ZMP

gspt1l

Ensembl ID:

ENSDARG00000014123

ZFIN ID:

ZDB-GENE-030131-4009

Description:

G1 to S phase transition 1, like [Source:RefSeq peptide;Acc:NP_942101]

Human Orthologues:

GSPT1, GSPT2

Human Descriptions:

G1 to S phase transition 1 [Source:HGNC Symbol;Acc:4621]
G1 to S phase transition 2 [Source:HGNC Symbol;Acc:4622]

Mouse Orthologues:

Gspt1, Gspt2

Mouse Descriptions:

G1 to S phase transition 1 Gene [Source:MGI Symbol;Acc:MGI:1316728]
G1 to S phase transition 2 Gene [Source:MGI Symbol;Acc:MGI:1316727]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa40114	Nonsense	Mutation detected in F1 DNA	Not yet available
sa26115	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa40114

Status:

Mutation detected in F1 DNA
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
ENSDART00000016780	Nonsense	182	577	5	14
ENSDART00000143755	None	None	166	None	4

Genomic Location (Zv9):

Chromosome 3 (position 36537755)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	36511349
GRCz11	3	36653207

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCTAATTCCGGCTCTCCACTGCAGGTATTTAACAGGAATGGTGGACAAA[C/T]GAACTCTGGAGAAGTATGAGAGAGAGGCCAAGGAGAAGAACAGGGAAACT

Long Flanking Sequence:

AATTTTCTCCGTTTTAATACTACATTAAAAGTCATACTAATGGTTTTCTGCAAACTCATGTTATTTGCTTGTTGACAAAAACATTTTACATTTCATCTTCATAAAACCAGCAGGCTTTATGGGATCATTGGACCCATTTGCTGAGATACTTTTCAGACTTGGCTCTAATATGTTTGGATTTGTTATATAACCTCTGTATTTTTAATCAGTTACCATCAAGGCATCTCGGTTCATGTCTGTCTCAAAAGCATCTTGGGGAATGTTTTAAAAATGTCTTTAGAGAGTAGCGTAGTGACCATTTTTACCTGTCCTGGCCTCACCCTATCTATTTCTTATCTCCCGTTTGTTCAGATGCTGGCAAGTCAACTATTGGAGGACAAATCATGTGAGTTGTTAAAGCTGACTCAGTGTTTTAGCAGATATTGTTTGTTTTTCCATCTATCTCTGATAGCCTAATTCCGGCTCTCCACTGCAGGTATTTAACAGGAATGGTGGACAAA[C/T]GAACTCTGGAGAAGTATGAGAGAGAGGCCAAGGAGAAGAACAGGGAAACTTGGTAATTACTGAAGTTAATATATTATTTTACCTGAACTTCTGCTGGCGGTCAGGCAGATTCCCTCCAAACAGAACTGAAATGTGTAGCACTTTTGTGAATGTTGTTTTTCACATTTTATAAAAAAAGGATTAGCATTTTTATGCTCAATTTTTTTCTCAGCCACCAAAATATGTAATTATTTTAGATCATGTCTGTGGTCAGAATAAAAACCCTTTTAAATCATGACCCAAATAAGTTTTATAAATTTTAAGTGTCATCTCTATCTCACTAGACTGACTCAAGGGCATTACTTGATGAAGAAACGTGGAAATGGCAGTACTAAGTTTTTTTTTCACTGACCAATTATTAATGTTATAAGAGGTTTATCAGGGCAAACCTTTGAAGATATATTTAAATACCAGAGATGGGGGACTGGAGTCACATGACTTGACTCAAGTCAGACTTAAGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa26115

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016780	Essential Splice Site	199	577	5	14
ENSDART00000143755	None	None	166	None	4

Genomic Location (Zv9):

Chromosome 3 (position 36537701)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	36511403
GRCz11	3	36653261

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCTGGAGAAGTATGAGAGAGAGGCCAAGGAGAAGAACAGGGAAACTTGG[T/G]AATTACTGAAGTTAATATATTATTTTACCTGAACTTCTGCTGGCGGTCAG

Long Flanking Sequence:

CTCATGTTATTTGCTTGTTGACAAAAACATTTTACATTTCATCTTCATAAAACCAGCAGGCTTTATGGGATCATTGGACCCATTTGCTGAGATACTTTTCAGACTTGGCTCTAATATGTTTGGATTTGTTATATAACCTCTGTATTTTTAATCAGTTACCATCAAGGCATCTCGGTTCATGTCTGTCTCAAAAGCATCTTGGGGAATGTTTTAAAAATGTCTTTAGAGAGTAGCGTAGTGACCATTTTTACCTGTCCTGGCCTCACCCTATCTATTTCTTATCTCCCGTTTGTTCAGATGCTGGCAAGTCAACTATTGGAGGACAAATCATGTGAGTTGTTAAAGCTGACTCAGTGTTTTAGCAGATATTGTTTGTTTTTCCATCTATCTCTGATAGCCTAATTCCGGCTCTCCACTGCAGGTATTTAACAGGAATGGTGGACAAACGAACTCTGGAGAAGTATGAGAGAGAGGCCAAGGAGAAGAACAGGGAAACTTGG[T/G]AATTACTGAAGTTAATATATTATTTTACCTGAACTTCTGCTGGCGGTCAGGCAGATTCCCTCCAAACAGAACTGAAATGTGTAGCACTTTTGTGAATGTTGTTTTTCACATTTTATAAAAAAAGGATTAGCATTTTTATGCTCAATTTTTTTCTCAGCCACCAAAATATGTAATTATTTTAGATCATGTCTGTGGTCAGAATAAAAACCCTTTTAAATCATGACCCAAATAAGTTTTATAAATTTTAAGTGTCATCTCTATCTCACTAGACTGACTCAAGGGCATTACTTGATGAAGAAACGTGGAAATGGCAGTACTAAGTTTTTTTTTCACTGACCAATTATTAATGTTATAAGAGGTTTATCAGGGCAAACCTTTGAAGATATATTTAAATACCAGAGATGGGGGACTGGAGTCACATGACTTGACTCAAGTCAGACTTAAGTCACAAAATTTAGGACTTGAGACTAGCTTGACAAATATCCAAAAAAGACTTGACT

Associated Phenotype:

Not determined