTAAAATATTCCACTGTTCAAGTGTTTGTTTTTACAGATAATGTGGGACGTTTATGTACTGCAGCACAATTACCCGACTGTGCTCCTGCAACTCTTCCTCATTTTAAACATGCATTAGTTTTGCAGTCTCTTCAGAAGTGGAGATCTCAGACTGCAGTTTGTGTGTTTGTGTCCGCAGGGAACCCAGAGAAGAATGAGGATACGGGGTTAGTGGAGTTCAGGCTGTCAGGGGCGCTGCAGTACATGACGTGGTATCACGCGGTGGGCTTGATCTGGATCAGTGAGTTCATCCTGGCCTGTCAGCAGATGACCGTCGCCGGAGCTGTGGTGACCTACTATTTCACAAG[G/T]TCGGTGTTTCTAGAGGAAAACTCTCATATGCTACTGGTCAACCTTTATTTTTTCTAGTTTATTTGTCAACTGAACAGTCAGTATAGTACTGTATAATAAGGATAGACATGAAAATGTACTGCTCGTTTACTCACCTTCAAATTTCAGACCTTCATAAATTTTTATTTTATTTTTTTTACATTGAACAGAAAAGAAGATATTTTGTAGAATGTTGAATGCCATTCATACTGTAGTAGGAAAACAACTACTATGGAAATCAATGGCTGCTGGTTTCTAATATTTTTCTATTATCATTAAGTTGAAAATCAAAGATATTTCCCATGTATCCAGGGATAAGACCAAACTGCCGGTGACGCCCATCCTGTCGTCGGTGCTGCGTTTGGTGCGGTATCACCTGGGCACTGTGGCCAAGGGCTCCTTCATCATCACCCTGGTCAAGATCCCGCGCCTCATTCTCATGTACATCCACAACCAGCTGAAAGGCAAGGTGAGGACACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38978
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 |
|---|---|---|---|---|---|
| ENSDART00000121552 | Essential Splice Site | 240 | 282 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 14 (position 6361499)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6048496 |
| GRCz11 | 14 | 6355330 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAACGGCACACCTGGAAGAGAGTTCTACATGGACAAGGCCCTGATG[G/A]TGAGTCACAGACGGAGAAAAGCTCGCAATCTGTCTGAAAAACGCCATAAA
Long Flanking Sequence:
CTAATTATCCTAACCTGCCAACCTAATTAGCCTAGTTAAAGACAAATGGATGACCATACTAGCATTGATATTGTTGCATGTCACTGTTTTTTTAAGATATATTCAACTCACCTGCTGTTTTCAAGATTACATGGTTGAAAAGTTGAAAGAAAAGTTTCCAGTAATGATCTGTTTGAGTTGTTCGAACCTGTGCTGTAAACACTGGTGCTTTATTGGTTACTTGGTTGCTCTACCTGCTAAATACTTGTCTGTTCCTTCTGCAGGTCCTGATCGTGACATGCACGGCGTTCGCCGGCGTTCTGGCGCTGAACTATCAGAGAGATTACACCGAGTGGGTCCTGCCGCTCATCATCGTGTGTCTGTTTGCGTTTCTGGTGGCCCACTGCTTCCTGTCCATCTTCGAGATCGTGGTGGACGTGCTCTTCCTCTGCTTCGCCATCGACACCAAATACAACAACGGCACACCTGGAAGAGAGTTCTACATGGACAAGGCCCTGATG[G/A]TGAGTCACAGACGGAGAAAAGCTCGCAATCTGTCTGAAAAACGCCATAAATAGTCTCAGTGTTGCGCGCACACTTGCCGTCTGAGTCACGTTCCTGTTTTGAGTTCGTTCGTTTTGAATGCAGGCTCTCTGCAGGCCTGGATATATTAATATTTTAAGATTCAGGTGGTGTCCCAGATATTCTCTCTGGACAACTTTCAGCTTTTGTTTTGAAAAGCTGGTTGATTCATTTATTGATTTAGTATTATTTTGTTGGAAAATCGACTTGTCTAATTACTCTAACTCGATTATAATTTTAATTACCTTAACATGATACCCTTACCTACACTTCCTGACAAAAGAAGTGTCGTCAATCCCAATTGTAAGAGAAACAAATAATAGCTTGACTTCTAGTTGATGATTTGGAAAAGTAGCAGAAGGTCGATTTTTCAGATGAATCATCTGTTGAGCTGCATCCCAATCATCACAAATACTGCAGACCAACTGGAACCCACATGGACC
Associated Phenotype:
Not determined